RNA Pol II-based regulations of chromosome folding.

IF 11.1 Q1 CELL BIOLOGY
Cell genomics Pub Date : 2025-10-08 Epub Date: 2025-08-08 DOI:10.1016/j.xgen.2025.100970
Christophe Chapard, Nathalie Bastié, Axel Cournac, Laura Chaptal, Henri Mboumba, Sophie Queille, Agnes Thierry, Olivier Gadal, Armelle Lengronne, Romain Koszul, Frédéric Beckouët
{"title":"RNA Pol II-based regulations of chromosome folding.","authors":"Christophe Chapard, Nathalie Bastié, Axel Cournac, Laura Chaptal, Henri Mboumba, Sophie Queille, Agnes Thierry, Olivier Gadal, Armelle Lengronne, Romain Koszul, Frédéric Beckouët","doi":"10.1016/j.xgen.2025.100970","DOIUrl":null,"url":null,"abstract":"<p><p>The spatial organization of eukaryotic genomes and its dynamics are of functional importance for gene expression, DNA replication, and segregation. Structural maintenance of chromosome (SMC) complexes are essential instruments of chromosome folding, enabling long-distance intra-chromatid DNA loops. The interplay between these processes is complex. For instance, cohesin, in addition to tethering sister chromatids, dynamically regulates gene expression in mammals by promoting interactions between distal regulatory elements and promoters, whereas transcription itself affects genome folding in many ways. Here, we comprehensively dissect the relative contributions of transcription and cohesin complexes, as well as their interplay, to yeast S. cerevisiae genome organization. In particular, we show that transcription (1) is not a motor required to push cohesin during DNA loop expansion, (2) specifically induces the appearance of DNA loops independently of SMC complexes, and (3) interferes with cohesin-mediated DNA loop expansion during their establishment.</p>","PeriodicalId":72539,"journal":{"name":"Cell genomics","volume":" ","pages":"100970"},"PeriodicalIF":11.1000,"publicationDate":"2025-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell genomics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.xgen.2025.100970","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/8 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The spatial organization of eukaryotic genomes and its dynamics are of functional importance for gene expression, DNA replication, and segregation. Structural maintenance of chromosome (SMC) complexes are essential instruments of chromosome folding, enabling long-distance intra-chromatid DNA loops. The interplay between these processes is complex. For instance, cohesin, in addition to tethering sister chromatids, dynamically regulates gene expression in mammals by promoting interactions between distal regulatory elements and promoters, whereas transcription itself affects genome folding in many ways. Here, we comprehensively dissect the relative contributions of transcription and cohesin complexes, as well as their interplay, to yeast S. cerevisiae genome organization. In particular, we show that transcription (1) is not a motor required to push cohesin during DNA loop expansion, (2) specifically induces the appearance of DNA loops independently of SMC complexes, and (3) interferes with cohesin-mediated DNA loop expansion during their establishment.

基于RNA Pol ii的染色体折叠调控。
真核生物基因组的空间组织及其动力学对基因表达、DNA复制和分离具有重要的功能。染色体结构维持(SMC)复合体是染色体折叠的重要工具,可以实现长距离的染色单体内DNA环。这些过程之间的相互作用是复杂的。例如,在哺乳动物中,内聚蛋白除了捆绑姐妹染色单体外,还通过促进远端调控元件和启动子之间的相互作用来动态调节基因表达,而转录本身则以多种方式影响基因组折叠。在这里,我们全面剖析了转录和内聚蛋白复合物的相对贡献,以及它们之间的相互作用,酵母酿酒酵母基因组组织。特别是,我们发现转录(1)在DNA环扩张过程中不是推动黏结蛋白所需的马达,(2)特异性地诱导独立于SMC复合物的DNA环的出现,以及(3)在DNA环的建立过程中干扰黏结蛋白介导的DNA环扩张。
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
CiteScore
7.10
自引率
0.00%
发文量
0
×
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