4.6 Article

Relationship between AMPK and the transcriptional balance of clock-related genes in skeletal muscle

Journal

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpendo.90510.2008

Keywords

adenosine 5 '-monophosphate-activated protein kinase; clock genes; circadian rhythm

Funding

  1. Swedish Research Council
  2. Swedish Diabetes Association
  3. Swedish Agency for Innovation Systems
  4. Foundation for Scientific Studies of Diabetology
  5. Swedish Centre for Sports Research
  6. Strategic Research Foundation
  7. Commission of the European Communities [LSHM-CT-2004-005272 EXGENESIS, LSHM-CT-2004-512013 EUGENE2]

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Vieira E, Nilsson EC, Nerstedt A, Ormestad M, Long YC, GarciaRoves PM, Zierath JR, Mahlapuu M. Relationship between AMPK and the transcriptional balance of clock-related genes in skeletal muscle. Am J Physiol Endocrinol Metab 295: E1032-E1037, 2008. First published August 26, 2008; doi:10.1152/ajpendo.90510.2008.-Circadian clocks coordinate physiological, behavioral, and biochemical events with predictable daily environmental changes by a self-sustained transcriptional feedback loop. CLOCK and ARNTL are transcriptional activators that regulate Per and Cry gene expression. PER and CRY inhibit their own transcription, and their turnover allows this cycle to restart. The transcription factors BHLHB2 and BHLHB3 repress Per activation, whereas orphan nuclear receptors of the NR1D and ROR families control Arntl expression. Here we show the AMP-activated protein kinase (AMPK)gamma(3) subunit is involved in the regulation of peripheral circadian clock function. AMPK gamma 3 knockout (Prkag3(-/-)) mice or wild-type littermates were injected with saline or an AMPK activator, 5-amino-4-imidazole-carboxamide riboside (AICAR), and white glycolytic gastrocnemius muscle was removed for gene expression analysis. Genes involved in the regulation of circadian rhythms (Cry2, Nr1d1, and Bhlhb2) were differentially regulated in response to AICAR in wild-type mice but remained unaltered in Prkag3(-/-) mice. Basal expression of Per1 was higher in Prkag3(-/-) mice compared with wild-type mice. Distinct diurnal changes in the respiratory exchange ratio (RER) between the light and dark phase of the day were observed in wild-type mice but not Prkag3(-/-) mice. In summary, the expression profile of clock-related genes in skeletal muscle in response to AICAR, as well as the diurnal shift in energy utilization, is impaired in AMPK gamma(3) subunit knockout mice. Our results indicate AMPK heterotrimeric complexes containing the AMPK gamma(3) subunit may play a specific role in linking circadian oscillators and energy metabolism in skeletal muscle.

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