<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Stewart MG</submitter><funding>NHGRI NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pubmed_abstract>Cells coordinate diverse events at anaphase onset, including separase activation, cohesin cleavage, chromosome separation, and spindle reorganization. Regulation of the XMAP215 family member and microtubule polymerase, Stu2, at the metaphase-anaphase transition determines a specific redistribution from kinetochores to spindle microtubules. We show that cells modulate Stu2 kinetochore-microtubule localization by Polo-like kinase1/Cdc5-mediated phosphorylation of T866, near the Stu2 C-terminus, thereby promoting dissociation from the kinetochore Ndc80 complex. Cdk/Cdc28 likely primes Cdc5:Stu2 interaction. Cdc28 activity is also required for Stu2 nuclear import. PP2A&lt;sup>Cdc55&lt;/sup> actively opposes Cdc5 activity on Stu2&lt;sup>T866&lt;/sup> during metaphase. This counter-regulation allows for swi</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2024.11.01.621564</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11566010</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A coordinated kinase and phosphatase network regulates Stu2 recruitment to yeast kinetochores.</pubmed_title><pmcid>PMC11566010</pmcid><funding_grant_id>F31 CA271740</funding_grant_id><funding_grant_id>R35 GM142749</funding_grant_id><funding_grant_id>P30 CA015704</funding_grant_id><funding_grant_id>T32 HG008962</funding_grant_id><pubmed_authors>Harrison SC</pubmed_authors><pubmed_authors>Carrier JS</pubmed_authors><pubmed_authors>Zahm JA</pubmed_authors><pubmed_authors>Stewart MG</pubmed_authors><pubmed_authors>Miller MP</pubmed_authors></additional><is_claimable>false</is_claimable><name>A coordinated kinase and phosphatase network regulates Stu2 recruitment to yeast kinetochores.</name><description>Cells coordinate diverse events at anaphase onset, including separase activation, cohesin cleavage, chromosome separation, and spindle reorganization. Regulation of the XMAP215 family member and microtubule polymerase, Stu2, at the metaphase-anaphase transition determines a specific redistribution from kinetochores to spindle microtubules. We show that cells modulate Stu2 kinetochore-microtubule localization by Polo-like kinase1/Cdc5-mediated phosphorylation of T866, near the Stu2 C-terminus, thereby promoting dissociation from the kinetochore Ndc80 complex. Cdk/Cdc28 likely primes Cdc5:Stu2 interaction. Cdc28 activity is also required for Stu2 nuclear import. PP2A&lt;sup>Cdc55&lt;/sup> actively opposes Cdc5 activity on Stu2&lt;sup>T866&lt;/sup> during metaphase. This counter-regulation allows for swi</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2026-04-08T18:44:25.077Z</modification><creation>2025-04-06T22:46:12.776Z</creation></dates><accession>S-EPMC11566010</accession><cross_references><pubmed>39553986</pubmed><doi>10.1101/2024.11.01.621564</doi></cross_references></HashMap>