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dc.contributor.authorHuarte, Maite
dc.contributor.authorGuttman, Mitchell
dc.contributor.authorFeldser, David M.
dc.contributor.authorGarber, Manuel
dc.contributor.authorKoziol, Magdalena J.
dc.contributor.authorKenzelmann-Broz, Daniela
dc.contributor.authorKhalil, Ahmad M.
dc.contributor.authorZuk, Or
dc.contributor.authorAmit, Ido
dc.contributor.authorRabani, Michal
dc.contributor.authorAttardi, Laura D.
dc.contributor.authorRegev, Aviv
dc.contributor.authorRinn, John L.
dc.contributor.authorLander, Eric Steven
dc.contributor.authorJacks, Tyler E
dc.date.accessioned2015-03-17T15:03:32Z
dc.date.available2015-03-17T15:03:32Z
dc.date.issued2010-08
dc.date.submitted2010-04
dc.identifier.issn00928674
dc.identifier.issn1097-4172
dc.identifier.urihttp://hdl.handle.net/1721.1/96038
dc.description.abstractRecently, more than 1000 large intergenic noncoding RNAs (lincRNAs) have been reported. These RNAs are evolutionarily conserved in mammalian genomes and thus presumably function in diverse biological processes. Here, we report the identification of lincRNAs that are regulated by p53. One of these lincRNAs (lincRNA-p21) serves as a repressor in p53-dependent transcriptional responses. Inhibition of lincRNA-p21 affects the expression of hundreds of gene targets enriched for genes normally repressed by p53. The observed transcriptional repression by lincRNA-p21 is mediated through the physical association with hnRNP-K. This interaction is required for proper genomic localization of hnRNP-K at repressed genes and regulation of p53 mediates apoptosis. We propose a model whereby transcription factors activate lincRNAs that serve as key repressors by physically associating with repressive complexes and modulate their localization to sets of previously active genes.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (New Innovator Award)en_US
dc.description.sponsorshipSmith Family Foundationen_US
dc.description.sponsorshipDamon Runyon Cancer Research Foundationen_US
dc.description.sponsorshipSearle Scholars Programen_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (1R01CA119176-01)en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.cell.2010.06.040en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceElsevieren_US
dc.titleA Large Intergenic Noncoding RNA Induced by p53 Mediates Global Gene Repression in the p53 Responseen_US
dc.typeArticleen_US
dc.identifier.citationHuarte, Maite, Mitchell Guttman, David Feldser, Manuel Garber, Magdalena J. Koziol, Daniela Kenzelmann-Broz, Ahmad M. Khalil, et al. “A Large Intergenic Noncoding RNA Induced by P53 Mediates Global Gene Repression in the P53 Response.” Cell 142, no. 3 (August 2010): 409–419. © 2010 Elsevier Inc.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorJacks, Tyler E.en_US
dc.contributor.mitauthorGuttman, Mitchellen_US
dc.contributor.mitauthorFeldser, David M.en_US
dc.contributor.mitauthorRegev, Aviven_US
dc.contributor.mitauthorLander, Eric S.en_US
dc.relation.journalCellen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsHuarte, Maite; Guttman, Mitchell; Feldser, David; Garber, Manuel; Koziol, Magdalena J.; Kenzelmann-Broz, Daniela; Khalil, Ahmad M.; Zuk, Or; Amit, Ido; Rabani, Michal; Attardi, Laura D.; Regev, Aviv; Lander, Eric S.; Jacks, Tyler; Rinn, John L.en_US
dc.identifier.orcidhttps://orcid.org/0000-0001-5785-8911
dc.identifier.orcidhttps://orcid.org/0000-0001-8567-2049
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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