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  • 1
    Publication Date: 2000-12-23
    Description: Recent studies suggest that insulin-degrading enzyme (IDE) in neurons and microglia degrades Abeta, the principal component of beta-amyloid and one of the neuropathological hallmarks of Alzheimer's disease (AD). We performed parametric and nonparametric linkage analyses of seven genetic markers on chromosome 10q, six of which map near the IDE gene, in 435 multiplex AD families. These analyses revealed significant evidence of linkage for adjacent markers (D10S1671, D10S583, D10S1710, and D10S566), which was most pronounced in late-onset families. Furthermore, we found evidence for allele-specific association between the putative disease locus and marker D10S583, which has recently been located within 195 kilobases of the IDE gene.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bertram, L -- Blacker, D -- Mullin, K -- Keeney, D -- Jones, J -- Basu, S -- Yhu, S -- McInnis, M G -- Go, R C -- Vekrellis, K -- Selkoe, D J -- Saunders, A J -- Tanzi, R E -- New York, N.Y. -- Science. 2000 Dec 22;290(5500):2302-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Genetics and Aging Unit, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA 02129, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11125142" target="_blank"〉PubMed〈/a〉
    Keywords: Age of Onset ; Aged ; Aged, 80 and over ; Alleles ; Alzheimer Disease/*genetics ; Apolipoproteins E/genetics ; Chromosome Mapping ; Chromosomes, Human, Pair 10/*genetics ; *Genetic Linkage ; Genetic Markers ; Humans ; Insulysin/*genetics ; Linkage Disequilibrium ; Middle Aged
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2000-12-23
    Description: Plasma Abeta42 (amyloid beta42 peptide) is invariably elevated in early-onset familial Alzheimer's disease (AD), and it is also increased in the first-degree relatives of patients with typical late-onset AD (LOAD). To detect LOAD loci that increase Abeta42, we used plasma Abeta42 as a surrogate trait and performed linkage analysis on extended AD pedigrees identified through a LOAD patient with extremely high plasma Abeta. Here, we report linkage to chromosome 10 with a maximal lod score of 3.93 at 81 centimorgans close to D10S1225. Remarkably, linkage to the same region was obtained independently in a genome-wide screen of LOAD sibling pairs. These results provide strong evidence for a novel LOAD locus on chromosome 10 that acts to increase Abeta.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ertekin-Taner, N -- Graff-Radford, N -- Younkin, L H -- Eckman, C -- Baker, M -- Adamson, J -- Ronald, J -- Blangero, J -- Hutton, M -- Younkin, S G -- AG06656/AG/NIA NIH HHS/ -- MH59490/MH/NIMH NIH HHS/ -- P50 AG16574/AG/NIA NIH HHS/ -- New York, N.Y. -- Science. 2000 Dec 22;290(5500):2303-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Mayo Clinic Jacksonville, Jacksonville, FL 32224, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11125143" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Age of Onset ; Aged ; Aged, 80 and over ; Alzheimer Disease/*blood/*genetics ; Amyloid beta-Peptides/*blood/genetics ; Chromosomes, Human, Pair 10/*genetics ; Female ; *Genetic Linkage ; Genetic Markers ; Genetic Predisposition to Disease ; Humans ; Lod Score ; Male ; Middle Aged ; Pedigree ; Peptide Fragments/*blood/genetics ; Phenotype ; *Quantitative Trait, Heritable
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 2000-12-23
    Description: In all eukaryotic organisms, inappropriate firing of replication origins during the G2 phase of the cell cycle is suppressed by cyclin-dependent kinases. Multicellular eukaryotes contain a second putative inhibitor of re-replication called geminin. Geminin is believed to block binding of the mini-chromosome maintenance (MCM) complex to origins of replication, but the mechanism of this inhibition is unclear. Here we show that geminin interacts tightly with Cdt1, a recently identified replication initiation factor necessary for MCM loading. The inhibition of DNA replication by geminin that is observed in cell-free DNA replication extracts is reversed by the addition of excess Cdt1. In the normal cell cycle, Cdt1 is present only in G1 and S, whereas geminin is present in S and G2 phases of the cell cycle. Together, these results suggest that geminin inhibits inappropriate origin firing by targeting Cdt1.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wohlschlegel, J A -- Dwyer, B T -- Dhar, S K -- Cvetic, C -- Walter, J C -- Dutta, A -- CA60499/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 2000 Dec 22;290(5500):2309-12.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, 75 Francis Street, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11125146" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Cell Cycle Proteins/chemistry/*metabolism/pharmacology ; Cell Nucleus/metabolism ; Cell-Free System ; Chromatin/metabolism ; *DNA Replication ; DNA-Binding Proteins/chemistry/*metabolism/pharmacology ; Evolution, Molecular ; G1 Phase ; G2 Phase ; Geminin ; HeLa Cells ; Humans ; *Interphase ; Molecular Sequence Data ; Molecular Weight ; Precipitin Tests ; Recombinant Fusion Proteins/metabolism ; Replication Origin ; *S Phase ; Xenopus ; Xenopus Proteins
    Print ISSN: 0036-8075
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 4
    Publication Date: 2000-12-23
    Description: Many areas of science depend on exploratory data analysis and visualization. The need to analyze large amounts of multivariate data raises the fundamental problem of dimensionality reduction: how to discover compact representations of high-dimensional data. Here, we introduce locally linear embedding (LLE), an unsupervised learning algorithm that computes low-dimensional, neighborhood-preserving embeddings of high-dimensional inputs. Unlike clustering methods for local dimensionality reduction, LLE maps its inputs into a single global coordinate system of lower dimensionality, and its optimizations do not involve local minima. By exploiting the local symmetries of linear reconstructions, LLE is able to learn the global structure of nonlinear manifolds, such as those generated by images of faces or documents of text.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Roweis, S T -- Saul, L K -- New York, N.Y. -- Science. 2000 Dec 22;290(5500):2323-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Gatsby Computational Neuroscience Unit, University College London, 17 Queen Square, London WC1N 3AR, UK. roweis@gatsby.ucl.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11125150" target="_blank"〉PubMed〈/a〉
    Keywords: *Algorithms ; Artificial Intelligence ; Face ; Humans ; Mathematics ; *Pattern Recognition, Visual
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  • 5
    Publication Date: 2000-12-23
    Description: The apolipoprotein E (APOE) gene is the only genetic risk factor that has so far been linked to risk for late-onset Alzheimer's disease (LOAD). However, 50 percent of Alzheimer's disease cases do not carry an APOE4 allele, suggesting that other risk factors must exist. We performed a two-stage genome-wide screen in sibling pairs with LOAD to detect other susceptibility loci. Here we report evidence for an Alzheimer's disease locus on chromosome 10. Our stage one multipoint lod score (logarithm of the odds ratio for linkage/no linkage) of 2.48 (266 sibling pairs) increased to 3.83 in stage 2 (429 sibling pairs) close to D10S1225 (79 centimorgans). This locus modifies risk for Alzheimer's disease independent of APOE genotype.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Myers, A -- Holmans, P -- Marshall, H -- Kwon, J -- Meyer, D -- Ramic, D -- Shears, S -- Booth, J -- DeVrieze, F W -- Crook, R -- Hamshere, M -- Abraham, R -- Tunstall, N -- Rice, F -- Carty, S -- Lillystone, S -- Kehoe, P -- Rudrasingham, V -- Jones, L -- Lovestone, S -- Perez-Tur, J -- Williams, J -- Owen, M J -- Hardy, J -- Goate, A M -- AG16208/AG/NIA NIH HHS/ -- AG5681/AG/NIA NIH HHS/ -- U24 AG021886/AG/NIA NIH HHS/ -- New York, N.Y. -- Science. 2000 Dec 22;290(5500):2304-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychiatry, Washington University School of Medicine, 660 S. Euclid, St. Louis, MO 63110, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11125144" target="_blank"〉PubMed〈/a〉
    Keywords: Age of Onset ; Aged ; Alleles ; Alzheimer Disease/*genetics ; Apolipoprotein E4 ; Apolipoproteins E/genetics ; Chromosomes, Human, Pair 10/*genetics ; Genetic Linkage ; Genetic Markers ; *Genetic Predisposition to Disease ; Genotype ; Humans ; Lod Score ; Nuclear Family ; Odds Ratio
    Print ISSN: 0036-8075
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 6
    Publication Date: 2000-12-23
    Description: Using functional magnetic resonance imaging, we investigated the mechanism by which cholinergic enhancement improves working memory. We studied the effect of the cholinesterase inhibitor physostigmine on subcomponents of this complex function. Cholinergic enhancement increased the selectivity of neural responses in extrastriate cortices during visual working memory, particularly during encoding. It also increased the participation of ventral extrastriate cortex during memory maintenance and decreased the participation of anterior prefrontal cortex. These results indicate that cholinergic enhancement improves memory performance by augmenting the selectivity of perceptual processing during encoding, thereby simplifying processing demands during memory maintenance and reducing the need for prefrontal participation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Furey, M L -- Pietrini, P -- Haxby, J V -- New York, N.Y. -- Science. 2000 Dec 22;290(5500):2315-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Brain and Cognition, National Institute of Mental Health, National Institutes of Health, Bethesda, MD, USA. furey@nih.gov〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11125148" target="_blank"〉PubMed〈/a〉
    Keywords: Acetylcholine/*physiology ; Brain Mapping ; Cerebral Cortex/drug effects/*physiology ; Cholinesterase Inhibitors/*pharmacology ; Cross-Over Studies ; Double-Blind Method ; Face ; Female ; Humans ; Male ; Memory, Short-Term/*drug effects/physiology ; Occipital Lobe/drug effects/physiology ; Pattern Recognition, Visual ; Physostigmine/*pharmacology ; Prefrontal Cortex/drug effects/*physiology ; Temporal Lobe/drug effects/physiology ; Visual Cortex/drug effects/physiology ; Visual Perception/drug effects
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  • 7
    Publication Date: 2000-12-23
    Description: Niemann-Pick type C2 disease (NP-C2) is a fatal hereditary disorder of unknown etiology characterized by defective egress of cholesterol from lysosomes. Here we show that the disease is caused by a deficiency in HE1, a ubiquitously expressed lysosomal protein identified previously as a cholesterol-binding protein. HE1 was undetectable in fibroblasts from NP-C2 patients but present in fibroblasts from unaffected controls and NP-C1 patients. Mutations in the HE1 gene, which maps to chromosome 14q24.3, were found in NP-C2 patients but not in controls. Treatment of NP-C2 fibroblasts with exogenous recombinant HE1 protein ameliorated lysosomal accumulation of low density lipoprotein-derived cholesterol.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Naureckiene, S -- Sleat, D E -- Lackland, H -- Fensom, A -- Vanier, M T -- Wattiaux, R -- Jadot, M -- Lobel, P -- DK45992/DK/NIDDK NIH HHS/ -- DK54317/DK/NIDDK NIH HHS/ -- NS37918/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 2000 Dec 22;290(5500):2298-301.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Advanced Biotechnology and Medicine, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, Piscataway, NJ, 08854, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11125141" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Biological Transport ; CHO Cells ; *Carrier Proteins ; Cell Membrane/metabolism ; Cells, Cultured ; Cholesterol/*metabolism ; Cricetinae ; Culture Media, Conditioned ; Fibroblasts/metabolism ; Glycoproteins/chemistry/*genetics/*metabolism/pharmacology ; Humans ; Lysosomes/*metabolism ; Molecular Sequence Data ; Mutation ; Niemann-Pick Diseases/*genetics/metabolism ; Rats ; Receptor, IGF Type 2/metabolism ; Recombinant Proteins/metabolism/pharmacology ; Transfection
    Print ISSN: 0036-8075
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  • 8
    Publication Date: 2000-12-23
    Description: Niemann-Pick C1 (NPC1) disease is characterized by cholesterol accumulation in lysosomes and aberrant feedback regulation of cellular cholesterol homeostasis. We provide evidence that the NPC1 protein has homology with the resistance-nodulation-division (RND) family of prokaryotic permeases and may normally function as a transmembrane efflux pump. Studies of acriflavine loading in normal and NPC1 fibroblasts indicated that NPC1 uses a proton motive force to remove accumulated acriflavine from the endosomal/lysosomal system. Expression of NPC1 in Escherichia coli (i) facilitated the transport of acriflavine across the plasma membrane, causing cytosolic accumulation, and (ii) resulted in transport of oleic acid but not cholesterol or cholesterol-oleate across the plasma membrane. These studies establish NPC1 as a eukaryotic member of the RND permease family.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Davies, J P -- Chen, F W -- Ioannou, Y A -- R01 DK54736/DK/NIDDK NIH HHS/ -- New York, N.Y. -- Science. 2000 Dec 22;290(5500):2295-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Human Genetics, Box 1498, The Mount Sinai School of Medicine, One Gustave L. Levy Place, New York, NY 10029, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11125140" target="_blank"〉PubMed〈/a〉
    Keywords: Acriflavine/metabolism ; Amino Acid Motifs ; Amino Acid Sequence ; Biological Transport ; *Carrier Proteins ; Cell Membrane/metabolism ; Cells, Cultured ; Cholesterol/metabolism ; Cholesterol Esters/metabolism ; Endosomes/metabolism ; Escherichia coli/genetics/metabolism ; Fibroblasts ; Fluorescence ; Fluorescent Dyes/metabolism ; Humans ; Lysosomes/metabolism ; *Membrane Glycoproteins ; Membrane Proteins/chemistry ; Membrane Transport Proteins/chemistry/*metabolism ; Molecular Sequence Data ; Niemann-Pick Diseases/genetics/*metabolism ; Oleic Acid/metabolism ; Protein Structure, Secondary ; Protein Structure, Tertiary ; Proteins/chemistry/*metabolism ; Proton-Motive Force ; Recombinant Proteins/metabolism ; Sequence Alignment
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  • 9
    Publication Date: 2000-12-23
    Description: Scientists working with large volumes of high-dimensional data, such as global climate patterns, stellar spectra, or human gene distributions, regularly confront the problem of dimensionality reduction: finding meaningful low-dimensional structures hidden in their high-dimensional observations. The human brain confronts the same problem in everyday perception, extracting from its high-dimensional sensory inputs-30,000 auditory nerve fibers or 10(6) optic nerve fibers-a manageably small number of perceptually relevant features. Here we describe an approach to solving dimensionality reduction problems that uses easily measured local metric information to learn the underlying global geometry of a data set. Unlike classical techniques such as principal component analysis (PCA) and multidimensional scaling (MDS), our approach is capable of discovering the nonlinear degrees of freedom that underlie complex natural observations, such as human handwriting or images of a face under different viewing conditions. In contrast to previous algorithms for nonlinear dimensionality reduction, ours efficiently computes a globally optimal solution, and, for an important class of data manifolds, is guaranteed to converge asymptotically to the true structure.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tenenbaum, J B -- de Silva, V -- Langford, J C -- New York, N.Y. -- Science. 2000 Dec 22;290(5500):2319-23.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychology, Stanford University, Stanford, CA 94305, USA. jbt@psych.stanford.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11125149" target="_blank"〉PubMed〈/a〉
    Keywords: *Algorithms ; Artificial Intelligence ; Face ; Humans ; Mathematics ; *Pattern Recognition, Visual ; *Visual Perception
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  • 10
    Publication Date: 2000-12-16
    Description: The retinoid X receptor (RXR) is a nuclear receptor that functions as a ligand-activated transcription factor. Little is known about the ligands that activate RXR in vivo. Here, we identified a factor in brain tissue from adult mice that activates RXR in cell-based assays. Purification and analysis of the factor by mass spectrometry revealed that it is docosahexaenoic acid (DHA), a long-chain polyunsaturated fatty acid that is highly enriched in the adult mammalian brain. Previous work has shown that DHA is essential for brain maturation, and deficiency of DHA in both rodents and humans leads to impaired spatial learning and other abnormalities. These data suggest that DHA may influence neural function through activation of an RXR signaling pathway.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉de Urquiza, A M -- Liu, S -- Sjoberg, M -- Zetterstrom, R H -- Griffiths, W -- Sjovall, J -- Perlmann, T -- New York, N.Y. -- Science. 2000 Dec 15;290(5499):2140-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Ludwig Institute for Cancer Research, Stockholm Branch, Box 240, S-171 77 Stockholm, Sweden.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11118147" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Assay ; Brain/growth & development/metabolism ; *Brain Chemistry ; Cell Line ; Chromatography, High Pressure Liquid ; Culture Media, Conditioned ; Dimerization ; Docosahexaenoic Acids/*isolation & purification/*metabolism/pharmacology ; Fatty Acids, Unsaturated/pharmacology ; Histone Acetyltransferases ; Humans ; Ligands ; Male ; Mice ; Nuclear Receptor Coactivator 1 ; Receptors, Retinoic Acid/genetics/*metabolism ; Recombinant Fusion Proteins/metabolism ; Retinoid X Receptors ; Signal Transduction ; Spectrometry, Mass, Electrospray Ionization ; Transcription Factors/genetics/*metabolism ; Transfection ; Tumor Cells, Cultured
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 11
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-12-09
    Description: Hepatitis C virus (HCV) infection is a global health problem affecting an estimated 170 million individuals worldwide. We report the identification of multiple independent adaptive mutations that cluster in the HCV nonstructural protein NS5A and confer increased replicative ability in vitro. Among these adaptive mutations were a single amino acid substitution that allowed HCV RNA replication in 10% of transfected hepatoma cells and a deletion of 47 amino acids encompassing the interferon (IFN) sensitivity determining region (ISDR). Independent of the ISDR, IFN-alpha rapidly inhibited HCV RNA replication in vitro. This work establishes a robust, cell-based system for genetic and functional analyses of HCV replication.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Blight, K J -- Kolykhalov, A A -- Rice, C M -- AI40034/AI/NIAID NIH HHS/ -- CA57973/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 2000 Dec 8;290(5498):1972-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Microbiology, Washington University School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110-1093, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11110665" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Substitution ; Hepacivirus/drug effects/genetics/*physiology ; Humans ; Interferon-alpha/pharmacology ; Mutation ; Phosphorylation ; Point Mutation ; RNA Replicase/genetics/metabolism ; RNA, Viral/*biosynthesis ; *Replicon ; Sequence Deletion ; Transfection ; Tumor Cells, Cultured ; Viral Nonstructural Proteins/*genetics/*metabolism ; Virus Replication
    Print ISSN: 0036-8075
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  • 12
    Publication Date: 2000-12-09
    Description: Tissue manipulation experiments in amphibians more than 50 years ago showed that induction of the inner ear requires two signals: a mesodermal signal followed by a neural signal. However, the molecules mediating this process have remained elusive. We present evidence for mesodermal initiation of otic development in higher vertebrates and show that the mesoderm can direct terminal differentiation of the inner ear in rostral ectoderm. Furthermore, we demonstrate the synergistic interactions of the extracellular polypeptide ligands FGF-19 and Wnt-8c as mediators of mesodermal and neural signals, respectively, initiating inner ear development.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ladher, R K -- Anakwe, K U -- Gurney, A L -- Schoenwolf, G C -- Francis-West, P H -- New York, N.Y. -- Science. 2000 Dec 8;290(5498):1965-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Craniofacial Development, King's College, London, SE1 9RT, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11110663" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Central Nervous System/embryology/metabolism ; Chick Embryo ; Culture Techniques ; Ear, Inner/*embryology/metabolism ; Ectoderm/cytology ; *Embryonic Induction ; Fibroblast Growth Factor 3 ; Fibroblast Growth Factors/genetics/*metabolism/pharmacology ; Gene Expression ; Homeodomain Proteins/genetics/metabolism ; Humans ; In Situ Hybridization ; Mesoderm/*metabolism ; Molecular Sequence Data ; Proto-Oncogene Proteins/genetics/*metabolism/pharmacology ; Quail/embryology ; Rhombencephalon/embryology/metabolism ; Signal Transduction ; Wnt Proteins ; *Zebrafish Proteins
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  • 13
    Publication Date: 2000-12-09
    Description: Genetic engineering of non-beta cells to release insulin upon feeding could be a therapeutic modality for patients with diabetes. A tumor-derived K-cell line was induced to produce human insulin by providing the cells with the human insulin gene linked to the 5'-regulatory region of the gene encoding glucose-dependent insulinotropic polypeptide (GIP). Mice expressing this transgene produced human insulin specifically in gut K cells. This insulin protected the mice from developing diabetes and maintained glucose tolerance after destruction of the native insulin-producing beta cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cheung, A T -- Dayanandan, B -- Lewis, J T -- Korbutt, G S -- Rajotte, R V -- Bryer-Ash, M -- Boylan, M O -- Wolfe, M M -- Kieffer, T J -- New York, N.Y. -- Science. 2000 Dec 8;290(5498):1959-62.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Medicine, University of Alberta, Edmonton, AB T6G 2S2, Canada.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11110661" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Blood Glucose/metabolism ; Cell Line ; Cloning, Molecular ; Diabetes Mellitus, Experimental/metabolism/*therapy ; Enteroendocrine Cells/*cytology/*metabolism ; Gastric Inhibitory Polypeptide/biosynthesis/genetics ; Gene Expression ; Genetic Engineering ; *Genetic Therapy ; Glucose/administration & dosage/*metabolism ; Glucose Tolerance Test ; Humans ; Insulin/biosynthesis/genetics/*metabolism ; Mice ; Mice, Transgenic ; Proinsulin/genetics ; Promoter Regions, Genetic ; Protein Precursors/genetics ; Stem Cells/cytology/metabolism ; Streptozocin ; Transfection ; Transgenes ; Tumor Cells, Cultured
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  • 14
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-12-02
    Description: Macroautophagy is a dynamic process involving the rearrangement of subcellular membranes to sequester cytoplasm and organelles for delivery to the lysosome or vacuole where the sequestered cargo is degraded and recycled. This process takes place in all eukaryotic cells. It is highly regulated through the action of various kinases, phosphatases, and guanosine triphosphatases (GTPases). The core protein machinery that is necessary to drive formation and consumption of intermediates in the macroautophagy pathway includes a ubiquitin-like protein conjugation system and a protein complex that directs membrane docking and fusion at the lysosome or vacuole. Macroautophagy plays an important role in developmental processes, human disease, and cellular response to nutrient deprivation.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2732363/" 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/PMC2732363/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Klionsky, D J -- Emr, S D -- CA58689/CA/NCI NIH HHS/ -- GM53396/GM/NIGMS NIH HHS/ -- R01 GM053396/GM/NIGMS NIH HHS/ -- R01 GM053396-11/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2000 Dec 1;290(5497):1717-21.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biology, University of Michigan, 830 North University, Ann Arbor, MI 48109-1048, USA. klionsky@umich.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11099404" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Autophagy ; Cytoplasm/*metabolism ; Humans ; Lysosomes/metabolism/ultrastructure ; Membrane Fusion ; Organelles/*metabolism/ultrastructure ; Phagosomes/*metabolism/ultrastructure ; Proteins/metabolism ; Yeasts/genetics/metabolism/ultrastructure
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  • 15
    Publication Date: 2000-12-02
    Description: Many apoptotic molecules relocate subcellularly in cells undergoing apoptosis. The pro-apoptotic protein BID underwent posttranslational (rather than classic cotranslational) N-myristoylation when cleavage by caspase 8 caused exposure of a glycine residue. N-myristoylation enabled the targeting of a complex of p7 and myristoylated p15 fragments of BID to artificial membranes bearing the lipid composition of mitochondria, as well as to intact mitochondria. This post-proteolytic N-myristoylation serves as an activating switch, enhancing BID-induced release of cytochrome c and cell death.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zha, J -- Weiler, S -- Oh, K J -- Wei, M C -- Korsmeyer, S J -- CA50239-13/CA/NCI NIH HHS/ -- K01 CA82231/CA/NCI NIH HHS/ -- T32 CA72320-01A1/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 2000 Dec 1;290(5497):1761-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Dana-Farber Cancer Institute, Departments of Pathology and Medicine, Harvard Medical School, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11099414" target="_blank"〉PubMed〈/a〉
    Keywords: Acyltransferases/genetics/metabolism ; Animals ; *Apoptosis ; BH3 Interacting Domain Death Agonist Protein ; Carrier Proteins/chemistry/*metabolism ; Caspase 8 ; Caspase 9 ; Caspases/metabolism ; Cytochrome c Group/metabolism ; Humans ; Intracellular Membranes/*metabolism ; Jurkat Cells ; Liposomes/metabolism ; Mice ; Mitochondria/*metabolism ; Myristic Acid/*metabolism ; Peptide Fragments/metabolism ; Protein Conformation ; Protein Processing, Post-Translational ; Protein Structure, Tertiary ; Protein Transport ; Recombinant Fusion Proteins/metabolism
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 16
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-12-02
    Description: Area 5 in the parietal lobe of the primate brain is thought to be involved in monitoring the posture and movement of the body. In this study, neurons in monkey area 5 were found to encode the position of the monkey's arm while it was covered from view. The same neurons also responded to the position of a visible, realistic false arm. The neurons were not sensitive to the sight of unrealistic substitutes for the arm and were able to distinguish a right from a left arm. These neurons appear to combine visual and somatosensory signals in order to monitor the configuration of the limbs. They could form the basis of the complex body schema that we constantly use to adjust posture and guide movement.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Graziano, M S -- Cooke, D F -- Taylor, C S -- 11347/PHS HHS/ -- New York, N.Y. -- Science. 2000 Dec 1;290(5497):1782-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychology, Princeton University, Princeton, NJ 08544, USA. graziano@princeton.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11099420" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arm ; *Body Image ; Cues ; Humans ; Macaca fascicularis ; Male ; Neural Pathways ; Neurons/*physiology ; Parietal Lobe/cytology/*physiology ; *Proprioception ; *Visual Perception
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  • 17
    Publication Date: 2000-12-02
    Description: In healthy individuals, acute changes in cholesterol intake produce modest changes in plasma cholesterol levels. A striking exception occurs in sitosterolemia, an autosomal recessive disorder characterized by increased intestinal absorption and decreased biliary excretion of dietary sterols, hypercholesterolemia, and premature coronary atherosclerosis. We identified seven different mutations in two adjacent, oppositely oriented genes that encode new members of the adenosine triphosphate (ATP)-binding cassette (ABC) transporter family (six mutations in ABCG8 and one in ABCG5) in nine patients with sitosterolemia. The two genes are expressed at highest levels in liver and intestine and, in mice, cholesterol feeding up-regulates expressions of both genes. These data suggest that ABCG5 and ABCG8 normally cooperate to limit intestinal absorption and to promote biliary excretion of sterols, and that mutated forms of these transporters predispose to sterol accumulation and atherosclerosis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Berge, K E -- Tian, H -- Graf, G A -- Yu, L -- Grishin, N V -- Schultz, J -- Kwiterovich, P -- Shan, B -- Barnes, R -- Hobbs, H H -- HL07360/HL/NHLBI NIH HHS/ -- HL20948/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 2000 Dec 1;290(5497):1771-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Genetics and McDermott Center for Human Growth and Development and Howard Hughes Medical Institute, University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Boulevard, Dallas, TX 75390-9046, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11099417" target="_blank"〉PubMed〈/a〉
    Keywords: ATP-Binding Cassette Transporters/chemistry/*genetics/metabolism ; Amino Acid Sequence ; Animals ; Bile/metabolism ; Cholesterol/blood ; Cholesterol, Dietary/administration & dosage/*metabolism ; Chromosome Mapping ; Chromosomes, Human, Pair 2 ; Codon ; DNA-Binding Proteins ; Expressed Sequence Tags ; Gene Expression Regulation ; Humans ; *Intestinal Absorption ; Intestines/metabolism ; Lipid Metabolism, Inborn Errors/*genetics/metabolism ; Lipoproteins/chemistry/*genetics/metabolism ; Liver/metabolism ; Mice ; Mice, Inbred C57BL ; Molecular Sequence Data ; Mutation ; Orphan Nuclear Receptors ; RNA, Messenger/genetics/metabolism ; Receptors, Cytoplasmic and Nuclear/metabolism ; Sitosterols/*blood/metabolism
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  • 18
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-12-02
    Description: Cholesterol plays an indispensable role in regulating the properties of cell membranes in mammalian cells. Recent advances suggest that cholesterol exerts many of its actions mainly by maintaining sphingolipid rafts in a functional state. How rafts contribute to cholesterol metabolism and transport in the cell is still an open issue. It has long been known that cellular cholesterol levels are precisely controlled by biosynthesis, efflux from cells, and influx of lipoprotein cholesterol into cells. The regulation of cholesterol homeostasis is now receiving a new focus, and this changed perspective may throw light on diseases caused by cholesterol excess, the prime example being atherosclerosis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Simons, K -- Ikonen, E -- New York, N.Y. -- Science. 2000 Dec 1;290(5497):1721-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Max Planck Institute for Molecular Cell Biology and Genetics, Pfotenhauerstrasse, 01307 Dresden, Germany. kai.simons@embl-heidelberg.de〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11099405" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Transport ; Cell Membrane/metabolism ; Cholesterol/biosynthesis/*metabolism ; Endoplasmic Reticulum/metabolism ; Golgi Apparatus/metabolism ; Homeostasis ; Humans ; Lipoproteins/metabolism ; Membrane Microdomains/*metabolism ; Models, Biological
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  • 19
    Publication Date: 2000-11-25
    Description: We generated a mutant of the red fluorescent protein drFP583. The mutant (E5) changes its fluorescence from green to red over time. The rate of color conversion is independent of protein concentration and therefore can be used to trace time-dependent expression. We used in vivo labeling with E5 to measure expression from the heat shock-dependent promoter in Caenorhabditis elegans and from the Otx-2 promoter in developing Xenopus embryos. Thus, E5 is a "fluorescent timer" that can be used to monitor both activation and down-regulation of target promoters on the whole-organism scale.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Terskikh, A -- Fradkov, A -- Ermakova, G -- Zaraisky, A -- Tan, P -- Kajava, A V -- Zhao, X -- Lukyanov, S -- Matz, M -- Kim, S -- Weissman, I -- Siebert, P -- 1 RO3 TW01362-01/TW/FIC NIH HHS/ -- New York, N.Y. -- Science. 2000 Nov 24;290(5496):1585-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉School of Medicine, Stanford University, Stanford, CA 94305, USA. Alexey.Terskikh@Stanford.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11090358" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Brain/embryology/metabolism ; Caenorhabditis elegans/embryology/genetics ; Cell Line ; Color ; Fluorescence ; Gene Expression Profiling/*methods ; *Gene Expression Regulation ; Gene Expression Regulation, Developmental ; Heat-Shock Proteins/genetics ; *Homeodomain Proteins ; Humans ; Luminescent Proteins/*chemistry/*genetics/metabolism ; Mutation ; Nerve Tissue Proteins/genetics ; Otx Transcription Factors ; *Promoter Regions, Genetic ; Temperature ; Time Factors ; Trans-Activators/genetics ; Xenopus laevis/embryology
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  • 20
    Publication Date: 2000-11-25
    Description: Evidence for a new signaling mechanism consisting of ligand-independent lateral propagation of receptor activation in the plasma membrane is presented. We visualized the phosphorylation of green fluorescent protein (GFP)-tagged ErbB1 (ErbB1-GFP) receptors in cells focally stimulated with epidermal growth factor (EGF) covalently attached to beads. This was achieved by quantitative imaging of protein reaction states in cells by fluorescence resonance energy transfer (FRET) with global analysis of fluorescence lifetime imaging microscopy (FLIM) data. The rapid and extensive propagation of receptor phosphorylation over the entire cell after focal stimulation demonstrates a signaling wave at the plasma membrane resulting in full activation of all receptors.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Verveer, P J -- Wouters, F S -- Reynolds, A R -- Bastiaens, P I -- New York, N.Y. -- Science. 2000 Nov 24;290(5496):1567-70.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Cell Biology and Cell Biophysics Program, European Molecular Biology Laboratory, Meyerhofstrasse 1, 69117 Heidelberg, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11090353" target="_blank"〉PubMed〈/a〉
    Keywords: Arsenicals/pharmacology ; Carbocyanines ; Cell Membrane/*metabolism ; Diffusion ; Dimerization ; Endocytosis ; Energy Transfer ; Enzyme Inhibitors/pharmacology ; Epidermal Growth Factor/*metabolism/pharmacology ; Fluorescence ; Fluorescent Dyes ; Green Fluorescent Proteins ; Humans ; Immunoglobulin Fab Fragments ; Ligands ; Luminescent Proteins ; Microscopy, Confocal ; Microscopy, Fluorescence ; Microspheres ; Phosphorylation ; Phosphotyrosine/immunology ; Protein Tyrosine Phosphatases/antagonists & inhibitors/metabolism ; Receptor, Epidermal Growth Factor/*metabolism ; *Signal Transduction ; Tumor Cells, Cultured
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  • 21
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-11-25
    Description: An enduring controversy in neuroscience concerns how the brain "binds" together separately coded stimulus features to form unitary representations of objects. Recent evidence has indicated a close link between this binding process and 40-hertz (gamma-band) oscillations generated by localized neural circuits. In a separate line of research, the ability of young infants to perceive objects as unitary and bounded has become a central focus for debates about the mechanisms of perceptual development. Here we demonstrate that binding-related 40-hertz oscillations are evident in the infant brain around 8 months of age, which is the same age at which behavioral and event-related potential evidence indicates the onset of perceptual binding of spatially separated static visual features.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Csibra, G -- Davis, G -- Spratling, M W -- Johnson, M H -- New York, N.Y. -- Science. 2000 Nov 24;290(5496):1582-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Centre for Brain and Cognitive Development, School of Psychology, Birkbeck College, University of London, Malet Street, London WC1E 7HX, UK. g.csibra@bbk.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11090357" target="_blank"〉PubMed〈/a〉
    Keywords: *Electroencephalography ; Evoked Potentials, Visual ; Female ; *Form Perception ; Frontal Lobe/*physiology ; Humans ; Infant ; Male ; Occipital Lobe/physiology ; Parietal Lobe/physiology
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  • 22
    Publication Date: 2000-11-25
    Description: Homologs of the Yersinia virulence effector YopJ are found in both plant and animal bacterial pathogens, as well as plant symbionts. These YopJ family members were shown to act as cysteine proteases. The catalytic triad of the protease was required for inhibition of the mitogen-activated protein kinase (MAPK) and nuclear factor kappaB (NF-kappaB) signaling in animal cells and for induction of localized cell death in plants. The substrates for YopJ were shown to be highly conserved ubiquitin-like molecules, which are covalently added to numerous regulatory proteins. YopJ family members exert their pathogenic effect on cells by disrupting this posttranslational modification.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Orth, K -- Xu, Z -- Mudgett, M B -- Bao, Z Q -- Palmer, L E -- Bliska, J B -- Mangel, W F -- Staskawicz, B -- Dixon, J E -- 18024/PHS HHS/ -- AI41599/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2000 Nov 24;290(5496):1594-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biological Chemistry, University of Michigan, Ann Arbor, Michigan 48109-0606, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11090361" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Bacterial Proteins/*chemistry/genetics/*metabolism ; Catalysis ; Catalytic Domain ; Cell Line ; Cysteine Endopeptidases/chemistry/genetics/*metabolism ; Humans ; *MAP Kinase Signaling System ; Mitogen-Activated Protein Kinases/metabolism ; Molecular Sequence Data ; NF-kappa B/*metabolism ; Plant Leaves/cytology/virology ; SUMO-1 Protein ; Sequence Alignment ; Signal Transduction ; Transfection ; Ubiquitins/metabolism ; Virulence ; Xanthomonas campestris/enzymology/pathogenicity ; Yersinia pseudotuberculosis/enzymology/metabolism/*pathogenicity
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  • 23
    Publication Date: 2000-11-25
    Description: beta-Arrestins, originally discovered in the context of heterotrimeric guanine nucleotide binding protein-coupled receptor (GPCR) desensitization, also function in internalization and signaling of these receptors. We identified c-Jun amino-terminal kinase 3 (JNK3) as a binding partner of beta-arrestin 2 using a yeast two-hybrid screen and by coimmunoprecipitation from mouse brain extracts or cotransfected COS-7 cells. The upstream JNK activators apoptosis signal-regulating kinase 1 (ASK1) and mitogen-activated protein kinase (MAPK) kinase 4 were also found in complex with beta-arrestin 2. Cellular transfection of beta-arrestin 2 caused cytosolic retention of JNK3 and enhanced JNK3 phosphorylation stimulated by ASK1. Moreover, stimulation of the angiotensin II type 1A receptor activated JNK3 and triggered the colocalization of beta-arrestin 2 and active JNK3 to intracellular vesicles. Thus, beta-arrestin 2 acts as a scaffold protein, which brings the spatial distribution and activity of this MAPK module under the control of a GPCR.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉McDonald, P H -- Chow, C W -- Miller, W E -- Laporte, S A -- Field, M E -- Lin, F T -- Davis, R J -- Lefkowitz, R J -- CA65861/CA/NCI NIH HHS/ -- CA85422/CA/NCI NIH HHS/ -- HL16037/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 2000 Nov 24;290(5496):1574-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute and Department of Medicine, Duke University Medical Center, Box 3821, Durham, NC 27710, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11090355" target="_blank"〉PubMed〈/a〉
    Keywords: Angiotensin II/metabolism/pharmacology ; Animals ; Arrestins/genetics/*metabolism ; COS Cells ; Cell Line ; Cell Nucleus/metabolism ; Cytosol/enzymology/metabolism ; Endosomes/enzymology/metabolism ; Enzyme Activation ; Humans ; *MAP Kinase Kinase 4 ; MAP Kinase Kinase Kinase 5 ; MAP Kinase Kinase Kinases/*metabolism ; *MAP Kinase Signaling System ; Mice ; Mitogen-Activated Protein Kinase 10 ; Mitogen-Activated Protein Kinase Kinases/metabolism ; Mitogen-Activated Protein Kinases/*metabolism ; Mutation ; Phosphorylation ; Protein-Tyrosine Kinases/*metabolism ; Proto-Oncogene Proteins c-jun/metabolism ; Rats ; Receptor, Angiotensin, Type 1 ; Receptors, Angiotensin/*metabolism ; Recombinant Fusion Proteins/metabolism ; Transfection ; Two-Hybrid System Techniques
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  • 24
    Publication Date: 2000-11-18
    Description: Despite the fact that Leishmania are transmitted exclusively by sand flies, none of the experimental models of leishmaniasis have established infection via sand fly bites. Here we describe a reproducible murine model of Leishmania major infection transmitted by Phlebotomus papatasi. Prior exposure of mice to bites of uninfected sand flies conferred powerful protection against Leishmania major that was associated with a strong delayed-type hypersensitivity response and with interferon-gamma production at the site of parasite delivery. These results have important implications for the epidemiology of cutaneous leishmaniasis and suggest a vaccination strategy against this and possibly other vector-borne diseases.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kamhawi, S -- Belkaid, Y -- Modi, G -- Rowton, E -- Sacks, D -- New York, N.Y. -- Science. 2000 Nov 17;290(5495):1351-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11082061" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Dermis/immunology/parasitology ; Disease Models, Animal ; Ear ; Epidermis/immunology/parasitology ; Female ; Humans ; Hypersensitivity, Delayed ; *Insect Bites and Stings ; *Insect Vectors/parasitology ; Interferon-gamma/biosynthesis ; Interleukins/biosynthesis ; *Leishmania major/physiology ; Leishmaniasis, Cutaneous/*immunology/parasitology/*transmission ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; *Phlebotomus/parasitology ; Saliva/immunology
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  • 25
    Publication Date: 2000-11-10
    Description: A genetic perspective of human history in Europe was derived from 22 binary markers of the nonrecombining Y chromosome (NRY). Ten lineages account for 〉95% of the 1007 European Y chromosomes studied. Geographic distribution and age estimates of alleles are compatible with two Paleolithic and one Neolithic migratory episode that have contributed to the modern European gene pool. A significant correlation between the NRY haplotype data and principal components based on 95 protein markers was observed, indicating the effectiveness of NRY binary polymorphisms in the characterization of human population composition and history.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Semino, O -- Passarino, G -- Oefner, P J -- Lin, A A -- Arbuzova, S -- Beckman, L E -- De Benedictis, G -- Francalacci, P -- Kouvatsi, A -- Limborska, S -- Marcikiae, M -- Mika, A -- Mika, B -- Primorac, D -- Santachiara-Benerecetti, A S -- Cavalli-Sforza, L L -- Underhill, P A -- GM 28428/GM/NIGMS NIH HHS/ -- GM 55273/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2000 Nov 10;290(5494):1155-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Dipartimento di Genetica e Microbiologia, Universita di Pavia, Via Ferrata 1, 27100 Pavia, Italy. semino@ipvgen.univp.it〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11073453" target="_blank"〉PubMed〈/a〉
    Keywords: Alleles ; Anthropology, Physical ; Climate ; DNA, Mitochondrial/genetics ; Emigration and Immigration ; Europe ; Female ; *Gene Pool ; Genetic Markers ; *Genetics, Population ; History, Ancient ; Humans ; Male ; Middle East ; *Y Chromosome
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  • 26
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-11-10
    Description: Gene duplication has generally been viewed as a necessary source of material for the origin of evolutionary novelties, but it is unclear how often gene duplicates arise and how frequently they evolve new functions. Observations from the genomic databases for several eukaryotic species suggest that duplicate genes arise at a very high rate, on average 0.01 per gene per million years. Most duplicated genes experience a brief period of relaxed selection early in their history, with a moderate fraction of them evolving in an effectively neutral manner during this period. However, the vast majority of gene duplicates are silenced within a few million years, with the few survivors subsequently experiencing strong purifying selection. Although duplicate genes may only rarely evolve new functions, the stochastic silencing of such genes may play a significant role in the passive origin of new species.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lynch, M -- Conery, J S -- R01-GM36827/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2000 Nov 10;290(5494):1151-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biology, University of Oregon, Eugene, OR 97403, USA. mlynch@oregon.uoregon.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11073452" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Substitution ; Animals ; Arabidopsis/genetics ; Base Sequence ; Caenorhabditis elegans/genetics ; Chickens/genetics ; Databases, Factual ; Drosophila melanogaster/genetics ; *Evolution, Molecular ; Gene Duplication ; Gene Silencing ; *Genes, Duplicate ; *Genome ; Humans ; Mice ; Models, Genetic ; Mutation ; Oryza/genetics ; Probability ; Proteins/chemistry/genetics ; Saccharomyces cerevisiae/genetics ; Selection, Genetic ; Stochastic Processes ; Time Factors
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  • 27
    Publication Date: 2000-11-10
    Description: The molecular mechanism(s) responsible for posttranscriptional gene silencing and RNA interference remain poorly understood. We have cloned a gene (Mut6) from the unicellular green alga Chlamydomonas reinhardtii that is required for the silencing of a transgene and two transposon families. Mut6 encodes a protein that is highly homologous to RNA helicases of the DEAH-box family. This protein is necessary for the degradation of certain aberrant RNAs, such as improperly processed transcripts, which are often produced by transposons and some transgenes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wu-Scharf, D -- Jeong, B -- Zhang, C -- Cerutti, H -- New York, N.Y. -- Science. 2000 Nov 10;290(5494):1159-62.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉School of Biological Sciences and Plant Science Initiative, University of Nebraska-Lincoln, E211 Beadle Center, Post Office Box 880666, Lincoln, NE 68588, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11073454" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Motifs ; Amino Acid Sequence ; Animals ; Chlamydomonas reinhardtii/enzymology/*genetics ; Cloning, Molecular ; *DNA Transposable Elements ; *Gene Silencing ; Humans ; Molecular Sequence Data ; RNA/metabolism ; RNA Helicases/chemistry/*genetics/*metabolism ; RNA, Messenger/metabolism ; Retroelements ; Reverse Transcriptase Polymerase Chain Reaction ; Sequence Alignment ; Sequence Homology, Amino Acid ; *Transgenes
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  • 28
    Publication Date: 2000-11-04
    Description: Aggregated alpha-synuclein proteins form brain lesions that are hallmarks of neurodegenerative synucleinopathies, and oxidative stress has been implicated in the pathogenesis of some of these disorders. Using antibodies to specific nitrated tyrosine residues in alpha-synuclein, we demonstrate extensive and widespread accumulations of nitrated alpha-synuclein in the signature inclusions of Parkinson's disease, dementia with Lewy bodies, the Lewy body variant of Alzheimer's disease, and multiple system atrophy brains. We also show that nitrated alpha-synuclein is present in the major filamentous building blocks of these inclusions, as well as in the insoluble fractions of affected brain regions of synucleinopathies. The selective and specific nitration of alpha-synuclein in these disorders provides evidence to directly link oxidative and nitrative damage to the onset and progression of neurodegenerative synucleinopathies.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Giasson, B I -- Duda, J E -- Murray, I V -- Chen, Q -- Souza, J M -- Hurtig, H I -- Ischiropoulos, H -- Trojanowski, J Q -- Lee, V M -- New York, N.Y. -- Science. 2000 Nov 3;290(5493):985-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Neurodegenerative Disease Research and Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11062131" target="_blank"〉PubMed〈/a〉
    Keywords: Alzheimer Disease/metabolism/pathology ; Antibodies, Monoclonal ; Blotting, Western ; Brain/*metabolism/pathology ; Brain Chemistry ; Enzyme-Linked Immunosorbent Assay ; Fluorescent Antibody Technique ; Humans ; Immunohistochemistry ; Lewy Bodies/chemistry ; Lewy Body Disease/metabolism/pathology ; Microscopy, Immunoelectron ; Multiple System Atrophy/metabolism/pathology ; Nerve Tissue Proteins/analysis/immunology/*metabolism ; Neurodegenerative Diseases/*metabolism/*pathology ; Neurons/chemistry/metabolism/ultrastructure ; *Oxidative Stress ; Parkinson Disease/metabolism/pathology ; Synucleins ; Tyrosine/*analogs & derivatives/analysis/immunology/*metabolism ; alpha-Synuclein
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  • 29
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-11-04
    Description: To assess the role of BAX in drug-induced apoptosis in human colorectal cancer cells, we generated cells that lack functional BAX genes. Such cells were partially resistant to the apoptotic effects of the chemotherapeutic agent 5-fluorouracil, but apoptosis was not abolished. In contrast, the absence of BAX completely abolished the apoptotic response to the chemopreventive agent sulindac and other nonsteroidal anti-inflammatory drugs (NSAIDs). NSAIDs inhibited the expression of the antiapoptotic protein Bcl-XL, resulting in an altered ratio of BAX to Bcl-XL and subsequent mitochondria-mediated cell death. These results establish an unambiguous role for BAX in apoptotic processes in human epithelial cancers and may have implications for cancer chemoprevention strategies.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zhang, L -- Yu, J -- Park, B H -- Kinzler, K W -- Vogelstein, B -- CA 43460/CA/NCI NIH HHS/ -- CA 57345/CA/NCI NIH HHS/ -- CA 62924/CA/NCI NIH HHS/ -- etc. -- New York, N.Y. -- Science. 2000 Nov 3;290(5493):989-92.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Oncology Center, and Program in Human Genetics, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11062132" target="_blank"〉PubMed〈/a〉
    Keywords: Anti-Inflammatory Agents, Non-Steroidal/*pharmacology ; Anticarcinogenic Agents/pharmacology ; Antimetabolites, Antineoplastic/*pharmacology ; *Apoptosis ; Colorectal Neoplasms/genetics/metabolism/*pathology ; Fluorouracil/*pharmacology ; Genes, p53 ; Humans ; Indomethacin/pharmacology ; Intracellular Membranes/drug effects/physiology ; Membrane Potentials/drug effects ; Mitochondria/drug effects/physiology ; Mutation ; Proto-Oncogene Proteins/genetics/*metabolism ; Proto-Oncogene Proteins c-bcl-2/metabolism ; Proto-Oncogenes ; Sulindac/pharmacology ; Tumor Cells, Cultured ; Tumor Suppressor Protein p53/metabolism ; bcl-2-Associated X Protein ; bcl-X Protein
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  • 30
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-10-29
    Description: The central nervous system functions primarily to convert patterns of activity in sensory receptors into patterns of muscle activity that constitute appropriate behavior. At the anatomical level this requires two complementary processes: a set of genetically encoded rules for building the basic network of connections, and a mechanism for subsequently fine tuning these connections on the basis of experience. Identifying the locus and mechanism of these structural changes has long been among neurobiology's major objectives. Evidence has accumulated implicating a particular class of contacts, excitatory synapses made onto dendritic spines, as the sites where connective plasticity occurs. New developments in light microscopy allow changes in spine morphology to be directly visualized in living neurons and suggest that a common mechanism, based on dynamic actin filaments, is involved in both the formation of dendritic spines during development and their structural plasticity at mature synapses.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Matus, A -- New York, N.Y. -- Science. 2000 Oct 27;290(5492):754-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Friedrich Miescher Institute, Maulbeerstrasse 66, 4058 Basel, Switzerland. matus@fmi.ch〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11052932" target="_blank"〉PubMed〈/a〉
    Keywords: Actin Cytoskeleton/*physiology ; Actins/*physiology ; Animals ; Brain/embryology/growth & development/physiology ; Calcium/metabolism ; Dendrites/*physiology/ultrastructure ; Humans ; Learning ; Long-Term Potentiation ; Neural Pathways ; *Neuronal Plasticity ; Receptors, Glutamate/metabolism ; Synapses/*physiology
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  • 31
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-10-29
    Description: Dendrites of individual neurons in the vertebrate central nervous system are contacted by thousands of synaptic terminals relaying information about the environment. The postsynaptic membrane at each synaptic terminal is the first place where information is processed as it converges on the dendrite. At the postsynaptic membrane of excitatory synapses, neurotransmitter receptors are attached to large protein "signaling machines" that delicately regulate the strength of synaptic transmission. These machines are visible in the electron microscope and are called the postsynaptic density. By changing synaptic strength in response to neural activity, the postsynaptic density contributes to information processing and the formation of memories.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kennedy, M B -- NS17660/NS/NINDS NIH HHS/ -- NS28710/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 2000 Oct 27;290(5492):750-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Biology, California Institute of Technology, Pasadena, CA 91125, USA. kennedym@its.caltech.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11052931" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Calcium-Calmodulin-Dependent Protein Kinase Type 2 ; Calcium-Calmodulin-Dependent Protein Kinases/metabolism ; Carrier Proteins/metabolism ; Dendrites/*physiology ; Humans ; Mental Processes/*physiology ; Models, Neurological ; Nerve Tissue Proteins/metabolism ; Neuropeptides/metabolism ; Presynaptic Terminals/physiology ; Receptors, N-Methyl-D-Aspartate/metabolism ; Receptors, Neurotransmitter/*metabolism ; *Signal Transduction ; Synaptic Membranes/*physiology ; *Synaptic Transmission
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  • 32
    Publication Date: 2000-10-29
    Description: The protein N-WASP [a homolog to the Wiskott-Aldrich syndrome protein (WASP)] regulates actin polymerization by stimulating the actin-nucleating activity of the actin-related protein 2/3 (Arp2/3) complex. N-WASP is tightly regulated by multiple signals: Only costimulation by Cdc42 and phosphatidylinositol (4,5)-bisphosphate (PIP2) yields potent polymerization. We found that regulation requires N-WASP's constitutively active output domain (VCA) and two regulatory domains: a Cdc42-binding domain and a previously undescribed PIP(2)-binding domain. In the absence of stimuli, the regulatory modules together hold the VCA-Arp2/3 complex in an inactive "closed" conformation. In this state, both the Cdc42- and PIP2-binding sites are masked. Binding of either input destabilizes the closed state and enhances binding of the other input. This cooperative activation mechanism shows how combinations of simple binding domains can be used to integrate and amplify coincident signals.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Prehoda, K E -- Scott, J A -- Mullins, R D -- Lim, W A -- New York, N.Y. -- Science. 2000 Oct 27;290(5492):801-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Cellular and Molecular Pharmacology, University of California, San Francisco, CA 94143-0450, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11052943" target="_blank"〉PubMed〈/a〉
    Keywords: Actin Cytoskeleton/metabolism ; Actin-Related Protein 2 ; Actin-Related Protein 3 ; Actins/*metabolism ; Amino Acid Motifs ; Binding Sites ; Biopolymers ; *Cytoskeletal Proteins ; GTP Phosphohydrolases/metabolism ; Humans ; Models, Biological ; Nerve Tissue Proteins/*chemistry/genetics/*metabolism ; Phosphatidylinositol 4,5-Diphosphate/metabolism ; Protein Binding ; Protein Conformation ; Protein Folding ; Protein Structure, Tertiary ; Recombinant Fusion Proteins/metabolism ; *Signal Transduction ; Thermodynamics ; Wiskott-Aldrich Syndrome Protein, Neuronal ; cdc42 GTP-Binding Protein/metabolism
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  • 33
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-10-29
    Description: Communication between neurons in the brain occurs primarily through synapses made onto elaborate treelike structures called dendrites. New electrical and optical recording techniques have led to tremendous advances in our understanding of how dendrites contribute to neuronal computation in the mammalian brain. The varied morphology and electrical and chemical properties of dendrites enable a spectrum of local and long-range signaling, defining the input-output relationship of neurons and the rules for induction of synaptic plasticity. In this way, diversity in dendritic signaling allows individual neurons to carry out specialized functions within their respective networks.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hausser, M -- Spruston, N -- Stuart, G J -- New York, N.Y. -- Science. 2000 Oct 27;290(5492):739-44.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Physiology, University College London, Gower Street, London WC1E 6BT, UK. m.hausser@ucl.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11052929" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials ; Animals ; Brain/physiology ; Calcium Signaling ; Dendrites/*physiology ; Electrophysiology ; Humans ; Ion Channel Gating ; Ion Channels/physiology ; *Neuronal Plasticity ; Neurons/physiology ; Neurotransmitter Agents/physiology ; Protein Biosynthesis ; *Signal Transduction ; Synapses/*physiology ; *Synaptic Transmission
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  • 34
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-10-29
    Description: Our understanding of the function of dendrites has been greatly enriched by an inspiring dialogue between theory and experiments. Rather than functionally ignoring dendrites, representing neurons as single summing points, we have realized that dendrites are electrically and chemically distributed nonlinear units and that this has important consequences for interpreting experimental data and for the role of neurons in information processing. Here, we examine the route to unraveling some of the enigmas of dendrites and highlight the main insights that have been gained. Future directions are discussed that will enable theory and models to keep shedding light on dendrites, where the most fundamental input-output adaptive processes take place.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Segev, I -- London, M -- New York, N.Y. -- Science. 2000 Oct 27;290(5492):744-50.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurobiology and Interdisciplinary Center for Neural Computation, The Hebrew University of Jerusalem, Jerusalem, 91904, Israel. idan@lobster.ls.huji.ac.il〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11052930" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Dendrites/*physiology ; Electrophysiology ; Humans ; Information Theory ; Ion Channel Gating ; Ion Channels/physiology ; Learning ; Mathematics ; Mental Processes ; *Models, Neurological ; Neuronal Plasticity ; Neurons/*physiology ; Synapses/*physiology ; *Synaptic Transmission
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  • 35
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-10-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stone, R -- New York, N.Y. -- Science. 2000 Sep 29;289(5488):2253-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11041782" target="_blank"〉PubMed〈/a〉
    Keywords: DNA, Mitochondrial/genetics ; Europe ; History, Ancient ; Humans ; Ice ; Italy ; Male ; *Mummies ; Paleodontology ; Paleopathology
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  • 36
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-10-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tisdale, M J -- New York, N.Y. -- Science. 2000 Sep 29;289(5488):2293-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Pharmaceutical Sciences Research Institute, Aston University, Birmingham B4 7ET, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11041796" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Blood Proteins/metabolism ; Cachexia/drug therapy/etiology/*metabolism/pathology ; Cell Differentiation ; Cysteine Endopeptidases/genetics/metabolism ; Cytokines/pharmacology ; Homeostasis ; Humans ; Interferon-gamma/pharmacology ; Mice ; Multienzyme Complexes/genetics/metabolism ; Muscle Proteins/*metabolism ; Muscle, Skeletal/cytology/*metabolism/pathology ; MyoD Protein/genetics/metabolism ; Myosins/genetics/metabolism ; NF-kappa B/*metabolism ; Neoplasms/*complications ; Promoter Regions, Genetic ; Proteasome Endopeptidase Complex ; Proteoglycans ; Transcription, Genetic ; Tumor Necrosis Factor-alpha/pharmacology ; Ubiquitins/metabolism
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  • 37
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-10-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshall, E -- New York, N.Y. -- Science. 2000 Sep 29;289(5488):2250.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11041779" target="_blank"〉PubMed〈/a〉
    Keywords: Brain/*anatomy & histology ; *Diagnostic Imaging ; Humans ; *Internet ; *Software
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  • 38
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-10-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mann, C C -- New York, N.Y. -- Science. 2000 Sep 29;289(5488):2251-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11041781" target="_blank"〉PubMed〈/a〉
    Keywords: *Anthropology ; Behavioral Research ; Books ; Brazil/epidemiology ; Disease Outbreaks ; Humans ; *Indians, South American ; Measles/epidemiology/etiology ; Measles Vaccine ; Publishing ; *Scientific Misconduct ; Vaccination ; Warfare
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  • 39
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-10-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holden, C -- New York, N.Y. -- Science. 2000 Sep 29;289(5488):2257.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11041786" target="_blank"〉PubMed〈/a〉
    Keywords: Bone and Bones ; Burial ; Government Agencies ; History, Ancient ; Humans ; *Indians, North American/genetics/history ; Jurisprudence ; Paleontology/*legislation & jurisprudence ; United States ; Washington
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  • 40
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-10-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sisodia, S S -- New York, N.Y. -- Science. 2000 Sep 29;289(5488):2296-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurobiology, Pharmacology and Physiology, University of Chicago, Chicago, IL 60637, USA. ssisodia@drugs.bsd.uchicago.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11041797" target="_blank"〉PubMed〈/a〉
    Keywords: Alzheimer Disease/genetics/metabolism ; Amino Acid Motifs ; Amino Acid Substitution ; Amyloid Precursor Protein Secretases ; Amyloid beta-Peptides/metabolism ; Amyloid beta-Protein Precursor/*metabolism ; Animals ; Aspartic Acid Endopeptidases ; Endopeptidases/genetics/*metabolism ; Endoplasmic Reticulum/metabolism ; Humans ; Membrane Proteins/chemistry/genetics/*metabolism ; Mice ; Neurons/*metabolism ; Presenilin-1 ; Presenilin-2 ; Protein Processing, Post-Translational
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  • 41
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-10-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Thomas, G A -- Williams, E D -- New York, N.Y. -- Science. 2000 Sep 29;289(5488):2283.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11041794" target="_blank"〉PubMed〈/a〉
    Keywords: DNA, Neoplasm ; Europe ; Humans ; International Cooperation ; Japan ; *Neoplasms, Radiation-Induced ; RNA, Neoplasm ; *Thyroid Neoplasms/etiology ; *Tissue Banks ; United States ; World Health Organization
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  • 42
    Publication Date: 2000-10-20
    Description: Ectodysplasin, a member of the tumor necrosis factor family, is encoded by the anhidrotic ectodermal dysplasia (EDA) gene. Mutations in EDA give rise to a clinical syndrome characterized by loss of hair, sweat glands, and teeth. EDA-A1 and EDA-A2 are two isoforms of ectodysplasin that differ only by an insertion of two amino acids. This insertion functions to determine receptor binding specificity, such that EDA-A1 binds only the receptor EDAR, whereas EDA-A2 binds only the related, but distinct, X-linked ectodysplasin-A2 receptor (XEDAR). In situ binding and organ culture studies indicate that EDA-A1 and EDA-A2 are differentially expressed and play a role in epidermal morphogenesis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yan, M -- Wang, L C -- Hymowitz, S G -- Schilbach, S -- Lee, J -- Goddard, A -- de Vos, A M -- Gao, W Q -- Dixit, V M -- New York, N.Y. -- Science. 2000 Oct 20;290(5491):523-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Oncology, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11039935" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Amino Acid Substitution ; Animals ; Binding Sites ; Cell Line ; DNA-Binding Proteins/metabolism ; Ectodermal Dysplasia/genetics ; Ectodysplasins ; Epidermis/embryology/*metabolism ; Humans ; *I-kappa B Proteins ; In Situ Hybridization ; Ligands ; Membrane Proteins/*chemistry/*metabolism ; Mice ; Models, Molecular ; Molecular Sequence Data ; Morphogenesis ; NF-kappa B/metabolism ; Phosphorylation ; Point Mutation ; Protein Conformation ; Proteins/metabolism ; Receptors, Cell Surface/chemistry/genetics/*metabolism ; Recombinant Fusion Proteins/metabolism ; Signal Transduction ; TNF Receptor-Associated Factor 6 ; Transfection
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  • 43
    Publication Date: 2000-10-20
    Description: Pseudomonas aeruginosa causes severe infections, particularly of the lung, that are life threatening. Here, we show that P. aeruginosa infection induces apoptosis of lung epithelial cells by activation of the endogenous CD95/CD95 ligand system. Deficiency of CD95 or CD95 ligand on epithelial cells prevented apoptosis of lung epithelial cells in vivo as well as in vitro. The importance of CD95/CD95 ligand-mediated lung epithelial cell apoptosis was demonstrated by the rapid development of sepsis in CD95- or CD95 ligand-deficient mice, but not in normal mice, after P. aeruginosa infection.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Grassme, H -- Kirschnek, S -- Riethmueller, J -- Riehle, A -- von Kurthy, G -- Lang, F -- Weller, M -- Gulbins, E -- New York, N.Y. -- Science. 2000 Oct 20;290(5491):527-30.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Physiology, University of Tuebingen, Gmelinstrasse 5, 72076 Tuebingen, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11039936" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antigens, CD95/genetics/*metabolism ; *Apoptosis ; Bone Marrow Transplantation ; Cell Line ; Epithelial Cells/*immunology/microbiology/pathology ; Fas Ligand Protein ; Humans ; In Situ Nick-End Labeling ; Lung/*immunology/microbiology/pathology ; Lung Diseases/*immunology/microbiology/pathology ; Membrane Glycoproteins/genetics/*metabolism ; Mice ; Mice, Inbred C3H ; Pseudomonas Infections/*immunology/microbiology/pathology ; Pseudomonas aeruginosa/immunology/*pathogenicity ; Sepsis/microbiology ; Spleen/microbiology
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  • 44
    Publication Date: 2000-10-20
    Description: With accumulating evidence indicating the importance of cytotoxic T lymphocytes (CTLs) in containing human immunodeficiency virus-1 (HIV-1) replication in infected individuals, strategies are being pursued to elicit virus-specific CTLs with prototype HIV-1 vaccines. Here, we report the protective efficacy of vaccine-elicited immune responses against a pathogenic SHIV-89.6P challenge in rhesus monkeys. Immune responses were elicited by DNA vaccines expressing SIVmac239 Gag and HIV-1 89.6P Env, augmented by the administration of the purified fusion protein IL-2/Ig, consisting of interleukin-2 (IL-2) and the Fc portion of immunoglobulin G (IgG), or a plasmid encoding IL-2/Ig. After SHIV-89.6P infection, sham-vaccinated monkeys developed weak CTL responses, rapid loss of CD4+ T cells, no virus-specific CD4+ T cell responses, high setpoint viral loads, significant clinical disease progression, and death in half of the animals by day 140 after challenge. In contrast, all monkeys that received the DNA vaccines augmented with IL-2/Ig were infected, but demonstrated potent secondary CTL responses, stable CD4+ T cell counts, preserved virus-specific CD4+ T cell responses, low to undetectable setpoint viral loads, and no evidence of clinical disease or mortality by day 140 after challenge.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Barouch, D H -- Santra, S -- Schmitz, J E -- Kuroda, M J -- Fu, T M -- Wagner, W -- Bilska, M -- Craiu, A -- Zheng, X X -- Krivulka, G R -- Beaudry, K -- Lifton, M A -- Nickerson, C E -- Trigona, W L -- Punt, K -- Freed, D C -- Guan, L -- Dubey, S -- Casimiro, D -- Simon, A -- Davies, M E -- Chastain, M -- Strom, T B -- Gelman, R S -- Montefiori, D C -- Lewis, M G -- Emini, E A -- Shiver, J W -- Letvin, N L -- AI-65301/AI/NIAID NIH HHS/ -- AI-85343/AI/NIAID NIH HHS/ -- CA-50139/CA/NCI NIH HHS/ -- P01 AI041521/AI/NIAID NIH HHS/ -- R01 CA050139/CA/NCI NIH HHS/ -- etc. -- New York, N.Y. -- Science. 2000 Oct 20;290(5491):486-92.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Avenue, Boston, MA 02215, USA. dan_barouch@hotmail.com〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11039923" target="_blank"〉PubMed〈/a〉
    Keywords: AIDS Vaccines/*therapeutic use ; Acquired Immunodeficiency Syndrome/*prevention & control ; Animals ; Antibodies, Viral/blood/immunology ; CD4 Lymphocyte Count ; CD4-Positive T-Lymphocytes/immunology ; Disease Progression ; HIV Antibodies/blood/immunology ; HIV Infections/immunology/*therapy/virology ; *HIV-1/genetics/immunology/physiology ; Humans ; Interleukin-2/genetics/immunology/*therapeutic use ; Lymphocyte Activation ; Macaca mulatta ; Neutralization Tests ; Recombinant Fusion Proteins/therapeutic use ; Simian Acquired Immunodeficiency Syndrome/immunology/prevention & ; control/therapy/virology ; Simian Immunodeficiency Virus/genetics/immunology/physiology ; T-Lymphocytes, Cytotoxic/immunology ; Vaccination ; Vaccines, DNA/*therapeutic use ; Viral Load ; Viremia ; Virus Replication
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  • 45
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-10-14
    Description: "Second-class citizen" is how researchers on soft money, who have to raise their salaries from grants, describe their position--even those who like their jobs. It can be fraught with financial insecurity, disrespect, and poor facilities--as well as some advantages, such as freedom from administrative duties. Those who have done it say that success requires a strong will, an accommodating department, friends in high places, and money in the bank as a cushion--not to mention emotional security and a tough skin.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Barinaga, M -- New York, N.Y. -- Science. 2000 Sep 22;289(5487):2024-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11032550" target="_blank"〉PubMed〈/a〉
    Keywords: *Career Mobility ; Faculty ; Humans ; *Job Satisfaction ; *Research Personnel ; *Research Support as Topic ; *Salaries and Fringe Benefits
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  • 46
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-10-14
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshall, E -- New York, N.Y. -- Science. 2000 Sep 22;289(5487):2023.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11032549" target="_blank"〉PubMed〈/a〉
    Keywords: Cytoplasm/transplantation ; DNA, Mitochondrial ; *Ethics, Medical ; *Genetic Therapy ; *Germ Cells ; Government Regulation ; Humans ; Ovum ; Public Policy ; Reproductive Techniques ; Research Support as Topic ; Societies, Scientific ; United States
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  • 47
    Publication Date: 2000-10-14
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Klenerman, P -- Lechner, F -- Kantzanou, M -- Ciurea, A -- Hengartner, H -- Zinkernagel, R -- New York, N.Y. -- Science. 2000 Sep 22;289(5487):2003.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Nuffield Department of Medicine, John Radcliffe Hospital, Oxford OX3 9DU, UK. klener@molbiol.ox.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11032545" target="_blank"〉PubMed〈/a〉
    Keywords: Acute Disease ; Animals ; Genetic Variation ; Hepacivirus/*genetics/immunology ; Hepatitis C/*immunology/virology ; Hepatitis C Antibodies/*immunology ; Humans ; Lymphocytic Choriomeningitis/immunology/virology ; Lymphocytic choriomeningitis virus/genetics/immunology ; Mice ; Mutation ; Neutralization Tests ; T-Lymphocytes, Cytotoxic/*immunology ; Viral Envelope Proteins/genetics/immunology
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  • 48
    Publication Date: 2000-10-13
    Description: Participants playing the computer game Tetris reported intrusive, stereotypical, visual images of the game at sleep onset. Three amnesic patients with extensive bilateral medial temporal lobe damage produced similar hypnagogic reports despite being unable to recall playing the game, suggesting that such imagery may arise without important contribution from the declarative memory system. In addition, control participants reported images from previously played versions of the game, demonstrating that remote memories can influence the images from recent waking experience.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stickgold, R -- Malia, A -- Maguire, D -- Roddenberry, D -- O'Connor, M -- MH-13,923/MH/NIMH NIH HHS/ -- MH-48,832/MH/NIMH NIH HHS/ -- NS26985/NS/NINDS NIH HHS/ -- R01 MH092638/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2000 Oct 13;290(5490):350-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Neurophysiology, Department of Psychiatry, Harvard Medical School, 74 Fenwood Road, Boston, MA 02115, USA. rstickgold@hms.harvard.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11030656" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Amnesia/*physiopathology ; Arousal ; Brain/*physiology ; Dreams/*physiology ; Hippocampus/physiology/physiopathology ; Humans ; Learning ; Memory/*physiology ; Middle Aged ; Sleep Stages/*physiology ; Temporal Lobe/physiology/physiopathology ; *Video Games
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  • 49
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-10-13
    Description: It has been suggested that sexual reproduction is maintained because it reduces the load imposed by recurrent deleterious mutations. If rates of deleterious mutation per diploid genome per generation (U) exceed 1, and mutations interact synergistically, then sexuals can overcome their inherent twofold disadvantage. We have tested this hypothesis by estimating genomic point mutation rates for protein-coding genes in a range of animal taxa. We find a positive linear relationship between U and generation time. In species with short generation times, U is predicted to be far below 1, suggesting that sex is not maintained by its capacity to purge the genome of deleterious mutations.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Keightley, P D -- Eyre-Walker, A -- New York, N.Y. -- Science. 2000 Oct 13;290(5490):331-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute of Cell, Animal and Population Biology, University of Edinburgh, West Mains Road, Edinburgh EH9 3JT, UK. p.keightley@ed.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11030650" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biological Evolution ; Birds/genetics/physiology ; Cats/genetics/physiology ; Cattle/genetics/physiology ; DNA Transposable Elements ; Dogs/genetics/physiology ; Drosophila/genetics/physiology ; Female ; Haplorhini/genetics/physiology ; Humans ; Male ; Mutation ; *Point Mutation ; Proteins/genetics ; Rodentia/genetics/physiology ; *Sex ; Sheep/genetics/physiology
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  • 50
    Publication Date: 2000-10-13
    Description: A nuclear isoform of myosin I beta that contains a unique 16-amino acid amino-terminal extension has been identified. An affinity-purified antibody to the 16-amino acid peptide demonstrated nuclear staining. Confocal and electron microscopy revealed that nuclear myosin I beta colocalized with RNA polymerase II in an alpha-amanitin- and actinomycin D-sensitive manner. The antibody coimmunoprecipitated RNA polymerase II and blocked in vitro RNA synthesis. This isoform of myosin I beta appears to be in a complex with RNA polymerase II and may affect transcription.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pestic-Dragovich, L -- Stojiljkovic, L -- Philimonenko, A A -- Nowak, G -- Ke, Y -- Settlage, R E -- Shabanowitz, J -- Hunt, D F -- Hozak, P -- de Lanerolle, P -- GM 37537/GM/NIGMS NIH HHS/ -- GM 56489/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2000 Oct 13;290(5490):337-41.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Physiology and Biophysics, University of Illinois at Chicago, Chicago, IL 60612, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11030652" target="_blank"〉PubMed〈/a〉
    Keywords: 3T3 Cells ; Actins/metabolism ; Amanitins/pharmacology ; Amino Acid Sequence ; Animals ; Base Sequence ; Cell Nucleus/*metabolism ; Cloning, Molecular ; Dactinomycin/pharmacology ; Exons ; HeLa Cells ; Humans ; Mice ; Microscopy, Confocal ; Microscopy, Electron ; *Molecular Motor Proteins ; Molecular Sequence Data ; Myosins/chemistry/genetics/immunology/*metabolism ; Nucleic Acid Synthesis Inhibitors/pharmacology ; Precipitin Tests ; Protein Isoforms/chemistry/genetics/immunology/metabolism ; RNA/*biosynthesis ; RNA Polymerase II/*metabolism ; *Transcription, Genetic
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  • 51
    Publication Date: 2000-10-13
    Description: Motivated by the rapid increase in atmospheric CO2 due to human activities since the Industrial Revolution, several international scientific research programs have analyzed the role of individual components of the Earth system in the global carbon cycle. Our knowledge of the carbon cycle within the oceans, terrestrial ecosystems, and the atmosphere is sufficiently extensive to permit us to conclude that although natural processes can potentially slow the rate of increase in atmospheric CO2, there is no natural "savior" waiting to assimilate all the anthropogenically produced CO2 in the coming century. Our knowledge is insufficient to describe the interactions between the components of the Earth system and the relationship between the carbon cycle and other biogeochemical and climatological processes. Overcoming this limitation requires a systems approach.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Falkowski, P -- Scholes, R J -- Boyle, E -- Canadell, J -- Canfield, D -- Elser, J -- Gruber, N -- Hibbard, K -- Hogberg, P -- Linder, S -- Mackenzie, F T -- Moore, B 3rd -- Pedersen, T -- Rosenthal, Y -- Seitzinger, S -- Smetacek, V -- Steffen, W -- New York, N.Y. -- Science. 2000 Oct 13;290(5490):291-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute of Marine and Coastal Sciences, Rutgers University, 71 Dudley Road, New Brunswick, NJ 08901, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11030643" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Atmosphere ; *Carbon/metabolism ; *Carbon Dioxide/metabolism ; *Climate ; *Earth (Planet) ; *Ecosystem ; Greenhouse Effect ; Humans
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  • 52
    Publication Date: 2000-10-06
    Description: Memapsin 2 (beta-secretase) is a membrane-associated aspartic protease involved in the production of beta-amyloid peptide in Alzheimer's disease and is a major target for drug design. We determined the crystal structure of the protease domain of human memapsin 2 complexed to an eight-residue inhibitor at 1.9 angstrom resolution. The active site of memapsin 2 is more open and less hydrophobic than that of other human aspartic proteases. The subsite locations from S4 to S2' are well defined. A kink of the inhibitor chain at P2' and the change of chain direction of P3' and P4' may be mimicked to provide inhibitor selectivity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hong, L -- Koelsch, G -- Lin, X -- Wu, S -- Terzyan, S -- Ghosh, A K -- Zhang, X C -- Tang, J -- New York, N.Y. -- Science. 2000 Oct 6;290(5489):150-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Protein Studies Program and Crystallography Program, Oklahoma Medical Research Foundation, 825 NE 13th Street, Oklahoma City, OK 73104, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11021803" target="_blank"〉PubMed〈/a〉
    Keywords: Amyloid Precursor Protein Secretases ; Aspartic Acid Endopeptidases/*chemistry/metabolism ; Catalytic Domain ; Crystallography, X-Ray ; Endopeptidases ; Humans ; Hydrogen Bonding ; Models, Molecular ; Oligopeptides/*metabolism ; Protease Inhibitors/chemistry/*metabolism ; Protein Conformation ; Protein Folding ; Protein Structure, Secondary ; Protein Structure, Tertiary ; Recombinant Proteins/chemistry/metabolism
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  • 53
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-10-06
    Description: Recent results emphasize the roles of T-independent antibody response in humoral defenses, for which B1 cells and marginal zone B cells are mostly responsible. We discuss how these cells are activated, migrate, and differentiate into antibody-producing cells in various lymphoid tissues. Based on recent findings in each of these areas of B cell biology, we propose a possible mechanism for peripheral tolerance of autoreactive B cells at target organs.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fagarasan, S -- Honjo, T -- New York, N.Y. -- Science. 2000 Oct 6;290(5489):89-92.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Medical Chemistry, Faculty of Medicine, Kyoto University, Yoshida, Sakyo-ku, Kyoto 606-8501, Japan.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11021805" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Antibody Formation ; Autoantibodies/biosynthesis ; B-Cell Activating Factor ; B-Lymphocytes/cytology/*immunology ; Cell Differentiation ; Cell Movement ; DNA-Binding Proteins/physiology ; Humans ; Immune Tolerance ; Immunity, Innate ; Immunity, Mucosal ; *Lymphocyte Activation ; Lymphoid Tissue/cytology/immunology ; *Membrane Proteins ; Models, Immunological ; Signal Transduction ; T-Lymphocytes/*immunology ; Tumor Necrosis Factor-alpha/physiology
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  • 54
    Publication Date: 2000-10-06
    Description: The signal transducers and activators of transcription (STAT) transcription factors become phosphorylated on tyrosine and translocate to the nucleus after stimulation of cells with growth factors or cytokines. We show that the Rac1 guanosine triphosphatase can bind to and regulate STAT3 activity. Dominant negative Rac1 inhibited STAT3 activation by growth factors, whereas activated Rac1 stimulated STAT3 phosphorylation on both tyrosine and serine residues. Moreover, activated Rac1 formed a complex with STAT3 in mammalian cells. Yeast two-hybrid analysis indicated that STAT3 binds directly to active but not inactive Rac1 and that the interaction occurs via the effector domain. Rac1 may serve as an alternate mechanism for targeting STAT3 to tyrosine kinase signaling complexes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Simon, A R -- Vikis, H G -- Stewart, S -- Fanburg, B L -- Cochran, B H -- Guan, K L -- GM-54304/GM/NIGMS NIH HHS/ -- K08-HL-03547/HL/NHLBI NIH HHS/ -- P30-DK34928/DK/NIDDK NIH HHS/ -- etc. -- New York, N.Y. -- Science. 2000 Oct 6;290(5489):144-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Pulmonary and Critical Care Division, Tupper Research Institute, New England Medical Center, Boston, MA 02111, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11021801" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Substitution ; Animals ; COS Cells ; Cell Line ; Cercopithecus aethiops ; DNA-Binding Proteins/genetics/*metabolism ; Enzyme Activation ; Epidermal Growth Factor/pharmacology ; Gene Expression Regulation ; Genes, Reporter ; Genetic Vectors ; Guanine Nucleotide Exchange Factors/genetics/metabolism ; Humans ; Janus Kinase 2 ; Mutation ; Neoplasm Proteins ; Phosphorylation ; Phosphoserine/metabolism ; Phosphotyrosine/metabolism ; Protein-Tyrosine Kinases/metabolism ; Proteins/genetics/metabolism ; *Proto-Oncogene Proteins ; Rats ; STAT3 Transcription Factor ; Signal Transduction ; Trans-Activators/genetics/*metabolism ; Transfection ; Two-Hybrid System Techniques ; rac1 GTP-Binding Protein/genetics/*metabolism
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  • 55
    Publication Date: 2000-10-06
    Description: Rearrangements involving the RET gene are common in radiation-associated papillary thyroid cancer (PTC). The RET/PTC1 type of rearrangement is an inversion of chromosome 10 mediated by illegitimate recombination between the RET and the H4 genes, which are 30 megabases apart. Here we ask whether despite the great linear distance between them, RET and H4 recombination might be promoted by their proximity in the nucleus. We used two-color fluorescence in situ hybridization and three-dimensional microscopy to map the positions of the RET and H4 loci within interphase nuclei. At least one pair of RET and H4 was juxtaposed in 35% of normal human thyroid cells and in 21% of peripheral blood lymphocytes, but only in 6% of normal mammary epithelial cells. Spatial contiguity of RET and H4 may provide a structural basis for generation of RET/PTC1 rearrangement by allowing a single radiation track to produce a double-strand break in each gene at the same site in the nucleus.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nikiforova, M N -- Stringer, J R -- Blough, R -- Medvedovic, M -- Fagin, J A -- Nikiforov, Y E -- CA 72597/CA/NCI NIH HHS/ -- P01 ES 05652-10/ES/NIEHS NIH HHS/ -- New York, N.Y. -- Science. 2000 Oct 6;290(5489):138-41.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pathology and Laboratory Medicine, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11021799" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Breast/cytology ; Cells, Cultured ; Chromosome Inversion ; Chromosomes, Human, Pair 10/*genetics ; Cytoskeletal Proteins ; *Drosophila Proteins ; Epithelial Cells ; Gene Rearrangement ; Humans ; In Situ Hybridization, Fluorescence ; Interphase ; Lymphocytes ; Neoplasms, Radiation-Induced/genetics ; Oncogene Proteins, Fusion/*genetics ; Protein-Tyrosine Kinases ; Proteins/*genetics ; Proto-Oncogene Proteins/*genetics ; Proto-Oncogene Proteins c-ret ; Receptor Protein-Tyrosine Kinases/*genetics ; *Recombination, Genetic ; Reverse Transcriptase Polymerase Chain Reaction ; Thyroid Gland/*cytology/*radiation effects ; Thyroid Neoplasms/genetics
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  • 56
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-10-06
    Description: Rather than being confined to the secondary lymphoid tissue of the spleen and lymph nodes, large numbers of lymphocytes are intrinsically associated with the epithelial surfaces of the body. The best studied is gut-associated lymphoid tissue, but distinct epithelium-associated lymphoid tissue also exists in the reproductive tract, the lung, and the skin. The multiple cell types and functions composing these lymphoid tissues are increasingly seen as the key to how antigens delivered to body surfaces can elicit either immunogenic or tolerogenic responses. In some instances, these responses occur purely within the local body surface tissue, yet in other cases both local and systemic responses are elicited.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hayday, A -- Viney, J L -- New York, N.Y. -- Science. 2000 Oct 6;290(5489):97-100.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Peter Gorer Department of Immunobiology, Guy's King's St Thomas' Medical School, University of London, Guy's Hospital, London, SE1 9RT, UK. adrian.hayday@kcl.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11021807" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cytokines/biosynthesis/immunology ; Epithelial Cells/immunology ; Humans ; Immune Tolerance ; *Immunity, Mucosal ; Lymphocytes/*immunology ; Lymphoid Tissue/*immunology ; T-Lymphocytes/*immunology
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  • 57
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-10-06
    Description: The immune response is initiated in organized lymphoid tissues where antigen-loaded dendritic cells (DCs) encounter antigen-specific T cells. DCs function as packets of information that must be decoded by the T cell before an appropriate immune response can be mounted. We discuss how the dynamics of DC-T cell encounter and the mechanism of T cell differentiation make the decoding of this information stochastic rather than determinate. This results in the generation of both terminally differentiated effector cells and intermediates that play distinctive roles in protection, immunoregulation, and immunological memory.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lanzavecchia, A -- Sallusto, F -- New York, N.Y. -- Science. 2000 Oct 6;290(5489):92-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute for Research in Biomedicine, Via Vincenzo Vela 6, CH-6500 Bellinzona, Switzerland. lanzavecchia@irb.unisi.ch〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11021806" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antigens/immunology ; Cell Differentiation ; Cytokines/biosynthesis/immunology ; Dendritic Cells/*immunology ; Humans ; *Immunologic Memory ; Lymphocyte Activation ; Lymphoid Tissue/immunology ; Receptors, Antigen, T-Cell/immunology ; Signal Transduction ; T-Lymphocyte Subsets/cytology/immunology ; T-Lymphocytes/cytology/*immunology ; T-Lymphocytes, Helper-Inducer/cytology/immunology
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-10-06
    Description: With the detailed description and analysis of several inhibitory receptor systems on lymphoid and myeloid cells, a central paradigm has emerged in which the pairing of activation and inhibition is necessary to initiate, amplify, and then terminate immune responses. In some cases, the activating and inhibitory receptors recognize similar ligands, and the net outcome is determined by the relative strength of these opposing signals. The importance of this modulation is demonstrated by the sometimes fatal autoimmune disorders observed in mice with targeted disruption of inhibitory receptors. The significance of these receptors is further evidenced by the conservation of immunoreceptor tyrosine-based inhibitory motifs during their evolution.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ravetch, J V -- Lanier, L L -- New York, N.Y. -- Science. 2000 Oct 6;290(5489):84-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Molecular Genetics and Immunology, Rockefeller University, New York, NY 10021, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11021804" target="_blank"〉PubMed〈/a〉
    Keywords: Abatacept ; Animals ; Antigens, CD/chemistry/immunology/metabolism ; Antigens, Differentiation/immunology ; Autoimmune Diseases/immunology ; B-Lymphocytes/immunology ; Blood Cells/immunology ; CTLA-4 Antigen ; Histocompatibility Antigens Class I/immunology/metabolism ; Humans ; *Immunity, Cellular ; *Immunoconjugates ; Killer Cells, Natural/immunology ; Lymphocyte Activation ; Phagocytes/immunology ; Receptors, IgG/immunology/metabolism ; Receptors, Immunologic/chemistry/*immunology/metabolism ; Signal Transduction ; T-Lymphocytes/immunology
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-30
    Description: Researchers have deciphered how a promising cancer drug acts like a smart bomb, homing in on only a very narrow range of its potential targets in the cell. The compound, known as STI-571, has shown remarkable success in early clinical trials on patients with chronic myelogenous leukemia. Now, in work reported on page 1938, scientists reveal just how the compound works--information that could aid in the design of similar cancer therapies.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marx, J -- New York, N.Y. -- Science. 2000 Sep 15;289(5486):1857-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11012350" target="_blank"〉PubMed〈/a〉
    Keywords: Antineoplastic Agents/chemistry/*therapeutic use ; Benzamides ; Catalytic Domain/drug effects ; Clinical Trials as Topic ; Enzyme Activation/drug effects ; Enzyme Inhibitors/therapeutic use ; Humans ; Imatinib Mesylate ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/*drug therapy/enzymology ; *Piperazines ; Protein Conformation ; Protein-Tyrosine Kinases/antagonists & inhibitors/chemistry ; Proto-Oncogene Proteins c-abl/*antagonists & inhibitors ; Pyrimidines/chemistry/*therapeutic use
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sinclair, A R -- Ludwig, D -- Clark, C W -- New York, N.Y. -- Science. 2000 Sep 15;289(5486):1875.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11012354" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Conservation of Natural Resources/methods ; *Ecosystem ; Humans ; Residence Characteristics
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yan, H -- Kinzler, K W -- Vogelstein, B -- New York, N.Y. -- Science. 2000 Sep 15;289(5486):1890-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute and the Johns Hopkins Oncology Center, Baltimore, MD 21231, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11012364" target="_blank"〉PubMed〈/a〉
    Keywords: Genetic Techniques ; *Genetic Testing/methods ; *Genetics, Medical/trends ; Humans ; Mutation ; Sociology
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marcus, M -- New York, N.Y. -- Science. 2000 Sep 15;289(5486):1878.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11012357" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Newborn/physiology ; Embryonic and Fetal Development ; Female ; *Food Preferences/physiology ; Humans ; Rats ; *Taste
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Korn, D -- New York, N.Y. -- Science. 2000 Sep 15;289(5486):1877.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11012355" target="_blank"〉PubMed〈/a〉
    Keywords: Embryo, Mammalian/cytology ; Guidelines as Topic ; Humans ; National Institutes of Health (U.S.) ; Research/*legislation & jurisprudence ; *Stem Cells ; United States
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hillis, D M -- New York, N.Y. -- Science. 2000 Sep 15;289(5486):1877-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11012356" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/*etiology ; Animals ; Drug Contamination ; Hiv-1 ; Humans ; Pan troglodytes/virology ; Poliovirus Vaccine, Oral/adverse effects ; Simian Immunodeficiency Virus
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ross, P S -- Vos, J G -- Birnbaum, L S -- Osterhaus, A D -- New York, N.Y. -- Science. 2000 Sep 15;289(5486):1878-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11012359" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Wild ; Diet ; Distemper Virus, Phocine ; Environmental Pollutants/analysis/*toxicity ; Europe ; Fishes ; Humans ; Morbillivirus Infections/etiology/mortality/*veterinary ; Polychlorinated Biphenyls/analysis/*toxicity ; *Seals, Earless
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    Publication Date: 2000-09-30
    Description: The open data release policy adopted by the large-scale DNA sequencing centers has made accessible valuable information that facilitates research. Herein, we argue that the data producers' rights to receive credit for at least some portion of the analyses of the data must be protected. We suggest that this protection take the form of a specification of the probable content of the primary paper the data producers intend to publish when the data gathering is complete. Rights to publish that paper ought then be restricted to the producers unless they give permission otherwise.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rowen, L -- Wong, G K -- Lane, R P -- Hood, L -- New York, N.Y. -- Science. 2000 Sep 15;289(5486):1881.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute for Systems Biology, Seattle, WA 98105, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11012360" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Databases, Factual ; *Human Genome Project ; Humans ; Information Services ; *Intellectual Property ; Mice ; *Publishing
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-30
    Description: Since the first report of a cloned animal (Dolly the sheep) 3 years ago, cloning mammals has become something of a cottage industry. As Prather discusses in his Perspective, pigs can now be added to the august list of cloned animals, which includes cows, goats, and mice. This is a particularly spectacular achievement because pig cloning has turned out to be notoriously difficult. The pig is also a valuable domestic animal to have cloned because, being physiologically close to humans, its organs can be used in xenotransplantation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Prather, R S -- New York, N.Y. -- Science. 2000 Sep 15;289(5486):1886-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Animal Sciences, University of Missouri-Columbia, Columbia, MO 65211, USA. pratherR@missouri.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11012362" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Genetically Modified ; Cell Differentiation ; *Cloning, Organism ; Culture Media ; Endogenous Retroviruses ; Female ; Fibroblasts/chemistry ; Humans ; Nuclear Transfer Techniques ; Oocytes/chemistry ; Swine/*virology ; Transplantation, Heterologous
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Frewer, A -- Hanefeld, F -- New York, N.Y. -- Science. 2000 Sep 15;289(5486):1878.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11012358" target="_blank"〉PubMed〈/a〉
    Keywords: Anthropometry ; Brain/abnormalities/*anatomy & histology ; History, 20th Century ; Humans ; Male ; Parietal Lobe/abnormalities ; Physics/*history ; Speech Disorders/etiology/history
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-30
    Description: Although there are elegants maps of the human brain that reveal differences in cellular architecture between different cortical regions, there is not much information about how corresponding cortical regions differ between the left and right hemispheres. As Gazzaniga explains in his Perspective, new results reveal the surprising finding of asymmetry in area 22 (which is important for language processing) of the left and right hemisphere (Galuske et al.). Clusters of neurons in area 22 of the left hemisphere are spaced farther apart and have longer axons cabling them together than neuronal clusters in area 22 of the right hemisphere.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gazzaniga, M S -- New York, N.Y. -- Science. 2000 Sep 15;289(5486):1887-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Cognitive Neuroscience, Dartmouth College, Hanover, NH 03755, USA. michael.s.gazzaniga@visen.dartmouth.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11012363" target="_blank"〉PubMed〈/a〉
    Keywords: *Brain Mapping ; Cerebral Cortex/*anatomy & histology/cytology/physiology ; Humans ; Neurons/physiology
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-30
    Description: At center stage at a meeting on the origin of the AIDS epidemic, held here this week at the Royal Society, was a controversial theory that a contaminated polio vaccine tested in Africa more than 40 years ago sparked the epidemic. The theory took a hit when researchers revealed that tests of old samples of the vaccine provided no supporting evidence, and the main proponent of the theory, British writer Edward Hooper, endured a verbal battering himself from several prominent scientists. But Hooper, unbowed, got in plenty of jabs of his own.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cohen, J -- New York, N.Y. -- Science. 2000 Sep 15;289(5486):1850-1.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11012346" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/epidemiology/*etiology ; Africa/epidemiology ; Animals ; DNA, Viral/analysis ; Disease Outbreaks ; Drug Contamination ; HIV/genetics/isolation & purification ; Haplorhini/genetics ; Humans ; Pan troglodytes/genetics ; Poliovirus Vaccine, Inactivated/*adverse effects
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-29
    Description: A fundamental question in aging research is whether humans and other species possess an immutable life-span limit. We examined the maximum age at death in Sweden, which rose from about 101 years during the 1860s to about 108 years during the 1990s. The pace of increase was 0.44 years per decade before 1969 but accelerated to 1. 11 years per decade after that date. More than 70 percent of the rise in the maximum age at death from 1861 to 1999 is attributable to reductions in death rates above age 70. The rest are due to increased numbers of survivors to old age (both larger birth cohorts and increased survivorship from infancy to age 70). The more rapid rise in the maximum age since 1969 is due to the faster pace of old-age mortality decline during recent decades.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wilmoth, J R -- Deegan, L J -- Lundstrom, H -- Horiuchi, S -- K02-AG00778/AG/NIA NIH HHS/ -- R01-AG11552/AG/NIA NIH HHS/ -- R01-AG14698/AG/NIA NIH HHS/ -- New York, N.Y. -- Science. 2000 Sep 29;289(5488):2366-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Demography, University of California, Berkeley, CA 94720-2120, USA. jrw@demog.berkeley.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11009426" target="_blank"〉PubMed〈/a〉
    Keywords: Aged ; Aged, 80 and over ; Cohort Studies ; Female ; Humans ; Life Expectancy/trends ; Life Tables ; *Longevity ; Male ; Mortality/trends ; Probability ; Sweden
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-23
    Description: The use of microarrays--slides or chips systematically dotted with DNA from thousands of genes--to determine gene expression patterns is providing a wealth of new information that should aid in cancer diagnosis and ultimately in therapy. In the past several months, researchers in several labs have used microarray technology to identify specific subtypes of a variety of cancers, including leukemias and lymphomas, the dangerous skin cancer melanoma, and breast cancer. In some cases, they can determine which cancers are likely to respond to current therapies and which aren't. In addition, the studies are giving researchers a fix on which genes are important for the development, maintenance, and spread of the various cancers, and are thus possible drug targets.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marx, J -- New York, N.Y. -- Science. 2000 Sep 8;289(5485):1670-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11001727" target="_blank"〉PubMed〈/a〉
    Keywords: Disease Progression ; *Gene Expression Profiling ; Gene Expression Regulation, Neoplastic ; Genes, Tumor Suppressor ; Humans ; Neoplasm Invasiveness ; Neoplasm Metastasis/genetics ; Neoplasms/*classification/diagnosis/*genetics/therapy ; *Oligonucleotide Array Sequence Analysis ; Oncogenes ; Prognosis
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Starck, W -- New York, N.Y. -- Science. 2000 Sep 8;289(5485):1691.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11001734" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Australia ; *Cnidaria ; Conservation of Natural Resources ; *Disasters ; *Ecosystem ; Humans
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Balter, M -- New York, N.Y. -- Science. 2000 Sep 8;289(5485):1663-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11001722" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Animals, Domestic ; Carrier State/*veterinary ; Cattle ; Creutzfeldt-Jakob Syndrome/epidemiology/prevention & control/*transmission ; Cricetinae ; Encephalopathy, Bovine Spongiform/epidemiology/prevention & control/*transmission ; Great Britain/epidemiology ; Humans ; Mice ; Prion Diseases/*transmission ; Species Specificity
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kelman, A -- Sequeira, L -- Nester, E W -- New York, N.Y. -- Science. 2000 Sep 8;289(5485):1689-91.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11001732" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Communicable Diseases/*history/microbiology ; History, 19th Century ; History, 20th Century ; Humans ; Molecular Biology/history ; Plant Diseases/*history/microbiology ; Tobacco Mosaic Virus
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-23
    Description: In this month's essay, Paul Nurse recapitulates the ontogeny of one of the most important theories in the history of biology, the cell theory, which proposes that all forms of life are composed of cells. Along the way, he lays out the wondrous molecular complexities and processes that he and others have discovered in the course of their studies of the lives of cells. In particular, Nurse focuses on the mechanisms and controls of cell reproduction that ultimately allow growth, development, and evolution to occur.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nurse, P -- New York, N.Y. -- Science. 2000 Sep 8;289(5485):1711-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Imperial Cancer Research Fund, London, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11001740" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Apoptosis ; Biological Evolution ; Catalysis ; Cell Biology/*history ; *Cell Cycle ; Cell Division ; *Cell Physiological Phenomena ; DNA Replication ; Energy Metabolism ; Enzymes/metabolism ; Genes ; History, 17th Century ; History, 18th Century ; History, 19th Century ; History, 20th Century ; Humans ; Neoplasms/genetics/pathology ; Organelles/metabolism ; Signal Transduction
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-23
    Description: As the world gets warmer, the predictions about the spread of vector-based diseases such as malaria get gloomier. However, in their timely Perspective, Dye and Reiter explain the implications of a new climate model (Randolph and Rogers), which predicts that the distribution of malaria is unlikely to change dramatically in the next 50 years even if the world does get hotter.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dye, C -- Reiter, P -- New York, N.Y. -- Science. 2000 Sep 8;289(5485):1697-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Communicable Diseases Control, Prevention and Eradication, World Health Organization (WHO), 1211 Geneva 27, Switzerland. dyec@who.ch〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11001735" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Anopheles/parasitology/physiology ; *Climate ; *Forecasting ; Greenhouse Effect ; Humans ; Humidity ; Insect Vectors/parasitology/physiology ; Malaria, Falciparum/*epidemiology/*transmission ; Models, Biological ; *Models, Statistical ; Multivariate Analysis ; Plasmodium falciparum/physiology ; Rain ; Regression Analysis ; Temperature
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Thompson, R L -- Sawtell, N M -- New York, N.Y. -- Science. 2000 Sep 8;289(5485):1651.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Genetics, University of Cincinnati Medical Center, Cincinnati, OH 45267-0524, USA. Richard.Thompson@UC.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11001720" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antibody Specificity ; *Apoptosis ; Blotting, Western ; Cell Nucleus/enzymology ; Cytoplasm/enzymology ; DNA Fragmentation ; Genes, Viral ; Herpesvirus 1, Human/genetics/*physiology ; Humans ; Immunohistochemistry ; In Situ Nick-End Labeling ; Mice ; Neurons/*cytology/*virology ; Poly(ADP-ribose) Polymerases/analysis/immunology ; Rabbits ; Virus Latency/*genetics
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holden, C -- New York, N.Y. -- Science. 2000 Sep 8;289(5485):1663.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11001721" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cannibalism/*history ; Colorado ; Feces/*chemistry ; History, Medieval ; Humans ; Indians, North American/*history ; Myoglobin/*analysis
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Silvergleid, A J -- New York, N.Y. -- Science. 2000 Sep 8;289(5485):1689-91.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11001733" target="_blank"〉PubMed〈/a〉
    Keywords: Blood Transfusion/*adverse effects ; Hepatitis C/*epidemiology/*transmission ; Humans ; Substance Abuse, Intravenous/complications ; United States/epidemiology
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-23
    Description: Triplet repeat diseases are disorders in which there is expansion of a repeat sequence of three nucleotides in the affected gene. Although the pathology usually results from production of a defective protein, myotonic dystrophy (DM) has proved to be a puzzle because the expanded repeats appear in a non-coding region of the affected DMPK gene. In a Perspective, Tapscott explains how findings from a new mouse model of DM (Mankodi et al.) could solve this paradox.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tapscott, S J -- New York, N.Y. -- Science. 2000 Sep 8;289(5485):1701-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA. stapscot@fhcrc.org〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11001736" target="_blank"〉PubMed〈/a〉
    Keywords: 3' Untranslated Regions ; Animals ; Anticipation, Genetic ; Cataract/etiology ; Chromosomes, Human, Pair 19 ; Chromosomes, Human, Pair 3 ; Disease Models, Animal ; Gene Expression Regulation ; Heart Conduction System/physiopathology ; Homeodomain Proteins/genetics ; Humans ; Mice ; Mice, Knockout ; Muscle, Skeletal/metabolism/pathology/physiopathology ; Myotonic Dystrophy/*genetics/metabolism/pathology/physiopathology ; Myotonin-Protein Kinase ; Phenotype ; Protein-Serine-Threonine Kinases/*genetics/metabolism ; RNA Processing, Post-Transcriptional ; RNA, Messenger/*genetics/metabolism ; RNA-Binding Proteins/metabolism ; *Trinucleotide Repeat Expansion
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-23
    Description: How do B cells generate the enormous diversity of antibodies that are able to recognize and bind to whichever antigen a B cell might happen to encounter in the body? Several genetic mechanisms that manipulate different combinations of immunoglobulin genes are known. In their Perspective, Neuberger and Scott, highlight another genetic mechanism called RNA editing now shown to be involved in the production of antibody diversity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Neuberger, M S -- Scott, J -- New York, N.Y. -- Science. 2000 Sep 8;289(5485):1705-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Medical Research Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11001738" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Antibody Diversity ; B-Lymphocytes/enzymology/*immunology ; Catalysis ; Cytidine Deaminase/chemistry/*genetics/*metabolism ; Evolution, Molecular ; Genes, Immunoglobulin ; Humans ; Immunoglobulin Class Switching ; Lymphocyte Activation ; Mice ; Mutation ; *RNA Editing ; RNA, Messenger/genetics/metabolism ; Tumor Cells, Cultured
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Smith, O -- New York, N.Y. -- Science. 2000 Sep 8;289(5485):1706.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11001739" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Autoimmune Diseases ; *Carrier Proteins ; HLA-DQ Antigens/analysis ; HLA-DQ beta-Chains ; Humans ; Hypothalamus/*metabolism/pathology ; *Intracellular Signaling Peptides and Proteins ; *Membrane Glycoproteins ; Narcolepsy/*etiology/immunology/metabolism/pathology ; Neurons/*metabolism/pathology ; *Neuropeptides ; Neurotransmitter Agents/cerebrospinal fluid/genetics/*metabolism ; Orexins ; Point Mutation ; Protein Precursors/genetics
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  • 84
    Publication Date: 2000-09-23
    Description: One of the major concerns with a potential change in climate is that an increase in extreme events will occur. Results of observational studies suggest that in many areas that have been analyzed, changes in total precipitation are amplified at the tails, and changes in some temperature extremes have been observed. Model output has been analyzed that shows changes in extreme events for future climates, such as increases in extreme high temperatures, decreases in extreme low temperatures, and increases in intense precipitation events. In addition, the societal infrastructure is becoming more sensitive to weather and climate extremes, which would be exacerbated by climate change. In wild plants and animals, climate-induced extinctions, distributional and phenological changes, and species' range shifts are being documented at an increasing rate. Several apparently gradual biological changes are linked to responses to extreme weather and climate events.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Easterling, D R -- Meehl, G A -- Parmesan, C -- Changnon, S A -- Karl, T R -- Mearns, L O -- New York, N.Y. -- Science. 2000 Sep 22;289(5487):2068-74.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉National Oceanic and Atmospheric Administration (NOAA)/National Climatic Data Center, 151 Patton Avenue, Asheville, NC 28801, USA. david.r.easterling@noaa.gov〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11000103" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Climate ; Demography ; *Disasters ; *Ecosystem ; Humans ; Insurance ; Models, Theoretical ; *Weather
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-19
    Description: Clinicians may soon be able to mount a multipronged attack against cholesterol, the artery-clogging lipid whose buildup in the body is a major contributor to heart attacks and other cardiovascular diseases. In work reported on page 1524, a team has pinpointed a biological master switch in mice that controls three pathways that work together to both rid the body of excess cholesterol and prevent its absorption from the intestine. The work suggests a new mechanism for reducing cholesterol, for example, with drugs that turn up the activity of the master switch, a protein known as the retinoid X receptor.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ferber, D -- New York, N.Y. -- Science. 2000 Sep 1;289(5484):1446-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10991725" target="_blank"〉PubMed〈/a〉
    Keywords: ATP Binding Cassette Transporter 1 ; ATP-Binding Cassette Transporters/*metabolism ; Animals ; Bile Acids and Salts ; Biological Transport/drug effects ; Cholesterol/*metabolism ; Cholesterol, Dietary/administration & dosage ; DNA-Binding Proteins/metabolism ; Glycoproteins/*metabolism ; Humans ; Intestinal Absorption/drug effects ; Intestines/drug effects/*metabolism ; Liver/metabolism ; Macrophages/metabolism ; Mice ; Orphan Nuclear Receptors ; *Receptors, Cytoplasmic and Nuclear ; Receptors, Retinoic Acid/*metabolism ; Receptors, Thyroid Hormone/metabolism ; Retinoid X Receptors ; Transcription Factors/*metabolism
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-19
    Description: A task force here has been studying cases of variant Creutzfeldt-Jakob disease (vCJD), an incurable malady of the brain and nervous system that has been linked to eating beef or other products from cattle infected with bovine spongiform encephalopathy or "mad cow disease." The team's goal is to find out just how the patients got infected and how many of them there may ultimately be. The number of confirmed or probable vCJD cases in the United Kingdom is still relatively small--a total of 80 as Science went to press--and recent estimates of the number of potential cases are lower than was once feared. Yet the task force's own recent results show that the incidence of vCJD is rising, and researchers remain determined to try to solve the riddles posed by vCJD.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Balter, M -- New York, N.Y. -- Science. 2000 Sep 1;289(5484):1452-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10991726" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bias (Epidemiology) ; Cattle ; Cluster Analysis ; Creutzfeldt-Jakob Syndrome/*epidemiology/transmission ; Disease Outbreaks ; Encephalopathy, Bovine Spongiform/epidemiology/transmission ; Female ; *Food ; Great Britain/epidemiology ; Humans ; Incidence ; Male ; Meat ; Surveys and Questionnaires
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-19
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kennedy, D -- New York, N.Y. -- Science. 2000 Sep 1;289(5484):1469.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10991729" target="_blank"〉PubMed〈/a〉
    Keywords: Bioethics ; Cell Line ; Embryo, Mammalian/*cytology ; *Guidelines as Topic ; Humans ; *National Institutes of Health (U.S.) ; Politics ; *Research/legislation & jurisprudence ; Research Support as Topic ; *Stem Cells ; United States
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-19
    Description: Cholera has been the scourge of humankind for centuries. Although most of the time Vibrio cholerae, the microbe that causes this disease, is a free-living organism inhabiting aquatic environments, it can invade human hosts causing severe diarrhea and often death. As DiRita explains in his Perspective, sequencing of the entire V. cholerae genome is revealing new facets of the pathogenesis of this dangerous microbe.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉DiRita, V J -- New York, N.Y. -- Science. 2000 Sep 1;289(5484):1488-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Microbiology and Immunology and Unit for Laboratory Animal Medicine, University of Michigan Medical School, Ann Arbor, MI 48109, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10991736" target="_blank"〉PubMed〈/a〉
    Keywords: Bacterial Proteins/genetics ; Bacterial Toxins/genetics ; Cholera/epidemiology/microbiology ; Cholera Toxin/genetics ; Chromosomes, Bacterial/genetics ; *Endopeptidases ; *Genome, Bacterial ; Humans ; Open Reading Frames ; Sequence Analysis, DNA ; Vibrio cholerae/*genetics/*pathogenicity/physiology ; Virulence/genetics
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-19
    Description: A plan to have scientists deposit functional magnetic resonance images of the brain in a public center at Dartmouth College as a condition of publication has drawn a flurry of objections. Brain scientists warn that if the project goes forward as planned, it could compromise the privacy of research subjects, get tangled up in technical knots, and rob authors of the credit they deserve. A new task force is attempting to elicit a consensus and draft a set of data-sharing guidelines supported by the entire field.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshall, E -- New York, N.Y. -- Science. 2000 Sep 1;289(5484):1458-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10991728" target="_blank"〉PubMed〈/a〉
    Keywords: Brain/*anatomy & histology/physiology ; *Brain Mapping ; *Databases, Factual ; Humans ; *Magnetic Resonance Imaging ; Periodicals as Topic ; Privacy ; Publishing ; Software
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-19
    Description: Microbiologists have long been puzzled by the finding that the gut mucosa does not respond to the myriad varieties of bacteria that normally reside in the gut. As Xavier and Podolsky explain in their Perspective, this may be because bacteria that are indigenous to the gut have learned ways to switch off pathways in gut epithelial cells that lead to switching on of genes involved in inflammation (Neish et al.).〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Xavier, R J -- Podolsky, D K -- New York, N.Y. -- Science. 2000 Sep 1;289(5484):1483-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Gastrointestinal Unit, Massachusetts General Hospital, 55 Fruit Street, GRJ-719, Boston, MA 02114, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10991734" target="_blank"〉PubMed〈/a〉
    Keywords: Cell Nucleus/metabolism ; Colon ; Cytokines/genetics ; Cytoplasm/metabolism ; Gene Expression Regulation ; Humans ; I-kappa B Proteins/*metabolism ; Inflammation ; Intestinal Mucosa/*metabolism/*microbiology ; NF-kappa B/*metabolism ; Salmonella/pathogenicity/*physiology ; Tumor Cells, Cultured ; Ubiquitins/metabolism
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-19
    Description: The National Institutes of Health (NIH) issued final guidelines last week allowing NIH-funded researchers to derive human pluripotent stem cells from fetal tissue, but not from embryos. Scientists may also work with embryonic stem cells, but may obtain them only from private sources and must ensure that derivation meets certain ethical conditions. The NIH spent nearly a year finalizing the guidelines, which researchers hope will allow work leading to the improved treatment of diabetes, Parkinson's, and other diseases.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vogel, G -- New York, N.Y. -- Science. 2000 Sep 1;289(5484):1442-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10991722" target="_blank"〉PubMed〈/a〉
    Keywords: Cell Line ; Embryo, Mammalian/*cytology ; *Guidelines as Topic ; Humans ; *National Institutes of Health (U.S.)/legislation & jurisprudence ; *Research/legislation & jurisprudence ; Research Support as Topic ; *Stem Cells ; United States
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-19
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 2000 Sep 1;289(5484):1471.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10991730" target="_blank"〉PubMed〈/a〉
    Keywords: Computational Biology ; *Databases, Factual ; *Genome, Human ; Humans ; *Internet
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-19
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Anderson, A -- New York, N.Y. -- Science. 2000 Sep 1;289(5484):1472-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10991732" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Archaeology ; *Birds ; Humans ; New Zealand ; Time Factors
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-19
    Description: Bone repair may be one of the first major applications of tissue engineering; efforts to encourage the growth of new bone using novel matrices, bone morphogenic proteins, gene therapy, and stem cells are all showing promise. But the commercial stakes are so high that some researchers are worried that patent claims, and a reluctance to test competing technologies in combination, could delay progress in the field.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Service, R F -- New York, N.Y. -- Science. 2000 Sep 1;289(5484):1498-500.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10991738" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biocompatible Materials ; *Biomedical Engineering ; *Biotechnology ; Bone Marrow Cells/cytology/*physiology ; Bone Marrow Transplantation ; Bone Morphogenetic Proteins/genetics/*therapeutic use ; *Bone Regeneration ; Cell Culture Techniques ; Clinical Trials as Topic ; Genetic Therapy ; Humans ; Osseointegration ; *Osteogenesis ; Parathyroid Hormone/genetics ; Stem Cell Transplantation ; Stem Cells/cytology/physiology
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    Publication Date: 2000-09-16
    Description: The inadvertent activation of the Abelson tyrosine kinase (Abl) causes chronic myelogenous leukemia (CML). A small-molecule inhibitor of Abl (STI-571) is effective in the treatment of CML. We report the crystal structure of the catalytic domain of Abl, complexed to a variant of STI-571. Critical to the binding of STI-571 is the adoption by the kinase of an inactive conformation, in which a centrally located "activation loop" is not phosphorylated. The conformation of this loop is distinct from that in active protein kinases, as well as in the inactive form of the closely related Src kinases. These results suggest that compounds that exploit the distinctive inactivation mechanisms of individual protein kinases can achieve both high affinity and high specificity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schindler, T -- Bornmann, W -- Pellicena, P -- Miller, W T -- Clarkson, B -- Kuriyan, J -- GM29362/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2000 Sep 15;289(5486):1938-42.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratories of Molecular Biophysics and Howard Hughes Medical Institute, The Rockefeller University, 1230 York Avenue, New York, NY 10021, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10988075" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antineoplastic Agents/chemistry/*pharmacology ; Benzamides ; Catalytic Domain ; Crystallography, X-Ray ; Enzyme Activation ; Enzyme Inhibitors/chemistry/*pharmacology ; Humans ; Imatinib Mesylate ; Mice ; Models, Molecular ; Phosphorylation ; *Piperazines ; Protein Conformation ; Proto-Oncogene Proteins c-abl/*antagonists & inhibitors/chemistry/metabolism ; Pyrimidines/chemistry/*pharmacology ; Recombinant Fusion Proteins ; Structure-Activity Relationship
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  • 96
    Publication Date: 2000-09-16
    Description: Mitochondrial import of a cytoplasmic transfer RNA (tRNA) in yeast requires the preprotein import machinery and cytosolic factors. We investigated whether the tRNA import pathway can be used to correct respiratory deficiencies due to mutations in the mitochondrial DNA and whether this system can be transferred into human cells. We show that cytoplasmic tRNAs with altered aminoacylation identity can be specifically targeted to the mitochondria and participate in mitochondrial translation. We also show that human mitochondria, which do not normally import tRNAs, are able to internalize yeast tRNA derivatives in vitro and that this import requires an essential yeast import factor.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kolesnikova, O A -- Entelis, N S -- Mireau, H -- Fox, T D -- Martin, R P -- Tarassov, I A -- GM29362/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2000 Sep 15;289(5486):1931-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉FRE 2168 du CNRS, Mecanismes Moleculaires de la Division Cellulaire et du Developpement, 21 rue Rene Descartes, 67084 Strasbourg, France.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10988073" target="_blank"〉PubMed〈/a〉
    Keywords: Acylation ; Base Sequence ; Biological Transport ; Cytoplasm/metabolism ; DNA, Mitochondrial/genetics/*metabolism ; Genes, Fungal ; Humans ; In Vitro Techniques ; Mitochondria/*metabolism ; Molecular Sequence Data ; Saccharomyces cerevisiae/genetics/metabolism ; Suppression, Genetic
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 97
    Publication Date: 2000-09-16
    Description: Language-relevant processing of auditory signals is lateralized and involves the posterior part of Brodmann area 22. We found that the functional lateralization in this area was accompanied by interhemispheric differences in the organization of the intrinsic microcircuitry. Neuronal tract tracing revealed a modular network of long-range intrinsic connections linking regularly spaced clusters of neurons. Although the cluster diameter was similar in both hemispheres, their spacing was about 20 percent larger in the left hemisphere. Assuming similar relations between functional and anatomical architecture as in visual cortex, the present data suggest that more functionally distinct columnar systems are included per surface unit in the left than in the right area 22.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Galuske, R A -- Schlote, W -- Bratzke, H -- Singer, W -- New York, N.Y. -- Science. 2000 Sep 15;289(5486):1946-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurophysiology, Max-Planck-Institute for Brain Research, Deutschordenstrasse 46, 60528 Frankfurt a.M., Germany. galuske@mpih-frankfurt.mpg.de〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10988077" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Aged, 80 and over ; Auditory Cortex/anatomy & histology/physiology ; *Brain Mapping ; Carbocyanines ; Female ; Fluorescent Dyes ; Humans ; Male ; Middle Aged ; Neural Pathways ; Temporal Lobe/*anatomy & histology/physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 98
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-09
    Description: Researchers are uncovering disturbing evidence that scientists and tourists are infecting wild primates with human pathogens. In response, ape specialists, including the American Society of Primatologists, are now calling for stricter health standards for researchers and tourists. They are also urging researchers to learn how to diagnose disease in their study animals.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ferber, D -- New York, N.Y. -- Science. 2000 Aug 25;289(5483):1277-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10979848" target="_blank"〉PubMed〈/a〉
    Keywords: Africa/epidemiology ; Animals ; Ape Diseases/epidemiology/*transmission ; Communicable Diseases/epidemiology/transmission/*veterinary ; *Gorilla gorilla ; Humans ; Parasitic Diseases, Animal/epidemiology/*transmission ; Primate Diseases/epidemiology/*transmission ; Primates ; Research Personnel ; Travel
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 99
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pennisi, E -- New York, N.Y. -- Science. 2000 Aug 25;289(5483):1267-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10979842" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Financing, Government ; *Genome ; Human Genome Project ; Humans ; Mice/genetics ; National Institutes of Health (U.S.)/economics ; Rats/*genetics ; Research Support as Topic ; *Sequence Analysis, DNA ; United States
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 100
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gibbons, A -- New York, N.Y. -- Science. 2000 Aug 25;289(5483):1267.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10979841" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Genome ; Humans ; Pan troglodytes/*genetics ; *Sequence Analysis, DNA
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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