The CST complex mediates a post-resection non-homologous end joining repair pathway and promotes local deletions in Saccharomyces cerevisiae
Year: 2025
Type: article
Abstract: The repair of a DNA double-strand break (DSB) by non-homologous end joining (NHEJ) generally leaves an intact or minimally modified sequence. Resection exposes single-stranded DNA and directs repair toward homology-dependent pathways and away from NHEJ. Here, we report that in Saccharomyces cerevisiae, the Cdc13/Stn1/Ten1 (CST) complex, characterized for its telomeric functions, acts after resection initiation to mediate a back-up NHEJ repair. We found a CST-specific mutation signature after repair characterized by deletions of 5-85 bp that were mostly dependent on NHEJ, with a subset dependent on microhomology-mediated end joining (MMEJ). The interaction between CST and Polα-primase is critical for these intermediate-size deletions, suggesting a role for fill-in synthesis, thus limiting extensive resection, which would otherwise lead to MMEJ-dependent deletions of several kilobases. Collectively, these results depict a complex picture of repair pathway choice where CST facilitates post-resection NHEJ repair, promoting local deletions but guarding against larger and potentially more deleterious deletions and rearrangements.
Source: Cell Genomics
Institutions: Centre National de la Recherche Scientifique, Sorbonne Université, Biologie Computationnelle, Quantitative et Synthétique, Institut de Biologie Paris-Seine, Inserm, Université Paris Cité, Commissariat à l'Énergie Atomique et aux Énergies Alternatives, Stabilité Génétique, Cellules Souches et Radiations, Institut Pasteur, Department of Genomes & Genetics
Language: English
Topic: DNA Repair Mechanisms
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $8,900
Funders: Intercollegiate Center for Management Science, Agence Nationale de la Recherche, Institut Pasteur, Fondation ARC pour la Recherche sur le Cancer, Ligue Contre le Cancer, Electricité de France, Sorbonne Université, Horizon 2020 Framework Programme, European Research Council, H2020 European Research Council, Institut du Cerveau et de la Moelle Epinière
OpenAlex ID: W4412478554
