Bauer W R, Hayes J J, White J H, Wolffe A P
Department of Microbiology, State University of New York, Stony Brook 11794-5222.
J Mol Biol. 1994 Feb 25;236(3):685-90. doi: 10.1006/jmbi.1994.1180.
We have measured the helical repeat of acetylated nucleosomes reconstituted with HeLa cell histone octamers and the 5 S RNA gene positioning sequence from Xenopus borealis. The hydroxyl radical footprinting experiments show that the helical repeat of nucleosome-bound DNA is unchanged upon acetylation, and that the extent of DNA-protein contacts remains unaltered. These results, combined with previous determinations of the linking number change in minichromosomes as a function of the extent of acetylation, are analyzed with surface linking theory. We demonstrate that the shape of the nucleosome changes upon acetylation, in such a way as to decrease the number of times the DNA winds around the nucleosome central axis.
我们测量了用HeLa细胞组蛋白八聚体和来自北方爪蟾的5S RNA基因定位序列重构的乙酰化核小体的螺旋重复。羟基自由基足迹实验表明,核小体结合的DNA的螺旋重复在乙酰化后不变,并且DNA-蛋白质接触的程度保持不变。这些结果与先前关于微型染色体中连接数变化作为乙酰化程度函数的测定相结合,用表面连接理论进行分析。我们证明,乙酰化后核小体的形状发生变化,从而减少DNA围绕核小体中心轴缠绕的次数。