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• W4310943621 abstract "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 diakinesis nuclei, whose formation depends on spo-11 function. These factors undergo a similar yet independent loading in developing oocytes, consistent with operating in different pathways. Abrogation of KU- or Theta-mediated end joining elicits opposite effects in brc-1; parg-1 doubles, suggesting a profound impact in influencing DNA repair pathway choice by BRC-1-PARG-1. Importantly, lack of PARG-1 catalytic activity suppresses untimely accumulation of RAD-51 foci in brc-1 mutants but is only partially required for fertility. Our data show that BRC-1/BRD-1–PARG-1 joint function is essential for genome integrity in meiotic cells by regulating multiple DNA repair pathways." @default.
• W4310943621 created "2022-12-21" @default.
• W4310943621 creator A5011489871 @default.
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• W4310943621 date "2022-11-28" @default.
• W4310943621 modified "2023-09-29" @default.
• W4310943621 title "PARG and BRCA1–BARD1 cooperative function regulates DNA repair pathway choice during gametogenesis" @default.
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• W4310943621 doi "https://doi.org/10.1093/nar/gkac1153" @default.
• W4310943621 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36478097" @default.
• W4310943621 hasPublicationYear "2022" @default.
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