Mutation-selection models of codon substitution and their use to estimate selective strengths on codon usage

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Mutation-selection models of codon substitution and their use to estimate selective strengths on codon usage. / Yang, Ziheng; Nielsen, Rasmus.

In: Molecular Biology and Evolution, Vol. 25, No. 3, 2008, p. 568-79.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Yang, Z & Nielsen, R 2008, 'Mutation-selection models of codon substitution and their use to estimate selective strengths on codon usage', Molecular Biology and Evolution, vol. 25, no. 3, pp. 568-79. https://doi.org/10.1093/molbev/msm284

APA

Yang, Z., & Nielsen, R. (2008). Mutation-selection models of codon substitution and their use to estimate selective strengths on codon usage. Molecular Biology and Evolution, 25(3), 568-79. https://doi.org/10.1093/molbev/msm284

Vancouver

Yang Z, Nielsen R. Mutation-selection models of codon substitution and their use to estimate selective strengths on codon usage. Molecular Biology and Evolution. 2008;25(3):568-79. https://doi.org/10.1093/molbev/msm284

Author

Yang, Ziheng ; Nielsen, Rasmus. / Mutation-selection models of codon substitution and their use to estimate selective strengths on codon usage. In: Molecular Biology and Evolution. 2008 ; Vol. 25, No. 3. pp. 568-79.

Bibtex

@article{eb90b280e6e911ddbf70000ea68e967b,
title = "Mutation-selection models of codon substitution and their use to estimate selective strengths on codon usage",
abstract = "Current models of codon substitution are formulated at the levels of nucleotide substitution and do not explicitly consider the separate effects of mutation and selection. They are thus incapable of inferring whether mutation or selection is responsible for evolution at silent sites. Here we implement a few population genetics models of codon substitution that explicitly consider mutation bias and natural selection at the DNA level. Selection on codon usage is modeled by introducing codon-fitness parameters, which together with mutation-bias parameters, predict optimal codon frequencies for the gene. The selective pressure may be for translational efficiency and accuracy or for fine-tuning translational kinetics to produce correct protein folding. We apply the models to compare mitochondrial and nuclear genes from several mammalian species. Model assumptions concerning codon usage are found to affect the estimation of sequence distances (such as the synonymous rate d(S), the nonsynonymous rate d(N), and the rate at the 4-fold degenerate sites d(4)), as found in previous studies, but the new models produced very similar estimates to some old ones. We also develop a likelihood ratio test to examine the null hypothesis that codon usage is due to mutation bias alone, not influenced by natural selection. Application of the test to the mammalian data led to rejection of the null hypothesis in most genes, suggesting that natural selection may be a driving force in the evolution of synonymous codon usage in mammals. Estimates of selection coefficients nevertheless suggest that selection on codon usage is weak and most mutations are nearly neutral. The sensitivity of the analysis on the assumed mutation model is discussed.",
author = "Ziheng Yang and Rasmus Nielsen",
note = "Keywords: Animals; Codon; Humans; Models, Genetic; Mutation; Selection (Genetics)",
year = "2008",
doi = "10.1093/molbev/msm284",
language = "English",
volume = "25",
pages = "568--79",
journal = "Molecular Biology and Evolution",
issn = "0737-4038",
publisher = "Oxford University Press",
number = "3",

}

RIS

TY - JOUR

T1 - Mutation-selection models of codon substitution and their use to estimate selective strengths on codon usage

AU - Yang, Ziheng

AU - Nielsen, Rasmus

N1 - Keywords: Animals; Codon; Humans; Models, Genetic; Mutation; Selection (Genetics)

PY - 2008

Y1 - 2008

N2 - Current models of codon substitution are formulated at the levels of nucleotide substitution and do not explicitly consider the separate effects of mutation and selection. They are thus incapable of inferring whether mutation or selection is responsible for evolution at silent sites. Here we implement a few population genetics models of codon substitution that explicitly consider mutation bias and natural selection at the DNA level. Selection on codon usage is modeled by introducing codon-fitness parameters, which together with mutation-bias parameters, predict optimal codon frequencies for the gene. The selective pressure may be for translational efficiency and accuracy or for fine-tuning translational kinetics to produce correct protein folding. We apply the models to compare mitochondrial and nuclear genes from several mammalian species. Model assumptions concerning codon usage are found to affect the estimation of sequence distances (such as the synonymous rate d(S), the nonsynonymous rate d(N), and the rate at the 4-fold degenerate sites d(4)), as found in previous studies, but the new models produced very similar estimates to some old ones. We also develop a likelihood ratio test to examine the null hypothesis that codon usage is due to mutation bias alone, not influenced by natural selection. Application of the test to the mammalian data led to rejection of the null hypothesis in most genes, suggesting that natural selection may be a driving force in the evolution of synonymous codon usage in mammals. Estimates of selection coefficients nevertheless suggest that selection on codon usage is weak and most mutations are nearly neutral. The sensitivity of the analysis on the assumed mutation model is discussed.

AB - Current models of codon substitution are formulated at the levels of nucleotide substitution and do not explicitly consider the separate effects of mutation and selection. They are thus incapable of inferring whether mutation or selection is responsible for evolution at silent sites. Here we implement a few population genetics models of codon substitution that explicitly consider mutation bias and natural selection at the DNA level. Selection on codon usage is modeled by introducing codon-fitness parameters, which together with mutation-bias parameters, predict optimal codon frequencies for the gene. The selective pressure may be for translational efficiency and accuracy or for fine-tuning translational kinetics to produce correct protein folding. We apply the models to compare mitochondrial and nuclear genes from several mammalian species. Model assumptions concerning codon usage are found to affect the estimation of sequence distances (such as the synonymous rate d(S), the nonsynonymous rate d(N), and the rate at the 4-fold degenerate sites d(4)), as found in previous studies, but the new models produced very similar estimates to some old ones. We also develop a likelihood ratio test to examine the null hypothesis that codon usage is due to mutation bias alone, not influenced by natural selection. Application of the test to the mammalian data led to rejection of the null hypothesis in most genes, suggesting that natural selection may be a driving force in the evolution of synonymous codon usage in mammals. Estimates of selection coefficients nevertheless suggest that selection on codon usage is weak and most mutations are nearly neutral. The sensitivity of the analysis on the assumed mutation model is discussed.

U2 - 10.1093/molbev/msm284

DO - 10.1093/molbev/msm284

M3 - Journal article

C2 - 18178545

VL - 25

SP - 568

EP - 579

JO - Molecular Biology and Evolution

JF - Molecular Biology and Evolution

SN - 0737-4038

IS - 3

ER -

ID: 9855321