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A maximum likelihood approach to the detection of selection from a phylogeny

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Summary

A large amount of information is contained within the phylogentic relationships between species. In addition to their branching patterns it is also possible to examine other aspects of the biology of the species. The influence that deleterious selection might have is determined here. The likelihood of different phylogenies in the presence of selection is explored to determine the properties of such a likelihood surface. The calculation of likelihoods for a phylogeny in the presence and absence of selection, permits the application of a likelihood ratio test to search for selection. It is shown that even a single selected site can have a strong effect on the likelihood. The method is illustrated with an example fromDrosophila melanogaster and suggests that delerious selection may be acting on transposable elements.

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References

  • Aquadro CF, Desse SF, Bland MM, Langley CH, Laurie-Ahlberg CC (1986) Molecular population genetics of the alcohol dehydrogenase gene region ofDrosophila melanogaster. Genetics 114:1165–1190

    PubMed  Google Scholar 

  • Avery PJ (1978) Selection effects in a model of two intermigrating colonies of finite size. Theor Pop Biol 13:24–39

    Google Scholar 

  • Birky GW, Walsh JB (1988) Effects of linkage on rates of molecular evolution. Proc Natl Acad Sci USA 85:6414–6418

    PubMed  Google Scholar 

  • Felsenstein J (1965) The effect of linkage on directional selection. Genetics 52:349–363

    PubMed  Google Scholar 

  • Felsenstein J (1981) Evolutionary trees from DNA sequences: a maximum likelihood approach. J Mol Evol 17:368–376

    PubMed  Google Scholar 

  • Felsenstein J (1988) Phylogenies from molecular sequences: inference and reliability. Annu Rev Genet 22:521–565

    PubMed  Google Scholar 

  • Fukami K, Tateno Y (1989) On the maximum, likelihood method for estimating molecular trees: uniqueness of the likelihood point. J Mol Evol 28:460–464

    PubMed  Google Scholar 

  • Gillespie JH (1984a) The molecular clock may be an episodic clock. Proc Natl Acad Sci USA 81:8009–8013

    PubMed  Google Scholar 

  • Gillespie JH (1984b) Molecular evolution over the mutational landscape. Evolution 38(5):1116–1129

    Google Scholar 

  • Gillespie JH (1986) Variability of evolutionary rates of DNA. Genetics 113:1077–1091

    PubMed  Google Scholar 

  • Gillespie JH (1989) Lineage effects and the index of dispersion of molecular evolution. Mol Biol Evol 6:636–648

    PubMed  Google Scholar 

  • Golding GB (1987) The detection of deleterious selection using ancestors inferred from a phylogenetic history. Genet Res Camb 49:71–82

    Google Scholar 

  • Golding GB, Aquadro CF, Langley CH (1986) Sequence evolution within populations under multiple types of mutation. Proc Natl Acad Sci USA 83:427–431

    PubMed  Google Scholar 

  • Graur D, Li WH (1989) Evolution of protein inhibitors of serine proteinases-positive Darwinian selection or compositional effects. J Mol Evol 28:131–135

    Google Scholar 

  • hartl DL, Dykhuizen DE, Dean AM (1985) Limits of adaptation: the evolution of selective neutrality. Genetics 111: 655–674

    PubMed  Google Scholar 

  • Hill RE, Hastie ND (1987) Accelerated evolution in the reactive centre regions of serine protease inhibitors. Nature 326:96–99

    PubMed  Google Scholar 

  • Hudson RR (1983) Testing the constant rate neutral allele model with protein sequence data. Evolution 37:203–217

    Google Scholar 

  • Iizuka M (1989) A population genetical model for sequence evolution under multiple types of mutation. Genet Res 54: 231–237

    PubMed  Google Scholar 

  • Kaplan NL, Brookfield JFY (1983) Transposable elements in Mendelian populations III. Statistical results. Genetics 104: 485–495

    Google Scholar 

  • Kimura M (1955) Solution of a process of random genetic drift with a continuous model. Proc Natl Acad Sci USA 41:144–150

    Google Scholar 

  • Kimura M (1962) On the probability of fixation of mutant genes in a population. Genetics 4:713–719

    Google Scholar 

  • Kimura M (1979) Model of effectively neutral mutations in which selective constraint is incorporated. Proc Natl Acad Sci USA 76:3440–3444

    Google Scholar 

  • Kimura M (1983) The neutral theory of molecular evolution. Cambridge University Press. New York

    Google Scholar 

  • Koop BF, Goodman M, Xer P, Chan K, Slightom JL (1986) Primate z-globin DNA sequences and man's place among the great apes. Nature 319:234–238

    PubMed  Google Scholar 

  • Langley CH, Fitch WM (1974) An examination of the constancy of the rate of molecular evolution. J Mol Evol 3:161–177

    PubMed  Google Scholar 

  • Maeda N, Wu C, Bliska J, Reneke J (1988) Molecular evolution of intergenic DNA in higher primates: pattern of DNA changes, molecular clock, and evolution of repetitive sequences. Mol Biol Evol 5(1):1–20

    PubMed  Google Scholar 

  • Montgomery EA, Langley CH (1983) Transposable elements in Mendelian populations II. Distribution of three copia-like elements in a natural population ofDrosophila melanogaster. Genetics 104:473–483

    Google Scholar 

  • Nei M (1987) Molecular evolutionary genetics. Columbia University Press, New York

    Google Scholar 

  • Ohta T (1973) Slightly deleterious mutant substitutions in evolution. Nature 246:96–98

    PubMed  Google Scholar 

  • Ohta T (1976) Role of very slightly deleterious mutations in molecular evolution and polymorphism. Theor Pop Biol 10: 254–275

    Google Scholar 

  • Ohta R, Kimura M (1971) On the constancy of the evolutionary rate of cistrons. J Mol Evol 1:18–25

    PubMed  Google Scholar 

  • Sawyer SA, Dykhuizen DE, Hartl DL (1987) Confidence interval for the number of selectively neutral amino acid polymorphisms. Proc Natl Acad Sci USA 84:6225–6228

    PubMed  Google Scholar 

  • Wilson AC, Carlson SS, White TJ (1977) Biochemical evolution. Annu Rev Biochem 46:573–639

    PubMed  Google Scholar 

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Golding, B., Felsenstein, J. A maximum likelihood approach to the detection of selection from a phylogeny. J Mol Evol 31, 511–523 (1990). https://doi.org/10.1007/BF02102078

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  • DOI: https://doi.org/10.1007/BF02102078

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