Wang G H, Wang C M, Wu X J, Chu T, Huang D W, Li J
School of Food and Biotechnology, Guangdong Industry Polytechnic, Guangzhou, 510300 China.
Department of Pharmacy, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 China.
Mol Biol (Mosk). 2024 Jan-Feb;58(1):157-159.
Streptococcus pyogenes Cas9 (SpCas9) is the most popular tool in gene editing; however, off-target mutagenesis is one of the biggest impediments in its application. In our previous study, we proposed the HH theory, which states that sgRNA/DNA hybrid (hybrid) extrusion-induced enhancement of hydrophobic interactions between the hybrid and REC3/HNH is a key factor in cleavage initiation. Based on the HH theory, we analyzed the interactions between the REC3 domain and hybrid and obtained 8 mutant sites. We designed 8 SpCas9 variants (V1-V8), used digital droplet PCR to assess SpCas9-induced DNA indels in human cells, and developed high-fidelity variants. Thus, the HH theory may be employed to further optimize SpCas9-mediated genome editing systems, and the resultant V3, V6, V7, and V8 SpCas9 variants may be valuable for applications requiring high-precision genome editing.
化脓性链球菌Cas9(SpCas9)是基因编辑中最常用的工具;然而,脱靶诱变是其应用中的最大障碍之一。在我们之前的研究中,我们提出了HH理论,该理论指出sgRNA/DNA杂交体(杂交体)挤出诱导杂交体与REC3/HNH之间疏水相互作用的增强是切割起始的关键因素。基于HH理论,我们分析了REC3结构域与杂交体之间的相互作用,并获得了8个突变位点。我们设计了8种SpCas9变体(V1-V8),使用数字液滴PCR评估SpCas9在人类细胞中诱导的DNA插入缺失,并开发了高保真变体。因此,HH理论可用于进一步优化SpCas9介导的基因组编辑系统,所得的V3、V6、V7和V8 SpCas9变体可能对需要高精度基因组编辑的应用有价值。