MacroH2A Allows ATP-Dependent Chromatin Remodeling by SWI/SNF and ACF Complexes but Specifically Reduces Recruitment of SWI/SNF

被引:44
|
作者
Chang, Evelyn Y. [2 ]
Ferreira, Helder [1 ]
Somers, Joanna [1 ]
Nusinow, Dmitri A. [2 ]
Owen-Hughes, Tom [1 ]
Narlikar, Geeta J. [2 ]
机构
[1] Univ Dundee, Coll Life Sci, Wellcome Trust Ctr Gene Regulat & Express, Dundee DD1 5EH, Scotland
[2] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94158 USA
基金
英国惠康基金;
关键词
D O I
10.1021/bi8016944
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
The variant histone macroH2A helps maintain X inactivation and gene silencing. Previous work implied that nucleosomes containing macroH2A cannot be remodeled by ISWI and SWI/SNF chromatin remodeling enzymes. Using approaches that prevent misassembly of macroH2A nucleosomes, we find that macroH2A nucleosomes are excellent substrates for both enzyme families. Interestingly, SWI/SNF, which is involved in gene activation, preferentially binds H2A nucleosomes over macroH2A nucleosomes, but ACF, an ISWI complex implicated in gene repression, shows no preference. Thus, macroH2A may help regulate the balance between activating and repressive remodeling complexes.
引用
收藏
页码:13726 / 13732
页数:7
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