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ABSTRACT: Background
In gene therapy via genome editing, it is essential to precisely repair disease-associated gene sequences without introducing random mutations. However, achieving highly accurate genome editing remains challenging owing to the low efficiency of homology-directed repair (HDR)-mediated gene repair, which relies on template DNA. Therefore, if Cas9 mutants capable of enhancing HDR can be identified, they could enable more precise gene therapies.Method
In this research project, we developed a screening system that uses the acquisition of diphtheria toxin resistance as an indicator of HDR efficiency in human cells and EGFP disruption as an indicator of off-target effect.Results
By screening a library of SpCas9 variants with random mutations introduced into its
SUBMITTER: Matsumoto D
PROVIDER: S-EPMC12673799 | biostudies-literature | 2025 Dec
REPOSITORIES: biostudies-literature