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
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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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