{"title":"Low-fecundity <i>dhc-1; mel-28 C. elegans</i> mutants do not have gonad mitosis defects.","authors":"Julia Stobierska, Anita G Fernandez","doi":"10.17912/micropub.biology.001445","DOIUrl":null,"url":null,"abstract":"<p><p>In <i>C. elegans , dhc-1 ( or283 ); mel-28 ( t1684 )</i> double mutants have a severely reduced brood size compared with each single mutant and compared to the wild type. To determine if this synthetic low-fecundity phenotype is due to reduced potential to produce gametes, we studied gonad length and distal gonad mitotic activity in <i>dhc-1 ( or283 )</i> mutants, <i>mel-28 ( t1684 )</i> mutants, wild-type animals, and <i>dhc-1 ( or283 ); mel-28 ( t1684 )</i> double mutants. Gonad length in <i>dhc-1 ; mel-28</i> double mutants was the same as the wild type. Using an antibody against phosphorylated histone H3 (PH3), we tracked mitotic activity in mutant and wild-type gonads. We found no significant difference in mitotic activity between the double mutant and the wild-type. These observations suggest that the reduced brood size in <i>dhc-1 ; mel-28</i> double mutants is not caused by a mitotically-inactive gonad and instead has a different and yet-to-be-determined basis.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2025 ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11795300/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"microPublication biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17912/micropub.biology.001445","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
In C. elegans , dhc-1 ( or283 ); mel-28 ( t1684 ) double mutants have a severely reduced brood size compared with each single mutant and compared to the wild type. To determine if this synthetic low-fecundity phenotype is due to reduced potential to produce gametes, we studied gonad length and distal gonad mitotic activity in dhc-1 ( or283 ) mutants, mel-28 ( t1684 ) mutants, wild-type animals, and dhc-1 ( or283 ); mel-28 ( t1684 ) double mutants. Gonad length in dhc-1 ; mel-28 double mutants was the same as the wild type. Using an antibody against phosphorylated histone H3 (PH3), we tracked mitotic activity in mutant and wild-type gonads. We found no significant difference in mitotic activity between the double mutant and the wild-type. These observations suggest that the reduced brood size in dhc-1 ; mel-28 double mutants is not caused by a mitotically-inactive gonad and instead has a different and yet-to-be-determined basis.