粘蛋白
CTCF公司
生物
染色体
染色体分离
染色体构象捕获
遗传学
折叠(DSP实现)
计算生物学
基因
基因表达
增强子
电气工程
工程类
作者
Pia Mach,Pavel Kos,Yinxiu Zhan,Julie Cramard,Simon Gaudin,Jana Tünnermann,Edoardo Marchi,Jan Eglinger,Jessica Zuin,Mariya Kryzhanovska,Sébastien A. Smallwood,Laurent Gelman,Grégory Roth,Elphège P. Nora,Guido Tiana,Luca Giorgetti
出处
期刊:Nature Genetics
[Nature Portfolio]
日期:2022-12-01
卷期号:54 (12): 1907-1918
被引量:63
标识
DOI:10.1038/s41588-022-01232-7
摘要
In mammals, interactions between sequences within topologically associating domains enable control of gene expression across large genomic distances. Yet it is unknown how frequently such contacts occur, how long they last and how they depend on the dynamics of chromosome folding and loop extrusion activity of cohesin. By imaging chromosomal locations at high spatial and temporal resolution in living cells, we show that interactions within topologically associating domains are transient and occur frequently during the course of a cell cycle. Interactions become more frequent and longer in the presence of convergent CTCF sites, resulting in suppression of variability in chromosome folding across time. Supported by physical models of chromosome dynamics, our data suggest that CTCF-anchored loops last around 10 min. Our results show that long-range transcriptional regulation might rely on transient physical proximity, and that cohesin and CTCF stabilize highly dynamic chromosome structures, facilitating selected subsets of chromosomal interactions.
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