The TFIIH complex is required to establish and maintain mitotic chromosome structure

Elife. 2022 Mar 16:11:e75475. doi: 10.7554/eLife.75475.

Abstract

Condensins compact chromosomes to promote their equal segregation during mitosis, but the mechanism of condensin engagement with and action on chromatin is incompletely understood. Here, we show that the general transcription factor TFIIH complex is continuously required to establish and maintain a compacted chromosome structure in transcriptionally silent Xenopus egg extracts. Inhibiting the DNA-dependent ATPase activity of the TFIIH complex subunit XPB rapidly and reversibly induces a complete loss of chromosome structure and prevents the enrichment of condensins I and II, but not topoisomerase II, on chromatin. In addition, inhibiting TFIIH prevents condensation of both mouse and Xenopus nuclei in Xenopus egg extracts, which suggests an evolutionarily conserved mechanism of TFIIH action. Reducing nucleosome density through partial histone depletion restores chromosome structure and condensin enrichment in the absence of TFIIH activity. We propose that the TFIIH complex promotes mitotic chromosome condensation by dynamically altering the chromatin environment to facilitate condensin loading and condensin-dependent loop extrusion.

Keywords: TFIIH; cell biology; chromosome condensation; chromosomes; condensin; gene expression; mitosis; mouse; nucleosomes; xenopus.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Animals
  • Chromatin
  • Chromosomes* / metabolism
  • DNA Topoisomerases, Type II* / metabolism
  • Histones
  • Mice
  • Mitosis
  • Nucleosomes
  • Xenopus laevis / metabolism

Substances

  • Chromatin
  • Histones
  • Nucleosomes
  • DNA Topoisomerases, Type II

Grants and funding

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.