粘蛋白
姐妹染色单体结合力的建立
生物
CTCF公司
染色单体
染色质
姐妹染色单体
遗传学
染色体分离
细胞生物学
突变体
DNA
染色体
转录因子
基因
增强子
作者
Kota Nagasaka,Iain F. Davidson,Roman R. Stocsits,Wen Tang,Gordana Wutz,Paul Batty,Mélanie Panarotto,Gabriele Litos,Alexander Schleiffer,Daniel W. Gerlich,Jan‐Michael Peters
出处
期刊:Molecular Cell
[Elsevier BV]
日期:2023-08-16
卷期号:83 (17): 3049-3063.e6
被引量:50
标识
DOI:10.1016/j.molcel.2023.07.024
摘要
Cohesin connects CTCF-binding sites and other genomic loci in cis to form chromatin loops and replicated DNA molecules in trans to mediate sister chromatid cohesion. Whether cohesin uses distinct or related mechanisms to perform these functions is unknown. Here, we describe a cohesin hinge mutant that can extrude DNA into loops but is unable to mediate cohesion in human cells. Our results suggest that the latter defect arises during cohesion establishment. The observation that cohesin's cohesion and loop extrusion activities can be partially separated indicates that cohesin uses distinct mechanisms to perform these two functions. Unexpectedly, the same hinge mutant can also not be stopped by CTCF boundaries as well as wild-type cohesin. This suggests that cohesion establishment and cohesin's interaction with CTCF boundaries depend on related mechanisms and raises the possibility that both require transient hinge opening to entrap DNA inside the cohesin ring.
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