Sturme Mark H J, van der Berg Jan Pieter, Bouwman Lianne M S, De Schrijver Adinda, de Maagd Ruud A, Kleter Gijs A, Battaglia-de Wilde Evy
Wageningen Food Safety Research, Wageningen University and Research, P.O. Box 230, 6700 AE Wageningen, The Netherlands.
Sciensano, Rue Juliette Wytsmanstraat 14, 1050 Brussels, Belgium.
ACS Agric Sci Technol. 2022 Apr 18;2(2):192-201. doi: 10.1021/acsagscitech.1c00270. Epub 2022 Mar 3.
CRISPR-Cas-based genome editing allows for precise and targeted genetic modification of plants. Nevertheless, unintended off-target edits can arise that might confer risks when present in gene-edited food crops. Through an extensive literature review we gathered information on CRISPR-Cas off-target edits in plants. Most observed off-target changes were small insertions or deletions (1-22 bp) or nucleotide substitutions, and large deletions (>100 bp) were rare. One study detected the insertion of vector-derived DNA sequences, which is important considering the risk assessment of gene-edited plants. Off-target sites had few mismatches (1-3 nt) with the target sequence and were mainly located in protein-coding regions, often in target gene homologues. Off-targets edits were predominantly detected via biased analysis of predicted off-target sites instead of unbiased genome-wide analysis. CRISPR-Cas-edited plants showed lower off-target mutation frequencies than conventionally bred plants. This Review can aid discussions on the relevance of evaluating off-target modifications for risk assessment of CRISPR-Cas-edited plants.
基于CRISPR-Cas的基因组编辑可实现对植物进行精确且有针对性的基因改造。然而,可能会出现意外的脱靶编辑,当这些编辑出现在基因编辑的粮食作物中时可能会带来风险。通过广泛的文献综述,我们收集了有关植物中CRISPR-Cas脱靶编辑的信息。观察到的大多数脱靶变化是小的插入或缺失(1-22个碱基对)或核苷酸替换,大的缺失(>100个碱基对)很少见。一项研究检测到载体衍生DNA序列的插入,这对于基因编辑植物的风险评估很重要。脱靶位点与靶序列的错配很少(1-3个核苷酸),主要位于蛋白质编码区域,通常在靶基因的同源物中。脱靶编辑主要是通过对预测的脱靶位点进行有偏分析而非无偏的全基因组分析来检测的。与传统培育的植物相比,CRISPR-Cas编辑的植物显示出更低的脱靶突变频率。本综述有助于讨论评估脱靶修饰对于CRISPR-Cas编辑植物风险评估的相关性。