PUBLICATION
Zebrafish genetic model of neuromuscular degeneration associated with Atrogin-1 expression
- Authors
- Menard, R., Morin, E., Morse, D., Halluin, C., Pende, M., Baanannou, A., Grendler, J., Fuqua, H., Li, J., Lancelot, L., Drent, J., Bonnet, F., Graber, J.H., Murawala, P., Dray, C., Pradère, J.P., Coffman, J.A., Madelaine, R.
- ID
- ZDB-PUB-260110-4
- Date
- 2026
- Source
- PLoS Genetics 22: e1012019e1012019 (Journal)
- Registered Authors
- Bonnet, Frederic, Coffman, James A., Grendler, Janelle, Madelaine, Romain, Menard, Romain, Pradere, Jean-Philippe
- Keywords
- none
- Datasets
- GEO:GSE274353
- MeSH Terms
-
- Aging/genetics
- Aging/pathology
- Animals
- Animals, Genetically Modified
- Disease Models, Animal
- Larva/genetics
- Muscle Fibers, Skeletal/metabolism
- Muscle Fibers, Skeletal/pathology
- Muscle Proteins*/genetics
- Muscle Proteins*/metabolism
- Muscle, Skeletal/metabolism
- Muscle, Skeletal/pathology
- Muscular Atrophy*/genetics
- Muscular Atrophy*/pathology
- SKP Cullin F-Box Protein Ligases*/genetics
- SKP Cullin F-Box Protein Ligases*/metabolism
- Sarcopenia*/genetics
- Sarcopenia*/pathology
- Zebrafish*/genetics
- Zebrafish Proteins*/genetics
- Zebrafish Proteins*/metabolism
- PubMed
- 41511973 Full text @ PLoS Genet.
Citation
Menard, R., Morin, E., Morse, D., Halluin, C., Pende, M., Baanannou, A., Grendler, J., Fuqua, H., Li, J., Lancelot, L., Drent, J., Bonnet, F., Graber, J.H., Murawala, P., Dray, C., Pradère, J.P., Coffman, J.A., Madelaine, R. (2026) Zebrafish genetic model of neuromuscular degeneration associated with Atrogin-1 expression. PLoS Genetics. 22:e1012019e1012019.
Abstract
The degenerative loss of muscle associated with aging leading to muscular atrophy is called sarcopenia. Currently, practicing regular physical exercise is the only efficient way to delay sarcopenia onset. Identification of therapeutic targets to alleviate the symptoms of aging requires in vivo model organisms of accelerated muscle degeneration and atrophy. The zebrafish undergoes aging, with hallmarks including mitochondrial dysfunction, telomere shortening, and accumulation of senescent cells. However, zebrafish age slowly, and no specific zebrafish models of accelerated muscle atrophy associated with molecular events of aging are currently available. We have developed a new genetic tool to efficiently accelerate muscle-fiber degeneration and muscle-tissue atrophy in zebrafish larvae and adults. We used a gain-of-function strategy with a molecule that has been shown to be necessary and sufficient to induce muscle atrophy and a sarcopenia phenotype in mammals: Atrogin-1 (also named Fbxo32). We report the generation, validation, and characterization of a zebrafish genetic model of accelerated neuromuscular atrophy, the atrofish. We demonstrated that Atrogin-1 expression specifically in skeletal muscle tissue induces a muscle atrophic phenotype associated with locomotion dysfunction in both larvae and adult fish. We identified degradation of the myosin light chain as an event occurring prior to muscle-fiber degeneration. Biological processes associated with muscle aging such as proteolysis, inflammation, stress response, extracellular matrix (ECM) remodeling, and apoptosis are upregulated in the atrofish. Surprisingly, we observed a strong correlation between muscle-fiber degeneration and reduced numbers of neuromuscular junctions in the peripheral nervous system, as well as neuronal cell bodies in the spinal cord, suggesting that muscle atrophy could underly a neurodegenerative phenotype in the central nervous system. Finally, while atrofish larvae can recover locomotive functions, adult atrofish have impaired regenerative capacities, as is observed in mammals during muscle aging. In the future, the atrofish could serve as a platform for testing molecules aimed at treating or alleviating the symptoms of muscle aging, thereby opening new therapeutic avenues in the fight against sarcopenia.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping