Up- and Downregulated Genes after Long-Term Muscle Atrophy Induced by Denervation in Mice Detected Using RNA-Seq.
Shoko SawanoMisaki FukushimaTaiki AkasakaMako NakamuraRyuichi TatsumiYoshihide IkeuchiWataru MizunoyaPublished in: Life (Basel, Switzerland) (2023)
Skeletal muscle atrophy occurs rapidly as a result of inactivity. Although there are many reports on changes in gene expression during the early phase of muscle atrophy, the patterns of up-and downregulated gene expression after long-term and equilibrated muscle atrophy are poorly understood. In this study, we comprehensively examined the changes in gene expression in long-term denervated mouse muscles using RNA-Seq. The murine right sciatic nerve was denervated, and the mice were housed for five weeks. The cross-sectional areas of the hind limb muscles were measured using an X-ray CT system 35 days after denervation. After 28 d of denervation, the cross-sectional area of the muscle decreased to approximately 65% of that of the intact left muscle and reached a plateau. Gene expression in the soleus and extensor digitorum longus (EDL) muscles on the 36th day was analyzed using RNA-Seq and validated using RT-qPCR. RNA-Seq analysis revealed that three genes- Adora1, E230016M11Rik , and Gm10718 -were upregulated and one gene- Gm20515 -was downregulated in the soleus muscle; additionally, four genes- Adora1 , E230016M11Rik , Pigh , and Gm15557 -were upregulated and one gene- Fzd7 -was downregulated in the EDL muscle (FDR < 0.05). Among these genes, E230016M11Rik , one of the long non-coding RNAs, was significantly upregulated in both the muscles. These findings indicate that E230016M11Rik could be a candidate gene for the maintenance of atrophied skeletal muscle size and an atrophic state.
Keyphrases
- rna seq
- skeletal muscle
- single cell
- gene expression
- genome wide
- dna methylation
- genome wide identification
- cross sectional
- insulin resistance
- long non coding rna
- computed tomography
- copy number
- bioinformatics analysis
- type diabetes
- emergency department
- high fat diet induced
- magnetic resonance
- contrast enhanced
- metabolic syndrome
- pet ct
- drug induced