Cargando…
CRISPR-induced exon skipping is dependent on premature termination codon mutations
In previous studies, CRISPR/Cas9 was shown to induce unexpected exon skipping; however, the mechanism by which this phenomenon is triggered is controversial. By analyzing 22 gene-edited rabbit lines generated using CRISPR/Cas9, we provide evidence of exon skipping at high frequency in premature term...
Autores principales: | Sui, Tingting, Song, Yuning, Liu, Zhiquan, Chen, Mao, Deng, Jichao, Xu, Yuanyuan, Lai, Liangxue, Li, Zhanjun |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6193291/ https://www.ncbi.nlm.nih.gov/pubmed/30333044 http://dx.doi.org/10.1186/s13059-018-1532-z |
Ejemplares similares
-
LMNA-mutated Rabbits: A Model of Premature Aging Syndrome with Muscular Dystrophy and Dilated Cardiomyopathy
por: Sui, Tingting, et al.
Publicado: (2019) -
Functional validation of the albinism-associated tyrosinase T373K SNP by CRISPR/Cas9-mediated homology-directed repair (HDR) in rabbits
por: Song, Yuning, et al.
Publicado: (2018) -
CRISPR Start-Loss: A Novel and Practical Alternative for Gene Silencing through Base-Editing-Induced Start Codon Mutations
por: Chen, Siyu, et al.
Publicado: (2020) -
CRISPR/Cas9-mediated mutation of tyrosinase (Tyr) 3′ UTR induce graying in rabbit
por: Song, Yuning, et al.
Publicado: (2017) -
CRISPR/Cas9-mediated GJA8 knockout in rabbits recapitulates human congenital cataracts
por: Yuan, Lin, et al.
Publicado: (2016)