Cyclin F-EXO1 axis controls cell cycle-dependent execution of double-strand break repair.
Journal
Science advances
ISSN: 2375-2548
Titre abrégé: Sci Adv
Pays: United States
ID NLM: 101653440
Informations de publication
Date de publication:
09 Aug 2024
09 Aug 2024
Historique:
medline:
9
8
2024
pubmed:
9
8
2024
entrez:
9
8
2024
Statut:
ppublish
Résumé
Ubiquitination is a crucial posttranslational modification required for the proper repair of DNA double-strand breaks (DSBs) induced by ionizing radiation (IR). DSBs are mainly repaired through homologous recombination (HR) when template DNA is present and nonhomologous end joining (NHEJ) in its absence. In addition, microhomology-mediated end joining (MMEJ) and single-strand annealing (SSA) provide backup DSBs repair pathways. However, the mechanisms controlling their use remain poorly understood. By using a high-resolution CRISPR screen of the ubiquitin system after IR, we systematically uncover genes required for cell survival and elucidate a critical role of the E3 ubiquitin ligase SCF
Identifiants
pubmed: 39121215
doi: 10.1126/sciadv.ado0636
doi:
Substances chimiques
Exodeoxyribonucleases
EC 3.1.-
Cyclins
0
EXO1 protein, human
EC 3.1.-
DNA Repair Enzymes
EC 6.5.1.-
CCNF protein, human
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM