Efficient Skipping of Single Exon Duplications in DMD Patient-Derived Cell Lines Using an Antisense Oligonucleotide Approach
| Autor: | Adeline Vulin, Nicolas Wein, Steve D. Wilton, Felecia Gumienny, Nianyuan Huang, Andrew R. Findlay, Kevin M. Flanigan |
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| Rok vydání: | 2017 |
| Předmět: |
0301 basic medicine
congenital hereditary and neonatal diseases and abnormalities Lineage (genetic) Duchenne muscular dystrophy Computational biology Cell Line Dystrophin 03 medical and health sciences Exon Gene Duplication Gene duplication medicine Humans Messenger RNA biology Exons Genetic Therapy Fibroblasts Oligonucleotides Antisense medicine.disease Exon skipping Muscular Dystrophy Duchenne 030104 developmental biology Neurology RNA splicing biology.protein Neurology (clinical) |
| Zdroj: | Journal of Neuromuscular Diseases. 4:199-207 |
| ISSN: | 2214-3602 2214-3599 |
| Popis: | Background:Exon skipping strategies in Duchenne muscular dystrophy (DMD) have largely been directed toward altering splicing of exons flanking out-of-frame deletions, with the goal of restoring an open mRNA reading frame that leads to production of an internally deleted but partially functional dystrophin protein. Objective:We sought to apply exon skipping to duplication mutations, assuming that the inherently limited efficiency of antisense oligonucleotide-induced exon skipping would more frequently skip a single copy of a duplicated exon, rather than both and result in significant amounts of wild-type DMD mRNA. Methods:We tested this hypothesis in fibroblast cell lines derived from patients with a variety of single or multiple exon duplications that have been modified to allow transdifferentiation into a myogenic lineage. Results:Using a variety of 2’O-methyl antisense oligonucleotides, significant skipping was induced for each duplication leading to a wild-type transcript as a major mRNA product. Conclusions:This study provides another proof of concept for the feasibility of therapeutic skipping in patients carrying exon duplications in order to express wild-type, full-length mRNA, although careful evaluation of the skipping efficiency should be performed as some exons are easier to skip than others. Such a personalized strategy is expected to be highly beneficial for this subset of DMD patients, compared to inducing expression of an internally-deleted dystrophin. |
| Databáze: | OpenAIRE |
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