Diagenode, SA, Liège Science Park, 4102 Seraing, Belgium.
Laboratoire de Signalisation Neurovasculaire, Faculté des Sciences, Université libre de Bruxelles (ULB), 12 rue des Profs. Jeener et Brachet, 6041 Gosselies, Belgium.
Biotechniques. 2019 Jun;66(6):295-302. doi: 10.2144/btn-2018-0187. Epub 2019 May 1.
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.
CRISPR/Cas9 技术已发展成为生成遗传模型的最有力方法,无论是基础研究还是临床前研究。尽管它看起来很简单,但基因组编辑实验的结果可能会受到技术参数和生物学因素的实质性影响。在这里,我们提供了优化 CRISPR/Cas9 基因组靶向效率和特异性的指南和工具。在进行基因组编辑实验之前,应仔细考虑目标基因座的性质、单指导 RNA 的设计以及递送方法的选择。也可以使用不同的方法来检测脱靶切割并降低意外突变的风险。这些经过优化的工具和适当的对照对于评估 CRISPR/Cas9 基因组编辑实验至关重要。