Biology Faculty, Lomonosov Moscow State University, 119992 Moscow, Russia.
Department of Pharmacology, Rutgers Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.
Cells. 2022 Aug 28;11(17):2678. doi: 10.3390/cells11172678.
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.
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。