Cas9-induced large deletions and small indels are controlled in a convergent fashion

Michael Kosicki, Felicity Allen, Frances Steward, Kärt Tomberg, Yangyang Pan and Allan Bradley ()
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Michael Kosicki: Lawrence Berkeley National Lab
Felicity Allen: Wellcome Sanger Institute
Frances Steward: Department of Medicine, University of Cambridge
Kärt Tomberg: Department of Medicine, University of Cambridge
Yangyang Pan: Department of Medicine, University of Cambridge
Allan Bradley: Department of Medicine, University of Cambridge

Nature Communications, 2022, vol. 13, issue 1, 1-11

Abstract: Abstract Repair of Cas9-induced double-stranded breaks results primarily in formation of small insertions and deletions (indels), but can also cause potentially harmful large deletions. While mechanisms leading to the creation of small indels are relatively well understood, very little is known about the origins of large deletions. Using a library of clonal NGS-validated mouse embryonic stem cells deficient for 32 DNA repair genes, we have shown that large deletion frequency increases in cells impaired for non-homologous end joining and decreases in cells deficient for the central resection gene Nbn and the microhomology-mediated end joining gene Polq. Across deficient clones, increase in large deletion frequency was closely correlated with the increase in the extent of microhomology and the size of small indels, implying a continuity of repair processes across different genomic scales. Furthermore, by targeting diverse genomic sites, we identified examples of repair processes that were highly locus-specific, discovering a role for exonuclease Trex1. Finally, we present evidence that indel sizes increase with the overall efficiency of Cas9 mutagenesis. These findings may have impact on both basic research and clinical use of CRISPR-Cas9, in particular in conjunction with repair pathway modulation.

Date: 2022
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DOI: 10.1038/s41467-022-30480-8

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