Comparison of Mutation Profiles in the Duchenne Muscular Dystrophy Gene among Populations: Implications for Potential Molecular Therapies
2015
Luz Berenice López-Hernández | Benjamín Gómez-Díaz | Alexandra Berenice Luna-Angulo | Mónica Anaya-Segura | David John Bunyan | Carolina Zúñiga-Guzman | Rosa Elena Escobar-Cedillo | Bladimir Roque-Ramírez | Luis Angel Ruano-Calderón | Héctor Rangel-Villalobos | Julia Angélica López-Hernández | Francisco Javier Estrada-Mena | Silvia García | Ramón Mauricio Coral-Vázquez
Novel therapeutic approaches are emerging to restore dystrophin function in Duchenne Muscular Dystrophy (DMD), a severe neuromuscular disease characterized by progressive muscle wasting and weakness. Some of the molecular therapies, such as exon skipping, stop codon read-through and internal ribosome entry site-mediated translation rely on the type and location of mutations. Hence, their potential applicability worldwide depends on mutation frequencies within populations. In view of this, we compared the mutation profiles of the populations represented in the DMD Leiden Open-source Variation Database with original data from Mexican patients (n = 162) with clinical diagnosis of the disease. Our data confirm that applicability of exon 51 is high in most populations, but also show that differences in theoretical applicability of exon skipping may exist among populations; Mexico has the highest frequency of potential candidates for the skipping of exons 44 and 46, which is different from other populations (p < 0.001). To our knowledge, this is the first comprehensive comparison of theoretical applicability of exon skipping targets among specific populations.
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