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RNA聚合酶II-核小体复合物重新包裹转录DNA的冷冻电镜结构。

Cryo-EM structures of RNA polymerase II-nucleosome complexes rewrapping transcribed DNA.

作者信息

Akatsu Munetaka, Ehara Haruhiko, Kujirai Tomoya, Fujita Risa, Ito Tomoko, Osumi Ken, Ogasawara Mitsuo, Takizawa Yoshimasa, Sekine Shun-Ichi, Kurumizaka Hitoshi

机构信息

Laboratory of Chromatin Structure and Function, Institute for Quantitative Biosciences, The University of Tokyo, Bunkyo, Tokyo, Japan; Department of Biological Sciences, Graduate School of Science, The University of Tokyo, Bunkyo, Tokyo, Japan.

Laboratory for Transcription Structural Biology, RIKEN Center for Biosystems Dynamics Research, Yokohama, Japan.

出版信息

J Biol Chem. 2023 Dec;299(12):105477. doi: 10.1016/j.jbc.2023.105477. Epub 2023 Nov 17.

DOI:10.1016/j.jbc.2023.105477
PMID:37981206
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10703601/
Abstract

RNA polymerase II (RNAPII) transcribes DNA wrapped in the nucleosome by stepwise pausing, especially at nucleosomal superhelical locations -5 and -1 [SHL(-5) and SHL(-1), respectively]. In the present study, we performed cryo-electron microscopy analyses of RNAPII-nucleosome complexes paused at a major nucleosomal pausing site, SHL(-1). We determined two previously undetected structures, in which the transcribed DNA behind RNAPII is sharply kinked at the RNAPII exit tunnel and rewrapped around the nucleosomal histones in front of RNAPII by DNA looping. This DNA kink shifts the DNA orientation toward the nucleosome, and the transcribed DNA region interacts with basic amino acid residues of histones H2A, H2B, and H3 exposed by the RNAPII-mediated nucleosomal DNA peeling. The DNA loop structure was not observed in the presence of the transcription elongation factors Spt4/5 and Elf1. These RNAPII-nucleosome structures provide important information for understanding the functional relevance of DNA looping during transcription elongation in the nucleosome.

摘要

RNA聚合酶II(RNAPII)通过逐步暂停转录包裹在核小体中的DNA,特别是在核小体超螺旋位置-5和-1处(分别为SHL(-5)和SHL(-1))。在本研究中,我们对在主要核小体暂停位点SHL(-1)处暂停的RNAPII-核小体复合物进行了冷冻电子显微镜分析。我们确定了两个以前未检测到的结构,其中RNAPII后面的转录DNA在RNAPII出口通道处急剧弯曲,并通过DNA环化重新缠绕在RNAPII前面的核小体组蛋白周围。这种DNA弯曲将DNA方向朝核小体转移,并且转录的DNA区域与由RNAPII介导的核小体DNA剥离所暴露的组蛋白H2A、H2B和H3的碱性氨基酸残基相互作用。在转录延伸因子Spt4/5和Elf1存在的情况下未观察到DNA环结构。这些RNAPII-核小体结构为理解核小体中转录延伸过程中DNA环化的功能相关性提供了重要信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8789/10703601/0c77cd663e9f/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8789/10703601/6a6dc0ec4b08/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8789/10703601/3bd6d6cfbbde/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8789/10703601/8b915952b8e8/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8789/10703601/0c77cd663e9f/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8789/10703601/6a6dc0ec4b08/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8789/10703601/3bd6d6cfbbde/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8789/10703601/8b915952b8e8/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8789/10703601/0c77cd663e9f/gr4.jpg

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