USH2A Gene Mutations in Rabbits Lead to Progressive Retinal Degeneration and Hearing Loss.

ABSTRACT:

Purpose

Mutations in USH2A gene are responsible for the greatest proportion of the Usher Syndrome (USH) population, among which more than 30% are frameshift mutations on exon 13. A clinically relevant animal model has been absent for USH2A-related vision loss. Here we sought to establish a rabbit model carrying USH2A frameshift mutation on exon 12 (human exon 13 equivalent).

Methods

CRISPR/Cas9 reagents targeting the rabbit USH2A exon 12 were delivered into rabbit embryos to produce an USH2A mutant rabbit line. The USH2A knockout animals were subjected to a series of functional and morphological analyses, including acoustic auditory brainstem responses, electroretinography, optical coherence tomography, fundus photography, fundus autofluorescence, histology, and immunohistoc

SUBMITTER: Nguyen VP 

PROVIDER: S-EPMC9940772 | biostudies-literature | 2023 Feb

REPOSITORIES: biostudies-literature