BAF complex-mediated chromatin relaxation is required for establishment of X chromosome inactivation.
Andrew KeniryNatasha JanszLinden J GearingIromi WanigasuriyaJoseph ChenChristian Maximilian NefzgerPeter F HickeyQuentin A GouilJoy LiuKelsey A BreslinMegan IminitoffTamara BeckAndres Tapia Del FierroLachlan W WhiteheadAndrew JarrattSarah A KinkelPhillippa C TaberlayTracy WillsonMiha PakuschMatthew E RitchieDouglas J HiltonMohammad Mahfuz ChowdhuryMarnie E BlewittPublished in: Nature communications (2022)
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.