Removal of TREX1 activity enhances CRISPR–Cas9-mediated homologous recombination

CRISPR-Cas9-mediated homology-directed repair (HDR) can introduce desired mutations at targeted genomic sites, but achieving high efficiencies is a major hurdle in many cell types, including cells deficient in DNA repair activity. In this study, we used genome-wide screening in Fanconi anemia patient lymphoblastic cell lines to uncover suppressors of CRISPR-Cas9-mediated HDR. We found that a single exonuclease, TREX1, reduces HDR efficiency when the repair template is a single-stranded or linearized double-stranded DNA. TREX1 expression serves as a biomarker for CRISPR-Cas9-mediated HDR in that the high TREX1 expression present in many different cell types (such as U2OS, Jurkat, MDA-MB-231 and primary T cells as well as hematopoietic stem and progenitor cells) predicts poor HDR. Here we demonstrate rescue of HDR efficiency (ranging from two-fold to eight-fold improvement) either by TREX1 knockout or by the use of single-stranded DNA templates chemically protected from TREX1 activity. Our data explain why some cell types are easier to edit than others and indicate routes for increasing CRISPR-Cas9-mediated HDR in TREX1-expressing contexts.

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Publication Details

Journal
Nature Biotechnology
Published
2024-08-12
DOI
https://doi.org/10.1038/s41587-024-02356-3
Citations
21
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
4.91

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article

Removal of TREX1 activity enhances CRISPR–Cas9-mediated homologous recombination

Mehmet E. Karasu, Grégoire Cullot, Eléonore Toufektchan, Yanyang Chen et al.
21 citations
Nature Biotechnology
CRISPR and Genetic Engineering
4.91
article

Removal of TREX1 activity enhances CRISPR–Cas9-mediated homologous recombination

Mehmet E. Karasu, Grégoire Cullot, Eléonore Toufektchan, Yanyang Chen, Jacob E. Corn, John Maciejowski, Alessandra Albertelli
article en
21 citations

Abstract

CRISPR-Cas9-mediated homology-directed repair (HDR) can introduce desired mutations at targeted genomic sites, but achieving high efficiencies is a major hurdle in many cell types, including cells deficient in DNA repair activity. In this study, we used genome-wide screening in Fanconi anemia patient lymphoblastic cell lines to uncover suppressors of CRISPR-Cas9-mediated HDR. We found that a single exonuclease, TREX1, reduces HDR efficiency when the repair template is a single-stranded or linearized double-stranded DNA. TREX1 expression serves as a biomarker for CRISPR-Cas9-mediated HDR in that the high TREX1 expression present in many different cell types (such as U2OS, Jurkat, MDA-MB-231 and primary T cells as well as hematopoietic stem and progenitor cells) predicts poor HDR. Here we demonstrate rescue of HDR efficiency (ranging from two-fold to eight-fold improvement) either by TREX1 knockout or by the use of single-stranded DNA templates chemically protected from TREX1 activity. Our data explain why some cell types are easier to edit than others and indicate routes for increasing CRISPR-Cas9-mediated HDR in TREX1-expressing contexts.

Nature BiotechnologyVol. 43(7)
Memorial Sloan Kettering Cancer Center (US), ETH Zurich (CH)
National Science Foundation, European Commission, Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, Eidgenössische Technische Hochschule Zürich, NOMIS Stiftung, Functional Genomics Center Zurich, National Cancer Institute
No poverty
Openalex Percentile: Top 4%
CRISPR and Genetic Engineering
4.91
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