The histone variant macroH2A interferes with transcription factor binding and SWI/SNF nucleosome remodeling

被引:218
|
作者
Angelov, D
Molla, A
Perche, PY
Hans, F
Côté, J
Khochbin, S
Bouvet, P
Dimitrov, S
机构
[1] INSERM, U309, Lab Biol Mol & Cellular Differenciat, Inst Albert Bonniot, F-38706 La Tronche, France
[2] Ecole Normale Super Lyon, CNRS, UMR 5665, F-69007 Lyon, France
[3] Univ Laval, Ctr Canc Res, Hotel Dieu Quebec, Quebec City, PQ G1R 2J6, Canada
关键词
D O I
10.1016/S1097-2765(03)00100-X
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 unusual histone variant macroH2A (mH2A) has been associated with repression of transcription, but the molecular mechanisms by which it exerts this function are unknown. Here we have identified a mechanism by which the different domains of mH2A may be involved in the repression of transcription. Evidence is presented that the presence of mH2A in a positioned nucleosome interferes with the binding of the transcription factor NF-kappaB. The nonhistone region of mH2A was identified to be associated with this interference. Importantly, the presence of macroH2A was found to severely impede SWI/SNF nucleosome remodeling and movement to neighboring DNA segments. This property of mH2A was demonstrated to reside only in its H2A-like domain. A hypothesis explaining the role of histone variants in transcriptional regulation is proposed.
引用
收藏
页码:1033 / 1041
页数:9
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