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. 1981 Nov;99(3-4):513–524. doi: 10.1093/genetics/99.3-4.513

Correlated Responses in Male Reproductive Traits in Mice Selected for Litter Size and Body Weight

E J Eisen 1, B H Johnson 1
PMCID: PMC1214518  PMID: 7200925

Abstract

Correlated responses in male reproductive traits were determined at 4, 6 and 8 weeks of age in lines of mice selected for large litter size (L+), large 6-week body weight (W+), large litter size and small body weight (L+W-) and small litter size and large body weight (L-W+), and in an unselected control (K). Concentration of serum testosterone and weights of testes, seminal vesicles, epididymides and adrenal glands increased with age. Line differences in testosterone concentration were not detected. L+ and W+ males exhibited positive correlated responses in testes, epididymides and seminal vescile weights. Testis weight adjusted for body weight was significantly larger for L+ than controls and approached significance for W+. Realized genetic correlation betestis weight and litter size was 0.60 ± 0.04, and the realized partial genetic correlation holding body weight constant was 0.42. Therefore, pleiotropic loci, acting via the hypothalamic-pituitary axis, affect testis weight and litter size independently of body weight. Additionally, genes influencing overall growth have a pleiotropic effect on testis weight and litter size in mice; the realized genetic correlations of body weight with testis weight and with litter size were 0.60 ± 0.03 and 0.52 ± 0.10. Testis weight increased in both L+W- and L-W+ males. The positive correlated response in L+W- may have resulted from changes in frequency of genes controlling reproductive processes; whereas, in L-W+ it could have been the result of changes in the frequency of genes associated with body weight.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Land R. B., Falconer D. S. Genetic studies of ovulation rate in the mouse. Genet Res. 1969 Feb;13(1):25–46. doi: 10.1017/s0016672300002718. [DOI] [PubMed] [Google Scholar]
  2. Land R. B. The expression of female sex-limited characters in the male. Nature. 1973 Jan 19;241(5386):208–209. doi: 10.1038/241208a0. [DOI] [PubMed] [Google Scholar]
  3. Payne A. H., Wong K. L., Vega M. M. Differential effects of single and repeated administrations of gonadotropins on luteinizing hormone receptors and testosterone synthesis in two populations of Leydig cells. J Biol Chem. 1980 Aug 10;255(15):7118–7122. [PubMed] [Google Scholar]
  4. Sustarsic D. L., Wolfe H. G. A genetic study of luteinizing hormone levels and induced lutenizing hormone release in male mice. J Hered. 1979 Jul-Aug;70(4):226–230. doi: 10.1093/oxfordjournals.jhered.a109243. [DOI] [PubMed] [Google Scholar]
  5. Tsuruhara T., Dufau M. L., Cigorraga S., Catt K. J. Hormonal regulation of testicular luteinizing hormone receptors. Effects on cyclic AMP and testosterone responses in isolated Leydig cells. J Biol Chem. 1977 Dec 25;252(24):9002–9009. [PubMed] [Google Scholar]
  6. Welsh T. H., McCraw R. L., Johnson B. H. Influence of corticosteroids on testosterone production in the bull. Biol Reprod. 1979 Oct;21(3):755–763. doi: 10.1095/biolreprod21.3.755. [DOI] [PubMed] [Google Scholar]

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