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棘霉素和偏端霉素诱导核小体核心DNA旋转。

Echinomycin and distamycin induce rotation of nucleosome core DNA.

作者信息

Low C M, Drew H R, Waring M J

出版信息

Nucleic Acids Res. 1986 Sep 11;14(17):6785-801. doi: 10.1093/nar/14.17.6785.

Abstract

When nucleosome cores reconstituted from chicken erythrocyte histones and a 160 bp DNA molecule are exposed to echinomycin, a bis-intercalating antitumour antibiotic, the DNA appears to rotate with respect to the histone octamer by about half a turn. New bands appear in patterns of DNAase I digestion at positions approximately mid-way between those characteristic of control core samples, while the control pattern is largely suppressed. Similar (but not identical) changes are produced when nucleosome cores are exposed to distamycin, a non-intercalating DNA-binding antibiotic. The effects of both ligands can be explained in terms of a change in rotational orientation of the core DNA, so as to place antibiotic binding sites on the inward-facing (concave) surface of the DNA supercoil. Presumably this serves to optimise non-bonded contacts with the polynucleotide backbone. These results establish that the positioning of DNA about the histone octamer is not absolutely determined by its nucleotide sequence, but may be modified by the binding of such relatively small molecules as antibiotics.

摘要

当由鸡红细胞组蛋白和一个160碱基对的DNA分子重构的核小体核心暴露于棘霉素(一种双嵌入抗肿瘤抗生素)时,DNA似乎相对于组蛋白八聚体旋转了约半圈。在DNA酶I消化模式中,新条带出现在大约介于对照核心样品特征位置中间的位置,而对照模式则在很大程度上受到抑制。当核小体核心暴露于偏端霉素(一种非嵌入性DNA结合抗生素)时,会产生类似(但不完全相同)的变化。两种配体的作用都可以用核心DNA旋转方向的改变来解释,从而使抗生素结合位点位于DNA超螺旋的向内(凹)表面。据推测,这有助于优化与多核苷酸主链的非键接触。这些结果表明,DNA围绕组蛋白八聚体的定位并非绝对由其核苷酸序列决定,而是可能会被诸如抗生素等相对小分子的结合所改变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8137/311699/ea9b05e5168c/nar00286-0018-a.jpg

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