CRISPR-Cas9-mediated therapeutic editing ofameliorates the disease phenotypes in a mouse model of Leber congenital amaurosis.

Abstract

Leber congenital amaurosis (LCA), one of the leading causes of childhood-onset blindness, is caused by autosomal recessive mutations in several genes including. In this study, we performed CRISPR-Cas9-mediated therapeutic correction of a disease-associated nonsense mutation ininmice, a model of human LCA. Subretinal injection of adeno-associated virus carrying CRISPR-Cas9 and donor DNA resulted in >1% homology-directed repair and ~1.6% deletion of the pathogenic stop codon inin retinal pigment epithelial tissues ofmice. The a- and b-waves of electroretinograms were recovered to levels up to 21.2 ± 4.1% and 39.8 ± 3.2% of their wild-type mice counterparts upon bright stimuli after dark adaptation 7 months after injection. There was no definite evidence of histologic perturbation or tumorigenesis during 7 months of observation. Collectively, we present the first therapeutic correction of annonsense mutation using CRISPR-Cas9, providing new insight for developing therapeutics for LCA.