<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Nago M</submitter><funding>Japan Society for the Promotion of Science</funding><pagination>e12622</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11751902</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(1)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>This study aimed to investigate the molecular mechanisms associated with chromosome segregation errors caused by intrinsic oxidative stress during in vitro oocyte maturation (IVM) using oocytes from &lt;i>Sod1&lt;/i>-deficient (&lt;i>Sod1&lt;/i>KO) mice.&lt;h4>Methods&lt;/h4>Ovulated or in vitro matured cumulus-cells oocyte complexes (COCs) were collected from wild-type (WT) and &lt;i>Sod1&lt;/i>KO mice and evaluated chromosome alignment, chromosome segregation, meiotic progression, and BUBR1 and REC8 protein expression levels.&lt;h4>Results&lt;/h4>In 21% O&lt;sub>2&lt;/sub> IVM, the &lt;i>Sod1&lt;/i>KO had significantly higher frequencies of chromosome misalignment and segregation errors compared to the WT, and they also reached Germinal Vesicle Break Down (GVBD) and M I stages peak earlier and showed a shorter M </pubmed_abstract><journal>Reproductive medicine and biology</journal><pubmed_title>&lt;i>Sod1&lt;/i> deficiency in mouse oocytes during in vitro maturation increases chromosome segregation errors with a reduced BUBR1 at kinetochore.</pubmed_title><pmcid>PMC11751902</pmcid><funding_grant_id>24580405</funding_grant_id><funding_grant_id>21580342</funding_grant_id><pubmed_authors>Ishii M</pubmed_authors><pubmed_authors>Odajima K</pubmed_authors><pubmed_authors>Yanai M</pubmed_authors><pubmed_authors>Nago M</pubmed_authors><pubmed_authors>Sato Y</pubmed_authors><pubmed_authors>Kimura N</pubmed_authors></additional><is_claimable>false</is_claimable><name>&lt;i>Sod1&lt;/i> deficiency in mouse oocytes during in vitro maturation increases chromosome segregation errors with a reduced BUBR1 at kinetochore.</name><description>&lt;h4>Purpose&lt;/h4>This study aimed to investigate the molecular mechanisms associated with chromosome segregation errors caused by intrinsic oxidative stress during in vitro oocyte maturation (IVM) using oocytes from &lt;i>Sod1&lt;/i>-deficient (&lt;i>Sod1&lt;/i>KO) mice.&lt;h4>Methods&lt;/h4>Ovulated or in vitro matured cumulus-cells oocyte complexes (COCs) were collected from wild-type (WT) and &lt;i>Sod1&lt;/i>KO mice and evaluated chromosome alignment, chromosome segregation, meiotic progression, and BUBR1 and REC8 protein expression levels.&lt;h4>Results&lt;/h4>In 21% O&lt;sub>2&lt;/sub> IVM, the &lt;i>Sod1&lt;/i>KO had significantly higher frequencies of chromosome misalignment and segregation errors compared to the WT, and they also reached Germinal Vesicle Break Down (GVBD) and M I stages peak earlier and showed a shorter M </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan-Dec</publication><modification>2026-06-12T05:17:44.049Z</modification><creation>2025-04-05T00:25:08.222Z</creation></dates><accession>S-EPMC11751902</accession><cross_references><pubmed>39845481</pubmed><doi>10.1002/rmb2.12622</doi></cross_references></HashMap>