| Literature DB >> 28985562 |
Suhas S P Rao1, Su-Chen Huang2, Brian Glenn St Hilaire3, Jesse M Engreitz4, Elizabeth M Perez4, Kyong-Rim Kieffer-Kwon5, Adrian L Sanborn6, Sarah E Johnstone7, Gavin D Bascom8, Ivan D Bochkov2, Xingfan Huang9, Muhammad S Shamim10, Jaeweon Shin9, Douglass Turner11, Ziyi Ye9, Arina D Omer2, James T Robinson12, Tamar Schlick13, Bradley E Bernstein7, Rafael Casellas14, Eric S Lander15, Erez Lieberman Aiden16.
Abstract
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.Entities:
Keywords: 4D Nucleome; CTCF; Hi-C; chromatin loops; cohesion; gene regulation; genome architecture; loop extrusion; nuclear compartments; superenhancers
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Year: 2017 PMID: 28985562 PMCID: PMC5846482 DOI: 10.1016/j.cell.2017.09.026
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582