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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.
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页码:384 / 397
页数:14
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