{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Kriz AJ"],"funding":["American Cancer Society","NICHD NIH HHS","Howard Hughes Medical Institute","National Institutes of Health","NIGMS NIH HHS"],"pagination":["1970-1987.e9"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8106664"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["81(9)"],"pubmed_abstract":["Depletion of architectural factors globally alters chromatin structure but only modestly affects gene expression. We revisit the structure-function relationship using the inactive X chromosome (Xi) as a model. We investigate cohesin imbalances by forcing its depletion or retention using degron-tagged RAD21 (cohesin subunit) or WAPL (cohesin release factor). Cohesin loss disrupts the Xi superstructure, unveiling superloops between escapee genes with minimal effect on gene repression. By contrast, forced cohesin retention markedly affects Xi superstructure, compromises spreading of Xist RNA-Polycomb complexes, and attenuates Xi silencing. Effects are greatest at distal chromosomal ends, where looping contacts with the Xist locus are weakened. Surprisingly, cohesin loss creates an Xi superloo"],"journal":["Molecular cell"],"pubmed_title":["Balancing cohesin eviction and retention prevents aberrant chromosomal interactions, Polycomb-mediated repression, and X-inactivation."],"pmcid":["PMC8106664"],"funding_grant_id":["F31 HD100109","R01 GM090278","R37 GM058839","R01 HD097665","R01 GM058839"],"pubmed_authors":["Nabet B","Sunwoo H","Lee JT","Colognori D","Kriz AJ"],"additional_accession":[]},"is_claimable":false,"name":"Balancing cohesin eviction and retention prevents aberrant chromosomal interactions, Polycomb-mediated repression, and X-inactivation.","description":"Depletion of architectural factors globally alters chromatin structure but only modestly affects gene expression. We revisit the structure-function relationship using the inactive X chromosome (Xi) as a model. We investigate cohesin imbalances by forcing its depletion or retention using degron-tagged RAD21 (cohesin subunit) or WAPL (cohesin release factor). Cohesin loss disrupts the Xi superstructure, unveiling superloops between escapee genes with minimal effect on gene repression. By contrast, forced cohesin retention markedly affects Xi superstructure, compromises spreading of Xist RNA-Polycomb complexes, and attenuates Xi silencing. Effects are greatest at distal chromosomal ends, where looping contacts with the Xist locus are weakened. Surprisingly, cohesin loss creates an Xi superloo","dates":{"release":"2021-01-01T00:00:00Z","publication":"2021 May","modification":"2026-05-30T18:50:33.317Z","creation":"2025-02-19T00:29:26.467Z"},"accession":"S-EPMC8106664","cross_references":{"pubmed":["33725485"],"doi":["10.1016/j.molcel.2021.02.031"]}}