<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Sorensen Turpin CG</submitter><funding>NHGRI NIH HHS</funding><funding>NIGMS NIH HHS</funding><funding>NIH HHS</funding><pubmed_abstract>Separase is a key regulator of the metaphase to anaphase transition with multiple functions. Separase cleaves cohesin to allow chromosome segregation and localizes to vesicles to promote exocytosis in mid-anaphase. The anaphase promoting complex/cyclosome (APC/C) activates separase by ubiquitinating its inhibitory chaperone, securin, triggering its degradation. How this pathway controls the exocytic function of separase has not been investigated. During meiosis I, securin is degraded over several minutes, while separase rapidly relocalizes from kinetochore structures at the spindle and cortex to sites of action on chromosomes and vesicles at anaphase onset. The loss of cohesin coincides with the relocalization of separase to the chromosome midbivalent at anaphase onset. APC/C depletion pre</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2023.12.12.571338</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10760073</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Securin Regulates the Spatiotemporal Dynamics of Separase.</pubmed_title><pmcid>PMC10760073</pmcid><funding_grant_id>R15 GM143731</funding_grant_id><funding_grant_id>P40 OD010440</funding_grant_id><funding_grant_id>R01 GM114471</funding_grant_id><funding_grant_id>R15 GM117548</funding_grant_id><funding_grant_id>U41 HG002223</funding_grant_id><pubmed_authors>LaForest M</pubmed_authors><pubmed_authors>Sorensen Turpin CG</pubmed_authors><pubmed_authors>Klebanow LU</pubmed_authors><pubmed_authors>Severson AF</pubmed_authors><pubmed_authors>Bembenek JN</pubmed_authors><pubmed_authors>Sloan D</pubmed_authors><pubmed_authors>Mitchell D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Securin Regulates the Spatiotemporal Dynamics of Separase.</name><description>Separase is a key regulator of the metaphase to anaphase transition with multiple functions. Separase cleaves cohesin to allow chromosome segregation and localizes to vesicles to promote exocytosis in mid-anaphase. The anaphase promoting complex/cyclosome (APC/C) activates separase by ubiquitinating its inhibitory chaperone, securin, triggering its degradation. How this pathway controls the exocytic function of separase has not been investigated. During meiosis I, securin is degraded over several minutes, while separase rapidly relocalizes from kinetochore structures at the spindle and cortex to sites of action on chromosomes and vesicles at anaphase onset. The loss of cohesin coincides with the relocalization of separase to the chromosome midbivalent at anaphase onset. APC/C depletion pre</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Dec</publication><modification>2026-04-08T04:03:37.32Z</modification><creation>2025-02-19T01:21:05.178Z</creation></dates><accession>S-EPMC10760073</accession><cross_references><pubmed>38168402</pubmed><doi>10.1101/2023.12.12.571338</doi></cross_references></HashMap>