Hibernating above the permafrost: effects of ambient temperature and season on expression of metabolic genes in liver and brown adipose tissue of arctic ground squirrels

SUMMARY Hibernating arctic ground squirrels (Urocitellus parryii), overwintering in frozen soils, maintain large gradients between ambient temperature (Ta) and body temperature (Tb) by substantially increasing metabolic rate during torpor while maintaining a subzero Tb. We used quantitative reverse-transcription PCR (qRT-PCR) to determine how the expression of 56 metabolic genes was affected by season (active in summer vs hibernating), metabolic load during torpor (imposed by differences in Ta: +2 vs –10°C) and hibernation state (torpid vs after arousal). Compared with active ground squirrels sampled in summer, liver from hibernators showed increased expression of genes associated with fatty acid catabolism (CPT1A, FABP1 and ACAT1), ketogenesis (HMGCS2) and gluconeogenesis (PCK1) and decreased expression of genes associated with fatty acid synthesis (ACACB, SCD and ELOVL6), amino acid metabolism, the urea cycle (PAH, BCKDHA and OTC), glycolysis (PDK1 and PFKM) and lipid metabolism (ACAT2). Stage of hibernation (torpid vs aroused) had a much smaller effect, with only one gene associated with glycogen synthesis (GSY1) in liver showing consistent differences in expression levels between temperature treatments. Despite the more than eightfold increase in energetic demand associated with defending Tb during torpor at a Ta of –10 vs +2°C, transcript levels in liver and brown adipose tissue differed little. Our results are inconsistent with a hypothesized switch to use of non-lipid fuels when ambient temperatures drop below freezing.

[1]  Timothy A. Dahl,et al.  Quantitative Analysis of Liver Protein Expression During Hibernation in the Golden-mantled Ground Squirrel*S , 2004, Molecular & Cellular Proteomics.

[2]  K. Nagy,et al.  Annual cycle of energy and time expenditure in a golden-mantled ground squirrel population , 1989, Oecologia.

[3]  C. Buck,et al.  Body temperature patterns during hibernation in a free-living Alaska marmot (Marmota broweri) , 2009 .

[4]  F. Geiser,et al.  Metabolic rate and body temperature reduction during hibernation and daily torpor. , 2004, Annual review of physiology.

[5]  Brian M. Barnes,et al.  Energetics of arousal episodes in hibernating arctic ground squirrels , 2009, Journal of Comparative Physiology B.

[6]  Brian M. Barnes,et al.  Temperatures of hibernacula and changes in body composition of arctic ground squirrels over winter , 1999 .

[7]  Thomas Ruf,et al.  Hibernation versus Daily Torpor in Mammals and Birds: Physiological Variables and Classification of Torpor Patterns , 1995, Physiological Zoology.

[8]  How Do Woodchucks (Marmota monax) Cope with Harsh Winter Conditions , 1996 .

[9]  R. Long,et al.  Simultaneous Collection of Body Temperature and Activity Data in Burrowing Mammals: a New Technique , 2007 .

[10]  T. Marr,et al.  Modulation of gene expression in hibernating arctic ground squirrels. , 2008, Physiological genomics.

[11]  D. Hittel,et al.  The translation state of differentially expressed mRNAs in the hibernating 13-lined ground squirrel (Spermophilus tridecemlineatus). , 2002, Archives of biochemistry and biophysics.

[12]  P. Pochet A Quantitative Analysis , 2006 .

[13]  Heng Tao Shen,et al.  Principal Component Analysis , 2009, Encyclopedia of Biometrics.

[14]  B. Rourke,et al.  Muscle plasticity in hibernating ground squirrels (Spermophilus lateralis) is induced by seasonal, but not low-temperature, mechanisms , 2010, Journal of Comparative Physiology B.

[15]  T. Marr,et al.  Detection of differential gene expression in brown adipose tissue of hibernating arctic ground squirrels with mouse microarrays. , 2006, Physiological genomics.

[16]  W. Galster,et al.  Gluconeogenesis in arctic ground squirrels between periods of hibernation. , 1975, The American journal of physiology.

[17]  H. Stephan,et al.  Freeze Avoidance in a Mammal: Body Temperatures Below 00C in an Arctic Hibernator , 1989 .

[18]  B. Barnes Freeze avoidance in a mammal: body temperatures below 0 degree C in an Arctic hibernator. , 1989, Science.

[19]  J. Knight,et al.  mRNA Stability and Polysome Loss in Hibernating Arctic Ground Squirrels (Spermophilus parryii) , 2000, Molecular and Cellular Biology.

[20]  Brian M. Barnes,et al.  Shotgun Proteomics Analysis of Hibernating Arctic Ground Squirrels* , 2009, Molecular & Cellular Proteomics.

[21]  S. Martin,et al.  Reversible depression of transcription during hibernation , 2002, Journal of Comparative Physiology B.

[22]  C. P. Lyman,et al.  Physiology of hibernation in mammals. , 1955, Physiological reviews.

[23]  C. I. Pogson,et al.  The flux control coefficient of carnitine palmitoyltransferase I on palmitate beta-oxidation in rat hepatocyte cultures. , 1997, The Biochemical journal.

[24]  J. R. Nestler Relationships between Respiratory Quotient and Metabolic Rate during Entry to and Arousal from Daily Torpor in Deer Mice (Peromyscus maniculatus) , 1990, Physiological Zoology.

[25]  Brian M. Barnes,et al.  Annual Cycle of Body Composition and Hibernation in Free-Living Arctic Ground Squirrels , 1999 .

[26]  P. J. Young Hibernating patterns of free-ranging Columbian ground squirrels , 1990, Oecologia.

[27]  K. Storey,et al.  Evidence for a reduced transcriptional state during hibernation in ground squirrels. , 2006, Cryobiology.

[28]  K. Storey,et al.  Metabolic rate depression in animals: transcriptional and translational controls , 2004, Biological reviews of the Cambridge Philosophical Society.

[29]  Michael W Pfaffl,et al.  RNA integrity and the effect on the real-time qRT-PCR performance. , 2006, Molecular aspects of medicine.

[30]  D. F. Hoyt,et al.  Disuse atrophy in the hibernating golden-mantled ground squirrel, Spermophilus lateralis. , 1991, The American journal of physiology.

[31]  F. Speleman,et al.  Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes , 2002, Genome Biology.

[32]  G. Denning,et al.  Identification of qRT-PCR reference genes for analysis of opioid gene expression in a hibernator , 2010, Journal of Comparative Physiology B.

[33]  N. Serkova,et al.  Quantitative analysis of liver metabolites in three stages of the circannual hibernation cycle in 13-lined ground squirrels by NMR. , 2007, Physiological genomics.

[34]  M. Willingham,et al.  Differential expression of ACAT1 and ACAT2 among cells within liver, intestine, kidney, and adrenal of nonhuman primates. , 2000, Journal of lipid research.

[35]  Weizhong Li,et al.  Seasonally hibernating phenotype assessed through transcript screening. , 2005, Physiological genomics.

[36]  Sandra L. Martin,et al.  Translational initiation is uncoupled from elongation at 18°C during mammalian hibernation , 2001 .

[37]  G. R. Michener Sexual differences in over-winter torpor patterns of Richardson's ground squirrels in natural hibernacula , 1992, Oecologia.

[38]  Y. Benjamini,et al.  Controlling the false discovery rate: a practical and powerful approach to multiple testing , 1995 .

[39]  Hannah V Carey,et al.  Seasonal proteomic changes reveal molecular adaptations to preserve and replenish liver proteins during ground squirrel hibernation. , 2010, American journal of physiology. Regulatory, integrative and comparative physiology.

[40]  J. M. Steffen,et al.  Morphometric and metabolic indices of disuse in muscles of hibernating ground squirrels. , 1991, Comparative biochemistry and physiology. B, Comparative biochemistry.

[41]  V. Zammit,et al.  Flux control exerted by mitochondrial outer membrane carnitine palmitoyltransferase over beta-oxidation, ketogenesis and tricarboxylic acid cycle activity in hepatocytes isolated from rats in different metabolic states. , 1996, The Biochemical journal.

[42]  W. Galster,et al.  Cyclic changes in carbohydrate concentrations during hibernation in the arctic ground squirrel. , 1970, The American journal of physiology.

[43]  Sandra L Martin,et al.  Mammalian hibernation: cellular and molecular responses to depressed metabolism and low temperature. , 2003, Physiological reviews.

[44]  G. Krause,et al.  Suppression of protein synthesis in brain during hibernation involves inhibition of protein initiation and elongation. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[45]  A. Malan,et al.  Intracellular pH in hibernation and respiratory acidosis in the European hamster , 2004, Journal of Comparative Physiology B.

[46]  M. Willis Metabolic Rate and Body Temperature Reduction during Hibernation , 2011 .

[47]  M. Pfaffl,et al.  A new mathematical model for relative quantification in real-time RT-PCR. , 2001, Nucleic acids research.

[48]  Claus Lindbjerg Andersen,et al.  Normalization of Real-Time Quantitative Reverse Transcription-PCR Data: A Model-Based Variance Estimation Approach to Identify Genes Suited for Normalization, Applied to Bladder and Colon Cancer Data Sets , 2004, Cancer Research.

[49]  C. Buck,et al.  Effects of ambient temperature on metabolic rate, respiratory quotient, and torpor in an arctic hibernator. , 2000, American journal of physiology. Regulatory, integrative and comparative physiology.