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Enzyme polymorphism inDrosophila melanogaster populations collected in two different habitats in Hungary

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Abstract

The level of enzyme polymorphism was compared in tenDrosophila melanogaster populations collected in farmyards and distilleries in two regions of Hungary. The total genetic diversity was partitioned into between-and within-population components at each investigated locus using Wright's F-statistics. Population differentiation was studied in two different ways. Genetic distances between pairs of populations were calculated and a hierarchical analysis of gene diversity was performed. Based on the F values gene flow was estimated among the populations at different levels of the hierarchy. The results indicated that our ‘farmyard populations’ collected within a region could be considered as parallel samples from a panmictic population rather than samples of distinct populations. In distilleries, the flies might be influenced by two different evolutionary forces: (i) selection due to the extremely high concentration of ethanol in the fermenting mash and (ii) genetic drift due to the combination of repeated founder effects and fluctuating population size. Our results suggested that ‘distillery populations’ could not be regarded as real populations either. They could be considered as peculiar cases: founder individuals taken from the total population (region) established special populations which survived in the distilleries for many generations. Thus the dominating force acting on the ‘distillery populations’ was genetic drift.

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References

  • Briscoe, D.A., A. Robertson & J.M. Malpica, 1975. Dominance at the Adh locus in response of adultDrosophila melanogaster to environmental alcohol. Nature 255: 148–149.

    PubMed  Google Scholar 

  • Cavalli-Sforza, L.L. & A.W.F. Edwards, 1967. Phylogenetic analysis: models and estimation procedures. Evolution 21: 550–570.

    Google Scholar 

  • David, J.R., 1988. Ethanol adaptation on alcohol dehydrogenase polymorphism inDrosophila: from phenotype functions to genetic structures, pp. 163–172 in Population Genetics and Evolution, edited by G. de Jong. Springer, Berlin.

    Google Scholar 

  • David, J.R., A. Alonso-Moraga, F. Borai, P. Capy, H. Mercot, S.F. McEvey, A. Munoz-Serrano & S. Tsakas, 1989. Latitudinal variation of Adh gene frequencies inDrosophila melanogaster: A Mediterranean instability. Heredity 62: 11–16.

    PubMed  Google Scholar 

  • Freriksen, J.W.M., 1992: Metabolic physiology and evolution of the alcohol dehydrogenase gene-enzyme system inDrosophila. Ph.D. thesis. University of Utrecht, The Netherlands.

    Google Scholar 

  • Geer, B.W., S.W. McKechnie & M.L. Langevin, 1983. Regulation of α-Glycerol-3-phosphate dehydrogenase inDrosophila melanogaster larvae by dietary ethanol and sucrose. J. Nutr. 113: 1632–1642.

    PubMed  Google Scholar 

  • Geer, B.W., M.L. Langevin & S.W. McKechnie, 1985. Dietary ethanol and lipid synthesis inDrosophila melanogaster. Biochem. Genet. 23: 607–622.

    PubMed  Google Scholar 

  • Geer, B.W., L. Dybas & L.J. Shanner, 1989. Alcohol dehydrogenase and ethanol tolerance at the cellular level inDrosophila melanogaster. J. Exp. Zool. 250: 22–39.

    PubMed  Google Scholar 

  • Geer, B.W., P.W.H. Heinstra & S.W. McKechnie, 1993. The biological basis of ethanol tolerance inDrosophila. Comp. Biochem. Physiol. 105B/2: 203–229.

    Google Scholar 

  • Gibson, J.B., T.W. May & A.V. Wilks, 1981. Genetic variation at the alcohol dehydrogenase locus inDrosophila melanogaster in relation to environmental variations: ethanol levels in breeding sites and allozyme frequencies. Oecologica 51: 191–198.

    Google Scholar 

  • Gibson, J.B. & A.V. Wilks, 1988. The alcohol dehydrogenase polymorphims ofDrosophila melanogaster in relation to environmental ethanol, ethanol tolerance and alcohol dehydrogenase activity. Heredity 60: 403–414.

    PubMed  Google Scholar 

  • Heinstra, P.W.H., 1993. Evolutionary genetics of theDrosophila alcohol dehydrogenase gene-enzyme system. Genetica 92: 1–22.

    PubMed  Google Scholar 

  • Heinstra, P.W.H., W. Scharloo & G.E.W. Thörig, 1987. Physiological significance of the alcohol dehydrogenase polymorphism in larvae ofDrosophila. Genetics 117: 75–84.

    PubMed  Google Scholar 

  • Heinstra, P.W.H., D. Seykens, A. Freriksen & B.W. Geer, 1990. Metabolic physiology of alcohol degradation and adaptation inDrosophila larvae as studied by means of carbon-13 nuclear magnetic resonance spectroscopy. Insect Biochem. 20: 343–348.

    Google Scholar 

  • Hickey, D.A. & M.D. McLean, 1980. Selection for ethanol tolerance and ADH allozymes in natural populations ofDrosophila melanogaster. Genet. Res. 36: 11–15.

    PubMed  Google Scholar 

  • Kojima, K., J. Gillespie & Y.N. Tobari, 1970. A profile ofDrosophila species' enzymes assayed by electrophoresis. I. Number of alleles, heterozygosity, and linkage disequilibrium. Biochem. Genet. 4: 627–637.

    PubMed  Google Scholar 

  • Marks, R.W., J.G. Brittnacher, J.F. McDonald, T. Prout & F.J. Ayala, 1980. Wineries,Drosophila, alcohol and ADH. Oecologica 47: 141–144.

    Google Scholar 

  • Middleton, R.J. & H. Kacser, 1983. Enzyme variation, metabolic flux and fitness: alcohol dehydrogenase inDrosophila melanogaster. Genetics 105: 633–650.

    PubMed  Google Scholar 

  • Nei, M., 1977. F-statistics and analysis of gene diversity in subdivided populations. Ann. Human. Genet. 41: 225–233.

    Google Scholar 

  • Nei, M., 1978. Estimation of average heterozygosity and genetic distance from a small number of individuals. Genetics 89: 583–590.

    Google Scholar 

  • Oakeshott, J.G., J.B. Gibson, P.R. Anderson, W.R. Knibb, D.G. Anderson & G.K. Chambers, 1982. Alcohol dehydrogenase and glycerol-3-phosphate dehydrogenase clines inDrosophila melanogaster on different continents. Evolution 36: 86–96.

    Google Scholar 

  • Oakeshott, J.G., J.B. Gibson & D.A. Willcocks, 1983. Latitudinal variation in octanol dehydrogenase and acid phosphatase allele frequencies inDrosophila melanogaster. Theor. Appl. Genet. 65: 191–196.

    Google Scholar 

  • O'Brien, S.J. & R.J. MacIntyre, 1969. An analysis of gene-enzyme variability in natural populations ofDrosophila melanogaster andDrosophila simulans. Am. Nat. 103: 97–114.

    Google Scholar 

  • Pecsene, K., 1989. A comparison of the level of enzyme polymorphism in cosmopolitanDrosophila species between populations collected in distilleries and in their surroundings in Hungary. Genet. Sel. Evol. 21: 147–157.

    Google Scholar 

  • Pecsenye, K. & G. Lörincz, 1988. Changes in gene frequencies at the octanol dehydrogenase locus ofDrosophila melanogaster imposed by environmental ethanol. Genetica 77: 171–177.

    PubMed  Google Scholar 

  • Pecsenye, K., L.P. Lefkovitch, B.E. Giles, & A. Saura, 1995. The influence of the Odh-Aldox region of the third chromosome on the response ofDrosophila melanogaster to environmental alcohol. Hereditas.

  • Pecsenye, K., L.P. Lefkovitch, B.E. Giles & A. Saura, 1995. Does the Odh-Aldox region of the third chromosome influence the response ofDrosophila melanogaster to alcohol stress? Hereditas.

  • Porter, A.H., 1990. Testing nominal species boundaries using gene flow statistics: The taxonomy of two hybridizing admiral butterflies (Limenitis: Nymphalidae). Syst. Zool. 39/2: 131–147.

    Google Scholar 

  • Singh, R.S., D.A. Hickey & J. David, 1982. Genetic differentiation between geographically distant populations ofDrosophila melanogaster. Genetics 101: 235–256.

    Google Scholar 

  • Slatkin, M. & N.H. Barton, 1989. A comparison of three indirect methods for estimating average levels of gene flow. Evolution 43: 1349–1368.

    Google Scholar 

  • Slatkin, M. & L. Voelm, 1991. F ST in a hierarchical island model. Genetics 127: 627–629.

    PubMed  Google Scholar 

  • Smith, D.B., C.H. Langley & F.M. Johnson, 1978. Variance component analysis of allozyme frequency data from eastern populations ofDrosophila melanogaster. Genetics 88: 121–137.

    PubMed  Google Scholar 

  • Sneath, P.H.A. & R.R. Sokal, 1973. Numerical Taxonomy. W.H. Freeman, San Francisco.

    Google Scholar 

  • Sokal, R.R. & F.J. Rohlf, 1969. Biometry. W.H. Freeman, San Francisco.

    Google Scholar 

  • Swofford, D.L. & R.B. Selander, 1989. A computer program for analysis of allelic variation in population genetics and biochemical systematics. Release 1.7. David L. Swofford, Illinois Natural History Survey.

  • Taylor, C.E. & J.R. Powel, 1983. Population structure ofDrosophila: genetics and ecology. In M. Ashburner & T.R.F. Wright (eds.), The Genetics and Biology ofDrosophila. Academic Press, London, Vol. 3d: 29–59.

    Google Scholar 

  • Wolf, P.G. & P.S. Soltis, 1992. Estimates of gene flow among populations, geographic races, and species in theImpomopsis aggredata complex. Genetics 130: 639–647.

    PubMed  Google Scholar 

  • Wright, S., 1951. The genetical structure of populations. Ann. Eugenics 15: 323–354

    Google Scholar 

  • Wright, S., 1965. The interpretation of population structure by F-statistics with special regard to systems of mating. Evolution 19: 395–420.

    Google Scholar 

  • Wright, S., 1978. Evolution and the genetics of populations. Vol. 4. Variability within and among natural populations. University of Chicago Press, Chicago.

    Google Scholar 

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Pecsenye, K., Meglécz, E. Enzyme polymorphism inDrosophila melanogaster populations collected in two different habitats in Hungary. Genetica 96, 257–268 (1995). https://doi.org/10.1007/BF01439580

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