Mitochondrial genes and mammalian phylogenies: Increasing the reliability of branch length estimation

被引:25
作者
Corneli, PS [1 ]
Ward, RH
机构
[1] Univ Utah, Dept Biol, Salt Lake City, UT 84112 USA
[2] Univ Oxford, Inst Biol Anthropol, Oxford OX1 2JD, England
关键词
maximum likelihood; mammalian phylogeny; complete mitochondrial genome; branch length estimates; mtDNA protein-coding genes;
D O I
10.1093/oxfordjournals.molbev.a026302
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Since branch lengths provide important information about the timing and the extent of evolutionary divergence among taxa, accurate resolution of evolutionary history depends as much on branch length estimates as on recovery of the correct topology. However, the empirical relationship between the choice of genes to sequence and the quality of branch length estimation remains ill defined. To address this issue, we evaluated the accuracy of branch lengths estimated from subsets of the mitochondrial genome for a mammalian phylogeny with known subordinal relationships. Using maximum-likelihood methods, we estimated branch lengths from an 11-kb sequence of all 13 protein-coding genes and compared them with estimates from single genes (0.2-1.8 kb) and from 7 different combinations of genes (2-3.5 kb). For each sequence, we separated the component of the log-likelihood deviation due to branch length differences associated with alternative topologies from that due to those that are independent of the topology. Even among the sequences that recovered the same tree topology, some produced significantly better branch length estimates than others did. The combination of comet topology and significantly better branch length estimation suggests that these gene combinations may prove useful in estimating phylogenetic relationships for mammalian divergences below the ordinal level. Thus, the proper choice of genes to sequence is a critical factor for reliable estimation of evolutionary history from molecular data.
引用
收藏
页码:224 / 234
页数:11
相关论文
共 56 条
[1]   The fossil record of North American mammals: Evidence for a Paleocene evolutionary radiation [J].
Alroy, J .
SYSTEMATIC BIOLOGY, 1999, 48 (01) :107-118
[2]   COMPLETE SEQUENCE OF BOVINE MITOCHONDRIAL-DNA - CONSERVED FEATURES OF THE MAMMALIAN MITOCHONDRIAL GENOME [J].
ANDERSON, S ;
DEBRUIJN, MHL ;
COULSON, AR ;
EPERON, IC ;
SANGER, F ;
YOUNG, IG .
JOURNAL OF MOLECULAR BIOLOGY, 1982, 156 (04) :683-717
[3]  
ARNASON U, 1993, J MOL EVOL, V37, P323
[4]  
ARNASON U, 1993, J MOL EVOL, V37, P312
[5]   Comparison between the complete mitochondrial DNA sequences of Homo and the common chimpanzee based on nonchimeric sequences [J].
Arnason, U ;
Xu, XF ;
Gullberg, A .
JOURNAL OF MOLECULAR EVOLUTION, 1996, 42 (02) :145-152
[6]   Phylogenetic analyses of mitochondrial DNA suggest a sister group relationship between Xenarthra (Edentata) and ferungulates [J].
Arnason, U ;
Gullberg, A ;
Janke, A .
MOLECULAR BIOLOGY AND EVOLUTION, 1997, 14 (07) :762-768
[7]   THE COMPLETE NUCLEOTIDE-SEQUENCE OF THE MITOCHONDRIAL-DNA OF THE FIN WHALE, BALAENOPTERA-PHYSALUS [J].
ARNASON, U ;
GULLBERG, A ;
WIDEGREN, B .
JOURNAL OF MOLECULAR EVOLUTION, 1991, 33 (06) :556-568
[8]   THE COMPLETE MITOCHONDRIAL-DNA SEQUENCE OF THE HARBOR SEAL, PHOCA-VITULINA [J].
ARNASON, U ;
JOHNSSON, E .
JOURNAL OF MOLECULAR EVOLUTION, 1992, 34 (06) :493-505
[9]   Pattern and timing of evolutionary divergences among hominoids based on analyses of complete mtDNAs [J].
Arnason, U ;
Gullberg, A ;
Janke, A ;
Xu, XF .
JOURNAL OF MOLECULAR EVOLUTION, 1996, 43 (06) :650-661
[10]   Conflict among individual mitochondrial proteins in resolving the phylogeny of eutherian orders [J].
Cao, Y ;
Janke, A ;
Waddell, PJ ;
Westerman, M ;
Takenaka, O ;
Murata, S ;
Okada, N ;
Pääbo, S ;
Hasegawa, M .
JOURNAL OF MOLECULAR EVOLUTION, 1998, 47 (03) :307-322