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ResearchIn-Press PreviewGeneticsMuscle biology Open Access | 10.1172/jci.insight.204742

PPMO therapy for dysferlinopathy induces pseudoexon skipping and restoration of functional protein

James E. Gooding,1 Gyeongsu Park,2 Atish Wagh,2 Jonathan K. Watts,2 Janice A. Dominov,1 and Robert H. Brown1

1Department of Neurology, University of Massachusetts Chan Medical School, Worcester, United States of America

2RNA Therapeutics Institute, University of Massachusetts Chan Medical School, Worcester, United States of America

Find articles by Gooding, J. in: PubMed | Google Scholar

1Department of Neurology, University of Massachusetts Chan Medical School, Worcester, United States of America

2RNA Therapeutics Institute, University of Massachusetts Chan Medical School, Worcester, United States of America

Find articles by Park, G. in: PubMed | Google Scholar

1Department of Neurology, University of Massachusetts Chan Medical School, Worcester, United States of America

2RNA Therapeutics Institute, University of Massachusetts Chan Medical School, Worcester, United States of America

Find articles by Wagh, A. in: PubMed | Google Scholar

1Department of Neurology, University of Massachusetts Chan Medical School, Worcester, United States of America

2RNA Therapeutics Institute, University of Massachusetts Chan Medical School, Worcester, United States of America

Find articles by Watts, J. in: PubMed | Google Scholar

1Department of Neurology, University of Massachusetts Chan Medical School, Worcester, United States of America

2RNA Therapeutics Institute, University of Massachusetts Chan Medical School, Worcester, United States of America

Find articles by Dominov, J. in: PubMed | Google Scholar

1Department of Neurology, University of Massachusetts Chan Medical School, Worcester, United States of America

2RNA Therapeutics Institute, University of Massachusetts Chan Medical School, Worcester, United States of America

Find articles by Brown, R. in: PubMed | Google Scholar

Published July 14, 2026 - More info

JCI Insight. https://doi.org/10.1172/jci.insight.204742.
Copyright © 2026, Gooding et al. This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
Published July 14, 2026 - Version history
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Abstract

The dysferlinopathies are a spectrum of autosomal recessive muscle diseases caused by mutations in the dysferlin gene (DYSF) gene. Clinical manifestations vary from asymptomatic hyperCKemia to severe muscle pathology and loss of muscle function. These are designated limb-girdle muscular dystrophy type 2R or LGMDR2 (formerly LGMD2B or Miyoshi myopathy). Among other functions, dysferlin is crucial for plasma membrane repair and maintenance of intracellular calcium homeostasis. In previous studies, we identified in two independent point mutations deep within introns that cause aberrant DYSF mRNA splicing and the inclusion of pseudoexons within transcripts that disrupt protein expression. In this study, we generated and characterized a novel mouse model for one of these mutations (within DYSF intron 44). In these mice, a segment of human DYSF DNA containing the mutant intronic sequence flanked by surrounding human exon sequences replaces the normal homologous mouse DNA. These mice exhibit aberrant Dysf pre-mRNA splicing, pseudoexon inclusion, loss of DYSF protein expression, and muscle pathology similar to that observed in patients. Using this new model, we identified antisense oligonucleotides and then a PPMO that blocks the mouse Dysf pre-mRNA splicing complexes from binding the mutant pre-mRNA, thereby restoring nearly normal muscle histology and function.

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