SMC complexes: Lifting the lid on loop extrusion

被引:24
|
作者
Higashi, Torahiko L. [1 ,2 ]
Uhlmann, Frank [1 ]
机构
[1] Francis Crick Inst, Chromosome Segregat Lab, London NW1 1AT, England
[2] Kyushu Univ, Dept Cellular Biochem, Fukuoka 8128582, Japan
基金
英国惠康基金; 英国医学研究理事会; 欧洲研究理事会;
关键词
HUMAN COHESIN; DNA ENTRY; CONDENSIN; ORGANIZATION; CHROMATIN; LOCALIZATION; GENES; SITES; RING; ACTS;
D O I
10.1016/j.ceb.2021.12.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Loop extrusion has emerged as a prominent hypothesis for how SMC complexes shape chromosomes - single molecule in vitro observations have yielded fascinating images of this process. When not extruding loops, SMC complexes are known to topologically entrap one or more DNAs. Here, we review how structural insight into the SMC complex cohesin has led to a molecular framework for both activities: a Brownian ratchet motion, associated with topological DNA entry, might repeat itself to elicit loop extrusion. After contrasting alternative loop extrusion models, we explore whether topological loading or loop extrusion is more adept at explaining in vivo SMC complex function. SMC variants that experimentally separate topological loading from loop extrusion will in the future probe their respective contributions to chromosome biology.
引用
收藏
页码:13 / 22
页数:10
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