BAF complex-mediated chromatin relaxation is required for establishment of X chromosome inactivation

Nat Commun. 2022 Mar 29;13(1):1658. doi: 10.1038/s41467-022-29333-1.

Abstract

The process of epigenetic silencing, while fundamentally important, is not yet completely understood. Here we report a replenishable female mouse embryonic stem cell (mESC) system, Xmas, that allows rapid assessment of X chromosome inactivation (XCI), the epigenetic silencing mechanism of one of the two X chromosomes that enables dosage compensation in female mammals. Through a targeted genetic screen in differentiating Xmas mESCs, we reveal that the BAF complex is required to create nucleosome-depleted regions at promoters on the inactive X chromosome during the earliest stages of establishment of XCI. Without this action gene silencing fails. Xmas mESCs provide a tractable model for screen-based approaches that enable the discovery of unknown facets of the female-specific process of XCI and epigenetic silencing more broadly.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chromatin / genetics
  • Dosage Compensation, Genetic
  • Epigenesis, Genetic
  • Female
  • Mice
  • RNA, Long Noncoding* / genetics
  • X Chromosome / genetics
  • X Chromosome Inactivation* / genetics

Substances

  • Chromatin
  • RNA, Long Noncoding