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Physiol. Genomics 24: 13-22, 2005. First published October 25, 2005; doi:10.1152/physiolgenomics.00301.2004
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Received 20 December 2004; accepted in final form 14 September 2005.
Physiological Genomics 24:13-22 (2005)
American Physiological Society © 2005 American Physiological Society

Seasonally hibernating phenotype assessed through transcript screening

Daryl R. Williams1, L. Elaine Epperson2, Weizhong Li1, Margaret A. Hughes1, Ruth Taylor3, Jane Rogers3, Sandra L. Martin2, Andrew R. Cossins1 and Andrew Y. Gracey1

1 School of Biological Sciences, University of Liverpool, United Kingdom
2 University of Colorado School of Medicine, Aurora, Colorado
3 The Wellcome Trust Sanger Institute, Hinxton, Cambridge, United Kingdom

Hibernation is a seasonally entrained and profound phenotypic transition to conserve energy in winter. It involves significant biochemical reprogramming, although our understanding of the underpinning molecular events is fragmentary and selective. We have conducted a large-scale gene expression screen of the golden-mantled ground squirrel, Spermophilus lateralis, to identify transcriptional responses associated specifically with the summer-winter transition and the torpid-arousal transition in winter. We used 112 cDNA microarrays comprising 12,288 probes that cover at least 5,109 genes. In liver, the profiles of torpid and active states in the winter were almost identical, although we identified 102 cDNAs that were differentially expressed between winter and summer, 90% of which were downregulated in the winter states. By contrast, in cardiac tissue, 59 and 115 cDNAs were elevated in interbout arousal and torpor, respectively, relative to the summer active condition, but only 7 were common to both winter states, and during arousal none was downregulated. In brain, 78 cDNAs were found to change in winter, 44 of which were upregulated. Thus transcriptional changes associated with hibernation are qualitatively modest and, since these changes are generally less than twofold, also quantitatively modest. Unbiased Gene Ontology profiling of the transcripts suggests a winter switch to ß-oxidation of lipids in liver and heart, a reduction in metabolism of toxic compounds and the urea cycle in liver, and downregulated electron transport in the brain. We identified just one strongly winter-induced transcript common to all tissues, namely an RNA-binding protein, RBM3. This analysis clearly differentiates responses of the principal tissues, identifies a large number of new genes undergoing regulation, and broadens our understanding of affected cellular processes that, in part, account for the winter-adaptive hibernating phenotype.

hibernation; torpor; microarray




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