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RNA聚合酶II通过过程中染色质重塑与恢复的机制。

Mechanism of chromatin remodeling and recovery during passage of RNA polymerase II.

作者信息

Kulaeva Olga I, Gaykalova Daria A, Pestov Nikolai A, Golovastov Viktor V, Vassylyev Dmitry G, Artsimovitch Irina, Studitsky Vasily M

机构信息

Department of Pharmacology, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, Piscataway, New Jersey, USA.

出版信息

Nat Struct Mol Biol. 2009 Dec;16(12):1272-8. doi: 10.1038/nsmb.1689. Epub 2009 Nov 22.

Abstract

Transcription of eukaryotic genes by RNA polymerase II (Pol II) is typically accompanied by nucleosome survival and minimal exchange of histones H3 and H4. The mechanism of nucleosome survival and recovery of chromatin structure remains obscure. Here we show how transcription through chromatin by Pol II is uniquely coupled with nucleosome survival. Structural modeling and functional analysis of the intermediates of transcription through a nucleosome indicated that when Pol II approaches an area of strong DNA-histone interactions, a small intranucleosomal DNA loop (zero-size or Ø-loop) containing transcribing enzyme is formed. During formation of the Ø-loop, the recovery of DNA-histone interactions behind Pol II is tightly coupled with their disruption ahead of the enzyme. This coupling is a distinct feature of the Pol II-type mechanism that allows further transcription through the nucleosome, prevents nucleosome translocation and minimizes displacement of H3 and H4 histones from DNA during enzyme passage.

摘要

RNA聚合酶II(Pol II)对真核基因的转录通常伴随着核小体的留存以及组蛋白H3和H4的极少交换。核小体留存及染色质结构恢复的机制仍不清楚。在此我们展示了Pol II通过染色质的转录如何独特地与核小体留存相耦合。对通过核小体的转录中间体的结构建模和功能分析表明,当Pol II接近DNA - 组蛋白强相互作用区域时,会形成一个包含转录酶的小核小体内DNA环(零大小或Ø环)。在Ø环形成过程中,Pol II后方DNA - 组蛋白相互作用的恢复与其前方相互作用的破坏紧密耦合。这种耦合是Pol II型机制的一个独特特征,它允许通过核小体进行进一步转录,防止核小体易位,并在酶通过期间使H3和H4组蛋白从DNA上的位移最小化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce39/2919570/eea4b5e7e151/nihms145199f1.jpg

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