Guidelines for optimized gene knockout using CRISPR/Cas9
Claude Van Campenhout,
Pauline Cabochette,
Anne-Clémence Veillard,
Miklos Laczik,
Agnieszka Zelisko-Schmidt,
Céline Sabatel,
Maxime Dhainaut,
Benoit Vanhollebeke,
Cyril Gueydan,
Véronique Kruys
Affiliations
Claude Van Campenhout
1Diagenode, SA, Liège Science Park, 4102 Seraing, Belgium
Pauline Cabochette
2Laboratoire de Signalisation Neurovasculaire, Faculté des Sciences, Université libre de Bruxelles (ULB), 12 rue des Profs. Jeener et Brachet, 6041 Gosselies, Belgium
Anne-Clémence Veillard
1Diagenode, SA, Liège Science Park, 4102 Seraing, Belgium
Miklos Laczik
1Diagenode, SA, Liège Science Park, 4102 Seraing, Belgium
Agnieszka Zelisko-Schmidt
1Diagenode, SA, Liège Science Park, 4102 Seraing, Belgium
Céline Sabatel
1Diagenode, SA, Liège Science Park, 4102 Seraing, Belgium
Maxime Dhainaut
3Precision Immunology Institute, Department of Genetics & Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA
Benoit Vanhollebeke
2Laboratoire de Signalisation Neurovasculaire, Faculté des Sciences, Université libre de Bruxelles (ULB), 12 rue des Profs. Jeener et Brachet, 6041 Gosselies, Belgium
Cyril Gueydan
5Laboratoire de Biologie Moléculaire du Gène, Faculté des Sciences, Université libre de Bruxelles (ULB), 12 rue des Profs. Jeener et Brachet, 6041 Gosselies, Belgium
Véronique Kruys
5Laboratoire de Biologie Moléculaire du Gène, Faculté des Sciences, Université libre de Bruxelles (ULB), 12 rue des Profs. Jeener et Brachet, 6041 Gosselies, Belgium
CRISPR/Cas9 technology has evolved as the most powerful approach to generate genetic models both for fundamental and preclinical research. Despite its apparent simplicity, the outcome of a genome-editing experiment can be substantially impacted by technical parameters and biological considerations. Here, we present guidelines and tools to optimize CRISPR/Cas9 genome-targeting efficiency and specificity. The nature of the target locus, the design of the single guide RNA and the choice of the delivery method should all be carefully considered prior to a genome-editing experiment. Different methods can also be used to detect off-target cleavages and decrease the risk of unwanted mutations. Together, these optimized tools and proper controls are essential to the assessment of CRISPR/Cas9 genome-editing experiments.