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  • 1
    Publication Date: 2008-09-20
    Description: During mouse embryogenesis, reversion of imprinted X chromosome inactivation in the pluripotent inner cell mass of the female blastocyst is initiated by the repression of Xist from the paternal X chromosome. Here we report that key factors supporting pluripotency-Nanog, Oct3/4, and Sox2-bind within Xist intron 1 in undifferentiated embryonic stem (ES) cells. Whereas Nanog null ES cells display a reversible and moderate up-regulation of Xist in the absence of any apparent modification of Oct3/4 and Sox2 binding, the drastic release of all three factors from Xist intron 1 triggers rapid ectopic accumulation of Xist RNA. We conclude that the three main genetic factors underlying pluripotency cooperate to repress Xist and thus couple X inactivation reprogramming to the control of pluripotency during embryogenesis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Navarro, Pablo -- Chambers, Ian -- Karwacki-Neisius, Violetta -- Chureau, Corinne -- Morey, Celine -- Rougeulle, Claire -- Avner, Philip -- Biotechnology and Biological Sciences Research Council/United Kingdom -- Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 2008 Sep 19;321(5896):1693-5. doi: 10.1126/science.1160952.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institut Pasteur, Unite de Genetique Moleculaire Murine, CNRS, URA2578, F-75015, Paris, France.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18802003" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Blastocyst Inner Cell Mass/metabolism ; Cell Differentiation ; Cell Line ; DNA-Binding Proteins/*metabolism ; Embryonic Stem Cells/cytology/*metabolism ; Female ; HMGB Proteins/*metabolism ; Homeodomain Proteins/genetics/*metabolism ; Introns ; Male ; Mice ; Octamer Transcription Factor-3/genetics/*metabolism ; Pluripotent Stem Cells/cytology/*metabolism ; RNA, Long Noncoding ; RNA, Untranslated/*genetics/metabolism ; SOXB1 Transcription Factors ; Transcription Factors/*metabolism ; Up-Regulation ; X Chromosome/physiology ; *X Chromosome Inactivation
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  • 2
    Publication Date: 2008-01-26
    Description: The hippocampus is an area of the brain involved in learning and memory. It contains parallel excitatory pathways referred to as the trisynaptic pathway (which carries information as follows: entorhinal cortex --〉 dentate gyrus --〉 CA3 --〉 CA1 --〉 entorhinal cortex) and the monosynaptic pathway (entorhinal cortex --〉 CA1 --〉 entorhinal cortex). We developed a generally applicable tetanus toxin-based method for transgenic mice that permits inducible and reversible inhibition of synaptic transmission and applied it to the trisynaptic pathway while preserving transmission in the monosynaptic pathway. We found that synaptic output from CA3 in the trisynaptic pathway is dispensable and the short monosynaptic pathway is sufficient for incremental spatial learning. In contrast, the full trisynaptic pathway containing CA3 is required for rapid one-trial contextual learning, for pattern completion-based memory recall, and for spatial tuning of CA1 cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nakashiba, Toshiaki -- Young, Jennie Z -- McHugh, Thomas J -- Buhl, Derek L -- Tonegawa, Susumu -- P50-MH58880/MH/NIMH NIH HHS/ -- R01-MH078821/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2008 Feb 29;319(5867):1260-4. doi: 10.1126/science.1151120. Epub 2008 Jan 24.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Picower Institute for Learning and Memory, Howard Hughes Medical Institute, RIKEN-MIT Neuroscience Research Center, Department of Biology and Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18218862" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials ; Animals ; Crosses, Genetic ; Dentate Gyrus/physiology ; Electrophysiology ; Entorhinal Cortex/physiology ; Excitatory Postsynaptic Potentials ; Female ; Hippocampus/*physiology ; Interneurons/physiology ; Male ; *Maze Learning ; Mental Recall ; Metalloendopeptidases/genetics ; Mice ; Mice, Transgenic ; Neural Pathways ; Pyramidal Cells/*physiology ; *Synaptic Transmission ; Tetanus Toxin/genetics
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  • 3
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-08-02
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 2008 Aug 1;321(5889):627. doi: 10.1126/science.321.5889.627b.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18669835" target="_blank"〉PubMed〈/a〉
    Keywords: Female ; Humans ; Male ; *Sex Characteristics ; *Sports
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  • 4
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-01-12
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schreiber, Hans -- Rowley, Donald A -- New York, N.Y. -- Science. 2008 Jan 11;319(5860):164-5. doi: 10.1126/science.1153713.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pathology, University of Chicago, Chicago, IL 60637, USA. hszz@midway.uchicago.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18187644" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antigen Presentation ; Antigens, Neoplasm/genetics/*immunology ; Autoantigens/*immunology ; Autoimmunity ; CD8-Positive T-Lymphocytes/*immunology ; Histones/*immunology ; Humans ; Immunotherapy, Adoptive ; Lymphocytes, Tumor-Infiltrating/*immunology ; Male ; Mice ; Mutation ; Peptide Fragments/immunology ; Prostatic Neoplasms/genetics/*immunology/therapy
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 5
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-08-02
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 2008 Aug 1;321(5889):625. doi: 10.1126/science.321.5889.625b.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18669831" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Aged ; *Aging ; *Athletic Performance ; Child ; Female ; Humans ; Male ; Middle Aged ; *Sports
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 6
    Publication Date: 2008-06-21
    Description: Astrocytes have long been thought to act as a support network for neurons, with little role in information representation or processing. We used two-photon imaging of calcium signals in the ferret visual cortex in vivo to discover that astrocytes, like neurons, respond to visual stimuli, with distinct spatial receptive fields and sharp tuning to visual stimulus features including orientation and spatial frequency. The stimulus-feature preferences of astrocytes were exquisitely mapped across the cortical surface, in close register with neuronal maps. The spatially restricted stimulus-specific component of the intrinsic hemodynamic mapping signal was highly sensitive to astrocyte activation, indicating that astrocytes have a key role in coupling neuronal organization to mapping signals critical for noninvasive brain imaging. Furthermore, blocking astrocyte glutamate transporters influenced the magnitude and duration of adjacent visually driven neuronal responses.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schummers, James -- Yu, Hongbo -- Sur, Mriganka -- New York, N.Y. -- Science. 2008 Jun 20;320(5883):1638-43. doi: 10.1126/science.1156120.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Picower Institute for Learning and Memory, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18566287" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Aspartic Acid/pharmacology ; Astrocytes/drug effects/*physiology ; Blood Volume ; Brain Mapping ; Calcium/metabolism ; Calcium Signaling ; Cerebrovascular Circulation ; Ferrets ; Fluorescent Dyes ; Glutamic Acid/metabolism ; Male ; Microscopy, Confocal ; Neurons/*physiology ; Neurotransmitter Agents/metabolism ; Photic Stimulation ; Synapses/physiology ; Visual Cortex/blood supply/cytology/*physiology
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  • 7
    Publication Date: 2008-12-17
    Description: Retinoic acid (RA) is an essential extrinsic inducer of meiotic initiation in mammalian germ cells. However, RA acts too widely in mammalian development to account, by itself, for the cell-type and temporal specificity of meiotic initiation. We considered parallels to yeast, in which extrinsic and intrinsic factors combine to restrict meiotic initiation. We demonstrate that, in mouse embryos, extrinsic and intrinsic factors together regulate meiotic initiation. The mouse RNA-binding protein DAZL, which is expressed by postmigratory germ cells, is a key intrinsic factor, enabling those cells to initiate meiosis in response to RA. Within a brief developmental window, Dazl-expressing germ cells in both XX and XY embryos actively acquire the ability to interpret RA as a meiosis-inducing signal.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lin, Yanfeng -- Gill, Mark E -- Koubova, Jana -- Page, David C -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2008 Dec 12;322(5908):1685-7. doi: 10.1126/science.1166340.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Whitehead Institute, and Department of Biology, Massachusetts Institute of Technology, 9 Cambridge Center, Cambridge, MA 02142, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19074348" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptor Proteins, Signal Transducing ; Animals ; Cell Cycle Proteins/metabolism ; Cell Nucleus/ultrastructure ; DNA Breaks ; DNA Repair ; Embryo, Mammalian/*cytology/physiology ; Endodeoxyribonucleases ; Esterases/metabolism ; Female ; Germ Cells/*cytology ; Male ; *Meiosis ; Mice ; Mice, Inbred C57BL ; Nuclear Proteins/genetics/metabolism ; Ovary/embryology/physiology ; Phosphoproteins/genetics/metabolism ; Proteins/metabolism ; RNA-Binding Proteins/genetics/*physiology ; Testis/embryology/physiology ; Tretinoin/pharmacology
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  • 8
    Publication Date: 2008-06-07
    Description: In mammals, dosage compensation is achieved by X-chromosome inactivation (XCI) in the female. The noncoding Xist gene initiates silencing of the X chromosome, whereas its antisense partner Tsix blocks silencing. The complementarity of Xist and Tsix RNAs has long suggested a role for RNA interference (RNAi). Here, we report that murine Xist and Tsix form duplexes in vivo. During XCI, the duplexes are processed to small RNAs (sRNAs), most likely on the active X (Xa) in a Dicer-dependent manner. Deleting Dicer compromises sRNA production and derepresses Xist. Furthermore, without Dicer, Xist RNA cannot accumulate and histone 3 lysine 27 trimethylation is blocked on the inactive X (Xi). The defects are partially rescued by truncating Tsix. Thus, XCI and RNAi intersect, down-regulating Xist on Xa and spreading silencing on Xi.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2584363/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2584363/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ogawa, Yuya -- Sun, Bryan K -- Lee, Jeannie T -- R01 GM058839/GM/NIGMS NIH HHS/ -- R01 GM058839-10/GM/NIGMS NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2008 Jun 6;320(5881):1336-41. doi: 10.1126/science.1157676.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Biology, Massachusetts General Hospital and Howard Hughes Medical Institute, Boston, MA 02114, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18535243" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Differentiation ; Cells, Cultured ; DEAD-box RNA Helicases/genetics/metabolism ; Embryonic Stem Cells ; Endoribonucleases/genetics/metabolism ; Female ; Histones/metabolism ; Male ; Methylation ; Mice ; *RNA Interference ; RNA, Double-Stranded/metabolism ; RNA, Long Noncoding ; RNA, Small Nuclear/metabolism ; RNA, Untranslated/genetics/*metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; Ribonuclease III ; X Chromosome/*genetics/metabolism ; *X Chromosome Inactivation
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  • 9
    Publication Date: 2008-05-31
    Description: The mapping of numbers onto space is fundamental to measurement and to mathematics. Is this mapping a cultural invention or a universal intuition shared by all humans regardless of culture and education? We probed number-space mappings in the Mundurucu, an Amazonian indigene group with a reduced numerical lexicon and little or no formal education. At all ages, the Mundurucu mapped symbolic and nonsymbolic numbers onto a logarithmic scale, whereas Western adults used linear mapping with small or symbolic numbers and logarithmic mapping when numbers were presented nonsymbolically under conditions that discouraged counting. This indicates that the mapping of numbers onto space is a universal intuition and that this initial intuition of number is logarithmic. The concept of a linear number line appears to be a cultural invention that fails to develop in the absence of formal education.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2610411/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2610411/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dehaene, Stanislas -- Izard, Veronique -- Spelke, Elizabeth -- Pica, Pierre -- New York, N.Y. -- Science. 2008 May 30;320(5880):1217-20. doi: 10.1126/science.1156540.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉INSERM, Cognitive Neuro-imaging Unit, Institut Federatif de Recherche (IFR) 49, Gif sur Yvette, France. stanislas.dehaene@cea.fr〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18511690" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Anthropology, Cultural ; Brazil ; Child ; *Cultural Evolution ; Educational Status ; Female ; Humans ; *Indians, South American ; *Intuition ; Male ; *Mathematics ; Middle Aged
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  • 10
    Publication Date: 2008-07-26
    Description: After disappointing results from all efficacy trials conducted to date, the field of microbicides research now faces substantial challenges. Poor coordination among interested parties and the choice of nonvalidated scientific targets for phase III studies have hampered progress and created mistrust about the use of microbicides as a method to prevent HIV-1 sexual transmission. Although new promising strategies are available, there will need to be serious reappraisals of how decisions are made to advance the next generations of candidates into clinical trials, and the use of appropriate animal models in this process will be critical.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2835691/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2835691/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Grant, Robert M -- Hamer, Dean -- Hope, Thomas -- Johnston, Rowena -- Lange, Joep -- Lederman, Michael M -- Lieberman, Judy -- Miller, Christopher J -- Moore, John P -- Mosier, Donald E -- Richman, Douglas D -- Schooley, Robert T -- Springer, Marty S -- Veazey, Ronald S -- Wainberg, Mark A -- U19 AI076981/AI/NIAID NIH HHS/ -- U19 AI076981-01/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2008 Jul 25;321(5888):532-4. doi: 10.1126/science.1160355.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉J. David Gladstone Institutes, University of California-San Francisco, San Francisco, CA 94518, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18653884" target="_blank"〉PubMed〈/a〉
    Keywords: Administration, Intravaginal ; Animals ; Anti-HIV Agents/*administration & dosage/pharmacology/therapeutic use ; Anti-Infective Agents, Local/*administration & dosage/pharmacology/therapeutic ; use ; Clinical Trials as Topic ; Disease Models, Animal ; Drug Evaluation, Preclinical ; Drug Therapy, Combination ; Female ; HIV Infections/drug therapy/*prevention & control/transmission ; HIV-1/*drug effects ; Humans ; Male ; Patient Compliance ; Polymers/*administration & dosage/pharmacology/therapeutic use ; Primates ; Reverse Transcriptase Inhibitors/*administration & ; dosage/pharmacology/therapeutic use ; Vaginal Diseases/drug therapy/*prevention & control
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  • 11
    Publication Date: 2008-10-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Travis, John -- New York, N.Y. -- Science. 2008 Oct 17;322(5900):368-9. doi: 10.1126/science.322.5900.368b.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18927371" target="_blank"〉PubMed〈/a〉
    Keywords: Bone and Bones/*chemistry ; Collagen/*chemistry ; History, 17th Century ; History, 18th Century ; Humans ; Hydroxyproline/*analysis ; Male ; Netherlands ; Scurvy/diagnosis/*history
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  • 12
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-08-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lyon, Bruce E -- Chaine, Alexis S -- Winkler, David W -- New York, N.Y. -- Science. 2008 Aug 22;321(5892):1051-2. doi: 10.1126/science.1159822.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Ecology and Evolutionary Biology, University of California, Santa Cruz, CA 95064, USA. lyon@biology.ucsc.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18719273" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Evolution ; *Climate ; Cues ; Environment ; Female ; Male ; *Oviposition ; Passeriformes/genetics/*physiology ; Phenotype ; Photoperiod ; Seasons ; Selection, Genetic ; Temperature ; Time Factors
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  • 13
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-11-29
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Machin, Stephen -- Pekkarinen, Tuomas -- New York, N.Y. -- Science. 2008 Nov 28;322(5906):1331-2. doi: 10.1126/science.1162573.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Economics, University College London, London, WC1 6BT, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19039123" target="_blank"〉PubMed〈/a〉
    Keywords: *Achievement ; Adolescent ; *Educational Measurement ; Female ; Humans ; Intelligence ; Internationality ; Male ; Mathematics ; Reading ; *Sex Characteristics
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  • 14
    Publication Date: 2008-03-01
    Description: Current theories hypothesize that dopamine neuronal firing encodes reward prediction errors. Although studies in nonhuman species provide direct support for this theory, functional magnetic resonance imaging (fMRI) studies in humans have focused on brain areas targeted by dopamine neurons [ventral striatum (VStr)] rather than on brainstem dopaminergic nuclei [ventral tegmental area (VTA) and substantia nigra]. We used fMRI tailored to directly image the brainstem. When primary rewards were used in an experiment, the VTA blood oxygen level-dependent (BOLD) response reflected a positive reward prediction error, whereas the VStr encoded positive and negative reward prediction errors. When monetary gains and losses were used, VTA BOLD responses reflected positive reward prediction errors modulated by the probability of winning. We detected no significant VTA BOLD response to nonrewarding events.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉D'Ardenne, Kimberlee -- McClure, Samuel M -- Nystrom, Leigh E -- Cohen, Jonathan D -- F32 MH072141/MH/NIMH NIH HHS/ -- P50 MH062196/MH/NIMH NIH HHS/ -- T32 MH065214/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2008 Feb 29;319(5867):1264-7. doi: 10.1126/science.1150605.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemistry, Princeton University, Princeton, NJ 08544, USA. dardenne@princeton.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18309087" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Basal Ganglia/physiology ; Conditioning, Classical ; Cues ; Dopamine/*physiology ; Female ; Humans ; Magnetic Resonance Imaging ; Male ; Mental Processes/*physiology ; Oxygen/blood ; Probability ; Reinforcement (Psychology) ; *Reward ; Ventral Tegmental Area/*physiology
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  • 15
    Publication Date: 2008-03-08
    Description: Chronic hyperglycemia contributes to the development of diabetes-associated complications. Increases in the concentration of circulating glucose activate the hexosamine biosynthetic pathway (HBP) and promote the O-glycosylation of proteins by O-glycosyl transferase (OGT). We show that OGT triggered hepatic gluconeogenesis through the O-glycosylation of the transducer of regulated cyclic adenosine monophosphate response element-binding protein (CREB) 2 (TORC2 or CRTC2). CRTC2 was O-glycosylated at sites that normally sequester CRTC2 in the cytoplasm through a phosphorylation-dependent mechanism. Decreasing amounts of O-glycosylated CRTC2 by expression of the deglycosylating enzyme O-GlcNAcase blocked effects of glucose on gluconeogenesis, demonstrating the importance of the HBP in the development of glucose intolerance.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dentin, Renaud -- Hedrick, Susan -- Xie, Jianxin -- Yates, John 3rd -- Montminy, Marc -- R01 GM037828/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2008 Mar 7;319(5868):1402-5. doi: 10.1126/science.1151363.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, CA 92037, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18323454" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Substitution ; Animals ; Blood Glucose/metabolism ; Cell Nucleus/metabolism ; Cells, Cultured ; Cyclic AMP Response Element-Binding Protein/metabolism ; Cytoplasm/metabolism ; Diabetes Mellitus/metabolism ; *Gluconeogenesis ; Glucose/*metabolism ; Glycosylation ; Glycosyltransferases/metabolism ; Hepatocytes/metabolism ; Humans ; Insulin/metabolism ; Liver/*metabolism ; Male ; Mice ; Mice, Inbred C57BL ; Phosphorylation ; RNA Interference ; Signal Transduction ; Trans-Activators/genetics/*metabolism ; Transcription Factors ; beta-N-Acetylhexosaminidases/metabolism
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  • 16
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-12-20
    Description: Nuclear reprogramming describes a switch in gene expression of one kind of cell to that of another unrelated cell type. Early studies in frog cloning provided some of the first experimental evidence for reprogramming. Subsequent procedures included mammalian somatic cell nuclear transfer, cell fusion, induction of pluripotency by ectopic gene expression, and direct reprogramming. Through these methods it becomes possible to derive one kind of specialized cell (such as a brain cell) from another, more accessible, tissue (such as skin) in the same individual. This has potential applications for cell replacement without the immunosuppression treatments that are required when cells are transferred between genetically different individuals. This article provides some background to this field, a discussion of mechanisms and efficiency, and comments on prospects for future nuclear reprogramming research.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gurdon, J B -- Melton, D A -- Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 2008 Dec 19;322(5909):1811-5. doi: 10.1126/science.1160810.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Wellcome Trust/Cancer Research UK Gurdon Institute and Department of Zoology, University of Cambridge, Cambridge CB2 12N, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19095934" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Dedifferentiation ; Cell Differentiation ; Cell Fusion ; Cell Lineage ; *Cellular Reprogramming ; Cloning, Organism ; DNA/metabolism ; DNA-Binding Proteins/metabolism ; Embryonic Stem Cells/cytology/physiology ; Female ; Gene Expression ; Humans ; Male ; Nuclear Transfer Techniques ; Oocytes/cytology ; Pluripotent Stem Cells/cytology/physiology ; Regulatory Sequences, Nucleic Acid ; Transcription Factors/genetics/metabolism
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  • 17
    Publication Date: 2008-12-20
    Description: The repeated discovery of adult dinosaurs in close association with egg clutches leads to speculation over the type and extent of care exhibited by these extinct animals for their eggs and young. To assess parental care in Cretaceous troodontid and oviraptorid dinosaurs, we examined clutch volume and the bone histology of brooding adults. In comparison to four archosaur care regressions, the relatively large clutch volumes of Troodon, Oviraptor, and Citipati scale most closely with a bird-paternal care model. Clutch-associated adults lack the maternal and reproductively associated histologic features common to extant archosaurs. Large clutch volumes and a suite of reproductive features shared only with birds favor paternal care, possibly within a polygamous mating system. Paternal care in both troodontids and oviraptorids indicates that this care system evolved before the emergence of birds and represents birds' ancestral condition. In extant birds and over most adult sizes, paternal and biparental care correspond to the largest and smallest relative clutch volumes, respectively.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Varricchio, David J -- Moore, Jason R -- Erickson, Gregory M -- Norell, Mark A -- Jackson, Frankie D -- Borkowski, John J -- New York, N.Y. -- Science. 2008 Dec 19;322(5909):1826-8. doi: 10.1126/science.1163245.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Earth Sciences, Montana State University, Bozeman, MT 59717, USA. djv@montana.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19095938" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Behavior, Animal ; *Biological Evolution ; *Birds/physiology ; Bone and Bones/anatomy & histology ; Clutch Size ; *Dinosaurs/physiology ; Female ; *Fossils ; Male ; Maternal Behavior ; *Nesting Behavior ; Paternal Behavior ; Regression Analysis ; *Sexual Behavior, Animal
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  • 18
    Publication Date: 2008-05-24
    Description: Taguchi et al. (Reports, 20 July 2007, p. 369) reported that mice heterozygous for a null mutation in insulin receptor substrate-2 (Irs2) display a 17% increase in median life span. However, using the same mouse model, we find no evidence for life-span extension and suggest that the findings of Taguchi et al. were due to atypical life-span profiles in their study animals.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Selman, Colin -- Lingard, Steven -- Gems, David -- Partridge, Linda -- Withers, Dominic J -- New York, N.Y. -- Science. 2008 May 23;320(5879):1012; author reply 1012. doi: 10.1126/science.1152366.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Centre for Diabetes and Endocrinology, Department of Medicine, University College London, Rayne Institute, 5 University Street, London WC1E 6JJ, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18497277" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Brain/*metabolism ; Crosses, Genetic ; Diet ; Female ; Homeostasis ; Insulin Receptor Substrate Proteins ; Intracellular Signaling Peptides and Proteins/genetics/*metabolism ; Kaplan-Meier Estimate ; *Longevity ; Male ; Mice ; Mice, Inbred C57BL ; Mutation ; Phosphoproteins/genetics/*metabolism ; Research Design ; Signal Transduction
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  • 19
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-09-20
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉De Lay, Paul R -- New York, N.Y. -- Science. 2008 Sep 19;321(5896):1631. doi: 10.1126/science.321.5896.1631a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18801980" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/*prevention & control ; Disease Outbreaks/*prevention & control ; Endemic Diseases ; Female ; Humans ; Male ; Preventive Health Services/*economics
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  • 20
    Publication Date: 2008-02-09
    Description: We have developed a biomechanical energy harvester that generates electricity during human walking with little extra effort. Unlike conventional human-powered generators that use positive muscle work, our technology assists muscles in performing negative work, analogous to regenerative braking in hybrid cars, where energy normally dissipated during braking drives a generator instead. The energy harvester mounts at the knee and selectively engages power generation at the end of the swing phase, thus assisting deceleration of the joint. Test subjects walking with one device on each leg produced an average of 5 watts of electricity, which is about 10 times that of shoe-mounted devices. The cost of harvesting-the additional metabolic power required to produce 1 watt of electricity-is less than one-eighth of that for conventional human power generation. Producing substantial electricity with little extra effort makes this method well-suited for charging powered prosthetic limbs and other portable medical devices.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Donelan, J M -- Li, Q -- Naing, V -- Hoffer, J A -- Weber, D J -- Kuo, A D -- New York, N.Y. -- Science. 2008 Feb 8;319(5864):807-10. doi: 10.1126/science.1149860.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉School of Kinesiology, Simon Fraser University (SFU), Burnaby, BC V5A 1S6, Canada. mdonelan@sfu.ca〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18258914" target="_blank"〉PubMed〈/a〉
    Keywords: *Bioelectric Energy Sources ; Biomechanical Phenomena ; *Electricity ; Energy Metabolism ; Humans ; Knee Joint/physiology ; Male ; Muscle, Skeletal/physiology ; *Walking
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  • 21
    Publication Date: 2008-09-06
    Description: Glioblastoma multiforme (GBM) is the most common and lethal type of brain cancer. To identify the genetic alterations in GBMs, we sequenced 20,661 protein coding genes, determined the presence of amplifications and deletions using high-density oligonucleotide arrays, and performed gene expression analyses using next-generation sequencing technologies in 22 human tumor samples. This comprehensive analysis led to the discovery of a variety of genes that were not known to be altered in GBMs. Most notably, we found recurrent mutations in the active site of isocitrate dehydrogenase 1 (IDH1) in 12% of GBM patients. Mutations in IDH1 occurred in a large fraction of young patients and in most patients with secondary GBMs and were associated with an increase in overall survival. These studies demonstrate the value of unbiased genomic analyses in the characterization of human brain cancer and identify a potentially useful genetic alteration for the classification and targeted therapy of GBMs.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2820389/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2820389/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Parsons, D Williams -- Jones, Sian -- Zhang, Xiaosong -- Lin, Jimmy Cheng-Ho -- Leary, Rebecca J -- Angenendt, Philipp -- Mankoo, Parminder -- Carter, Hannah -- Siu, I-Mei -- Gallia, Gary L -- Olivi, Alessandro -- McLendon, Roger -- Rasheed, B Ahmed -- Keir, Stephen -- Nikolskaya, Tatiana -- Nikolsky, Yuri -- Busam, Dana A -- Tekleab, Hanna -- Diaz, Luis A Jr -- Hartigan, James -- Smith, Doug R -- Strausberg, Robert L -- Marie, Suely Kazue Nagahashi -- Shinjo, Sueli Mieko Oba -- Yan, Hai -- Riggins, Gregory J -- Bigner, Darell D -- Karchin, Rachel -- Papadopoulos, Nick -- Parmigiani, Giovanni -- Vogelstein, Bert -- Velculescu, Victor E -- Kinzler, Kenneth W -- 5P50-NS-20023/NS/NINDS NIH HHS/ -- CA09547/CA/NCI NIH HHS/ -- CA108786/CA/NCI NIH HHS/ -- CA11898/CA/NCI NIH HHS/ -- CA121113/CA/NCI NIH HHS/ -- CA43460/CA/NCI NIH HHS/ -- CA57345/CA/NCI NIH HHS/ -- CA62924/CA/NCI NIH HHS/ -- NS052507/NS/NINDS NIH HHS/ -- P50 CA062924/CA/NCI NIH HHS/ -- P50 CA062924-160017/CA/NCI NIH HHS/ -- R01 CA121113/CA/NCI NIH HHS/ -- R01 CA121113-04/CA/NCI NIH HHS/ -- R01 CA140316/CA/NCI NIH HHS/ -- R37 CA043460/CA/NCI NIH HHS/ -- R37 CA043460-27/CA/NCI NIH HHS/ -- R37 CA057345/CA/NCI NIH HHS/ -- R37 CA057345-13/CA/NCI NIH HHS/ -- R37 CA057345-17/CA/NCI NIH HHS/ -- R37 CA057345-18/CA/NCI NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2008 Sep 26;321(5897):1807-12. doi: 10.1126/science.1164382. Epub 2008 Sep 4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Ludwig Center for Cancer Genetics and Therapeutics, and Howard Hughes Medical Institute at Johns Hopkins Kimmel Cancer Center, Baltimore, MD 21231, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18772396" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Brain Neoplasms/*genetics/mortality ; Female ; Gene Amplification ; Gene Dosage ; Gene Expression Profiling ; Gene Expression Regulation, Neoplastic ; Genome, Human ; Glioblastoma/*genetics/mortality ; Humans ; Isocitrate Dehydrogenase/chemistry/*genetics ; Male ; Middle Aged ; *Mutation ; Mutation, Missense ; Oligonucleotide Array Sequence Analysis ; Polymorphism, Single Nucleotide ; Sequence Analysis, DNA ; Signal Transduction ; Survival Rate
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  • 22
    Publication Date: 2008-09-06
    Description: A long-standing conjecture in neuroscience is that aspects of cognition depend on the brain's ability to self-generate sequential neuronal activity. We found that reliably and continually changing cell assemblies in the rat hippocampus appeared not only during spatial navigation but also in the absence of changing environmental or body-derived inputs. During the delay period of a memory task, each moment in time was characterized by the activity of a particular assembly of neurons. Identical initial conditions triggered a similar assembly sequence, whereas different conditions gave rise to different sequences, thereby predicting behavioral choices, including errors. Such sequences were not formed in control (nonmemory) tasks. We hypothesize that neuronal representations, evolved for encoding distance in spatial navigation, also support episodic recall and the planning of action sequences.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2570043/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2570043/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pastalkova, Eva -- Itskov, Vladimir -- Amarasingham, Asohan -- Buzsaki, Gyorgy -- MH54671/MH/NIMH NIH HHS/ -- NS34994/NS/NINDS NIH HHS/ -- R01 MH054671/MH/NIMH NIH HHS/ -- R01 MH054671-10/MH/NIMH NIH HHS/ -- R01 NS034994/NS/NINDS NIH HHS/ -- R01 NS034994-11/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 2008 Sep 5;321(5894):1322-7. doi: 10.1126/science.1159775.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Molecular and Behavioral Neuroscience, Rutgers, State University of New Jersey, 197 University Avenue, Newark, NJ 07102, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18772431" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials ; Animals ; Behavior, Animal ; Choice Behavior ; Cues ; Hippocampus/*cytology/*physiology ; Interneurons/physiology ; Male ; Maze Learning ; *Memory ; *Mental Recall ; Models, Neurological ; Motor Activity ; Pyramidal Cells/*physiology ; Rats ; Rats, Long-Evans
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  • 23
    Publication Date: 2008-08-02
    Description: MyD88 is a key downstream adapter for most Toll-like receptors (TLRs) and interleukin-1 receptors (IL-1Rs). MyD88 deficiency in mice leads to susceptibility to a broad range of pathogens in experimental settings of infection. We describe a distinct situation in a natural setting of human infection. Nine children with autosomal recessive MyD88 deficiency suffered from life-threatening, often recurrent pyogenic bacterial infections, including invasive pneumococcal disease. However, these patients were otherwise healthy, with normal resistance to other microbes. Their clinical status improved with age, but not due to any cellular leakiness in MyD88 deficiency. The MyD88-dependent TLRs and IL-1Rs are therefore essential for protective immunity to a small number of pyogenic bacteria, but redundant for host defense to most natural infections.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2688396/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2688396/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉von Bernuth, Horst -- Picard, Capucine -- Jin, Zhongbo -- Pankla, Rungnapa -- Xiao, Hui -- Ku, Cheng-Lung -- Chrabieh, Maya -- Mustapha, Imen Ben -- Ghandil, Pegah -- Camcioglu, Yildiz -- Vasconcelos, Julia -- Sirvent, Nicolas -- Guedes, Margarida -- Vitor, Artur Bonito -- Herrero-Mata, Maria Jose -- Arostegui, Juan Ignacio -- Rodrigo, Carlos -- Alsina, Laia -- Ruiz-Ortiz, Estibaliz -- Juan, Manel -- Fortuny, Claudia -- Yague, Jordi -- Anton, Jordi -- Pascal, Mariona -- Chang, Huey-Hsuan -- Janniere, Lucile -- Rose, Yoann -- Garty, Ben-Zion -- Chapel, Helen -- Issekutz, Andrew -- Marodi, Laszlo -- Rodriguez-Gallego, Carlos -- Banchereau, Jacques -- Abel, Laurent -- Li, Xiaoxia -- Chaussabel, Damien -- Puel, Anne -- Casanova, Jean-Laurent -- U19 AI057234/AI/NIAID NIH HHS/ -- U19 AI057234-02/AI/NIAID NIH HHS/ -- U19 AIO57234-02/PHS HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2008 Aug 1;321(5889):691-6. doi: 10.1126/science.1158298.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Human Genetics of Infectious Diseases, INSERM U550, Paris, France.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18669862" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Animals ; Bacterial Infections/*genetics/*immunology ; Cell Line, Transformed ; Child ; Child, Preschool ; Cytokines/metabolism ; Disease Susceptibility ; Female ; Gene Deletion ; Humans ; Immunity, Innate ; Male ; Mice ; Mutation, Missense ; Myeloid Differentiation Factor 88/*deficiency/genetics/metabolism ; Pneumococcal Infections/genetics/immunology ; Pseudomonas Infections/genetics/immunology ; Receptors, Interleukin-1/immunology/metabolism ; Signal Transduction ; Staphylococcal Infections/genetics/immunology ; Toll-Like Receptors/immunology/metabolism ; Transfection
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  • 24
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-03-15
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉King, Peter -- New York, N.Y. -- Science. 2008 Mar 14;319(5869):1483. doi: 10.1126/science.319.5869.1483b.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18339919" target="_blank"〉PubMed〈/a〉
    Keywords: Humans ; Larynx/*physiology ; *Learning ; Male ; *Music ; Pitch Perception ; Sound
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  • 25
    Publication Date: 2008-08-09
    Description: To sustain or repair cooperation during a social exchange, adaptive creatures must understand social gestures and the consequences when shared expectations about fair exchange are violated by accident or intent. We recruited 55 individuals afflicted with borderline personality disorder (BPD) to play a multiround economic exchange game with healthy partners. Behaviorally, individuals with BPD showed a profound incapacity to maintain cooperation, and were impaired in their ability to repair broken cooperation on the basis of a quantitative measure of coaxing. Neurally, activity in the anterior insula, a region known to respond to norm violations across affective, interoceptive, economic, and social dimensions, strongly differentiated healthy participants from individuals with BPD. Healthy subjects showed a strong linear relation between anterior insula response and both magnitude of monetary offer received from their partner (input) and the amount of money repaid to their partner (output). In stark contrast, activity in the anterior insula of BPD participants was related only to the magnitude of repayment sent back to their partner (output), not to the magnitude of offers received (input). These neural and behavioral data suggest that norms used in perception of social gestures are pathologically perturbed or missing altogether among individuals with BPD. This game-theoretic approach to psychopathology may open doors to new ways of characterizing and studying a range of mental illnesses.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105006/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105006/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉King-Casas, Brooks -- Sharp, Carla -- Lomax-Bream, Laura -- Lohrenz, Terry -- Fonagy, Peter -- Montague, P Read -- DA11723/DA/NIDA NIH HHS/ -- F32 MH078485/MH/NIMH NIH HHS/ -- MH078485/MH/NIMH NIH HHS/ -- MH52797/MH/NIMH NIH HHS/ -- NS045790/NS/NINDS NIH HHS/ -- R01 DA011723/DA/NIDA NIH HHS/ -- R01 MH052797/MH/NIMH NIH HHS/ -- R01 NS045790/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 2008 Aug 8;321(5890):806-10. doi: 10.1126/science.1156902.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Computational Psychiatry Unit and Department of Neuroscience, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18687957" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Borderline Personality Disorder/*physiopathology/*psychology ; Cerebral Cortex/*physiopathology ; *Cooperative Behavior ; Female ; Frontal Lobe/physiopathology ; *Games, Experimental ; Humans ; Magnetic Resonance Imaging ; Male ; Parietal Lobe/physiopathology ; Social Behavior ; Trust/*psychology
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  • 26
    Publication Date: 2008-04-26
    Description: The mammalian vomeronasal organ detects complex chemical signals that convey information about gender, strain, and the social and reproductive status of an individual. How these signals are encoded is poorly understood. We developed transgenic mice expressing the calcium indicator G-CaMP2 and analyzed population responses of vomeronasal neurons to urine from individual animals. A substantial portion of cells was activated by either male or female urine, but only a small population of cells responded exclusively to gender-specific cues shared across strains and individuals. Female cues activated more cells and were subject to more complex hormonal regulations than male cues. In contrast to gender, strain and individual information was encoded by the combinatorial activation of neurons such that urine from different individuals activated distinctive cell populations.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2602951/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2602951/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉He, Jie -- Ma, Limei -- Kim, Sangseong -- Nakai, Junichi -- Yu, C Ron -- NIDCD 008003/PHS HHS/ -- R01 DC008003/DC/NIDCD NIH HHS/ -- R01 DC008003-03/DC/NIDCD NIH HHS/ -- New York, N.Y. -- Science. 2008 Apr 25;320(5875):535-8. doi: 10.1126/science.1154476.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Stowers Institute for Medical Research, 1000 East 50th Street, Kansas City, MO 64110, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18436787" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Behavior, Animal ; Calcium/metabolism ; Cluster Analysis ; Cues ; Female ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Inbred CBA ; Neurons, Afferent/*physiology ; *Pheromones ; Principal Component Analysis ; Receptors, Pheromone/physiology ; Sex Characteristics ; *Urine/chemistry ; Vomeronasal Organ/cytology/*physiology
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  • 27
    Publication Date: 2008-03-29
    Description: Schizophrenia is a devastating neurodevelopmental disorder whose genetic influences remain elusive. We hypothesize that individually rare structural variants contribute to the illness. Microdeletions and microduplications 〉100 kilobases were identified by microarray comparative genomic hybridization of genomic DNA from 150 individuals with schizophrenia and 268 ancestry-matched controls. All variants were validated by high-resolution platforms. Novel deletions and duplications of genes were present in 5% of controls versus 15% of cases and 20% of young-onset cases, both highly significant differences. The association was independently replicated in patients with childhood-onset schizophrenia as compared with their parents. Mutations in cases disrupted genes disproportionately from signaling networks controlling neurodevelopment, including neuregulin and glutamate pathways. These results suggest that multiple, individually rare mutations altering genes in neurodevelopmental pathways contribute to schizophrenia.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Walsh, Tom -- McClellan, Jon M -- McCarthy, Shane E -- Addington, Anjene M -- Pierce, Sarah B -- Cooper, Greg M -- Nord, Alex S -- Kusenda, Mary -- Malhotra, Dheeraj -- Bhandari, Abhishek -- Stray, Sunday M -- Rippey, Caitlin F -- Roccanova, Patricia -- Makarov, Vlad -- Lakshmi, B -- Findling, Robert L -- Sikich, Linmarie -- Stromberg, Thomas -- Merriman, Barry -- Gogtay, Nitin -- Butler, Philip -- Eckstrand, Kristen -- Noory, Laila -- Gochman, Peter -- Long, Robert -- Chen, Zugen -- Davis, Sean -- Baker, Carl -- Eichler, Evan E -- Meltzer, Paul S -- Nelson, Stanley F -- Singleton, Andrew B -- Lee, Ming K -- Rapoport, Judith L -- King, Mary-Claire -- Sebat, Jonathan -- HD043569/HD/NICHD NIH HHS/ -- M01 RR000046/RR/NCRR NIH HHS/ -- MH061355/MH/NIMH NIH HHS/ -- MH061464/MH/NIMH NIH HHS/ -- MH061528/MH/NIMH NIH HHS/ -- NS052108/NS/NINDS NIH HHS/ -- R01 HD043569/HD/NICHD NIH HHS/ -- RR000046/RR/NCRR NIH HHS/ -- RR025014/RR/NCRR NIH HHS/ -- U01 MH061355/MH/NIMH NIH HHS/ -- U01 MH061464/MH/NIMH NIH HHS/ -- U01 MH061528/MH/NIMH NIH HHS/ -- U24 NS052108/NS/NINDS NIH HHS/ -- UL1 RR025014/RR/NCRR NIH HHS/ -- Howard Hughes Medical Institute/ -- Intramural NIH HHS/ -- New York, N.Y. -- Science. 2008 Apr 25;320(5875):539-43. doi: 10.1126/science.1155174. Epub 2008 Mar 27.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Medicine, University of Washington, Seattle, WA 98195, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18369103" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Age of Onset ; Amino Acid Sequence ; Brain/cytology/*growth & development/metabolism ; Case-Control Studies ; Child ; Excitatory Amino Acid Transporter 1/chemistry/genetics/physiology ; Female ; *Gene Deletion ; *Gene Duplication ; Genetic Predisposition to Disease ; Genome, Human ; Humans ; Male ; Molecular Sequence Data ; *Mutation ; Neurons/cytology/physiology ; Oligonucleotide Array Sequence Analysis ; Polymorphism, Single Nucleotide ; Receptor, Epidermal Growth Factor/chemistry/genetics/physiology ; Receptor, ErbB-4 ; Schizophrenia/*genetics/physiopathology ; Signal Transduction
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  • 28
    Publication Date: 2008-07-19
    Description: Sleep is an essential process conserved from flies to humans. The importance of sleep is underscored by its tight homeostatic control. Through a forward genetic screen, we identified a gene, sleepless, required for sleep in Drosophila. The sleepless gene encodes a brain-enriched, glycosylphosphatidylinositol-anchored protein. Loss of SLEEPLESS protein caused an extreme (〉80%) reduction in sleep; a moderate reduction in SLEEPLESS had minimal effects on baseline sleep but markedly reduced the amount of recovery sleep after sleep deprivation. Genetic and molecular analyses revealed that quiver, a mutation that impairs Shaker-dependent potassium current, is an allele of sleepless. Consistent with this finding, Shaker protein levels were reduced in sleepless mutants. We propose that SLEEPLESS is a signaling molecule that connects sleep drive to lowered membrane excitability.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2771549/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2771549/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Koh, Kyunghee -- Joiner, William J -- Wu, Mark N -- Yue, Zhifeng -- Smith, Corinne J -- Sehgal, Amita -- AG017628/AG/NIA NIH HHS/ -- P01 AG017628/AG/NIA NIH HHS/ -- P01 AG017628-070004/AG/NIA NIH HHS/ -- R01 NS072431/NS/NINDS NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2008 Jul 18;321(5887):372-6. doi: 10.1126/science.1155942.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Department of Neuroscience, University of Pennsylvania, Philadelphia, PA 19104, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18635795" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Animals, Genetically Modified ; Behavior, Animal ; Brain/metabolism ; Cell Membrane/metabolism ; DNA Transposable Elements ; Drosophila Proteins/chemistry/*genetics/*physiology ; Drosophila melanogaster/genetics/*physiology ; Female ; *Genes, Insect ; Glycosylphosphatidylinositols ; Homeostasis ; Longevity ; Male ; Membrane Proteins/chemistry/*genetics/*physiology ; *Models, Animal ; Molecular Sequence Data ; Mutation ; Phenotype ; Shaker Superfamily of Potassium Channels/physiology ; Signal Transduction ; *Sleep/genetics/physiology ; Sleep Deprivation ; Transgenes
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  • 29
    Publication Date: 2008-03-01
    Description: Amyotrophic lateral sclerosis (ALS) is a fatal motor neuron disorder characterized pathologically by ubiquitinated TAR DNA binding protein (TDP-43) inclusions. The function of TDP-43 in the nervous system is uncertain, and a mechanistic role in neurodegeneration remains speculative. We identified neighboring mutations in a highly conserved region of TARDBP in sporadic and familial ALS cases. TARDBPM337V segregated with disease within one kindred and a genome-wide scan confirmed that linkage was restricted to chromosome 1p36, which contains the TARDBP locus. Mutant forms of TDP-43 fragmented in vitro more readily than wild type and, in vivo, caused neural apoptosis and developmental delay in the chick embryo. Our evidence suggests a pathophysiological link between TDP-43 and ALS.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sreedharan, Jemeen -- Blair, Ian P -- Tripathi, Vineeta B -- Hu, Xun -- Vance, Caroline -- Rogelj, Boris -- Ackerley, Steven -- Durnall, Jennifer C -- Williams, Kelly L -- Buratti, Emanuele -- Baralle, Francisco -- de Belleroche, Jacqueline -- Mitchell, J Douglas -- Leigh, P Nigel -- Al-Chalabi, Ammar -- Miller, Christopher C -- Nicholson, Garth -- Shaw, Christopher E -- G0500289/Medical Research Council/United Kingdom -- G0501573/Medical Research Council/United Kingdom -- G0600974/Medical Research Council/United Kingdom -- Medical Research Council/United Kingdom -- Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 2008 Mar 21;319(5870):1668-72. doi: 10.1126/science.1154584. Epub 2008 Feb 28.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Clinical Neuroscience, King's College London, Medical Research Council (MRC) Centre for Neurodegeneration Research, and Institute of Psychiatry, London, SE5 8AF, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18309045" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Amino Acid Sequence ; Amino Acid Substitution ; Amyotrophic Lateral Sclerosis/*genetics ; Animals ; Apoptosis ; CHO Cells ; Chick Embryo ; Chromosomes, Human, Pair 1/genetics ; Cricetinae ; Cricetulus ; DNA-Binding Proteins/chemistry/*genetics/physiology ; Embryonic Development ; Female ; Humans ; Male ; Microsatellite Repeats ; Middle Aged ; Molecular Sequence Data ; Mutant Proteins/chemistry/physiology ; *Mutation, Missense ; Neurons/cytology/physiology
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  • 30
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-10-25
    Description: "Warmth" is the most powerful personality trait in social judgment, and attachment theorists have stressed the importance of warm physical contact with caregivers during infancy for healthy relationships in adulthood. Intriguingly, recent research in humans points to the involvement of the insula in the processing of both physical temperature and interpersonal warmth (trust) information. Accordingly, we hypothesized that experiences of physical warmth (or coldness) would increase feelings of interpersonal warmth (or coldness), without the person's awareness of this influence. In study 1, participants who briefly held a cup of hot (versus iced) coffee judged a target person as having a "warmer" personality (generous, caring); in study 2, participants holding a hot (versus cold) therapeutic pad were more likely to choose a gift for a friend instead of for themselves.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2737341/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2737341/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Williams, Lawrence E -- Bargh, John A -- MH-R01-60767/MH/NIMH NIH HHS/ -- R01 MH060767-09/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2008 Oct 24;322(5901):606-7. doi: 10.1126/science.1162548.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Leeds School of Business, University of Colorado at Boulder, UCB 419, Boulder, CO, 80309-0419, USA. lawrence.williams@colorado.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18948544" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Cerebral Cortex/physiology ; Cold Temperature ; Emotions ; Female ; Hot Temperature ; Humans ; *Interpersonal Relations ; Judgment ; Male ; Personality ; Social Behavior ; *Social Perception ; *Thermosensing ; *Trust
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  • 31
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-05-31
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Balter, Michael -- New York, N.Y. -- Science. 2008 May 30;320(5880):1146-7. doi: 10.1126/science.320.5880.1146b.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18511664" target="_blank"〉PubMed〈/a〉
    Keywords: Asian Continental Ancestry Group/genetics ; *DNA, Mitochondrial ; Emigration and Immigration ; Freezing ; Genetic Markers ; Greenland ; Hair/*chemistry ; History, Ancient ; Humans ; Inuits/*genetics ; Male
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  • 32
    Publication Date: 2008-09-27
    Description: Pluripotent stem cells have been generated from mouse and human somatic cells by viral expression of the transcription factors Oct4, Sox2, Klf4, and c-Myc. A major limitation of this technology is the use of potentially harmful genome-integrating viruses. We generated mouse induced pluripotent stem (iPS) cells from fibroblasts and liver cells by using nonintegrating adenoviruses transiently expressing Oct4, Sox2, Klf4, and c-Myc. These adenoviral iPS (adeno-iPS) cells show DNA demethylation characteristic of reprogrammed cells, express endogenous pluripotency genes, form teratomas, and contribute to multiple tissues, including the germ line, in chimeric mice. Our results provide strong evidence that insertional mutagenesis is not required for in vitro reprogramming. Adenoviral reprogramming may provide an improved method for generating and studying patient-specific stem cells and for comparing embryonic stem cells and iPS cells.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3987909/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3987909/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stadtfeld, Matthias -- Nagaya, Masaki -- Utikal, Jochen -- Weir, Gordon -- Hochedlinger, Konrad -- DP2 OD003266/OD/NIH HHS/ -- New York, N.Y. -- Science. 2008 Nov 7;322(5903):945-9. doi: 10.1126/science.1162494. Epub 2008 Sep 25.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Massachusetts General Hospital Cancer Center and Center for Regenerative Medicine, 185 Cambridge Street, Boston, MA 02114, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18818365" target="_blank"〉PubMed〈/a〉
    Keywords: Adenoviridae/*genetics/physiology ; Animals ; Cell Differentiation ; Cell Line ; *Cellular Reprogramming ; Chimera ; Cloning, Molecular ; Female ; Fibroblasts/*cytology/metabolism/virology ; Genes, myc ; *Genetic Vectors ; Hepatocytes/*cytology/metabolism/virology ; Kruppel-Like Transcription Factors/genetics/metabolism ; Liver/cytology/embryology ; Male ; Mice ; Mice, SCID ; Octamer Transcription Factor-3/genetics/metabolism ; *Pluripotent Stem Cells/cytology/metabolism/transplantation ; Proto-Oncogene Proteins c-myc/genetics/metabolism ; SOXB1 Transcription Factors/genetics/metabolism ; Teratoma/etiology ; Transgenes ; Virus Integration
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  • 33
    Publication Date: 2008-02-09
    Description: Previous studies have reported that related human couples tend to produce more children than unrelated couples but have been unable to determine whether this difference is biological or stems from socioeconomic variables. Our results, drawn from all known couples of the Icelandic population born between 1800 and 1965, show a significant positive association between kinship and fertility, with the greatest reproductive success observed for couples related at the level of third and fourth cousins. Owing to the relative socioeconomic homogeneity of Icelanders, and the observation of highly significant differences in the fertility of couples separated by very fine intervals of kinship, we conclude that this association is likely to have a biological basis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Helgason, Agnar -- Palsson, Saebjorn -- Gudbjartsson, Daniel F -- Kristjansson, Thornordur -- Stefansson, Kari -- New York, N.Y. -- Science. 2008 Feb 8;319(5864):813-6. doi: 10.1126/science.1150232.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉deCODE Genetics, Sturlugata 8, 101 Reykjavik, Iceland. agnar@decode.is〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18258915" target="_blank"〉PubMed〈/a〉
    Keywords: Consanguinity ; *Family ; *Family Characteristics ; Female ; *Fertility ; Humans ; Iceland ; Male ; Socioeconomic Factors
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  • 34
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-02-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Shoubridge, Eric A -- Wai, Timothy -- New York, N.Y. -- Science. 2008 Feb 15;319(5865):914-5. doi: 10.1126/science.1154515.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Montreal Neurological Institute and Department of Human Genetics, McGill University, Montreal, Quebec H3A 2B4, Canada. eric@ericpc.mni.mcgill.ca〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18276880" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Autophagy ; Cell Line ; DNA, Mitochondrial/*genetics ; DNA-Directed DNA Polymerase/genetics ; Electron Transport Complex IV/*genetics ; Embryonic Stem Cells ; Female ; Frameshift Mutation ; *Germ-Line Mutation ; Male ; Mice ; Mitochondria/physiology ; NADH Dehydrogenase/*genetics ; Oocytes/*physiology ; Oogenesis ; *Selection, Genetic
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  • 35
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-11-08
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pennisi, Elizabeth -- New York, N.Y. -- Science. 2008 Nov 7;322(5903):838. doi: 10.1126/science.322.5903.838.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18988816" target="_blank"〉PubMed〈/a〉
    Keywords: African Continental Ancestry Group/genetics ; Asian Continental Ancestry Group/genetics ; Costs and Cost Analysis ; Female ; *Genome, Human ; *Genomics/economics/methods ; Humans ; Leukemia, Myeloid, Acute/genetics ; Male ; *Polymorphism, Single Nucleotide ; *Sequence Analysis, DNA/economics/methods
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  • 36
    Publication Date: 2008-10-11
    Description: Naturally occurring Foxp3+CD4+ regulatory T cells (Tregs) are essential for maintaining immunological self-tolerance and immune homeostasis. Here, we show that a specific deficiency of cytotoxic T lymphocyte antigen 4 (CTLA-4) in Tregs results in spontaneous development of systemic lymphoproliferation, fatal T cell-mediated autoimmune disease, and hyperproduction of immunoglobulin E in mice, and it also produces potent tumor immunity. Treg-specific CTLA-4 deficiency impairs in vivo and in vitro suppressive function of Tregs-in particular, Treg-mediated down-regulation of CD80 and CD86 expression on dendritic cells. Thus, natural Tregs may critically require CTLA-4 to suppress immune responses by affecting the potency of antigen-presenting cells to activate other T cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wing, Kajsa -- Onishi, Yasushi -- Prieto-Martin, Paz -- Yamaguchi, Tomoyuki -- Miyara, Makoto -- Fehervari, Zoltan -- Nomura, Takashi -- Sakaguchi, Shimon -- New York, N.Y. -- Science. 2008 Oct 10;322(5899):271-5. doi: 10.1126/science.1160062.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Experimental Pathology, Institute for Frontier Medical Sciences, Kyoto University, Kyoto 606-8507, Japan.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18845758" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antigen-Presenting Cells/immunology ; Antigens, CD/genetics/immunology/*metabolism ; Antigens, CD80/metabolism ; Antigens, CD86/metabolism ; Autoimmune Diseases/immunology ; *Autoimmunity ; CD8-Positive T-Lymphocytes/immunology ; CTLA-4 Antigen ; Dendritic Cells/immunology ; Down-Regulation ; Female ; Forkhead Transcription Factors/genetics/metabolism ; *Immune Tolerance ; Immunoglobulin E/blood ; Immunoglobulin G/blood ; Leukemia/immunology ; Lymphocyte Activation ; Lymphocytes/immunology ; Male ; Mice ; Mice, Inbred BALB C ; T-Lymphocytes, Regulatory/*immunology
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  • 37
    Publication Date: 2008-07-19
    Description: The frontal eye field (FEF) is one of several cortical regions thought to modulate sensory inputs. Moreover, several hypotheses suggest that the FEF can only modulate early visual areas in the presence of a visual stimulus. To test for bottom-up gating of frontal signals, we microstimulated subregions in the FEF of two monkeys and measured the effects throughout the brain with functional magnetic resonance imaging. The activity of higher-order visual areas was strongly modulated by FEF stimulation, independent of visual stimulation. In contrast, FEF stimulation induced a topographically specific pattern of enhancement and suppression in early visual areas, but only in the presence of a visual stimulus. Modulation strength depended on stimulus contrast and on the presence of distractors. We conclude that bottom-up activation is needed to enable top-down modulation of early visual cortex and that stimulus saliency determines the strength of this modulation.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011100/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011100/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ekstrom, Leeland B -- Roelfsema, Pieter R -- Arsenault, John T -- Bonmassar, Giorgio -- Vanduffel, Wim -- P41 RR014075/RR/NCRR NIH HHS/ -- P41 RR014075-13/RR/NCRR NIH HHS/ -- P41RR14075/RR/NCRR NIH HHS/ -- R01 EB000790/EB/NIBIB NIH HHS/ -- R01 EB000790-05/EB/NIBIB NIH HHS/ -- New York, N.Y. -- Science. 2008 Jul 18;321(5887):414-7. doi: 10.1126/science.1153276.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Charlestown, MA 02129, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18635806" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Brain Mapping ; Electric Stimulation ; Fixation, Ocular ; Frontal Lobe/*physiology ; Macaca mulatta ; Magnetic Resonance Imaging ; Male ; Photic Stimulation ; Saccades ; Visual Cortex/*physiology ; Visual Pathways
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  • 38
    Publication Date: 2008-06-21
    Description: The control of innate immune responses through activation of the nuclear transcription factor NF-kappaB is essential for the elimination of invading microbial pathogens. We showed that the bacterial N-(3-oxo-dodecanoyl) homoserine lactone (C12) selectively impairs the regulation of NF-kappaB functions in activated mammalian cells. The consequence is specific repression of stimulus-mediated induction of NF-kappaB-responsive genes encoding inflammatory cytokines and other immune regulators. These findings uncover a strategy by which C12-producing opportunistic pathogens, such as Pseudomonas aeruginosa, attenuate the innate immune system to establish and maintain local persistent infection in humans, for example, in cystic fibrosis patients.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kravchenko, Vladimir V -- Kaufmann, Gunnar F -- Mathison, John C -- Scott, David A -- Katz, Alexander Z -- Grauer, David C -- Lehmann, Mandy -- Meijler, Michael M -- Janda, Kim D -- Ulevitch, Richard J -- New York, N.Y. -- Science. 2008 Jul 11;321(5886):259-63. doi: 10.1126/science.1156499. Epub 2008 Jun 19.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Immunology and Microbial Sciences, Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18566250" target="_blank"〉PubMed〈/a〉
    Keywords: 4-Butyrolactone/*analogs & derivatives/physiology ; Adult ; Animals ; Cyclic AMP Response Element-Binding Protein/metabolism ; Cystic Fibrosis/microbiology ; Female ; *Gene Expression Regulation ; Homoserine/*analogs & derivatives/physiology ; Humans ; I-kappa B Kinase/metabolism ; I-kappa B Proteins/metabolism ; Immunity, Innate ; Interferon-gamma/immunology ; Lipopolysaccharides/immunology ; Macrophage Activation ; Macrophages/*immunology/*metabolism ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Middle Aged ; NF-kappa B/*metabolism ; Phosphorylation ; Pseudomonas Infections/immunology/microbiology ; Pseudomonas aeruginosa/immunology/*pathogenicity/physiology ; *Signal Transduction ; Toll-Like Receptors/metabolism ; Transcription Factor RelA/metabolism
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  • 39
    Publication Date: 2008-02-16
    Description: The majority of mitochondrial DNA (mtDNA) mutations that cause human disease are mild to moderately deleterious, yet many random mtDNA mutations would be expected to be severe. To determine the fate of the more severe mtDNA mutations, we introduced mtDNAs containing two mutations that affect oxidative phosphorylation into the female mouse germ line. The severe ND6 mutation was selectively eliminated during oogenesis within four generations, whereas the milder COI mutation was retained throughout multiple generations even though the offspring consistently developed mitochondrial myopathy and cardiomyopathy. Thus, severe mtDNA mutations appear to be selectively eliminated from the female germ line, thereby minimizing their impact on population fitness.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3049809/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3049809/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fan, Weiwei -- Waymire, Katrina G -- Narula, Navneet -- Li, Peng -- Rocher, Christophe -- Coskun, Pinar E -- Vannan, Mani A -- Narula, Jagat -- Macgregor, Grant R -- Wallace, Douglas C -- AG13154/AG/NIA NIH HHS/ -- AG16573/AG/NIA NIH HHS/ -- AG24373/AG/NIA NIH HHS/ -- DK73691/DK/NIDDK NIH HHS/ -- HD45913/HD/NICHD NIH HHS/ -- NS21328/NS/NINDS NIH HHS/ -- U01 HD045913-01/HD/NICHD NIH HHS/ -- U01 HD045913-02/HD/NICHD NIH HHS/ -- U01 HD045913-03/HD/NICHD NIH HHS/ -- U01 HD045913-04/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 2008 Feb 15;319(5865):958-62. doi: 10.1126/science.1147786.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Molecular and Mitochondrial Medicine and Genetics, University of California, Irvine, CA 92697, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18276892" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cardiomyopathies/genetics/pathology ; Cell Line ; Crosses, Genetic ; DNA, Mitochondrial/*genetics ; Electron Transport Complex I/metabolism ; Electron Transport Complex IV/*genetics/metabolism ; Embryonic Stem Cells ; Female ; Frameshift Mutation ; *Germ-Line Mutation ; Litter Size ; Male ; Mice ; Mitochondria/physiology ; Mitochondrial Myopathies/*genetics/pathology ; Mutation, Missense ; Myocardium/pathology ; NADH Dehydrogenase/*genetics ; Oocytes/*physiology ; Oogenesis ; Oxidative Phosphorylation ; Oxygen Consumption ; Point Mutation ; *Selection, Genetic
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  • 40
    Publication Date: 2008-11-29
    Description: Hepatic glucose production is critical for basal brain function and survival when dietary glucose is unavailable. Glucose-6-phosphatase (G6Pase) is an essential, rate-limiting enzyme that serves as a terminal gatekeeper for hepatic glucose release into the plasma. Mutations in G6Pase result in Von Gierke's disease (glycogen storage disease-1a), a potentially fatal genetic disorder. We have identified the transcriptional coactivator SRC-2 as a regulator of fasting hepatic glucose release, a function that SRC-2 performs by controlling the expression of hepatic G6Pase. SRC-2 modulates G6Pase expression directly by acting as a coactivator with the orphan nuclear receptor RORalpha. In addition, SRC-2 ablation, in both a whole-body and liver-specific manner, resulted in a Von Gierke's disease phenotype in mice. Our results position SRC-2 as a critical regulator of mammalian glucose production.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2668604/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2668604/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chopra, Atul R -- Louet, Jean-Francois -- Saha, Pradip -- An, Jie -- Demayo, Franco -- Xu, Jianming -- York, Brian -- Karpen, Saul -- Finegold, Milton -- Moore, David -- Chan, Lawrence -- Newgard, Christopher B -- O'Malley, Bert W -- DK58242/DK/NIDDK NIH HHS/ -- HL51586/HL/NHLBI NIH HHS/ -- P01 DK059820/DK/NIDDK NIH HHS/ -- P01 DK059820-08/DK/NIDDK NIH HHS/ -- P01 DK58398/DK/NIDDK NIH HHS/ -- P01 DK59820/DK/NIDDK NIH HHS/ -- R01 DK056239/DK/NIDDK NIH HHS/ -- R01 DK056239-08/DK/NIDDK NIH HHS/ -- U19 DK062434/DK/NIDDK NIH HHS/ -- U19 DK062434-07/DK/NIDDK NIH HHS/ -- New York, N.Y. -- Science. 2008 Nov 28;322(5906):1395-9. doi: 10.1126/science.1164847.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular and Cellular Biology, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19039140" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cells, Cultured ; Fasting ; Female ; Gene Expression Profiling ; Gene Expression Regulation, Enzymologic ; Glucose/*metabolism ; Glucose-6-Phosphatase/*genetics/metabolism ; Glycogen Storage Disease Type I/*genetics/metabolism ; Hepatocytes/metabolism ; Kidney/metabolism ; Liver/*metabolism ; Liver Glycogen/metabolism ; Male ; Mice ; Mice, Knockout ; Nuclear Receptor Coactivator 2/genetics/*metabolism ; RNA Interference ; Receptors, Retinoic Acid/metabolism ; Response Elements ; Transcription, Genetic ; Triglycerides/metabolism
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  • 41
    Publication Date: 2008-07-26
    Description: High copy number and random segregation confound genetic analysis of the mitochondrial genome. We developed an efficient selection for heritable mitochondrial genome (mtDNA) mutations in Drosophila, thereby enhancing a metazoan model for study of mitochondrial genetics and mutations causing human mitochondrial disease. Targeting a restriction enzyme to mitochondria in the germline compromised fertility, but escaper progeny carried homoplasmic mtDNA mutations lacking the cleavage site. Among mutations eliminating a site in the cytochrome c oxidase gene, mt:CoI(A302T) was healthy, mt:CoI(R301L) was male sterile but otherwise healthy, and mt:CoI(R301S) exhibited a wide range of defects, including growth retardation, neurodegeneration, muscular atrophy, male sterility, and reduced life span. Thus, germline expression of mitochondrial restriction enzymes creates a powerful selection and has allowed direct isolation of mitochondrial mutants in a metazoan.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2754248/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2754248/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Xu, Hong -- DeLuca, Steven Z -- O'Farrell, Patrick H -- R01 AI060102/AI/NIAID NIH HHS/ -- R01 AI060102-08/AI/NIAID NIH HHS/ -- R01 GM037193/GM/NIGMS NIH HHS/ -- R01 GM037193-22/GM/NIGMS NIH HHS/ -- R01 GM086854/GM/NIGMS NIH HHS/ -- R01 GM086854-09A1/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2008 Jul 25;321(5888):575-7. doi: 10.1126/science.1160226.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry and Biophysics, University of California at San Francisco, San Francisco, CA 94158-2200, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18653897" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Genetically Modified ; Bacterial Proteins/genetics/metabolism ; DNA Restriction Enzymes/genetics/*metabolism ; DNA, Mitochondrial/*genetics/metabolism ; Deoxyribonucleases, Type II Site-Specific/genetics/*metabolism ; Drosophila melanogaster/embryology/*genetics/growth & development/metabolism ; Embryo, Nonmammalian/metabolism ; Eye/anatomy & histology/growth & development ; Female ; Genome, Insect ; *Genome, Mitochondrial ; Infertility, Male ; Male ; Mitochondrial Diseases/genetics/metabolism ; Morphogenesis ; Muscles/ultrastructure ; Muscular Dystrophy, Animal ; *Mutation ; Spermatogenesis
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  • 42
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-12-20
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Prum, Richard O -- New York, N.Y. -- Science. 2008 Dec 19;322(5909):1799-800. doi: 10.1126/science.1168808.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Ecology and Evolutionary Biology and Peabody Museum of Natural History, Post Office Box 208105, Yale University, New Haven, CT 06520, USA. richard.prum@yale.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19095929" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Behavior, Animal ; *Biological Evolution ; *Birds/physiology ; Clutch Size ; *Dinosaurs/physiology ; Female ; *Fossils ; Male ; *Nesting Behavior ; Paternal Behavior ; Sexual Behavior, Animal
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  • 43
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-08-09
    Description: Our ability to remember what we have seen is very limited. Most current views characterize this limit as a fixed number of items-only four objects-that can be held in visual working memory. We show that visual memory capacity is not fixed by the number of objects, but rather is a limited resource that is shared out dynamically between all items in the visual scene. This resource can be shifted flexibly between objects, with allocation biased by selective attention and toward targets of upcoming eye movements. The proportion of resources allocated to each item determines the precision with which it is remembered, a relation that we show is governed by a simple power law, allowing quantitative estimates of resource distribution in a scene.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2532743/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2532743/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bays, Paul M -- Husain, Masud -- 061140/Wellcome Trust/United Kingdom -- Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 2008 Aug 8;321(5890):851-4. doi: 10.1126/science.1158023.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute of Cognitive Neuroscience, University College London, 17 Queen Square, London WC1N 3AR, UK. p.bays@ion.ucl.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18687968" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; *Attention ; Female ; Fixation, Ocular ; Humans ; Male ; *Memory, Short-Term ; *Mental Recall ; Models, Neurological ; *Saccades ; Vision, Ocular ; *Visual Perception
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  • 44
    Publication Date: 2008-05-31
    Description: Close relatedness has long been considered crucial to the evolution of eusociality. However, it has recently been suggested that close relatedness may be a consequence, rather than a cause, of eusociality. We tested this idea with a comparative analysis of female mating frequencies in 267 species of eusocial bees, wasps, and ants. We found that mating with a single male, which maximizes relatedness, is ancestral for all eight independent eusocial lineages that we investigated. Mating with multiple males is always derived. Furthermore, we found that high polyandry (〉2 effective mates) occurs only in lineages whose workers have lost reproductive totipotency. These results provide the first evidence that monogamy was critical in the evolution of eusociality, strongly supporting the prediction of inclusive fitness theory.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hughes, William O H -- Oldroyd, Benjamin P -- Beekman, Madeleine -- Ratnieks, Francis L W -- New York, N.Y. -- Science. 2008 May 30;320(5880):1213-6. doi: 10.1126/science.1156108.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute of Integrative and Comparative Biology, University of Leeds, Leeds, LS2 9JT, UK. w.o.h.hughes@leeds.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18511689" target="_blank"〉PubMed〈/a〉
    Keywords: Altruism ; Animals ; Ants ; Bees ; *Biological Evolution ; Female ; Male ; Phylogeny ; *Sexual Behavior, Animal ; *Social Behavior ; Sociobiology ; Wasps
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  • 45
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-07-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holden, Constance -- New York, N.Y. -- Science. 2008 Jul 25;321(5888):487. doi: 10.1126/science.321.5888.487a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18653860" target="_blank"〉PubMed〈/a〉
    Keywords: Brain/*anatomy & histology ; Cephalometry ; Female ; *Friends ; Head/anatomy & histology ; Humans ; Intelligence ; Male ; Organ Size ; Personality ; *Social Behavior
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  • 46
    Publication Date: 2008-07-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hyde, Janet S -- Lindberg, Sara M -- Linn, Marcia C -- Ellis, Amy B -- Williams, Caroline C -- New York, N.Y. -- Science. 2008 Jul 25;321(5888):494-5. doi: 10.1126/science.1160364.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychology, University of Wisconsin, 1202 West Johnson Street, Madison, WI 53706, USA. jshyde@wisc.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18653867" target="_blank"〉PubMed〈/a〉
    Keywords: *Achievement ; Adolescent ; Aptitude ; Career Choice ; Child ; Educational Measurement ; Ethnic Groups ; Female ; Humans ; *Learning ; Male ; *Mathematics ; Problem Solving ; *Sex Characteristics
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  • 47
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-08-02
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cho, Adrian -- New York, N.Y. -- Science. 2008 Aug 1;321(5889):625. doi: 10.1126/science.321.5889.625a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18669830" target="_blank"〉PubMed〈/a〉
    Keywords: *Athletic Performance ; *Body Temperature ; Cold Temperature ; Female ; Humans ; Male ; *Running
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  • 48
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-09-13
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stone, Richard -- New York, N.Y. -- Science. 2008 Sep 12;321(5895):1441. doi: 10.1126/science.321.5895.1441.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18787147" target="_blank"〉PubMed〈/a〉
    Keywords: Animal Migration ; Animals ; Asia ; *Birds/anatomy & histology/physiology ; Conservation of Natural Resources ; Crime ; *Extinction, Biological ; Female ; Male ; Population Dynamics ; Reproduction
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  • 49
    Publication Date: 2008-04-05
    Description: Whereas gamma-band neuronal oscillations clearly appear integral to visual attention, the role of lower-frequency oscillations is still being debated. Mounting evidence indicates that a key functional property of these oscillations is the rhythmic shifting of excitability in local neuronal ensembles. Here, we show that when attended stimuli are in a rhythmic stream, delta-band oscillations in the primary visual cortex entrain to the rhythm of the stream, resulting in increased response gain for task-relevant events and decreased reaction times. Because of hierarchical cross-frequency coupling, delta phase also determines momentary power in higher-frequency activity. These instrumental functions of low-frequency oscillations support a conceptual framework that integrates numerous earlier findings.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lakatos, Peter -- Karmos, George -- Mehta, Ashesh D -- Ulbert, Istvan -- Schroeder, Charles E -- MH060358/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2008 Apr 4;320(5872):110-3. doi: 10.1126/science.1154735.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Cognitive Neuroscience and Schizophrenia Program, Nathan Kline Institute, Orangeburg, NY 10962, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18388295" target="_blank"〉PubMed〈/a〉
    Keywords: Acoustic Stimulation ; Animals ; Attention/*physiology ; Cues ; Delta Rhythm ; Electroencephalography ; Electrophysiology ; Macaca fascicularis ; Male ; Neurons/*physiology ; Periodicity ; Photic Stimulation ; Reaction Time ; Visual Cortex/*physiology ; Visual Perception
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  • 50
    Publication Date: 2008-12-17
    Description: Helgason et al. (Reports, 8 February 2008, p. 813) reported a positive association between kinship and fertility in the Icelandic population. We point out that the data further suggest that fertility initially increases with kinship and then decays. This is supported by another large study on the Danish population suggesting a superposition of effects of inbreeding and outbreeding depression on human fertility.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Labouriau, Rodrigo -- Amorim, Antonio -- New York, N.Y. -- Science. 2008 Dec 12;322(5908):1634; author reply 1634. doi: 10.1126/science.1161907.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Genetics and Biotechnology, Faculty of Agricultural Sciences, Aarhus University, DK-8830 Tjele, Denmark. rodrigo.labouriau@agrsci.dk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19074330" target="_blank"〉PubMed〈/a〉
    Keywords: Consanguinity ; Denmark ; *Family ; *Family Characteristics ; Female ; *Fertility ; Humans ; Iceland ; Male ; Socioeconomic Factors
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  • 51
    Publication Date: 2008-11-22
    Description: Metabolic regulation in mammals requires communication between multiple organs and tissues. The rise in the incidence of obesity and associated metabolic disorders, including type 2 diabetes, has renewed interest in interorgan communication. We used mouse models to explore the mechanism whereby obesity enhances pancreatic beta cell mass, pathophysiological compensation for insulin resistance. We found that hepatic activation of extracellular regulated kinase (ERK) signaling induced pancreatic beta cell proliferation through a neuronal-mediated relay of metabolic signals. This metabolic relay from the liver to the pancreas is involved in obesity-induced islet expansion. In mouse models of insulin-deficient diabetes, liver-selective activation of ERK signaling increased beta cell mass and normalized serum glucose levels. Thus, interorgan metabolic relay systems may serve as valuable targets in regenerative treatments for diabetes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Imai, Junta -- Katagiri, Hideki -- Yamada, Tetsuya -- Ishigaki, Yasushi -- Suzuki, Toshinobu -- Kudo, Hirohito -- Uno, Kenji -- Hasegawa, Yutaka -- Gao, Junhong -- Kaneko, Keizo -- Ishihara, Hisamitsu -- Niijima, Akira -- Nakazato, Masamitsu -- Asano, Tomoichiro -- Minokoshi, Yasuhiko -- Oka, Yoshitomo -- New York, N.Y. -- Science. 2008 Nov 21;322(5905):1250-4. doi: 10.1126/science.1163971.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Molecular Metabolism and Diabetes, Tohoku University Graduate School of Medicine, Sendai 980-8575, Japan.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19023081" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Proliferation ; Central Nervous System/metabolism ; Diabetes Mellitus, Experimental/metabolism ; Hyperplasia ; Insulin/metabolism ; Insulin Resistance ; Insulin-Secreting Cells/*metabolism/pathology ; Liver/*metabolism ; MAP Kinase Kinase 1/*metabolism ; *MAP Kinase Signaling System ; Male ; Mice ; Mice, Inbred C57BL ; Neurons/*metabolism ; Obesity/*metabolism ; Pancreas/innervation ; Recombinant Proteins/metabolism ; Vagus Nerve/cytology/metabolism ; Xenopus
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  • 52
    Publication Date: 2008-08-09
    Description: Parasitism can be a major constraint on host condition and an important selective force. Theoretical and empirical evidence shows that maternal condition affects relative investment in sons and daughters; however, the effect of parasitism on sex ratio in vertebrates is seldom considered. We demonstrate experimentally that parasitism constrains the ability of mothers to rear sons in a long-lived seabird, the European shag Phalacrocorax aristotelis. The effect contributes to the decline in offspring survival as the breeding season progresses and hence has important population-level consequences for this, and potentially other, seasonal breeders.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Reed, T E -- Daunt, F -- Hall, M E -- Phillips, R A -- Wanless, S -- Cunningham, E J A -- New York, N.Y. -- Science. 2008 Sep 19;321(5896):1681-2. doi: 10.1126/science.1159466. Epub 2008 Aug 7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute of Evolutionary Biology, University of Edinburgh, Edinburgh EH9 3JT, UK. tomreed@u.washington.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18687923" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antinematodal Agents/therapeutic use ; Ascaridida Infections/drug therapy/physiopathology/*veterinary ; Ascaridoidea ; Bird Diseases/drug therapy/*physiopathology ; Birds/*parasitology/*physiology ; Feeding Behavior ; Female ; Ivermectin/*therapeutic use ; Male ; *Nesting Behavior ; Reproduction ; Sex Characteristics ; *Sex Ratio ; Survival Rate
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 53
    Publication Date: 2008-12-17
    Description: Models of cognitive control posit a key modulatory role for the pontine locus coeruleus-norepinephrine (LC-NE) system. In nonhuman primates, phasic LC-NE activity confers adaptive adjustments in cortical gain in task-relevant brain networks, and in performance, on a trial-by-trial basis. This model has remained untested in humans. We used the pharmacological agent modafinil to promote low-tonic/high-phasic LC-NE activity in healthy humans performing a cognitive control task during event-related functional magnetic resonance imaging (fMRI). Modafanil administration was associated with decreased task-independent, tonic LC activity, increased task-related LC and prefrontal cortex (PFC) activity, and enhanced LC-PFC functional connectivity. These results confirm in humans the role of the LC-NE system in PFC function and cognitive control and suggest a mechanism for therapeutic action of procognitive noradrenergic agents.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Minzenberg, Michael J -- Watrous, Andrew J -- Yoon, Jong H -- Ursu, Stefan -- Carter, Cameron S -- MH059883/MH/NIMH NIH HHS/ -- UL1 RR024146/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 2008 Dec 12;322(5908):1700-2. doi: 10.1126/science.1164908.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychiatry, University of California, Davis School of Medicine, Sacramento, CA, USA. michael.minzenberg@ucdmc.ucdavis.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19074351" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Benzhydryl Compounds/administration & dosage/*pharmacology ; Brain Mapping ; Central Nervous System Stimulants/pharmacology ; *Cognition/drug effects ; Female ; Humans ; Locus Coeruleus/drug effects/*physiology ; Magnetic Resonance Imaging ; Male ; Neurons/drug effects/physiology ; Norepinephrine/*metabolism ; Norepinephrine Plasma Membrane Transport Proteins/antagonists & ; inhibitors/metabolism ; Prefrontal Cortex/physiology ; Task Performance and Analysis
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  • 54
    Publication Date: 2008-05-31
    Description: The question of how the human brain represents conceptual knowledge has been debated in many scientific fields. Brain imaging studies have shown that different spatial patterns of neural activation are associated with thinking about different semantic categories of pictures and words (for example, tools, buildings, and animals). We present a computational model that predicts the functional magnetic resonance imaging (fMRI) neural activation associated with words for which fMRI data are not yet available. This model is trained with a combination of data from a trillion-word text corpus and observed fMRI data associated with viewing several dozen concrete nouns. Once trained, the model predicts fMRI activation for thousands of other concrete nouns in the text corpus, with highly significant accuracies over the 60 nouns for which we currently have fMRI data.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mitchell, Tom M -- Shinkareva, Svetlana V -- Carlson, Andrew -- Chang, Kai-Min -- Malave, Vicente L -- Mason, Robert A -- Just, Marcel Adam -- New York, N.Y. -- Science. 2008 May 30;320(5880):1191-5. doi: 10.1126/science.1152876.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Machine Learning Department, School of Computer Science, Carnegie Mellon University, Pittsburgh, PA 15213, USA. Tom.Mitchell@cs.cmu.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18511683" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Brain/*physiology ; Brain Mapping ; Computational Biology ; Female ; Humans ; *Language ; Magnetic Resonance Imaging ; Male ; Models, Neurological ; Models, Statistical ; Semantics ; Speech Perception/*physiology
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  • 55
    Publication Date: 2008-07-26
    Description: Duane's retraction syndrome (DRS) is a complex congenital eye movement disorder caused by aberrant innervation of the extraocular muscles by axons of brainstem motor neurons. Studying families with a variant form of the disorder (DURS2-DRS), we have identified causative heterozygous missense mutations in CHN1, a gene on chromosome 2q31 that encodes alpha2-chimaerin, a Rac guanosine triphosphatase-activating protein (RacGAP) signaling protein previously implicated in the pathfinding of corticospinal axons in mice. We found that these are gain-of-function mutations that increase alpha2-chimaerin RacGAP activity in vitro. Several of the mutations appeared to enhance alpha2-chimaerin translocation to the cell membrane or enhance its ability to self-associate. Expression of mutant alpha2-chimaerin constructs in chick embryos resulted in failure of oculomotor axons to innervate their target extraocular muscles. We conclude that alpha2-chimaerin has a critical developmental function in ocular motor axon pathfinding.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2593867/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2593867/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Miyake, Noriko -- Chilton, John -- Psatha, Maria -- Cheng, Long -- Andrews, Caroline -- Chan, Wai-Man -- Law, Krystal -- Crosier, Moira -- Lindsay, Susan -- Cheung, Michelle -- Allen, James -- Gutowski, Nick J -- Ellard, Sian -- Young, Elizabeth -- Iannaccone, Alessandro -- Appukuttan, Binoy -- Stout, J Timothy -- Christiansen, Stephen -- Ciccarelli, Maria Laura -- Baldi, Alfonso -- Campioni, Mara -- Zenteno, Juan C -- Davenport, Dominic -- Mariani, Laura E -- Sahin, Mustafa -- Guthrie, Sarah -- Engle, Elizabeth C -- G9900837/Medical Research Council/United Kingdom -- G9900989/Medical Research Council/United Kingdom -- R01 EY015298/EY/NEI NIH HHS/ -- R01 EY015298-01/EY/NEI NIH HHS/ -- R01 EY015298-02/EY/NEI NIH HHS/ -- R01 EY015298-03/EY/NEI NIH HHS/ -- R01 EY015298-04/EY/NEI NIH HHS/ -- R01 EY015298-05/EY/NEI NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2008 Aug 8;321(5890):839-43. doi: 10.1126/science.1156121. Epub 2008 Jul 24.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Medicine (Genetics), Children's Hospital Boston, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18653847" target="_blank"〉PubMed〈/a〉
    Keywords: Abducens Nerve/abnormalities ; Amino Acid Sequence ; Animals ; Axons/physiology ; Cell Line ; Cell Membrane/metabolism ; Chick Embryo ; Chimerin 1/chemistry/*genetics/*metabolism ; Duane Retraction Syndrome/*genetics ; Female ; Gene Expression Profiling ; Heterozygote ; Humans ; Male ; Molecular Sequence Data ; *Mutation, Missense ; Oculomotor Muscles/embryology/innervation/metabolism ; Oculomotor Nerve/abnormalities/embryology ; Pedigree
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  • 56
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-01-05
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rice, William R -- Friberg, Urban -- New York, N.Y. -- Science. 2008 Jan 4;319(5859):42-3. doi: 10.1126/science.1153482.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Ecology, Evolution, and Marine Biology, University of California, Santa Barbara, CA 93106, USA. rice@lifesci.ucsb.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18174425" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Evolution ; Drosophila melanogaster/*genetics ; Female ; *Gene Expression Regulation ; Gene Silencing ; Genes, Insect ; Male ; Mutation ; Selection, Genetic ; Y Chromosome/*genetics
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  • 57
    Publication Date: 2008-06-07
    Description: The brain processes objects through a series of regions along the ventral visual pathway, but the circuitry subserving the analysis of specific complex forms remains unknown. One complex form category, faces, selectively activates six patches of cortex in the macaque ventral pathway. To identify the connectivity of these face patches, we used electrical microstimulation combined with simultaneous functional magnetic resonance imaging. Stimulation of each of four targeted face patches produced strong activation, specifically within a subset of the other face patches. Stimulation outside the face patches produced an activation pattern that spared the face patches. These results suggest that the face patches form a strongly and specifically interconnected hierarchical network.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Moeller, Sebastian -- Freiwald, Winrich A -- Tsao, Doris Y -- New York, N.Y. -- Science. 2008 Jun 6;320(5881):1355-9. doi: 10.1126/science.1157436.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute for Brain Research and Center for Advanced Imaging, University of Bremen, Post Office Box 330440, D-28334 Bremen, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18535247" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Brain Mapping ; Electric Stimulation ; Electrophysiology ; *Face ; *Form Perception ; Macaca mulatta ; Magnetic Resonance Imaging ; Male ; Pattern Recognition, Visual ; Photic Stimulation ; Recognition (Psychology) ; Temporal Lobe/anatomy & histology/*physiology ; Visual Pathways
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  • 58
    Publication Date: 2008-11-01
    Description: To equalize X-chromosome dosages between the sexes, the female mammal inactivates one of her two X chromosomes. X-chromosome inactivation (XCI) is initiated by expression of Xist, a 17-kb noncoding RNA (ncRNA) that accumulates on the X in cis. Because interacting factors have not been isolated, the mechanism by which Xist induces silencing remains unknown. We discovered a 1.6-kilobase ncRNA (RepA) within Xist and identified the Polycomb complex, PRC2, as its direct target. PRC2 is initially recruited to the X by RepA RNA, with Ezh2 serving as the RNA binding subunit. The antisense Tsix RNA inhibits this interaction. RepA depletion abolishes full-length Xist induction and trimethylation on lysine 27 of histone H3 of the X. Likewise, PRC2 deficiency compromises Xist up-regulation. Therefore, RepA, together with PRC2, is required for the initiation and spread of XCI. We conclude that a ncRNA cofactor recruits Polycomb complexes to their target locus.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2748911/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2748911/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zhao, Jing -- Sun, Bryan K -- Erwin, Jennifer A -- Song, Ji-Joon -- Lee, Jeannie T -- R01 GM058839/GM/NIGMS NIH HHS/ -- R01 GM058839-10/GM/NIGMS NIH HHS/ -- R01 GM110090/GM/NIGMS NIH HHS/ -- R01GM58839/GM/NIGMS NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2008 Oct 31;322(5902):750-6. doi: 10.1126/science.1163045.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18974356" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Differentiation ; Cell Line ; Chromatin Immunoprecipitation ; Electrophoretic Mobility Shift Assay ; Embryonic Stem Cells ; Female ; Fibroblasts ; Male ; Mice ; Mice, Transgenic ; Molecular Sequence Data ; Polycomb-Group Proteins ; Polymerase Chain Reaction ; RNA, Long Noncoding ; RNA, Untranslated/genetics/*metabolism ; Repetitive Sequences, Nucleic Acid ; Repressor Proteins/*metabolism ; Up-Regulation ; X Chromosome/*metabolism ; X Chromosome Inactivation
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  • 59
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-12-06
    Description: Experiments have shown that punishment enhances socially beneficial cooperation but that the costs of punishment outweigh the gains from cooperation. This challenges evolutionary models of altruistic cooperation and punishment, which predict that punishment will be beneficial. We compared 10- and 50-period cooperation experiments. With the longer time horizon, punishment is unambiguously beneficial.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gachter, Simon -- Renner, Elke -- Sefton, Martin -- New York, N.Y. -- Science. 2008 Dec 5;322(5907):1510. doi: 10.1126/science.1164744.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Centre for Decision Research and Experimental Economics, University of Nottingham, School of Economics, Sir Clive Granger Building, University Park, Nottingham NG7 2RD, UK. simon.gaechter@nottingham.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19056978" target="_blank"〉PubMed〈/a〉
    Keywords: *Cooperative Behavior ; Female ; Games, Experimental ; Humans ; Male ; *Punishment ; Young Adult
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  • 60
    Publication Date: 2008-05-20
    Description: Development of axonal tracts requires interactions between growth cones and the environment. Tracts such as the anterior commissure and internal capsule are defective in mice with null mutation of Celsr3. We generated a conditional Celsr3 allele, allowing regional inactivation. Inactivation in telencephalon, ventral forebrain, or cortex demonstrated essential roles for Celsr3 in neurons that project axons to the anterior commissure and subcerebral targets, as well as in cells that guide axons through the internal capsule. When Celsr3 was inactivated in cortex, subcerebral projections failed to grow, yet corticothalamic axons developed normally, indicating that besides guidepost cells, additional Celsr3-independent cues can assist their progression. These observations provide in vivo evidence that Celsr3-mediated interactions between axons and guidepost cells govern axonal tract formation in mammals.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2746700/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2746700/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zhou, Libing -- Bar, Isabelle -- Achouri, Younes -- Campbell, Kenneth -- De Backer, Olivier -- Hebert, Jean M -- Jones, Kevin -- Kessaris, Nicoletta -- de Rouvroit, Catherine Lambert -- O'Leary, Dennis -- Richardson, William D -- Goffinet, Andre M -- Tissir, Fadel -- G0501173/Medical Research Council/United Kingdom -- G0800575/Medical Research Council/United Kingdom -- G9708005/Medical Research Council/United Kingdom -- R01 MH086147/MH/NIMH NIH HHS/ -- R01 MH086147-05/MH/NIMH NIH HHS/ -- R37 NS031558/NS/NINDS NIH HHS/ -- R37 NS031558-15/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 2008 May 16;320(5878):946-9. doi: 10.1126/science.1155244.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Developmental Neurobiology, Universite Catholique de Louvain, 1200 Bruxelles, Belgique.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18487195" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Axons/*physiology ; Cadherins/*genetics/*physiology ; Cerebral Cortex/cytology/embryology ; Female ; Gene Silencing ; Internal Capsule/cytology/embryology/physiology ; Male ; Mice ; Neural Pathways/*embryology/physiology ; Neurons/*physiology ; Prosencephalon/cytology/*embryology/physiology ; Receptors, Cell Surface/*genetics/*physiology ; Septal Nuclei/embryology/physiology ; Thalamus/cytology/embryology ; Tissue Culture Techniques
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  • 61
    Publication Date: 2008-08-23
    Description: Common wisdom holds that choice decisions are based on conscious deliberations of the available information about choice options. On the basis of recent insights about unconscious influences on information processing, we tested whether automatic mental associations of undecided individuals bias future choices in a manner such that these choices reflect the evaluations implied by earlier automatic associations. With the use of a computer-based, speeded categorization task to assess automatic mental associations (i.e., associations that are activated unintentionally, difficult to control, and not necessarily endorsed at a conscious level) and self-report measures to assess consciously endorsed beliefs and choice preferences, automatic associations of undecided participants predicted changes in consciously reported beliefs and future choices over a period of 1 week. Conversely, for decided participants, consciously reported beliefs predicted changes in automatic associations and future choices over the same period. These results indicate that decision-makers sometimes have already made up their mind at an unconscious level, even when they consciously indicate that they are still undecided.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Galdi, Silvia -- Arcuri, Luciano -- Gawronski, Bertram -- New York, N.Y. -- Science. 2008 Aug 22;321(5892):1100-2. doi: 10.1126/science.1160769.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Developmental Psychology and Socialization, University of Padova, Via Venezia 8, 35131 Padova, Italy. silvia.galdi@unipd.it〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18719288" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Aged ; Attitude ; *Choice Behavior ; Culture ; *Decision Making ; Female ; Humans ; Longitudinal Studies ; Male ; *Mental Processes ; Middle Aged ; Politics ; *Unconscious (Psychology)
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  • 62
    Publication Date: 2008-09-20
    Description: Using sensory information for the prediction of future events is essential for survival. Midbrain dopamine neurons are activated by environmental cues that predict rewards, but the cellular mechanisms that underlie this phenomenon remain elusive. We used in vivo voltammetry and in vitro patch-clamp electrophysiology to show that both dopamine release to reward predictive cues and enhanced synaptic strength onto dopamine neurons develop over the course of cue-reward learning. Increased synaptic strength was not observed after stable behavioral responding. Thus, enhanced synaptic strength onto dopamine neurons may act to facilitate the transformation of neutral environmental stimuli to salient reward-predictive cues.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2613864/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2613864/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stuber, Garret D -- Klanker, Marianne -- de Ridder, Bram -- Bowers, M Scott -- Joosten, Ruud N -- Feenstra, Matthijs G -- Bonci, Antonello -- DA015096/DA/NIDA NIH HHS/ -- DA021937/DA/NIDA NIH HHS/ -- R01 DA015096/DA/NIDA NIH HHS/ -- R01 DA015096-06/DA/NIDA NIH HHS/ -- New York, N.Y. -- Science. 2008 Sep 19;321(5896):1690-2. doi: 10.1126/science.1160873.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Ernest Gallo Clinic and Research Center, Department of Neurology, University of California, San Francisco, Emeryville, CA 94608, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18802002" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Conditioning (Psychology) ; Cues ; Dopamine/*physiology ; Excitatory Postsynaptic Potentials ; *Learning ; Long-Term Potentiation ; Male ; Mesencephalon/cytology/*physiology ; Neurons/*physiology ; Nucleus Accumbens/*physiology ; Patch-Clamp Techniques ; Rats ; Receptors, AMPA/metabolism ; Receptors, N-Methyl-D-Aspartate/metabolism ; *Reward ; Signal Transduction ; Synapses/*physiology ; Synaptic Transmission
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  • 63
    Publication Date: 2008-05-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Morell, Virginia -- New York, N.Y. -- Science. 2008 May 9;320(5877):742-3. doi: 10.1126/science.320.5877.742.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18467568" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Animals, Wild ; *Conservation of Natural Resources ; Female ; Male ; Population Dynamics
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  • 64
    Publication Date: 2008-01-12
    Description: Angiogenesis-mediated progression of micrometastasis to lethal macrometastasis is the major cause of death in cancer patients. Here, using mouse models of pulmonary metastasis, we identify bone marrow (BM)-derived endothelial progenitor cells (EPCs) as critical regulators of this angiogenic switch. We show that tumors induce expression of the transcription factor Id1 in the EPCs and that suppression of Id1 after metastatic colonization blocked EPC mobilization, caused angiogenesis inhibition, impaired pulmonary macrometastases, and increased survival of tumor-bearing animals. These findings establish the role of EPCs in metastatic progression in preclinical models and suggest that selective targeting of EPCs may merit investigation as a therapy for cancer patients with lung metastases.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gao, Dingcheng -- Nolan, Daniel J -- Mellick, Albert S -- Bambino, Kathryn -- McDonnell, Kevin -- Mittal, Vivek -- New York, N.Y. -- Science. 2008 Jan 11;319(5860):195-8. doi: 10.1126/science.1150224.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Cancer Genome Research Center, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18187653" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bone Marrow Cells/cytology/physiology ; Carcinoma, Lewis Lung/*blood supply/pathology/*secondary ; Disease Progression ; Endothelial Cells/cytology/*physiology ; Female ; Gene Expression ; Inhibitor of Differentiation Protein 1/genetics/metabolism ; Lung Neoplasms/blood supply/pathology/*secondary ; Male ; Mammary Neoplasms, Animal/blood supply/pathology ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Neoplasm Metastasis/*pathology ; Neoplasm Transplantation ; *Neovascularization, Pathologic ; Stem Cells/cytology/*physiology
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  • 65
    Publication Date: 2008-04-05
    Description: Recent experiments with rats suggest that they show episodic-like or what-where-when memory for a preferred food found on a radial maze. Although memory for when a salient event occurred suggests that rats can mentally travel in time to a moment in the past, an alternative possibility is that they remember how long ago the food was found. Three groups of rats were tested for memory of previously encountered food. The different groups could use only the cues of when, how long ago, or when + how long ago. Only the cue of how long ago food was encountered was used successfully. These results suggest that episodic-like memory in rats is qualitatively different from human episodic memory.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Roberts, William A -- Feeney, Miranda C -- Macpherson, Krista -- Petter, Mark -- McMillan, Neil -- Musolino, Evanya -- New York, N.Y. -- Science. 2008 Apr 4;320(5872):113-5. doi: 10.1126/science.1152709.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychology, University of Western Ontario, London, Ontario, N6A 5C2, Canada. roberts@uwo.ca〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18388296" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cues ; Male ; Maze Learning ; *Memory ; Random Allocation ; Rats ; Rats, Long-Evans ; Time Factors
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 66
    Publication Date: 2008-07-16
    Description: To find inherited causes of autism-spectrum disorders, we studied families in which parents share ancestors, enhancing the role of inherited factors. We mapped several loci, some containing large, inherited, homozygous deletions that are likely mutations. The largest deletions implicated genes, including PCDH10 (protocadherin 10) and DIA1 (deleted in autism1, or c3orf58), whose level of expression changes in response to neuronal activity, a marker of genes involved in synaptic changes that underlie learning. A subset of genes, including NHE9 (Na+/H+ exchanger 9), showed additional potential mutations in patients with unrelated parents. Our findings highlight the utility of "homozygosity mapping" in heterogeneous disorders like autism but also suggest that defective regulation of gene expression after neural activity may be a mechanism common to seemingly diverse autism mutations.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586171/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586171/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Morrow, Eric M -- Yoo, Seung-Yun -- Flavell, Steven W -- Kim, Tae-Kyung -- Lin, Yingxi -- Hill, Robert Sean -- Mukaddes, Nahit M -- Balkhy, Soher -- Gascon, Generoso -- Hashmi, Asif -- Al-Saad, Samira -- Ware, Janice -- Joseph, Robert M -- Greenblatt, Rachel -- Gleason, Danielle -- Ertelt, Julia A -- Apse, Kira A -- Bodell, Adria -- Partlow, Jennifer N -- Barry, Brenda -- Yao, Hui -- Markianos, Kyriacos -- Ferland, Russell J -- Greenberg, Michael E -- Walsh, Christopher A -- 1K01MH71801/MH/NIMH NIH HHS/ -- 1K23MH080954-01/MH/NIMH NIH HHS/ -- 1R01 MH083565/MH/NIMH NIH HHS/ -- 5P30HD018655-26/HD/NICHD NIH HHS/ -- 5R01NS048276-05/NS/NINDS NIH HHS/ -- K01 MH071801/MH/NIMH NIH HHS/ -- K01 MH071801-04/MH/NIMH NIH HHS/ -- K01 MH071801-05/MH/NIMH NIH HHS/ -- K23 MH080954/MH/NIMH NIH HHS/ -- K23 MH080954-01/MH/NIMH NIH HHS/ -- MH64547/MH/NIMH NIH HHS/ -- N01-HG-65403/HG/NHGRI NIH HHS/ -- R01 MH083565/MH/NIMH NIH HHS/ -- R01 NS048276/NS/NINDS NIH HHS/ -- R01 NS048276-01/NS/NINDS NIH HHS/ -- R01 NS048276-02/NS/NINDS NIH HHS/ -- R01 NS048276-03/NS/NINDS NIH HHS/ -- R01 NS048276-04/NS/NINDS NIH HHS/ -- R01 NS048276-05/NS/NINDS NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2008 Jul 11;321(5886):218-23. doi: 10.1126/science.1157657.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Genetics, Children's Hospital Boston and Harvard Medical School, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18621663" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptor Proteins, Signal Transducing/genetics ; Animals ; Autistic Disorder/*genetics/physiopathology ; Brain/metabolism ; Cadherins/genetics ; *Chromosome Mapping ; Consanguinity ; Female ; Gene Deletion ; Gene Dosage ; Gene Expression Regulation ; Genes, Recessive ; Genetic Predisposition to Disease ; Homozygote ; Humans ; Lod Score ; Male ; *Mutation ; Neurons/physiology ; Oligonucleotide Array Sequence Analysis ; Pedigree ; Polymorphism, Single Nucleotide ; Rats ; Sodium-Hydrogen Antiporter/genetics ; Transcription Factors/genetics/metabolism
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  • 67
    Publication Date: 2008-09-27
    Description: Almost two decades after CFTR was identified as the gene responsible for cystic fibrosis (CF), we still lack answers to many questions about the pathogenesis of the disease, and it remains incurable. Mice with a disrupted CFTR gene have greatly facilitated CF studies, but the mutant mice do not develop the characteristic manifestations of human CF, including abnormalities of the pancreas, lung, intestine, liver, and other organs. Because pigs share many anatomical and physiological features with humans, we generated pigs with a targeted disruption of both CFTR alleles. Newborn pigs lacking CFTR exhibited defective chloride transport and developed meconium ileus, exocrine pancreatic destruction, and focal biliary cirrhosis, replicating abnormalities seen in newborn humans with CF. The pig model may provide opportunities to address persistent questions about CF pathogenesis and accelerate discovery of strategies for prevention and treatment.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2570747/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2570747/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rogers, Christopher S -- Stoltz, David A -- Meyerholz, David K -- Ostedgaard, Lynda S -- Rokhlina, Tatiana -- Taft, Peter J -- Rogan, Mark P -- Pezzulo, Alejandro A -- Karp, Philip H -- Itani, Omar A -- Kabel, Amanda C -- Wohlford-Lenane, Christine L -- Davis, Greg J -- Hanfland, Robert A -- Smith, Tony L -- Samuel, Melissa -- Wax, David -- Murphy, Clifton N -- Rieke, August -- Whitworth, Kristin -- Uc, Aliye -- Starner, Timothy D -- Brogden, Kim A -- Shilyansky, Joel -- McCray, Paul B Jr -- Zabner, Joseph -- Prather, Randall S -- Welsh, Michael J -- AI076671/AI/NIAID NIH HHS/ -- DK54759/DK/NIDDK NIH HHS/ -- HL07638/HL/NHLBI NIH HHS/ -- HL51670/HL/NHLBI NIH HHS/ -- K08 AI076671/AI/NIAID NIH HHS/ -- K08 AI076671-01/AI/NIAID NIH HHS/ -- P01 HL051670/HL/NHLBI NIH HHS/ -- P01 HL051670-15/HL/NHLBI NIH HHS/ -- P30 DK054759/DK/NIDDK NIH HHS/ -- P30 DK054759-10/DK/NIDDK NIH HHS/ -- P30 DK054759-109004/DK/NIDDK NIH HHS/ -- R01 DK051315/DK/NIDDK NIH HHS/ -- T32 HL007638/HL/NHLBI NIH HHS/ -- T32 HL007638-23/HL/NHLBI NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2008 Sep 26;321(5897):1837-41. doi: 10.1126/science.1163600.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Internal Medicine, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18818360" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Newborn ; Chlorides/metabolism ; *Cystic Fibrosis/genetics/pathology/physiopathology ; Cystic Fibrosis Transmembrane Conductance Regulator/*genetics/metabolism ; *Disease Models, Animal ; Female ; Gallbladder/pathology ; Ileus/pathology/physiopathology ; Intestines/pathology ; Ion Transport ; Liver/pathology ; Liver Cirrhosis, Biliary/pathology ; Lung/pathology ; Male ; Pancreas, Exocrine/pathology ; Recombination, Genetic ; *Swine
    Print ISSN: 0036-8075
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  • 68
    Publication Date: 2008-03-29
    Description: The synaptic response waveform, which determines signal integration properties in the brain, depends on the spatiotemporal profile of neurotransmitter in the synaptic cleft. Here, we show that electrophoretic interactions between AMPA receptor-mediated excitatory currents and negatively charged glutamate molecules accelerate the clearance of glutamate from the synaptic cleft, speeding up synaptic responses. This phenomenon is reversed upon depolarization and diminished when intracleft electric fields are weakened through a decrease in the AMPA receptor density. In contrast, the kinetics of receptor-mediated currents evoked by direct application of glutamate are voltage-independent, as are synaptic currents mediated by the electrically neutral neurotransmitter GABA. Voltage-dependent temporal tuning of excitatory synaptic responses may thus contribute to signal integration in neural circuits.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2685065/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2685065/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sylantyev, Sergiy -- Savtchenko, Leonid P -- Niu, Yin-Ping -- Ivanov, Anton I -- Jensen, Thomas P -- Kullmann, Dimitri M -- Xiao, Min-Yi -- Rusakov, Dmitri A -- 071179/Wellcome Trust/United Kingdom -- G0400627/Medical Research Council/United Kingdom -- G0400627(71256)/Medical Research Council/United Kingdom -- G0400627(76527)/Medical Research Council/United Kingdom -- G0600368/Medical Research Council/United Kingdom -- G0600368(77987)/Medical Research Council/United Kingdom -- G116/147/Medical Research Council/United Kingdom -- Medical Research Council/United Kingdom -- Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 2008 Mar 28;319(5871):1845-9. doi: 10.1126/science.1154330.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute of Neurology, University College London, Queen Square, London, WC1N 3BG, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18369150" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cells, Cultured ; Dendrites/physiology ; Diffusion ; Dipeptides/pharmacology ; *Excitatory Postsynaptic Potentials ; Glutamic Acid/*metabolism ; Magnesium/pharmacology ; Male ; Monte Carlo Method ; Patch-Clamp Techniques ; Pyramidal Cells/*physiology ; Quinoxalines/pharmacology ; Rats ; Rats, Sprague-Dawley ; Receptors, AMPA/antagonists & inhibitors/*metabolism ; Receptors, GABA/metabolism ; Synapses/*physiology ; gamma-Aminobutyric Acid/metabolism
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  • 69
    Publication Date: 2008-02-02
    Description: Recombination plays a crucial role in meiosis, ensuring the proper segregation of chromosomes. Recent linkage disequilibrium (LD) and sperm-typing studies suggest that recombination rates vary tremendously across the human genome, with most events occurring in narrow "hotspots." To examine variation in fine-scale recombination patterns among individuals, we used dense, genome-wide single-nucleotide polymorphism data collected in nuclear families to localize crossovers with high spatial resolution. This analysis revealed that overall recombination hotspot usage is similar in males and females, with individual hotspots often active in both sexes. Across the genome, roughly 60% of crossovers occurred in hotspots inferred from LD studies. Notably, however, we found extensive and heritable variation among both males and females in the proportion of crossovers occurring in these hotspots.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Coop, Graham -- Wen, Xiaoquan -- Ober, Carole -- Pritchard, Jonathan K -- Przeworski, Molly -- GM83098/GM/NIGMS NIH HHS/ -- HD21244/HD/NICHD NIH HHS/ -- HG002772/HG/NHGRI NIH HHS/ -- HL56399/HL/NHLBI NIH HHS/ -- HL56533/HL/NHLBI NIH HHS/ -- R01 HG002772/HG/NHGRI NIH HHS/ -- New York, N.Y. -- Science. 2008 Mar 7;319(5868):1395-8. doi: 10.1126/science.1151851. Epub 2008 Jan 31.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Human Genetics, University of Chicago, 920 East 58th Street, Cummings Life Science Center, Chicago, IL 60637, USA. gcoop@uchicago.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18239090" target="_blank"〉PubMed〈/a〉
    Keywords: *Crossing Over, Genetic ; Female ; Genetic Variation ; *Genome, Human ; Genotype ; Haplotypes ; Humans ; Linkage Disequilibrium ; Male ; Maternal Age ; Meiosis ; Paternal Age ; Pedigree ; Polymorphism, Single Nucleotide ; *Recombination, Genetic ; Sex Characteristics ; Transcription Initiation Site
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  • 70
    Publication Date: 2008-01-05
    Description: The paucity of polymorphisms in single-copy genes on the Y chromosome of Drosophila contrasts with data indicating that this chromosome has polymorphic phenotypic effects on sex ratio, temperature sensitivity, behavior, and fitness. We show that the Y chromosome of D. melanogaster harbors substantial genetic diversity in the form of polymorphisms for genetic elements that differentially affect the expression of hundreds of X-linked and autosomal genes. The affected genes are more highly expressed in males, more meagerly expressed in females, and more highly divergent between species. Functionally, they affect microtubule stability, lipid and mitochondrial metabolism, and the thermal sensitivity of spermatogenesis. Our findings provide a mechanism for adaptive phenotypic variation associated with the Y chromosome.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lemos, Bernardo -- Araripe, Luciana O -- Hartl, Daniel L -- GM065169/GM/NIGMS NIH HHS/ -- GM068465/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2008 Jan 4;319(5859):91-3. doi: 10.1126/science.1148861.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Organismic and Evolutionary Biology, Harvard University, 16 Divinity Avenue, Cambridge, MA 02138, USA. blemos@oeb.harvard.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18174442" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Evolution ; Climate ; DNA Transposable Elements ; Drosophila/*genetics/physiology ; Drosophila melanogaster/*genetics/physiology ; Epigenesis, Genetic ; Female ; *Gene Expression Regulation ; Genes, Insect ; Genetic Linkage ; Genetic Variation ; Heterochromatin/genetics ; Male ; *Polymorphism, Genetic ; Spermatogenesis ; Temperature ; Y Chromosome/*genetics
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  • 71
    Publication Date: 2008-02-16
    Description: Alcohol dependence is a major public health challenge in need of new treatments. As alcoholism evolves, stress systems in the brain play an increasing role in motivating continued alcohol use and relapse. We investigated the role of the neurokinin 1 receptor (NK1R), a mediator of behavioral stress responses, in alcohol dependence and treatment. In preclinical studies, mice genetically deficient in NK1R showed a marked decrease in voluntary alcohol consumption and had an increased sensitivity to the sedative effects of alcohol. In a randomized controlled experimental study, we treated recently detoxified alcoholic inpatients with an NK1R antagonist (LY686017; n = 25) or placebo (n = 25). LY686017 suppressed spontaneous alcohol cravings, improved overall well-being, blunted cravings induced by a challenge procedure, and attenuated concomitant cortisol responses. Brain functional magnetic resonance imaging responses to affective stimuli likewise suggested beneficial LY686017 effects. Thus, as assessed by these surrogate markers of efficacy, NK1R antagonism warrants further investigation as a treatment in alcoholism.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉George, David T -- Gilman, Jodi -- Hersh, Jacqueline -- Thorsell, Annika -- Herion, David -- Geyer, Christopher -- Peng, Xiaomei -- Kielbasa, William -- Rawlings, Robert -- Brandt, John E -- Gehlert, Donald R -- Tauscher, Johannes T -- Hunt, Stephen P -- Hommer, Daniel -- Heilig, Markus -- Intramural NIH HHS/ -- New York, N.Y. -- Science. 2008 Mar 14;319(5869):1536-9. doi: 10.1126/science.1153813. Epub 2008 Feb 14.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Clinical and Translational Studies, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD 20892, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18276852" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; *Alcohol Drinking/drug therapy ; Alcoholism/*drug therapy ; Animals ; Behavior, Addictive/drug therapy ; Brain/drug effects/physiology ; Emotions/drug effects ; Ethanol/administration & dosage/pharmacology ; Female ; Humans ; Hydrocortisone/blood ; Magnetic Resonance Imaging ; Male ; Mice ; Mice, Inbred C57BL ; Middle Aged ; *Neurokinin-1 Receptor Antagonists ; Pyridines/administration & dosage/pharmacology/*therapeutic use ; Receptors, Neurokinin-1/deficiency/genetics/*physiology ; Triazoles/administration & dosage/pharmacology/*therapeutic use
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  • 72
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-05-03
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2008 May 2;320(5876):606-7. doi: 10.1126/science.320.5876.606.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18451279" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Animals ; Blindness/genetics/*therapy ; Carrier Proteins/genetics ; Child ; Clinical Trials as Topic ; Dogs ; Eye Proteins/genetics ; *Genetic Therapy ; Humans ; Infant ; Male ; Retinal Diseases/genetics/*therapy ; cis-trans-Isomerases
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  • 73
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-09-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Leslie, Mitch -- New York, N.Y. -- Science. 2008 Sep 26;321(5897):1764-5. doi: 10.1126/science.321.5897.1764.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18818335" target="_blank"〉PubMed〈/a〉
    Keywords: *Aging/genetics ; Cause of Death ; Family ; Female ; Humans ; Life Style ; *Longevity/genetics ; Male
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  • 74
    Publication Date: 2008-12-17
    Description: A central goal of evolutionary biology is to identify the genes and evolutionary forces that cause speciation, the emergence of reproductive isolation between populations. Despite the identification of several genes that cause hybrid sterility or inviability-many of which have evolved rapidly under positive Darwinian selection-little is known about the ecological or genomic forces that drive the evolution of postzygotic isolation. Here, we show that the same gene, Overdrive, causes both male sterility and segregation distortion in F1 hybrids between the Bogota and U.S. subspecies of Drosophila pseudoobscura. This segregation distorter gene is essential for hybrid sterility, a strong reproductive barrier between these young taxa. Our results suggest that genetic conflict may be an important evolutionary force in speciation.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2628965/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2628965/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Phadnis, Nitin -- Orr, H Allen -- GM51932/GM/NIGMS NIH HHS/ -- R01 GM051932/GM/NIGMS NIH HHS/ -- R01 GM051932-13/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2009 Jan 16;323(5912):376-9. doi: 10.1126/science.1163934. Epub 2008 Dec 11.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biology, University of Rochester, Rochester, NY 14627-0211, USA. pdns@mail.rochester.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19074311" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Carrier Proteins/chemistry/*genetics/physiology ; Chromosome Mapping ; Chromosome Segregation/*genetics ; Crosses, Genetic ; Drosophila/*genetics ; Drosophila Proteins/chemistry/*genetics/physiology ; Female ; Gene Flow ; *Genes, Insect ; *Genetic Speciation ; *Hybridization, Genetic ; Infertility, Male/genetics ; Male ; Meiosis ; Microsatellite Repeats ; Molecular Sequence Data ; Sex Ratio ; Transgenes
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  • 75
    Publication Date: 2008-12-17
    Description: Speciation genes restrict gene flow between the incipient species and related taxa. Three decades ago, we mapped a mammalian speciation gene, hybrid sterility 1 (Hst1), in the intersubspecific hybrids of house mouse. Here, we identify this gene as Prdm9, encoding a histone H3 lysine 4 trimethyltransferase. We rescued infertility in male hybrids with bacterial artificial chromosomes carrying Prdm9 from a strain with the "fertility" Hst1(f) allele. Sterile hybrids display down-regulated microrchidia 2B (Morc2b) and fail to compartmentalize gammaH2AX into the pachynema sex (XY) body. These defects, seen also in Prdm9-null mutants, are rescued by the Prdm9 transgene. Identification of a vertebrate hybrid sterility gene reveals a role for epigenetics in speciation and opens a window to a hybrid sterility gene network.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mihola, Ondrej -- Trachtulec, Zdenek -- Vlcek, Cestmir -- Schimenti, John C -- Forejt, Jiri -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2009 Jan 16;323(5912):373-5. doi: 10.1126/science.1163601. Epub 2008 Dec 11.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, Videnska 1083, 142 20 Prague, Czech Republic.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19074312" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Chromosome Mapping ; Chromosomes, Artificial, Bacterial ; Crosses, Genetic ; Epigenesis, Genetic ; Female ; Gene Expression Regulation ; *Genetic Speciation ; Histone-Lysine N-Methyltransferase/chemistry/*genetics/*metabolism ; Histones/metabolism ; Hybridization, Genetic ; Infertility, Male/*genetics ; Male ; *Meiosis ; Methylation ; Mice ; Mice, Inbred C3H ; Mice, Transgenic ; Molecular Sequence Data ; Ovary/enzymology ; Testis/enzymology
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  • 76
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-12-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ley, Timothy J -- Hamilton, Barton H -- New York, N.Y. -- Science. 2008 Dec 5;322(5907):1472-4. doi: 10.1126/science.1165878.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Medicine, Washington University Medical School, St. Louis, MO 63130, USA. timley@wustl.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19056961" target="_blank"〉PubMed〈/a〉
    Keywords: *Biomedical Research/economics ; *Career Mobility ; Education, Graduate ; Education, Medical ; Female ; Humans ; Male ; National Institutes of Health (U.S.)/economics/*statistics & numerical data ; Research Support as Topic/*statistics & numerical data ; Sex Factors ; United States
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  • 77
    Publication Date: 2008-11-08
    Description: A number of large noncoding RNAs (ncRNAs) epigenetically silence genes through unknown mechanisms. The Air ncRNA is imprinted--monoallelically expressed from the paternal allele. Air is required for allele-specific silencing of the cis-linked Slc22a3, Slc22a2, and Igf2r genes in mouse placenta. We show that Air interacts with the Slc22a3 promoter chromatin and the H3K9 histone methyltransferase G9a in placenta. Air accumulates at the Slc22a3 promoter in correlation with localized H3K9 methylation and transcriptional repression. Genetic ablation of G9a results in nonimprinted, biallelic transcription of Slc22a3. Truncated Air fails to accumulate at the Slc22a3 promoter, which results in reduced G9a recruitment and biallelic transcription. Our results suggest that Air, and potentially other large ncRNAs, target repressive histone-modifying activities through molecular interaction with specific chromatin domains to epigenetically silence transcription.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nagano, Takashi -- Mitchell, Jennifer A -- Sanz, Lionel A -- Pauler, Florian M -- Ferguson-Smith, Anne C -- Feil, Robert -- Fraser, Peter -- BB/D014050/1/Biotechnology and Biological Sciences Research Council/United Kingdom -- BBS/E/B/0000C151/Biotechnology and Biological Sciences Research Council/United Kingdom -- G0400156/Medical Research Council/United Kingdom -- Biotechnology and Biological Sciences Research Council/United Kingdom -- Medical Research Council/United Kingdom -- New York, N.Y. -- Science. 2008 Dec 12;322(5908):1717-20. doi: 10.1126/science.1163802. Epub 2008 Nov 6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Chromatin and Gene Expression, Babraham Institute, Babraham Research Campus, Cambridge CB22 3AT, UK. takashi.nagano@bbsrc.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18988810" target="_blank"〉PubMed〈/a〉
    Keywords: Alleles ; Animals ; Chromatin/*metabolism ; Epigenesis, Genetic ; Female ; Genomic Imprinting ; Histone-Lysine N-Methyltransferase/*metabolism ; Histones/metabolism ; In Situ Hybridization, Fluorescence ; Male ; Methylation ; Mice ; Mice, Inbred BALB C ; Myocardium/metabolism ; Organic Cation Transport Proteins/*genetics ; Placenta/*metabolism ; Pregnancy ; Promoter Regions, Genetic ; *RNA Interference ; RNA, Untranslated/*genetics/metabolism ; *Transcription, Genetic
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  • 78
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-10-11
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Couzin, Jennifer -- New York, N.Y. -- Science. 2008 Oct 10;322(5899):180-1. doi: 10.1126/science.322.5899.180.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18845721" target="_blank"〉PubMed〈/a〉
    Keywords: Attitude ; *Data Collection ; Female ; Humans ; Male ; *Politics ; *Prejudice ; *Public Opinion ; United States
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  • 79
    Publication Date: 2008-05-31
    Description: The Paleo-Eskimo Saqqaq and Independence I cultures, documented from archaeological remains in Northern Canada and Greenland, represent the earliest human expansion into the New World's northern extremes. However, their origin and genetic relationship to later cultures are unknown. We sequenced a mitochondrial genome from a Paleo-Eskimo human by using 3400-to 4500-year-old frozen hair excavated from an early Greenlandic Saqqaq settlement. The sample is distinct from modern Native Americans and Neo-Eskimos, falling within haplogroup D2a1, a group previously observed among modern Aleuts and Siberian Sireniki Yuit. This result suggests that the earliest migrants into the New World's northern extremes derived from populations in the Bering Sea area and were not directly related to Native Americans or the later Neo-Eskimos that replaced them.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gilbert, M Thomas P -- Kivisild, Toomas -- Gronnow, Bjarne -- Andersen, Pernille K -- Metspalu, Ene -- Reidla, Maere -- Tamm, Erika -- Axelsson, Erik -- Gotherstrom, Anders -- Campos, Paula F -- Rasmussen, Morten -- Metspalu, Mait -- Higham, Thomas F G -- Schwenninger, Jean-Luc -- Nathan, Roger -- De Hoog, Cees-Jan -- Koch, Anders -- Moller, Lone Nukaaraq -- Andreasen, Claus -- Meldgaard, Morten -- Villems, Richard -- Bendixen, Christian -- Willerslev, Eske -- New York, N.Y. -- Science. 2008 Jun 27;320(5884):1787-9. doi: 10.1126/science.1159750. Epub 2008 May 29.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Ancient Genetics, Department of Biology, Universitetsparken 15, DK-2100 Copenhagen, Denmark.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18511654" target="_blank"〉PubMed〈/a〉
    Keywords: Asian Continental Ancestry Group/genetics ; DNA, Mitochondrial/*genetics ; Emigration and Immigration ; Female ; Genetics, Population ; *Genome, Mitochondrial ; Greenland ; Hair/chemistry ; Haplotypes ; History, Ancient ; Humans ; Indians, North American/genetics ; Inuits/classification/*genetics/history ; Male ; Molecular Sequence Data ; Polymorphism, Single Nucleotide ; Sequence Analysis, DNA
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  • 80
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-02-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2008 Feb 8;319(5864):754-5. doi: 10.1126/science.319.5864.754.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18258900" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Child ; Child, Preschool ; Cities ; *Education ; Female ; *Government Programs/economics ; *Health Promotion/economics ; Humans ; Infant ; Male ; Mexico ; New York City ; *Nutritional Status ; Poverty/*prevention & control ; Poverty Areas ; *Social Welfare/economics
    Print ISSN: 0036-8075
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  • 81
    Publication Date: 2008-09-13
    Description: Object recognition is challenging because each object produces myriad retinal images. Responses of neurons from the inferior temporal cortex (IT) are selective to different objects, yet tolerant ("invariant") to changes in object position, scale, and pose. How does the brain construct this neuronal tolerance? We report a form of neuronal learning that suggests the underlying solution. Targeted alteration of the natural temporal contiguity of visual experience caused specific changes in IT position tolerance. This unsupervised temporal slowness learning (UTL) was substantial, increased with experience, and was significant in single IT neurons after just 1 hour. Together with previous theoretical work and human object perception experiments, we speculate that UTL may reflect the mechanism by which the visual stream builds and maintains tolerant object representations.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3307055/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3307055/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Li, Nuo -- DiCarlo, James J -- R01 EY014970/EY/NEI NIH HHS/ -- R01 EY014970-01A1/EY/NEI NIH HHS/ -- R01-EY014970/EY/NEI NIH HHS/ -- New York, N.Y. -- Science. 2008 Sep 12;321(5895):1502-7. doi: 10.1126/science.1160028.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉McGovern Institute for Brain Research and Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18787171" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Form Perception ; *Learning ; Macaca mulatta ; Male ; Models, Neurological ; Neuronal Plasticity ; Neurons/*physiology ; Saccades ; Temporal Lobe/*physiology ; Visual Cortex/*physiology ; *Visual Perception
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  • 82
    Publication Date: 2008-03-29
    Description: Learning to associate sensory cues with threats is critical for minimizing aversive experience. The ecological benefit of associative learning relies on accurate perception of predictive cues, but how aversive learning enhances perceptual acuity of sensory signals, particularly in humans, is unclear. We combined multivariate functional magnetic resonance imaging with olfactory psychophysics to show that initially indistinguishable odor enantiomers (mirror-image molecules) become discriminable after aversive conditioning, paralleling the spatial divergence of ensemble activity patterns in primary olfactory (piriform) cortex. Our findings indicate that aversive learning induces piriform plasticity with corresponding gains in odor enantiomer discrimination, underscoring the capacity of fear conditioning to update perceptual representation of predictive cues, over and above its well-recognized role in the acquisition of conditioned responses. That completely indiscriminable sensations can be transformed into discriminable percepts further accentuates the potency of associative learning to enhance sensory cue perception and support adaptive behavior.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2756335/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2756335/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Li, Wen -- Howard, James D -- Parrish, Todd B -- Gottfried, Jay A -- DC007653/DC/NIDCD NIH HHS/ -- K08 DC007653/DC/NIDCD NIH HHS/ -- K08 DC007653-03/DC/NIDCD NIH HHS/ -- New York, N.Y. -- Science. 2008 Mar 28;319(5871):1842-5. doi: 10.1126/science.1152837.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Cognitive Neurology and Alzheimer's Disease Center, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA. wenli@northwestern.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18369149" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; *Association Learning ; Brain Mapping ; *Conditioning, Classical ; Cues ; *Discrimination Learning ; Fear ; Female ; Humans ; Magnetic Resonance Imaging ; Male ; *Odors ; Olfactory Pathways/*physiology ; *Perception ; Smell/*physiology ; Stereoisomerism
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  • 83
    Publication Date: 2008-05-03
    Description: Several studies have shown that healthy individuals with fasting plasma glucose (FPG) levels at the high end of the normal range have an increased risk of mortality. To identify genetic determinants that contribute to interindividual variation in FPG, we tested 392,935 single-nucleotide polymorphisms (SNPs) in 654 normoglycemic participants for association with FPG, and we replicated the most strongly associated SNP (rs560887, P = 4 x 10(-7)) in 9353 participants. SNP rs560887 maps to intron 3 of the G6PC2 gene, which encodes glucose-6-phosphatase catalytic subunit-related protein (also known as IGRP), a protein selectively expressed in pancreatic islets. This SNP was associated with FPG (linear regression coefficient beta = -0.06 millimoles per liter per A allele, combined P = 4 x 10(-23)) and with pancreatic beta cell function (Homa-B model, combined P = 3 x 10(-13)) in three populations; however, it was not associated with type 2 diabetes risk. We speculate that G6PC2 regulates FPG by modulating the set point for glucose-stimulated insulin secretion in pancreatic beta cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bouatia-Naji, Nabila -- Rocheleau, Ghislain -- Van Lommel, Leentje -- Lemaire, Katleen -- Schuit, Frans -- Cavalcanti-Proenca, Christine -- Marchand, Marion -- Hartikainen, Anna-Liisa -- Sovio, Ulla -- De Graeve, Franck -- Rung, Johan -- Vaxillaire, Martine -- Tichet, Jean -- Marre, Michel -- Balkau, Beverley -- Weill, Jacques -- Elliott, Paul -- Jarvelin, Marjo-Riitta -- Meyre, David -- Polychronakos, Constantin -- Dina, Christian -- Sladek, Robert -- Froguel, Philippe -- New York, N.Y. -- Science. 2008 May 23;320(5879):1085-8. doi: 10.1126/science.1156849. Epub 2008 May 1.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉CNRS UMR 8090 Institute of Biology, Pasteur Institute of Lille and Lille 2 Droit et Sante University, 59019 Lille, France.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18451265" target="_blank"〉PubMed〈/a〉
    Keywords: Alleles ; Blood Glucose/*metabolism ; Body Mass Index ; Diabetes Mellitus, Type 2/genetics ; Fasting ; Female ; Genetic Predisposition to Disease ; Glucose-6-Phosphatase/*genetics/metabolism ; Humans ; Insulin/blood/secretion ; Insulin-Secreting Cells/physiology ; Introns ; Linear Models ; Male ; Meta-Analysis as Topic ; *Polymorphism, Single Nucleotide
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  • 84
    Publication Date: 2008-06-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gormley, William T Jr -- Phillips, Deborah -- Gayer, Ted -- New York, N.Y. -- Science. 2008 Jun 27;320(5884):1723-4. doi: 10.1126/science.1156019.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18583597" target="_blank"〉PubMed〈/a〉
    Keywords: Child Development ; Child, Preschool ; *Cognition ; *Early Intervention (Education) ; Educational Measurement ; Faculty/standards ; Female ; Humans ; Male ; Oklahoma ; *Schools, Nursery ; Socioeconomic Factors
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  • 85
    Publication Date: 2008-04-19
    Description: Mercury has contaminated rivers worldwide, with health consequences for aquatic organisms and humans who consume them. Researchers have focused on aquatic birds as sentinels for mercury. However, trophic transfer between adjacent ecosystems could lead to the export of aquatic mercury to terrestrial habitats. Along a mercury-contaminated river in Virginia, United States, terrestrial birds had significantly elevated levels of mercury in their blood, similar to their aquatic-feeding counterparts. Diet analysis revealed that spiders delivered much of the dietary mercury. We conclude that aquatic mercury pollution can move into terrestrial habitats, where it biomagnifies to levels in songbirds that may cause adverse effects. Rivers contaminated with mercury may pose a threat to the many bird species that feed on predatory invertebrates in adjacent riparian habitats.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cristol, Daniel A -- Brasso, Rebecka L -- Condon, Anne M -- Fovargue, Rachel E -- Friedman, Scott L -- Hallinger, Kelly K -- Monroe, Adrian P -- White, Ariel E -- New York, N.Y. -- Science. 2008 Apr 18;320(5874):335. doi: 10.1126/science.1154082.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute for Integrative Bird Behavior Studies, Department of Biology, College of William and Mary, Williamsburg, VA 23185, USA. dacris@wm.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18420925" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Birds/blood/metabolism ; Diet ; *Ecosystem ; Feathers/chemistry ; Feeding Behavior ; Female ; *Food Chain ; Grasshoppers/chemistry ; Lepidoptera/chemistry ; Male ; Mercury/*analysis/blood ; Methylmercury Compounds/*analysis ; *Songbirds/blood ; Spiders/chemistry ; Virginia ; Water Pollutants, Chemical/analysis
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  • 86
    Publication Date: 2008-06-07
    Description: Serotonin (5-HT) has long been implicated in social behavior and impulsivity, but the mechanisms through which it modulates self-control remain unclear. We observed the effects of manipulating 5-HT function on behavior in the ultimatum game, where players must decide whether to accept or reject fair or unfair monetary offers from another player. Participants with depleted 5-HT levels rejected a greater proportion of unfair offers, but not fair offers, without showing changes in mood, fairness judgment, basic reward processing, or response inhibition. Our results suggest that 5-HT plays a critical role in regulating emotion during social decision-making.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2504725/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2504725/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Crockett, Molly J -- Clark, Luke -- Tabibnia, Golnaz -- Lieberman, Matthew D -- Robbins, Trevor W -- 076244/Wellcome Trust/United Kingdom -- 076274/Wellcome Trust/United Kingdom -- G0001354/Medical Research Council/United Kingdom -- Medical Research Council/United Kingdom -- Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 2008 Jun 27;320(5884):1739. doi: 10.1126/science.1155577. Epub 2008 Jun 5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Experimental Psychology, University of Cambridge, Cambridge CB2 3EB, UK. mc536@cam.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18535210" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Decision Making/physiology ; *Emotions ; Games, Experimental ; Humans ; Male ; Prefrontal Cortex/physiology ; Serotonin/*physiology ; *Social Behavior ; *Social Perception
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  • 87
    Publication Date: 2008-01-12
    Description: Substantial evidence exists that many tumors can be specifically recognized by CD8+ T lymphocytes. The definition of antigens targeted by these cells is paramount for the development of effective immunotherapeutic strategies for treating human cancers. In a screen for endogenous tumor-associated T cell responses in a primary mouse model of prostatic adenocarcinoma, we identified a naturally arising CD8+ T cell response that is reactive to a peptide derived from histone H4. Despite the ubiquitous nature of histones, T cell recognition of histone H4 peptide was specifically associated with the presence of prostate cancer in these mice. Thus, the repertoire of antigens recognized by tumor-infiltrating T cells is broader than previously thought and includes peptides derived from ubiquitous self antigens that are normally sequestered from immune detection.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Savage, Peter A -- Vosseller, Keith -- Kang, Chulho -- Larimore, Kevin -- Riedel, Elyn -- Wojnoonski, Kathleen -- Jungbluth, Achim A -- Allison, James P -- New York, N.Y. -- Science. 2008 Jan 11;319(5860):215-20. doi: 10.1126/science.1148886.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Immunology, Howard Hughes Medical Institute, and Ludwig Center for Cancer Immunotherapy, Memorial Sloan-Kettering Cancer Center (MSKCC), New York, NY 10021, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18187659" target="_blank"〉PubMed〈/a〉
    Keywords: Adenocarcinoma/*immunology ; Adoptive Transfer ; Animals ; Antigen Presentation ; Antigens, Neoplasm/*immunology ; Autoantigens/*immunology ; CD8-Positive T-Lymphocytes/*immunology ; Cell Line ; Epitopes, T-Lymphocyte/immunology ; Histones/*immunology ; Hybridomas ; Lymphocytes, Tumor-Infiltrating/*immunology ; Male ; Mice ; Mice, Transgenic ; Peptide Fragments/immunology ; Prostatic Neoplasms/*immunology ; Receptors, Antigen, T-Cell, alpha-beta/immunology
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  • 88
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-10-25
    Description: The development of queen and worker phenotypes in ants has been believed to be largely determined from environmental effects. We provide evidence that the production of discrete phenotypes is also influenced by genetic interaction effects. During the development of eggs into adults, some patrilines among offspring of multiply mated Pogonomyrmex rugosus ant queens became more common in workers while others became overrepresented in queens. Controlled crosses showed that these changes stem from some parental genome combinations being compatible for producing one phenotype but less compatible for the other. Genetic interaction effects on caste may be maintained over evolutionary time because the fitness of an allele depends on its genetic background.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schwander, Tanja -- Keller, Laurent -- New York, N.Y. -- Science. 2008 Oct 24;322(5901):552. doi: 10.1126/science.1162590.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Ecology and Evolution, University of Lausanne, CH-1015 Lausanne, Switzerland. tanja.schwander@gmail.com〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18948532" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Ants/*genetics/*physiology ; Crosses, Genetic ; Female ; *Genes, Insect ; Hierarchy, Social ; Male ; Ovum/physiology ; Reproduction/genetics
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  • 89
    Publication Date: 2008-09-27
    Description: Having repeatedly retrieved an object from a location, human infants tend to search the same place even when they observe the object being hidden at another location. This perseverative error is usually explained by infants' inability to inhibit a previously rewarded search response or to recall the new location. We show that the tendency to commit this error is substantially reduced (from 81 to 41%) when the object is hidden in front of 10-month-old infants without the experimenter using the communicative cues that normally accompany object hiding in this task. We suggest that this improvement is due to an interpretive bias that normally helps infants learn from demonstrations but misleads them in the context of a hiding game. Our finding provides an alternative theoretical perspective on the nature of infants' perseverative search errors.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Topal, Jozsef -- Gergely, Gyorgy -- Miklosi, Adam -- Erdohegyi, Agnes -- Csibra, Gergely -- G9715587/Medical Research Council/United Kingdom -- New York, N.Y. -- Science. 2008 Sep 26;321(5897):1831-4. doi: 10.1126/science.1161437.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Research Institute for Psychology, Hungarian Academy of Sciences, Budapest H-1132, Hungary. topaljozsef@gmail.com〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18818358" target="_blank"〉PubMed〈/a〉
    Keywords: *Cognition ; Communication ; Concept Formation ; Cues ; Female ; Humans ; Infant ; Infant Behavior/*psychology ; *Learning ; Male ; Memory ; Mental Recall
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  • 90
    facet.materialart.
    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-11-22
    Description: Imagine that the neighborhood you are living in is covered with graffiti, litter, and unreturned shopping carts. Would this reality cause you to litter more, trespass, or even steal? A thesis known as the broken windows theory suggests that signs of disorderly and petty criminal behavior trigger more disorderly and petty criminal behavior, thus causing the behavior to spread. This may cause neighborhoods to decay and the quality of life of its inhabitants to deteriorate. For a city government, this may be a vital policy issue. But does disorder really spread in neighborhoods? So far there has not been strong empirical support, and it is not clear what constitutes disorder and what may make it spread. We generated hypotheses about the spread of disorder and tested them in six field experiments. We found that, when people observe that others violated a certain social norm or legitimate rule, they are more likely to violate other norms or rules, which causes disorder to spread.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Keizer, Kees -- Lindenberg, Siegwart -- Steg, Linda -- New York, N.Y. -- Science. 2008 Dec 12;322(5908):1681-5. doi: 10.1126/science.1161405. Epub 2008 Nov 20.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Faculty of Behavioral and Social Sciences, University of Groningen, 9712 TS Groningen, Netherlands. K.E.Keizer@rug.nl〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19023045" target="_blank"〉PubMed〈/a〉
    Keywords: Cities ; Crime ; Environment ; Female ; Humans ; Male ; Netherlands ; Refuse Disposal ; *Residence Characteristics ; *Social Behavior ; *Social Control, Formal ; Social Environment ; *Social Problems
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  • 91
    Publication Date: 2008-01-19
    Description: The evolutionary changes that occur over a small number of generations in natural populations often run counter to what is expected on the basis of the heritability of traits and the selective forces acting upon them. In Soay sheep, dark coat color is associated with large size, which is heritable and positively correlated with fitness, yet the frequency of dark sheep has decreased. This unexpected microevolutionary trend is explained by genetic linkage between the causal mutation underlying the color polymorphism and quantitative trait loci with antagonistic effects on size and fitness. As a consequence, homozygous dark sheep are large, but have reduced fitness relative to phenotypically indistinguishable dark heterozygotes and light sheep. This result demonstrates the importance of understanding the genetic basis of fitness variation when making predictions about the microevolutionary consequences of selection.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gratten, J -- Wilson, A J -- McRae, A F -- Beraldi, D -- Visscher, P M -- Pemberton, J M -- Slate, J -- New York, N.Y. -- Science. 2008 Jan 18;319(5861):318-20. doi: 10.1126/science.1151182.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Animal and Plant Sciences, University of Sheffield, Sheffield S10 2TN, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18202287" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Wild/genetics/physiology ; *Biological Evolution ; Birth Weight/genetics ; Body Size/genetics ; Female ; Genetic Linkage ; Genotype ; Hair Color/*genetics ; Heterozygote ; Homozygote ; Linear Models ; Male ; Oxidoreductases/genetics ; Phenotype ; Quantitative Trait Loci ; Reproduction ; Scotland ; Selection, Genetic ; Sheep/*genetics/physiology
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  • 92
    Publication Date: 2008-08-16
    Description: Much of the genetic predisposition to colorectal cancer (CRC) in humans is unexplained. Studying a Caucasian-dominated population in the United States, we showed that germline allele-specific expression (ASE) of the gene encoding transforming growth factor-beta (TGF-beta) type I receptor, TGFBR1, is a quantitative trait that occurs in 10 to 20% of CRC patients and 1 to 3% of controls. ASE results in reduced expression of the gene, is dominantly inherited, segregates in families, and occurs in sporadic CRC cases. Although subtle, the reduction in constitutive TGFBR1 expression alters SMAD-mediated TGF-beta signaling. Two major TGFBR1 haplotypes are predominant among ASE cases, which suggests ancestral mutations, but causative germline changes have not been identified. Conservative estimates suggest that ASE confers a substantially increased risk of CRC (odds ratio, 8.7; 95% confidence interval, 2.6 to 29.1), but these estimates require confirmation and will probably show ethnic differences.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2672914/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2672914/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Valle, Laura -- Serena-Acedo, Tarsicio -- Liyanarachchi, Sandya -- Hampel, Heather -- Comeras, Ilene -- Li, Zhongyuan -- Zeng, Qinghua -- Zhang, Hong-Tao -- Pennison, Michael J -- Sadim, Maureen -- Pasche, Boris -- Tanner, Stephan M -- de la Chapelle, Albert -- CA108741/CA/NCI NIH HHS/ -- CA112520/CA/NCI NIH HHS/ -- CA16058/CA/NCI NIH HHS/ -- CA67941/CA/NCI NIH HHS/ -- R01 CA108741/CA/NCI NIH HHS/ -- R01 CA108741-01A2/CA/NCI NIH HHS/ -- R01 CA112520/CA/NCI NIH HHS/ -- R01 CA112520-01A1/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 2008 Sep 5;321(5894):1361-5. doi: 10.1126/science.1159397. Epub 2008 Aug 14.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Human Cancer Genetics Program, Comprehensive Cancer Center, Ohio State University, Columbus, OH 43210, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18703712" target="_blank"〉PubMed〈/a〉
    Keywords: 3' Untranslated Regions ; Adult ; Aged ; Aged, 80 and over ; Alleles ; Cell Line ; Colorectal Neoplasms/*genetics ; Female ; *Gene Expression ; *Genetic Predisposition to Disease ; Haplotypes ; Heterozygote ; Humans ; Linkage Disequilibrium ; Male ; Middle Aged ; Polymorphism, Single Nucleotide ; Protein-Serine-Threonine Kinases/*genetics ; Quantitative Trait, Heritable ; Receptors, Transforming Growth Factor beta/*genetics ; Risk Factors ; Signal Transduction ; Smad3 Protein/metabolism ; Transforming Growth Factor beta/metabolism
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  • 93
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-05-31
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Guiso, Luigi -- Monte, Ferdinando -- Sapienza, Paola -- Zingales, Luigi -- New York, N.Y. -- Science. 2008 May 30;320(5880):1164-5. doi: 10.1126/science.1154094.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉European University Institute, Villa San Paolo, Via della Piazzuola 43, 50133 Florence, Italy.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18511674" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Cultural Diversity ; *Culture ; Educational Measurement ; Female ; *Gender Identity ; Humans ; Internationality ; Male ; *Mathematics ; Reading ; *Sex Characteristics ; Women's Rights
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 94
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-11-29
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Greenberger, Phyllis -- New York, N.Y. -- Science. 2008 Nov 28;322(5906):1325-6. doi: 10.1126/science.322.5906.1325b.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19039120" target="_blank"〉PubMed〈/a〉
    Keywords: Clinical Trials as Topic/*statistics & numerical data ; Female ; Humans ; Male ; *Patient Selection ; Research Design/*statistics & numerical data ; *Sex Characteristics ; Sex Distribution ; *Women's Health
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  • 95
    Publication Date: 2008-01-12
    Description: Natural selection is expected to eliminate genetic incompatibilities from interbreeding populations. We have discovered a globally distributed incompatibility in the primarily selfing species Caenorhabditis elegans that has been maintained despite its negative consequences for fitness. Embryos homozygous for a naturally occurring deletion of the zygotically acting gene zeel-1 arrest if their sperm parent carries an incompatible allele of a second, paternal-effect locus, peel-1. The two interacting loci are tightly linked, with incompatible alleles occurring in linkage disequilibrium in two common haplotypes. These haplotypes exhibit elevated sequence divergence, and population genetic analyses of this region indicate that natural selection is preserving both haplotypes in the population. Our data suggest that long-term maintenance of a balanced polymorphism has permitted the incompatibility to persist despite gene flow across the rest of the genome.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2421010/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2421010/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Seidel, Hannah S -- Rockman, Matthew V -- Kruglyak, Leonid -- GM071508/GM/NIGMS NIH HHS/ -- R01 HG004321/HG/NHGRI NIH HHS/ -- R01 HG004321-01/HG/NHGRI NIH HHS/ -- R37 MH059520/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2008 Feb 1;319(5863):589-94. doi: 10.1126/science.1151107. Epub 2008 Jan 10.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Lewis-Sigler Institute for Integrative Genomics and Department of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ 08544, USA. hseidel@princeton.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18187622" target="_blank"〉PubMed〈/a〉
    Keywords: Alleles ; Animals ; Animals, Genetically Modified ; Caenorhabditis elegans/embryology/*genetics ; Cloning, Molecular ; Crosses, Genetic ; Disorders of Sex Development ; Embryo, Nonmammalian/physiology ; Embryonic Development ; Gene Flow ; Genes, Helminth ; Genetic Linkage ; Genome, Helminth ; Haplotypes ; Linkage Disequilibrium ; Male ; Molecular Sequence Data ; Penetrance ; Polymorphism, Single Nucleotide ; *Selection, Genetic
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  • 96
    Publication Date: 2008-02-09
    Description: The diversity and complexity of food webs (the networks of feeding relationships within an ecological community) are considered to be important factors determining ecosystem function and stability. However, the biological processes driving these factors are poorly understood. Resource quality affects species interactions by limiting energy transfer to consumers and their predators, affecting life history and morphological traits. We show that differences in plant traits affect the structure of an entire food web through a series of direct and indirect effects. Three trophic levels of consumers were influenced by plant quality, as shown by quantitative herbivore-parasitoid-secondary parasitoid food webs. We conclude, on the basis of our data, that changes in the food web are dependent on both trait- and density-mediated interactions among species.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bukovinszky, Tibor -- van Veen, F J Frank -- Jongema, Yde -- Dicke, Marcel -- New York, N.Y. -- Science. 2008 Feb 8;319(5864):804-7. doi: 10.1126/science.1148310.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Entomology, Wageningen University, Post Office Box 8031, 6700 EH Wageningen, Netherlands. tibor.bukovinszky@wur.nl〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18258913" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Aphids/anatomy & histology/parasitology/*physiology ; Body Size ; *Brassica/anatomy & histology/chemistry/physiology ; Feeding Behavior ; Female ; *Food Chain ; Male ; Plant Leaves/chemistry ; Wasps/parasitology/*physiology
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  • 97
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2008-02-09
    Description: Reproducing in cities has always been costly, leading to lower fertility (that is, lower birth rates) in urban than in rural areas. Historically, although cities provided job opportunities, initially residents incurred the penalty of higher infant mortality, but as mortality rates fell at the end of the 19th century, European birth rates began to plummet. Fertility decline in Africa only started recently and has been dramatic in some cities. Here it is argued that both historical and evolutionary demographers are interpreting fertility declines across the globe in terms of the relative costs of child rearing, which increase to allow children to outcompete their peers. Now largely free from the fear of early death, postindustrial societies may create an environment that generates runaway parental investment, which will continue to drive fertility ever lower.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mace, Ruth -- New York, N.Y. -- Science. 2008 Feb 8;319(5864):764-6. doi: 10.1126/science.1153960.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Anthropology, University College London, Taviton Street, London WC1H 0BW, UK. r.mace@ucl.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18258904" target="_blank"〉PubMed〈/a〉
    Keywords: *Birth Rate ; Child ; Child Rearing ; *Cities ; Family Characteristics ; Female ; Fertility ; Humans ; Male ; *Urban Population
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  • 98
    Publication Date: 2008-04-29
    Description: Homozygous deletion of the survival motor neuron 1 gene (SMN1) causes spinal muscular atrophy (SMA), the most frequent genetic cause of early childhood lethality. In rare instances, however, individuals are asymptomatic despite carrying the same SMN1 mutations as their affected siblings, thereby suggesting the influence of modifier genes. We discovered that unaffected SMN1-deleted females exhibit significantly higher expression of plastin 3 (PLS3) than their SMA-affected counterparts. We demonstrated that PLS3 is important for axonogenesis through increasing the F-actin level. Overexpression of PLS3 rescued the axon length and outgrowth defects associated with SMN down-regulation in motor neurons of SMA mouse embryos and in zebrafish. Our study suggests that defects in axonogenesis are the major cause of SMA, thereby opening new therapeutic options for SMA and similar neuromuscular diseases.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Oprea, Gabriela E -- Krober, Sandra -- McWhorter, Michelle L -- Rossoll, Wilfried -- Muller, Stefan -- Krawczak, Michael -- Bassell, Gary J -- Beattie, Christine E -- Wirth, Brunhilde -- HD055835/HD/NICHD NIH HHS/ -- R01 HD055835/HD/NICHD NIH HHS/ -- R01NS50414/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 2008 Apr 25;320(5875):524-7. doi: 10.1126/science.1155085.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute of Human Genetics, University of Cologne, 50931 Cologne, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18440926" target="_blank"〉PubMed〈/a〉
    Keywords: Actins/blood/*genetics/*metabolism ; Animals ; Axons/metabolism/*physiology/ultrastructure ; Cell Differentiation ; Cell Line ; Cyclic AMP Response Element-Binding Protein/genetics/metabolism ; Female ; Gene Expression ; Growth Cones/metabolism/ultrastructure ; Humans ; Male ; Membrane Glycoproteins ; Mice ; Microfilament Proteins ; Muscular Atrophy, Spinal/*genetics ; Nerve Tissue Proteins/genetics/metabolism ; Pedigree ; Phosphoproteins/blood/*genetics/*metabolism ; RNA-Binding Proteins/genetics/metabolism ; SMN Complex Proteins ; Spinal Cord/metabolism ; Survival of Motor Neuron 1 Protein ; Transcription, Genetic ; Zebrafish/embryology/genetics
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  • 99
    Publication Date: 2008-11-29
    Description: In plants and mammals, small RNAs indirectly mediate epigenetic inheritance by specifying cytosine methylation. We found that small RNAs themselves serve as vectors for epigenetic information. Crosses between Drosophila strains that differ in the presence of a particular transposon can produce sterile progeny, a phenomenon called hybrid dysgenesis. This phenotype manifests itself only if the transposon is paternally inherited, suggesting maternal transmission of a factor that maintains fertility. In both P- and I-element-mediated hybrid dysgenesis models, daughters show a markedly different content of Piwi-interacting RNAs (piRNAs) targeting each element, depending on their parents of origin. Such differences persist from fertilization through adulthood. This indicates that maternally deposited piRNAs are important for mounting an effective silencing response and that a lack of maternal piRNA inheritance underlies hybrid dysgenesis.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2805124/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2805124/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Brennecke, Julius -- Malone, Colin D -- Aravin, Alexei A -- Sachidanandam, Ravi -- Stark, Alexander -- Hannon, Gregory J -- P01 CA013106/CA/NCI NIH HHS/ -- P01 CA013106-37/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 2008 Nov 28;322(5906):1387-92. doi: 10.1126/science.1165171.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Watson School of Biological Sciences, Howard Hughes Medical Institute, Cold Spring Harbor Laboratory (CSHL), 1 Bungtown Road, Cold Spring Harbor, NY 11724, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19039138" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Argonaute Proteins ; Crosses, Genetic ; *DNA Transposable Elements ; Drosophila Proteins/genetics/metabolism ; Drosophila melanogaster/embryology/*genetics/physiology ; *Epigenesis, Genetic ; Female ; Fertility ; Hybridization, Genetic ; Male ; Ovary/metabolism ; Peptide Initiation Factors/genetics/metabolism ; *RNA Interference ; RNA, Small Interfering/*genetics/metabolism
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  • 100
    Publication Date: 2008-11-15
    Description: Enhancer of zeste homolog 2 (EZH2) is a mammalian histone methyltransferase that contributes to the epigenetic silencing of target genes and regulates the survival and metastasis of cancer cells. EZH2 is overexpressed in aggressive solid tumors by mechanisms that remain unclear. Here we show that the expression and function of EZH2 in cancer cell lines are inhibited by microRNA-101 (miR-101). Analysis of human prostate tumors revealed that miR-101 expression decreases during cancer progression, paralleling an increase in EZH2 expression. One or both of the two genomic loci encoding miR-101 were somatically lost in 37.5% of clinically localized prostate cancer cells (6 of 16) and 66.7% of metastatic disease cells (22 of 33). We propose that the genomic loss of miR-101 in cancer leads to overexpression of EZH2 and concomitant dysregulation of epigenetic pathways, resulting in cancer progression.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2684823/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2684823/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Varambally, Sooryanarayana -- Cao, Qi -- Mani, Ram-Shankar -- Shankar, Sunita -- Wang, Xiaosong -- Ateeq, Bushra -- Laxman, Bharathi -- Cao, Xuhong -- Jing, Xiaojun -- Ramnarayanan, Kalpana -- Brenner, J Chad -- Yu, Jindan -- Kim, Jung H -- Han, Bo -- Tan, Patrick -- Kumar-Sinha, Chandan -- Lonigro, Robert J -- Palanisamy, Nallasivam -- Maher, Christopher A -- Chinnaiyan, Arul M -- K99 CA129565/CA/NCI NIH HHS/ -- K99 CA129565-01A1/CA/NCI NIH HHS/ -- P50 CA069568/CA/NCI NIH HHS/ -- P50 CA069568-06A10016/CA/NCI NIH HHS/ -- P50CA69568/CA/NCI NIH HHS/ -- U01 CA111275/CA/NCI NIH HHS/ -- U01 CA111275-04/CA/NCI NIH HHS/ -- UO1 111275/PHS HHS/ -- New York, N.Y. -- Science. 2008 Dec 12;322(5908):1695-9. doi: 10.1126/science.1165395. Epub 2008 Nov 13.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Michigan Center for Translational Pathology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19008416" target="_blank"〉PubMed〈/a〉
    Keywords: 3' Untranslated Regions ; Algorithms ; Breast Neoplasms/genetics/metabolism ; Cell Line, Tumor ; DNA-Binding Proteins/*genetics/metabolism ; Disease Progression ; Epigenesis, Genetic ; Female ; *Gene Expression Regulation, Neoplastic ; Genome, Human ; Histones/*metabolism ; Humans ; Lysine/metabolism ; Male ; Methylation ; MicroRNAs/*genetics/metabolism ; Neoplasm Metastasis ; Neoplasms/*genetics/metabolism ; Polycomb Repressive Complex 2 ; Promoter Regions, Genetic ; Prostatic Neoplasms/*genetics/metabolism/pathology ; RNA, Small Interfering/genetics ; Stomach Neoplasms/genetics/metabolism ; Transcription Factors/*genetics/metabolism
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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