α-Satellite RNA maintains centromeric cohesion through R-loops.

IF 16 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Molecular Cell Pub Date : 2026-08-20 Epub Date: 2026-08-05 DOI:10.1016/j.molcel.2026.07.023
Lu Yang, Qian Zhang, Zhen Teng, Erin Moran, Zhen Lin, P Todd Stukenberg, Hong Liu
{"title":"α-Satellite RNA maintains centromeric cohesion through R-loops.","authors":"Lu Yang, Qian Zhang, Zhen Teng, Erin Moran, Zhen Lin, P Todd Stukenberg, Hong Liu","doi":"10.1016/j.molcel.2026.07.023","DOIUrl":null,"url":null,"abstract":"<p><p>Tandemly repeated satellite DNAs provide the building blocks for centromeres, but whether and how their transcripts regulate chromosome segregation remain poorly defined. Here, we show that human α-satellite RNAs (α-SatRNAs) are required for maintaining centromeric cohesion during mitosis. α-SatRNAs localize to centromeres and physically associate with α-satellite chromatin to form R-loops both in cis and in trans. Disruption of these R-loops by RNase H1 overexpression causes centromeric cohesion defects, phenocopying α-SatRNA knockdown, which can be rescued by the expression of an α-satellite consensus sequence, supporting a major role for α-SatRNA-formed R-loops in centromeric cohesion. Furthermore, ectopic targeting of the cohesion protector Shugoshin (Sgo)1 to centromeric α-SatDNAs largely rescues centromeric cohesion defects caused by α-SatRNA knockdown or RNase H1 overexpression. Our findings reveal a critical pathway comprising α-SatRNAs, R-loops, and Sgo1 in regulating centromeric cohesion, thus providing an important mechanism to explain how satellite transcripts regulate chromosomal stability.</p>","PeriodicalId":18950,"journal":{"name":"Molecular Cell","volume":" ","pages":"3198-3212.e6"},"PeriodicalIF":16.0000,"publicationDate":"2026-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13532348/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Cell","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.molcel.2026.07.023","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/8/5 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Tandemly repeated satellite DNAs provide the building blocks for centromeres, but whether and how their transcripts regulate chromosome segregation remain poorly defined. Here, we show that human α-satellite RNAs (α-SatRNAs) are required for maintaining centromeric cohesion during mitosis. α-SatRNAs localize to centromeres and physically associate with α-satellite chromatin to form R-loops both in cis and in trans. Disruption of these R-loops by RNase H1 overexpression causes centromeric cohesion defects, phenocopying α-SatRNA knockdown, which can be rescued by the expression of an α-satellite consensus sequence, supporting a major role for α-SatRNA-formed R-loops in centromeric cohesion. Furthermore, ectopic targeting of the cohesion protector Shugoshin (Sgo)1 to centromeric α-SatDNAs largely rescues centromeric cohesion defects caused by α-SatRNA knockdown or RNase H1 overexpression. Our findings reveal a critical pathway comprising α-SatRNAs, R-loops, and Sgo1 in regulating centromeric cohesion, thus providing an important mechanism to explain how satellite transcripts regulate chromosomal stability.

Abstract Image

α-卫星RNA通过r环维持着丝粒内聚。
连续重复的卫星dna为着丝粒提供了构建模块,但是它们的转录物是否以及如何调节染色体分离仍然没有明确的定义。在这里,我们发现人类α-卫星rna (α-SatRNAs)是有丝分裂期间维持着丝粒内聚所必需的。α-卫星rna定位于着丝粒,并与α-卫星染色质物理结合形成顺式和反式r环。RNase H1过表达对这些r环的破坏导致着丝粒内聚缺陷,表现为α-SatRNA敲低,可通过α-卫星一致序列的表达来修复,支持α-SatRNA形成的r环在着丝粒内聚中的主要作用。此外,内聚保护因子Shugoshin (Sgo)1异位靶向着丝粒α- satdna,很大程度上挽救了由α-SatRNA敲低或RNase H1过表达引起的着丝粒内聚缺陷。我们的研究结果揭示了一个由α-SatRNAs、R-loops和Sgo1组成的调节着丝粒内聚的关键途径,从而为解释卫星转录本如何调节染色体稳定性提供了重要的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Molecular Cell
Molecular Cell 生物-生化与分子生物学
CiteScore
26.00
自引率
3.80%
发文量
389
审稿时长
1 months
期刊介绍: Molecular Cell is a companion to Cell, the leading journal of biology and the highest-impact journal in the world. Launched in December 1997 and published monthly. Molecular Cell is dedicated to publishing cutting-edge research in molecular biology, focusing on fundamental cellular processes. The journal encompasses a wide range of topics, including DNA replication, recombination, and repair; Chromatin biology and genome organization; Transcription; RNA processing and decay; Non-coding RNA function; Translation; Protein folding, modification, and quality control; Signal transduction pathways; Cell cycle and checkpoints; Cell death; Autophagy; Metabolism.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书