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. 1995 Feb;139(2):993–1005. doi: 10.1093/genetics/139.2.993

A Space-Time Process Model for the Evolution of DNA Sequences

Z Yang 1
PMCID: PMC1206396  PMID: 7713447

Abstract

We describe a model for the evolution of DNA sequences by nucleotide substitution, whereby nucleotide sites in the sequence evolve over time, whereas the rates of substitution are variable and correlated over sites. The temporal process used to describe substitutions between nucleotides is a continuous-time Markov process, with the four nucleotides as the states. The spatial process used to describe variation and dependence of substitution rates over sites is based on a serially correlated gamma distribution, i.e., an auto-gamma model assuming Markov-dependence of rates at adjacent sites. To achieve computational efficiency, we use several equal-probability categories to approximate the gamma distribution, and the result is an auto-discrete-gamma model for rates over sites. Correlation of rates at sites then is modeled by the Markov chain transition of rates at adjacent sites from one rate category to another, the states of the chain being the rate categories. Two versions of nonparametric models, which place no restrictions on the distributional forms of rates for sites, also are considered, assuming either independence or Markov dependence. The models are applied to data of a segment of mitochondrial genome from nine primate species. Model parameters are estimated by the maximum likelihood method, and models are compared by the likelihood ratio test. Tremendous variation of rates among sites in the sequence is revealed by the analyses, and when rate differences for different codon positions are appropriately accounted for in the models, substitution rates at adjacent sites are found to be strongly (positively) correlated. Robustness of the results to uncertainty of the phylogenetic tree linking the species is examined.

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Selected References

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  1. Brown W. M., Prager E. M., Wang A., Wilson A. C. Mitochondrial DNA sequences of primates: tempo and mode of evolution. J Mol Evol. 1982;18(4):225–239. doi: 10.1007/BF01734101. [DOI] [PubMed] [Google Scholar]
  2. Felsenstein J. Evolutionary trees from DNA sequences: a maximum likelihood approach. J Mol Evol. 1981;17(6):368–376. doi: 10.1007/BF01734359. [DOI] [PubMed] [Google Scholar]
  3. Goldman N. Simple diagnostic statistical tests of models for DNA substitution. J Mol Evol. 1993 Dec;37(6):650–661. doi: 10.1007/BF00182751. [DOI] [PubMed] [Google Scholar]
  4. Jin L., Nei M. Limitations of the evolutionary parsimony method of phylogenetic analysis. Mol Biol Evol. 1990 Jan;7(1):82–102. doi: 10.1093/oxfordjournals.molbev.a040588. [DOI] [PubMed] [Google Scholar]
  5. Leroux B. G., Puterman M. L. Maximum-penalized-likelihood estimation for independent and Markov-dependent mixture models. Biometrics. 1992 Jun;48(2):545–558. [PubMed] [Google Scholar]
  6. Tamura K., Nei M. Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees. Mol Biol Evol. 1993 May;10(3):512–526. doi: 10.1093/oxfordjournals.molbev.a040023. [DOI] [PubMed] [Google Scholar]
  7. Wakeley J. Substitution-rate variation among sites and the estimation of transition bias. Mol Biol Evol. 1994 May;11(3):436–442. doi: 10.1093/oxfordjournals.molbev.a040124. [DOI] [PubMed] [Google Scholar]
  8. Wolfe K. H., Sharp P. M., Li W. H. Mutation rates differ among regions of the mammalian genome. Nature. 1989 Jan 19;337(6204):283–285. doi: 10.1038/337283a0. [DOI] [PubMed] [Google Scholar]
  9. Yang Z., Goldman N., Friday A. Comparison of models for nucleotide substitution used in maximum-likelihood phylogenetic estimation. Mol Biol Evol. 1994 Mar;11(2):316–324. doi: 10.1093/oxfordjournals.molbev.a040112. [DOI] [PubMed] [Google Scholar]
  10. Yang Z. Maximum-likelihood estimation of phylogeny from DNA sequences when substitution rates differ over sites. Mol Biol Evol. 1993 Nov;10(6):1396–1401. doi: 10.1093/oxfordjournals.molbev.a040082. [DOI] [PubMed] [Google Scholar]

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