Journal Article

Dystrophin myonuclear domain restoration governs treatment efficacy in dystrophic muscle

Stantzou, Amalia, Matouk, Meriem, Richard, Isabelle, Garcia, Luis, Morin, Adrien, Hildyard, John, Schuelke, Markus, Amthor, Helge, Petrova, Olga N., Goyenvalle, Aurélie, Falcone, Sestina, Piercy, Richard J., Tensorer, Thomas, Petkova, Mina V., Manoliu, Tudor, Laplace-Builhé, Corinne

2023

Overview

Dystrophin is essential for muscle health: its sarcolemmal absence causes the fatal, X-linked condition, Duchenne muscular dystrophy (DMD). However, its normal, spatial organization remains poorly understood, which hinders the interpretation of efficacy of its therapeutic restoration. Using female reporter mice heterozygous for fluorescently tagged dystrophin (DmdEGFP ), we here reveal that dystrophin distribution is unexpectedly compartmentalized, being restricted to myonuclear-defined sarcolemmal territories extending ~80 μm, which we called “basal sarcolemmal dystrophin units (BSDUs).” These territories were further specialized at myotendinous junctions, where both Dmd transcripts and dystrophin protein were enriched. Genome-level correction in X-linked muscular dystrophy mice via CRISPR/Cas9 gene editing restored a mosaic of separated dystrophin domains, whereas transcript-level Dmd correction, following treatment with tricyclo-DNA antisense oligonucleotides, restored dystrophin initially at junctions before extending along the entire fiber—with levels ~2% sufficient to moderate the dystrophic process. We conclude that widespread restoration of fiber dystrophin is likely critical for therapeutic success in DMD, perhaps most importantly, at muscle–tendon junctions.

• Publisher: National Academy of Sciences
• Subject: Animals / Antisense DNA / Antisense oligonucleotides / Biological Sciences / Cell Biology / CRISPR / Disease Models, Animal / Domains / Duchenne's muscular dystrophy / Dystrophin / Dystrophin - genetics / Dystrophin - metabolism / Dystrophy / Effectiveness / Female / Gene Editing / Genetic modification / Genomes / Life Sciences / Mice / Mice, Inbred mdx / Muscle, Skeletal - metabolism / Muscles / Muscles - metabolism / Muscular dystrophy / Muscular Dystrophy, Duchenne - genetics / Muscular Dystrophy, Duchenne - metabolism / Muscular Dystrophy, Duchenne - therapy / Oligonucleotides / Restoration / Treatment Outcome