Cyclin F–EXO1 axis controls cell cycle–dependent execution of double-strand break repair

• Published in: Science advances Vol. 10; no. 32; p. eado0636
• Main Authors: Yang, Hongbin, Fouad, Shahd, Smith, Paul, Bae, Eun Young, Ji, Yu, Lan, Xinhui, Van Ess, Ava, Buffa, Francesca M., Fischer, Roman, Vendrell, Iolanda, Kessler, Benedikt M., D’Angiolella, Vincenzo
• Format: Journal Article
• Language: English
• Published: 09.08.2024
• ISSN: 2375-2548; 2375-2548
• DOI: 10.1126/sciadv.ado0636

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 cyclin F in cell cycle–dependent DSB repair. We show that SCF cyclin F –mediated EXO1 degradation prevents DNA end resection in mitosis, allowing MMEJ to take place. Moreover, we identify a conserved cyclin F recognition motif, distinct from the one used by other cyclins, with broad implications in cyclin specificity for cell cycle control. E3 ubiquitin ligase cyclin F induces degradation of EXO1 in mitosis for correct deployment of microhomology-mediated end joining.