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  • Animals  (809)
  • Analytical Chemistry and Spectroscopy
  • Inorganic Chemistry
  • Surface physics, nanoscale physics, low-dimensional systems
  • Nature Publishing Group (NPG)  (809)
  • 2015-2019
  • 2010-2014  (809)
  • 1990-1994
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  • 2010-2014  (809)
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  • 101
    Publication Date: 2012-08-03
    Description: Motor axons receive retrograde signals from skeletal muscle that are essential for the differentiation and stabilization of motor nerve terminals. Identification of these retrograde signals has proved elusive, but their production by muscle depends on the receptor tyrosine kinase, MuSK (muscle, skeletal receptor tyrosine-protein kinase), and Lrp4 (low-density lipoprotein receptor (LDLR)-related protein 4), an LDLR family member that forms a complex with MuSK, binds neural agrin and stimulates MuSK kinase activity. Here we show that Lrp4 also functions as a direct muscle-derived retrograde signal for early steps in presynaptic differentiation. We demonstrate that Lrp4 is necessary, independent of MuSK activation, for presynaptic differentiation in vivo, and we show that Lrp4 binds to motor axons and induces clustering of synaptic-vesicle and active-zone proteins. Thus, Lrp4 acts bidirectionally and coordinates synapse formation by binding agrin, activating MuSK and stimulating postsynaptic differentiation, and functioning in turn as a muscle-derived retrograde signal that is necessary and sufficient for presynaptic differentiation.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3448831/" 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/PMC3448831/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yumoto, Norihiro -- Kim, Natalie -- Burden, Steven J -- 5 P30CA16087-31/CA/NCI NIH HHS/ -- NS36193/NS/NINDS NIH HHS/ -- R01 NS036193/NS/NINDS NIH HHS/ -- England -- Nature. 2012 Sep 20;489(7416):438-42. doi: 10.1038/nature11348. Epub 2012 Aug 1.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Molecular Neurobiology Program, Helen L. and Martin S. Kimmel Center for Biology and Medicine at the Skirball Institute of Biomolecular Medicine, New York University Medical School, New York, New York, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22854782" target="_blank"〉PubMed〈/a〉
    Keywords: Amyotrophic Lateral Sclerosis ; Animals ; *Cell Differentiation ; Cells, Cultured ; Coculture Techniques ; Diaphragm ; Mice ; Motor Neurons/metabolism ; Muscle, Skeletal/cytology/*innervation/metabolism ; Neural Tube/cytology/metabolism ; Neuromuscular Junction/*cytology/*metabolism ; Presynaptic Terminals/*metabolism ; Protein Binding ; Receptor Protein-Tyrosine Kinases/metabolism ; Receptors, LDL/*metabolism ; Sarcopenia ; *Signal Transduction ; Synapsins/metabolism ; Tissue Culture Techniques
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  • 102
    Publication Date: 2012-05-04
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gentilella, Antonio -- Thomas, George -- England -- Nature. 2012 May 2;485(7396):50-1. doi: 10.1038/485050a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22552093" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Gene Expression Regulation ; Humans ; Male ; *Models, Biological ; Multiprotein Complexes ; *Neoplasm Metastasis ; Prostatic Neoplasms/*pathology ; *Protein Biosynthesis ; Proteins/*metabolism ; *Signal Transduction ; TOR Serine-Threonine Kinases/*metabolism
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  • 103
    Publication Date: 2012-04-13
    Description: Understanding the molecular and cellular mechanisms that mediate magnetosensation in vertebrates is a formidable scientific problem. One hypothesis is that magnetic information is transduced into neuronal impulses by using a magnetite-based magnetoreceptor. Previous studies claim to have identified a magnetic sense system in the pigeon, common to avian species, which consists of magnetite-containing trigeminal afferents located at six specific loci in the rostral subepidermis of the beak. These studies have been widely accepted in the field and heavily relied upon by both behavioural biologists and physicists. Here we show that clusters of iron-rich cells in the rostro-medial upper beak of the pigeon Columbia livia are macrophages, not magnetosensitive neurons. Our systematic characterization of the pigeon upper beak identified iron-rich cells in the stratum laxum of the subepidermis, the basal region of the respiratory epithelium and the apex of feather follicles. Using a three-dimensional blueprint of the pigeon beak created by magnetic resonance imaging and computed tomography, we mapped the location of iron-rich cells, revealing unexpected variation in their distribution and number--an observation that is inconsistent with a role in magnetic sensation. Ultrastructure analysis of these cells, which are not unique to the beak, showed that their subcellular architecture includes ferritin-like granules, siderosomes, haemosiderin and filopodia, characteristics of iron-rich macrophages. Our conclusion that these cells are macrophages and not magnetosensitive neurons is supported by immunohistological studies showing co-localization with the antigen-presenting molecule major histocompatibility complex class II. Our work necessitates a renewed search for the true magnetite-dependent magnetoreceptor in birds.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Treiber, Christoph Daniel -- Salzer, Marion Claudia -- Riegler, Johannes -- Edelman, Nathaniel -- Sugar, Cristina -- Breuss, Martin -- Pichler, Paul -- Cadiou, Herve -- Saunders, Martin -- Lythgoe, Mark -- Shaw, Jeremy -- Keays, David Anthony -- England -- Nature. 2012 Apr 11;484(7394):367-70. doi: 10.1038/nature11046.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute of Molecular Pathology, Dr Bohr-Gasse, 1030 Vienna, Austria.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22495303" target="_blank"〉PubMed〈/a〉
    Keywords: Animal Migration ; Animals ; Beak/anatomy & histology/*cytology ; Columbidae/*anatomy & histology/physiology ; Feathers/cytology/ultrastructure ; Ferrocyanides/analysis ; Immunohistochemistry ; Iron/analysis/*metabolism ; Macrophages/*metabolism/ultrastructure ; *Magnetic Fields ; Magnetic Resonance Imaging ; Neurons/metabolism ; Orientation ; Respiratory Mucosa/cytology/ultrastructure ; *Sensation ; Tomography, Emission-Computed, Single-Photon
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  • 104
    Publication Date: 2012-03-31
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lieberman, Daniel E -- England -- Nature. 2012 Mar 28;483(7391):550-1. doi: 10.1038/483550a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22460898" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptation, Physiological/*physiology ; Animals ; Foot/*anatomy & histology/*physiology ; Gait/*physiology ; Hominidae/*anatomy & histology/*physiology ; Humans ; Walking/*physiology
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  • 105
    Publication Date: 2012-03-01
    Description: The human X and Y chromosomes evolved from an ordinary pair of autosomes during the past 200-300 million years. The human MSY (male-specific region of Y chromosome) retains only three percent of the ancestral autosomes' genes owing to genetic decay. This evolutionary decay was driven by a series of five 'stratification' events. Each event suppressed X-Y crossing over within a chromosome segment or 'stratum', incorporated that segment into the MSY and subjected its genes to the erosive forces that attend the absence of crossing over. The last of these events occurred 30 million years ago, 5 million years before the human and Old World monkey lineages diverged. Although speculation abounds regarding ongoing decay and looming extinction of the human Y chromosome, remarkably little is known about how many MSY genes were lost in the human lineage in the 25 million years that have followed its separation from the Old World monkey lineage. To investigate this question, we sequenced the MSY of the rhesus macaque, an Old World monkey, and compared it to the human MSY. We discovered that during the last 25 million years MSY gene loss in the human lineage was limited to the youngest stratum (stratum 5), which comprises three percent of the human MSY. In the older strata, which collectively comprise the bulk of the human MSY, gene loss evidently ceased more than 25 million years ago. Likewise, the rhesus MSY has not lost any older genes (from strata 1-4) during the past 25 million years, despite its major structural differences to the human MSY. The rhesus MSY is simpler, with few amplified gene families or palindromes that might enable intrachromosomal recombination and repair. We present an empirical reconstruction of human MSY evolution in which each stratum transitioned from rapid, exponential loss of ancestral genes to strict conservation through purifying selection.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3292678/" 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/PMC3292678/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hughes, Jennifer F -- Skaletsky, Helen -- Brown, Laura G -- Pyntikova, Tatyana -- Graves, Tina -- Fulton, Robert S -- Dugan, Shannon -- Ding, Yan -- Buhay, Christian J -- Kremitzki, Colin -- Wang, Qiaoyan -- Shen, Hua -- Holder, Michael -- Villasana, Donna -- Nazareth, Lynne V -- Cree, Andrew -- Courtney, Laura -- Veizer, Joelle -- Kotkiewicz, Holland -- Cho, Ting-Jan -- Koutseva, Natalia -- Rozen, Steve -- Muzny, Donna M -- Warren, Wesley C -- Gibbs, Richard A -- Wilson, Richard K -- Page, David C -- R01 HG000257/HG/NHGRI NIH HHS/ -- R01 HG000257-17/HG/NHGRI NIH HHS/ -- U54 HG003273/HG/NHGRI NIH HHS/ -- Howard Hughes Medical Institute/ -- England -- Nature. 2012 Feb 22;483(7387):82-6. doi: 10.1038/nature10843.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Department of Biology, Massachusetts Institute of Technology, 9 Cambridge Center, Cambridge, Massachusetts 02142, USA. jhughes@wi.mit.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22367542" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Chromosomes, Human, Y/*genetics ; Conserved Sequence/*genetics ; Crossing Over, Genetic/genetics ; *Evolution, Molecular ; Gene Amplification/genetics ; *Gene Deletion ; Humans ; In Situ Hybridization, Fluorescence ; Macaca mulatta/*genetics ; Male ; Models, Genetic ; Molecular Sequence Data ; Pan troglodytes/genetics ; Radiation Hybrid Mapping ; Selection, Genetic/genetics ; Time Factors ; Y Chromosome/*genetics
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  • 106
    Publication Date: 2012-09-14
    Description: The link between the microbes in the human gut and the development of obesity, cardiovascular disease and metabolic syndromes, such as type 2 diabetes, is becoming clearer. However, because of the complexity of the microbial community, the functional connections are less well understood. Studies in both mice and humans are helping to show what effect the gut microbiota has on host metabolism by improving energy yield from food and modulating dietary or the host-derived compounds that alter host metabolic pathways. Through increased knowledge of the mechanisms involved in the interactions between the microbiota and its host, we will be in a better position to develop treatments for metabolic disease.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tremaroli, Valentina -- Backhed, Fredrik -- England -- Nature. 2012 Sep 13;489(7415):242-9. doi: 10.1038/nature11552.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Wallenberg Laboratory for Cardiovascular and Metabolic Research, Sahlgrenska University Hospital, 413 45 Gothenburg, Sweden.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22972297" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Diet ; *Energy Metabolism ; Fermentation ; Humans ; Immunity, Innate ; Inflammation/metabolism/microbiology ; Intestines/immunology/*metabolism/*microbiology ; Metabolic Syndrome X/metabolism/microbiology ; Metagenome/immunology/*physiology ; Obesity/metabolism/microbiology
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  • 107
    Publication Date: 2012-10-05
    Description: The substantia nigra pars compacta and ventral tegmental area contain the two largest populations of dopamine-releasing neurons in the mammalian brain. These neurons extend elaborate projections in the striatum, a large subcortical structure implicated in motor planning and reward-based learning. Phasic activation of dopaminergic neurons in response to salient or reward-predicting stimuli is thought to modulate striatal output through the release of dopamine to promote and reinforce motor action. Here we show that activation of dopamine neurons in striatal slices rapidly inhibits action potential firing in both direct- and indirect-pathway striatal projection neurons through vesicular release of the inhibitory transmitter GABA (gamma-aminobutyric acid). GABA is released directly from dopaminergic axons but in a manner that is independent of the vesicular GABA transporter VGAT. Instead, GABA release requires activity of the vesicular monoamine transporter VMAT2, which is the vesicular transporter for dopamine. Furthermore, VMAT2 expression in GABAergic neurons lacking VGAT is sufficient to sustain GABA release. Thus, these findings expand the repertoire of synaptic mechanisms used by dopamine neurons to influence basal ganglia circuits, show a new substrate whose transport is dependent on VMAT2 and demonstrate that GABA can function as a bona fide co-transmitter in monoaminergic neurons.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944587/" 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/PMC3944587/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tritsch, Nicolas X -- Ding, Jun B -- Sabatini, Bernardo L -- 4R00NS075136/NS/NINDS NIH HHS/ -- NS046579/NS/NINDS NIH HHS/ -- R00 NS075136/NS/NINDS NIH HHS/ -- R01 NS046579/NS/NINDS NIH HHS/ -- T32 NS007484/NS/NINDS NIH HHS/ -- Howard Hughes Medical Institute/ -- England -- Nature. 2012 Oct 11;490(7419):262-6. doi: 10.1038/nature11466. Epub 2012 Oct 3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurobiology, Howard Hughes Medical Institute, Harvard Medical School, 220 Longwood Avenue, Boston, Massachusetts 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23034651" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Corpus Striatum/cytology/*metabolism ; Dopaminergic Neurons/*metabolism ; GABA Plasma Membrane Transport Proteins/*metabolism ; Gene Expression Profiling ; Gene Expression Regulation ; Gene Knock-In Techniques ; Mice ; Mice, Transgenic ; Vesicular Monoamine Transport Proteins/metabolism ; gamma-Aminobutyric Acid/*metabolism
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  • 108
    Publication Date: 2012-02-22
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Clifford, Steven C -- England -- Nature. 2012 Feb 15;482(7386):481-2. doi: 10.1038/nature10949.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22343899" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Clonal Evolution/*genetics ; Humans ; Medulloblastoma/*genetics/*pathology ; Neoplasm Metastasis/*genetics/*pathology
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  • 109
    Publication Date: 2012-05-04
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zaidi, Mone -- Iqbal, Jameel -- England -- Nature. 2012 May 2;485(7396):47-8. doi: 10.1038/485047a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22552091" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Bone Resorption ; *Cytoprotection ; Female ; Male ; Osteoblasts/*cytology ; Osteoclasts/*cytology ; *Osteogenesis ; Semaphorin-3A/*metabolism
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  • 110
    Publication Date: 2012-05-25
    Description: Oligodendrocytes, the myelin-forming glial cells of the central nervous system, maintain long-term axonal integrity. However, the underlying support mechanisms are not understood. Here we identify a metabolic component of axon-glia interactions by generating conditional Cox10 (protoheme IX farnesyltransferase) mutant mice, in which oligodendrocytes and Schwann cells fail to assemble stable mitochondrial cytochrome c oxidase (COX, also known as mitochondrial complex IV). In the peripheral nervous system, Cox10 conditional mutants exhibit severe neuropathy with dysmyelination, abnormal Remak bundles, muscle atrophy and paralysis. Notably, perturbing mitochondrial respiration did not cause glial cell death. In the adult central nervous system, we found no signs of demyelination, axonal degeneration or secondary inflammation. Unlike cultured oligodendrocytes, which are sensitive to COX inhibitors, post-myelination oligodendrocytes survive well in the absence of COX activity. More importantly, by in vivo magnetic resonance spectroscopy, brain lactate concentrations in mutants were increased compared with controls, but were detectable only in mice exposed to volatile anaesthetics. This indicates that aerobic glycolysis products derived from oligodendrocytes are rapidly metabolized within white matter tracts. Because myelinated axons can use lactate when energy-deprived, our findings suggest a model in which axon-glia metabolic coupling serves a physiological function.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613737/" 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/PMC3613737/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Funfschilling, Ursula -- Supplie, Lotti M -- Mahad, Don -- Boretius, Susann -- Saab, Aiman S -- Edgar, Julia -- Brinkmann, Bastian G -- Kassmann, Celia M -- Tzvetanova, Iva D -- Mobius, Wiebke -- Diaz, Francisca -- Meijer, Dies -- Suter, Ueli -- Hamprecht, Bernd -- Sereda, Michael W -- Moraes, Carlos T -- Frahm, Jens -- Goebbels, Sandra -- Nave, Klaus-Armin -- 078415/Wellcome Trust/United Kingdom -- England -- Nature. 2012 Apr 29;485(7399):517-21. doi: 10.1038/nature11007.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Max Planck Institute of Experimental Medicine, Department of Neurogenetics, Hermann-Rein-Strasse 3, D-37075 Gottingen, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22622581" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials ; Alkyl and Aryl Transferases/deficiency/genetics/metabolism ; Animals ; Axons/*physiology ; Brain/cytology/metabolism ; Cell Respiration ; Cell Survival ; Demyelinating Diseases/enzymology/genetics/metabolism/pathology ; Electron Transport Complex IV/antagonists & inhibitors/genetics/metabolism ; *Glycolysis ; Lactic Acid/metabolism ; Magnetic Resonance Spectroscopy ; Membrane Proteins/deficiency/genetics/metabolism ; Mice ; Mitochondria/enzymology/genetics/metabolism/pathology ; Mutant Proteins/genetics/metabolism ; Myelin Sheath/*metabolism ; Oligodendroglia/cytology/drug effects/enzymology/*metabolism ; Protons ; Schwann Cells/enzymology/metabolism ; Time Factors
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  • 111
    Publication Date: 2012-06-09
    Description: Evidence is mounting that extinctions are altering key processes important to the productivity and sustainability of Earth's ecosystems. Further species loss will accelerate change in ecosystem processes, but it is unclear how these effects compare to the direct effects of other forms of environmental change that are both driving diversity loss and altering ecosystem function. Here we use a suite of meta-analyses of published data to show that the effects of species loss on productivity and decomposition--two processes important in all ecosystems--are of comparable magnitude to the effects of many other global environmental changes. In experiments, intermediate levels of species loss (21-40%) reduced plant production by 5-10%, comparable to previously documented effects of ultraviolet radiation and climate warming. Higher levels of extinction (41-60%) had effects rivalling those of ozone, acidification, elevated CO(2) and nutrient pollution. At intermediate levels, species loss generally had equal or greater effects on decomposition than did elevated CO(2) and nitrogen addition. The identity of species lost also had a large effect on changes in productivity and decomposition, generating a wide range of plausible outcomes for extinction. Despite the need for more studies on interactive effects of diversity loss and environmental changes, our analyses clearly show that the ecosystem consequences of local species loss are as quantitatively significant as the direct effects of several global change stressors that have mobilized major international concern and remediation efforts.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hooper, David U -- Adair, E Carol -- Cardinale, Bradley J -- Byrnes, Jarrett E K -- Hungate, Bruce A -- Matulich, Kristin L -- Gonzalez, Andrew -- Duffy, J Emmett -- Gamfeldt, Lars -- O'Connor, Mary I -- England -- Nature. 2012 May 2;486(7401):105-8. doi: 10.1038/nature11118.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biology, Western Washington University, Bellingham, Washington 98225-9160, USA. hooper@biol.wwu.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22678289" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biodiversity ; Ecology ; *Ecosystem ; *Extinction, Biological ; Models, Biological
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  • 112
    Publication Date: 2012-11-16
    Description: Metabolic phenotyping involves the comprehensive analysis of biological fluids or tissue samples. This analysis allows biochemical classification of a person's physiological or pathological states that relate to disease diagnosis or prognosis at the individual level and to disease risk factors at the population level. These approaches are currently being implemented in hospital environments and in regional phenotyping centres worldwide. The ultimate aim of such work is to generate information on patient biology using techniques such as patient stratification to better inform clinicians on factors that will enhance diagnosis or the choice of therapy. There have been many reports of direct applications of metabolic phenotyping in a clinical setting.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nicholson, Jeremy K -- Holmes, Elaine -- Kinross, James M -- Darzi, Ara W -- Takats, Zoltan -- Lindon, John C -- England -- Nature. 2012 Nov 15;491(7424):384-92. doi: 10.1038/nature11708.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Surgery and Cancer, Faculty of Medicine, Imperial College London, South Kensington, London SW7 2AZ, UK. j.nicholson@imperial.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23151581" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biomarkers/analysis ; Body Fluids/*chemistry/metabolism ; Cells/metabolism ; General Surgery/*methods ; Humans ; Metabolic Diseases/diagnosis ; *Metabolome ; *Phenotype ; Precision Medicine
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  • 113
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    Nature Publishing Group (NPG)
    Publication Date: 2012-06-22
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Trivedi, Bijal P -- England -- Nature. 2012 Jun 20;486(7403):S7-9. doi: 10.1038/486S7a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22717403" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Appetite/physiology ; Blood Glucose/metabolism ; Food Habits/physiology ; Gastrointestinal Tract/metabolism ; Humans ; Memory/physiology ; Receptors, G-Protein-Coupled/metabolism ; Taste/*physiology ; Taste Perception/*physiology
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  • 114
    Publication Date: 2012-02-03
    Description: Natural materials are renowned for exquisite designs that optimize function, as illustrated by the elasticity of blood vessels, the toughness of bone and the protection offered by nacre. Particularly intriguing are spider silks, with studies having explored properties ranging from their protein sequence to the geometry of a web. This material system, highly adapted to meet a spider's many needs, has superior mechanical properties. In spite of much research into the molecular design underpinning the outstanding performance of silk fibres, and into the mechanical characteristics of web-like structures, it remains unknown how the mechanical characteristics of spider silk contribute to the integrity and performance of a spider web. Here we report web deformation experiments and simulations that identify the nonlinear response of silk threads to stress--involving softening at a yield point and substantial stiffening at large strain until failure--as being crucial to localize load-induced deformation and resulting in mechanically robust spider webs. Control simulations confirmed that a nonlinear stress response results in superior resistance to structural defects in the web compared to linear elastic or elastic-plastic (softening) material behaviour. We also show that under distributed loads, such as those exerted by wind, the stiff behaviour of silk under small deformation, before the yield point, is essential in maintaining the web's structural integrity. The superior performance of silk in webs is therefore not due merely to its exceptional ultimate strength and strain, but arises from the nonlinear response of silk threads to strain and their geometrical arrangement in a web.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cranford, Steven W -- Tarakanova, Anna -- Pugno, Nicola M -- Buehler, Markus J -- England -- Nature. 2012 Feb 1;482(7383):72-6. doi: 10.1038/nature10739.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory for Atomistic and Molecular Mechanics, Department of Civil and Environmental Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22297972" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biomechanical Phenomena ; Elasticity ; Hardness ; Models, Biological ; Silk/*chemistry ; *Spiders/physiology ; *Tensile Strength ; Wind
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  • 115
    Publication Date: 2012-02-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zare, Richard N -- England -- Nature. 2012 Feb 15;482(7385):312-3. doi: 10.1038/482312a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22337044" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Carbon Dioxide/analysis/metabolism ; Carbon Radioisotopes/*analysis/metabolism ; Chemistry Techniques, Analytical/*methods ; Radiometric Dating/*methods
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  • 116
    Publication Date: 2012-07-31
    Description: Dendritic arborizations of many neurons are patterned by a process called self-avoidance, in which branches arising from a single neuron repel each other. By minimizing gaps and overlaps within the arborization, self-avoidance facilitates complete coverage of a neuron's territory by its neurites. Remarkably, some neurons that display self-avoidance interact freely with other neurons of the same subtype, implying that they discriminate self from non-self. Here we demonstrate roles for the clustered protocadherins (Pcdhs) in dendritic self-avoidance and self/non-self discrimination. The Pcdh locus encodes 58 related cadherin-like transmembrane proteins, at least some of which exhibit isoform-specific homophilic adhesion in heterologous cells and are expressed stochastically and combinatorially in single neurons. Deletion of all 22 Pcdh genes in the mouse gamma-subcluster (Pcdhg genes) disrupts self-avoidance of dendrites in retinal starburst amacrine cells (SACs) and cerebellar Purkinje cells. Further genetic analysis of SACs showed that Pcdhg proteins act cell-autonomously during development, and that replacement of the 22 Pcdhg proteins with a single isoform restores self-avoidance. Moreover, expression of the same single isoform in all SACs decreases interactions among dendrites of neighbouring SACs (heteroneuronal interactions). These results suggest that homophilic Pcdhg interactions between sibling neurites (isoneuronal interactions) generate a repulsive signal that leads to self-avoidance. In this model, heteroneuronal interactions are normally permitted because dendrites seldom encounter a matched set of Pcdhg proteins unless they emanate from the same soma. In many respects, our results mirror those reported for Dscam1 (Down syndrome cell adhesion molecule) in Drosophila: this complex gene encodes thousands of recognition molecules that exhibit stochastic expression and isoform-specific interactions, and mediate both self-avoidance and self/non-self discrimination. Thus, although insect Dscam and vertebrate Pcdh proteins share no sequence homology, they seem to underlie similar strategies for endowing neurons with distinct molecular identities and patterning their arborizations.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3427422/" 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/PMC3427422/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lefebvre, Julie L -- Kostadinov, Dimitar -- Chen, Weisheng V -- Maniatis, Tom -- Sanes, Joshua R -- F31 NS078893/NS/NINDS NIH HHS/ -- R01 EY022073/EY/NEI NIH HHS/ -- R01 NS029169/NS/NINDS NIH HHS/ -- R01EY022073/EY/NEI NIH HHS/ -- R01NS029169/NS/NINDS NIH HHS/ -- R01NS043915/NS/NINDS NIH HHS/ -- T32 EY007110/EY/NEI NIH HHS/ -- England -- Nature. 2012 Aug 23;488(7412):517-21. doi: 10.1038/nature11305.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Brain Science and Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22842903" target="_blank"〉PubMed〈/a〉
    Keywords: Amacrine Cells/*cytology/*metabolism ; Animals ; Cadherins/genetics/*metabolism ; Cell Adhesion Molecules/genetics/metabolism ; Cells, Cultured ; Dendrites/*metabolism ; Drosophila Proteins/genetics/metabolism ; Drosophila melanogaster/genetics/metabolism ; Evolution, Molecular ; Mice ; Mice, Transgenic ; Protein Isoforms/genetics/metabolism ; Purkinje Cells/*cytology/*metabolism
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  • 117
    Publication Date: 2012-03-27
    Description: Alternative messenger RNA splicing is the main reason that vast mammalian proteomic complexity can be achieved with a limited number of genes. Splicing is physically and functionally coupled to transcription, and is greatly affected by the rate of transcript elongation. As the nascent pre-mRNA emerges from transcribing RNA polymerase II (RNAPII), it is assembled into a messenger ribonucleoprotein (mRNP) particle; this is the functional form of the nascent pre-mRNA and determines the fate of the mature transcript. However, factors that connect the transcribing polymerase with the mRNP particle and help to integrate transcript elongation with mRNA splicing remain unclear. Here we characterize the human interactome of chromatin-associated mRNP particles. This led us to identify deleted in breast cancer 1 (DBC1) and ZNF326 (which we call ZNF-protein interacting with nuclear mRNPs and DBC1 (ZIRD)) as subunits of a novel protein complex--named DBIRD--that binds directly to RNAPII. DBIRD regulates alternative splicing of a large set of exons embedded in (A + T)-rich DNA, and is present at the affected exons. RNA-interference-mediated DBIRD depletion results in region-specific decreases in transcript elongation, particularly across areas encompassing affected exons. Together, these data indicate that the DBIRD complex acts at the interface between mRNP particles and RNAPII, integrating transcript elongation with the regulation of alternative splicing.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3378035/" 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/PMC3378035/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Close, Pierre -- East, Philip -- Dirac-Svejstrup, A Barbara -- Hartmann, Holger -- Heron, Mark -- Maslen, Sarah -- Chariot, Alain -- Soding, Johannes -- Skehel, Mark -- Svejstrup, Jesper Q -- A3560/Cancer Research UK/United Kingdom -- Cancer Research UK/United Kingdom -- England -- Nature. 2012 Mar 25;484(7394):386-9. doi: 10.1038/nature10925.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Mechanisms of Transcription Laboratory, Cancer Research UK London Research Institute, Clare Hall Laboratories, South Mimms EN6 3LD, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22446626" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptor Proteins, Signal Transducing/genetics/metabolism ; *Alternative Splicing ; Animals ; Carrier Proteins/genetics/metabolism ; Chromatin/genetics/metabolism ; Exons/genetics ; HEK293 Cells ; Heterogeneous-Nuclear Ribonucleoproteins/deficiency/metabolism ; Humans ; Mice ; Multiprotein Complexes/*chemistry/genetics/*metabolism ; RNA Interference ; RNA Polymerase II/*metabolism ; RNA, Messenger/*biosynthesis/*genetics/metabolism ; Ribonucleoproteins/chemistry/genetics/metabolism ; *Transcription, Genetic
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  • 118
    facet.materialart.
    Unknown
    Nature Publishing Group (NPG)
    Publication Date: 2012-09-22
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nijhuis, Michelle -- England -- Nature. 2012 Sep 20;489(7416):352-4. doi: 10.1038/489352a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22996530" target="_blank"〉PubMed〈/a〉
    Keywords: Alaska ; Animals ; Desert Climate ; *Ecosystem ; Fires/prevention & control/*statistics & numerical data ; Global Warming/statistics & numerical data ; Insects/physiology ; Montana ; Southwestern United States ; Trees/*metabolism/parasitology
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  • 119
    Publication Date: 2012-06-05
    Description: Adult stem cells support tissue homeostasis and repair throughout the life of an individual. During ageing, numerous intrinsic and extrinsic changes occur that result in altered stem-cell behaviour and reduced tissue maintenance and regeneration. In the Drosophila testis, ageing results in a marked decrease in the self-renewal factor Unpaired (Upd), leading to a concomitant loss of germline stem cells. Here we demonstrate that IGF-II messenger RNA binding protein (Imp) counteracts endogenous small interfering RNAs to stabilize upd (also known as os) RNA. However, similar to upd, Imp expression decreases in the hub cells of older males, which is due to the targeting of Imp by the heterochronic microRNA let-7. In the absence of Imp, upd mRNA therefore becomes unprotected and susceptible to degradation. Understanding the mechanistic basis for ageing-related changes in stem-cell behaviour will lead to the development of strategies to treat age-onset diseases and facilitate stem-cell-based therapies in older individuals.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Toledano, Hila -- D'Alterio, Cecilia -- Czech, Benjamin -- Levine, Erel -- Jones, D Leanne -- R01 AG028092/AG/NIA NIH HHS/ -- R01 AG040288/AG/NIA NIH HHS/ -- England -- Nature. 2012 May 23;485(7400):605-10. doi: 10.1038/nature11061.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Genetics, The Salk Institute for Biological Studies, La Jolla, California 92037, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22660319" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Argonaute Proteins/metabolism ; Base Sequence ; Cell Aging/*physiology ; Drosophila Proteins/biosynthesis/genetics/*metabolism ; Drosophila melanogaster/*cytology/genetics/*metabolism ; Female ; Male ; MicroRNAs/*genetics ; Organ Specificity ; RNA Helicases/metabolism ; RNA, Messenger/genetics/metabolism ; RNA, Small Interfering/antagonists & inhibitors/genetics/metabolism ; RNA-Binding Proteins/biosynthesis/genetics/*metabolism ; Ribonuclease III/metabolism ; Stem Cell Niche/genetics/*physiology ; Testis/*cytology ; Transcription Factors/genetics/metabolism
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  • 120
    facet.materialart.
    Unknown
    Nature Publishing Group (NPG)
    Publication Date: 2012-11-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Trounson, Alan -- England -- Nature. 2012 Nov 8;491(7423):193. doi: 10.1038/491193a.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉California Institute for Regenerative Medicine, San Francisco, California 94107, USA. atrounson@cirm.ca.gov〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23135461" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Awards and Prizes ; Cellular Reprogramming ; Cloning, Organism/*history ; Embryonic Stem Cells/physiology ; Female ; Great Britain ; History, 20th Century ; Induced Pluripotent Stem Cells/physiology ; Sheep ; Swine
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  • 121
    Publication Date: 2012-07-06
    Description: Autism spectrum disorders (ASDs) are highly prevalent neurodevelopmental disorders, but the underlying pathogenesis remains poorly understood. Recent studies have implicated the cerebellum in these disorders, with post-mortem studies in ASD patients showing cerebellar Purkinje cell (PC) loss, and isolated cerebellar injury has been associated with a higher incidence of ASDs. However, the extent of cerebellar contribution to the pathogenesis of ASDs remains unclear. Tuberous sclerosis complex (TSC) is a genetic disorder with high rates of comorbid ASDs that result from mutation of either TSC1 or TSC2, whose protein products dimerize and negatively regulate mammalian target of rapamycin (mTOR) signalling. TSC is an intriguing model to investigate the cerebellar contribution to the underlying pathogenesis of ASDs, as recent studies in TSC patients demonstrate cerebellar pathology and correlate cerebellar pathology with increased ASD symptomatology. Functional imaging also shows that TSC patients with ASDs display hypermetabolism in deep cerebellar structures, compared to TSC patients without ASDs. However, the roles of Tsc1 and the sequelae of Tsc1 dysfunction in the cerebellum have not been investigated so far. Here we show that both heterozygous and homozygous loss of Tsc1 in mouse cerebellar PCs results in autistic-like behaviours, including abnormal social interaction, repetitive behaviour and vocalizations, in addition to decreased PC excitability. Treatment of mutant mice with the mTOR inhibitor, rapamycin, prevented the pathological and behavioural deficits. These findings demonstrate new roles for Tsc1 in PC function and define a molecular basis for a cerebellar contribution to cognitive disorders such as autism.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3615424/" 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/PMC3615424/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tsai, Peter T -- Hull, Court -- Chu, YunXiang -- Greene-Colozzi, Emily -- Sadowski, Abbey R -- Leech, Jarrett M -- Steinberg, Jason -- Crawley, Jacqueline N -- Regehr, Wade G -- Sahin, Mustafa -- K12 NS079414/NS/NINDS NIH HHS/ -- P30HD18655/HD/NICHD NIH HHS/ -- R01 NS032405/NS/NINDS NIH HHS/ -- R01NS032405/NS/NINDS NIH HHS/ -- R01NS58956/NS/NINDS NIH HHS/ -- T32 MH020017/MH/NIMH NIH HHS/ -- T32 NS007473/NS/NINDS NIH HHS/ -- Howard Hughes Medical Institute/ -- Intramural NIH HHS/ -- England -- Nature. 2012 Aug 30;488(7413):647-51. doi: 10.1038/nature11310.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉The F.M. Kirby Neurobiology Center, Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA. peter.tsai@childrens.harvard.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22763451" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Autistic Disorder/complications/genetics/pathology/*physiopathology ; Behavior, Animal/drug effects ; Cell Count ; Cell Shape/drug effects ; Cerebellum/drug effects/pathology/*physiopathology ; Grooming/drug effects/physiology ; Heterozygote ; Maze Learning/drug effects/physiology ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mutation/genetics ; Purkinje Cells/drug effects/*metabolism ; Rotarod Performance Test ; Sirolimus/pharmacology ; Synapses/metabolism ; TOR Serine-Threonine Kinases/antagonists & inhibitors/metabolism ; Tuberous Sclerosis/complications/genetics ; Tumor Suppressor Proteins/deficiency/*genetics/*metabolism ; Vocalization, Animal/drug effects/physiology
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  • 122
    Publication Date: 2012-09-18
    Description: Antiviral responses must be tightly regulated to defend rapidly against infection while minimizing inflammatory damage. Type 1 interferons (IFN-I) are crucial mediators of antiviral responses and their transcription is regulated by a variety of transcription factors; principal among these is the family of interferon regulatory factors (IRFs). The IRF gene regulatory networks are complex and contain multiple feedback loops. The tools of systems biology are well suited to elucidate the complex interactions that give rise to precise coordination of the interferon response. Here we have used an unbiased systems approach to predict that a member of the forkhead family of transcription factors, FOXO3, is a negative regulator of a subset of antiviral genes. This prediction was validated using macrophages isolated from Foxo3-null mice. Genome-wide location analysis combined with gene deletion studies identified the Irf7 gene as a critical target of FOXO3. FOXO3 was identified as a negative regulator of Irf7 transcription and we have further demonstrated that FOXO3, IRF7 and IFN-I form a coherent feed-forward regulatory circuit. Our data suggest that the FOXO3-IRF7 regulatory circuit represents a novel mechanism for establishing the requisite set points in the interferon pathway that balances the beneficial effects and deleterious sequelae of the antiviral response.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3556990/" 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/PMC3556990/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Litvak, Vladimir -- Ratushny, Alexander V -- Lampano, Aaron E -- Schmitz, Frank -- Huang, Albert C -- Raman, Ayush -- Rust, Alistair G -- Bergthaler, Andreas -- Aitchison, John D -- Aderem, Alan -- HHSN272200700038C/AI/NIAID NIH HHS/ -- HHSN272200700038C/PHS HHS/ -- HHSN272200800058C/AI/NIAID NIH HHS/ -- HSN272200800058C/PHS HHS/ -- R01 AI025032/AI/NIAID NIH HHS/ -- R01 AI032972/AI/NIAID NIH HHS/ -- R01AI025032/AI/NIAID NIH HHS/ -- R01AI032972/AI/NIAID NIH HHS/ -- U19 AI100627/AI/NIAID NIH HHS/ -- U54 GM103511/GM/NIGMS NIH HHS/ -- U54 RR022220/RR/NCRR NIH HHS/ -- U54GM103511/GM/NIGMS NIH HHS/ -- England -- Nature. 2012 Oct 18;490(7420):421-5. doi: 10.1038/nature11428. Epub 2012 Sep 16.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Seattle Biomedical Research Institute, Seattle, Washington 98109, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22982991" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Female ; Forkhead Transcription Factors/deficiency/genetics/*metabolism ; Gene Deletion ; Gene Expression Regulation/*immunology ; Inflammation/genetics/*immunology/*pathology ; Interferon Regulatory Factor-7/deficiency/genetics/*metabolism ; Interferon Type I/immunology ; Lung/immunology/pathology/virology ; Macrophages/immunology ; Mice ; Mice, Inbred C57BL ; Reproducibility of Results ; Vesiculovirus/*immunology
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  • 123
    Publication Date: 2012-07-20
    Description: Animals approach stimuli that predict a pleasant outcome. After the paired presentation of an odour and a reward, Drosophila melanogaster can develop a conditioned approach towards that odour. Despite recent advances in understanding the neural circuits for associative memory and appetitive motivation, the cellular mechanisms for reward processing in the fly brain are unknown. Here we show that a group of dopamine neurons in the protocerebral anterior medial (PAM) cluster signals sugar reward by transient activation and inactivation of target neurons in intact behaving flies. These dopamine neurons are selectively required for the reinforcing property of, but not a reflexive response to, the sugar stimulus. In vivo calcium imaging revealed that these neurons are activated by sugar ingestion and the activation is increased on starvation. The output sites of the PAM neurons are mainly localized to the medial lobes of the mushroom bodies (MBs), where appetitive olfactory associative memory is formed. We therefore propose that the PAM cluster neurons endow a positive predictive value to the odour in the MBs. Dopamine in insects is known to mediate aversive reinforcement signals. Our results highlight the cellular specificity underlying the various roles of dopamine and the importance of spatially segregated local circuits within the MBs.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Liu, Chang -- Placais, Pierre-Yves -- Yamagata, Nobuhiro -- Pfeiffer, Barret D -- Aso, Yoshinori -- Friedrich, Anja B -- Siwanowicz, Igor -- Rubin, Gerald M -- Preat, Thomas -- Tanimoto, Hiromu -- R01 MH081982/MH/NIMH NIH HHS/ -- Howard Hughes Medical Institute/ -- England -- Nature. 2012 Aug 23;488(7412):512-6. doi: 10.1038/nature11304.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Max-Planck-Institut fur Neurobiologie, Martinsried 82152, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22810589" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Appetitive Behavior/physiology ; Calcium Signaling ; Dendrites/physiology ; Dopamine/metabolism ; Dopaminergic Neurons/cytology/*physiology ; Drosophila melanogaster/*cytology/*physiology ; Memory/*physiology ; Mushroom Bodies/cytology/metabolism ; Odors/*analysis ; *Reward ; Smell/genetics/physiology
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  • 124
    Publication Date: 2012-06-09
    Description: Synaptic neurotransmitter release is driven by Ca(2+) influx through active zone voltage-gated calcium channels (VGCCs). Control of active zone VGCC abundance and function remains poorly understood. Here we show that a trafficking step probably sets synaptic VGCC levels in rats, because overexpression of the pore-forming alpha1(A) VGCC subunit fails to change synaptic VGCC abundance or function. alpha2deltas are a family of glycosylphosphatidylinositol (GPI)-anchored VGCC-associated subunits that, in addition to being the target of the potent neuropathic analgesics gabapentin and pregabalin (alpha2delta-1 and alpha2delta-2), were also identified in a forward genetic screen for pain genes (alpha2delta-3). We show that these proteins confer powerful modulation of presynaptic function through two distinct molecular mechanisms. First, alpha2delta subunits set synaptic VGCC abundance, as predicted from their chaperone-like function when expressed in non-neuronal cells. Second, alpha2deltas configure synaptic VGCCs to drive exocytosis through an extracellular metal ion-dependent adhesion site (MIDAS), a conserved set of amino acids within the predicted von Willebrand A domain of alpha2delta. Expression of alpha2delta with an intact MIDAS motif leads to an 80% increase in release probability, while simultaneously protecting exocytosis from blockade by an intracellular Ca(2+) chelator. alpha2deltas harbouring MIDAS site mutations still drive synaptic accumulation of VGCCs; however, they no longer change release probability or sensitivity to intracellular Ca(2+) chelators. Our data reveal dual functionality of these clinically important VGCC subunits, allowing synapses to make more efficient use of Ca(2+) entry to drive neurotransmitter release.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3376018/" 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/PMC3376018/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hoppa, Michael B -- Lana, Beatrice -- Margas, Wojciech -- Dolphin, Annette C -- Ryan, Timothy A -- G0700368/Medical Research Council/United Kingdom -- G0801756/Medical Research Council/United Kingdom -- G0901758/Medical Research Council/United Kingdom -- R01 MH085783/MH/NIMH NIH HHS/ -- R01 MH085783-01A1/MH/NIMH NIH HHS/ -- R01 MH085783-02/MH/NIMH NIH HHS/ -- R01 MH085783-03/MH/NIMH NIH HHS/ -- R01 MH085783-04/MH/NIMH NIH HHS/ -- England -- Nature. 2012 May 13;486(7401):122-5. doi: 10.1038/nature11033.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry, Weill Cornell Medical College, New York, New York 10023, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22678293" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials ; Animals ; Calcium Channels/biosynthesis/*genetics/*metabolism ; Calcium Signaling ; *Exocytosis ; Mice ; Neurotransmitter Agents/metabolism/*secretion ; Presynaptic Terminals/*metabolism/*secretion ; Probability ; Rats
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  • 125
    Publication Date: 2012-03-13
    Description: Many bacterial pathogens can enter various host cells and then survive intracellularly, transiently evade humoral immunity, and further disseminate to other cells and tissues. When bacteria enter host cells and replicate intracellularly, the host cells sense the invading bacteria as damage-associated molecular patterns (DAMPs) and pathogen-associated molecular patterns (PAMPs) by way of various pattern recognition receptors. As a result, the host cells induce alarm signals that activate the innate immune system. Therefore, bacteria must modulate host inflammatory signalling and dampen these alarm signals. How pathogens do this after invading epithelial cells remains unclear, however. Here we show that OspI, a Shigella flexneri effector encoded by ORF169b on the large plasmid and delivered by the type IotaIotaIota secretion system, dampens acute inflammatory responses during bacterial invasion by suppressing the tumour-necrosis factor (TNF)-receptor-associated factor 6 (TRAF6)-mediated signalling pathway. OspI is a glutamine deamidase that selectively deamidates the glutamine residue at position 100 in UBC13 to a glutamic acid residue. Consequently, the E2 ubiquitin-conjugating activity required for TRAF6 activation is inhibited, allowing S. flexneri OspI to modulate the diacylglycerol-CBM (CARD-BCL10-MALT1) complex-TRAF6-nuclear-factor-kappaB signalling pathway. We determined the 2.0 A crystal structure of OspI, which contains a putative cysteine-histidine-aspartic acid catalytic triad. A mutational analysis showed this catalytic triad to be essential for the deamidation of UBC13. Our results suggest that S. flexneri inhibits acute inflammatory responses in the initial stage of infection by targeting the UBC13-TRAF6 complex.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sanada, Takahito -- Kim, Minsoo -- Mimuro, Hitomi -- Suzuki, Masato -- Ogawa, Michinaga -- Oyama, Akiho -- Ashida, Hiroshi -- Kobayashi, Taira -- Koyama, Tomohiro -- Nagai, Shinya -- Shibata, Yuri -- Gohda, Jin -- Inoue, Jun-ichiro -- Mizushima, Tsunehiro -- Sasakawa, Chihiro -- England -- Nature. 2012 Mar 11;483(7391):623-6. doi: 10.1038/nature10894.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Infectious Disease Control, International Research Center for Infectious Diseases, University of Tokyo, Minato-ku, Tokyo 108-8639, Japan.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22407319" target="_blank"〉PubMed〈/a〉
    Keywords: *Adaptor Proteins, Signal Transducing/metabolism ; Amidohydrolases/*chemistry/genetics/*metabolism ; Amino Acid Sequence ; Animals ; Aspartic Acid/metabolism ; Biocatalysis ; Caspases/metabolism ; Catalytic Domain/genetics ; Crystallography, X-Ray ; Cysteine/metabolism ; DNA Mutational Analysis ; Diglycerides/antagonists & inhibitors/metabolism ; Dysentery, Bacillary/microbiology ; Glutamic Acid/metabolism ; Glutamine/metabolism ; HEK293 Cells ; HeLa Cells ; Histidine/metabolism ; Humans ; Immunity, Innate ; Inflammation/enzymology/*immunology/*metabolism ; Mice ; Models, Molecular ; Molecular Sequence Data ; NF-kappa B/metabolism ; Neoplasm Proteins/metabolism ; Shigella flexneri/*enzymology/genetics/*immunology/pathogenicity ; TNF Receptor-Associated Factor 6/deficiency/genetics/metabolism ; Ubiquitin-Conjugating Enzymes/chemistry/genetics/*metabolism ; Virulence Factors/metabolism
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  • 126
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    Unknown
    Nature Publishing Group (NPG)
    Publication Date: 2012-07-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Turnbaugh, Peter J -- England -- Nature. 2012 Jul 4;487(7405):47-8. doi: 10.1038/487047a.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉FAS Center for Systems Biology, Harvard University, Cambridge, Massachusetts 02138, USA. pturnbaugh@fas.harvard.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22763552" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bilophila/*drug effects ; Colitis/*chemically induced/*microbiology ; Dietary Fats/*pharmacology ; Interleukin-10/*deficiency ; Metagenome/*drug effects ; Taurocholic Acid/*metabolism
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  • 127
    Publication Date: 2012-11-09
    Description: Regulatory T (T(reg)) cells, characterized by expression of the transcription factor forkhead box P3 (Foxp3), maintain immune homeostasis by suppressing self-destructive immune responses. Foxp3 operates as a late-acting differentiation factor controlling T(reg) cell homeostasis and function, whereas the early T(reg)-cell-lineage commitment is regulated by the Akt kinase and the forkhead box O (Foxo) family of transcription factors. However, whether Foxo proteins act beyond the T(reg)-cell-commitment stage to control T(reg) cell homeostasis and function remains largely unexplored. Here we show that Foxo1 is a pivotal regulator of T(reg )cell function. T(reg) cells express high amounts of Foxo1 and display reduced T-cell-receptor-induced Akt activation, Foxo1 phosphorylation and Foxo1 nuclear exclusion. Mice with T(reg)-cell-specific deletion of Foxo1 develop a fatal inflammatory disorder similar in severity to that seen in Foxp3-deficient mice, but without the loss of T(reg) cells. Genome-wide analysis of Foxo1 binding sites reveals ~300 Foxo1-bound target genes, including the pro-inflammatory cytokine Ifng, that do not seem to be directly regulated by Foxp3. These findings show that the evolutionarily ancient Akt-Foxo1 signalling module controls a novel genetic program indispensable for T(reg) cell function.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3771531/" 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/PMC3771531/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ouyang, Weiming -- Liao, Will -- Luo, Chong T -- Yin, Na -- Huse, Morgan -- Kim, Myoungjoo V -- Peng, Min -- Chan, Pamela -- Ma, Qian -- Mo, Yifan -- Meijer, Dies -- Zhao, Keji -- Rudensky, Alexander Y -- Atwal, Gurinder -- Zhang, Michael Q -- Li, Ming O -- HG001696/HG/NHGRI NIH HHS/ -- R01 HG001696/HG/NHGRI NIH HHS/ -- Howard Hughes Medical Institute/ -- England -- Nature. 2012 Nov 22;491(7425):554-9. doi: 10.1038/nature11581. Epub 2012 Nov 7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Immunology Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10065, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23135404" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Binding Sites ; Cell Nucleus/metabolism/pathology ; Female ; Forkhead Transcription Factors/*metabolism ; Gene Expression Regulation/genetics ; Genome/genetics ; Immune Tolerance/genetics/immunology ; Interferon-gamma/deficiency/genetics ; Male ; Mice ; Mice, Inbred C57BL ; Proto-Oncogene Proteins c-akt/metabolism ; Receptors, Antigen, T-Cell/immunology/metabolism ; Signal Transduction ; T-Lymphocytes, Regulatory/*immunology/*metabolism/pathology ; *Transcription, Genetic
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  • 128
    Publication Date: 2012-11-07
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bolker, Jessica -- England -- Nature. 2012 Nov 1;491(7422):31-3. doi: 10.1038/491031a.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biological Sciences, University of New Hampshire, Durham 03824, New Hampshire, USA. jessica.bolker@unh.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23128209" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Animals, Laboratory ; Arabidopsis ; Caenorhabditis elegans ; Disease Models, Animal ; Drosophila melanogaster/genetics/growth & development/physiology ; Environment ; Genotype ; Mice ; *Models, Animal ; *Models, Biological ; Phenotype ; Rats ; Reproducibility of Results ; Research Design/*standards ; Species Specificity
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  • 129
    Publication Date: 2012-05-25
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Owen, Richard -- Jobling, Susan -- England -- Nature. 2012 May 23;485(7399):441. doi: 10.1038/485441a.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉University of Exeter Business School, Exeter EX4 4PU, UK. r.j.owen@exeter.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22622553" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Wild ; Aquatic Organisms/*drug effects ; Contraceptives, Oral, Hormonal/adverse effects/chemistry ; Disorders of Sex Development/*chemically induced ; Endocrine Disruptors/*adverse effects/analysis ; Environmental Monitoring/economics ; Environmental Policy/*economics ; Ethinyl Estradiol/*adverse effects/analysis ; Europe ; Female ; Fishes ; Fresh Water/chemistry ; Humans
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  • 130
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    Unknown
    Nature Publishing Group (NPG)
    Publication Date: 2012-11-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gilbert, Natasha -- England -- Nature. 2012 Nov 22;491(7425):503-4. doi: 10.1038/491503a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23172189" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Aquatic Organisms/drug effects ; Disorders of Sex Development/chemically induced/epidemiology/*veterinary ; Endocrine Disruptors/*adverse effects/*isolation & purification/poisoning ; Environmental Restoration and Remediation/economics/*legislation & jurisprudence ; Ethinyl Estradiol/adverse effects/isolation & purification/poisoning ; European Union/economics ; Female ; Fishes/abnormalities ; Great Britain ; Male ; Rivers/chemistry ; Water Pollution/*adverse effects/economics/*legislation & jurisprudence ; Water Purification/economics/*legislation & jurisprudence/methods
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  • 131
    Publication Date: 2012-02-22
    Description: Human neurodegenerative diseases have the temporal hallmark of afflicting the elderly population. Ageing is one of the most prominent factors to influence disease onset and progression, yet little is known about the molecular pathways that connect these processes. To understand this connection it is necessary to identify the pathways that functionally integrate ageing, chronic maintenance of the brain and modulation of neurodegenerative disease. MicroRNAs (miRNA) are emerging as critical factors in gene regulation during development; however, their role in adult-onset, age-associated processes is only beginning to be revealed. Here we report that the conserved miRNA miR-34 regulates age-associated events and long-term brain integrity in Drosophila, providing a molecular link between ageing and neurodegeneration. Fly mir-34 expression exhibits adult-onset, brain-enriched and age-modulated characteristics. Whereas mir-34 loss triggers a gene profile of accelerated brain ageing, late-onset brain degeneration and a catastrophic decline in survival, mir-34 upregulation extends median lifespan and mitigates neurodegeneration induced by human pathogenic polyglutamine disease protein. Some of the age-associated effects of miR-34 require adult-onset translational repression of Eip74EF, an essential ETS domain transcription factor involved in steroid hormone pathways. Our studies indicate that miRNA-dependent pathways may have an impact on adult-onset, age-associated events by silencing developmental genes that later have a deleterious influence on adult life cycle and disease, and highlight fly miR-34 as a key miRNA with a role in this process.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3326599/" 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/PMC3326599/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Liu, Nan -- Landreh, Michael -- Cao, Kajia -- Abe, Masashi -- Hendriks, Gert-Jan -- Kennerdell, Jason R -- Zhu, Yongqing -- Wang, Li-San -- Bonini, Nancy M -- AG010124/AG/NIA NIH HHS/ -- R01 NS043578/NS/NINDS NIH HHS/ -- R01 NS043578-05/NS/NINDS NIH HHS/ -- R01-NS043578/NS/NINDS NIH HHS/ -- RC2 AG036528/AG/NIA NIH HHS/ -- RC2 AG036528-01/AG/NIA NIH HHS/ -- RC2-AG036528-01/AG/NIA NIH HHS/ -- T32 AG000255/AG/NIA NIH HHS/ -- T32 AG000255-02/AG/NIA NIH HHS/ -- T32 AG00255/AG/NIA NIH HHS/ -- U01 AG032984/AG/NIA NIH HHS/ -- U01 AG032984-02/AG/NIA NIH HHS/ -- U01-AG-032984-02/AG/NIA NIH HHS/ -- Howard Hughes Medical Institute/ -- England -- Nature. 2012 Feb 15;482(7386):519-23. doi: 10.1038/nature10810.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biology, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22343898" target="_blank"〉PubMed〈/a〉
    Keywords: Aging/*genetics ; Animals ; Brain/metabolism/pathology ; *Disease Models, Animal ; Down-Regulation ; Drosophila Proteins/biosynthesis/genetics ; Drosophila melanogaster/*genetics/*physiology ; Female ; Gene Expression Regulation/*genetics ; Hot Temperature ; Humans ; Longevity/genetics ; Male ; MicroRNAs/*genetics ; Mutation ; Neurodegenerative Diseases/*genetics/pathology ; Protein Biosynthesis ; RNA, Messenger/analysis/genetics ; Survival Analysis ; Time Factors ; Transcription Factors/biosynthesis/genetics ; Up-Regulation
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  • 132
    Publication Date: 2012-11-20
    Description: The mammalian gastrointestinal tract provides a complex and competitive environment for the microbiota. Successful colonization by pathogens requires scavenging nutrients, sensing chemical signals, competing with the resident bacteria and precisely regulating the expression of virulence genes. The gastrointestinal pathogen enterohaemorrhagic Escherichia coli (EHEC) relies on inter-kingdom chemical sensing systems to regulate virulence gene expression. Here we show that these systems control the expression of a novel two-component signal transduction system, named FusKR, where FusK is the histidine sensor kinase and FusR the response regulator. FusK senses fucose and controls expression of virulence and metabolic genes. This fucose-sensing system is required for robust EHEC colonization of the mammalian intestine. Fucose is highly abundant in the intestine. Bacteroides thetaiotaomicron produces multiple fucosidases that cleave fucose from host glycans, resulting in high fucose availability in the gut lumen. During growth in mucin, B. thetaiotaomicron contributes to EHEC virulence by cleaving fucose from mucin, thereby activating the FusKR signalling cascade, modulating the virulence gene expression of EHEC. Our findings suggest that EHEC uses fucose, a host-derived signal made available by the microbiota, to modulate EHEC pathogenicity and metabolism.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518558/" 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/PMC3518558/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pacheco, Alline R -- Curtis, Meredith M -- Ritchie, Jennifer M -- Munera, Diana -- Waldor, Matthew K -- Moreira, Cristiano G -- Sperandio, Vanessa -- 5 T32 AI7520-14/AI/NIAID NIH HHS/ -- AI053067/AI/NIAID NIH HHS/ -- AI077613/AI/NIAID NIH HHS/ -- AI42347/AI/NIAID NIH HHS/ -- AI77853/AI/NIAID NIH HHS/ -- R01 AI053067/AI/NIAID NIH HHS/ -- R01 AI077613/AI/NIAID NIH HHS/ -- R37 AI042347/AI/NIAID NIH HHS/ -- England -- Nature. 2012 Dec 6;492(7427):113-7. doi: 10.1038/nature11623. Epub 2012 Nov 18.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, Texas 75390-9048, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23160491" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bacterial Proteins/*metabolism ; Bacteroides/enzymology/growth & development/*metabolism ; Enterohemorrhagic Escherichia coli/genetics/*growth & development/pathogenicity ; Escherichia coli Proteins/genetics/metabolism ; Fucose/*metabolism ; Gastrointestinal Tract/metabolism/*microbiology ; Gene Expression Regulation, Bacterial ; Mucins/metabolism ; Protein Kinases/genetics/metabolism ; Rabbits ; Receptors, Adrenergic/metabolism ; Signal Transduction ; Transcription Factors/genetics/metabolism ; Virulence/genetics ; Virulence Factors/genetics ; alpha-L-Fucosidase/metabolism
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  • 133
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    Nature Publishing Group (NPG)
    Publication Date: 2012-05-04
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉England -- Nature. 2012 May 2;485(7396):6. doi: 10.1038/485006b.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22552052" target="_blank"〉PubMed〈/a〉
    Keywords: Americas ; Animals ; Archaeology/*standards ; Emigrants and Immigrants/history ; Emigration and Immigration/*history ; History, Ancient ; Humans ; Models, Theoretical
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  • 134
    Publication Date: 2012-03-24
    Description: A specific memory is thought to be encoded by a sparse population of neurons. These neurons can be tagged during learning for subsequent identification and manipulation. Moreover, their ablation or inactivation results in reduced memory expression, suggesting their necessity in mnemonic processes. However, the question of sufficiency remains: it is unclear whether it is possible to elicit the behavioural output of a specific memory by directly activating a population of neurons that was active during learning. Here we show in mice that optogenetic reactivation of hippocampal neurons activated during fear conditioning is sufficient to induce freezing behaviour. We labelled a population of hippocampal dentate gyrus neurons activated during fear learning with channelrhodopsin-2 (ChR2) and later optically reactivated these neurons in a different context. The mice showed increased freezing only upon light stimulation, indicating light-induced fear memory recall. This freezing was not detected in non-fear-conditioned mice expressing ChR2 in a similar proportion of cells, nor in fear-conditioned mice with cells labelled by enhanced yellow fluorescent protein instead of ChR2. Finally, activation of cells labelled in a context not associated with fear did not evoke freezing in mice that were previously fear conditioned in a different context, suggesting that light-induced fear memory recall is context specific. Together, our findings indicate that activating a sparse but specific ensemble of hippocampal neurons that contribute to a memory engram is sufficient for the recall of that memory. Moreover, our experimental approach offers a general method of mapping cellular populations bearing memory engrams.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3331914/" 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/PMC3331914/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Liu, Xu -- Ramirez, Steve -- Pang, Petti T -- Puryear, Corey B -- Govindarajan, Arvind -- Deisseroth, Karl -- Tonegawa, Susumu -- P50 MH058880/MH/NIMH NIH HHS/ -- P50 MH058880-10/MH/NIMH NIH HHS/ -- P50-MH58880/MH/NIMH NIH HHS/ -- R01 MH078821/MH/NIMH NIH HHS/ -- R01 MH078821-17/MH/NIMH NIH HHS/ -- R01-MH078821/MH/NIMH NIH HHS/ -- England -- Nature. 2012 Mar 22;484(7394):381-5. doi: 10.1038/nature11028.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉RIKEN-MIT Center for Neural Circuit Genetics at the Picower Institute for Learning and Memory, Department of Biology and Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22441246" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bacterial Proteins/genetics/metabolism ; Conditioning (Psychology)/physiology/radiation effects ; Dentate Gyrus/cytology/physiology/radiation effects ; Fear/*physiology/*radiation effects ; Female ; Freezing Reaction, Cataleptic/physiology/radiation effects ; Gene Expression Regulation ; Hippocampus/cytology/*physiology/*radiation effects ; Light ; Luminescent Proteins/genetics/metabolism ; Male ; Mental Recall/*radiation effects ; Mice ; Mice, Transgenic ; Rhodopsin/genetics/metabolism
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  • 135
    Publication Date: 2012-09-29
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Infante, Francisco -- Perez, Jeanneth -- Vega, Fernando E -- England -- Nature. 2012 Sep 27;489(7417):502. doi: 10.1038/489502a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23018957" target="_blank"〉PubMed〈/a〉
    Keywords: Agriculture/economics/*methods ; Animals ; Beetles/drug effects/microbiology/*pathogenicity ; Coffea/*parasitology ; Coffee/economics ; Insect Control/economics/*methods ; Seeds/parasitology
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  • 136
    Publication Date: 2012-07-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Padian, Kevin -- England -- Nature. 2012 Jul 19;487(7407):310-11. doi: 10.1038/nature11382.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22763457" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bone Development/*physiology ; *Bone and Bones ; Dinosaurs/*physiology ; *Seasons
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  • 137
    Publication Date: 2012-03-02
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Collins, James -- England -- Nature. 2012 Feb 29;483(7387):S11. doi: 10.1038/483S11a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22378119" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bioengineering/economics/*trends ; Bioreactors ; Genetic Engineering/trends ; Humans ; Metagenome ; Mice ; Neoplasms/genetics/immunology/pathology ; Synthetic Biology/economics/*trends
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  • 138
    Publication Date: 2012-11-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Houllier, Francois -- England -- Nature. 2012 Nov 15;491(7424):327. doi: 10.1038/491327a.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉INRA, Paris, France. francois.houllier@paris.inra.fr〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23151562" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biotechnology/ethics/*standards ; *Organisms, Genetically Modified ; Periodicals as Topic ; Public Opinion ; Research/*standards
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  • 139
    Publication Date: 2012-01-17
    Description: Hair cells of the inner ear are not normally replaced during an animal's life, and must continually renew components of their various organelles. Among these are the stereocilia, each with a core of several hundred actin filaments that arise from their apical surfaces and that bear the mechanotransduction apparatus at their tips. Actin turnover in stereocilia has previously been studied by transfecting neonatal rat hair cells in culture with a beta-actin-GFP fusion, and evidence was found that actin is replaced, from the top down, in 2-3 days. Overexpression of the actin-binding protein espin causes elongation of stereocilia within 12-24 hours, also suggesting rapid regulation of stereocilia lengths. Similarly, the mechanosensory 'tip links' are replaced in 5-10 hours after cleavage in chicken and mammalian hair cells. In contrast, turnover in chick stereocilia in vivo is much slower. It might be that only certain components of stereocilia turn over quickly, that rapid turnover occurs only in neonatal animals, only in culture, or only in response to a challenge like breakage or actin overexpression. Here we quantify protein turnover by feeding animals with a (15)N-labelled precursor amino acid and using multi-isotope imaging mass spectrometry to measure appearance of new protein. Surprisingly, in adult frogs and mice and in neonatal mice, in vivo and in vitro, the stereocilia were remarkably stable, incorporating newly synthesized protein at 〈10% per day. Only stereocilia tips had rapid turnover and no treadmilling was observed. Other methods confirmed this: in hair cells expressing beta-actin-GFP we bleached fiducial lines across hair bundles, but they did not move in 6 days. When we stopped expression of beta- or gamma-actin with tamoxifen-inducible recombination, neither actin isoform left the stereocilia, except at the tips. Thus, rapid turnover in stereocilia occurs only at the tips and not by a treadmilling process.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3267870/" 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/PMC3267870/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zhang, Duan-Sun -- Piazza, Valeria -- Perrin, Benjamin J -- Rzadzinska, Agnieszka K -- Poczatek, J Collin -- Wang, Mei -- Prosser, Haydn M -- Ervasti, James M -- Corey, David P -- Lechene, Claude P -- 2P41RR0112553-12/RR/NCRR NIH HHS/ -- F32DC009539/DC/NIDCD NIH HHS/ -- P41EB001974/EB/NIBIB NIH HHS/ -- P41RR14579/RR/NCRR NIH HHS/ -- R01 AR042423/AR/NIAMS NIH HHS/ -- R01 AR042423-08/AR/NIAMS NIH HHS/ -- R01 AR049899/AR/NIAMS NIH HHS/ -- R01 DC000033/DC/NIDCD NIH HHS/ -- R01 DC002281/DC/NIDCD NIH HHS/ -- R01AR049899/AR/NIAMS NIH HHS/ -- R01D K58762/PHS HHS/ -- R01DC00033/DC/NIDCD NIH HHS/ -- R01DC02281/DC/NIDCD NIH HHS/ -- R01DC03463/DC/NIDCD NIH HHS/ -- R01DC04179/DC/NIDCD NIH HHS/ -- R01EY12963/EY/NEI NIH HHS/ -- R01GM47214/GM/NIGMS NIH HHS/ -- R37DK39773/DK/NIDDK NIH HHS/ -- WT079643/Wellcome Trust/United Kingdom -- Howard Hughes Medical Institute/ -- England -- Nature. 2012 Jan 15;481(7382):520-4. doi: 10.1038/nature10745.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurobiology, Harvard Medical School and Howard Hughes Medical Institute, Boston, Massachusetts 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22246323" target="_blank"〉PubMed〈/a〉
    Keywords: Actins/metabolism ; Animals ; Animals, Newborn ; Bleaching Agents ; Chickens ; Epithelium/drug effects/metabolism ; Fiducial Markers ; Hair Cells, Auditory, Inner/*cytology ; Homologous Recombination/drug effects ; Mass Spectrometry/*methods ; Mice ; Mice, Inbred C57BL ; Proteins/*metabolism ; Rana catesbeiana ; Stereocilia/*metabolism ; Tamoxifen/pharmacology
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  • 140
    Publication Date: 2012-10-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tollefson, Jeff -- England -- Nature. 2012 Oct 25;490(7421):458-9. doi: 10.1038/490458a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23099379" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Aquatic Organisms/metabolism ; Canada ; Carbon Dioxide/metabolism ; *Carbon Sequestration ; Ecology ; Environmental Policy/*legislation & jurisprudence ; Oceans and Seas ; Phytoplankton/growth & development/metabolism ; Politics ; Salmon/*growth & development ; Seawater/*chemistry ; Uncertainty
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  • 141
    Publication Date: 2012-06-09
    Description: Human activities are causing Earth's sixth major extinction event-an accelerating decline of the world's stocks of biological diversity at rates 100 to 1,000 times pre-human levels. Historically, low-impact intrusion into species habitats arose from local demands for food, fuel and living space. However, in today's increasingly globalized economy, international trade chains accelerate habitat degradation far removed from the place of consumption. Although adverse effects of economic prosperity and economic inequality have been confirmed, the importance of international trade as a driver of threats to species is poorly understood. Here we show that a significant number of species are threatened as a result of international trade along complex routes, and that, in particular, consumers in developed countries cause threats to species through their demand of commodities that are ultimately produced in developing countries. We linked 25,000 Animalia species threat records from the International Union for Conservation of Nature Red List to more than 15,000 commodities produced in 187 countries and evaluated more than 5 billion supply chains in terms of their biodiversity impacts. Excluding invasive species, we found that 30% of global species threats are due to international trade. In many developed countries, the consumption of imported coffee, tea, sugar, textiles, fish and other manufactured items causes a biodiversity footprint that is larger abroad than at home. Our results emphasize the importance of examining biodiversity loss as a global systemic phenomenon, instead of looking at the degrading or polluting producers in isolation. We anticipate that our findings will facilitate better regulation, sustainable supply-chain certification and consumer product labelling.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lenzen, M -- Moran, D -- Kanemoto, K -- Foran, B -- Lobefaro, L -- Geschke, A -- England -- Nature. 2012 Jun 6;486(7401):109-12. doi: 10.1038/nature11145.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉ISA, School of Physics A28, The University of Sydney, New South Wales 2006, Australia. m.lenzen@physics.usyd.edu.au〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22678290" target="_blank"〉PubMed〈/a〉
    Keywords: Agriculture/economics/statistics & numerical data ; Animals ; *Biodiversity ; Commerce/economics/*statistics & numerical data ; Crops, Agricultural/economics/supply & distribution ; Developed Countries/economics/statistics & numerical data ; *Developing Countries/economics/statistics & numerical data ; Endangered Species/*statistics & numerical data ; Fisheries/statistics & numerical data ; Forestry/economics/statistics & numerical data ; Industry/economics/*statistics & numerical data ; *Internationality
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  • 142
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    Nature Publishing Group (NPG)
    Publication Date: 2012-08-04
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Borrell, Brendan -- England -- Nature. 2012 Aug 2;488(7409):18. doi: 10.1038/488018a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22859181" target="_blank"〉PubMed〈/a〉
    Keywords: Aging/*drug effects/metabolism ; Animals ; Astragalus membranaceus/chemistry ; Biotechnology/economics/*legislation & jurisprudence ; Dietary Supplements/adverse effects ; Employee Grievances/*legislation & jurisprudence ; Humans ; Male ; Mice ; Plant Extracts/adverse effects/economics/*pharmacology ; Prostatic Neoplasms/chemically induced ; *Rejuvenation ; Telomerase/deficiency/genetics/metabolism ; Telomere/*drug effects/enzymology/metabolism ; Unemployment
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  • 143
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    Nature Publishing Group (NPG)
    Publication Date: 2012-11-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Borthwick, Lindsay -- England -- Nature. 2012 Nov 1;491(7422):S10-1.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23136653" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Aged ; *Aging ; Animals ; Autistic Disorder/diagnosis/economics/*physiopathology/therapy ; Baclofen/analogs & derivatives/therapeutic use ; Benzamides/therapeutic use ; Child ; Humans ; Imidazoles/therapeutic use ; Intelligence Tests ; Longitudinal Studies ; Mice ; Middle Aged ; Patient Advocacy ; Personal Health Services/statistics & numerical data/supply & distribution ; Prevalence ; Prognosis ; Pyridines/therapeutic use ; Speech ; Young Adult
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  • 144
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    Nature Publishing Group (NPG)
    Publication Date: 2012-01-13
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gilbert, Natasha -- England -- Nature. 2012 Jan 10;481(7380):125. doi: 10.1038/481125a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22237084" target="_blank"〉PubMed〈/a〉
    Keywords: Agriculture/*legislation & jurisprudence/*methods ; Animals ; *Animals, Domestic/microbiology ; Anti-Bacterial Agents/*administration & dosage/pharmacology ; Antibiotic Prophylaxis/utilization/veterinary ; Cephalosporins/administration & dosage/pharmacology ; Drug Resistance, Bacterial/drug effects ; European Union ; Humans ; United States ; United States Food and Drug Administration
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  • 145
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    Nature Publishing Group (NPG)
    Publication Date: 2012-02-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pagel, Mark -- England -- Nature. 2012 Feb 15;482(7385):297-9. doi: 10.1038/482297a.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉School of Biological Sciences, University of Reading, UK. m.pagel@reading.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22337031" target="_blank"〉PubMed〈/a〉
    Keywords: Altruism ; Animals ; *Communication/history ; *Cultural Evolution/history ; History, Ancient ; Humans ; Knowledge ; *Language/history ; Learning ; *Social Behavior/history ; Social Justice/psychology ; Survival
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  • 146
    Publication Date: 2012-02-14
    Description: Neisseria are obligate human pathogens causing bacterial meningitis, septicaemia and gonorrhoea. Neisseria require iron for survival and can extract it directly from human transferrin for transport across the outer membrane. The transport system consists of TbpA, an integral outer membrane protein, and TbpB, a co-receptor attached to the cell surface; both proteins are potentially important vaccine and therapeutic targets. Two key questions driving Neisseria research are how human transferrin is specifically targeted, and how the bacteria liberate iron from transferrin at neutral pH. To address these questions, we solved crystal structures of the TbpA-transferrin complex and of the corresponding co-receptor TbpB. We characterized the TbpB-transferrin complex by small-angle X-ray scattering and the TbpA-TbpB-transferrin complex by electron microscopy. Our studies provide a rational basis for the specificity of TbpA for human transferrin, show how TbpA promotes iron release from transferrin, and elucidate how TbpB facilitates this process.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3292680/" 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/PMC3292680/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Noinaj, Nicholas -- Easley, Nicole C -- Oke, Muse -- Mizuno, Naoko -- Gumbart, James -- Boura, Evzen -- Steere, Ashley N -- Zak, Olga -- Aisen, Philip -- Tajkhorshid, Emad -- Evans, Robert W -- Gorringe, Andrew R -- Mason, Anne B -- Steven, Alasdair C -- Buchanan, Susan K -- P41 RR005969/RR/NCRR NIH HHS/ -- P41-RR05969/RR/NCRR NIH HHS/ -- R01 GM086749/GM/NIGMS NIH HHS/ -- R01-DK21739/DK/NIDDK NIH HHS/ -- R01-GM086749/GM/NIGMS NIH HHS/ -- U54 GM087519/GM/NIGMS NIH HHS/ -- U54-GM087519/GM/NIGMS NIH HHS/ -- ZIA DK036143-04/Intramural NIH HHS/ -- England -- Nature. 2012 Feb 12;483(7387):53-8. doi: 10.1038/nature10823.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, US National Institutes of Health, Bethesda, Maryland 20892, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22327295" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Apoproteins/chemistry/metabolism ; Bacterial Proteins/*chemistry/metabolism/ultrastructure ; Binding Sites ; Biological Transport ; Cattle ; Crystallography, X-Ray ; Humans ; Iron/*metabolism ; Mice ; Models, Molecular ; Molecular Dynamics Simulation ; Neisseria/*metabolism/pathogenicity ; Protein Conformation ; Scattering, Small Angle ; Species Specificity ; Structure-Activity Relationship ; Transferrin/chemistry/metabolism/ultrastructure ; Transferrin-Binding Protein A/*chemistry/*metabolism/ultrastructure ; Transferrin-Binding Protein B/*chemistry/*metabolism/ultrastructure ; X-Ray Diffraction
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  • 147
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    Nature Publishing Group (NPG)
    Publication Date: 2012-07-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉England -- Nature. 2012 Jul 25;487(7408):405-6. doi: 10.1038/487405b.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22836960" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biodiversity ; Conservation of Natural Resources/*statistics & numerical data ; Data Collection ; Interviews as Topic ; Surveys and Questionnaires ; *Wilderness
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  • 148
    Publication Date: 2012-02-02
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Berns, Kenneth I -- Casadevall, Arturo -- Cohen, Murray L -- Ehrlich, Susan A -- Enquist, Lynn W -- Fitch, J Patrick -- Franz, David R -- Fraser-Liggett, Claire M -- Grant, Christine M -- Imperiale, Michael J -- Kanabrocki, Joseph -- Keim, Paul S -- Lemon, Stanley M -- Levy, Stuart B -- Lumpkin, John R -- Miller, Jeffery F -- Murch, Randall -- Nance, Mark E -- Osterholm, Michael T -- Relman, David A -- Roth, James A -- Vidaver, Anne K -- England -- Nature. 2012 Jan 31;482(7384):153-4. doi: 10.1038/482153a.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉US National Science Advisory Board for Biosecurity, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22294204" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bioterrorism/prevention & control/*trends ; Humans ; Influenza A Virus, H5N1 Subtype/*genetics/*pathogenicity/physiology ; Influenza, Human/*transmission/*virology ; Public Health ; Risk Assessment ; Zoonoses/transmission/virology
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  • 149
    Publication Date: 2012-04-28
    Description: Allergies are generally thought to be a detrimental outcome of a mistargeted immune response that evolved to provide immunity to macroparasites. Here we present arguments to suggest that allergic immunity has an important role in host defence against noxious environmental substances, including venoms, haematophagous fluids, environmental xenobiotics and irritants. We argue that appropriately targeted allergic reactions are beneficial, although they can become detrimental when excessive. Furthermore, we suggest that allergic hypersensitivity evolved to elicit anticipatory responses and to promote avoidance of suboptimal environments.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596087/" 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/PMC3596087/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Palm, Noah W -- Rosenstein, Rachel K -- Medzhitov, Ruslan -- R01 AI055502/AI/NIAID NIH HHS/ -- R01 AI089771/AI/NIAID NIH HHS/ -- R01 DK071754/DK/NIDDK NIH HHS/ -- T32 AR007107/AR/NIAMS NIH HHS/ -- Howard Hughes Medical Institute/ -- England -- Nature. 2012 Apr 25;484(7395):465-72. doi: 10.1038/nature11047.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06510, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22538607" target="_blank"〉PubMed〈/a〉
    Keywords: Allergens/adverse effects/immunology ; Animals ; Biological Evolution ; Environmental Exposure ; Humans ; Hypersensitivity/*immunology ; Inflammation/immunology ; *Models, Immunological ; Th2 Cells/*immunology ; Xenobiotics/adverse effects/immunology
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  • 150
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    Nature Publishing Group (NPG)
    Publication Date: 2012-08-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cyranoski, David -- England -- Nature. 2012 Aug 9;488(7410):139. doi: 10.1038/488139a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22874941" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Specimen Banks/economics/*organization & administration ; Cell Line ; Clinical Trials as Topic ; Fetal Blood/cytology ; Humans ; Induced Pluripotent Stem Cells/*cytology ; Japan ; Mice
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  • 151
    Publication Date: 2012-10-23
    Description: Reported widespread declines of wild and managed insect pollinators have serious consequences for global ecosystem services and agricultural production. Bees contribute approximately 80% of insect pollination, so it is important to understand and mitigate the causes of current declines in bee populations . Recent studies have implicated the role of pesticides in these declines, as exposure to these chemicals has been associated with changes in bee behaviour and reductions in colony queen production. However, the key link between changes in individual behaviour and the consequent impact at the colony level has not been shown. Social bee colonies depend on the collective performance of many individual workers. Thus, although field-level pesticide concentrations can have subtle or sublethal effects at the individual level, it is not known whether bee societies can buffer such effects or whether it results in a severe cumulative effect at the colony level. Furthermore, widespread agricultural intensification means that bees are exposed to numerous pesticides when foraging, yet the possible combinatorial effects of pesticide exposure have rarely been investigated. Here we show that chronic exposure of bumblebees to two pesticides (neonicotinoid and pyrethroid) at concentrations that could approximate field-level exposure impairs natural foraging behaviour and increases worker mortality leading to significant reductions in brood development and colony success. We found that worker foraging performance, particularly pollen collecting efficiency, was significantly reduced with observed knock-on effects for forager recruitment, worker losses and overall worker productivity. Moreover, we provide evidence that combinatorial exposure to pesticides increases the propensity of colonies to fail.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3495159/" 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/PMC3495159/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gill, Richard J -- Ramos-Rodriguez, Oscar -- Raine, Nigel E -- 094886/Wellcome Trust/United Kingdom -- BB/I000178/1/Biotechnology and Biological Sciences Research Council/United Kingdom -- Biotechnology and Biological Sciences Research Council/United Kingdom -- Wellcome Trust/United Kingdom -- England -- Nature. 2012 Nov 1;491(7422):105-8. doi: 10.1038/nature11585. Epub 2012 Oct 21.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉School of Biological Sciences, Royal Holloway, University of London, Egham, Surrey, TW20 0EX, UK. richard.gill@rhul.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23086150" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bees/*drug effects/*physiology ; Behavior, Animal/*drug effects/physiology ; Feeding Behavior/drug effects ; Female ; Imidazoles/pharmacology ; Insecticides/*pharmacology ; Male ; Nitro Compounds/pharmacology ; Pollen/metabolism ; Pollination/drug effects ; Pyrethrins/pharmacology ; *Social Behavior ; Social Dominance ; Survival Analysis
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  • 152
    Publication Date: 2012-03-01
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lombard, David B -- Miller, Richard A -- R01 GM101171/GM/NIGMS NIH HHS/ -- England -- Nature. 2012 Mar 7;483(7388):166-7. doi: 10.1038/nature10950.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22367538" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Female ; Longevity/*physiology ; Male ; *Sex Characteristics ; Sirtuins/*metabolism
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  • 153
    Publication Date: 2012-06-05
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Palpant, Nathan J -- Murry, Charles E -- England -- Nature. 2012 May 31;485(7400):585-6. doi: 10.1038/485585a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22660313" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Cell Transdifferentiation ; *Cellular Reprogramming ; Female ; Fibroblasts/*cytology ; Heart/*physiology ; Male ; Myocardial Infarction/*therapy ; Myocytes, Cardiac/*cytology/*physiology ; Regenerative Medicine/*methods ; Transcription Factors/*metabolism
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  • 154
    Publication Date: 2012-07-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schoeninger, Margaret J -- England -- Nature. 2012 Jul 4;487(7405):42-3. doi: 10.1038/487042a.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Anthropology, University of California, San Diego, La Jolla, California 92093, USA. mjschoen@ucsd.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22763547" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Diet/*veterinary ; *Food Preferences ; *Fossils ; *Fruit ; *Hominidae ; *Plant Bark ; *Plant Leaves
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  • 155
    Publication Date: 2012-03-17
    Description: Neuroectodermal signalling centres induce and pattern many novel vertebrate brain structures but are absent, or divergent, in invertebrate chordates. This has led to the idea that signalling-centre genetic programs were first assembled in stem vertebrates and potentially drove morphological innovations of the brain. However, this scenario presumes that extant cephalochordates accurately represent ancestral chordate characters, which has not been tested using close chordate outgroups. Here we report that genetic programs homologous to three vertebrate signalling centres-the anterior neural ridge, zona limitans intrathalamica and isthmic organizer-are present in the hemichordate Saccoglossus kowalevskii. Fgf8/17/18 (a single gene homologous to vertebrate Fgf8, Fgf17 and Fgf18), sfrp1/5, hh and wnt1 are expressed in vertebrate-like arrangements in hemichordate ectoderm, and homologous genetic mechanisms regulate ectodermal patterning in both animals. We propose that these genetic programs were components of an unexpectedly complex, ancient genetic regulatory scaffold for deuterostome body patterning that degenerated in amphioxus and ascidians, but was retained to pattern divergent structures in hemichordates and vertebrates.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3719855/" 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/PMC3719855/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pani, Ariel M -- Mullarkey, Erin E -- Aronowicz, Jochanan -- Assimacopoulos, Stavroula -- Grove, Elizabeth A -- Lowe, Christopher J -- 1F31NS074738-01A1/NS/NINDS NIH HHS/ -- 1T32HD055164-01A1/HD/NICHD NIH HHS/ -- F31 NS074738/NS/NINDS NIH HHS/ -- R01 HD042330/HD/NICHD NIH HHS/ -- R01 HD42330/HD/NICHD NIH HHS/ -- R37 MH059962/MH/NIMH NIH HHS/ -- T32 HD055164/HD/NICHD NIH HHS/ -- England -- Nature. 2012 Mar 14;483(7389):289-94. doi: 10.1038/nature10838.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Committee on Evolutionary Biology, The University of Chicago, 1025 East 57th Street, Chicago, Illinois 60637, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22422262" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biological Evolution ; Brain/*anatomy & histology/*embryology/physiology ; Chordata/*anatomy & histology/*embryology/genetics/physiology ; Fibroblast Growth Factors/metabolism ; Hedgehog Proteins/metabolism ; Mice ; *Signal Transduction ; Vertebrates/*anatomy & histology/*embryology/genetics/physiology ; Wnt Signaling Pathway
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  • 156
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    Unknown
    Nature Publishing Group (NPG)
    Publication Date: 2012-12-12
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bourzac, Katherine -- England -- Nature. 2012 Dec 6;492(7427):S18-20. doi: 10.1038/492S18a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23222670" target="_blank"〉PubMed〈/a〉
    Keywords: Age of Onset ; Aging/*drug effects/genetics/*physiology ; Animal Diseases/epidemiology/genetics/prevention & control ; Animals ; Biomedical Research ; *Caloric Restriction ; Cardiovascular Diseases/prevention & control ; Female ; Gene Expression Profiling ; Geriatrics/methods ; Humans ; Longevity/*drug effects/genetics/*physiology ; Macaca mulatta/physiology ; Male ; Mice ; Models, Animal ; Neoplasms/prevention & control ; Oligonucleotide Array Sequence Analysis ; Reproducibility of Results ; Sirolimus/adverse effects/analogs & derivatives/immunology/*pharmacology ; Sirtuins/deficiency/genetics/metabolism ; Somatomedins/genetics/metabolism ; Stilbenes/pharmacology ; TOR Serine-Threonine Kinases/metabolism
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  • 157
    Publication Date: 2012-02-24
    Description: Packaging of proteins from the endoplasmic reticulum into COPII vesicles is essential for secretion. In cells, most COPII vesicles are approximately 60-80 nm in diameter, yet some must increase their size to accommodate 300-400 nm procollagen fibres or chylomicrons. Impaired COPII function results in collagen deposition defects, cranio-lenticulo-sutural dysplasia, or chylomicron retention disease, but mechanisms to enlarge COPII coats have remained elusive. Here, we identified the ubiquitin ligase CUL3-KLHL12 as a regulator of COPII coat formation. CUL3-KLHL12 catalyses the monoubiquitylation of the COPII-component SEC31 and drives the assembly of large COPII coats. As a result, ubiquitylation by CUL3-KLHL12 is essential for collagen export, yet less important for the transport of small cargo. We conclude that monoubiquitylation controls the size and function of a vesicle coat.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3292188/" 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/PMC3292188/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Jin, Lingyan -- Pahuja, Kanika Bajaj -- Wickliffe, Katherine E -- Gorur, Amita -- Baumgartel, Christine -- Schekman, Randy -- Rape, Michael -- DP2 OD003088/OD/NIH HHS/ -- DP2 OD003088-01/OD/NIH HHS/ -- R01 GM083064/GM/NIGMS NIH HHS/ -- R01 GM083064-04/GM/NIGMS NIH HHS/ -- Howard Hughes Medical Institute/ -- England -- Nature. 2012 Feb 22;482(7386):495-500. doi: 10.1038/nature10822.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular and Cell Biology, University of California at Berkeley, California 94720, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22358839" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; COP-Coated Vesicles/*chemistry/*metabolism ; Cell Line ; Cell Shape ; Collagen/metabolism ; Cullin Proteins/genetics/metabolism ; Embryonic Stem Cells/cytology/metabolism ; HeLa Cells ; Humans ; Mice ; Microfilament Proteins/genetics/metabolism ; Protein Transport ; Ubiquitin/*metabolism ; Ubiquitination ; Vesicular Transport Proteins/genetics/metabolism
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  • 158
    Publication Date: 2012-04-24
    Description: Cell transplantation is a potential strategy for treating blindness caused by the loss of photoreceptors. Although transplanted rod-precursor cells are able to migrate into the adult retina and differentiate to acquire the specialized morphological features of mature photoreceptor cells, the fundamental question remains whether transplantation of photoreceptor cells can actually improve vision. Here we provide evidence of functional rod-mediated vision after photoreceptor transplantation in adult Gnat1-/- mice, which lack rod function and are a model of congenital stationary night blindness. We show that transplanted rod precursors form classic triad synaptic connections with second-order bipolar and horizontal cells in the recipient retina. The newly integrated photoreceptor cells are light-responsive with dim-flash kinetics similar to adult wild-type photoreceptors. By using intrinsic imaging under scotopic conditions we demonstrate that visual signals generated by transplanted rods are projected to higher visual areas, including V1. Moreover, these cells are capable of driving optokinetic head tracking and visually guided behaviour in the Gnat1-/- mouse under scotopic conditions. Together, these results demonstrate the feasibility of photoreceptor transplantation as a therapeutic strategy for restoring vision after retinal degeneration.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3888831/" 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/PMC3888831/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pearson, R A -- Barber, A C -- Rizzi, M -- Hippert, C -- Xue, T -- West, E L -- Duran, Y -- Smith, A J -- Chuang, J Z -- Azam, S A -- Luhmann, U F O -- Benucci, A -- Sung, C H -- Bainbridge, J W -- Carandini, M -- Yau, K-W -- Sowden, J C -- Ali, R R -- 082217/Wellcome Trust/United Kingdom -- EY016805/EY/NEI NIH HHS/ -- EY06837/EY/NEI NIH HHS/ -- EY11307/EY/NEI NIH HHS/ -- G03000341/Medical Research Council/United Kingdom -- G0901550/Medical Research Council/United Kingdom -- MR/J004553/1/Medical Research Council/United Kingdom -- NIHR-RP-011-003/Department of Health/United Kingdom -- R01 EY011307/EY/NEI NIH HHS/ -- R01 EY011307-18/EY/NEI NIH HHS/ -- R01 EY016805/EY/NEI NIH HHS/ -- R01 EY016805-07/EY/NEI NIH HHS/ -- Department of Health/United Kingdom -- England -- Nature. 2012 May 3;485(7396):99-103. doi: 10.1038/nature10997.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Genetics, UCL Institute of Ophthalmology, University College London, 11-43 Bath Street, London, EC1V 9EL, UK. rachael.pearson@ucl.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22522934" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; GTP-Binding Protein alpha Subunits/deficiency/genetics ; Light ; Maze Learning ; Mice ; Retinal Bipolar Cells/ultrastructure ; Retinal Horizontal Cells/ultrastructure ; Retinal Rod Photoreceptor Cells/cytology/*physiology/radiation ; effects/*transplantation ; Transducin/deficiency/genetics ; Vision, Ocular/*physiology/radiation effects ; Visual Cortex/physiology/radiation effects
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  • 159
    Publication Date: 2012-06-09
    Description: The complexity of cancer has led to recent interest in polypharmacological approaches for developing kinase-inhibitor drugs; however, optimal kinase-inhibition profiles remain difficult to predict. Using a Ret-kinase-driven Drosophila model of multiple endocrine neoplasia type 2 and kinome-wide drug profiling, here we identify that AD57 rescues oncogenic Ret-induced lethality, whereas related Ret inhibitors imparted reduced efficacy and enhanced toxicity. Drosophila genetics and compound profiling defined three pathways accounting for the mechanistic basis of efficacy and dose-limiting toxicity. Inhibition of Ret plus Raf, Src and S6K was required for optimal animal survival, whereas inhibition of the 'anti-target' Tor led to toxicity owing to release of negative feedback. Rational synthetic tailoring to eliminate Tor binding afforded AD80 and AD81, compounds featuring balanced pathway inhibition, improved efficacy and low toxicity in Drosophila and mammalian multiple endocrine neoplasia type 2 models. Combining kinase-focused chemistry, kinome-wide profiling and Drosophila genetics provides a powerful systems pharmacology approach towards developing compounds with a maximal therapeutic index.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3703503/" 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/PMC3703503/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dar, Arvin C -- Das, Tirtha K -- Shokat, Kevan M -- Cagan, Ross L -- P01 CA081403-11/CA/NCI NIH HHS/ -- R01 CA084309/CA/NCI NIH HHS/ -- R01 CA109730/CA/NCI NIH HHS/ -- R01 EB001987/EB/NIBIB NIH HHS/ -- R01CA084309/CA/NCI NIH HHS/ -- R01CA109730/CA/NCI NIH HHS/ -- R01EB001987/EB/NIBIB NIH HHS/ -- Howard Hughes Medical Institute/ -- England -- Nature. 2012 Jun 6;486(7401):80-4. doi: 10.1038/nature11127.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute and Department of Cellular and Molecular Pharmacology, University of California, San Francisco, California 94158, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22678283" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Benzenesulfonates/pharmacology ; Cell Transformation, Neoplastic/drug effects/pathology ; Disease Models, Animal ; Drosophila Proteins/antagonists & inhibitors/genetics/metabolism ; Drosophila melanogaster/drug effects/genetics ; Drug Evaluation, Preclinical ; Drug-Related Side Effects and Adverse Reactions ; Extracellular Signal-Regulated MAP Kinases/antagonists & inhibitors/metabolism ; Heterocyclic Compounds with 4 or More Rings/adverse ; effects/chemistry/pharmacology/therapeutic use ; Humans ; Male ; *Molecular Targeted Therapy ; Multiple Endocrine Neoplasia Type 2b/*drug therapy/enzymology/*genetics ; Niacinamide/analogs & derivatives ; Phenylurea Compounds ; *Polypharmacy ; Protein Kinase Inhibitors/adverse effects/chemistry/pharmacology/therapeutic use ; Proto-Oncogene Proteins c-ret/genetics/metabolism ; Pyridines/pharmacology ; Receptor Protein-Tyrosine Kinases/antagonists & inhibitors ; Signal Transduction/drug effects ; Survival Rate ; Xenograft Model Antitumor Assays ; src-Family Kinases/antagonists & inhibitors/metabolism
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  • 160
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    Unknown
    Nature Publishing Group (NPG)
    Publication Date: 2012-03-03
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉England -- Nature. 2012 Feb 29;483(7387):5-6. doi: 10.1038/483005b.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22382938" target="_blank"〉PubMed〈/a〉
    Keywords: Amish/genetics ; Animals ; Child ; Genetic Diseases, Inborn/diagnosis/economics/*genetics ; Genetics, Medical/*trends ; Humans ; Pediatrics/trends ; Rare Diseases/diagnosis/economics/*genetics ; Syndrome
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  • 161
    facet.materialart.
    Unknown
    Nature Publishing Group (NPG)
    Publication Date: 2012-10-19
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pennings, Steven C -- England -- Nature. 2012 Oct 18;490(7420):352-3. doi: 10.1038/490352a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23075984" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Eutrophication/*physiology ; *Food ; *Salts ; *Wetlands
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  • 162
    Publication Date: 2012-06-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gardner, Elie -- England -- Nature. 2012 Jun 20;486(7403):306-7. doi: 10.1038/486306a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22722169" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Chemical Fractionation/methods ; Conservation of Natural Resources/methods ; Diet/adverse effects ; Ecosystem ; *Environment ; Environmental Restoration and Remediation ; Fishes ; Gold/chemistry/*isolation & purification ; Humans ; Mercury/adverse effects/analysis/chemistry/isolation & purification ; Mercury Poisoning/*epidemiology/prevention & control ; Mining/*legislation & jurisprudence/standards ; Peru/epidemiology
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  • 163
    Publication Date: 2012-03-01
    Description: The mammalian target of rapamycin (mTOR) kinase is a master regulator of protein synthesis that couples nutrient sensing to cell growth and cancer. However, the downstream translationally regulated nodes of gene expression that may direct cancer development are poorly characterized. Using ribosome profiling, we uncover specialized translation of the prostate cancer genome by oncogenic mTOR signalling, revealing a remarkably specific repertoire of genes involved in cell proliferation, metabolism and invasion. We extend these findings by functionally characterizing a class of translationally controlled pro-invasion messenger RNAs that we show direct prostate cancer invasion and metastasis downstream of oncogenic mTOR signalling. Furthermore, we develop a clinically relevant ATP site inhibitor of mTOR, INK128, which reprograms this gene expression signature with therapeutic benefit for prostate cancer metastasis, for which there is presently no cure. Together, these findings extend our understanding of how the 'cancerous' translation machinery steers specific cancer cell behaviours, including metastasis, and may be therapeutically targeted.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3663483/" 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/PMC3663483/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hsieh, Andrew C -- Liu, Yi -- Edlind, Merritt P -- Ingolia, Nicholas T -- Janes, Matthew R -- Sher, Annie -- Shi, Evan Y -- Stumpf, Craig R -- Christensen, Carly -- Bonham, Michael J -- Wang, Shunyou -- Ren, Pingda -- Martin, Michael -- Jessen, Katti -- Feldman, Morris E -- Weissman, Jonathan S -- Shokat, Kevan M -- Rommel, Christian -- Ruggero, Davide -- R01 CA140456/CA/NCI NIH HHS/ -- R01 CA154916/CA/NCI NIH HHS/ -- Howard Hughes Medical Institute/ -- England -- Nature. 2012 Feb 22;485(7396):55-61. doi: 10.1038/nature10912.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉School of Medicine and Department of Urology, Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, California 94158, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22367541" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptor Proteins, Signal Transducing/metabolism ; Animals ; Benzoxazoles/pharmacology ; Cell Line, Tumor ; Cell Movement/drug effects/genetics ; Eukaryotic Initiation Factor-4E/metabolism ; Eukaryotic Initiation Factors/metabolism ; Gene Expression Regulation, Neoplastic/drug effects/genetics ; Genome/genetics ; Humans ; Male ; Mice ; Mice, Inbred C57BL ; Neoplasm Invasiveness/genetics ; *Neoplasm Metastasis/drug therapy/genetics ; Phosphoproteins/metabolism ; Prostatic Neoplasms/drug therapy/genetics/*pathology ; *Protein Biosynthesis ; Pyrimidines/pharmacology ; RNA, Messenger/genetics/metabolism ; Repressor Proteins/metabolism ; *Signal Transduction ; TOR Serine-Threonine Kinases/antagonists & inhibitors/*metabolism
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  • 164
    Publication Date: 2012-02-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cooke, Justin G -- Leaper, Russell -- Papastavrou, Vassili -- England -- Nature. 2012 Feb 15;482(7385):308. doi: 10.1038/482308c.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22337038" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Commerce ; Conservation of Natural Resources/*economics/*legislation & jurisprudence ; *Whales
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  • 165
    Publication Date: 2012-04-17
    Description: As with many other viruses, the initial cell attachment of rotaviruses, which are the major causative agent of infantile gastroenteritis, is mediated by interactions with specific cellular glycans. The distally located VP8* domain of the rotavirus spike protein VP4 (ref. 5) mediates such interactions. The existing paradigm is that 'sialidase-sensitive' animal rotavirus strains bind to glycans with terminal sialic acid (Sia), whereas 'sialidase-insensitive' human rotavirus strains bind to glycans with internal Sia such as GM1 (ref. 3). Although the involvement of Sia in the animal strains is firmly supported by crystallographic studies, it is not yet known how VP8* of human rotaviruses interacts with Sia and whether their cell attachment necessarily involves sialoglycans. Here we show that VP8* of a human rotavirus strain specifically recognizes A-type histo-blood group antigen (HBGA) using a glycan array screen comprised of 511 glycans, and that virus infectivity in HT-29 cells is abrogated by anti-A-type antibodies as well as significantly enhanced in Chinese hamster ovary cells genetically modified to express the A-type HBGA, providing a novel paradigm for initial cell attachment of human rotavirus. HBGAs are genetically determined glycoconjugates present in mucosal secretions, epithelia and on red blood cells, and are recognized as susceptibility and cell attachment factors for gastric pathogens like Helicobacter pylori and noroviruses. Our crystallographic studies show that the A-type HBGA binds to the human rotavirus VP8* at the same location as the Sia in the VP8* of animal rotavirus, and suggest how subtle changes within the same structural framework allow for such receptor switching. These results raise the possibility that host susceptibility to specific human rotavirus strains and pathogenesis are influenced by genetically controlled expression of different HBGAs among the world's population.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3350622/" 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/PMC3350622/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hu, Liya -- Crawford, Sue E -- Czako, Rita -- Cortes-Penfield, Nicolas W -- Smith, David F -- Le Pendu, Jacques -- Estes, Mary K -- Prasad, B V Venkataram -- AI 080656/AI/NIAID NIH HHS/ -- AI36040/AI/NIAID NIH HHS/ -- GM62116/GM/NIGMS NIH HHS/ -- P30 DK056338/DK/NIDDK NIH HHS/ -- P30 DK56338/DK/NIDDK NIH HHS/ -- P41 GM103694/GM/NIGMS NIH HHS/ -- R01 AI080656/AI/NIAID NIH HHS/ -- U54 GM062116/GM/NIGMS NIH HHS/ -- U54 GM062116-01A1/GM/NIGMS NIH HHS/ -- England -- Nature. 2012 Apr 15;485(7397):256-9. doi: 10.1038/nature10996.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Verna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, Texas 77030, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22504179" target="_blank"〉PubMed〈/a〉
    Keywords: ABO Blood-Group System/chemistry/genetics/immunology/*metabolism ; Amino Acid Sequence ; Animals ; CHO Cells ; Cricetinae ; Crystallography, X-Ray ; Erythrocytes/metabolism/virology ; Host Specificity/*physiology ; Humans ; Models, Molecular ; Molecular Sequence Data ; N-Acetylneuraminic Acid/antagonists & inhibitors/chemistry/immunology/metabolism ; RNA-Binding Proteins/chemistry/*metabolism ; Receptors, Virus/chemistry/genetics/*metabolism ; *Rotavirus/chemistry/classification/metabolism/pathogenicity ; Viral Nonstructural Proteins/chemistry/*metabolism
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  • 166
    Publication Date: 2012-12-14
    Description: The clinical efficacy and safety of a drug is determined by its activity profile across many proteins in the proteome. However, designing drugs with a specific multi-target profile is both complex and difficult. Therefore methods to design drugs rationally a priori against profiles of several proteins would have immense value in drug discovery. Here we describe a new approach for the automated design of ligands against profiles of multiple drug targets. The method is demonstrated by the evolution of an approved acetylcholinesterase inhibitor drug into brain-penetrable ligands with either specific polypharmacology or exquisite selectivity profiles for G-protein-coupled receptors. Overall, 800 ligand-target predictions of prospectively designed ligands were tested experimentally, of which 75% were confirmed to be correct. We also demonstrate target engagement in vivo. The approach can be a useful source of drug leads when multi-target profiles are required to achieve either selectivity over other drug targets or a desired polypharmacology.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3653568/" 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/PMC3653568/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Besnard, Jeremy -- Ruda, Gian Filippo -- Setola, Vincent -- Abecassis, Keren -- Rodriguiz, Ramona M -- Huang, Xi-Ping -- Norval, Suzanne -- Sassano, Maria F -- Shin, Antony I -- Webster, Lauren A -- Simeons, Frederick R C -- Stojanovski, Laste -- Prat, Annik -- Seidah, Nabil G -- Constam, Daniel B -- Bickerton, G Richard -- Read, Kevin D -- Wetsel, William C -- Gilbert, Ian H -- Roth, Bryan L -- Hopkins, Andrew L -- 083481/Wellcome Trust/United Kingdom -- BB/FOF/PF/15/09/Biotechnology and Biological Sciences Research Council/United Kingdom -- BB/J010510/1/Biotechnology and Biological Sciences Research Council/United Kingdom -- MH082441/MH/NIMH NIH HHS/ -- R01 DA017204/DA/NIDA NIH HHS/ -- R01 MH061887/MH/NIMH NIH HHS/ -- U19 MH082441/MH/NIMH NIH HHS/ -- WT 083481/Wellcome Trust/United Kingdom -- England -- Nature. 2012 Dec 13;492(7428):215-20. doi: 10.1038/nature11691.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Biological Chemistry and Drug Discovery, College of Life Sciences, University of Dundee, Dundee DD1 5EH, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23235874" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Automation ; Drug Delivery Systems ; *Drug Design ; Female ; *Ligands ; Male ; Mice ; Mice, Inbred C57BL ; Models, Theoretical ; Pharmacological Phenomena ; Reproducibility of Results
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  • 167
    Publication Date: 2012-06-29
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Levin, I -- Veidt, C -- Vaughn, B H -- Brailsford, G -- Bromley, T -- Heinz, R -- Lowe, D -- Miller, J B -- Poss, C -- White, J W C -- England -- Nature. 2012 Jun 27;486(7404):E3-4; discussion E4. doi: 10.1038/nature11175.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institut fur Umweltphysik, Heidelberg University, 69120 Heidelberg, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22739319" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Atmosphere/*chemistry ; *Geography ; Methane/*analysis ; Microbial Consortia/*physiology
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  • 168
    Publication Date: 2012-10-13
    Description: Calcium-dependent exocytosis of synaptic vesicles mediates the release of neurotransmitters. Important proteins in this process have been identified such as the SNAREs, synaptotagmins, complexins, Munc18 and Munc13. Structural and functional studies have yielded a wealth of information about the physiological role of these proteins. However, it has been surprisingly difficult to arrive at a unified picture of the molecular sequence of events from vesicle docking to calcium-triggered membrane fusion. Using mainly a biochemical and biophysical perspective, we briefly survey the molecular mechanisms in an attempt to functionally integrate the key proteins into the emerging picture of the neuronal fusion machine.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4461657/" 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/PMC4461657/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Jahn, Reinhard -- Fasshauer, Dirk -- 3P01GM072694-05S1/GM/NIGMS NIH HHS/ -- P01 GM072694/GM/NIGMS NIH HHS/ -- England -- Nature. 2012 Oct 11;490(7419):201-7. doi: 10.1038/nature11320.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurobiology, Max-Planck-Institute for Biophysical Chemistry, 37077 Gottingen, Germany. rjahn@gwdg.de〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23060190" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Calcium/metabolism ; Exocytosis/*physiology ; Humans ; Lipid Metabolism ; Models, Biological ; SNARE Proteins/chemistry/metabolism ; Synaptic Vesicles/*physiology
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  • 169
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    Publication Date: 2012-04-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Git, Anna -- England -- Nature. 2012 Apr 25;484(7395):439-40. doi: 10.1038/484439a.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Cancer Research UK, Cambridge Research Institute, Li Ka Shing Centre, Cambridge CB2 0RE, UK. anna.git@cancer.org.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22538584" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biotechnology/economics/*standards ; *Confidentiality ; *Disclosure ; Efficiency ; Humans ; Indicators and Reagents/economics/*standards ; Mice ; MicroRNAs/biosynthesis/genetics ; Patents as Topic ; Reference Standards ; Research/economics/*standards
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  • 170
    Publication Date: 2012-10-02
    Description: The genome-wide identification of pairs of interacting proteins is an important step in the elucidation of cell regulatory mechanisms. Much of our present knowledge derives from high-throughput techniques such as the yeast two-hybrid assay and affinity purification, as well as from manual curation of experiments on individual systems. A variety of computational approaches based, for example, on sequence homology, gene co-expression and phylogenetic profiles, have also been developed for the genome-wide inference of protein-protein interactions (PPIs). Yet comparative studies suggest that the development of accurate and complete repertoires of PPIs is still in its early stages. Here we show that three-dimensional structural information can be used to predict PPIs with an accuracy and coverage that are superior to predictions based on non-structural evidence. Moreover, an algorithm, termed PrePPI, which combines structural information with other functional clues, is comparable in accuracy to high-throughput experiments, yielding over 30,000 high-confidence interactions for yeast and over 300,000 for human. Experimental tests of a number of predictions demonstrate the ability of the PrePPI algorithm to identify unexpected PPIs of considerable biological interest. The surprising effectiveness of three-dimensional structural information can be attributed to the use of homology models combined with the exploitation of both close and remote geometric relationships between proteins.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3482288/" 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/PMC3482288/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zhang, Qiangfeng Cliff -- Petrey, Donald -- Deng, Lei -- Qiang, Li -- Shi, Yu -- Thu, Chan Aye -- Bisikirska, Brygida -- Lefebvre, Celine -- Accili, Domenico -- Hunter, Tony -- Maniatis, Tom -- Califano, Andrea -- Honig, Barry -- CA082683/CA/NCI NIH HHS/ -- CA121852/CA/NCI NIH HHS/ -- DK057539/DK/NIDDK NIH HHS/ -- GM030518/GM/NIGMS NIH HHS/ -- GM094597/GM/NIGMS NIH HHS/ -- R01 CA082683/CA/NCI NIH HHS/ -- R01 DK057539/DK/NIDDK NIH HHS/ -- R01 GM030518/GM/NIGMS NIH HHS/ -- R01 NS043915/NS/NINDS NIH HHS/ -- R01NS043915/NS/NINDS NIH HHS/ -- U54 CA121852/CA/NCI NIH HHS/ -- U54 GM094597/GM/NIGMS NIH HHS/ -- Howard Hughes Medical Institute/ -- England -- Nature. 2012 Oct 25;490(7421):556-60. doi: 10.1038/nature11503. Epub 2012 Sep 30.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Columbia University, New York, New York 10032, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23023127" target="_blank"〉PubMed〈/a〉
    Keywords: *Algorithms ; Animals ; Bayes Theorem ; Brain/metabolism ; Cadherins/metabolism ; High-Throughput Screening Assays ; Humans ; Matrix Attachment Region Binding Proteins/metabolism ; Mice ; Models, Molecular ; PPAR gamma/metabolism ; Phylogeny ; Protein Binding ; Protein Conformation ; Protein Interaction Mapping/*methods ; *Protein Interaction Maps ; Protein Kinases/chemistry/metabolism ; Proteins/*chemistry/*metabolism ; Proteome/chemistry/metabolism ; Proteomics/*methods ; ROC Curve ; Reproducibility of Results ; Saccharomyces cerevisiae/chemistry/metabolism ; Suppressor of Cytokine Signaling Proteins/metabolism ; Transcription Factors/metabolism
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  • 171
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    Publication Date: 2012-02-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cooper, Barry -- England -- Nature. 2012 Feb 22;482(7386):465. doi: 10.1038/482465a.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉School of Mathematics, University of Leeds, Leeds LS2 9JT, UK. pmt6sbc@leeds.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22358814" target="_blank"〉PubMed〈/a〉
    Keywords: *Algorithms ; Animals ; Artificial Intelligence ; Brain/physiology ; *Computer Simulation ; Computers/history ; History, 20th Century ; Humans ; Mathematics/history ; Morphogenesis ; Quantum Theory/history
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  • 172
    Publication Date: 2012-12-12
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schughart, Klaus -- Libert, Claude -- Kas, Martien J -- England -- Nature. 2012 Dec 6;492(7427):41. doi: 10.1038/492041c.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23222600" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Animals, Laboratory ; *Models, Animal ; *Models, Biological ; Research Design/*standards
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  • 173
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    Nature Publishing Group (NPG)
    Publication Date: 2012-06-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Park, Soo Bin -- England -- Nature. 2012 Jun 5;486(7401):14. doi: 10.1038/486014a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22678257" target="_blank"〉PubMed〈/a〉
    Keywords: Academies and Institutes ; Animals ; *Biological Evolution ; Biology/*education ; Birds/physiology ; Humans ; Phylogeny ; *Religion and Science ; Republic of Korea ; *Textbooks as Topic
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  • 174
    Publication Date: 2012-11-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gladwin, Mark T -- Kim-Shapiro, Daniel B -- England -- Nature. 2012 Nov 15;491(7424):344-5. doi: 10.1038/nature11640. Epub 2012 Oct 31.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23123855" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Endothelial Cells/*metabolism ; *Gene Expression Regulation ; Hemoglobins/*metabolism ; Humans ; Nitric Oxide/*metabolism ; Peptide Fragments/*metabolism ; *Signal Transduction
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  • 175
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    Nature Publishing Group (NPG)
    Publication Date: 2012-03-31
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉England -- Nature. 2012 Mar 28;483(7391):509-10. doi: 10.1038/483509b.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22460860" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Global Health ; Humans ; Influenza A Virus, H5N1 Subtype/genetics/isolation & purification/pathogenicity ; Influenza, Human/*epidemiology/transmission/*virology ; Population Surveillance/*methods ; Poultry/virology ; Swine/virology ; Zoonoses/epidemiology/transmission/virology
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  • 176
    Publication Date: 2012-07-18
    Description: The inflammasome regulates the release of caspase activation-dependent cytokines, including interleukin (IL)-1beta, IL-18 and high-mobility group box 1 (HMGB1). By studying HMGB1 release mechanisms, here we identify a role for double-stranded RNA-dependent protein kinase (PKR, also known as EIF2AK2) in inflammasome activation. Exposure of macrophages to inflammasome agonists induced PKR autophosphorylation. PKR inactivation by genetic deletion or pharmacological inhibition severely impaired inflammasome activation in response to double-stranded RNA, ATP, monosodium urate, adjuvant aluminium, rotenone, live Escherichia coli, anthrax lethal toxin, DNA transfection and Salmonella typhimurium infection. PKR deficiency significantly inhibited the secretion of IL-1beta, IL-18 and HMGB1 in E. coli-induced peritonitis. PKR physically interacts with several inflammasome components, including NOD-like receptor (NLR) family pyrin domain-containing 3 (NLRP3), NLRP1, NLR family CARD domain-containing protein 4 (NLRC4), absent in melanoma 2 (AIM2), and broadly regulates inflammasome activation. PKR autophosphorylation in a cell-free system with recombinant NLRP3, apoptosis-associated speck-like protein containing a CARD (ASC, also known as PYCARD) and pro-caspase-1 reconstitutes inflammasome activity. These results show a crucial role for PKR in inflammasome activation, and indicate that it should be possible to pharmacologically target this molecule to treat inflammation.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4163918/" 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/PMC4163918/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lu, Ben -- Nakamura, Takahisa -- Inouye, Karen -- Li, Jianhua -- Tang, Yiting -- Lundback, Peter -- Valdes-Ferrer, Sergio I -- Olofsson, Peder S -- Kalb, Thomas -- Roth, Jesse -- Zou, Yongrui -- Erlandsson-Harris, Helena -- Yang, Huan -- Ting, Jenny P-Y -- Wang, Haichao -- Andersson, Ulf -- Antoine, Daniel J -- Chavan, Sangeeta S -- Hotamisligil, Gokhan S -- Tracey, Kevin J -- DK052539/DK/NIDDK NIH HHS/ -- G0700654/Medical Research Council/United Kingdom -- R01 DK052539/DK/NIDDK NIH HHS/ -- R01 GM057226/GM/NIGMS NIH HHS/ -- R01 GM062508/GM/NIGMS NIH HHS/ -- R01 GM62508/GM/NIGMS NIH HHS/ -- England -- Nature. 2012 Aug 30;488(7413):670-4. doi: 10.1038/nature11290.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Biomedical Science, The Feinstein Institute for Medical Research, 350 Community Drive, Manhasset, New York 11030, USA. blu@nshs.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22801494" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptor Proteins, Signal Transducing/metabolism ; Adenosine Triphosphate/pharmacology ; Animals ; Antigens, Bacterial/pharmacology ; Apoptosis Regulatory Proteins/metabolism ; Bacterial Toxins/pharmacology ; CARD Signaling Adaptor Proteins/metabolism ; Calcium-Binding Proteins/metabolism ; Carrier Proteins/metabolism ; Cell Line ; Cells, Cultured ; Crystallins/metabolism ; Escherichia coli/immunology/physiology ; Escherichia coli Infections/immunology/metabolism ; Female ; HMGB1 Protein/blood/*secretion ; Humans ; Inflammasomes/agonists/*metabolism ; Interleukin-18/blood ; Interleukin-1beta/blood ; Interleukin-6/analysis/blood ; Macrophages, Peritoneal/drug effects/metabolism ; Male ; Membrane Proteins/metabolism ; Mice ; Mice, Inbred C57BL ; Peritonitis/metabolism ; Phosphorylation ; RNA, Double-Stranded/immunology/pharmacology ; Rotenone/pharmacology ; Salmonella Infections/immunology/metabolism ; Salmonella typhimurium/immunology/physiology ; Transfection ; Uric Acid/pharmacology ; eIF-2 Kinase/antagonists & inhibitors/deficiency/genetics/*metabolism
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  • 177
    Publication Date: 2012-11-16
    Description: Cancer metabolism has received a substantial amount of interest over the past decade. The advances in analytical tools have, along with the rapid progress of cancer genomics, generated an increasingly complex understanding of metabolic reprogramming in cancer. As numerous connections between oncogenic signalling pathways and metabolic activities emerge, the importance of metabolic reprogramming in cancer is being increasingly recognized. The identification of metabolic weaknesses of cancer cells has been used to create strategies for treating cancer, but there are still challenges to be faced in bringing the drugs that target cancer metabolism to the clinic.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schulze, Almut -- Harris, Adrian L -- 11359/Cancer Research UK/United Kingdom -- NF-SI-0611-10163/Department of Health/United Kingdom -- Cancer Research UK/United Kingdom -- England -- Nature. 2012 Nov 15;491(7424):364-73. doi: 10.1038/nature11706.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Gene Expression Analysis Laboratory, Cancer Research UK, London Research Institute, 44 Lincoln's Inn Fields, London WC2A 3LY, UK. almut.schulze@cancer.org.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23151579" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Proliferation ; Humans ; Lipids/biosynthesis ; Mitochondria/metabolism ; Neoplasms/diagnosis/*metabolism/physiopathology/therapy ; Oncogenes/physiology ; Signal Transduction ; Tumor Suppressor Proteins/metabolism
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  • 178
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    Publication Date: 2012-02-03
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bowman, David -- England -- Nature. 2012 Feb 1;482(7383):30. doi: 10.1038/482030a.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉School for Plant Science, University of Tasmania, Private Bag 55 Hobart, Tasmania 7001, Australia. david.bowman@utas.edu.au〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22297953" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Australia ; Conservation of Natural Resources/*methods ; Elephants/*physiology ; Extinction, Biological ; Fires/*prevention & control/statistics & numerical data ; *Food Chain ; Herbivory ; Introduced Species/statistics & numerical data ; Poaceae/growth & development ; Predatory Behavior
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  • 179
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    Publication Date: 2012-03-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉England -- Nature. 2012 Mar 21;483(7390):373-4. doi: 10.1038/483373b.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22437570" target="_blank"〉PubMed〈/a〉
    Keywords: Aircraft ; Animal Experimentation/*ethics/*legislation & jurisprudence ; Animal Rights/legislation & jurisprudence ; Animal Welfare/standards ; Animals ; *Animals, Laboratory ; Biomedical Research/*ethics/standards ; Great Britain ; Humans ; Primates ; *Public Opinion ; *Research Personnel ; Transportation/*legislation & jurisprudence
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  • 180
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    Publication Date: 2012-05-25
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Maher, Brendan -- England -- Nature. 2012 May 23;485(7399):431-4. doi: 10.1038/485431a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22622550" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biohazard Release/*prevention & control ; Bioterrorism/*prevention & control ; Birds/virology ; Guidelines as Topic ; Humans ; Influenza A Virus, H5N1 Subtype/genetics/pathogenicity/physiology ; Influenza in Birds/*transmission/*virology ; Influenza, Human/*transmission/*virology ; International Cooperation ; Mammals/virology ; National Institutes of Health (U.S.) ; Risk Assessment ; Security Measures/*organization & administration/standards ; United States
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  • 181
    Publication Date: 2012-12-14
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vaux, David L -- England -- Nature. 2012 Dec 13;492(7428):180-1. doi: 10.1038/492180a.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Walter and Eliza Hall Institute of Medical Research and at the University of Melbourne, Parkville, Victoria 3052, Australia. vaux@wehi.edu.au〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23235861" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Editorial Policies ; Humans ; Peer Review, Research/standards ; Research/education/*standards ; Research Personnel/*education/standards ; *Statistics as Topic
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  • 182
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    Publication Date: 2012-05-25
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gozlan, Rodolphe -- England -- Nature. 2012 May 23;485(7399):446. doi: 10.1038/485446d.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22622560" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Communicable Diseases, Emerging/*microbiology ; *Ecosystem ; Fungi/*pathogenicity ; Humans ; Mycoses/*epidemiology/*veterinary ; Plants/*microbiology
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  • 183
    Publication Date: 2012-11-09
    Description: Defects in the availability of haem substrates or the catalytic activity of the terminal enzyme in haem biosynthesis, ferrochelatase (Fech), impair haem synthesis and thus cause human congenital anaemias. The interdependent functions of regulators of mitochondrial homeostasis and enzymes responsible for haem synthesis are largely unknown. To investigate this we used zebrafish genetic screens and cloned mitochondrial ATPase inhibitory factor 1 (atpif1) from a zebrafish mutant with profound anaemia, pinotage (pnt (tq209)). Here we describe a direct mechanism establishing that Atpif1 regulates the catalytic efficiency of vertebrate Fech to synthesize haem. The loss of Atpif1 impairs haemoglobin synthesis in zebrafish, mouse and human haematopoietic models as a consequence of diminished Fech activity and elevated mitochondrial pH. To understand the relationship between mitochondrial pH, redox potential, [2Fe-2S] clusters and Fech activity, we used genetic complementation studies of Fech constructs with or without [2Fe-2S] clusters in pnt, as well as pharmacological agents modulating mitochondrial pH and redox potential. The presence of [2Fe-2S] cluster renders vertebrate Fech vulnerable to perturbations in Atpif1-regulated mitochondrial pH and redox potential. Therefore, Atpif1 deficiency reduces the efficiency of vertebrate Fech to synthesize haem, resulting in anaemia. The identification of mitochondrial Atpif1 as a regulator of haem synthesis advances our understanding of the mechanisms regulating mitochondrial haem homeostasis and red blood cell development. An ATPIF1 deficiency may contribute to important human diseases, such as congenital sideroblastic anaemias and mitochondriopathies.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504625/" 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/PMC3504625/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Shah, Dhvanit I -- Takahashi-Makise, Naoko -- Cooney, Jeffrey D -- Li, Liangtao -- Schultz, Iman J -- Pierce, Eric L -- Narla, Anupama -- Seguin, Alexandra -- Hattangadi, Shilpa M -- Medlock, Amy E -- Langer, Nathaniel B -- Dailey, Tamara A -- Hurst, Slater N -- Faccenda, Danilo -- Wiwczar, Jessica M -- Heggers, Spencer K -- Vogin, Guillaume -- Chen, Wen -- Chen, Caiyong -- Campagna, Dean R -- Brugnara, Carlo -- Zhou, Yi -- Ebert, Benjamin L -- Danial, Nika N -- Fleming, Mark D -- Ward, Diane M -- Campanella, Michelangelo -- Dailey, Harry A -- Kaplan, Jerry -- Paw, Barry H -- K01 DK085217/DK/NIDDK NIH HHS/ -- P01 HL032262/HL/NHLBI NIH HHS/ -- P30 DK072437/DK/NIDDK NIH HHS/ -- R01 DK052380/DK/NIDDK NIH HHS/ -- R01 DK070838/DK/NIDDK NIH HHS/ -- R01 DK096051/DK/NIDDK NIH HHS/ -- R01 HL082945/HL/NHLBI NIH HHS/ -- T32 GM007223/GM/NIGMS NIH HHS/ -- England -- Nature. 2012 Nov 22;491(7425):608-12. doi: 10.1038/nature11536. Epub 2012 Nov 7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Medicine, Division of Hematology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23135403" target="_blank"〉PubMed〈/a〉
    Keywords: Anemia, Sideroblastic/genetics/metabolism/pathology ; Animals ; Disease Models, Animal ; Erythroblasts/cytology/*metabolism ; *Erythropoiesis ; Ferrochelatase/metabolism ; Genetic Complementation Test ; Heme/*biosynthesis ; Humans ; Hydrogen-Ion Concentration ; Mice ; Mitochondria/*metabolism/pathology ; Mitochondrial Proteins/deficiency/genetics/*metabolism ; Oxidation-Reduction ; Proteins/genetics/*metabolism ; Zebrafish/metabolism
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  • 184
    facet.materialart.
    Unknown
    Nature Publishing Group (NPG)
    Publication Date: 2012-04-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Graber, Cynthia -- England -- Nature. 2012 Apr 12;484(7393):S7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22509508" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Disease Progression ; Humans ; Inflammation/drug therapy/immunology/pathology ; Magnetic Resonance Imaging ; Multiple Sclerosis/*diagnosis/drug therapy/immunology/pathology ; Myelin Sheath/immunology/pathology
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  • 185
    Publication Date: 2012-05-19
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Malhotra, Dheeraj -- Sebat, Jonathan -- England -- Nature. 2012 May 16;485(7398):318-9. doi: 10.1038/485318a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22596152" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Chromosomes, Human, Pair 16/*genetics ; DNA Copy Number Variations/*genetics ; Gene Dosage/*genetics ; Head/*abnormalities ; Humans ; Microcephaly/*genetics ; Nuclear Proteins/*genetics ; *Phenotype
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  • 186
    Publication Date: 2012-06-23
    Description: Over the past 16 years, vast plantings of transgenic crops producing insecticidal proteins from the bacterium Bacillus thuringiensis (Bt) have helped to control several major insect pests and reduce the need for insecticide sprays. Because broad-spectrum insecticides kill arthropod natural enemies that provide biological control of pests, the decrease in use of insecticide sprays associated with Bt crops could enhance biocontrol services. However, this hypothesis has not been tested in terms of long-term landscape-level impacts. On the basis of data from 1990 to 2010 at 36 sites in six provinces of northern China, we show here a marked increase in abundance of three types of generalist arthropod predators (ladybirds, lacewings and spiders) and a decreased abundance of aphid pests associated with widespread adoption of Bt cotton and reduced insecticide sprays in this crop. We also found evidence that the predators might provide additional biocontrol services spilling over from Bt cotton fields onto neighbouring crops (maize, peanut and soybean). Our work extends results from general studies evaluating ecological effects of Bt crops by demonstrating that such crops can promote biocontrol services in agricultural landscapes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lu, Yanhui -- Wu, Kongming -- Jiang, Yuying -- Guo, Yuyuan -- Desneux, Nicolas -- England -- Nature. 2012 Jul 19;487(7407):362-5. doi: 10.1038/nature11153.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, 100193 China.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22722864" target="_blank"〉PubMed〈/a〉
    Keywords: *Agriculture/trends ; Animals ; Aphids/physiology ; Arthropods/physiology ; Bacillus thuringiensis/genetics ; China ; Food Chain ; *Gossypium/genetics/parasitology ; *Insecticides ; Pest Control, Biological/*trends ; *Plants, Genetically Modified ; Population Density ; Time Factors
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  • 187
    Publication Date: 2012-05-12
    Description: 〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4034543/" 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/PMC4034543/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Shaker, Anisa -- Rubin, Deborah C -- K08 CA153036/CA/NCI NIH HHS/ -- England -- Nature. 2012 May 9;485(7397):181-2. doi: 10.1038/485181a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22575955" target="_blank"〉PubMed〈/a〉
    Keywords: Adult Stem Cells/cytology/*transplantation ; Animals ; Colitis, Ulcerative/*pathology/*therapy ; Humans ; Intestines/*cytology/pathology ; Mice ; Organoids/cytology/transplantation ; Regenerative Medicine/*methods ; Stem Cell Transplantation ; Tissue Engineering/methods
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  • 188
    Publication Date: 2012-02-10
    Description: A balance between pro- and anti-inflammatory mechanisms at mucosal interfaces, which are sites of constitutive exposure to microbes and non-microbial foreign substances, allows for efficient protection against pathogens yet prevents adverse inflammatory responses associated with allergy, asthma and intestinal inflammation. Regulatory T (T(reg)) cells prevent systemic and tissue-specific autoimmunity and inflammatory lesions at mucosal interfaces. These cells are generated in the thymus (tT(reg) cells) and in the periphery (induced (i)T(reg) cells), and their dual origin implies a division of labour between tT(reg) and iT(reg) cells in immune homeostasis. Here we show that a highly selective blockage in differentiation of iT(reg) cells in mice did not lead to unprovoked multi-organ autoimmunity, exacerbation of induced tissue-specific autoimmune pathology, or increased pro-inflammatory responses of T helper 1 (T(H)1) and T(H)17 cells. However, mice deficient in iT(reg) cells spontaneously developed pronounced T(H)2-type pathologies at mucosal sites--in the gastrointestinal tract and lungs--with hallmarks of allergic inflammation and asthma. Furthermore, iT(reg)-cell deficiency altered gut microbial communities. These results suggest that whereas T(reg) cells generated in the thymus appear sufficient for control of systemic and tissue-specific autoimmunity, extrathymic differentiation of T(reg) cells affects commensal microbiota composition and serves a distinct, essential function in restraint of allergic-type inflammation at mucosal interfaces.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3485072/" 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/PMC3485072/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Josefowicz, Steven Z -- Niec, Rachel E -- Kim, Hye Young -- Treuting, Piper -- Chinen, Takatoshi -- Zheng, Ye -- Umetsu, Dale T -- Rudensky, Alexander Y -- 1F31NS073203-01/NS/NINDS NIH HHS/ -- F31 NS073203/NS/NINDS NIH HHS/ -- GM07739/GM/NIGMS NIH HHS/ -- R37 AI034206/AI/NIAID NIH HHS/ -- T32 GM007739/GM/NIGMS NIH HHS/ -- Howard Hughes Medical Institute/ -- England -- Nature. 2012 Feb 8;482(7385):395-9. doi: 10.1038/nature10772.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute and Immunology Program, Sloan Kettering Institute, New York, New York 10021, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22318520" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Asthma/immunology/pathology ; Cell Differentiation ; Enhancer Elements, Genetic/genetics ; Female ; Forkhead Transcription Factors/genetics ; Immunity, Mucosal/*immunology ; Inflammation/*immunology/pathology ; Intestines/immunology/microbiology/pathology ; Lung/immunology/pathology ; Male ; Mice ; Organ Specificity ; Stomach/immunology/microbiology/pathology ; T-Lymphocytes, Regulatory/*cytology/*immunology ; Th2 Cells/*immunology ; Thymus Gland
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  • 189
    facet.materialart.
    Unknown
    Nature Publishing Group (NPG)
    Publication Date: 2012-02-18
    Description: The discovery of microRNAs (miRNAs) almost two decades ago established a new paradigm of gene regulation. During the past ten years these tiny non-coding RNAs have been linked to virtually all known physiological and pathological processes, including cancer. In the same way as certain key protein-coding genes, miRNAs can be deregulated in cancer, in which they can function as a group to mark differentiation states or individually as bona fide oncogenes or tumour suppressors. Importantly, miRNA biology can be harnessed experimentally to investigate cancer phenotypes or used therapeutically as a target for drugs or as the drug itself.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3509753/" 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/PMC3509753/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lujambio, Amaia -- Lowe, Scott W -- P01 CA013106/CA/NCI NIH HHS/ -- P30 CA008748/CA/NCI NIH HHS/ -- R01 AG016379/AG/NIA NIH HHS/ -- Howard Hughes Medical Institute/ -- England -- Nature. 2012 Feb 15;482(7385):347-55. doi: 10.1038/nature10888.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Cancer Biology and Genetics Program, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, New York 10065, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22337054" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Gene Expression Regulation, Neoplastic ; Humans ; MicroRNAs/biosynthesis/*genetics/therapeutic use ; Neoplasm Metastasis ; Neoplasms/diagnosis/drug therapy/*genetics/pathology ; Oncogenes/genetics ; Tumor Suppressor Protein p53/metabolism
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  • 190
    Publication Date: 2012-07-20
    Description: Cardiac hypertrophy is initiated as an adaptive response to sustained overload but progresses pathologically as heart failure ensues. Here we report that genetic loss of APJ, a G-protein-coupled receptor, confers resistance to chronic pressure overload by markedly reducing myocardial hypertrophy and heart failure. In contrast, mice lacking apelin (the endogenous APJ ligand) remain sensitive, suggesting an apelin-independent function of APJ. Freshly isolated APJ-null cardiomyocytes exhibit an attenuated response to stretch, indicating that APJ is a mechanosensor. Activation of APJ by stretch increases cardiomyocyte cell size and induces molecular markers of hypertrophy. Whereas apelin stimulates APJ to activate Galphai and elicits a protective response, stretch signals in an APJ-dependent, G-protein-independent fashion to induce hypertrophy. Stretch-mediated hypertrophy is prevented by knockdown of beta-arrestins or by pharmacological doses of apelin acting through Galphai. Taken together, our data indicate that APJ is a bifunctional receptor for both mechanical stretch and the endogenous peptide apelin. By sensing the balance between these stimuli, APJ occupies a pivotal point linking sustained overload to cardiomyocyte hypertrophy.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3422434/" 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/PMC3422434/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Scimia, Maria Cecilia -- Hurtado, Cecilia -- Ray, Saugata -- Metzler, Scott -- Wei, Ke -- Wang, Jianming -- Woods, Chris E -- Purcell, Nicole H -- Catalucci, Daniele -- Akasaka, Takeshi -- Bueno, Orlando F -- Vlasuk, George P -- Kaliman, Perla -- Bodmer, Rolf -- Smith, Layton H -- Ashley, Euan -- Mercola, Mark -- Brown, Joan Heller -- Ruiz-Lozano, Pilar -- NS05422/NS/NINDS NIH HHS/ -- P01 HL085577/HL/NHLBI NIH HHS/ -- R01 HL054732/HL/NHLBI NIH HHS/ -- R01 HL086879/HL/NHLBI NIH HHS/ -- R01HL054732/HL/NHLBI NIH HHS/ -- R01HL083463/HL/NHLBI NIH HHS/ -- R01HL086879/HL/NHLBI NIH HHS/ -- R01HL28143/HL/NHLBI NIH HHS/ -- R37 HL028143/HL/NHLBI NIH HHS/ -- R37HL059502/HL/NHLBI NIH HHS/ -- England -- Nature. 2012 Aug 16;488(7411):394-8. doi: 10.1038/nature11263.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Sanford-Burnham Medical Research Institute, La Jolla, California 92037, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22810587" target="_blank"〉PubMed〈/a〉
    Keywords: Adipokines ; Animals ; Aorta/pathology ; Arrestins/deficiency/genetics/metabolism ; Blood Pressure ; Cardiomegaly/*metabolism/pathology/physiopathology/prevention & control ; Female ; GTP-Binding Protein alpha Subunits, Gi-Go/metabolism ; Intercellular Signaling Peptides and ; Proteins/deficiency/genetics/metabolism/pharmacology ; Male ; Mechanoreceptors/metabolism ; Mechanotransduction, Cellular/drug effects/physiology ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Myocytes, Cardiac/drug effects/pathology ; Receptors, G-Protein-Coupled/agonists/deficiency/genetics/*metabolism ; Signal Transduction/drug effects
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  • 191
    Publication Date: 2012-06-23
    Description: Trophic interactions govern biomass fluxes in ecosystems, and stability in food webs. Knowledge of how trophic interaction strengths are affected by differences among habitats is crucial for understanding variation in ecological systems. Here we show how substantial variation in consumption-rate data, and hence trophic interaction strengths, arises because consumers tend to encounter resources more frequently in three dimensions (3D) (for example, arboreal and pelagic zones) than two dimensions (2D) (for example, terrestrial and benthic zones). By combining new theory with extensive data (376 species, with body masses ranging from 5.24 x 10(-14) kg to 800 kg), we find that consumption rates scale sublinearly with consumer body mass (exponent of approximately 0.85) for 2D interactions, but superlinearly (exponent of approximately 1.06) for 3D interactions. These results contradict the currently widespread assumption of a single exponent (of approximately 0.75) in consumer-resource and food-web research. Further analysis of 2,929 consumer-resource interactions shows that dimensionality of consumer search space is probably a major driver of species coexistence, and the stability and abundance of populations.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pawar, Samraat -- Dell, Anthony I -- Savage, Van M -- England -- Nature. 2012 Jun 28;486(7404):485-9. doi: 10.1038/nature11131.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biomathematics, David Geffen School of Medicine, University of California, Los Angeles, California 90095-1766, USA. samraat@ucla.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22722834" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biomass ; Birds/physiology ; Body Size ; Body Weight ; Eating/physiology ; *Ecosystem ; Energy Metabolism ; Feeding Behavior/*physiology ; Fishes/physiology ; Flight, Animal ; *Food Chain ; Locomotion/physiology ; *Models, Biological ; Population Dynamics ; Predatory Behavior/physiology ; Reproduction/physiology ; Ruminants/physiology
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  • 192
    Publication Date: 2012-11-06
    Description: Current global patterns of biodiversity result from processes that operate over both space and time and thus require an integrated macroecological and macroevolutionary perspective. Molecular time trees have advanced our understanding of the tempo and mode of diversification and have identified remarkable adaptive radiations across the tree of life. However, incomplete joint phylogenetic and geographic sampling has limited broad-scale inference. Thus, the relative prevalence of rapid radiations and the importance of their geographic settings in shaping global biodiversity patterns remain unclear. Here we present, analyse and map the first complete dated phylogeny of all 9,993 extant species of birds, a widely studied group showing many unique adaptations. We find that birds have undergone a strong increase in diversification rate from about 50 million years ago to the near present. This acceleration is due to a number of significant rate increases, both within songbirds and within other young and mostly temperate radiations including the waterfowl, gulls and woodpeckers. Importantly, species characterized with very high past diversification rates are interspersed throughout the avian tree and across geographic space. Geographically, the major differences in diversification rates are hemispheric rather than latitudinal, with bird assemblages in Asia, North America and southern South America containing a disproportionate number of species from recent rapid radiations. The contribution of rapidly radiating lineages to both temporal diversification dynamics and spatial distributions of species diversity illustrates the benefits of an inclusive geographical and taxonomical perspective. Overall, whereas constituent clades may exhibit slowdowns, the adaptive zone into which modern birds have diversified since the Cretaceous may still offer opportunities for diversification.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Jetz, W -- Thomas, G H -- Joy, J B -- Hartmann, K -- Mooers, A O -- England -- Nature. 2012 Nov 15;491(7424):444-8. doi: 10.1038/nature11631. Epub 2012 Oct 31.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Ecology and Evolutionary Biology, Yale University, 165 Prospect Street, New Haven, Connecticut 06520-8106, USA. walter.jetz@yale.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23123857" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biodiversity ; Birds/*classification/genetics/physiology ; *Phylogeny
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  • 193
    Publication Date: 2012-02-18
    Description: Species diversity can be lost through two different but potentially interacting extinction processes: demographic decline and speciation reversal through introgressive hybridization. To investigate the relative contribution of these processes, we analysed historical and contemporary data of replicate whitefish radiations from 17 pre-alpine European lakes and reconstructed changes in genetic species differentiation through time using historical samples. Here we provide evidence that species diversity evolved in response to ecological opportunity, and that eutrophication, by diminishing this opportunity, has driven extinctions through speciation reversal and demographic decline. Across the radiations, the magnitude of eutrophication explains the pattern of species loss and levels of genetic and functional distinctiveness among remaining species. We argue that extinction by speciation reversal may be more widespread than currently appreciated. Preventing such extinctions will require that conservation efforts not only target existing species but identify and protect the ecological and evolutionary processes that generate and maintain species.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vonlanthen, P -- Bittner, D -- Hudson, A G -- Young, K A -- Muller, R -- Lundsgaard-Hansen, B -- Roy, D -- Di Piazza, S -- Largiader, C R -- Seehausen, O -- England -- Nature. 2012 Feb 15;482(7385):357-62. doi: 10.1038/nature10824.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Aquatic Ecology and Evolution, Institute of Ecology and Evolution, University of Bern, Baltzerstrasse 6, CH-3012 Bern, Switzerland.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22337055" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biodiversity ; *Biological Evolution ; Europe ; Eutrophication/*physiology ; *Extinction, Biological ; *Genetic Speciation ; Lakes ; Models, Biological ; Phenotype ; Salmonidae/genetics/*physiology
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  • 194
    Publication Date: 2012-11-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Shimizu, Kazumichi -- Stopfer, Mark -- England -- Nature. 2012 Dec 6;492(7427):44-5. doi: 10.1038/nature11757. Epub 2012 Nov 21.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23172148" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Female ; Neural Inhibition/*physiology ; Olfactory Pathways/*physiology ; Olfactory Receptor Neurons/*metabolism ; *Synapses
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  • 195
    Publication Date: 2012-05-19
    Description: Copy number variants (CNVs) are major contributors to genetic disorders. We have dissected a region of the 16p11.2 chromosome--which encompasses 29 genes--that confers susceptibility to neurocognitive defects when deleted or duplicated. Overexpression of each human transcript in zebrafish embryos identified KCTD13 as the sole message capable of inducing the microcephaly phenotype associated with the 16p11.2 duplication, whereas suppression of the same locus yielded the macrocephalic phenotype associated with the 16p11.2 deletion, capturing the mirror phenotypes of humans. Analyses of zebrafish and mouse embryos suggest that microcephaly is caused by decreased proliferation of neuronal progenitors with concomitant increase in apoptosis in the developing brain, whereas macrocephaly arises by increased proliferation and no changes in apoptosis. A role for KCTD13 dosage changes is consistent with autism in both a recently reported family with a reduced 16p11.2 deletion and a subject reported here with a complex 16p11.2 rearrangement involving de novo structural alteration of KCTD13. Our data suggest that KCTD13 is a major driver for the neurodevelopmental phenotypes associated with the 16p11.2 CNV, reinforce the idea that one or a small number of transcripts within a CNV can underpin clinical phenotypes, and offer an efficient route to identifying dosage-sensitive loci.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3366115/" 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/PMC3366115/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Golzio, Christelle -- Willer, Jason -- Talkowski, Michael E -- Oh, Edwin C -- Taniguchi, Yu -- Jacquemont, Sebastien -- Reymond, Alexandre -- Sun, Mei -- Sawa, Akira -- Gusella, James F -- Kamiya, Atsushi -- Beckmann, Jacques S -- Katsanis, Nicholas -- F32MH087123/MH/NIMH NIH HHS/ -- HD06286/HD/NICHD NIH HHS/ -- MH-084018/MH/NIMH NIH HHS/ -- MH-091230/MH/NIMH NIH HHS/ -- P50 MH094268/MH/NIMH NIH HHS/ -- P50 MH094268-02/MH/NIMH NIH HHS/ -- R01 MH091230/MH/NIMH NIH HHS/ -- R01 MH092443/MH/NIMH NIH HHS/ -- England -- Nature. 2012 May 16;485(7398):363-7. doi: 10.1038/nature11091.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Human Disease Modeling and Department of Cell biology, Duke University, Durham, North Carolina 27710, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22596160" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Apoptosis/genetics ; Cell Proliferation ; Chromosomes, Human, Pair 16/*genetics ; DNA Copy Number Variations/*genetics ; Gene Dosage/*genetics ; Gene Duplication/genetics ; Head/*abnormalities/embryology ; Humans ; Mice ; Microcephaly/*genetics ; Nuclear Proteins/*genetics/metabolism ; Organ Size/genetics ; *Phenotype ; RNA, Messenger/genetics/metabolism ; Sequence Deletion/genetics ; Transcription, Genetic ; Up-Regulation ; Zebrafish/abnormalities/embryology/genetics
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    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 196
    Publication Date: 2012-10-13
    Description: The nervous system provides a fundamental source of data for understanding the evolutionary relationships between major arthropod groups. Fossil arthropods rarely preserve neural tissue. As a result, inferring sensory and motor attributes of Cambrian taxa has been limited to interpreting external features, such as compound eyes or sensilla decorating appendages, and early-diverging arthropods have scarcely been analysed in the context of nervous system evolution. Here we report exceptional preservation of the brain and optic lobes of a stem-group arthropod from 520 million years ago (Myr ago), Fuxianhuia protensa, exhibiting the most compelling neuroanatomy known from the Cambrian. The protocerebrum of Fuxianhuia is supplied by optic lobes evidencing traces of three nested optic centres serving forward-viewing eyes. Nerves from uniramous antennae define the deutocerebrum, and a stout pair of more caudal nerves indicates a contiguous tritocerebral component. Fuxianhuia shares a tripartite pre-stomodeal brain and nested optic neuropils with extant Malacostraca and Insecta, demonstrating that these characters were present in some of the earliest derived arthropods. The brain of Fuxianhuia impacts molecular analyses that advocate either a branchiopod-like ancestor of Hexapoda or remipedes and possibly cephalocarids as sister groups of Hexapoda. Resolving arguments about whether the simple brain of a branchiopod approximates an ancestral insect brain or whether it is the result of secondary simplification has until now been hindered by lack of fossil evidence. The complex brain of Fuxianhuia accords with cladistic analyses on the basis of neural characters, suggesting that Branchiopoda derive from a malacostracan-like ancestor but underwent evolutionary reduction and character reversal of brain centres that are common to hexapods and malacostracans. The early origin of sophisticated brains provides a probable driver for versatile visual behaviours, a view that accords with compound eyes from the early Cambrian that were, in size and resolution, equal to those of modern insects and malacostracans.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ma, Xiaoya -- Hou, Xianguang -- Edgecombe, Gregory D -- Strausfeld, Nicholas J -- England -- Nature. 2012 Oct 11;490(7419):258-61. doi: 10.1038/nature11495.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Yunnan Key Laboratory for Palaeobiology, Yunnan University, Kunming 650091, China. x.ma@nhm.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23060195" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arthropods/*anatomy & histology/classification ; Brain/anatomy & histology ; *Fossils ; Optic Lobe, Nonmammalian/anatomy & histology
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    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 197
    Publication Date: 2012-01-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Shestopalov, Ilya A -- Zon, Leonard I -- England -- Nature. 2012 Jan 25;481(7382):453-5. doi: 10.1038/481453a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22281591" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Endothelium/*cytology/*metabolism ; Hematopoietic Stem Cells/*cytology/*metabolism ; Stem Cell Niche/*physiology ; Stromal Cells/*cytology/*metabolism
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    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 198
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    Unknown
    Nature Publishing Group (NPG)
    Publication Date: 2012-04-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gravitz, Lauren -- England -- Nature. 2012 Apr 12;484(7393):S2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22509503" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Blood-Brain Barrier/pathology ; Brain/pathology ; Disease Susceptibility ; Humans ; Middle Aged ; Models, Immunological ; Models, Neurological ; Multiple Sclerosis/*etiology/genetics/immunology/physiopathology
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    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 199
    Publication Date: 2012-04-17
    Description: The development and maintenance of an epithelium requires finely balanced rates of growth and cell death. However, the mechanical and biochemical mechanisms that ensure proper feedback control of tissue growth, which when deregulated contribute to tumorigenesis, are poorly understood. Here we use the fly notum as a model system to identify a novel process of crowding-induced cell delamination that balances growth to ensure the development of well-ordered cell packing. In crowded regions of the tissue, a proportion of cells undergo a serial loss of cell-cell junctions and a progressive loss of apical area, before being squeezed out by their neighbours. This path of delamination is recapitulated by a simple computational model of epithelial mechanics, in which stochastic cell loss relieves overcrowding as the system tends towards equilibrium. We show that this process of delamination is mechanistically distinct from apoptosis-mediated cell extrusion and precedes the first signs of cell death. Overall, this analysis reveals a simple mechanism that buffers epithelia against variations in growth. Because live-cell delamination constitutes a mechanistic link between epithelial hyperplasia and cell invasion, this is likely to have important implications for our understanding of the early stages of cancer development.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marinari, Eliana -- Mehonic, Aida -- Curran, Scott -- Gale, Jonathan -- Duke, Thomas -- Baum, Buzz -- 9786/Cancer Research UK/United Kingdom -- Cancer Research UK/United Kingdom -- England -- Nature. 2012 Apr 15;484(7395):542-5. doi: 10.1038/nature10984.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Medical Research Council Laboratory of Molecular Cell Biology, University College London, Gower Street, London WC1E 6BT, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22504180" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Apoptosis ; Cell Communication ; Cell Count ; Cell Death ; Cell Growth Processes ; Cell Survival ; Drosophila melanogaster/*cytology ; Epithelial Cells/*cytology ; Female ; Male ; Models, Biological ; Neoplasms/pathology ; Stochastic Processes
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  • 200
    Publication Date: 2012-03-31
    Description: Past sea-level records provide invaluable information about the response of ice sheets to climate forcing. Some such records suggest that the last deglaciation was punctuated by a dramatic period of sea-level rise, of about 20 metres, in less than 500 years. Controversy about the amplitude and timing of this meltwater pulse (MWP-1A) has, however, led to uncertainty about the source of the melt water and its temporal and causal relationships with the abrupt climate changes of the deglaciation. Here we show that MWP-1A started no earlier than 14,650 years ago and ended before 14,310 years ago, making it coeval with the Bolling warming. Our results, based on corals drilled offshore from Tahiti during Integrated Ocean Drilling Project Expedition 310, reveal that the increase in sea level at Tahiti was between 12 and 22 metres, with a most probable value between 14 and 18 metres, establishing a significant meltwater contribution from the Southern Hemisphere. This implies that the rate of eustatic sea-level rise exceeded 40 millimetres per year during MWP-1A.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Deschamps, Pierre -- Durand, Nicolas -- Bard, Edouard -- Hamelin, Bruno -- Camoin, Gilbert -- Thomas, Alexander L -- Henderson, Gideon M -- Okuno, Jun'ichi -- Yokoyama, Yusuke -- England -- Nature. 2012 Mar 28;483(7391):559-64. doi: 10.1038/nature10902.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉CEREGE, UMR Aix-Marseille Universite - CNRS - IRD - College de France, Technopole de l'Arbois, BP 80, 13545 Aix-en-Provence Cedex 4, France. deschamps@cerege.fr〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22460900" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Anthozoa ; Coral Reefs ; Freezing ; Global Warming/*history ; History, Ancient ; *Ice Cover ; Oceans and Seas ; Polynesia ; Seawater/*analysis ; Time Factors ; Uncertainty
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    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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