Cohesin Removal Reprograms Gene Expression upon Mitotic Entry

Mol Cell. 2020 Apr 2;78(1):127-140.e7. doi: 10.1016/j.molcel.2020.01.023. Epub 2020 Feb 7.

Abstract

As cells enter mitosis, the genome is restructured to facilitate chromosome segregation, accompanied by dramatic changes in gene expression. However, the mechanisms that underlie mitotic transcriptional regulation are unclear. In contrast to transcribed genes, centromere regions retain transcriptionally active RNA polymerase II (Pol II) in mitosis. Here, we demonstrate that chromatin-bound cohesin is necessary to retain elongating Pol II at centromeres. We find that WAPL-mediated removal of cohesin from chromosome arms during prophase is required for the dissociation of Pol II and nascent transcripts, and failure of this process dramatically alters mitotic gene expression. Removal of cohesin/Pol II from chromosome arms in prophase is important for accurate chromosome segregation and normal activation of gene expression in G1. We propose that prophase cohesin removal is a key step in reprogramming gene expression as cells transition from G2 through mitosis to G1.

Keywords: RNA Pol II; WAPL; centromere; cohesin; mitotic transcription; prophase pathway.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anaphase / genetics
  • Animals
  • Aurora Kinase B / analysis
  • Cell Cycle
  • Cell Cycle Proteins / analysis
  • Cell Cycle Proteins / physiology*
  • Cell Line
  • Centromere / enzymology
  • Chromosomal Proteins, Non-Histone / physiology*
  • Chromosome Segregation
  • Cohesins
  • G1 Phase / genetics
  • G2 Phase Cell Cycle Checkpoints / genetics
  • Gene Expression Regulation*
  • Humans
  • Metaphase / genetics
  • Mitosis / genetics*
  • Prophase
  • RNA Polymerase II / metabolism
  • Transcription, Genetic*
  • Xenopus laevis

Substances

  • Cell Cycle Proteins
  • Chromosomal Proteins, Non-Histone
  • Aurora Kinase B
  • RNA Polymerase II