Transcriptional Silencers: Driving Gene Expression with the Brakes On

被引:47
作者
Segert, Julian A. [1 ,2 ,3 ]
Gisselbrecht, Stephen S. [1 ,2 ]
Bulyk, Martha L. [1 ,2 ,3 ,4 ]
机构
[1] Brigham & Womens Hosp, Dept Med, Div Genet, 75 Francis St, Boston, MA 02115 USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Harvard Univ, Program Biol & Biomed Sci, Cambridge, MA 02138 USA
[4] Brigham & Womens Hosp, Dept Pathol, 75 Francis St, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
E-CADHERIN; FACULTATIVE HETEROCHROMATIN; TRANSPOSABLE ELEMENTS; ENHANCERS; DISEASE; BINDING; REST; REPRESSION; SNAIL; LONG;
D O I
10.1016/j.tig.2021.02.002
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Silencers are regulatory DNA elements that reduce transcription from their target promoters; they are the repressive counterparts of enhancers. Although discovered decades ago, and despite evidence of their importance in development and disease, silencers have been much less studied than enhancers. Recently, however, a series of papers have reported systematic studies of silencers in various model systems. Silencers are often bifunctional regulatory elements that can also act as enhancers, depending on cellular context, and are enriched for expression quantitative trait loci (eQTLs) and disease-associated variants. There is not yet evidence of a 'silencer chromatin signature', in the distribution of histone modifications or associated proteins, that is common to all silencers; instead, silencers may fall into various subclasses, acting by distinct (and possibly overlapping) mechanisms.
引用
收藏
页码:514 / 527
页数:14
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