Functional delineation of three groups of the ATP-dependent family of chromatin remodeling enzymes
Graduate School of Biomedical Sciences; Department of Cell Biology; Program in Molecular Medicine
Life Sciences | Medicine and Health Sciences
ATP-dependent chromatin remodeling enzymes antagonize the inhibitory effects of chromatin. We compare 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.
DOI of Published Version
J Biol Chem. 2000 Jun 23;275(25):18864-70. Link to article on publisher's site
The Journal of biological chemistry
Boyer LA, Logie C, Bonte E, Becker PB, Wade PA, Wolffe AP, Wu C, Imbalzano AN, Peterson CL. (2000). Functional delineation of three groups of the ATP-dependent family of chromatin remodeling enzymes. GSBS Student Publications. https://doi.org/10.1074/jbc.M002810200. Retrieved from https://escholarship.umassmed.edu/gsbs_sp/119