2022
PARG and BRCA1-BARD1 cooperative function regulates DNA repair pathway choice during gametogenesis
TRIVEDI, Shalini, Jitka BLAŽÍČKOVÁ a Nicola SILVAZákladní údaje
Originální název
PARG and BRCA1-BARD1 cooperative function regulates DNA repair pathway choice during gametogenesis
Autoři
TRIVEDI, Shalini (356 Indie, domácí), Jitka BLAŽÍČKOVÁ (203 Česká republika, domácí) a Nicola SILVA (380 Itálie, garant, domácí)
Vydání
Nucleic acids research, Oxford, Oxford University Press, 2022, 0305-1048
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10608 Biochemistry and molecular biology
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 14.900
Kód RIV
RIV/00216224:14110/22:00128165
Organizační jednotka
Lékařská fakulta
UT WoS
000894104000001
Klíčová slova anglicky
PARG; BRCA1–BARD1; DNA repair pathway choice; gametogenesis
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 29. 8. 2024 23:16, Mgr. Michal Petr
Anotace
V originále
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.
Návaznosti
GA20-08819S, projekt VaV |
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LM2018129, projekt VaV |
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