Hostname: page-component-cd9895bd7-jn8rn Total loading time: 0 Render date: 2024-12-26T17:23:45.687Z Has data issue: false hasContentIssue false

Responses to divergent selection for plasma concentrations of insulin-like growth factor-1 in mice

Published online by Cambridge University Press:  14 April 2009

S. N. McCutcheon
Affiliation:
Department of Animal Science, Massey University, Palmerston North, New Zealand
D. D. S. Mackenzie
Affiliation:
Department of Animal Science, Massey University, Palmerston North, New Zealand
P. D. Gluckman
Affiliation:
Department of Paediatrics, University of Auckland Medical School, Auckland, New Zealand
J. E. Ormsby
Affiliation:
Small Animal Production Unit, Massey University, Palmerston North, New Zealand
B. H. Brier
Affiliation:
Department of Paediatrics, University of Auckland Medical School, Auckland, New Zealand
Rights & Permissions [Opens in a new window]

Summary

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

A divergent selection experiment with mice, using plasma concentrations of insulin-like growth factor-1 (IGF-1) at 42 days of age as the selection criterion, was undertaken for 7 generations. Lines were not replicated. To obtain sufficient plasma for the IGF-1 assay, blood from four individuals was volumetrically bulked to obtain a litter mean IGF-1 concentration. This necessitated the use of between family selection. Although inbreeding accumulated in a linear fashion in each of the high, control and low lines, the rates were different for each line (3·6, 1·6 and 5·3% per generation for the high, control and low lines, respectively). As a consequence, the effects of selection and inbreeding are confounded in this experiment. Divergence between the high and low lines in plasma concentrations of IGF-1 continued steadily until generation 5. In generations 6 and 7, there was a reduced degree of divergence and this contributed towards the low realized heritability value of 0.15 ± 0.12. Six-week liveweight showed a steady positive correlated response to selection for or against plasma concentrations of IGF-1 until generation 4 (high-low difference = 1·7 g = 12%). In generation 5, a substantial drop in 6-week liveweight in the low line relative to both the high and control lines occurred (high-low difference, 3·9; g, 25%). This difference was maintained until generation 7.

This experiment suggests that genetic variation exists at 6 weeks of age in plasma concentrations of IGF-1 in mice. Furthermore, genetic covariation between plasma IGF-1 concentrations and liveweight at 6 weeks of age is likely to be positive. Further experiments have been initiated to examine these theories.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1989

References

Adashi, E. Y., Resnick, C. E., D'Ercole, A. J., Svoboda, M. E. & van Wyk, J. J. (1985). Insulin-like growth factors as intraovarian regulators of granulosa cell growth and function. Endocrine Reviews 6, 400420.CrossRefGoogle Scholar
Anon. (1987) Mouse News Letter 79, 25.Google Scholar
Blair, H. T., McCutcheon, S. N., Mackenzie, D. D. S., Gluckman, P. D. & Ormsby, J. E. (1987). Variation in plasma concentration of insulin-like growth factor-1 and its covariation with liveweight in mice. Australian Journal of Biological Sciences 40, 287293.CrossRefGoogle ScholarPubMed
Breier, B. H., Bass, H. J., Butler, J. H. & Gluckman, P. D. (1986). The somatomedin axis in young steers: influence of nutritional status on pulsatile release of GH and circulating concentrations of IGF-1. Journal of Endocrinology 111, 209215.CrossRefGoogle Scholar
Buonomo, F. C., Lauterio, T. J., Baile, C. A. & Campion, D. R. (1987). Determination of insulin-like growth factor-1 (IGF-1) and IGF binding protein protein levels in swine. Domestic Animal Endocrinology 4, 2331.CrossRefGoogle ScholarPubMed
Cockrem, F. (1959). Selection for relationships opposite to those predicted by the genetic correlation between two traits in the house mouse (Mus musculus). Nature 183, 342343.CrossRefGoogle ScholarPubMed
Eigenmann, J. E., Patterson, D. F. & Froesch, E. R. (1984). Body-size parallels insulin-like growth factor-1 levels but not growth hormone secretory capacity. Acta Endocrinologica 106, 448453.Google Scholar
Falconer, D. S. (1981). Introduction to Quantitative Genetics. Longman Group Ltd, U.K.Google Scholar
Flux, D. S. (1957). The growth-stimulating effect of growth hormone and l-thyroxine on the mammary glands and uterus of the mouse. Journal of Endocrinology 15, 266272.CrossRefGoogle ScholarPubMed
Flux, D. S. & Munford, R. E. (1957). The effect of adrenocorticotrophin on the mammary glands of intact mature female mice of the CHI strain. Journal of Endocrinology 14, 343347.CrossRefGoogle ScholarPubMed
Froesch, E. R., Schmid, C., Schwander, J. & Zapf, J. (1985). Actions of insulin-like growth factors. Annual Reviews of Physiology 47, 443467.CrossRefGoogle ScholarPubMed
Gilmour, A. R. (1985). REG – A Generalized Linear Models Program. New South Wales Department of Agriculture, Australia.Google Scholar
Gluckman, P. D., Breier, B. H. & Davis, S. R. (1987). Physiology of the somatotropic axis with particular reference to the ruminant. Journal of Dairy Science 70, 442466.CrossRefGoogle Scholar
Gluckman, P. D. & Butler, J. H. (1983). Parturition related changes in the insulin-like growth factors 1 and 2 in the perinatal lamb. Journal of Endocrinology 99, 223232.CrossRefGoogle ScholarPubMed
Hall, K. & Sara, V. R. (1983). Growth and somatomedins. Vitamins and Hormones 40, 175233.CrossRefGoogle ScholarPubMed
Hill, W. G. (1972). Estimation of realised heritabilities from selection experiments I. Divergent selection. Biometrics 28, 747765.CrossRefGoogle ScholarPubMed
Holder, A. T. & Wallis, M. (1977). Actions of growth hormone, prolactin and thyroxine on serum somatomedin-like activity and growth in hypopituitary dwarf mice. Journal of Endocrinology 74, 223229.CrossRefGoogle ScholarPubMed
Huybrechts, L. M., King, D. B., Lauterio, T. J., Marsh, J. and Scanes, C. B. (1985). Plasma concentrations of somatomedin-C in hypophysectomized, dwarf and intact growing domestic fowl as determined by heterologous radioimmunoassay. Journal of Endocrinology 104, 233239.CrossRefGoogle ScholarPubMed
Lund-Larsen, T. R. & Bakke, H. (1975). Growth hormone and somatomedin activities in lines of pigs selected for rate of gain and thickness of backfat. Acta Agriculture Scandinavica 25, 231234.CrossRefGoogle Scholar
Merimee, T. J., Zapf, J., Hewlett, B. & Cavalii-Sforza, L. L. (1987). Insulin-like growth factors in pygmies. The New England Journal of Medicine 316, 906911.CrossRefGoogle ScholarPubMed
Nilsson, A., Isgaard, J., Lindahl, A., Dahlstrom, A., Skottner, A. & Isaksson, O. G. P. (1986). Regulation by growth hormone of number of chondrocytes containing IGF-1 in rat growth plate. Science 233, 571574.CrossRefGoogle ScholarPubMed
Willeberg, P., Kastrup, K. W. & Andresen, E. (1975). Pituitary dwarfism in German Shepherd dogs: studies on somatomedin activity. Nordisk Veterinaer Medicin 27, 448454.Google ScholarPubMed