Department of Chemistry, Hanyang University, Seoul, 04763, South Korea.
Research Institute for Convergence of Basic Sciences, Hanyang University, Seoul, 04763, South Korea.
Sci Rep. 2019 Mar 20;9(1):4939. doi: 10.1038/s41598-019-41356-1.
Molecular cloning is an essential technique in molecular biology and biochemistry, but it is frequently laborious when adequate restriction enzyme recognition sites are absent. Cas9 endonucleases can induce site-specific DNA double-strand breaks at sites homologous to their guide RNAs, rendering an alternative to restriction enzymes. Here, by combining DNA cleavage via a Cas9 endonuclease and DNA ligation via Gibson assembly, we demonstrate a precise and practical DNA cloning method for replacing part of a backbone plasmid. We first replaced a resistance marker gene as a proof of concept and next generated DNA plasmids that encode engineered Cas9 variants (VQR, VRER and SpCas9-NG), which target non-canonical NGA, NGCG and NG protospacer-adjacent motif (PAM) sequences, fused with adenosine deaminases for adenine base editing (named VQR-ABE, VRER-ABE and NG-ABE, respectively). Ultimately, we confirmed that the re-constructed plasmids can successfully convert adenosine to guanine at endogenous target sites containing the non-canonical NGA, NGCG and NG PAMs, expanding the targetable range of the adenine base editing.
分子克隆是分子生物学和生物化学中的一项基本技术,但当缺乏足够的限制性内切酶识别位点时,它通常很繁琐。Cas9 内切酶可以在与其向导 RNA 同源的位点诱导特异性 DNA 双链断裂,为限制性内切酶提供了一种替代方法。在这里,我们通过 Cas9 内切酶介导的 DNA 切割和 Gibson 组装介导的 DNA 连接相结合,展示了一种用于替换骨架质粒部分的精确而实用的 DNA 克隆方法。我们首先以替换抗性标记基因为概念验证,然后生成了编码工程化 Cas9 变体(VQR、VRER 和 SpCas9-NG)的 DNA 质粒,这些变体靶向非经典的 NGA、NGCG 和 NG 原间隔邻近基序 (PAM) 序列,并与腺苷脱氨酶融合用于腺嘌呤碱基编辑(分别命名为 VQR-ABE、VRER-ABE 和 NG-ABE)。最终,我们证实了重构的质粒可以在含有非经典 NGA、NGCG 和 NG PAMs 的内源性靶位点成功地将腺嘌呤转换为鸟嘌呤,从而扩展了腺嘌呤碱基编辑的靶向范围。