Register      Login
Australian Journal of Zoology Australian Journal of Zoology Society
Evolutionary, molecular and comparative zoology
RESEARCH ARTICLE

Do genomic datasets resolve the correct relationship among the placental, marsupial and monotreme lineages?

Gavin Huttley
+ Author Affiliations
- Author Affiliations

John Curtin School of Medical Research, The Australian National University, Canberra, ACT 0200, Australia. Email: gavin.huttley@anu.edu.au

Australian Journal of Zoology 57(4) 167-174 https://doi.org/10.1071/ZO09049
Submitted: 16 April 2009  Accepted: 19 June 2009   Published: 26 October 2009

Abstract

Did the mammal radiation arise through initial divergence of prototherians from a common ancestor of metatherians and eutherians, the Theria hypothesis, or of eutherians from a common ancestor of metatherians and prototherians, the Marsupionta hypothesis? Molecular phylogenetic analyses of point substitutions applied to this problem have been contradictory – mtDNA-encoded sequences supported Marsupionta, nuclear-encoded sequences and RY (purine–pyrimidine)-recoded mtDNA supported Theria. The consistency property of maximum likelihood guarantees convergence on the true tree only with longer alignments. Results from analyses of genome datasets should therefore be impervious to choice of outgroup. We assessed whether important hypotheses concerning mammal evolution, including Theria/Marsupionta and the branching order of rodents, carnivorans and primates, are resolved by phylogenetic analyses using ~2.3 megabases of protein-coding sequence from genome projects. In each case, only two tree topologies were being compared and thus inconsistency in resolved topologies can only derive from flawed models of sequence divergence. The results from all substitution models strongly supported Theria. For the eutherian lineages, all models were sensitive to the outgroup. We argue that phylogenetic inference from point substitutions will remain unreliable until substitution models that better match biological mechanisms of sequence divergence have been developed.


References

Belov, K. , Hellman, L. , and Cooper, D. W. (2002). Characterization of immunoglobulin gamma 1 from a monotreme, Tachyglossus aculeatus. Immunogenetics 53, 1065–1071.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed | Felsenstein J. (2003). ‘Inferring Phylogenies.’ (Sinauer Associates: Sunderland, MA.)

Goldman, N. (1993). Simple diagnostic statistical tests of models for DNA substitution. Journal of Molecular Evolution 37, 650–661.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed | Kosiol C. (2006). Markov models for protein sequence evolution. Ph.D. Thesis, EMBL–European Bioinformatics Institute, University of Cambridge, Cambridge.

Krawczak, M. , Ball, E. V. , and Cooper, D. N. (1998). Neighboring-nucleotide effects on the rates of germ-line single-base-pair substitution in human genes. American Journal of Human Genetics 63, 474–488.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed | Penny D , Hendy MD , Steel MA (1991). Testing the theory of descent. In ‘Phylogenetic Analysis of DNA Sequences’. (Eds M. M. Miyamoto and J. Cracraft.) pp. 155–183. (Oxford University Press: Oxford.)

Phillips, M. J. , and Penny, D. (2003). The root of the mammalian tree inferred from whole mitochondrial genomes. Molecular Phylogenetics and Evolution 28, 171–185.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Phillips, M. J. , Delsuc, F. , and Penny, D. (2004). Genome-scale phylogeny and the detection of systematic biases. Molecular Biology and Evolution 21, 1455–1458.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Pond, S. K. , and Muse, S. V. (2005). Site-to-site variation of synonymous substitution rates. Molecular Biology and Evolution 22, 2375–2385.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Posada, D. , and Crandall, K. A. (1998). MODELTEST: testing the model of DNA substitution. Bioinformatics 14, 817–818.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Powell, M. J. D. (1964). An efficient method for finding the minimum of a function of several variables without calculating derivatives. The Computer Journal 7, 155–162.
Crossref | GoogleScholarGoogle Scholar |

Proffitt, J. H. , Davie, J. R. , Swinton, D. , and Hattman, S. (1984). 5-Methylcytosine is not detectable in Saccharomyces cerevisiae DNA. Molecular and Cellular Biology 4, 985–988.
CAS | PubMed |

Schranz, H. W. , Yap, V. B. , Easteal, S. , Knight, R. , and Huttley, G. A. (2008). Pathological rate matrices: from primates to pathogens. BMC Bioinformatics 9, 550.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Sueoka, N. (1962). On the genetic basis of variation and heterogeneity of DNA base composition. Proceedings of the National Academy of Sciences of the United States of America 48, 582–592.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

van Rheede, T. , Bastiaans, T. , Boone, D. N. , Hedges, S. B. , de Jong, W. W. , and Madsen, O. (2006). The platypus in its place: nuclear genes and indels confirm the sister group relation of monotremes and therians. Molecular Biology and Evolution 23, 587–597.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Warren, W. C. , Hillier, L. W. , Graves, J. A. M. , Birney, E. , and Ponting, C. P., , et al. (2008). Genome analysis of the platypus reveals unique signatures of evolution. Nature 453, 175–183.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Whelan, S. , Lio, P. , and Goldman, N. (2001). Molecular phylogenetics: state-of-the-art methods for looking into the past. Trends in Genetics 17, 262–272.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Yang, Z. (1994). Maximum likelihood phylogenetic estimation from DNA sequences with variable rates over sites: approximate methods. Journal of Molecular Evolution 39, 306–314.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Yang, Z. (1997). How often do wrong models produce better phylogenies? Molecular Biology and Evolution 14(1), 105–108.
PubMed |

Zuckerkandl, E. , and Pauling, L. (1965). Molecules as documents of evolutionary history. Journal of Theoretical Biology 8, 357–366.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |

Zurawski, G. , and Clegg, M. T. (1984). The barley chloroplast DNA atpBE, trnM2, and trnV1 loci. Nucleic Acids Research 12, 2549–2559.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed |