Gene expression profiling of skeletal muscle in exercise-trained and sedentary rats with inborn high and low VO2max

Anja Bye, Morten A. Høydal, Daniele Catalucci, Mette Langaas, Ole Johan Kemi, Vidar Beisvag, Lauren G. Koch, Steven L. Britton, Øyvind Ellingsen, Ulrik Wisløff

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

The relationship between inborn maximal oxygen uptake (VO2max) and skeletal muscle gene expression is unknown. Since low VO2max is a strong predictor of cardiovascular mortality, genes related to low VO 2max might also be involved in cardiovascular disease. To establish the relationship between inborn VO2max and gene expression, we performed microarray analysis of the soleus muscle of rats artificially selected for high- and low running capacity (HCR and LCR, respectively). In LCR, a low VO2max was accompanied by aggregation of cardiovascular risk factors similar to the metabolic syndrome. Although sedentary HCR were able to maintain a 120% higher running speed at VO2max than sedentary LCR, only three transcripts were differentially expressed (FDR ≤ 0.05) between the groups. Sedentary LCR expressed high levels of a transcript with strong homology to human leucyl-transfer RNA synthetase, of whose overexpression has been associated with a mutation linked to mitochondrial dysfunction. Moreover, we studied exercise-induced alterations in soleus gene expression, since accumulating evidence indicates that long-term endurance training has beneficial effects on the metabolic syndrome. In terms of gene expression, the response to exercise training was more pronounced in HCR than LCR. HCR upregulated several genes associated with lipid metabolism and fatty acid elongation, whereas LCR upregulated only one transcript after exercise training. The results indicate only minor differences in soleus muscle gene expression between sedentary HCR and LCR. However, the inborn level of fitness seems to influence the transcriptional adaption to exercise, as more genes were upregulated after exercise training in HCR than LCR.

Original languageEnglish
Pages (from-to)213-221
Number of pages9
JournalPhysiol Genomics
Volume35
Issue number3
DOIs
Publication statusPublished - Nov 2008

Fingerprint

Gene Expression Profiling
Skeletal Muscle
Gene Expression
Exercise
Genes
Amino Acyl-tRNA Synthetases
Microarray Analysis
Lipid Metabolism
Running
Cardiovascular Diseases
Fatty Acids
Oxygen
Mutation
Mortality

Keywords

  • Gene ontology
  • MELAS
  • Metabolic syndrome
  • Microarray analysis
  • Soleus muscle

ASJC Scopus subject areas

  • Physiology
  • Genetics

Cite this

Gene expression profiling of skeletal muscle in exercise-trained and sedentary rats with inborn high and low VO2max. / Bye, Anja; Høydal, Morten A.; Catalucci, Daniele; Langaas, Mette; Kemi, Ole Johan; Beisvag, Vidar; Koch, Lauren G.; Britton, Steven L.; Ellingsen, Øyvind; Wisløff, Ulrik.

In: Physiol Genomics, Vol. 35, No. 3, 11.2008, p. 213-221.

Research output: Contribution to journalArticle

Bye, A, Høydal, MA, Catalucci, D, Langaas, M, Kemi, OJ, Beisvag, V, Koch, LG, Britton, SL, Ellingsen, Ø & Wisløff, U 2008, 'Gene expression profiling of skeletal muscle in exercise-trained and sedentary rats with inborn high and low VO2max', Physiol Genomics, vol. 35, no. 3, pp. 213-221. https://doi.org/10.1152/physiolgenomics.90282.2008
Bye, Anja ; Høydal, Morten A. ; Catalucci, Daniele ; Langaas, Mette ; Kemi, Ole Johan ; Beisvag, Vidar ; Koch, Lauren G. ; Britton, Steven L. ; Ellingsen, Øyvind ; Wisløff, Ulrik. / Gene expression profiling of skeletal muscle in exercise-trained and sedentary rats with inborn high and low VO2max. In: Physiol Genomics. 2008 ; Vol. 35, No. 3. pp. 213-221.
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