组蛋白H3
PRC2
EZH2型
组蛋白甲基化
组蛋白
色域
生物
组蛋白H2A
细胞生物学
甲基化
组蛋白甲基转移酶
基因沉默
多组蛋白
DNA甲基化
遗传学
基因
抑制因子
基因表达
核糖核酸
解旋酶
作者
Ru Cao,Liangjun Wang,Hengbin Wang,Li Xia,Hediye Erdjument‐Bromage,Paul Tempst,Richard S. Jones,Yi Zhang
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2002-11-01
卷期号:298 (5595): 1039-1043
被引量:3491
标识
DOI:10.1126/science.1076997
摘要
Polycomb group (PcG) proteins play important roles in maintaining the silent state of HOX genes. Recent studies have implicated histone methylation in long-term gene silencing. However, a connection between PcG-mediated gene silencing and histone methylation has not been established. Here we report the purification and characterization of an EED-EZH2 complex, the human counterpart of the Drosophila ESC-E(Z) complex. We demonstrate that the complex specifically methylates nucleosomal histone H3 at lysine 27 (H3-K27). Using chromatin immunoprecipitation assays, we show that H3-K27 methylation colocalizes with, and is dependent on, E(Z) binding at an Ultrabithorax ( Ubx ) Polycomb response element (PRE), and that this methylation correlates with Ubx repression. Methylation on H3-K27 facilitates binding of Polycomb (PC), a component of the PRC1 complex, to histone H3 amino-terminal tail. Thus, these studies establish a link between histone methylation and PcG-mediated gene silencing.
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