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[Preprint]. 2023 Feb 24:2023.02.24.529205. [Version 1] doi: 10.1101/2023.02.24.529205

EXO1-mediated DNA repair by single-strand annealing is essential for BRCA1-deficient cells

B van de Kooij, A Schreuder, RS Pavani, V Garzero, A Van Hoeck, M San Martin Alonso, D Koerse, TJ Wendel, E Callen, J Boom, H Mei, E Cuppen, A Nussenzweig, H van Attikum, SM Noordermeer
PMCID: PMC10503826  PMID: 37720033

Summary

Deficiency for the repair of DNA double-strand breaks (DSBs) via homologous recombination (HR) leads to chromosomal instability and diseases such as cancer. Yet, defective HR also results in vulnerabilities that can be exploited for targeted therapy. Here, we identify such a vulnerability and show that BRCA1-deficient cells are dependent on the long-range end-resection factor EXO1 for survival. EXO1 loss results in DNA replication-induced lesions decorated by poly(ADP-ribose)-chains. In cells that lack both BRCA1 and EXO1, this is accompanied by unresolved DSBs due to impaired single-strand annealing (SSA), a DSB repair process that requires the activity of both proteins. In contrast, BRCA2-deficient cells have increased SSA, also in the absence of EXO1, and hence are not dependent on EXO1 for survival. In agreement with our mechanistic data, BRCA1-mutated tumours have elevated EXO1 expression and contain more genomic signatures of SSA compared to BRCA1-proficient tumours. Collectively, our data indicate that EXO1 is a promising novel target for treatment of BRCA1-deficient tumours.

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