Suppr超能文献

组蛋白尾部和单链 DNA 断裂在核小体阻止 RNA 聚合酶中的作用。

Role of Histone Tails and Single Strand DNA Breaks in Nucleosomal Arrest of RNA Polymerase.

机构信息

Institute of Gene Biology, Russian Academy of Sciences, 119334 Moscow, Russia.

Faculty of Biology, Lomonosov Moscow State University, 119234 Moscow, Russia.

出版信息

Int J Mol Sci. 2023 Jan 24;24(3):2295. doi: 10.3390/ijms24032295.

Abstract

Transcription through nucleosomes by RNA polymerases (RNAP) is accompanied by formation of small intranucleosomal DNA loops (i-loops). The i-loops form more efficiently in the presence of single-strand breaks or gaps in a non-template DNA strand (NT-SSBs) and induce arrest of transcribing RNAP, thus allowing detection of NT-SSBs by the enzyme. Here we examined the role of histone tails and extranucleosomal NT-SSBs in i-loop formation and arrest of RNAP during transcription of promoter-proximal region of nucleosomal DNA. NT-SSBs present in linker DNA induce arrest of RNAP +1 to +15 bp in the nucleosome, suggesting formation of the i-loops; the arrest is more efficient in the presence of the histone tails. Consistently, DNA footprinting reveals formation of an i-loop after stalling RNAP at the position +2 and backtracking to position +1. The data suggest that histone tails and NT-SSBs present in linker DNA strongly facilitate formation of the i-loops during transcription through the promoter-proximal region of nucleosomal DNA.

摘要

RNA 聚合酶(RNAP)在核小体上进行转录时会伴随形成小的核小体内部 DNA 环(i-环)。在非模板 DNA 链(NT-SSB)上存在单链断裂或缺口的情况下,i-环的形成效率更高,并诱导转录的 RNAP 停滞,从而使该酶能够检测到 NT-SSB。在这里,我们研究了组蛋白尾部和核小体外的 NT-SSB 在转录起始点附近核小体 DNA 转录过程中 i-环形成和 RNAP 停滞中的作用。连接 DNA 中存在的 NT-SSB 诱导 RNAP 在核小体中停滞在+1 到+15bp 处,表明 i-环的形成;在存在组蛋白尾部的情况下,停滞更为有效。一致地,DNA 足迹分析表明,在 RNAP 停滞在+2 位置并回溯到+1 位置后,形成了 i-环。数据表明,连接 DNA 中存在的组蛋白尾部和 NT-SSB 可强烈促进转录起始点附近核小体 DNA 区域中 i-环的形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/101a/9917218/f40e9940cce8/ijms-24-02295-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验