WAG, a Functional Partner of RNF20/40, Regulates Histone H2B Ubiquitination and Gene Transcription

被引:124
作者
Zhang, Feng [1 ]
Yu, Xiaochun [1 ]
机构
[1] Univ Michigan, Sch Med, Div Mol Med & Genet, Dept Internal Med, Ann Arbor, MI 48109 USA
关键词
RNA-POLYMERASE-II; H3; METHYLATION; PAF1; COMPLEX; CHROMATIN MODIFICATIONS; PROCESSING FACTORS; HUMAN-CELLS; WW DOMAINS; YEAST; MONOUBIQUITINATION; UBIQUITYLATION;
D O I
10.1016/j.molcel.2011.01.024
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
Histone H2B ubiquitination plays an important role in regulating chromatin organization during gene transcription. It has been shown that RNF20/40 regulates H2B ubiquitination. Here, using protein affinity purification, we have identified WAC as a functional partner of RNF20/40. Depletion of WAC abolishes H2B ubiquitination. WAG interacts with RNF20/40 through its C-terminal coiled-coil region and promotes RNF20/40 s E3 ligase activity for H2B ubiquitination. The N-terminal WW domain of WAC recognizes RNA polymerase II. During gene transcription, WAG targets RNF20/40 to associate with RNA polymerase II complex for H2B ubiquitination at active transcription sites, which regulates transcription. Moreover, WAG-dependent transcription is important for cell-cycle checkpoint activation in response to genotoxic stress. Taken together, our results demonstrate an important regulator for transcription-coupled histone H2B ubiquitination.
引用
收藏
页码:384 / 397
页数:14
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