A conserved Swi2/Snf2 ATPase motif couples ATP hydrolysis to chromatin remodeling

被引:72
作者
Smith, CL [1 ]
Peterson, CL [1 ]
机构
[1] Univ Massachusetts, Sch Med, Program Mol Med, Interdisciplinary Grad Program, Worcester, MA 01605 USA
关键词
D O I
10.1128/MCB.25.14.5880-5892.2005
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
Yeast (Saccharomyces cerevisiae) SWI/SNF is a prototype for a large family of ATP-dependent chromatin-remodeling enzymes that facilitate numerous DNA-mediated processes. Swi2/Snf2 is the catalytic subunit of SWI/SNF, and it is the founding member of a novel subfamily of the SF2 superfamily of DNA helicase/ATPases. Here we present a functional analysis of the diagnostic set of helicase/ATPase sequence motifs found within all Swi2p/Snf2p family members. Whereas many of these motifs play key roles in ATP binding and/or hydrolysis, we identify residues within conserved motif V that are specifically required to couple ATP hydrolysis to chromatin-remodeling activity. Interestingly, motif V of the human Swi2p/Snf2p homolog, Brg1p, has been shown to be a possible hot spot for mutational alterations associated with cancers.
引用
收藏
页码:5880 / 5892
页数:13
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