Modification of Enhancer Chromatin: What, How, and Why?

被引:1014
|
作者
Calo, Eliezer [1 ]
Wysocka, Joanna [1 ,2 ]
机构
[1] Stanford Univ, Sch Med, Dept Chem & Syst Biol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
关键词
HISTONE H3; DNA METHYLATION; TRANSCRIPTION FACTORS; BINDING PROTEIN; GENE-EXPRESSION; METHYLTRANSFERASE COMPLEX; EPIGENETIC SIGNATURES; REGULATORY ELEMENTS; START SITES; CPG ISLANDS;
D O I
10.1016/j.molcel.2013.01.038
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Emergence of form and function during embryogenesis arises in large part through cell-type- and cell-state-specific variation in gene expression patterns, mediated by specialized cis-regulatory elements called enhancers. Recent large-scale epigenomic mapping revealed unexpected complexity and dynamics of enhancer utilization patterns, with 400,000 putative human enhancers annotated by the ENCODE project alone. These large-scale efforts were largely enabled through the understanding that enhancers share certain stereotypical chromatin features. However, an important question still lingers: what is the functional significance of enhancer chromatin modification? Here we give an overview of enhancer-associated modifications of histones and DNA and discuss enzymatic activities involved in their dynamic deposition and removal. We describe potential downstream effectors of these marks and propose models for exploring functions of chromatin modification in regulating enhancer activity during development.
引用
收藏
页码:825 / 837
页数:13
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