Deconstructing repression: evolving models of co-repressor action

被引:405
作者
Perissi, Valentina [1 ]
Jepsen, Kristen [1 ]
Glass, Christopher K. [2 ]
Rosenfeld, Michael G. [1 ]
机构
[1] Univ Calif San Diego, Dept Med, Howard Hughes Med Inst, Sch Med, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Cellular & Mol Med, Sch Med, La Jolla, CA 92093 USA
关键词
NUCLEAR RECEPTOR-COREPRESSOR; THYROID-HORMONE RECEPTOR; II HISTONE DEACETYLASES; EMBRYONIC STEM-CELLS; NF-KAPPA-B; MOUSE DEVELOPMENT; TRANSCRIPTIONAL REPRESSION; GENE-EXPRESSION; DNA-DAMAGE; MEDIATED REPRESSION;
D O I
10.1038/nrg2736
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A crucial aspect of development, homeostasis and prevention of disease is the strict maintenance of patterns of gene repression. Gene repression is largely achieved by the combinatorial action of various enzymatic complexes-known as co-repressor complexes-that are recruited to DNA by transcription factors and often act through enzymatic modification of histone protein tails. Our understanding of how co-repressors act has begun to change over recent years owing to the increased availability of genome-scale data. Here, we consider specific strategies that underlie repression events-for example, those mediated by the nuclear receptor co-repressor (NCoR, also known as NCOR1) and silencing mediator of retinoic acid and thyroid hormone receptor (SMRT, also known as NCOR2) co-repressor complexes-and discuss emerging themes in gene repression.
引用
收藏
页码:109 / 123
页数:15
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