New methods for detecting positive selection at single amino acid sites

被引:62
作者
Suzuki, Y
机构
[1] Penn State Univ, Inst Mol Evolut Genet, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Biol, University Pk, PA 16802 USA
关键词
positive selection; ancestral sequence; parsimony; Bayesian; likelihood;
D O I
10.1007/s00239-004-2599-6
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
Inferring positive selection at single amino acid sites is of particular importance for studying evolutionary mechanisms of a protein. For this purpose, Suzuki and Gojobori (1999) developed a method (SG method) for comparing the rates of synonymous and nonsynonymous substitutions at each codon site in a protein-coding nucleotide sequence, using ancestral codons at interior nodes of the phylogenctic tree as inferred by the maximum parsimony method. In the SG method, however, selective neutrality of nucleotide substitutions cannot be tested at codon sites, where only termination codons are inferred at any interior node or the number of equally parsimonious inferences of ancestral codons at all interior nodes exceeds 10,000. Here I present a modified SG method which is free from these problems. Specifically, I use the distance-based Bayesian method for inferring :the single most likely ancestral codon from 61 :sense codons at each interior node. In the computer simulation and real data analysis, the modified SG method showed a higher overall efficiency of detecting positive selection than the original SG method, particularly at highly polymorphic codon sites. These results indicate that the modified SG method is useful for inferring positive selection at codon sites where neutrality cannot be tested by the original SG method. I also discuss that the p-distance is preferable to the number of synonymous substitutions for inferring the phylogenetic tree in the SG method, and present a maximum likelihood method for detecting positive selection at single amino acid sites, which produced reasonable results in the real data analysis.
引用
收藏
页码:11 / 19
页数:9
相关论文
共 37 条
[11]   JAPANESE ISOLATES OF THE NON-A, NON-B HEPATITIS VIRAL GENOME SHOW SEQUENCE VARIATIONS FROM THE ORIGINAL ISOLATE IN THE USA [J].
KATO, N ;
OHKOSHI, S ;
SHIMOTOHNO, K .
PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES, 1989, 65 (09) :219-223
[12]   MOLECULAR-CLONING OF THE HUMAN HEPATITIS-C VIRUS GENOME FROM JAPANESE PATIENTS WITH NON-A, NON-B HEPATITIS [J].
KATO, N ;
HIJIKATA, M ;
OOTSUYAMA, Y ;
NAKAGAWA, M ;
OHKOSHI, S ;
SUGIMURA, T ;
SHIMOTOHNO, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (24) :9524-9528
[14]  
Lechmann M, 1996, HEPATOLOGY, V24, P790
[15]  
MUSE SV, 1994, MOL BIOL EVOL, V11, P715
[16]   The optimization principle in phylogenetic analysis tends to give incorrect topologies when the number of nucleotides or amino acids used is small [J].
Nei, M ;
Kumar, S ;
Takahashi, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (21) :12390-12397
[17]  
NEI M, 1986, MOL BIOL EVOL, V3, P418
[18]  
Nei M, 2000, MOL EVOLUTIONARY PHY
[19]   Classification, nomenclature, and database development for hepatitis C virus (HCV) and related viruses: proposals for standardization [J].
Robertson, B ;
Myers, G ;
Howard, C ;
Brettin, T ;
Bukh, J ;
Gaschen, B ;
Gojobori, T ;
Maertens, G ;
Mizokami, M ;
Nainan, O ;
Netesov, S ;
Nishioka, K ;
Shin-i, T ;
Simmonds, P ;
Smith, D ;
Stuyver, L ;
Weiner, A .
ARCHIVES OF VIROLOGY, 1998, 143 (12) :2493-2503
[20]   THE NEIGHBOR-JOINING METHOD - A NEW METHOD FOR RECONSTRUCTING PHYLOGENETIC TREES [J].
SAITOU, N ;
NEI, M .
MOLECULAR BIOLOGY AND EVOLUTION, 1987, 4 (04) :406-425