Transcriptional regulation by coactivators in embryonic stem cells

被引:22
|
作者
Fong, Yick W. [1 ]
Cattoglio, Claudia [1 ]
Yamaguchi, Teppei [1 ]
Tjian, Robert [1 ,2 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Howard Hughes Med Inst, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Li Ka Shing Ctr Biomed & Hlth Sci, Berkeley, CA 94720 USA
关键词
self-renewal; pluripotency; transcription activation; Mediator; TFIID; DNA repair; PROTEIN-INTERACTION NETWORK; MEDIATOR COMPLEX; CHROMATIN MODIFICATION; REPAIR COMPLEX; SELF-RENEWAL; RNAI SCREEN; DNA-REPAIR; GENES; PLURIPOTENCY; PROMOTER;
D O I
10.1016/j.tcb.2012.04.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Embryonic stem (ES) cells, like all cell types, are defined by their unique transcriptional signatures. The ability of ES cells to self-renew or exit the pluripotent state and enter differentiation requires extensive changes in their transcriptome and epigenome. Remarkably, transcriptional programs governing each cell fate must remain sufficiently malleable so that expression of only a handful of transcriptional activators can override the preexisting state by collaborating with an unexpectedly elaborate collection of coactivators to specify, restrict and stabilize the new state. Here, we discuss recent advances in our understanding of how the same coactivator can interpret multiple lines of information encoded by different activators and integrate signals from diverse regulators into stem cell-specific transcriptional outputs.
引用
收藏
页码:292 / 298
页数:7
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