粘蛋白
生物
CTCF公司
遗传学
循环(图论)
染色体
组蛋白
舱室(船)
染色体分离
细胞生物学
基因
转录因子
海洋学
数学
增强子
组合数学
地质学
作者
Suhas S.P. Rao,Su Chen Huang,Brian Glenn St Hilaire,Jesse M. Engreitz,Elizabeth M. Perez,Kyong Rim Kieffer-Kwon,Adrian L. Sanborn,Sarah E. Johnstone,Gavin Bascom,Ivan D. Bochkov,Xingfan Huang,Muhammad S. Shamim,Jaeweon Shin,Douglass Turner,Ziyi Ye,Arina D. Omer,James T. Robinson,Tamar Schlick,B Bernstein,Rafael Casellas,Eric S. Lander,E Aiden
出处
期刊:Cell
[Cell Press]
日期:2017-10-01
卷期号:171 (2): 305-320.e24
被引量:1452
标识
DOI:10.1016/j.cell.2017.09.026
摘要
The human genome folds to create thousands of intervals, called “contact domains,” that exhibit enhanced contact frequency within themselves. “Loop domains” form because of tethering between two loci—almost always bound by CTCF and cohesin—lying on the same chromosome. “Compartment domains” form when genomic intervals with similar histone marks co-segregate. Here, we explore the effects of degrading cohesin. All loop domains are eliminated, but neither compartment domains nor histone marks are affected. Loss of loop domains does not lead to widespread ectopic gene activation but does affect a significant minority of active genes. In particular, cohesin loss causes superenhancers to co-localize, forming hundreds of links within and across chromosomes and affecting the regulation of nearby genes. We then restore cohesin and monitor the re-formation of each loop. Although re-formation rates vary greatly, many megabase-sized loops recovered in under an hour, consistent with a model where loop extrusion is rapid.
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