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Am J Physiol Regul Integr Comp Physiol 293: R2315-R2322, 2007. First published September 26, 2007; doi:10.1152/ajpregu.00505.2007
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DEVELOPMENTAL PHYSIOLOGY AND PREGNANCY

Molecular mechanisms underlying the development of endothermy in birds (Gallus gallus): a new role of PGC-1{alpha}?

Isabel Walter and Frank Seebacher

Integrative Physiology, School of Biological Sciences, The University of Sydney, Sydney, Australia

Submitted 11 July 2007 ; accepted in final form 25 September 2007

In endotherms, plasticity of internal heat production in response to environmental variability is an important component of thermoregulation. During embryogenesis endotherms cannot regulate their body temperature metabolically and are therefore similar to ectotherms. The transition from ectothermy to endothermy occurs by the development of metabolic capacity during embryogenesis. Here we test the hypothesis that the development of metabolism during embryogenesis in birds is under transcriptional control and that metabolic capacity is upregulated in colder environments. The peroxisome proliferator-activated receptor-{gamma} (PPAR{gamma}) coactivator-1{alpha} (PGC-1{alpha}) is the major metabolic regulator in mammals. PGC-1{alpha} and its target PPAR{gamma} were significantly elevated during development in pectoral muscle and liver of chickens (Gallus gallus) compared with adults. However, the timing of upregulation of PGC-1{alpha} and PPAR{gamma} was not in synchrony. In cool incubation temperatures (35°C) both PGC-1{alpha} and PPAR{gamma} gene expression was increased in liver but not in skeletal muscle, compared with a 38°C incubation treatment. Cytochrome c oxidase and citrate synthase enzyme activities and ATP synthase gene expression increased during embryonic development in liver and muscle, and there was a significant effect of incubation temperature on these parameters. Our findings suggest that PGC-1{alpha} might be important for establishing endothermic metabolic capacity during embryogenesis in birds.

metabolism; peroxisome proliferator-activated receptor-{gamma}; oxidative capacity; hypothermic; cytochrome c oxidase



Address for reprint requests and other correspondence: I. Walter, Integrative Physiology, School of Biological Sciences A08, The Univ. of Sydney, NSW 2006, Australia (e-mail: iwal9728{at}usyd.edu.au)







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