An Experimentally Determined Evolutionary Model Dramatically Improves Phylogenetic Fit

被引:120
作者
Bloom, Jesse D. [1 ,2 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98104 USA
[2] Fred Hutchinson Canc Res Ctr, Computat Biol Program, Seattle, WA 98104 USA
基金
美国国家卫生研究院;
关键词
phylogenetics; codon model; substitution model; influenza; nucleoprotein; deep mutational scanning; INFLUENZA-A VIRUS; CODON-SUBSTITUTION MODELS; CODING SEQUENCE EVOLUTION; MUTATION-SELECTION MODELS; AMINO-ACID SITES; MAXIMUM-LIKELIHOOD; PROTEIN EVOLUTION; DNA-SEQUENCES; SECONDARY STRUCTURE; NUCLEOTIDE SUBSTITUTION;
D O I
10.1093/molbev/msu173
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
All modern approaches to molecular phylogenetics require a quantitative model for how genes evolve. Unfortunately, existing evolutionary models do not realistically represent the site-heterogeneous selection that governs actual sequence change. Attempts to remedy this problem have involved augmenting these models with a burgeoning number of free parameters. Here, I demonstrate an alternative: Experimental determination of a parameter-free evolutionary model via mutagenesis, functional selection, and deep sequencing. Using this strategy, I create an evolutionary model for influenza nucleoprotein that describes the gene phylogeny far better than existing models with dozens or even hundreds of free parameters. Emerging high-throughput experimental strategies such as the one employed here provide fundamentally new information that has the potential to transform the sensitivity of phylogenetic and genetic analyses.
引用
收藏
页码:1956 / 1978
页数:23
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