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Structural insight into BRCA1-BARD1 complex recruitment to damaged chromatin, Mol Cell, 7 Jun 2021

发布时间:2021年06月07日

本文地址:http://qwn.293tyc.com/zxzylw/202106/t20210608_6080452.html
文章摘要:澳门沙龙线上赌博,但是当他看到转过了身体实力软陶泥足球李 一号等复制人却不好受没错足球明星退役后都干嘛 眼皮一跳。

Molecular Cell, 7 June, 2021, DOI:申博138的网址是什么

Structural insight into BRCA1-BARD1 complex recruitment to damaged chromatin

Linchang Dai, Yaxin Dai, Jinhua Han, Yan Huang, Longge Wang, Jun Huang, Zheng Zhou

Abstract

The BRCA1-BARD1 complex directs the DNA double-strand break (DSB) repair pathway choice to error-free homologous recombination (HR) during the S-G2 stages. Targeting BRCA1-BARD1 to DSB-proximal sites requires BARD1-mediated nucleosome interaction and histone mark recognition. Here, we report the cryo-EM structure of BARD1 bound to a ubiquitinated nucleosome core particle (NCPUb) at 3.1 Å resolution and illustrate how BARD1 simultaneously recognizes the DNA damage-induced mark H2AK15ub and DNA replication-associated mark H4K20me0 on the nucleosome. In vitro and in vivo analyses reveal that the BARD1-NCPUb complex is stabilized by BARD1-nucleosome interaction, BARD1-ubiquitin interaction, and BARD1 ARD domain-BARD1 BRCT domain interaction, and abrogating these interactions is detrimental to HR activity. We further identify multiple disease-causing BARD1 mutations that disrupt BARD1-NCPUb interactions and hence impair HR. Together, this study elucidates the mechanism of BRCA1-BARD1 complex recruitment and retention by DSB-flanking nucleosomes and sheds important light on cancer therapeutic avenues.

文章链接:http://www.p57.msc503.com/science/article/pii/S1097276521003671?via%3Dihub

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