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Transcriptomic Insights into Post-Spawning Death and Muscle Atrophy in Ayu (Plecoglossus altivelis)
Jiancheng Liang1, Minoru Fujisawa1, Shogo Toma1
1Graduate School of Agricultural and Life Sciences, The University of Tokyo, Bunkyo 113-8657, Tokyo, Japan.
International Journal of Molecular Sciences
|January 25, 2025
Summary
Post-spawning ayu experience rapid muscle atrophy and metabolic dysfunction due to significant gene expression changes. Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) may drive accelerated aging and death in this semelparous species.
Area of Science:
- Molecular Biology
- Fish Physiology
- Genomics
Background:
- Semelparous species, such as ayu (Plecoglossus altivelis), exhibit post-spawning mortality.
- The molecular underpinnings of this rapid physiological decline and death are not well understood.
Purpose of the Study:
- To investigate transcriptomic alterations in ayu skeletal muscle before and after spawning.
- To identify key genes and pathways involved in post-spawning muscle atrophy and metabolic dysfunction.
Main Methods:
- RNA sequencing was employed to analyze gene expression profiles.
- Differential Gene Expression (DEG) analysis, Gene Set Enrichment Analysis (GSEA), KEGG pathway analysis, and Protein-Protein Interaction (PPI) network analysis were performed.
Main Results:
- Over 3000 differentially expressed genes (DEGs) were identified.
- Significant downregulation of energy metabolism and protein degradation pathways was observed.
- Post-spawning ayu showed decreased body weight, reduced myosin heavy chain gene expression, and signs of muscle atrophy.
- Decreased expression of AP-1 transcription factors and the identification of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as a key factor in muscle atrophy and aging were noted.
Conclusions:
- Ayu skeletal muscle undergoes severe metabolic disorders and cellular stress responses post-spawning.
- These molecular changes provide insights into the mechanisms driving post-spawning death in ayu.
- GAPDH may play a critical role in the accelerated aging and muscle atrophy observed.

