selective constraints on amino acids estimated by a mechanistic codon substitution model with multiple nucleotide changes选择性限制氨基酸估计机械密码子替换模型与多个核苷酸的变化.pdfVIP

selective constraints on amino acids estimated by a mechanistic codon substitution model with multiple nucleotide changes选择性限制氨基酸估计机械密码子替换模型与多个核苷酸的变化.pdf

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selective constraints on amino acids estimated by a mechanistic codon substitution model with multiple nucleotide changes选择性限制氨基酸估计机械密码子替换模型与多个核苷酸的变化

Selective Constraints on Amino Acids Estimated by a Mechanistic Codon Substitution Model with Multiple Nucleotide Changes Sanzo Miyazawa* Graduate School of Engineering, Gunma University, Kiryu, Gunma, Japan Abstract Background: Empirical substitution matrices represent the average tendencies of substitutions over various protein families by sacrificing gene-level resolution. We develop a codon-based model, in which mutational tendencies of codon, a genetic code, and the strength of selective constraints against amino acid replacements can be tailored to a given gene. First, selective constraints averaged over proteins are estimated by maximizing the likelihood of each 1-PAM matrix of empirical amino acid (JTT, WAG, and LG) and codon (KHG) substitution matrices. Then, selective constraints specific to given proteins are approximated as a linear function of those estimated from the empirical substitution matrices. Results: Akaike information criterion (AIC) values indicate that a model allowing multiple nucleotide changes fits the empirical substitution matrices significantly better. Also, the ML estimates of transition-transversion bias obtained from these empirical matrices are not so large as previously estimated. The selective constraints are characteristic of proteins rather than species. However, their relative strengths among amino acid pairs can be approximated not to depend very much on protein families but amino acid pairs, because the present model, in which selective constraints are approximated to be a linear function of those estimated from the JTT/WAG/LG/KHG matrices, can provide a good fit to other empirical substitution matrices including cpREV for chloroplast proteins and mtREV for vertebrate mitochondrial proteins. Conclusions/Significance: The present codon-based model with the M

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