<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ali A</submitter><funding>Human Frontier Science Program (HFSP)</funding><pagination>289</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9879976</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(1)</volume><pubmed_abstract>Organization of microtubule arrays requires spatio-temporal regulation of the microtubule nucleator γ-tubulin ring complex (γTuRC) at microtubule organizing centers (MTOCs). MTOC-localized adapter proteins are thought to recruit and activate γTuRC, but the molecular underpinnings remain obscure. Here we show that at interphase centrosomes, rather than adapters, the microtubule polymerase ch-TOG (also named chTOG or CKAP5) ultimately controls γTuRC recruitment and activation. ch-TOG co-assembles with γTuRC to stimulate nucleation around centrioles. In the absence of ch-TOG, γTuRC fails to localize to these sites, but not the centriole lumen. However, whereas some ch-TOG is stably bound at subdistal appendages, it only transiently associates with PCM. ch-TOG's dynamic behavior requires its tubulin-binding TOG domains and a C-terminal region involved in localization. In addition, ch-TOG also promotes nucleation from the Golgi. Thus, at interphase centrosomes stimulation of nucleation and γTuRC attachment are mechanistically coupled through transient recruitment of ch-TOG, and ch-TOG's nucleation-promoting activity is not restricted to centrosomes.</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Microtubule nucleation and γTuRC centrosome localization in interphase cells require ch-TOG.</pubmed_title><pmcid>PMC9879976</pmcid><funding_grant_id>LT000181/2018-L</funding_grant_id><pubmed_authors>Vineethakumari C</pubmed_authors><pubmed_authors>Lacasa C</pubmed_authors><pubmed_authors>Ali A</pubmed_authors><pubmed_authors>Luders J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Microtubule nucleation and γTuRC centrosome localization in interphase cells require ch-TOG.</name><description>Organization of microtubule arrays requires spatio-temporal regulation of the microtubule nucleator γ-tubulin ring complex (γTuRC) at microtubule organizing centers (MTOCs). MTOC-localized adapter proteins are thought to recruit and activate γTuRC, but the molecular underpinnings remain obscure. Here we show that at interphase centrosomes, rather than adapters, the microtubule polymerase ch-TOG (also named chTOG or CKAP5) ultimately controls γTuRC recruitment and activation. ch-TOG co-assembles with γTuRC to stimulate nucleation around centrioles. In the absence of ch-TOG, γTuRC fails to localize to these sites, but not the centriole lumen. However, whereas some ch-TOG is stably bound at subdistal appendages, it only transiently associates with PCM. ch-TOG's dynamic behavior requires its tubulin-binding TOG domains and a C-terminal region involved in localization. In addition, ch-TOG also promotes nucleation from the Golgi. Thus, at interphase centrosomes stimulation of nucleation and γTuRC attachment are mechanistically coupled through transient recruitment of ch-TOG, and ch-TOG's nucleation-promoting activity is not restricted to centrosomes.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-04T20:35:37.414Z</modification><creation>2025-04-04T20:35:37.414Z</creation></dates><accession>S-EPMC9879976</accession><cross_references><pubmed>36702836</pubmed><doi>10.1038/s41467-023-35955-w</doi></cross_references></HashMap>