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PMID: 23582322 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Master transcription factors and mediator establish super-enhancers at key cell identity genes.

Cell ·Vol. 153 ·No. 2 ·2013-04-11 ·Pages 307-19

Whyte WA, Orlando DA, Hnisz D, Abraham BJ, Lin CY, Kagey MH, Rahl PB, Lee TI, Young RA

Abstract

Master 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.

MeSH Terms
Animals B-Lymphocytes/metabolism Cell Line Cell Lineage Embryonic Stem Cells/metabolism Enhancer Elements, Genetic Gene Expression Regulation Gene Knockdown Techniques Humans Mediator Complex/metabolism Mice Transcription Factors/metabolism Transcription, Genetic
Chemicals
Mediator Complex Transcription Factors
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Whyte Warren A
Whitehead Institute for Biomedical Research, 9 Cambridge Center, Cambridge, MA 02142, USA.
Orlando David A
Hnisz Denes
Abraham Brian J
Lin Charles Y
Kagey Michael H
Rahl Peter B
Lee Tong Ihn
Young Richard A
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Article Info
Journal
Cell
Abbr.
Cell
ISSN
1097-4172
Published
2013-04-11
Pages
307-19
Language
English
Region
United States
NLM ID
0413066
PMCID
PMC3653129
Subset
IM
Grants
NCI NIH HHS · R01 CA146445 · United States
NCI NIH HHS · P30 CA014051 · United States
NHGRI NIH HHS · R01 HG002668 · United States
NHGRI NIH HHS · HG002668 · United States
NCI NIH HHS · CA146445 · United States
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