<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Stubenvoll MD</submitter><funding>National Institutes of Health</funding><funding>NIGMS NIH HHS</funding><pagination>e1006370</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5045193</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(9)</volume><pubmed_abstract>Centrosomes are critical sites for orchestrating microtubule dynamics, and exhibit dynamic changes in size during the cell cycle. As cells progress to mitosis, centrosomes recruit more microtubules (MT) to form mitotic bipolar spindles that ensure proper chromosome segregation. We report a new role for ATX-2, a C. elegans ortholog of Human Ataxin-2, in regulating centrosome size and MT dynamics. ATX-2, an RNA-binding protein, forms a complex with SZY-20 in an RNA-independent fashion. Depleting ATX-2 results in embryonic lethality and cytokinesis failure, and restores centrosome duplication to zyg-1 mutants. In this pathway, SZY-20 promotes ATX-2 abundance, which inversely correlates with centrosome size. Centrosomes depleted of ATX-2 exhibit elevated levels of centrosome factors (ZYG-1, SP</pubmed_abstract><journal>PLoS genetics</journal><pubmed_title>ATX-2, the C. elegans Ortholog of Human Ataxin-2, Regulates Centrosome Size and Microtubule Dynamics.</pubmed_title><pmcid>PMC5045193</pmcid><funding_grant_id>7R15GM101633-02</funding_grant_id><funding_grant_id>R15 GM101633</funding_grant_id><pubmed_authors>Medley JC</pubmed_authors><pubmed_authors>Song MH</pubmed_authors><pubmed_authors>Stubenvoll MD</pubmed_authors><pubmed_authors>Irwin M</pubmed_authors></additional><is_claimable>false</is_claimable><name>ATX-2, the C. elegans Ortholog of Human Ataxin-2, Regulates Centrosome Size and Microtubule Dynamics.</name><description>Centrosomes are critical sites for orchestrating microtubule dynamics, and exhibit dynamic changes in size during the cell cycle. As cells progress to mitosis, centrosomes recruit more microtubules (MT) to form mitotic bipolar spindles that ensure proper chromosome segregation. We report a new role for ATX-2, a C. elegans ortholog of Human Ataxin-2, in regulating centrosome size and MT dynamics. ATX-2, an RNA-binding protein, forms a complex with SZY-20 in an RNA-independent fashion. Depleting ATX-2 results in embryonic lethality and cytokinesis failure, and restores centrosome duplication to zyg-1 mutants. In this pathway, SZY-20 promotes ATX-2 abundance, which inversely correlates with centrosome size. Centrosomes depleted of ATX-2 exhibit elevated levels of centrosome factors (ZYG-1, SP</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Sep</publication><modification>2025-04-18T18:36:48.263Z</modification><creation>2019-03-26T22:45:04Z</creation></dates><accession>S-EPMC5045193</accession><cross_references><pubmed>27689799</pubmed><doi>10.1371/journal.pgen.1006370</doi></cross_references></HashMap>