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Generation of a more efficient prime editor 2 by addition of the Rad51 DNA-binding domain.

Myungjae SongJung Min LimSeonwoo MinJeong-Seok OhDong Young KimJae-Sung WooHiroshi NishimasuSung-Rae ChoSungroh YoonHyongbum Henry Kim
Published in: Nature communications (2021)
Although prime editing is a promising genome editing method, the efficiency of prime editor 2 (PE2) is often insufficient. Here we generate a more efficient variant of PE2, named hyPE2, by adding the Rad51 DNA-binding domain. When tested at endogenous sites, hyPE2 shows a median of 1.5- or 1.4- fold (range, 0.99- to 2.6-fold) higher efficiencies than PE2; furthermore, at sites where PE2-induced prime editing is very inefficient (efficiency < 1%), hyPE2 enables prime editing with efficiencies ranging from 1.1% to 2.9% at up to 34% of target sequences, potentially facilitating prime editing applications.
Keyphrases
  • crispr cas
  • genome editing
  • dna binding
  • transcription factor
  • dna damage
  • dna repair
  • oxidative stress
  • high glucose