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dc.contributor.authorHnisz, Denes
dc.contributor.authorAbraham, Brian Joseph
dc.contributor.authorLee, Tong Ihn
dc.contributor.authorLau, Ashley
dc.contributor.authorSaint-Andre, Violaine
dc.contributor.authorSigova, Alla A.
dc.contributor.authorHoke, Heather Ashley
dc.contributor.authorYoung, Richard A.
dc.date.accessioned2016-08-10T15:24:18Z
dc.date.available2016-08-10T15:24:18Z
dc.date.issued2013-11
dc.date.submitted2013-09
dc.identifier.issn00928674
dc.identifier.urihttp://hdl.handle.net/1721.1/103877
dc.description.abstractSuper-enhancers are large clusters of transcriptional enhancers that drive expression of genes that define cell identity. Improved understanding of the roles that super-enhancers play in biology would be afforded by knowing the constellation of factors that constitute these domains and by identifying super-enhancers across the spectrum of human cell types. We describe here the population of transcription factors, cofactors, chromatin regulators, and transcription apparatus occupying super-enhancers in embryonic stem cells and evidence that super-enhancers are highly transcribed. We produce a catalog of super-enhancers in a broad range of human cell types and find that super-enhancers associate with genes that control and define the biology of these cells. Interestingly, disease-associated variation is especially enriched in the super-enhancers of disease-relevant cell types. Furthermore, we find that cancer cells generate super-enhancers at oncogenes and other genes important in tumor pathogenesis. Thus, super-enhancers play key roles in human cell identity in health and in disease.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH grant HG002668)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH grant CA109901)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH grant CA146445)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH Roadmap Epigenome Projects and the Rush Alzheimer’s Disease Center at Rush University Medical Center, Chicago (P30AG10161)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH Roadmap Epigenome Projects and the Rush Alzheimer’s Disease Center at Rush University Medical Center, Chicago (R01AG36042)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH Roadmap Epigenome Projects and the Rush Alzheimer’s Disease Center at Rush University Medical Center, Chicago (RC2AG36547)en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.cell.2013.09.053en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleSuper-Enhancers in the Control of Cell Identity and Diseaseen_US
dc.typeArticleen_US
dc.identifier.citationHnisz, Denes, Brian J. Abraham, Tong Ihn Lee, Ashley Lau, Violaine Saint-André, Alla A. Sigova, Heather A. Hoke, and Richard A. Young. “Super-Enhancers in the Control of Cell Identity and Disease.” Cell 155, no. 4 (November 2013): 934–947.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentWhitehead Institute for Biomedical Researchen_US
dc.contributor.mitauthorHnisz, Denesen_US
dc.contributor.mitauthorAbraham, Brian Josephen_US
dc.contributor.mitauthorLee, Tong Ihnen_US
dc.contributor.mitauthorLau, Ashleyen_US
dc.contributor.mitauthorSaint-Andre, Violaineen_US
dc.contributor.mitauthorSigova, Alla A.en_US
dc.contributor.mitauthorHoke, Heather Ashleyen_US
dc.contributor.mitauthorYoung, Richard A.en_US
dc.relation.journalCellen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsHnisz, Denes; Abraham, Brian J.; Lee, Tong Ihn; Lau, Ashley; Saint-André, Violaine; Sigova, Alla A.; Hoke, Heather A.; Young, Richard A.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-4549-5425
dc.identifier.orcidhttps://orcid.org/0000-0001-8855-8647
mit.licensePUBLISHER_CCen_US


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