F1000Research
F1000Research
5 years ago

From disease modelling to personalised therapy in patients with CEP290 mutations [version 1; referees: 2 approved]

Simon A. Ramsbottom, Elisa Molinari, John A. Sayer, Shalabh Srivastava
Mutations that give rise to premature termination codons are a common cause of inherited genetic diseases. When transcripts containing these changes are generated, they are usually rapidly removed by the cell through the process of nonsense-mediated decay. Here we discuss observed changes in transcripts of the centrosomal protein CEP290 resulting not from degradation, but from changes in exon usage. We also comment on a landmark paper (Drivas et al. Sci Transl Med. 2015) where modelling this process of exon usage may be used to predict disease severity in CEP290 ciliopathies, and how understanding this process may potentially be used for therapeutic benefit in the future.

Publisher URL: https://f1000research.com/articles/6-669/v1

DOI: 10.12688/f1000research.11553.1

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