Dual sgRNAs facilitate CRISPR/Cas9-mediated mouse genome targeting


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Abstract

The bacterial clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated 9 (Cas9) system is a versatile RNA-guided mammalian genome modification system. One-step generation of mouse genome targeting has been achieved by co-microinjection of one-cell stage embryos with Cas9 mRNA and small/single guide (sg)RNA. Many studies have focused on enhancing the efficiency of this system. In the present study, we report that simultaneous use of dual sgRNAs to target an individual gene significantly improved the Cas9-mediated genome targeting with a bi-allelic modification efficiency of up to 78%. We further observed that the target gene modifications were characterized by efficient germline transmission and site-dependent off-target effects, and also that the apolipoprotein E gene knockout-mediated defects in blood biochemical parameters were recapitulated by CRISPR/Cas9-mediated heritable gene modification. Our results provide a dual sgRNAs strategy to facilitate CRISPR/Cas9-mediated mouse genome targeting.Clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated 9 (Cas9) endonuclease, also known as an RNA-guided endonuclease (RGEN), is increasingly being used for eukaryote genome targeting; however, its efficiency, specificity and versatility needs to be optimized. In this issue, Zhou et al. report an improved method for CRISPR/Cas9-mediated gene targeting, and show that the simultaneous use of dual sgRNAs to target an individual mouse gene is a more efficient and specific method than using just a single sgRNA. This new dual sgRNAs strategy will facilitate CRISPR/Cas9-mediated mammalian genome targeting.

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