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dc.contributor.authorWhyte, Warren A.
dc.contributor.authorOrlando, David A.
dc.contributor.authorHnisz, Denes
dc.contributor.authorAbraham, Brian J.
dc.contributor.authorLin, Charles Y.
dc.contributor.authorKagey, Michael H.
dc.contributor.authorRahl, Peter B.
dc.contributor.authorLee, Tong Ihn
dc.contributor.authorYoung, Richard A.
dc.contributor.authorYoung, Richard A.
dc.date.accessioned2016-08-11T15:32:10Z
dc.date.available2016-08-11T15:32:10Z
dc.date.issued2013-04
dc.date.submitted2013-02
dc.identifier.issn00928674
dc.identifier.urihttp://hdl.handle.net/1721.1/103896
dc.description.abstractMaster transcription factors Oct4, Sox2, and Nanog bind enhancer elements and recruit Mediator to activate much of the gene expression program of pluripotent embryonic stem cells (ESCs). We report here that the ESC master transcription factors form unusual enhancer domains at most genes that control the pluripotent state. These domains, which we call super-enhancers, consist of clusters of enhancers that are densely occupied by the master regulators and Mediator. Super-enhancers differ from typical enhancers in size, transcription factor density and content, ability to activate transcription, and sensitivity to perturbation. Reduced levels of Oct4 or Mediator cause preferential loss of expression of super-enhancer-associated genes relative to other genes, suggesting how changes in gene expression programs might be accomplished during development. In other more differentiated cells, super-enhancers containing cell-type-specific master transcription factors are also found at genes that define cell identity. Super-enhancers thus play key roles in the control of mammalian cell identity.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 CA146445)en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.cell.2013.03.035en_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.titleMaster Transcription Factors and Mediator Establish Super-Enhancers at Key Cell Identity Genesen_US
dc.typeArticleen_US
dc.identifier.citationWhyte, Warren A., David A. Orlando, Denes Hnisz, Brian J. Abraham, Charles Y. Lin, Michael H. Kagey, Peter B. Rahl, Tong Ihn Lee, and Richard A. Young. “Master Transcription Factors and Mediator Establish Super-Enhancers at Key Cell Identity Genes.” Cell 153, no. 2 (April 2013): 307–319.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentWhitehead Institute for Biomedical Researchen_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.orderedauthorsWhyte, Warren A.; Orlando, David A.; Hnisz, Denes; Abraham, Brian J.; Lin, Charles Y.; Kagey, Michael H.; Rahl, Peter B.; Lee, Tong Ihn; Young, Richard A.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0001-8855-8647
mit.licensePUBLISHER_CCen_US


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