CRISPR/Cas9-mediated genome editing induces exon skipping by alternative splicing or exon deletion

Volume: 18, Issue: 1
Published: Jun 14, 2017
Abstract
CRISPR is widely used to disrupt gene function by inducing small insertions and deletions. Here, we show that some single-guide RNAs (sgRNAs) can induce exon skipping or large genomic deletions that delete exons. For example, CRISPR-mediated editing of β-catenin exon 3, which encodes an autoinhibitory domain, induces partial skipping of the in-frame exon and nuclear accumulation of β-catenin. A single sgRNA can induce small insertions or...
Paper Details
Title
CRISPR/Cas9-mediated genome editing induces exon skipping by alternative splicing or exon deletion
Published Date
Jun 14, 2017
Volume
18
Issue
1
Citation AnalysisPro
  • Scinapse’s Top 10 Citation Journals & Affiliations graph reveals the quality and authenticity of citations received by a paper.
  • Discover whether citations have been inflated due to self-citations, or if citations include institutional bias.