Guyon J R, Narlikar G J, Sif S, Kingston R E
Department of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts 02114, USA.
Mol Cell Biol. 1999 Mar;19(3):2088-97. doi: 10.1128/MCB.19.3.2088.
The histone N-terminal tails have been shown previously to be important for chromatin assembly, remodeling, and stability. We have tested the ability of human SWI-SNF (hSWI-SNF) to remodel nucleosomes whose tails have been cleaved through a limited trypsin digestion. We show that hSWI-SNF is able to remodel tailless mononucleosomes and nucleosomal arrays, although hSWI-SNF remodeling of tailless nucleosomes is less effective than remodeling of nucleosomes with tails. Analogous to previous observations with tailed nucleosomal templates, we show both (i) that hSWI-SNF-remodeled trypsinized mononucleosomes and arrays are stable for 30 min in the remodeled conformation after removal of ATP and (ii) that the remodeled tailless mononucleosome can be isolated on a nondenaturing acrylamide gel as a novel species. Thus, nucleosome remodeling by hSWI-SNF can occur via interactions with a tailless nucleosome core.
先前已表明组蛋白N端尾巴对于染色质组装、重塑及稳定性很重要。我们测试了人类SWI-SNF(hSWI-SNF)重塑经有限胰蛋白酶消化其尾巴已被切割的核小体的能力。我们发现hSWI-SNF能够重塑无尾单核小体和核小体阵列,尽管hSWI-SNF对无尾核小体的重塑效果不如对有尾核小体的重塑。与先前对有尾核小体模板的观察类似,我们表明:(i)去除ATP后,hSWI-SNF重塑的经胰蛋白酶处理的单核小体和阵列在重塑构象下可稳定30分钟;(ii)重塑的无尾单核小体可作为一种新物种在非变性聚丙烯酰胺凝胶上分离出来。因此,hSWI-SNF介导的核小体重塑可通过与无尾核小体核心的相互作用发生。