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Variation in a natural population of Schizophyllum commune
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  • Original Article
  • Published: 01 December 1976

Variation in a natural population of Schizophyllum commune

II. Variation within the extreme isolates for growth rate

  • S Williams1 nAff2,
  • M M Verma1,3,
  • J L Jinks1 &
  • …
  • C M Brasier1 nAff4 

Heredity volume 37, pages 365–375 (1976)Cite this article

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Summary

Two extreme dikaryotic isolates chosen from a large sample of a localised population of Schizophyllum commune exhibited a considerable amount of genetical variation for growth rate at the near ambient temperature of 20°C and at the higher temperature of 30°C. The potential variation within these extreme isolates was greater than the variation observed in the whole sample. Regression analysis of the variation in growth rate of the dikaryotic progeny of the extreme isolates on that of their component monokaryons showed that the nature of gene action was not the same in these two stages of the life cycle.

The simple additive-dominance model of gene action was adequate to explain the variation in growth rate in both of the extreme isolates at both of the temperatures. The small deviations from this model could be accounted for by unequal gene frequencies due to small sample size although a low incidence of non-allelic interactions could not be ruled out. Directional dominance for growth rate was detected in both isolates at the more normal temperature and it was opposing in direction in the two isolates. In the slow growing isolate the dominance was for faster growth and in the fast growing isolate it was for slower growth. This is expected for a character which displays overall ambi-directional dominance if isolates with more extreme growth rates than those recovered in the population sample are eliminated by stabilising selection. The dominance is temperature dependent being ambi-directional in both isolates at the higher temperature.

Environmental heterogeneity, the buffering effects of directional dominance and genotype-environment interactions and opposing selective forces operating on the monokaryotic and dikaryotic stages of the life cycle are possible contributory factors to the considerable free and potential variability displayed in this small, localised population.

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References

  • Barnes, B W. 1966. Environment and selection in Drosophila melanogaster. Ph.D. Thesis, University of Birmingham, England.

  • Barnes, B W. 1968. Stabilising selection in Drosophila melanogaster. Heredity, 23, 433–442.

    Article  CAS  Google Scholar 

  • Brasier, C M. 1970. Variation in natural population of Schizophyllum commune. Amer Nat, 104, 191–204.

    Article  Google Scholar 

  • Breese, E L, and Mather, K. 1957. The organisation of polygenic activity within a chromosome in Drosophila. I. Hair characters. Heredity, 11, 373–395.

    Article  Google Scholar 

  • Connolly, V, and Jinks, J L. 1975. The genetical architecture of general and specific environmental sensitivity. Heredity, 35, 249–259.

    Article  Google Scholar 

  • Jinks, J L. 1954. The analysis of continuous variation in a diallel cross of Nicotiana rustica varieties. I. The analysis of F1 data. Genetics, 39, 767–788.

    CAS  PubMed  PubMed Central  Google Scholar 

  • Jinks, J L, and Broadhurst, P L. 1963. Diallel analysis of litter size and body weight in rats. Heredity, 18, 319–336.

    Article  Google Scholar 

  • Jinks, J L, and Connolly, V. 1973. Selection for specific and general response to environmental differences. Heredity, 30, 33–40.

    Article  Google Scholar 

  • Kearsey, M J, and Barnes, B W. 1970. Variation for metrical characters in Drosophila populations. II. Natural selection. Heredity, 25, 11–21.

    Article  CAS  Google Scholar 

  • Kearsey, M J, and Kojima, K. 1967. The genetic architecture of body weight and egg hatchability in Drosophila melanogaster. Genetics, 56, 23–37.

    CAS  PubMed  PubMed Central  Google Scholar 

  • Lawrence, M J. 1965. Variation in wild populations of Papaver dubium. I. Variation within populations: diallel crosses. Heredity, 20, 183–204.

    Article  Google Scholar 

  • Mather, K. 1953. The genetical structure of populations. Symp Soc Expt Biol, 7, 66–95.

    Google Scholar 

  • Mather, K. 1960. Evolution in polygenic systems. Evolution e Genetica Accad Nazionale die Lincei, 47, 131–152.

    Google Scholar 

  • Mather, K. 1973. Genetical Structure of Populations. Chapman and Hall, London.

    Google Scholar 

  • Mather, K, and Jinks, J L. 1971. Biometrical Genetics. Chapman and Hall, London.

    Book  Google Scholar 

  • Perkins, J M, and Jinks, J L. 1968. Environmental and genotype-environmental components of variability. III. Multiple lines and crosses. Heredity, 23, 339–356.

    Article  CAS  Google Scholar 

  • Simchen, G. 1965. Variation in a dikaryotic population of Collybia velutipes. Amer Nat, 92, 221–232.

    Google Scholar 

  • Simchen, G. 1966. Fruiting and growth rate among dikaryotic progeny of single wild isolates of Schizophyllum commune. Genetics, 53, 1151–1165.

    CAS  PubMed  PubMed Central  Google Scholar 

  • Simchen, G, and Jinks, J L. 1964. The determination of dikaryotic growth rate in the Basidiomycete Schizophyllum commune: a biometrical analysis. Heredity, 19, 629–649.

    Article  CAS  Google Scholar 

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Author information

Author notes
  1. S Williams

    Present address: Normal College, Bangor, North Wales

  2. C M Brasier

    Present address: Forest Research Station, Alice Holt Lodge, Farnham, Surrey, England

Authors and Affiliations

  1. Department of Genetics, University of Birmingham, Birmingham, B15 2TT

    S Williams, M M Verma, J L Jinks & C M Brasier

  2. Department of Plant Breeding, Punjab Agricultural University, Ludhiana, India

    M M Verma

Authors
  1. S Williams
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  2. M M Verma
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  3. J L Jinks
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  4. C M Brasier
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Williams, S., Verma, M., Jinks, J. et al. Variation in a natural population of Schizophyllum commune. Heredity 37, 365–375 (1976). https://doi.org/10.1038/hdy.1976.101

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  • Received: 12 April 1976

  • Issue date: 01 December 1976

  • DOI: https://doi.org/10.1038/hdy.1976.101

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