<HashMap><database>bioimages</database><scores/><additional><omics_type>Unknown</omics_type><submitter/><species>Homo sapiens (human)</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-BIAD368</full_dataset_link><repository>bioimages</repository><figure_sub>Protocols</figure_sub><figure_sub>Funding</figure_sub><figure_sub>Study Component</figure_sub><figure_sub>organisation</figure_sub><pubmed_authors>Ying Li</pubmed_authors><pubmed_authors>Bastiaan Dekker</pubmed_authors><pubmed_authors>Sergey V. Venev</pubmed_authors><pubmed_authors>Denis L. Lafontaine</pubmed_authors><pubmed_authors>A. Nicole Fox</pubmed_authors><pubmed_authors>Erica M Hildebrand</pubmed_authors><pubmed_authors>Yu Liu</pubmed_authors><pubmed_authors>Job Dekker</pubmed_authors><pubmed_authors>Kirill Polovnikov</pubmed_authors><pubmed_authors>Leonid Mirny</pubmed_authors></additional><is_claimable>false</is_claimable><name>Directed Topoisomerase II activity disentangles interphase compartment domains</name><description>The topological state of chromosomes determines their mechanical properties, dynamics, and function. Recent work indicated that interphase chromosomes are largely free of entanglements. Here, we use Hi-C, polymer simulations and multi-contact 3C, and propose that, in contrast, mitotic chromosomes are self-entangled. We explore how a mitotic self-entangled state is converted into an unentangled interphase state during mitotic exit. Most mitotic entanglements are removed during anaphase/telophase, with remaining ones removed during early G1, in a Topoisomerase II-dependent process. Polymer models suggest a two-stage disentanglement pathway: first, decondensation of mitotic chromosomes with remaining condensin loops produces entropic forces that bias Topoisomerase II activity towards decatena</description><dates><release>2023-03-10T00:00:00Z</release><modification>2024-03-07T20:16:12.23Z</modification><creation>2022-03-11T15:46:07.77Z</creation></dates><accession>S-BIAD368</accession><cross_references/></HashMap>