| Literature DB >> 30466729 |
Matías Montes1, Brianne L Sanford2, Daniel F Comiskey1, Dawn S Chandler3.
Abstract
Alternative splicing of pre-mRNA increases genetic diversity, and recent studies estimate that most human multiexon genes are alternatively spliced. If this process is not highly regulated and accurate, it leads to mis-splicing events, which may result in proteins with altered function. A growing body of work has implicated mis-splicing events in a range of diseases, including cancer, neurodegenerative diseases, and muscular dystrophies. Understanding the mechanisms that cause aberrant splicing events and how this leads to disease is vital for designing effective therapeutic strategies. In this review, we focus on advances in therapies targeting splicing, and highlight the animal models developed to recapitulate disease phenotypes as a model for testing these therapies.Entities:
Keywords: RNA splicing; animal models; disease
Mesh:
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Year: 2018 PMID: 30466729 PMCID: PMC6339821 DOI: 10.1016/j.tig.2018.10.002
Source DB: PubMed Journal: Trends Genet ISSN: 0168-9525 Impact factor: 11.639