Generation and Analysis of Xenopus laevis Models of Retinal Degeneration Using CRISPR/Cas9.
Methods in molecular biology (Clifton, N.J.), 1834: 193-207 PMID 30324446 DOI 10.1007/978-1-4939-8669-9_14
Abstract
Xenopus laevis have proven to be a useful system for rapid generation and analysis of transgenic models of human retinal disease. However, experimental approaches in this system were limited by lack of a robust knockdown or knockout technology. Here we describe a protocol for generation of Cas9-edited X. laevis embryos. The technique introduces point mutations into the genome of X. laevis resulting in in-frame and out-of-frame insertions and deletions that allow modeling of both dominant and recessive human diseases and efficiently generates gene knockdown and knockout. Our techniques can produce high-frequency gene editing in X. laevis, permitting analysis in the F0 generation.