Functional delineation of three groups of the ATP-dependent family of chromatin remodeling enzymes

被引:100
作者
Boyer, LA
Logie, C
Bonte, E
Becker, PB
Wade, PA
Wolffe, AP
Wu, C
Imbalzano, AN
Peterson, CL
机构
[1] Univ Massachusetts, Sch Med, Program Mol Med, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Dept Biochem & Mol Biol, Worcester, MA 01605 USA
[3] NICHD, Mol Embryol Lab, NIH, Bethesda, MD 20892 USA
[4] Adolf Butenandt Inst, D-80336 Munich, Germany
[5] Univ Massachusetts, Sch Med, Dept Cell Biol, Worcester, MA 01655 USA
[6] NCI, Mol Cell Biol Lab, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1074/jbc.M002810200
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
ATP-dependent chromatin remodeling enzymes antagonize the inhibitory effects of chromatin. We com pare six different remodeling complexes: ySWI/SNF, yRSC, hSWI/SNF, xMi-2, dCHRAC, and dNURF. We find that each complex uses similar amounts of ATP to remodel nucleosomal arrays at nearly identical rates. We also perform assays with arrays reconstituted with hyperacetylated or trypsinized histones and isolated histone (H3/H4)(2) tetramers. The results define three groups of the ATP-dependent family of remodeling enzymes. In addition we investigate the ability of an acidic activator to recruit remodeling complexes to nucleosomal arrays. We propose that ATP-dependent chromatin remodeling enzymes share a common reaction mechanism and that a key distinction between complexes is in their mode of regulation or recruitment.
引用
收藏
页码:18864 / 18870
页数:7
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