Novel Role of Tieg1 in Muscle Metabolism and Mitochondrial Oxidative Capacities - Université de technologie de Compiègne Access content directly
Journal Articles Acta Physiologica Year : 2020

Novel Role of Tieg1 in Muscle Metabolism and Mitochondrial Oxidative Capacities

Malek Kammoun
Lydie Nadal-Desbarats
Sandra Même
Philippe Pouletaut
William Même
Frédéric Szeremeta
Sabine Bensamoun


Aim Tieg1 is involved in multiple signalling pathways, human diseases, and is highly expressed in muscle where its functions are poorly understood. Methods We have utilized Tieg1 knockout (KO) mice to identify novel and important roles for this transcription factor in regulating muscle ultrastructure, metabolism and mitochondrial functions in the soleus and extensor digitorum longus (EDL) muscles. RNA sequencing, immunoblotting, transmission electron microscopy, MRI, NMR, histochemical and mitochondrial function assays were performed. Results Loss of Tieg1 expression resulted in altered sarcomere organization and a significant decrease in mitochondrial number. Histochemical analyses demonstrated an absence of succinate dehydrogenase staining and a decrease in cytochrome c oxidase (COX) enzyme activity in KO soleus with similar, but diminished, effects in the EDL. Decreased complex I, COX and citrate synthase (CS) activities were detected in the soleus muscle of KO mice indicating altered mitochondrial function. Complex I activity was also diminished in KO EDL. Significant decreases in CS and respiratory chain complex activities were identified in KO soleus. 1H‐NMR spectra revealed no significant metabolic difference between wild‐type and KO muscles. However, 31P spectra revealed a significant decrease in phosphocreatine and ATPγ. Altered expression of 279 genes, many of which play roles in mitochondrial and muscle function, were identified in KO soleus muscle. Ultimately, all of these changes resulted in an exercise intolerance phenotype in Tieg1 KO mice. Conclusion Our findings have implicated novel roles for Tieg1 in muscle including regulation of gene expression, metabolic activity and organization of tissue ultrastructure. This muscle phenotype resembles diseases associated with exercise intolerance and myopathies of unknown consequence.
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Dates and versions

hal-02304067 , version 1 (16-11-2020)
hal-02304067 , version 2 (25-06-2021)



Malek Kammoun, Vladimir Veksler, Lydie Nadal-Desbarats, Sandra Même, Jérôme Piquereau, et al.. Novel Role of Tieg1 in Muscle Metabolism and Mitochondrial Oxidative Capacities. Acta Physiologica, 2020, 228 (3), pp.e13394. ⟨10.1111/apha.13394⟩. ⟨hal-02304067v1⟩
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