Plant Genome. 2016 Nov;9(3). doi: 10.3835/plantgenome2016.05.0047.
The CRISPR-Cas9 system (clustered regularly interspaced short palindromic repeats with associated Cas9 protein) has been used to generate targeted changes for direct modification of endogenous genes in an increasing number of plant species; but development of plant genome editing has not yet fully considered potential off-target mismatches that may lead to unintended changes within the genome. Assessing the specificity of CRISPR-Cas9 for increasing editing efficiency as well as the potential for unanticipated downstream effects from off-target mutations is an important regulatory consideration for agricultural applications. Increasing genome-editing specificity entails developing improved design methods that better predict the prevalence of off-target mutations as a function of genome composition and design of the engineered ribonucleoprotein (RNP). Early results from CRISPR-Cas9 genome editing in plant systems indicate that the incidence of off-target mutation frequencies is quite low; however, by analyzing CRISPR-edited plant lines and improving both computational tools and reagent design, it may be possible to further decrease unanticipated effects at potential mismatch sites within the genome. This will provide assurance that CRISPR-Cas9 reagents can be designed and targeted with a high degree of specificity. Improved and experimentally validated design tools for discriminating target and potential off-target positions that incorporate consideration of the designed nuclease fidelity and selectivity will help to increase confidence for regulatory decision making for genome-edited plants.
CRISPR-Cas9 系统(成簇规律间隔短回文重复序列与相关 Cas9 蛋白)已被用于生成靶向变化,以直接修饰越来越多的植物物种的内源性基因;但是,植物基因组编辑的发展尚未充分考虑可能导致基因组内非预期变化的潜在脱靶错配。评估 CRISPR-Cas9 提高编辑效率的特异性以及脱靶突变的潜在意外下游效应,是农业应用的一个重要监管考虑因素。提高基因组编辑特异性需要开发改进的设计方法,这些方法可以更好地预测脱靶突变的流行程度,作为基因组组成和工程核糖核蛋白(RNP)设计的函数。植物系统中 CRISPR-Cas9 基因组编辑的早期结果表明,脱靶突变频率的发生率相当低;然而,通过分析 CRISPR 编辑的植物系和改进计算工具和试剂设计,有可能进一步降低基因组中潜在错配位点的意外影响。这将确保可以用高度特异性来设计和靶向 CRISPR-Cas9 试剂。用于区分靶标和潜在脱靶位置的改进和经过实验验证的设计工具,考虑了设计核酸酶的保真度和选择性,这将有助于提高对经过基因组编辑的植物的监管决策的信心。