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转录偶联核小体组装

Transcription-coupled nucleosome assembly.

作者信息

Robert François, Jeronimo Célia

机构信息

Institut de recherches cliniques de Montréal, 110 Avenue des Pins Ouest, Montréal, QC H2W 1R7, Canada; Département de Médecine, Faculté de Médecine, Université de Montréal, 2900 Boul. Édouard-Montpetit, Montréal, QC H3T 1J4, Canada; Faculty of Medicine, Division of Experimental Medicine, McGill University, Montréal, QC H3A 1A3, Canada.

Institut de recherches cliniques de Montréal, 110 Avenue des Pins Ouest, Montréal, QC H2W 1R7, Canada.

出版信息

Trends Biochem Sci. 2023 Nov;48(11):978-992. doi: 10.1016/j.tibs.2023.08.003. Epub 2023 Aug 30.

Abstract

Eukaryotic transcription occurs on chromatin, where RNA polymerase II encounters nucleosomes during elongation. These nucleosomes must unravel for the DNA to enter the active site. However, in most transcribed genes, nucleosomes remain intact due to transcription-coupled chromatin assembly mechanisms. These mechanisms primarily involve the local reassembly of displaced nucleosomes to prevent (epi)genomic instability and the emergence of cryptic transcription. As a fail-safe mechanism, cells can assemble nucleosomes de novo, particularly in highly transcribed genes, but this may result in the loss of epigenetic information. This review examines transcription-coupled chromatin assembly, with an emphasis on studies in yeast and recent structural studies. These studies shed light on how elongation factors and histone chaperones coordinate to enable nucleosome recycling during transcription.

摘要

真核生物转录发生在染色质上,在延伸过程中RNA聚合酶II会遇到核小体。这些核小体必须解开,以便DNA进入活性位点。然而,在大多数转录基因中,由于转录偶联的染色质组装机制,核小体保持完整。这些机制主要涉及移位核小体的局部重新组装,以防止(表观)基因组不稳定和隐秘转录的出现。作为一种故障安全机制,细胞可以从头组装核小体,特别是在高度转录的基因中,但这可能导致表观遗传信息的丢失。本综述探讨转录偶联的染色质组装,重点是酵母中的研究和最近的结构研究。这些研究揭示了延伸因子和组蛋白伴侣如何协同作用,以在转录过程中实现核小体循环利用。

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