Functional coupling between writers, erasers and readers of histone and DNA methylation

被引:114
|
作者
Torres, Idelisse Ortiz [1 ,2 ]
Fujimori, Danica Galonic [1 ,3 ]
机构
[1] Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, Chem & Chem Biol Grad Program, San Francisco, CA 94158 USA
[3] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94158 USA
关键词
EPIGENETIC MARKS; GENE REPRESSION; BINDING MODULES; TUDOR DOMAIN; H3; RECOGNITION; CHROMATIN; METHYLTRANSFERASE; HETEROCHROMATIN; COMPLEX;
D O I
10.1016/j.sbi.2015.09.007
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
DNA and histone lysine methylation are dynamic chemical modifications that play a crucial role in the establishment of gene expression patterns during development. Both types of genomic methylation patterns are enzymatically regulated by the opposing activities of enzymes that introduce and remove these marks, known as methylation 'writers' and 'erasers', respectively. The appropriate localization and activity of these enzymes on chromatin is, in part, regulated by chromatin 'readers', protein modules that recognize histone and DNA modifications. Such reading modules are either encoded within the same polypeptide as the catalytic domains of writers and erasers, or present in protein partners that associate with them. Here, we review recent structural, biochemical and biological studies that demonstrate that there are multiple mechanisms by which reader domains can regulate the writers and erasers of histone and DNA methylation.
引用
收藏
页码:68 / 75
页数:8
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