Patterns of nucleotide substitution in mitochondrial protein coding genes of vertebrates.

Maximum likelihood methods were used to study the differences in substitution rates among the four nucleotides and among different nucleotide sites in mitochondrial protein-coding genes of vertebrates. In the 1st + 2nd codon position data, the frequency of nucleotide G is negatively correlated with evolutionary rates of genes, substitution rates vary substantially among sites, and the transition/transversion rate bias (R) is two to five times larger than that expected at random. Generally, largest transition biases and greatest differences in substitution rates among sites are found in the highly conserved genes. The 3rd positions in placental mammal genes exhibit strong nucleotide composition biases and the transitional rates exceed transversional rates by one to two orders of magnitude. Tamura-Nei and Hasegawa-Kishino-Yano models with gamma distributed variable rates among sites (gamma parameter, alpha) adequately describe the nucleotide substitution process in 1st+2nd position data. In these data, ignoring differences in substitution rates among sites leads to largest biases while estimating substitution rates. Kimura's two-parameter model with variable-rates among sites performs satisfactorily in likelihood estimation of R, alpha, and overall amount of evolution for 1st+2nd position data. It can also be used to estimate pairwise distances with appropriate values of alpha for a majority of genes.

[1]  M. Nei,et al.  Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees. , 1993, Molecular biology and evolution.

[2]  S. Tavaré Some probabilistic and statistical problems in the analysis of DNA sequences , 1986 .

[3]  P. Gingerich,et al.  New whale from the Eocene of Pakistan and the origin of cetacean swimming , 1994, Nature.

[4]  Nicholas W. Gillham,et al.  Organelle Genes and Genomes , 1994 .

[5]  B. Crespi,et al.  Evolution, weighting, and phylogenetic utility of mitochondrial gene sequences and a compilation of conserved polymerase chain reaction primers , 1994 .

[6]  H. Kishino,et al.  Heterogeneity of tempo and mode of mitochondrial DNA evolution among mammalian orders. , 1989, Idengaku zasshi.

[7]  Rainer Fuchs,et al.  CLUSTAL V: improved software for multiple sequence alignment , 1992, Comput. Appl. Biosci..

[8]  A Rzhetsky,et al.  Tests of applicability of several substitution models for DNA sequence data. , 1995, Molecular biology and evolution.

[9]  C. Ragan Structure of NADH-Ubiquinone Reductase (Complex I) , 1987 .

[10]  J. Wakeley,et al.  Substitution-rate variation among sites and the estimation of transition bias. , 1994, Molecular biology and evolution.

[11]  John C. Avise,et al.  Molecular Markers, Natural History and Evolution , 1993, Springer US.

[12]  N. Perna,et al.  Unequal Base Frequencies and the Estimation of Substitution Rates , 1995 .

[13]  D. A. Clayton,et al.  Sequence and gene organization of mouse mitochondrial DNA , 1981, Cell.

[14]  A. Wilson,et al.  Sequence Evolution of Mitochondrial DNA in Humans and Chimpanzees: Control Region and a Protein-Coding Region , 1991 .

[15]  S. Hedges,et al.  Monophyly of the order Rodentia inferred from mitochondrial DNA sequences of the genes for 12S rRNA, 16S rRNA, and tRNA-valine. , 1995, Molecular biology and evolution.

[16]  G A Churchill,et al.  Methods for inferring phylogenies from nucleic acid sequence data by using maximum likelihood and linear invariants. , 1991, Molecular biology and evolution.

[17]  M. Nei Age of the common ancestor of human mitochondrial DNA. , 1992, Molecular biology and evolution.

[18]  B. Roe,et al.  The complete nucleotide sequence of the Xenopus laevis mitochondrial genome. , 1985, The Journal of biological chemistry.

[19]  Sudhir Kumar,et al.  MEGA: Molecular Evolutionary Genetics Analysis software for microcomputers , 1994, Comput. Appl. Biosci..

[20]  T. Jukes CHAPTER 24 – Evolution of Protein Molecules , 1969 .

[21]  W. J. Dakin General Zoölogy , 1926, Nature.

[22]  M. Clegg,et al.  Evolutionary Analysis of Plant DNA Sequences , 1987, The American Naturalist.

[23]  N. Takahata,et al.  Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[24]  G. Estabrook,et al.  Compositional Effects and Weighting of Nucleotide Sequences for Phylogenetic Analysis , 1994 .

[25]  N Takezaki,et al.  Efficiencies of different genes and different tree-building methods in recovering a known vertebrate phylogeny. , 1996, Molecular biology and evolution.

[26]  K. Hawkes,et al.  African populations and the evolution of human mitochondrial DNA. , 1991, Science.

[27]  M. Nei,et al.  Relative efficiencies of the maximum-likelihood, neighbor-joining, and maximum-parsimony methods when substitution rate varies with site. , 1994, Molecular biology and evolution.

[28]  S. Vries,et al.  Mitochondrial cytochrome b: evolution and structure of the protein. , 1993, Biochimica et biophysica acta.

[29]  A Janke,et al.  The marsupial mitochondrial genome and the evolution of placental mammals. , 1994, Genetics.

[30]  H Kishino,et al.  Converting distance to time: application to human evolution. , 1990, Methods in enzymology.

[31]  G. B. Golding,et al.  Estimates of DNA and protein sequence divergence: an examination of some assumptions. , 1983, Molecular biology and evolution.

[32]  E. Simons,et al.  Hind Limbs of Eocene Basilosaurus: Evidence of Feet in Whales , 1990, Science.

[33]  F. Sanger,et al.  Complete sequence of bovine mitochondrial DNA. Conserved features of the mammalian mitochondrial genome. , 1982, Journal of molecular biology.

[34]  P. Desjardins,et al.  Sequence and gene organization of the chicken mitochondrial genome. A novel gene order in higher vertebrates. , 1990, Journal of molecular biology.

[35]  K. Tamura,et al.  Model selection in the estimation of the number of nucleotide substitutions. , 1994, Molecular biology and evolution.

[36]  Z. Yang,et al.  On the use of nucleic acid sequences to infer early branchings in the tree of life. , 1995, Molecular biology and evolution.

[37]  R. Martin Primate origins: plugging the gaps , 1993, Nature.

[38]  C Saccone,et al.  Influence of base composition on quantitative estimates of gene evolution. , 1990, Methods in enzymology.

[39]  Robert L. Carroll,et al.  Vertebrate Paleontology and Evolution , 1988 .

[40]  P. C. Huang,et al.  The complete nucleotide sequence of the Crossostoma lacustre mitochondrial genome: conservation and variations among vertebrates. , 1992, Nucleic acids research.

[41]  M. Lynch,et al.  A method for calibrating molecular clocks and its application to animal mitochondrial DNA. , 1993, Genetics.