Two histone fold proteins, CHRAC-14 and CHRAC-16, are developmentally regulated subunits of chromatin accessibility complex (CHRAC)

被引:63
作者
Corona, DFV
Eberharter, A
Budde, A
Deuring, R
Ferrari, S
Varga-Weisz, P
Wilm, M
Tamkun, J
Becker, PB
机构
[1] Adolf Butenandt Inst, D-80336 Munich, Germany
[2] European Mol Biol Lab, D-69117 Heidelberg, Germany
[3] EMBL Int PhD Programme, Santa Cruz, CA 95064 USA
[4] Univ Calif Santa Cruz, Dept Biol, Santa Cruz, CA 95064 USA
关键词
CHRAC; chromatin; histone fold; ISWI; nucleosome;
D O I
10.1093/emboj/19.12.3049
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 ISWI ATPase of Drosophila is a molecular engine that can drive a range of nucleosome remodelling reactions ire vitro. ISWI is important for cell viability, developmental gene expression and chromosome structure. It interacts with other proteins to form several distinct nucleosome remodelling machines. The chromatin accessibility complex (CHRAC) is a biochemical entity containing ISWI in association with several other proteins. Here we report on the identification of the two smallest CHRAC subunits, CHRAC-14 and CHRAC-16. They contain histone fold domains most closely related to those found in sequence-specific transcription factors NF-YB and NF-YC, respectively, CHRAC-14 and CHRAC-16 interact directly with each other as well as with ISWI, and are associated with functionally active CHRAC. The developmental expression profiles of both subunits suggest specialized roles in chromatin remodelling reactions in the early embryo for both histone fold subunits.
引用
收藏
页码:3049 / 3059
页数:11
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