[基于 HH 理论开发高特异性和高效率的 SpCas9 变体]。

G H Wang, C M Wang, X J Wu, T Chu, D W Huang, J Li
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引用次数: 0

摘要

化脓性链球菌Cas9(SpCas9)是基因编辑领域最流行的工具,然而,脱靶诱变是其应用的最大障碍之一。在之前的研究中,我们提出了 HH 理论,即 sgRNA/DNA 杂交(杂交)挤压引起的杂交与 REC3/HNH 之间疏水相互作用的增强是裂解启动的关键因素。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个SpCas9变体(V1-V8),利用数字液滴PCR技术评估了人体细胞中SpCas9诱导的DNA indels,并开发出了高保真变体。因此,HH 理论可用于进一步优化 SpCas9 介导的基因组编辑系统,由此产生的 V3、V6、V7 和 V8 SpCas9 变体可能对需要高精度基因组编辑的应用很有价值。
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[The Development of SpCas9 Variants with High Specificity and Efficiency Based on the HH Theory].

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.

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来源期刊
Molekulyarnaya Biologiya
Molekulyarnaya Biologiya Medicine-Medicine (all)
CiteScore
0.70
自引率
0.00%
发文量
131
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