Skip to main content

A reanalysis of protein polymorphism in Drosophila melanogaster, D. simulans, D. sechellia and D. mauritiana: effects of population size and selection

  • Chapter
Drosophila melanogaster, Drosophila simulans: So Similar, So Different

Part of the book series: Contemporary Issues in Genetics and Evolution ((CIGE,volume 11))

  • 368 Accesses

Abstract

Comparison of synonymous and nonsynonymous variation/substitution within and between species at individual genes has become a widely used general approach to detect the effect of selection versus drift. The sibling species group comprised of two cosmopolitan (Drosophila melanogaster and Drosophila simulans) and two island (Drosophila mauritiana and Drosophila sechellia) species has become a model system for such studies. In the present study we reanalyzed the pattern of protein variation in these species, and the results were compared against the patterns of nucleotide variation obtained from the literature, mostly available for melanogaster and simulans. We have mainly focused on the contrasting patterns of variation between the cosmopolitan pair. The results can be summarized as follows: (1) As expected the island species D. mauritiana and D. sechellia showed much less variation than the cosmopolitan species D. melanogaster and D. simulans. (2) The chromosome 2 showed significantly less variation than chromosome 3 and X in all four species which may indicate effects of past selective sweeps. (3) In contrast to its overall low variation, D. mauritiana showed highest variation for X-linked loci which may indicate introgression from its sibling, D. simulans. (4) An average population of D. simulans was as heterozygous as that of D. melanogaster (14.4% v.s. 13.9%) but the difference was large and significant when considering only polymorphic loci (37.2% v.s. 26.1%). (5) The species-wise pooled populations of these two species showed similar results (all loci= 18.3% v.s. 20.0%, polymorphic loci = 47.2% v.s. 37.6%). (6) An average population of D. simulans had more low- frequency alleles than D. melanogaster, and the D. simulans alleles were found widely distributed in all populations whereas the D. melanogaster alleles were limited to local populations. As a results of this, pooled populations of D. melanogaster showed more polymorphic loci than those of D. simulans (48.0% v.s. 32.0%) but the difference was reduced when the comparison was made on the basis of an average population (29.1 % v.s. 21.4%). (7) While the allele frequency distributions within populations were nonsignificant in both D. melanogaster and D. simulans, melanogaster had fewer than simulans, but more than expected from the neutral theory, low frequency alleles. (8) Diallelic loci with the second allele with a frequency less than 20% had similar frequencies in all four species but those with the second allele with a frequency higher than 20% were limited to only melanogaster. the latter group of loci have clinal (latitudinal) patterns of variation indicative of balancing selection. (9) The comparison of D. simulans/D. melanogaster protein variation gave a ratio of 1.04 for all loci and 1.42 for polymorphic loci, against a ratio of approximately 2-fold difference for silent nucleotide sites. This suggests that the species ratios of protein and silent nucleotide polymorphism are too close to call for selective difference between silent and allozyme variation in D. simulans. In conclusion, the contrasting levels of allozyme polymorphism, distribution of rare alleles, number of diallelic loci and the patterns of geographic differentiation between the two species suggest the role of natural selection in D. melanogaster, and of possibly ancient population structure and recent worldwide migration in D. simulans. Population size differences alone are insufficient as an explanation for the patterns of variation between these two species.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 129.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 169.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 169.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  • Akashi, H., 1994. Synonymous codon usage in Drosophila melano-gaster. natural selection and translational accuracy. Genetics 136: 927–935. Akashi, H., 1995. Inferring weak selection from patterns of polymorphism and divergence at’ silent’ sites in Drosophila DNA. Genetics 139: 1067-1076. Akashi, H., 1996. Molecular evolution between Drosophila melano-gaster and D. simulans: reduced codon bias, faster rates of amino acid substitution and larger proteins in D. melanogaster. Genetics 144: 1297-1307.

    PubMed  CAS  Google Scholar 

  • Andolfatto, P., J.D. Wall & M. Kreitman, 1999. Unusual haplotype structure at the proximal breakpoint of In(2L)t in a natural population of Drosophila melanogaster. Genetics 153: 1297–1311. Aquadro, C.F., 1992. Why is the genome variable? Insights from Drosophila. TIG 8: 355-362. Aquadro, C.F., 1997. Insights into the evolutionary process from patterns of DNA sequence variability. Curr. Opin. Genet. Dev. 7: 835-840. Aquadro, C.F., K.M. Lado & W.A. Noon, 1988. The rosy region of D. melanogaster and Drosophila simulans. I. Contrasting levels of naturally occurring DNA restriction map variation and divergence. Genetics 119: 875-888. Aquadro, C.F., D.I. Begun & E.C. Kindahl, 1994. Selection, recombination, and DNA polymorphism in Drosophila, pp. 46-56 in Non-neutral Evolution Theories and Molecular Data, edited by B. Golding. Chapman & Hall, New York, USA. Aulard, S., J.R. David & F. Lemeunier, 2002. Chromosomal inversion polymorphism in Afrotropical populations of Drosophila melanogaster. Genet. Res. Camb. 79: 49-63. Baba-Aissa, F., M. Solignac, N. Dennebouy & J.R. David, 1988. Mitochondrial DNA variability in Drosophila simulans. I. Contrasting levels of naturally occurring DNA restriction map variation and divergence. Genetics 119: 1165-1190. Begun, DJ. & C.F. Aquadro, 1992. Levels of naturally occurring DNA polymorphism correlate with recombination rates in D. melanogaster. Nature 356: 519-520. Begun, D.J. & C.F. Aquadro, 1993. African and North American populations of Drosophila melanogaster are very different at the DNA level. Nature 365: 548-550.

    PubMed  CAS  Google Scholar 

  • Bellard, J.W.O., 2000. Comparative genomics of Mitochondrial DNA in Drosophila simulans. J. Mol. Evol. 51:64–75. Bellard, J.W.O., J. Hatzidakis, T.L. Karr & M. Kreitman, 1996. Reduced variation in Drosophila simulans Mitochondrial DNA. Genetics 144: 1519-1528. Benassi, V. & M. Veuille, 1995. Comparative population structure of molecular and allozyme variation of Drosophila melanogaster Adh between Europe, West Africa and East Africa. Genet. Res. Camb. 65: 95-103. Berry, A. & M. Kreitman, 1993. Molecular analysis of an allozyme cline: alcohol dehydrogenase in Drosophila melanogaster on the East coast of North America. Genetics 134: 869-893. Cappy, P., E. Pla & J.R. David, 1993. Phenotypic and genetic variability of morphometrical traits in natural populations of Drosophila melanogaster and D. simulans. I. Geographic variations. Genet. Sei. Evol. 25:517-536. Chambers, G.K., 1988. The Drosophila alcohol dehydrogenase gene-enzyme system. Adv. Genet. 25: 39-107. Charlesworfh, B., 1996. Background selection and patterns of genetic diversity in Drosophila melanogaster. Genet. Res. Camb. 68: 131-149. Charlesworth B., M.T. Morgan & D. Charlesworth, 1993. The effect of deleterious mutations on neutral molecular variation. Genetics 134: 1289-1303. Choudhary, M., 1987. Genetic structure and species divergence between populations of Drosophila melanogaster, and its sibling species Drosophila simulans. PhD Thesis, McMaster University. Choudhary, M. & R.S. Singh, 1987. A comparative study of genetic variation in natural populations of Drosophila melanogaster. III. Variations in genetic structure and their causes between Drosophila melanogaster and its sibling species Drosophila simulans. Genetics 117:697-710. Crow, J.F. & M. Kimura, 1970. An Introduction to Population Genetics Theory. Harper & Row, New York. Dainou, O., M.L. Cariou, J.M. Goux & J.R. David, 1993. Amylase polymorphism in Drosophila melanogaster. haplotype frequencies in tropical African and American populations. Genet. Sei. Evol. 25: 133-151. David, J.R. & P. Capy, 1988. Genetic variation of Drosophila melanogaster natural populations. TIG 4: 106-111. David, J.R., C. Bocquet & E. Pia, 1976. New results on the genetic characteristics of the Far East race of Drosophila melanogaster. Genet. Res. 28: 253-260. Eanes, W.A., M. Kirchner & J. Yoon, 1993. Evidence for the adap-tive evolution of the G6pd gene in the Drosophila melanogaster and Drosophila simulans lineages. Proc. Natl. Acad. Sei. USA 90: 7475-7479. Eanes, W.A., M. Kirchner, J. Yoon, C.H. Biermann, I.-N. Wang, M.A. McCartney & B.C. Verrelli, 1996. Historical selection, amino acid polymorphism and lineage-specific divergence at the G6pd locus in Drosophila melanogaster and D. simulans. Genetics 144: 1027-1041.

    Google Scholar 

  • Ewens, W.J., 1972. The sampling theory of selectively neutral alleres. Theor. Pop. Biol. 3:87–112. Hamblin, M.T. & M. Veuille, 1999. Population structure among African and derived populations of Drosophila simulans: Evidence for ancient subdivision and recent admixture. Genetics 153:305-317. Hudson, R.R., 1994. How can the low levels of DNA sequence variation in regions of the Drosophila genome with low recombination rates be explained? Proc. Natl. Acad. Sci. USA 91: 6815-6818. Hudson, R.R. & N.L. Kaplan, 1995. Deleterious background selection with recombination. Genetics 141: 1605-1617. Hudson, R.R., Säez & F.J. Ayala, 1997. DNA variation at the Sod locus of Drosophila melanogaster. an unfolding story of natural selection. Proc. Natl. Acad. Sei. USA 94: 7725-7729. Kliman R.M. & J. Hey, 1993. Reduced natural selection associated with low recombination in Drosophila melanogaster. Mol. Biol. Evol. 10: 1239-1258. Kliman, R.M. & J. Hey, 1994. The effects of mutation and natural selection on codon bias in the genes of Drosophila. Genetics 137: 1049-1056. Kulathinal, R. & R.S. Singh, 1998. Cytological characterization of premeiotic versus postmeiotic defects producing male hybrid sterility among sibling species of the Drosophila melanogaster complex. Evolution 52: 1067-1079. Lachaise, D., M.-L. Cariou, J.R. David, F. Lemeunier, L. Tsacas & M. Ashburner, 1988. Historical biogeography of the Drosophila melanogaster species subgroup. Evol. Biol. 22: 159-225. Lemeunier, F. & S. Aulard, 1992. Inversion polymorphism in Drosophila melanogaster, pp. 339-405 in Drosophila Inversion Polymorphism, Chapter 6, edited by C.B. Krimbas & J.R. Powell. CRC Press, Boca Raton, FL. Li, W.-H., 1979. Maintenance of genetic variability under pressure of neutral and deleterious mutations in a finite population. Genetics 92: 647-667. Long, A.D., 1993. A correction for allele frequency estimates derived from isofemale lines. Biochem. Genet. 31: 61-74. Moriyama, E.N. & J.R. Powell, 1996. Intraspecific nuclear DNA variation in Drosophila. Mol. Biol. Evol. 13: 261-277. Oakeshott, J.G., G.K. Chambers, J.B. Gibson, W.F. Eanes & D.A. Willcocks, 1983. Geographic variation in G6pd and Pgd allele frequencies in Drosophila melanogaster. Heredity 50: 62-72.

    Google Scholar 

  • Ohta, T., 1976. Role of very slightly deleterious mutations in molecular evolution and polymorphism. Theor. Pop. Biol. 10: 254–275. Ohta, T., 1987. Very slightly deleterious mutations and the molecular clock. J. Mol. Evol. 26: 1-6. Shields, D.C., P.M. Sharp, D.G. Higgins & F. Wright, 1988.’ silent’ sites in Drosophila genes are not neutral: evidence of selection among synonymous codons. Mol. Biol. Evol. 5: 704-716. Singh, R.S., 1989. Population genetics and evolution of species related to Drosophila melanogaster. Ann. Rev. Genet. 23: 425 53. Singh, R.S. & A.D. Long, 1992. Geographic variation in Drosophila: from molecules to morphology and back. TREE 7: 340-345. Singh, R.S. & L.R. Rhomberg, 1987a. A comprehensive study of genetic variation in natural populations of D. melanogaster. I. Estimates of gene flow from rare alleles. Genetics 115: 313-322. Singh, R.S. & L.R. Rhomberg, 1987b. A comprehensive study of genetic variation in natural populations of D. melanogaster. II. Estimates of heterozygosity and patterns of geographic differentiation. Genetics 117: 255-271. Singh, R.S., D.A. Hickey & J. David, 1982. Genetic differentiation between geographically distant populations of Drosophila melanogaster. Genetics 101: 235-256. Slatkin, M., 1981. Rare alleles as indicators of gene flow. Evolution 39: 53-65. Smith, J.M. & J. Haigh, 1974. The hitch-hiking effect of a favourable gene. Genet. Res. Camb. 23: 23-35. True, J.R., J.M. Mercer & C.C. Laurie, 1996. Differences in crossover frequency and distribution among three sibling species of Drosophila. Genetics 142: 507-523. Veuille, M., V. Bénassi, S. Autlard & F. Depaulis, 1998. Allele-specific population structure of Drosophila melanogaster alcohol dehydrogenase at the molecular level. Genetics 149: 971-981. Vouidibio, J., P. Cappy, D. Defaye, E. Pia, J. Sandrin, A. Csink & J.R. David, 1989. Short-range genetic structure of Drosophila melanogaster populations in an Afrotropical urban area and its significance. Proc. Natl. Acad. Sci. USA 86: 8442-8446. Wiehe, T.H.E. & W. Stephan, 1993. Analysis of a genetic hitchhiking model, and its application to DNA polymorphism data from Drosophila melanogaster. Mol. Biol. Evol. 10: 842-854.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

P. Capy P. Gibert I. Boussy

Rights and permissions

Reprints and permissions

Copyright information

© 2004 Springer Science+Business Media Dordrecht

About this chapter

Cite this chapter

Morton, R.A., Choudhary, M., Cariou, ML., Singh, R.S. (2004). A reanalysis of protein polymorphism in Drosophila melanogaster, D. simulans, D. sechellia and D. mauritiana: effects of population size and selection. In: Capy, P., Gibert, P., Boussy, I. (eds) Drosophila melanogaster, Drosophila simulans: So Similar, So Different. Contemporary Issues in Genetics and Evolution, vol 11. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-0965-2_9

Download citation

  • DOI: https://doi.org/10.1007/978-94-007-0965-2_9

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-3755-6

  • Online ISBN: 978-94-007-0965-2

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics