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新生霉素在体外抑制被动染色质组装。

Novobiocin inhibits passive chromatin assembly in vitro.

作者信息

Sealy L, Cotten M, Chalkley R

出版信息

EMBO J. 1986 Dec 1;5(12):3305-11. doi: 10.1002/j.1460-2075.1986.tb04644.x.

Abstract

Novobiocin, an inhibitor of prokaryotic DNA gyrase and eukaryotic type II topoisomerase enzymes, interferes with in vitro chromatin assembly using purified histones, DNA and nucleoplasmin. The target of inhibition is not topoisomerase II; this energy-independent assembly system lacks any ATP and Mg2+-dependent type II topoisomerase or gyrase activities. Rather, novobiocin interacts with histones, disrupting histone-histone associations required for octamer formation, and causing histones to precipitate from both nucleoplasmin-histone and histone-DNA complexes. Thus, novobiocin is able to generate 'dynamic' chromatin in vitro in the absence of ATP and Mg2+ by removing histones from previously assembled static chromatin, so that the DNA supercoils, previously constrained by conventional nucleosomes, become susceptible to removal by topoisomerase I.

摘要

新生霉素是一种原核生物DNA促旋酶和真核生物II型拓扑异构酶的抑制剂,它使用纯化的组蛋白、DNA和核质蛋白干扰体外染色质组装。抑制的靶点不是拓扑异构酶II;这个不依赖能量的组装系统缺乏任何ATP和Mg2+依赖性II型拓扑异构酶或促旋酶活性。相反,新生霉素与组蛋白相互作用,破坏八聚体形成所需的组蛋白-组蛋白结合,并导致组蛋白从核质蛋白-组蛋白和组蛋白-DNA复合物中沉淀出来。因此,新生霉素能够在没有ATP和Mg2+的情况下,通过从先前组装的静态染色质中去除组蛋白,在体外产生“动态”染色质,从而使先前受传统核小体限制的DNA超螺旋变得易于被拓扑异构酶I去除。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc52/1167327/9efdcb3c8bfe/emboj00175-0237-a.jpg

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