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. 1988 Dec;120(4):1043–1051. doi: 10.1093/genetics/120.4.1043

Linkage Disequilibrium in Natural and Experimental Populations of Drosophila Melanogaster

Z Smit-McBride 1, A Moya 1, F J Ayala 1
PMCID: PMC1203567  PMID: 3147215

Abstract

We have studied linkage disequilibrium in Drosophila melanogaster in two samples from a wild population and in four large laboratory populations derived from the wild samples. We have assayed four polymorphic enzyme loci, fairly closely linked in the third chromosome: Sod, Est-6, Pgm, and Odh. The assay method used allows us to identify the allele associations separately in each of the two homologous chromosomes from each male sampled. We have detected significant linkage disequilibrium between two loci in 16.7% of the cases in the wild samples and in 27.8% of the cases in the experimental populations, considerably more than would be expected by chance alone. We have also found three-locus disequilibria in more instances than would be expected by chance. Some disequilibria present in the wild samples disappear in the experimental populations derived from them, but new ones appear over the generations. The effective population sizes required to generate the observed disequilibria by randomness range from 40 to more than 60,000 individuals in the natural population, depending on which locus pair is considered, and from 100 to more than 60,000 in the experimental populations. These population sizes are unrealistic; moreover, the fact that different locus-pairs yield disparate estimates within the same population argues against the likelihood that the disequilibria may have arisen as a consequence of population bottlenecks. Migration, or population mixing, cannot be excluded as the process generating the disequilibria in the wild samples, but can in the experimental populations. We conclude that linkage disequilibrium in these populations is most likely due to natural selection acting on the allozymes, or on loci very tightly linked to them.

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Selected References

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

  1. Baker W. K. Linkage disequilibrium over space and time in natural populations of Drosophila montana. Proc Natl Acad Sci U S A. 1975 Oct;72(10):4095–4099. doi: 10.1073/pnas.72.10.4095. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Barker J. S. Inter-locus interactions: a review of experimental evidence. Theor Popul Biol. 1979 Dec;16(3):323–346. doi: 10.1016/0040-5809(79)90021-2. [DOI] [PubMed] [Google Scholar]
  3. Birley A. J., Haley C. S. The Genetical Response to Natural Selection by Varied Environments. IV. Gametic Disequilibrium in Spatially Varied Environments. Genetics. 1987 Feb;115(2):295–303. doi: 10.1093/genetics/115.2.295. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Charlesworth B., Charlesworth D. A study of linkage disequilibrium in populations of Drosophila melanogaster. Genetics. 1973 Feb;73(2):351–359. doi: 10.1093/genetics/73.2.351. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Clegg M. T., Allard R. W. Patterns of Genetic Differentiation in the Slender Wild Oat Species Avena barbata. Proc Natl Acad Sci U S A. 1972 Jul;69(7):1820–1824. doi: 10.1073/pnas.69.7.1820. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Clegg M. T., Kidwell J. F., Horch C. R. Dynamics of Correlated Genetic Systems. V. Rates of Decay of Linkage Disequilibria in Experimental Populations of DROSOPHILA MELANOGASTER. Genetics. 1980 Jan;94(1):217–234. doi: 10.1093/genetics/94.1.217. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Epperson B. K., Allard R. W. Linkage Disequilibrium between Allozymes in Natural Populations of Lodgepole Pine. Genetics. 1987 Feb;115(2):341–352. doi: 10.1093/genetics/115.2.341. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hedrick P. W., Thomson G. A two-locus neutrality test: applications to humans, E. coli and lodgepole pine. Genetics. 1986 Jan;112(1):135–156. doi: 10.1093/genetics/112.1.135. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Hudson R. R. Properties of a neutral allele model with intragenic recombination. Theor Popul Biol. 1983 Apr;23(2):183–201. doi: 10.1016/0040-5809(83)90013-8. [DOI] [PubMed] [Google Scholar]
  10. Langley C. H., Smith D. B., Johnson F. M. Analysis of linkage disequilibria between allozyme loci in natural populations of Drosophila melanogaster. Genet Res. 1978 Nov;32(3):215–229. doi: 10.1017/s0016672300018711. [DOI] [PubMed] [Google Scholar]
  11. Laurie-Ahlberg C. C., Weir B. S. Allozymic Variation and Linkage Disequilibrium in Some Laboratory Populations of DROSOPHILA MELANOGASTER. Genetics. 1979 Aug;92(4):1295–1314. doi: 10.1093/genetics/92.4.1295. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Mitton J. B., Koehn R. K. Population genetics of marine pelecypods. 3. Epistasis between functionally related isoenzymes of Mytilus edulis. Genetics. 1973 Mar;73(3):487–496. doi: 10.1093/genetics/73.3.487. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Ohta T. Linkage disequilibrium between amino acid sites in immunoglobulin genes and other multigene families. Genet Res. 1980 Oct;36(2):181–197. doi: 10.1017/s0016672300019790. [DOI] [PubMed] [Google Scholar]
  14. Ohta T. Linkage disequilibrium with the island model. Genetics. 1982 May;101(1):139–155. doi: 10.1093/genetics/101.1.139. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Selander R. K., Levin B. R. Genetic diversity and structure in Escherichia coli populations. Science. 1980 Oct 31;210(4469):545–547. doi: 10.1126/science.6999623. [DOI] [PubMed] [Google Scholar]
  16. Zhang Q., Tibayrenc M., Ayala F. J. Linkage disequilibrium in natural populations of Trypanosoma cruzi (flagellate), the agent of Chagas' disease. J Protozool. 1988 Feb;35(1):81–85. doi: 10.1111/j.1550-7408.1988.tb04081.x. [DOI] [PubMed] [Google Scholar]
  17. van der Loo W., Arthur C. P., Richardson B. J., Wallage-Drees M., Hamers R. Nonrandom allele associations between unlinked protein loci: are the polymorphisms of the immunoglobulin constant regions adaptive? Proc Natl Acad Sci U S A. 1987 May;84(9):3075–3079. doi: 10.1073/pnas.84.9.3075. [DOI] [PMC free article] [PubMed] [Google Scholar]

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