<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang X</submitter><funding>Eunice Kennedy Shriver National Institute of Child Health and Human Development</funding><funding>NICHD NIH HHS</funding><funding>University of Georgia</funding><funding>National Science Foundation</funding><pagination>jcs256297</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8325960</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>134(14)</volume><pubmed_abstract>Oocyte-specific knockdown of pericentrin (PCNT) in transgenic (Tg) mice disrupts acentriolar microtubule-organizing center (aMTOC) formation, leading to spindle instability and error-prone meiotic division. Here, we show that PCNT-depleted oocytes lack phosphorylated Aurora A (pAURKA) at spindle poles, while overall levels are unaltered. To test aMTOC-associated AURKA function, metaphase II (MII) control (WT) and Tg oocytes were briefly exposed to a specific AURKA inhibitor (MLN8237). Similar defects were observed in Tg and MLN8237-treated WT oocytes, including altered spindle structure, increased chromosome misalignment and impaired microtubule regrowth. Yet, AURKA inhibition had a limited effect on Tg oocytes, revealing a critical role for aMTOC-associated AURKA in regulating spindle sta</pubmed_abstract><journal>Journal of cell science</journal><pubmed_title>Loss of acentriolar MTOCs disrupts spindle pole Aurora A and assembly of the liquid-like meiotic spindle domain in oocytes.</pubmed_title><pmcid>PMC8325960</pmcid><funding_grant_id>HD093383</funding_grant_id><funding_grant_id>HD092857</funding_grant_id><funding_grant_id>R56 HD093383</funding_grant_id><funding_grant_id>R03 HD092857</funding_grant_id><pubmed_authors>Baumann C</pubmed_authors><pubmed_authors>De La Fuente R</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Viveiros MM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Loss of acentriolar MTOCs disrupts spindle pole Aurora A and assembly of the liquid-like meiotic spindle domain in oocytes.</name><description>Oocyte-specific knockdown of pericentrin (PCNT) in transgenic (Tg) mice disrupts acentriolar microtubule-organizing center (aMTOC) formation, leading to spindle instability and error-prone meiotic division. Here, we show that PCNT-depleted oocytes lack phosphorylated Aurora A (pAURKA) at spindle poles, while overall levels are unaltered. To test aMTOC-associated AURKA function, metaphase II (MII) control (WT) and Tg oocytes were briefly exposed to a specific AURKA inhibitor (MLN8237). Similar defects were observed in Tg and MLN8237-treated WT oocytes, including altered spindle structure, increased chromosome misalignment and impaired microtubule regrowth. Yet, AURKA inhibition had a limited effect on Tg oocytes, revealing a critical role for aMTOC-associated AURKA in regulating spindle sta</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jul</publication><modification>2025-04-19T20:45:18.217Z</modification><creation>2025-02-19T00:25:42.004Z</creation></dates><accession>S-EPMC8325960</accession><cross_references><pubmed>34152366</pubmed><doi>10.1242/jcs.256297</doi></cross_references></HashMap>