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Exon skipping as a therapeutic strategy applied to an RYR1 mutation with pseudo-exon inclusion causing a severe core myopathy.

John Rendu 1 Julie Brocard 2 Eric Denarier 3, 4 Nicole Monnier 3, 5 France Piétri-Rouxel 6 Cyriaque Beley 6 Nathalie Roux-Buisson 3, 5 Brigitte Gilbert-Dussardier 7 Marie José Perez 8 Norma Romero 6, 9 Luis Garcia 6 Joël Lunardi 10 Julien Fauré 1 Anne Fourest-Lieuvin 11 Isabelle Marty 2, *
* Corresponding author
1 INSERM U836, équipe 4, Muscles et pathologies
GIN - Grenoble Institut des Neurosciences, Biochimie Génétique et Moléculaire
2 INSERM U836, équipe 4, Muscles et pathologies
GIN - Grenoble Institut des Neurosciences
3 GIN - Grenoble Institut des Neurosciences
4 GPC - Groupe Physiopathologie du Cytosquelette
5 Biochimie Génétique et Moléculaire
6 Thérapie des maladies du muscle strié
7 Génétique Médicale
8 Foetopathologie
9 Institut de Myologie
10 INSERM U836, équipe 1, Physiopathologie du cytosquelette
GIN - Grenoble Institut des Neurosciences, Biochimie Génétique et Moléculaire
11 ANTE-INSERM U836, équipe 13, Régulation dynamique et structurale du cytosquelette
GPC - Groupe Physiopathologie du Cytosquelette, GIN - Grenoble Institut des Neurosciences
Abstract : Central core disease is a myopathy often arising from mutations in the type 1 ryanodine receptor (RYR1) gene, encoding the sarcoplasmic reticulum calcium release channel RyR1. No treatment is currently available for this disease. We studied the pathological situation of a severely affected child with two recessive mutations, which resulted in a massive reduction in the amount of RyR1. The paternal mutation induced the inclusion of a new in-frame pseudo-exon in RyR1 mRNA that resulted in the insertion of additional amino acids leading to the instability of the protein. We hypothesized that skipping this additional exon would be sufficient to restore RyR1 expression and to normalize calcium releases. We therefore developed U7-AON lentiviral vectors to force exon skipping on affected primary muscle cells. The efficiency of the exon skipping was evaluated at the mRNA level, at the protein level, and at the functional level using calcium imaging. In these affected cells, we observed a decreased inclusion of the pseudo-exon, an increased RyR1 protein expression, and a restoration of calcium releases of normal amplitude either upon direct RyR1 stimulation or in response to membrane depolarization. This study is the first demonstration of the potential of exon-skipping strategy for the therapy of central core disease, from the molecular to the functional level.
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https://www.hal.inserm.fr/inserm-00904818
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Submitted on : Friday, November 15, 2013 - 11:56:24 AM
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CEA | CNRS | UGA | U836 | UPMC | U974 | SORBONNE-UNIVERSITE | SU-MEDECINE | IRIG | CEA-GRE

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John Rendu, Julie Brocard, Eric Denarier, Nicole Monnier, France Piétri-Rouxel, et al.. Exon skipping as a therapeutic strategy applied to an RYR1 mutation with pseudo-exon inclusion causing a severe core myopathy.. Human Gene Therapy, Mary Ann Liebert, 2013, 24 (7), pp.702-13. ⟨10.1089/hum.2013.052⟩. ⟨inserm-00904818⟩

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