Cohesin Loss Eliminates All Loop Domains

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 D. Bascom, Ivan D. Bochkov, Xingfan Huang, Muhammad S. Shamim, Jaeweon Shin, Douglass Turner, Ziyi Ye, Arina D. Omer, James T. Robinson, Tamar Schlick, Bradley E. Bernstein, Rafael CasellasEric S. Lander, Erez Lieberman Aiden

Research output: Contribution to journalArticlepeer-review

1055 Scopus citations

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. Mapping the nucleome in 4D during cohesin loss and recovery reveals that cohesin degradation eliminates loop domains but has only modest transcriptional consequences.

Original languageEnglish (US)
Pages (from-to)305-320.e24
JournalCell
Volume171
Issue number2
DOIs
StatePublished - Oct 5 2017
Externally publishedYes

Keywords

  • 4D Nucleome
  • chromatin loops
  • cohesion
  • CTCF
  • gene regulation
  • genome architecture
  • Hi-C
  • loop extrusion
  • nuclear compartments
  • superenhancers

ASJC Scopus subject areas

  • General Biochemistry, Genetics and Molecular Biology

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