NatureMolecular BiologyPeer-reviewed journal article
In vivo CRISPR-Cas gene editing with no detectable genome-wide off-target mutations
Pınar AkçakayaiD, Maggie L. Bobbin, Jimmy A. GuoiD, Jose Malagon-Lopez, Kendell ClementiD, Sara P. GarciaiD, Mick D. FellowsiD, Michelle J. PorrittiD, Mike A. Firth, Alba CarrerasiD, Tania BaccegaiD, Frank SeeligeriD, Mikael BjurselliD, Shengdar Q. TsaiiD, Nathalie T. NguyeniD, Roberto NitschiD, Lorenz M. Mayr, Luca PinelloiD, Mohammad Bohlooly‐YiD, Martin J. AryeeiD, Marcello MarescaiD, J. Keith JoungiD
Abstract
CRISPR-Cas genome-editing nucleases hold substantial promise for human therapeutics1-5 but identifying unwanted off-target mutations remains an important requirement for clinical translation6, 7. For ex vivo therapeutic applications, previously published cell-based genome-wide methods provide potentially useful strategies to identify and quantify these off-target mutation sites8-12. However, a well-validated method that can reliably identify off-targets in vivo has not been described to date, leaving the question of whether and how frequently these types of mutations occur. Here we describe Verification of In Vivo Off-targets (VIVO), a highly sensitive, unbiased, and generalizable strategy that we show can robustly identify genome-wide CRISPR-Cas nuclease off-target effects in vivo. To our knowledge, these studies provide the first demonstration that CRISPR-Cas nucleases can induce substantial off-target mutations in vivo, a result we obtained using a deliberately promiscuous guide RNA (gRNA). More importantly, we used VIVO to show that appropriately designed gRNAs can direct efficient in vivo editing without inducing detectable off-target mutations. Our findings provide strong support for and should encourage further development of in vivo genome editing therapeutic strategies.
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- 322
- FWCI
- 18.76
- Field percentile
- top 1%
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