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克服转录延伸过程中的核小体障碍。

Overcoming the nucleosome barrier during transcript elongation.

机构信息

Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, USA.

出版信息

Trends Genet. 2012 Jun;28(6):285-94. doi: 10.1016/j.tig.2012.02.005. Epub 2012 Mar 31.

Abstract

RNA polymerase II (Pol II) must break the nucleosomal barrier to gain access to DNA and transcribe genes efficiently. New single-molecule techniques have elucidated many molecular details of nucleosome disassembly and what happens once Pol II encounters a nucleosome. Our review highlights mechanisms that Pol II utilizes to transcribe through nucleosomes, including the roles of chromatin remodelers, histone chaperones, post-translational modifications of histones, incorporation of histone variants into nucleosomes, and activation of the poly(ADP-ribose) polymerase (PARP) enzyme. Future studies need to assess the molecular details and the contribution of each of these mechanisms, individually and in combination, to transcription across the genome to understand how cells are able to regulate transcription in response to developmental, environmental and nutritional cues.

摘要

RNA 聚合酶 II(Pol II)必须打破核小体障碍才能有效地进入 DNA 并转录基因。新的单分子技术已经阐明了核小体解体的许多分子细节,以及 Pol II 遇到核小体后会发生什么。我们的综述强调了 Pol II 利用的穿过核小体进行转录的机制,包括染色质重塑因子、组蛋白伴侣、组蛋白的翻译后修饰、组蛋白变体掺入核小体以及聚(ADP-核糖)聚合酶(PARP)酶的激活。未来的研究需要评估这些机制中的每一个在基因组范围内转录中的分子细节和贡献,单独和组合,以了解细胞如何能够响应发育、环境和营养线索调节转录。

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