PRC2
H3K4me3
组蛋白
核小体
细胞生物学
组蛋白H3
生物
化学
表观遗传学
遗传学
DNA
基因表达
基因
发起人
作者
Vignesh Kasinath,Curtis Beck,Paul Sauer,Simon Poepsel,Jennifer Kosmatka,Marco Faini,Daniel B. Toso,Ruedi Aebersold,Eva Nogales
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2021-01-21
卷期号:371 (6527)
被引量:179
标识
DOI:10.1126/science.abc3393
摘要
Polycomb repressive complexes 1 and 2 (PRC1 and PRC2) cooperate to determine cell identity by epigenetic gene expression regulation. However, the mechanism of PRC2 recruitment by means of recognition of PRC1-mediated H2AK119ub1 remains poorly understood. Our PRC2 cryo-electron microscopy structure with cofactors JARID2 and AEBP2 bound to a H2AK119ub1-containing nucleosome reveals a bridge helix in EZH2 that connects the SET domain, H3 tail, and nucleosomal DNA. JARID2 and AEBP2 each interact with one ubiquitin and the H2A-H2B surface. JARID2 stimulates PRC2 through interactions with both the polycomb protein EED and the H2AK119-ubiquitin, whereas AEBP2 has an additional scaffolding role. The presence of these cofactors partially overcomes the inhibitory effect that H3K4me3 and H3K36me3 exert on core PRC2 (in the absence of cofactors). Our results support a key role for JARID2 and AEBP2 in the cross-talk between histone modifications and PRC2 activity.
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