scispace - formally typeset
Search or ask a question
Institution

Cold Spring Harbor Laboratory

NonprofitCold Spring Harbor, New York, United States
About: Cold Spring Harbor Laboratory is a nonprofit organization based out in Cold Spring Harbor, New York, United States. It is known for research contribution in the topics: Gene & Genome. The organization has 3772 authors who have published 6603 publications receiving 1010873 citations. The organization is also known as: CSHL.
Topics: Gene, Genome, RNA, DNA, Cancer


Papers
More filters
Journal ArticleDOI
06 Oct 1994-Nature
TL;DR: It is shown that p21 does not block PCNA-dependent nucleotide-excision repair, in contrast to its inhibition of simian virus 40 DNA replication, and the short gap-filling DNA synthesis by PC NA-dependent DNA polymerases δ and ɛ is less sensitive to inhibition by p21 than is long primer-extension synthesis.
Abstract: In mammalian cells, DNA damage increases the levels of the nuclear tumour-suppressor p53, resulting in elevated synthesis of p21, an inhibitor of cyclin-dependent kinases (CDK). p21 may also directly block DNA replication by inhibiting the proliferating-cell nuclear antigen (PCNA), an essential DNA replication protein. However, PCNA is also required for nucleotide-excision repair of DNA, an intrinsic part of the cellular response to ultraviolet irradiation. Using an in vitro system, we now show that p21 does not block PCNA-dependent nucleotide-excision repair, in contrast to its inhibition of simian virus 40 DNA replication. Furthermore, the short gap-filling DNA synthesis by PCNA-dependent DNA polymerases delta and epsilon is less sensitive to inhibition by p21 than is long primer-extension synthesis. The ability of p21 to inhibit the role of PCNA in DNA replication but not in DNA repair rationalizes in vivo data showing that genetic damage leads to inactivation of chromosomal replication while allowing damage-responsive repair.

668 citations

Journal ArticleDOI
TL;DR: The results indicate that GFP‐positive cells in transgenic animals accurately represent neural stem and progenitor cells and suggest that these nestin‐GFP–expressing cells encompass the majority of the neural stem cells in the adult brain.
Abstract: Neural stem cells generate a wide spectrum of cell types in developing and adult nervous systems. These cells are marked by expression of the intermediate filament nestin. We used the regulatory elements of the nestin gene to generate transgenic mice in which neural stem cells of the embryonic and adult brain are marked by the expression of green fluorescent protein (GFP). We used these animals as a reporter line for studying neural stem and progenitor cells in the developing and adult nervous systems. In these nestin-GFP animals, we found that GFP-positive cells reflect the distribution of nestin-positive cells and accurately mark the neurogenic areas of the adult brain. Nestin-GFP cells can be isolated with high purity by using fluorescent-activated cell sorting and can generate multipotential neurospheres. In the adult brain, nestin-GFP cells are approximately 1,400-fold more efficient in generating neurospheres than are GFP-negative cells and, despite their small number, give rise to 70 times more neurospheres than does the GFP-negative population. We characterized the expression of a panel of differentiation markers in GFP-positive cells in the nestin-GFP transgenics and found that these cells can be divided into two groups based on the strength of their GFP signal: GFP-bright cells express glial fibrillary acidic protein (GFAP) but not betaIII-tubulin, whereas GFP-dim cells express betaIII-tubulin but not GFAP. These two classes of cells represent distinct classes of neuronal precursors in the adult mammalian brain, and may reflect different stages of neuronal differentiation. We also found unusual features of nestin-GFP-positive cells in the subgranular cell layer of the dentate gyrus. Together, our results indicate that GFP-positive cells in our transgenic animals accurately represent neural stem and progenitor cells and suggest that these nestin-GFP-expressing cells encompass the majority of the neural stem cells in the adult brain.

667 citations

Journal ArticleDOI
TL;DR: The nearly complete genomic sequence and comparative analyses of the closely related species Caenorhabditis briggsae have been integrated into WormBase, including gene predictions, ortholog assignments and a new synteny viewer to display the relationships between the two species.
Abstract: WormBase (http://www.wormbase.org/) is the central data repository for information about Caenorhabditis elegans and related nematodes. As a model organism database, WormBase extends beyond the genomic sequence, integrating experimental results with extensively annotated views of the genome. The WormBase Consortium continues to expand the biological scope and utility of WormBase with the inclusion of large-scale genomic analyses, through active data and literature curation, through new analysis and visualization tools, and through refinement of the user interface. Over the past year, the nearly complete genomic sequence and comparative analyses of the closely related species Caenorhabditis briggsae have been integrated into WormBase, including gene predictions, ortholog assignments and a new synteny viewer to display the relationships between the two species. Extensive site-wide refinement of the user interface now provides quick access to the most frequently accessed resources and a consistent browsing experience across the site. Unified single-page views now provide complete summaries of commonly accessed entries like genes. These advances continue to increase the utility of WormBase for C.elegans researchers, as well as for those researchers exploring problems in functional and comparative genomics in the context of a powerful genetic system.

664 citations

Journal ArticleDOI
Damian Smedley1, Syed Haider2, Steffen Durinck3, Luca Pandini4, Paolo Provero5, Paolo Provero4, James E. Allen6, Olivier Arnaiz7, Mohammad Awedh8, Richard Baldock9, Giulia Barbiera4, Philippe Bardou10, Tim Beck11, Andrew Blake, Merideth Bonierbale12, Anthony J. Brookes11, Gabriele Bucci4, Iwan Buetti4, Sarah W. Burge6, Cédric Cabau10, Joseph W. Carlson13, Claude Chelala14, Charalambos Chrysostomou11, Davide Cittaro4, Olivier Collin15, Raul Cordova12, Rosalind J. Cutts14, Erik Dassi16, Alex Di Genova17, Anis Djari10, Anthony Esposito18, Heather Estrella18, Eduardo Eyras19, Eduardo Eyras20, Julio Fernandez-Banet18, Simon A. Forbes1, Robert C. Free11, Takatomo Fujisawa, Emanuela Gadaleta14, Jose Manuel Garcia-Manteiga4, David Goodstein13, Kristian Gray6, José Afonso Guerra-Assunção14, Bernard Haggarty9, Dong Jin Han21, Byung Woo Han21, Todd W. Harris22, Jayson Harshbarger, Robert K. Hastings11, Richard D. Hayes13, Claire Hoede10, Shen Hu23, Zhi-Liang Hu24, Lucie N. Hutchins, Zhengyan Kan18, Hideya Kawaji, Aminah Keliet10, Arnaud Kerhornou6, Sunghoon Kim21, Rhoda Kinsella6, Christophe Klopp10, Lei Kong25, Daniel Lawson6, Dejan Lazarevic4, Ji Hyun Lee21, Thomas Letellier10, Chuan-Yun Li25, Pietro Liò26, Chu Jun Liu25, Jie Luo6, Alejandro Maass17, Jérôme Mariette10, Thomas Maurel6, Stefania Merella4, Azza M. Mohamed8, François Moreews10, Ibounyamine Nabihoudine10, Nelson Ndegwa27, Céline Noirot10, Cristian Perez-Llamas20, Michael Primig28, Alessandro Quattrone16, Hadi Quesneville10, Davide Rambaldi4, James M. Reecy24, Michela Riba4, Steven Rosanoff6, Amna A. Saddiq8, Elisa Salas12, Olivier Sallou15, Rebecca Shepherd1, Reinhard Simon12, Linda Sperling7, William Spooner29, Daniel M. Staines6, Delphine Steinbach10, Kevin R. Stone, Elia Stupka4, Jon W. Teague1, Abu Z. Dayem Ullah14, Jun Wang25, Doreen Ware29, Marie Wong-Erasmus, Ken Youens-Clark29, Amonida Zadissa6, Shi Jian Zhang25, Arek Kasprzyk8, Arek Kasprzyk4 
TL;DR: The latest version of the BioMart Community Portal comes with many new databases that have been created by the ever-growing community and comes with better support and extensibility for data analysis and visualization tools.
Abstract: The BioMart Community Portal (www.biomart.org) is a community-driven effort to provide a unified interface to biomedical databases that are distributed worldwide. The portal provides access to numerous database projects supported by 30 scientific organizations. It includes over 800 different biological datasets spanning genomics, proteomics, model organisms, cancer data, ontology information and more. All resources available through the portal are independently administered and funded by their host organizations. The BioMart data federation technology provides a unified interface to all the available data. The latest version of the portal comes with many new databases that have been created by our ever-growing community. It also comes with better support and extensibility for data analysis and visualization tools. A new addition to our toolbox, the enrichment analysis tool is now accessible through graphical and web service interface. The BioMart community portal averages over one million requests per day. Building on this level of service and the wealth of information that has become available, the BioMart Community Portal has introduced a new, more scalable and cheaper alternative to the large data stores maintained by specialized organizations.

664 citations

Journal ArticleDOI
TL;DR: Analysis of sequence motifs found in metazoan protein factors involved in constitutive pre-mRNA splicing and in alternative splicing regulation indicates that the RRM is an ancient conserved region (ACR) that has diversified by duplication of genes and intragenic domains.
Abstract: We present a systematic analysis of sequence motifs found in metazoan protein factors involved in constitutive pre-mRNA splicing and in alternative splicing regulation. Using profile analysis we constructed a database enriched in protein sequences containing one or more presumptive copies of the RNA-recognition motif (RRM). We provide an accurate alignment of RRMs and structure-based criteria for identifying new RRMs, including many that lack the prototype RNP-1 submotif. We present a comprehensive table of 125 sequences containing 252 RRMs, including 22 previously unreported RRMs in 17 proteins. The presence of a putative RRM in these proteins, which are implicated in a variety of cellular processes, strongly suggests that their function involves binding to RNA. Unreported homologies in the RRM-enriched database to the metazoan SR family of splicing factors are described for an Arg-rich human nuclear protein and two yeast proteins (S. pombe mei2 and S. cerevisiae Npl3). We have rigorously tested the phylogenetic relationships of a large sample of RRMs. This analysis indicates that the RRM is an ancient conserved region (ACR) that has diversified by duplication of genes and intragenic domains. Statistical analyses and classification of repeated Arg-Ser (RS) and RGG domains in various protein splicing factors are presented.

663 citations


Authors

Showing all 3800 results

NameH-indexPapersCitations
Phillip A. Sharp172614117126
Gregory J. Hannon165421140456
Ian A. Wilson15897198221
Marco A. Marra153620184684
Michael E. Greenberg148316114317
Tom Maniatis143318299495
Detlef Weigel14251684670
Kim Nasmyth14229459231
Arnold J. Levine139485116005
Joseph E. LeDoux13947891500
Gerald R. Fink13831670868
Ramnik J. Xavier138597101879
Harold E. Varmus13749676320
David A. Jackson136109568352
Scott W. Lowe13439689376
Network Information
Related Institutions (5)
Howard Hughes Medical Institute
34.6K papers, 5.2M citations

99% related

Salk Institute for Biological Studies
13.1K papers, 1.6M citations

98% related

European Bioinformatics Institute
10.5K papers, 999.6K citations

96% related

Laboratory of Molecular Biology
24.2K papers, 2.1M citations

96% related

Broad Institute
11.6K papers, 1.5M citations

95% related

Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202316
202239
2021292
2020350
2019315
2018288