“…With CRISPR-Cas-assisted accurate cleavage in target DNA sequences and thus introducing double-stranded DNA (dsDNA) breaks (DSBs), the genome engineering efficiency can be greatly improved. Up to date, both the type II Cas9 system and type V Cas12a system have been widely applied in genome editing in a large number of species ( Cong et al, 2013 ; Jiang et al, 2014 , 2015 ; Cobb et al, 2015 ; Huang et al, 2015 ; Matsu-Ura et al, 2015 ; Low et al, 2016 ; Jia et al, 2017 ; Harrison and Hart, 2018 ; Hu et al, 2019 ). Compared to Cas9, Cas12a has several distinct features, including the preference of T-rich PAM sequences and the staggered cleavage pattern against target dsDNA ( Zetsche et al, 2015 ; Yamano et al, 2016 ).…”