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Open Access Highly Accessed Research

Time- and exercise-dependent gene regulation in human skeletal muscle

Alexander C Zambon1, Erin L McDearmon2, Nathan Salomonis1, Karen M Vranizan14, Kirsten L Johansen3, Deborah Adey3, Joseph S Takahashi2, Morris Schambelan3 and Bruce R Conklin13*

Author Affiliations

1 Gladstone Institute of Cardiovascular Disease, Department of Medicine, University of California, San Francisco, CA 94141, USA

2 Howard Hughes Medical Institute, Department of Neurobiology and Physiology, Northwestern University, Evanston, IL 60208, USA

3 Department of Medicine, University of California, San Francisco, CA 94141, USA

4 Functional Genomics Lab, University of California, Berkeley, CA 94720, USA

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Genome Biology 2003, 4:R61  doi:10.1186/gb-2003-4-10-r61

Published: 25 September 2003

Abstract

Background

Skeletal muscle remodeling is a critical component of an organism's response to environmental changes. Exercise causes structural changes in muscle and can induce phase shifts in circadian rhythms, fluctuations in physiology and behavior with a period of around 24 hours that are maintained by a core clock mechanism. Both exercise-induced remodeling and circadian rhythms rely on the transcriptional regulation of key genes.

Results

We used DNA microarrays to determine the effects of resistance exercise (RE) on gene regulation in biopsy samples of human quadriceps muscle obtained 6 and 18 hours after an acute bout of isotonic exercise with one leg. We also profiled diurnal gene regulation at the same time points (2000 and 0800 hours) in the non-exercised leg. Comparison of our results with published circadian gene profiles in mice identified 44 putative genes that were regulated in a circadian fashion. We then used quantitative PCR to validate the circadian expression of selected gene orthologs in mouse skeletal muscle.

Conclusions

The coordinated regulation of the circadian clock genes Cry1, Per2, and Bmal1 6 hours after RE and diurnal genes 18 hours after RE in the exercised leg suggest that RE may directly modulate circadian rhythms in human skeletal muscle.