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dc.contributor.authorHnisz, Denes
dc.contributor.authorYoung, Richard A.
dc.contributor.authorChakraborty, Arup K.
dc.contributor.authorSharp, Phillip A.
dc.contributor.authorShrinivas, Krishna,Ph. D.Massachusetts Institute of Technology.
dc.date.accessioned2018-07-09T17:57:51Z
dc.date.available2018-07-09T17:57:51Z
dc.date.issued2017-03
dc.identifier.issn0092-8674
dc.identifier.issn1097-4172
dc.identifier.urihttp://hdl.handle.net/1721.1/116858
dc.description.abstractPhase-separated multi-molecular assemblies provide a general regulatory mechanism to compartmentalize biochemical reactions within cells. We propose that a phase separation model explains established and recently described features of transcriptional control. These features include the formation of super-enhancers, the sensitivity of super-enhancers to perturbation, the transcriptional bursting patterns of enhancers, and the ability of an enhancer to produce simultaneous activation at multiple genes. This model provides a conceptual framework to further explore principles of gene control in mammals. Keywords: super-enhancer; enhancer; phase separation; transcription; nuclear body; gene control; bursting; transcriptional burst; co-operativityen_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant HG002668)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant P01-CA042063)en_US
dc.description.sponsorshipNational Cancer Institute (U.S.) (Grant P30-CA14051)en_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/J.CELL.2017.02.007en_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.titleA Phase Separation Model for Transcriptional Controlen_US
dc.typeArticleen_US
dc.identifier.citationHnisz, Denes, et al. “A Phase Separation Model for Transcriptional Control.” Cell 169, 1 (March 2017): 13–23 © 2017 Elsevier Incen_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Medical Engineering & Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Physicsen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorShrinivas, Krishna
dc.contributor.mitauthorYoung, Richard A.
dc.contributor.mitauthorChakraborty, Arup K.
dc.contributor.mitauthorSharp, Phillip A.
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
dc.date.updated2018-07-09T15:36:21Z
dspace.orderedauthorsHnisz, Denes; Shrinivas, Krishna; Young, Richard A.; Chakraborty, Arup K.; Sharp, Phillip A.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-4167-9385
dc.identifier.orcidhttps://orcid.org/0000-0001-8855-8647
dc.identifier.orcidhttps://orcid.org/0000-0003-1268-9602
dc.identifier.orcidhttps://orcid.org/0000-0003-1465-1691
dspace.mitauthor.errortrue
mit.licensePUBLISHER_CCen_US


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