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RNA聚合酶II转录过程中组蛋白存活的机制。

Mechanism of histone survival during transcription by RNA polymerase II.

作者信息

Kulaeva Olga I, Studitsky Vasily M

机构信息

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

出版信息

Transcription. 2010 Sep-Oct;1(2):85-8. doi: 10.4161/trns.1.2.12519.

Abstract

This work is related to and stems from our recent NSMB paper, "Mechanism of chromatin remodeling and recovery during passage of RNA polymerase II" (December 2009). Synopsis. Recent genomic studies from many laboratories have suggested that nucleosomes are not displaced from moderately transcribed genes. Furthermore, histones H3/H4 carrying the primary epigenetic marks are not displaced or exchanged (in contrast to H2A/H2B histones) during moderate transcription by RNA polymerase II (Pol II) in vivo. These exciting observations suggest that the large molecule of Pol II passes through chromatin structure without even transient displacement of H3/H4 histones. The most recent analysis of the RNA polymerase II (Pol II)-type mechanism of chromatin remodeling in vitro (described in our NSMB 2009 paper) suggests that nucleosome survival is tightly coupled with formation of a novel intermediate: a very small intranucleosomal DNA loop (Ø-loop) containing transcribing Pol II. In the submitted manuscript we critically evaluate one of the key predictions of this model: the lack of even transient displacement of histones H3/H4 during Pol II transcription in vitro. The data suggest that, indeed, histones H3/H4 are not displaced during Pol II transcription in vitro. These studies are directly connected with the observation in vivo on the lack of exchange of histones H3/H4 during Pol II transcription.

摘要

这项工作与我们最近发表在《自然结构与分子生物学》(NSMB)上的论文“RNA聚合酶II转录过程中染色质重塑与恢复的机制”(2009年12月)相关且源于该论文。概述。许多实验室近期的基因组研究表明,核小体不会从中度转录的基因上被置换下来。此外,在体内RNA聚合酶II(Pol II)进行中度转录期间,携带主要表观遗传标记的组蛋白H3/H4不会被置换或交换(与组蛋白H2A/H2B相反)。这些令人兴奋的观察结果表明,Pol II的大分子穿过染色质结构时,甚至不会使H3/H4组蛋白发生短暂置换。最近对体外染色质重塑的RNA聚合酶II(Pol II)型机制的分析(在我们2009年的NSMB论文中有描述)表明,核小体的存活与一种新中间体的形成紧密相关:一种包含正在转录的Pol II的非常小的核小体内DNA环(Ø环)。在提交的手稿中,我们批判性地评估了该模型的一个关键预测:在体外Pol II转录过程中组蛋白H3/H4甚至不会发生短暂置换。数据表明,实际上,在体外Pol II转录过程中组蛋白H3/H4不会被置换。这些研究与体内观察到的在Pol II转录过程中组蛋白H3/H4缺乏交换直接相关。

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