Cloning and expression of PPARγ and PGC-1α from the hibernating ground squirrel, Spermophilus tridecemlineatus

The peroxisome proliferator-activated receptor (PPAR) family of transcription factors play a key role in lipid metabolism and have been implicated in a number of disease states, most notably of which is obesity. Controlled regulation of lipid metabolism is a key ingredient for successful hibernation. Partial cDNA sequences for one of the PPAR proteins, PPARγ and the PPARγ co-activator (PGC-1α) have been cloned from the hibernating ground squirrel, Spermophilus tridecemlineatus and show differential regulation during hibernation at the mRNA level using relative RT-PCR and at the protein level via immunoblotting in brown adipose tissue (BAT), heart, skeletal muscle and white adipose tissue (WAT). The cDNA sequence for PGC-1α revealed a number of amino acid substitutions and two were worthy of note, one resulting in the loss of a potential protein kinase C (PKC) site, while another resulted in the creation of a PKC site, suggesting that PKC may be important in regulating PGC-1α. RT-PCR revealed a near 2-fold up-regulation of PPARγ in BAT and to a lesser extent (< 1.5-fold) in heart and WAT, while PGC-1α displayed significantly higher levels of expression in skeletal muscle during hibernation (3.1-fold, p < 0.005). The protein levels of PPARγ were significantly increased in BAT and WAT (1.5 and 1.8-fold, respectively) while PGC-1α displayed significant changes in expression in heart (3.5-fold) and skeletal muscle (1.8-fold). Our current findings indicate a role for increased expression of PPARγ and PGC-1α in hibernating animals. (Mol Cell Biochem 269: 175–182, 2005)

[1]  T. Willson,et al.  Comprehensive Messenger Ribonucleic Acid Profiling Reveals That Peroxisome Proliferator-Activated Receptor γ Activation Has Coordinate Effects on Gene Expression in Multiple Insulin-Sensitive Tissues. , 2001, Endocrinology.

[2]  P. Puigserver,et al.  A Cold-Inducible Coactivator of Nuclear Receptors Linked to Adaptive Thermogenesis , 1998, Cell.

[3]  J. Saffitz,et al.  Peroxisome proliferator-activated receptor gamma coactivator-1 promotes cardiac mitochondrial biogenesis. , 2000, The Journal of clinical investigation.

[4]  Guillaume Adelmant,et al.  Control of hepatic gluconeogenesis through the transcriptional coactivator PGC-1 , 2001, Nature.

[5]  Y. Nishizuka,et al.  Studies on the phosphorylation of myelin basic protein by protein kinase C and adenosine 3':5'-monophosphate-dependent protein kinase. , 1985, The Journal of biological chemistry.

[6]  Kenneth B Storey,et al.  Differential expression of Akt, PPARgamma, and PGC-1 during hibernation in bats. , 2003, Biochemistry and cell biology = Biochimie et biologie cellulaire.

[7]  D. Hittel,et al.  Differential expression of mitochondria-encoded genes in a hibernating mammal. , 2002, The Journal of experimental biology.

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

[9]  L. Sokoloff,et al.  Local Cerebral Blood Flow during Hibernation, a Model of Natural Tolerance to “Cerebral Ischemia” , 1994, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[10]  Ricardo Cavicchioli,et al.  Cold-adapted enzymes. , 2006, Annual review of biochemistry.

[11]  Jiandie D. Lin,et al.  Transcriptional co-activator PGC-1α drives the formation of slow-twitch muscle fibres , 2002, Nature.

[12]  K. Storey,et al.  Metabolic regulation in mammalian hibernation: enzyme and protein adaptations. , 1997, Comparative biochemistry and physiology. Part A, Physiology.

[13]  K. Storey,et al.  The optimal depot fat composition for hibernation by golden-mantled ground squirrels (Spermophilus lateralis) , 2004, Journal of Comparative Physiology B.

[14]  R. Bassel-Duby,et al.  Regulation of Mitochondrial Biogenesis in Skeletal Muscle by CaMK , 2002, Science.

[15]  K. Storey,et al.  Freeze-induced expression of a novel gene, fr47, in the liver of the freeze-tolerant wood frog, Rana sylvatica. , 2003, Biochimica et biophysica acta.

[16]  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.

[17]  Kenneth B. Storey,et al.  Differential expression of Akt, PPARγ, and PGC-1 during hibernation in bats , 2003 .

[18]  K L Gould,et al.  Substrate specificity of protein kinase C. Use of synthetic peptides corresponding to physiological sites as probes for substrate recognition requirements. , 1986, European journal of biochemistry.

[19]  K. Storey,et al.  Comparisons of the effects of temperature on the liver fatty acid binding proteins from hibernator and nonhibernator mammals. , 1998, Biochemistry and cell biology = Biochimie et biologie cellulaire.

[20]  K. Frerichs,et al.  Cerebral Sinus and Venous Thrombosis in Rats Induces Long-Term Deficits in Brain Function and Morphology—Evidence for a Cytotoxic Genesis , 1994, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[21]  T. Willson,et al.  Comprehensive messenger ribonucleic acid profiling reveals that peroxisome proliferator-activated receptor gamma activation has coordinate effects on gene expression in multiple insulin-sensitive tissues. , 2001, Endocrinology.

[22]  K. Storey Mammalian hibernation. Transcriptional and translational controls. , 2003, Advances in experimental medicine and biology.

[23]  J. Berger,et al.  The mechanisms of action of PPARs. , 2002, Annual review of medicine.

[24]  S. Egginton,et al.  Differential Effects of Cold Exposure on Muscle Fibre Composition and Capillary Supply in Hibernator and Non‐Hibernator Rodents , 2001, Experimental physiology.

[25]  D. Bernlohr,et al.  Fatty Acid-binding Protein-Hormone-sensitive Lipase Interaction , 2003, Journal of Biological Chemistry.

[26]  S. Patel,et al.  Characterization of the Functional Interaction of Adipocyte Lipid-binding Protein with Hormone-sensitive Lipase* , 2001, The Journal of Biological Chemistry.

[27]  K. Storey,et al.  Up-regulation of fatty acid-binding proteins during hibernation in the little brown bat, Myotis lucifugus. , 2004, Biochimica et biophysica acta.

[28]  K. Storey,et al.  Gene up-regulation in heart during mammalian hibernation. , 2000, Cryobiology.

[29]  N. Willassen,et al.  Cold adapted enzymes. , 2000, Biotechnology annual review.

[30]  M. B. Rollins,et al.  Low-temperature carbon utilization is regulated by novel gene activity in the heart of a hibernating mammal. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[31]  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.

[32]  S. Kimball,et al.  Amino acid effects on translational repressor 4E-BP1 are mediated primarily by l-leucine in isolated adipocytes. , 1998, American journal of physiology. Cell physiology.

[33]  D. Hittel,et al.  Differential expression of adipose- and heart-type fatty acid binding proteins in hibernating ground squirrels. , 2001, Biochimica et biophysica acta.

[34]  B. Lowell,et al.  Differential regulation of uncoupling protein gene homologues in multiple tissues of hibernating ground squirrels. , 1998, The American journal of physiology.

[35]  D. Langin,et al.  Conversion from white to brown adipocytes: a strategy for the control of fat mass? , 2003, Trends in Endocrinology & Metabolism.