dc.contributor.author | Hnisz, Denes | |
dc.contributor.author | Young, Richard A. | |
dc.contributor.author | Chakraborty, Arup K. | |
dc.contributor.author | Sharp, Phillip A. | |
dc.contributor.author | Shrinivas, Krishna,Ph. D.Massachusetts Institute of Technology. | |
dc.date.accessioned | 2018-07-09T17:57:51Z | |
dc.date.available | 2018-07-09T17:57:51Z | |
dc.date.issued | 2017-03 | |
dc.identifier.issn | 0092-8674 | |
dc.identifier.issn | 1097-4172 | |
dc.identifier.uri | http://hdl.handle.net/1721.1/116858 | |
dc.description.abstract | Phase-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-operativity | en_US |
dc.description.sponsorship | National Institutes of Health (U.S.) (Grant HG002668) | en_US |
dc.description.sponsorship | National Institutes of Health (U.S.) (Grant P01-CA042063) | en_US |
dc.description.sponsorship | National Cancer Institute (U.S.) (Grant P30-CA14051) | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1016/J.CELL.2017.02.007 | en_US |
dc.rights | Creative Commons Attribution-NonCommercial-NoDerivs License | en_US |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | en_US |
dc.source | PMC | en_US |
dc.title | A Phase Separation Model for Transcriptional Control | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Hnisz, Denes, et al. “A Phase Separation Model for Transcriptional Control.” Cell 169, 1 (March 2017): 13–23 © 2017 Elsevier Inc | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Institute for Medical Engineering & Science | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Biological Engineering | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Biology | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Chemical Engineering | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Chemistry | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Physics | en_US |
dc.contributor.department | Koch Institute for Integrative Cancer Research at MIT | en_US |
dc.contributor.mitauthor | Shrinivas, Krishna | |
dc.contributor.mitauthor | Young, Richard A. | |
dc.contributor.mitauthor | Chakraborty, Arup K. | |
dc.contributor.mitauthor | Sharp, Phillip A. | |
dc.relation.journal | Cell | en_US |
dc.eprint.version | Author's final manuscript | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dc.date.updated | 2018-07-09T15:36:21Z | |
dspace.orderedauthors | Hnisz, Denes; Shrinivas, Krishna; Young, Richard A.; Chakraborty, Arup K.; Sharp, Phillip A. | en_US |
dspace.embargo.terms | N | en_US |
dc.identifier.orcid | https://orcid.org/0000-0002-4167-9385 | |
dc.identifier.orcid | https://orcid.org/0000-0001-8855-8647 | |
dc.identifier.orcid | https://orcid.org/0000-0003-1268-9602 | |
dc.identifier.orcid | https://orcid.org/0000-0003-1465-1691 | |
dspace.mitauthor.error | true | |
mit.license | PUBLISHER_CC | en_US |