Acknowledgments This work was supported by grants from the Strategic Priority Research Program of Chinese Academy of Sciences (XDB11010500), the External Cooperation Program of BIC, Chinese Academy of Sciences (GJHZ201305) and the National Natural Science Foundation of China (31420103918 and 31372257).
Custom-designed nuclease technologies such as the clustered regularly in- terspaced short palindromic repeat (CRISPR)-associated (Cas) system provide attractive genome editing tools for insect functional genetics....