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RESEARCH ARTICLE

Genotypic and nutritional regulation of gene expression in two sheep hindlimb muscles with distinct myofibre and metabolic characteristics

G. S. Nattrass A D , S. P. Quigley A , G. E. Gardner C , C. S. Bawden A , C. J. McLaughlan A , R. S. Hegarty B and P. L. Greenwood B
+ Author Affiliations
- Author Affiliations

Australian Sheep Industry Cooperative Research Centre, Armidale, NSW 2350, Australia.

A South Australian Research and Development Institute—Livestock Systems, Roseworthy, SA 5371, Australia.

B NSW Department of Primary Industries Beef Industry Centre of Excellence, University of New England, Armidale, NSW 2351, Australia.

C School of Rural Science and Natural Resources, University of New England, Armidale, NSW 2351, Australia; Present address: School of Veterinary and Biomedical Sciences, Murdoch University, Murdoch, WA 6150, Australia.

D Corresponding author. Email: nattrass.greg@saugov.sa.gov.au

Australian Journal of Agricultural Research 57(6) 691-698 https://doi.org/10.1071/AR05101
Submitted: 21 March 2005  Accepted: 10 May 2006   Published: 20 June 2006

Abstract

This study investigated whether the expression profile of GDF8 (myostatin), myogenic regulatory factors (MRFs: MYF5, MYOD1, MYOG (myogenin), and MYF6), and IGF-system (IGF1, IGF2, IGF1R) genes are correlated with anatomical muscle, nutrition level, and estimated breeding values (EBVs) for muscling, growth, and/or fatness. Real-time PCR was employed to quantitatively measure the mRNA levels of these genes in the semimembranosus (SM) and semitendinosus (ST) muscles of growing lambs. The lambs were sired by Poll Dorset rams with differing EBVs for growth, muscling, and fatness, and were fed either high or low quality and availability pasture from birth to ~8 months of age. With the exception of MYOD1, the mRNA levels of all genes examined in this study showed varying degrees of nutritional regulation. All the MRF mRNA levels were higher in the SM muscle than the ST muscle, whereas myostatin mRNA was higher in the ST muscle than the SM muscle. Interactions between muscle type and nutrition were detected for IGF2, MYF6, and myogenin, while positive correlations between IGF2 and IGF1R and between MYOD1 and myogenin mRNA levels were apparent in both muscles. At the genotypic level, subtle differences in mRNA levels suggested interactions between nutrition and sire EBV. The findings of this study confirm that the MRFs, IGFs, and myostatin genes are differentially affected by a variety of factors that include nutrition, muscle type, and sire EBVs. Together, these data suggest that this suite of genes has important roles during postnatal muscle growth, even at quite late stages of growth and development.

Additional keywords: myogenic regulatory factors, myostatin, insulin-like growth factors, satellite cells, estimated breeding values.


Acknowledgments

We would like to thank the Australian Sheep Industry Cooperative Research Centre for providing the funds to conduct this research and to Meat and Livestock Australia (MLA) for funding the original Management Solutions experiment, which provided the muscle samples used in our study. We also thank the following technicians, Reg Woodgate, Joe Brunner, Bill Johns, and Steve Sinclair from the NSW Department of Primary Industries Beef Industry Centre of Excellence, who helped manage the nutritional requirements of the sheep and collect the muscle biopsy samples prior to slaughter. We also wish to acknowledge the considerable inputs of Dr David Hopkins in providing constructive criticisms and suggestions during the development and revision of this paper.


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