<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pereira AL</submitter><funding>Wellcome Trust</funding><funding>PHS HHS</funding><funding>NIGMS NIH HHS</funding><pagination>4526-42</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC1635371</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(10)</volume><pubmed_abstract>CLASPs are widely conserved microtubule plus-end-tracking proteins with essential roles in the local regulation of microtubule dynamics. In yeast, Drosophila, and Xenopus, a single CLASP orthologue is present, which is required for mitotic spindle assembly by regulating microtubule dynamics at the kinetochore. In mammals, however, only CLASP1 has been directly implicated in cell division, despite the existence of a second paralogue, CLASP2, whose mitotic roles remain unknown. Here, we show that CLASP2 localization at kinetochores, centrosomes, and spindle throughout mitosis is remarkably similar to CLASP1, both showing fast microtubule-independent turnover rates. Strikingly, primary fibroblasts from Clasp2 knockout mice show numerous spindle and chromosome segregation defects that can be p</pubmed_abstract><journal>Molecular biology of the cell</journal><pubmed_title>Mammalian CLASP1 and CLASP2 cooperate to ensure mitotic fidelity by regulating spindle and kinetochore function.</pubmed_title><pmcid>PMC1635371</pmcid><funding_grant_id>073915</funding_grant_id><funding_grant_id>R37 GM040198-22</funding_grant_id><funding_grant_id>GMS 40198</funding_grant_id><funding_grant_id>R37 GM040198</funding_grant_id><pubmed_authors>Stepanova T</pubmed_authors><pubmed_authors>Hergert PJ</pubmed_authors><pubmed_authors>Rieder CL</pubmed_authors><pubmed_authors>Galjart N</pubmed_authors><pubmed_authors>Sayas CL</pubmed_authors><pubmed_authors>Earnshaw WC</pubmed_authors><pubmed_authors>Duque C</pubmed_authors><pubmed_authors>Drabek K</pubmed_authors><pubmed_authors>Matos I</pubmed_authors><pubmed_authors>Pereira AL</pubmed_authors><pubmed_authors>Lince-Faria M</pubmed_authors><pubmed_authors>Pereira AJ</pubmed_authors><pubmed_authors>Maiato H</pubmed_authors><pubmed_authors>Maia AR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mammalian CLASP1 and CLASP2 cooperate to ensure mitotic fidelity by regulating spindle and kinetochore function.</name><description>CLASPs are widely conserved microtubule plus-end-tracking proteins with essential roles in the local regulation of microtubule dynamics. In yeast, Drosophila, and Xenopus, a single CLASP orthologue is present, which is required for mitotic spindle assembly by regulating microtubule dynamics at the kinetochore. In mammals, however, only CLASP1 has been directly implicated in cell division, despite the existence of a second paralogue, CLASP2, whose mitotic roles remain unknown. Here, we show that CLASP2 localization at kinetochores, centrosomes, and spindle throughout mitosis is remarkably similar to CLASP1, both showing fast microtubule-independent turnover rates. Strikingly, primary fibroblasts from Clasp2 knockout mice show numerous spindle and chromosome segregation defects that can be p</description><dates><release>2006-01-01T00:00:00Z</release><publication>2006 Oct</publication><modification>2025-04-04T13:41:02.32Z</modification><creation>2019-03-27T01:46:13Z</creation></dates><accession>S-EPMC1635371</accession><cross_references><pubmed>16914514</pubmed><doi>10.1091/mbc.e06-07-0579</doi><doi>10.1091/mbc.E06-07-0579</doi></cross_references></HashMap>