| Literature DB >> 33247095 |
Yajing Liu1,2, Changyang Zhou2, Shisheng Huang1,3, Lu Dang4, Yu Wei2,3, Jun He1,3, Yingsi Zhou2, Shaoshuai Mao2, Wanyu Tao1,3, Yu Zhang1, Hui Yang5, Xingxu Huang6, Tian Chi7.
Abstract
DNA base editors, typically comprising editing enzymes fused to the N-terminus of nCas9, display off-target effects on DNA and/or RNA, which have remained an obstacle to their clinical applications. Off-target edits are typically countered via rationally designed point mutations, but the approach is tedious and not always effective. Here, we report that the off-target effects of both A > G and C > T editors can be dramatically reduced without compromising the on-target editing simply by inserting the editing enzymes into the middle of nCas9 at tolerant sites identified using a transposon-based genetic screen. Furthermore, employing this Cas-embedding strategy, we have created a highly specific editor capable of efficient C > T editing at methylated and GC-rich sequences.Entities:
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Year: 2020 PMID: 33247095 PMCID: PMC7695861 DOI: 10.1038/s41467-020-19690-0
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919