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转录过程中感应 DNA 损伤的核小体 DNA 环的结构。

Structure of an Intranucleosomal DNA Loop That Senses DNA Damage during Transcription.

机构信息

Biology Faculty, Lomonosov Moscow State University, 119992 Moscow, Russia.

Department of Pharmacology, Rutgers Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.

出版信息

Cells. 2022 Aug 28;11(17):2678. doi: 10.3390/cells11172678.

Abstract

Transcription through chromatin by RNA polymerase II (Pol II) is accompanied by the formation of small intranucleosomal DNA loops containing the enzyme (i-loops) that are involved in survival of core histones on the DNA and arrest of Pol II during the transcription of damaged DNA. However, the structures of i-loops have not been determined. Here, the structures of the intermediates formed during transcription through a nucleosome containing intact or damaged DNA were studied using biochemical approaches and electron microscopy. After RNA polymerase reaches position +24 from the nucleosomal boundary, the enzyme can backtrack to position +20, where DNA behind the enzyme recoils on the surface of the histone octamer, forming an i-loop that locks Pol II in the arrested state. Since the i-loop is formed more efficiently in the presence of SSBs positioned behind the transcribing enzyme, the loop could play a role in the transcription-coupled repair of DNA damage hidden in the chromatin structure.

摘要

RNA 聚合酶 II(Pol II)通过染色质进行转录伴随着形成包含酶的小核小体 DNA 环(i-环),这些环参与 DNA 上核心组蛋白的存活和受损 DNA 转录过程中 Pol II 的停滞。然而,i-环的结构尚未确定。在这里,使用生化方法和电子显微镜研究了在包含完整或受损 DNA 的核小体上进行转录时形成的中间产物的结构。当 RNA 聚合酶从核小体边界到达+24 位置后,酶可以回溯到+20 位置,此时酶后面的 DNA 在组蛋白八聚体表面回卷,形成一个 i-环,将 Pol II 锁定在停滞状态。由于 i-环在位于转录酶后面的 SSB 存在时更有效地形成,因此该环可能在转录偶联修复隐藏在染色质结构中的 DNA 损伤中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71d9/9454427/db29b46760d8/cells-11-02678-g001.jpg

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