Author:
Keniry Andrew,Jansz Natasha,Gearing Linden J.,Wanigasuriya Iromi,Chen Joseph,Nefzger Christian M.,Hickey Peter F.,Gouil Quentin,Liu Joy,Breslin Kelsey A.,Iminitoff Megan,Beck Tamara,Tapia del Fierro Andres,Whitehead Lachlan,Kinkel Sarah A.,Taberlay Phillippa C.,Willson Tracy,Pakusch Miha,Ritchie Matthew E.,Hilton Douglas J.,Polo Jose M.,Blewitt Marnie E.
Abstract
SummaryAlthough female pluripotency significantly differs to male, complications with in vitro culture of female embryonic stem cells (ESC) have severely limited the use and study of these cells. We report a replenishable female ESC system, Xmas, that has enabled us to optimise a protocol for preserving the XX karyotype. Our protocol also improves male ESC fitness. We utilised our Xmas ESC system to screen for regulators of the female-specific process of X chromosome inactivation, revealing chromatin remodellers Smarcc1 and Smarca4 as key regulators of establishment of X inactivation. The remodellers create a nucleosome depleted region at gene promotors on the inactive X during exit from pluripotency, without which gene silencing fails. Our female ESC system provides a tractable model for XX ESC culture that will expedite study of female pluripotency and has enabled us to discover new features of the female-specific process of X inactivation.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献