dc.contributor.author | Shrinivas, Krishna | |
dc.contributor.author | Sabari, Benjamin R | |
dc.contributor.author | Coffey, Eliot L | |
dc.contributor.author | Klein, Isaac A | |
dc.contributor.author | Boija, Ann | |
dc.contributor.author | Zamudio, Alicia V | |
dc.contributor.author | Schuijers, Jurian | |
dc.contributor.author | Hannett, Nancy M | |
dc.contributor.author | Sharp, Phillip A | |
dc.contributor.author | Young, Richard A | |
dc.contributor.author | Chakraborty, Arup K | |
dc.date.accessioned | 2021-10-27T20:04:39Z | |
dc.date.available | 2021-10-27T20:04:39Z | |
dc.date.issued | 2019 | |
dc.identifier.uri | https://hdl.handle.net/1721.1/134369 | |
dc.description.abstract | © 2019 Elsevier Inc. Enhancers are DNA elements that are bound by transcription factors (TFs), which recruit coactivators and the transcriptional machinery to genes. Phase-separated condensates of TFs and coactivators have been implicated in assembling the transcription machinery at particular enhancers, yet the role of DNA sequence in this process has not been explored. We show that DNA sequences encoding TF binding site number, density, and affinity above sharply defined thresholds drive condensation of TFs and coactivators. A combination of specific structured (TF-DNA) and weak multivalent (TF-coactivator) interactions allows for condensates to form at particular genomic loci determined by the DNA sequence and the complement of expressed TFs. DNA features found to drive condensation promote enhancer activity and transcription in cells. Our study provides a framework to understand how the genome can scaffold transcriptional condensates at specific loci and how the universal phenomenon of phase separation might regulate this process. Shrinivas et al. demonstrate that specific types of motif compositions encoded in DNA drive localized formation of transcriptional condensates. These findings explain how phase separation can occur at specific genomic locations and shed light on why only some genomic loci become highly active enhancers. | |
dc.language.iso | en | |
dc.publisher | Elsevier BV | |
dc.relation.isversionof | 10.1016/J.MOLCEL.2019.07.009 | |
dc.rights | Creative Commons Attribution-NonCommercial-NoDerivs License | |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.source | PMC | |
dc.title | Enhancer Features that Drive Formation of Transcriptional Condensates | |
dc.type | Article | |
dc.contributor.department | Massachusetts Institute of Technology. Department of Chemical Engineering | |
dc.contributor.department | Massachusetts Institute of Technology. Institute for Medical Engineering & Science | |
dc.contributor.department | Whitehead Institute for Biomedical Research | |
dc.contributor.department | Massachusetts Institute of Technology. Department of Biology | |
dc.contributor.department | Koch Institute for Integrative Cancer Research at MIT | |
dc.contributor.department | Massachusetts Institute of Technology. Department of Physics | |
dc.contributor.department | Ragon Institute of MGH, MIT and Harvard | |
dc.contributor.department | Massachusetts Institute of Technology. Department of Chemistry | |
dc.relation.journal | Molecular Cell | |
dc.eprint.version | Author's final manuscript | |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
eprint.status | http://purl.org/eprint/status/PeerReviewed | |
dc.date.updated | 2021-08-04T16:54:32Z | |
dspace.orderedauthors | Shrinivas, K; Sabari, BR; Coffey, EL; Klein, IA; Boija, A; Zamudio, AV; Schuijers, J; Hannett, NM; Sharp, PA; Young, RA; Chakraborty, AK | |
dspace.date.submission | 2021-08-04T16:54:34Z | |
mit.journal.volume | 75 | |
mit.journal.issue | 3 | |
mit.license | PUBLISHER_CC | |
mit.metadata.status | Authority Work and Publication Information Needed | |