A codon-based model designed to describe lentiviral evolution

被引:28
作者
Pedersen, AMK
Wiuf, C
Christiansen, FB
机构
[1] Aarhus Univ, Inst Biol Sci, Dept Ecol & Genet, DK-8000 Aarhus C, Denmark
[2] Tech Univ Denmark, Dept Chem, Ctr Biol Sequence Anal, Lyngby, Denmark
关键词
codon-based model; lentivirus; CpG depression; codon usage; HIV1; goodness of fit;
D O I
10.1093/oxfordjournals.molbev.a026006
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
A codon-based model designed to describe lentiviral evolution is developed. The model incorporates unequal base compositions in the three codon positions and selection against the CpG dinucleotide within codons to account for a deficit of this dinucleotide exhibited by lentiviral genes. The model is, to a large extent, able to account for the pattern of codon usage exhibited by the HIV1 genes gag, pol, and env, in spite of its parameter paucity. The model is extended to a similar model which operates on pentets (codons and their neighboring bases). The results obtained by the pentet model establish the importance of depression of CpGs across codon boundaries as well as within codons. The goodness of fit of the CpG depression model to the observed evolution in pairwise alignments of HIV1 sequences is assessed. The model provides a significantly better description of the observed evolution than the simpler models examined. The parameter estimates indicate that part of the unusually large biases in nucleotide frequencies observed in HIV1 genes is caused by selection against CpGs, We find that the estimates of expected numbers of substitutions, of transitions to transversions, and of synonymous to nonsynonymous substitution rates are robust to CpG depression, whereas the ratio of CpG-generating substitutions to other substitutions is strongly influenced by the choice of model.
引用
收藏
页码:1069 / 1081
页数:13
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