<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Trivedi S</submitter><funding>Department of Biology of Masaryk University, Faculty of Medicine</funding><funding>Czech Science Foundation</funding><pubmed_abstract>Meiotic chromosome segregation relies on programmed DNA double-strand break induction. These are in turn repaired by homologous recombination, generating physical attachments between the parental chromosomes called crossovers. A subset of breaks yields recombinant outcomes, while crossover-independent mechanisms repair the majority of lesions. The balance between different repair pathways is crucial to ensure genome integrity. We show that Caenorhabditis elegans BRC-1/BRCA1-BRD-1/BARD1 and PARG-1/PARG form a complex in vivo, essential for accurate DNA repair in the germline. Simultaneous depletion of BRC-1 and PARG-1 causes synthetic lethality due to reduced crossover formation and impaired break repair, evidenced by hindered RPA-1 removal and presence of aberrant chromatin bodies in diaki</pubmed_abstract><journal>Nucleic acids research</journal><pagination>gkac1153</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9757042</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>PARG and BRCA1-BARD1 cooperative function regulates DNA repair pathway choice during gametogenesis.</pubmed_title><pmcid>PMC9757042</pmcid><funding_grant_id>GA20-08819S</funding_grant_id><pubmed_authors>Trivedi S</pubmed_authors><pubmed_authors>Blazickova J</pubmed_authors><pubmed_authors>Silva N</pubmed_authors></additional><is_claimable>false</is_claimable><name>PARG and BRCA1-BARD1 cooperative function regulates DNA repair pathway choice during gametogenesis.</name><description>Meiotic chromosome segregation relies on programmed DNA double-strand break induction. These are in turn repaired by homologous recombination, generating physical attachments between the parental chromosomes called crossovers. A subset of breaks yields recombinant outcomes, while crossover-independent mechanisms repair the majority of lesions. The balance between different repair pathways is crucial to ensure genome integrity. We show that Caenorhabditis elegans BRC-1/BRCA1-BRD-1/BARD1 and PARG-1/PARG form a complex in vivo, essential for accurate DNA repair in the germline. Simultaneous depletion of BRC-1 and PARG-1 causes synthetic lethality due to reduced crossover formation and impaired break repair, evidenced by hindered RPA-1 removal and presence of aberrant chromatin bodies in diaki</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-04T08:56:00.818Z</modification><creation>2025-04-04T08:56:00.818Z</creation></dates><accession>S-EPMC9757042</accession><cross_references><pubmed>36478097</pubmed><doi>10.1093/nar/gkac1153</doi></cross_references></HashMap>