Base editors (BEs) are developed by combining different nucleotide deaminase family members, including cytidine deaminase family members (e.g., APOBECs) and adenosine deaminase family members (e.g., Adenosine deaminases acting on RNA, ADARs), with the CRISPR-Cas system (e.g., CRISPR/Cas9 and CRISPR/Cpf1).

Various BEs have been used for targeted C-to-T/A-to-G base editing in different species. While numerous human diseases have been reported to be driven by point mutations in genomic DNA, these disease-related point mutations can be potentially corrected with recently developed BEs, providing new therapeutic options.

A research team led by Dr. YANG Li at the CAS-MPG Partner Institute for Computational Biology of Chinese Academy of Sciences and Dr. CHEN Jia and Dr. HUANG Xingxu at ShanghaiTech University has developed a series of novel base editors based on a spectrum of cytidine deaminases from different species, including human apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like (APOBEC3A, hA3A) cytidine deaminase family members.

By analyzing disease-related T-to-C mutations that can be theoretically reverted to thymines by BEs, researchers found that ~ 43% of them are on cytosines in the context of CpG dinucleotides.

It is well known that C of CpG is usually methylated in mammalian cells, and methylation of C strongly suppresses cytidine deamination activity of some APOBEC/AID deaminases. Therefore, previously developed BEs that are based on rat APOBEC1 (rA1) cytidine deaminase are inefficient in editing cytosines in highly-methylated regions.

To develop BEs for efficient C-to-T base editing in highly methylated regions, researchers developed a series of BEs by fusing Cas9 nickase with a dozen of different APOBEC/AID deaminases, and then showed that most of them can be used for C-to-T base editing.

Importantly, a novel BE based on hA3A (hA3A-BE) and its engineered versions with narrower editing windows were found to mediate efficient C-to-T base editing in regions with high methylation levels and other examined regions with different contexts.

These newly developed hA3A-BEs can comprehensively induce efficient base editing in all examined contexts, including both methylated DNA regions and GpC dinucleotides.

The study was published online in Nature Biotechnology. It was supported by grants from the National Natural Science Foundation of China, Ministry of Science and Technology, Shanghai Municipal Science and Technology Commission, and ShanghaiTech University.