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氨基酸替换模型及其在线粒体蛋白质进化中的应用。

Models of amino acid substitution and applications to mitochondrial protein evolution.

作者信息

Yang Z, Nielsen R, Hasegawa M

机构信息

Department of Biology (Galton Laboratory), University College London, England.

出版信息

Mol Biol Evol. 1998 Dec;15(12):1600-11. doi: 10.1093/oxfordjournals.molbev.a025888.

DOI:10.1093/oxfordjournals.molbev.a025888
PMID:9866196
Abstract

Models of amino acid substitution were developed and compared using maximum likelihood. Two kinds of models are considered. "Empirical" models do not explicitly consider factors that shape protein evolution, but attempt to summarize the substitution pattern from large quantities of real data. "Mechanistic" models are formulated at the codon level and separate mutational biases at the nucleotide level from selective constraints at the amino acid level. They account for features of sequence evolution, such as transition-transversion bias and base or codon frequency biases, and make use of physicochemical distances between amino acids to specify nonsynonymous substitution rates. A general approach is presented that transforms a Markov model of codon substitution into a model of amino acid replacement. Protein sequences from the entire mitochondrial genomes of 20 mammalian species were analyzed using different models. The mechanistic models were found to fit the data better than empirical models derived from large databases. Both the mutational distance between amino acids (determined by the genetic code and mutational biases such as the transition-transversion bias) and the physicochemical distance are found to have strong effects on amino acid substitution rates. A significant proportion of amino acid substitutions appeared to have involved more than one codon position, indicating that nucleotide substitutions at neighboring sites may be correlated. Rates of amino acid substitution were found to be highly variable among sites.

摘要

利用最大似然法开发并比较了氨基酸替换模型。考虑了两种模型。“经验”模型没有明确考虑影响蛋白质进化的因素,而是试图从大量实际数据中总结替换模式。“机制”模型是在密码子水平上构建的,将核苷酸水平的突变偏差与氨基酸水平的选择限制区分开来。它们考虑了序列进化的特征,如转换-颠换偏差以及碱基或密码子频率偏差,并利用氨基酸之间的物理化学距离来确定非同义替换率。提出了一种将密码子替换的马尔可夫模型转化为氨基酸替换模型的通用方法。使用不同模型分析了20种哺乳动物整个线粒体基因组的蛋白质序列。发现机制模型比从大型数据库得出的经验模型更适合数据。氨基酸之间的突变距离(由遗传密码和转换-颠换偏差等突变偏差决定)和物理化学距离都对氨基酸替换率有强烈影响。相当一部分氨基酸替换似乎涉及不止一个密码子位置,这表明相邻位点的核苷酸替换可能是相关的。发现氨基酸替换率在不同位点之间变化很大。

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