Efficient base editing in methylated regions with a human APOBEC3A-Cas9 fusion
- PMID: 30125268
- DOI: 10.1038/nbt.4198
Efficient base editing in methylated regions with a human APOBEC3A-Cas9 fusion
Abstract
Base editors (BEs) enable the generation of targeted single-nucleotide mutations, but currently used rat APOBEC1-based BEs are relatively inefficient in editing cytosines in highly methylated regions or in GpC contexts. By screening a variety of APOBEC and AID deaminases, we show that human APOBEC3A-conjugated BEs and versions we engineered to have narrower editing windows can mediate efficient C-to-T base editing in regions with high methylation levels and GpC dinucleotide content.
Comment in
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Better base editors.Nat Methods. 2018 Oct;15(10):763. doi: 10.1038/s41592-018-0154-4. Nat Methods. 2018. PMID: 30275576 No abstract available.
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