Physiol. Genomics 32: 170-181, 2008.
First published October 9, 2007; doi:10.1152/physiolgenomics.00075.2007
1094-8341/08 $8.00
Received 31 March 2007;
accepted in final form 27 September 2007.
Physiological Genomics 32:170-181 (2008)
1094-8341/08 $8.00 © 2008 American Physiological Society
Modulation of gene expression in hibernating arctic ground squirrels
Jun Yan1,2,
Brian M. Barnes1,
Franziska Kohl1 and
Thomas G. Marr1,3
1 Institute of Arctic Biology, University of Alaska Fairbanks, Fairbanks, Alaska
2 CAS-MPG Partner Institute for Computational Biology, Shanghai Institutes of Biological Sciences, Shanghai, China
3 Hiberna Corporation, Boulder, Colorado
We performed a broadscale screening of differential gene expression using both high-throughput bead-array technology and real-time PCR assay in brown adipose tissue, liver, heart, hypothalamus, and skeletal muscle in hibernating arctic ground squirrels, comparing animals sampled after two durations of steady-state torpor, during two stages of spontaneous arousal episodes, and in animals after they ended hibernation. Significant seasonal and torpor-arousal cycle differences of gene expression were detected in genes involved in glycolysis, fatty acid metabolism, gluconeogenesis, amino acid metabolism, molecular transport, detoxification, cardiac contractility, circadian rhythm, cell growth and apoptosis, muscle dystrophy, and RNA and protein protection. We observed, for the first time, complex modulation of gene expression during multiple stages of torpor-arousal cycles. The mRNA levels of certain metabolic genes drop significantly during the transition from late torpor to early arousal, perhaps due to the rapid turnover of mRNA transcripts resulting from the translational demands during thermogenesis in early arousal, whereas the mRNA levels of genes related to circadian rhythm, cell growth, and apoptosis rise significantly in the early or late arousal phases during torpor-arousal cycle, suggesting the resumption of circadian rhythm and cell cycle during arousal.
metabolism; cardiac contractility; circadian rhythm; muscle dystrophy; cell cycle
Copyright © 2008 by the American Physiological Society.