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PMID: 2120449 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Mitochondrial DNA evolution in primates: transition rate has been extremely low in the lemur.

Journal of molecular evolution ·Vol. 31 ·No. 2 ·1990-08-00 ·Pages 113-21

Hasegawa M, Kishino H, Hayasaka K, Horai S

Abstract

Based on mitochondrial DNA (mt-DNA) sequence data from a wide range of primate species, branching order in the evolution of primates was inferred by the maximum likelihood method of Felsenstein without assuming rate constancy among lineages. Bootstrap probabilities for the maximum likelihood tree topology among alternatives were estimated without performing a maximum likelihood estimation for each resampled data set. Variation in the evolutionary rate among lineages was examined for the maximum likelihood tree by a method developed by Kishino and Hasegawa. From these analyses it appears that the transition rate of mtDNA evolution in the lemur has been extremely low, only about 1/10 that in other primate lines, whereas the transversion rate does not differ significantly from that of other primates. Furthermore, the transition rate in catarrhines, except the gibbon, is higher than those in the tarsier and in platyrrhines, and the transition rate in the gibbon is lower than those in other catarrhines. Branching dates in primate evolution were estimated by a molecular clock analysis of mtDNA, taking into account the rate of variation among different lines, and the results were compared with those estimated from nuclear DNA. Under the most likely model, where the evolutionary rate of mtDNA has been uniform within a great apes/human clade, human/chimpanzee clustering is preferred to the alternative branching orders among human, chimpanzee, and gorilla.

MeSH Terms
Animals Biological Evolution DNA, Mitochondrial/analysis Gene Frequency Genetic Variation Lemur/genetics Primates/genetics
Chemicals
DNA, Mitochondrial
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Hasegawa M
Institute of Statistical Mathematics, Tokyo, Japan.
Kishino H
Hayasaka K
Horai S
References (34)
34 references, click to expand
  1. Fossil evidence on human origins and dispersal.
    Cold Spring Harb Symp Quant Biol. 1986;51 Pt 1:419-28 PMID: 3107877
  2. Sequence and organization of the human mitochondrial genome.
    Nature. 1981 Apr 9;290(5806):457-65 PMID: 7219534
  3. Evolution of DNA sequences has been retarded in Malagasy primates.
    Nature. 1980 Jul 24;286(5771):420-3 PMID: 6772964
  4. The neighbor-joining method: a new method for reconstructing phylogenetic trees.
    Mol Biol Evol. 1987 Jul;4(4):406-25 PMID: 3447015
  5. Mitochondrial DNA sequences of primates: tempo and mode of evolution.
    J Mol Evol. 1982;18(4):225-39 PMID: 6284948
  6. Mitochondrial nucleic acids and their relation to the biogenesis of mitochondria.
    Physiol Rev. 1970 Jul;50(3):376-427 PMID: 4912905
  7. Recombination and balanced chromosome polymorphism suggested by DNA sequences 5' to the human delta-globin gene.
    Proc Natl Acad Sci U S A. 1983 Aug;80(16):5012-6 PMID: 6308666
  8. The molecular clock runs more slowly in man than in apes and monkeys.
    Nature. 1987 Mar 5-11;326(6108):93-6 PMID: 3102974
  9. DNA DIVERGENCE AMONG HOMINOIDS.
    Evolution. 1989 Aug;43(5):925-942 PMID: 28564151
  10. CONFIDENCE LIMITS ON THE MAXIMUM-LIKELIHOOD ESTIMATE OF THE HOMINOID TREE FROM MITOCHONDRIAL-DNA SEQUENCES.
    Evolution. 1989 May;43(3):672-677 PMID: 28568382
  11. Evidence for higher rates of nucleotide substitution in rodents than in man.
    Proc Natl Acad Sci U S A. 1985 Mar;82(6):1741-5 PMID: 3856856
  12. Complete sequence of bovine mitochondrial DNA. Conserved features of the mammalian mitochondrial genome.
    J Mol Biol. 1982 Apr 25;156(4):683-717 PMID: 7120390
  13. Dating of the human-ape splitting by a molecular clock of mitochondrial DNA.
    J Mol Evol. 1985;22(2):160-74 PMID: 3934395
  14. An improved method for determining codon variability in a gene and its application to the rate of fixation of mutations in evolution.
    Biochem Genet. 1970 Oct;4(5):579-93 PMID: 5489762
  15. Nuclear and mitochondrial DNA comparisons reveal extreme rate variation in the molecular clock.
    Science. 1986 Oct 10;234(4773):194-6 PMID: 3018931
  16. Heterogeneity of tempo and mode of mitochondrial DNA evolution among mammalian orders.
    Jpn J Genet. 1989 Aug;64(4):243-58 PMID: 2483667
  17. The spider monkey psi eta-globin gene and surrounding sequences: recent or ancient insertions of LINEs and SINEs?
    Genomics. 1988 Oct;3(3):237-55 PMID: 2852163
  18. The phylogeny of the hominoid primates, as indicated by DNA-DNA hybridization.
    J Mol Evol. 1984;20(1):2-15 PMID: 6429338
  19. Rates of DNA sequence evolution differ between taxonomic groups.
    Science. 1986 Mar 21;231(4744):1393-8 PMID: 3082006
  20. Temporal scaling of molecular evolution in primates and other mammals.
    Mol Biol Evol. 1986 May;3(3):205-21 PMID: 3444400
  21. Converting distance to time: application to human evolution.
    Methods Enzymol. 1990;183:550-70 PMID: 2314292
  22. Sequence and gene organization of mouse mitochondrial DNA.
    Cell. 1981 Oct;26(2 Pt 2):167-80 PMID: 7332926
  23. Primate eta-globin DNA sequences and man's place among the great apes.
    Nature. 1986 Jan 16-22;319(6050):234-8 PMID: 3945312
  24. Phylogenies from molecular sequences: inference and reliability.
    Annu Rev Genet. 1988;22:521-65 PMID: 3071258
  25. DNA hybridization evidence of hominoid phylogeny: results from an expanded data set.
    J Mol Evol. 1987;26(1-2):99-121 PMID: 3125341
  26. Molecular phylogeny and evolution of primate mitochondrial DNA.
    Mol Biol Evol. 1988 Nov;5(6):626-44 PMID: 3146681
  27. Phylogenetic relations of humans and African apes from DNA sequences in the psi eta-globin region.
    Science. 1987 Oct 16;238(4825):369-73 PMID: 3116671
  28. Man's place in Hominoidea as inferred from molecular clocks of DNA.
    J Mol Evol. 1987;26(1-2):132-47 PMID: 3125331
  29. Molecular evolution of intergenic DNA in higher primates: pattern of DNA changes, molecular clock, and evolution of repetitive sequences.
    Mol Biol Evol. 1988 Jan;5(1):1-20 PMID: 3357413
  30. Biochemical evolution.
    Annu Rev Biochem. 1977;46:573-639 PMID: 409339
  31. Evolutionary trees from DNA sequences: a maximum likelihood approach.
    J Mol Evol. 1981;17(6):368-76 PMID: 7288891
  32. Molecular systematics of higher primates: genealogical relations and classification.
    Proc Natl Acad Sci U S A. 1988 Oct;85(20):7627-31 PMID: 3174657
  33. Immunological time scale for hominid evolution.
    Science. 1967 Dec 1;158(3805):1200-3 PMID: 4964406
  34. Evaluation of the maximum likelihood estimate of the evolutionary tree topologies from DNA sequence data, and the branching order in hominoidea.
    J Mol Evol. 1989 Aug;29(2):170-9 PMID: 2509717
Article Info
Journal
Journal of molecular evolution
Abbr.
J Mol Evol
ISSN
0022-2844
Published
1990-08-00
Pages
113-21
Language
English
Region
Germany
NLM ID
0360051
Subset
IM
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