| Literature DB >> 29706539 |
Giulia Furlan1, Nancy Gutierrez Hernandez1, Christophe Huret1, Rafael Galupa2, Joke Gerarda van Bemmel3, Antonio Romito1, Edith Heard2, Céline Morey4, Claire Rougeulle5.
Abstract
Accumulation of the Xist long noncoding RNA (lncRNA) on one X chromosome is the trigger for X chromosome inactivation (XCI) in female mammals. Xist expression, which needs to be tightly controlled, involves a cis-acting region, the X-inactivation center (Xic), containing many lncRNA genes that evolved concomitantly to Xist from protein-coding ancestors through pseudogeneization and loss of coding potential. Here, we uncover an essential role for the Xic-linked noncoding gene Ftx in the regulation of Xist expression. We show that Ftx is required in cis to promote Xist transcriptional activation and establishment of XCI. Importantly, we demonstrate that this function depends on Ftx transcription and not on the RNA products. Our findings illustrate the multiplicity of layers operating in the establishment of XCI and highlight the diversity in the modus operandi of the noncoding players.Entities:
Keywords: 3D interactions; CTCF; X chromosome inactivation; long noncoding RNAs; mouse embryonic stem cell differentiation
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Year: 2018 PMID: 29706539 DOI: 10.1016/j.molcel.2018.03.024
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970