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Dual base editor catalyzes both cytosine and adenine base conversions in human cells.
Nature Biotechnology ( IF 46.9 ) Pub Date : 2020-06-01 , DOI: 10.1038/s41587-020-0527-y
Xiaohui Zhang 1 , Biyun Zhu 1 , Liang Chen 1 , Ling Xie 1 , Weishi Yu 1, 2 , Ying Wang 3 , Linxi Li 1 , Shuming Yin 1 , Lei Yang 1 , Handan Hu 1 , Honghui Han 4 , Yongmei Li 1 , Liren Wang 1 , Geng Chen 1 , Xueyun Ma 1 , Hongquan Geng 5 , Wanfeng Huang 1 , Xiufeng Pang 1 , Zuozhen Yang 2 , Yuxuan Wu 1 , Stefan Siwko 6 , Ryo Kurita 7 , Yukio Nakamura 8 , Li Yang 3 , Mingyao Liu 1 , Dali Li 1
Affiliation  

Although base editors are useful tools for precise genome editing, current base editors can only convert either adenines or cytosines. We developed a dual adenine and cytosine base editor (A&C-BEmax) by fusing both deaminases with a Cas9 nickase to achieve C-to-T and A-to-G conversions at the same target site. Compared to single base editors, A&C-BEmax’s activity on adenines is slightly reduced, whereas activity on cytosines is higher and RNA off-target activity is substantially decreased.



中文翻译:

双碱基编辑器催化人体细胞中的胞嘧啶和腺嘌呤碱基转换。

尽管碱基编辑器是精确基因组编辑的有用工具,但当前的碱基编辑器只能转换腺嘌呤或胞嘧啶。我们通过将两种脱氨酶与 Cas9 切口酶融合,开发了双腺嘌呤和胞嘧啶碱基编辑器 (A&C-BEmax),以在同一靶位点实现 C 到 T 和 A 到 G 的转换。与单碱基编辑器相比,A&C-BEmax 对腺嘌呤的活性略有降低,而对胞嘧啶的活性较高,并且 RNA 脱靶活性大幅降低。

更新日期:2020-06-01
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