Norton V G, Imai B S, Yau P, Bradbury E M
Department of Biological Chemistry, School of Medicine, University of California, Davis 95616.
Cell. 1989 May 5;57(3):449-57. doi: 10.1016/0092-8674(89)90920-3.
Nucleosome core particles differing in their levels of histone acetylation have been formed on a closed circular DNA that contains a tandemly repeated 207 bp nucleosome positioning sequence. The effect of acetylation on the linking number per nucleosome particle has been determined. With increasing levels of acetylation, the negative linking number change per nucleosome decreases from -1.04 +/- 0.08 for control to -0.82 +/- 0.05 for highly acetylated nucleosomes. These results indicate that histone acetylation has the ability to release negative supercoils previously constrained by nucleosomes into a closed chromatin loop and in effect function as a eukaryotic gyrase.
在含有串联重复的207 bp核小体定位序列的闭环DNA上,已经形成了组蛋白乙酰化水平不同的核小体核心颗粒。已经确定了乙酰化对每个核小体颗粒连接数的影响。随着乙酰化水平的增加,每个核小体的负连接数变化从对照的-1.04±0.08降至高度乙酰化核小体的-0.82±0.05。这些结果表明,组蛋白乙酰化能够将先前受核小体限制的负超螺旋释放到封闭的染色质环中,实际上起到了真核生物促旋酶的作用。