{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["13(1)"],"submitter":["Yang T"],"funding":["This work was supported by the Whitehead Scholar Award (E.Y.) and Start-up funds by the Department of Cell Biology Duke Medical Center"],"pubmed_abstract":["X chromosome inactivation (XCI) is a dosage compensation phenomenon that occurs in females. Initiation of XCI depends on Xist RNA, which triggers silencing of one of the two X chromosomes, except for XCI escape genes that continue to be biallelically expressed. In the soma XCI is stably maintained with continuous Xist expression. How Xist impacts XCI maintenance remains an open question. Here we conditionally delete Xist in hematopoietic system of mice and report differentiation and cell cycle defects in female hematopoietic stem and progenitor cells (HSPCs). By utilizing female HSPCs and mouse embryonic fibroblasts, we find that X-linked genes show variable tolerance to Xist loss. Specifically, XCI escape genes exhibit preferential transcriptional upregulation, which associates with low H"],"journal":["Nature communications"],"pagination":["4464"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9343370"],"repository":["biostudies-literature"],"pubmed_title":["Xist exerts gene-specific silencing during XCI maintenance and impacts lineage-specific cell differentiation and proliferation during hematopoiesis."],"pmcid":["PMC9343370"],"pubmed_authors":["Ou J","Yildirim E","Yang T"],"additional_accession":[]},"is_claimable":false,"name":"Xist exerts gene-specific silencing during XCI maintenance and impacts lineage-specific cell differentiation and proliferation during hematopoiesis.","description":"X chromosome inactivation (XCI) is a dosage compensation phenomenon that occurs in females. Initiation of XCI depends on Xist RNA, which triggers silencing of one of the two X chromosomes, except for XCI escape genes that continue to be biallelically expressed. In the soma XCI is stably maintained with continuous Xist expression. How Xist impacts XCI maintenance remains an open question. Here we conditionally delete Xist in hematopoietic system of mice and report differentiation and cell cycle defects in female hematopoietic stem and progenitor cells (HSPCs). By utilizing female HSPCs and mouse embryonic fibroblasts, we find that X-linked genes show variable tolerance to Xist loss. Specifically, XCI escape genes exhibit preferential transcriptional upregulation, which associates with low H","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Aug","modification":"2026-06-01T02:17:58.206Z","creation":"2025-04-05T12:12:09.027Z"},"accession":"S-EPMC9343370","cross_references":{"pubmed":["35915095"],"doi":["10.1038/s41467-022-32273-5"]}}