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Publication : An inducible knockout of Dicer in adult mice does not affect endurance exercise-induced muscle adaptation.

First Author  Oikawa S Year  2019
Journal  Am J Physiol Cell Physiol Volume  316
Issue  2 Pages  C285-C292
PubMed ID  30540495 Mgi Jnum  J:272748
Mgi Id  MGI:6280176 Doi  10.1152/ajpcell.00278.2018
Citation  Oikawa S, et al. (2019) An inducible knockout of Dicer in adult mice does not affect endurance exercise-induced muscle adaptation. Am J Physiol Cell Physiol 316(2):C285-C292
abstractText  The contractile and metabolic properties of adult skeletal muscle change in response to endurance exercise. The mechanisms of transcriptional regulation in exercise-induced skeletal muscle adaptation, including fiber-type switching and mitochondrial biogenesis, have been investigated intensively, whereas the role of microRNA (miRNA)-mediated posttranscriptional gene regulation is less well understood. We used tamoxifen-inducible Dicer1 knockout (iDicer KO) mice to reduce the global expression of miRNAs in adult skeletal muscle and subjected these mice to 2 wk of voluntary wheel running. Dicer mRNA expression was completely depleted in fast-twitch plantaris muscle after tamoxifen injection. However, several muscle-enriched miRNAs, including miR-1 and miR-133a, were reduced by only 30-50% in both the slow and fast muscles. The endurance exercise-induced changes that occurred for many parameters (i.e., fast-to-slow fiber-type switch and increases in succinate dehydrogenase, respiratory chain complex II, and citrate synthase activity) in wild type (WT) also occurred in the iDicer KO mice. Protein expression of myosin heavy chain IIa, peroxisome proliferator-activated receptor-gamma coactivator-1alpha, and cytochrome c complex IV was also increased in the iDicer KO mice by the voluntary running. Furthermore, there was no significant difference in oxygen consumption rate in the isolated mitochondria between the WT and iDicer KO mice. These data indicate that muscle-enriched miRNAs were detectable even after 4 wk of tamoxifen treatment and there was no apparent specific endurance-exercise-induced muscle phenotype in the iDicer KO mice.
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