Literature DB >> 18586695

Likelihood-based clustering (LiBaC) for codon models, a method for grouping sites according to similarities in the underlying process of evolution.

Le Bao1, Hong Gu, Katherine A Dunn, Joseph P Bielawski.   

Abstract

Models of codon evolution are useful for investigating the strength and direction of natural selection via a parameter for the nonsynonymous/synonymous rate ratio (omega = d(N)/d(S)). Different codon models are available to account for diversity of the evolutionary patterns among sites. Codon models that specify data partitions as fixed effects allow the most evolutionary diversity among sites but require that site partitions are a priori identifiable. Models that use a parametric distribution to express the variability in the omega ratio across site do not require a priori partitioning of sites, but they permit less among-site diversity in the evolutionary process. Simulation studies presented in this paper indicate that differences among sites in estimates of omega under an overly simplistic analytical model can reflect more than just natural selection pressure. We also find that the classic likelihood ratio tests for positive selection have a high false-positive rate in some situations. In this paper, we developed a new method for assigning codon sites into groups where each group has a different model, and the likelihood over all sites is maximized. The method, called likelihood-based clustering (LiBaC), can be viewed as a generalization of the family of model-based clustering approaches to models of codon evolution. We report the performance of several LiBaC-based methods, and selected alternative methods, over a wide variety of scenarios. We find that LiBaC, under an appropriate model, can provide reliable parameter estimates when the process of evolution is very heterogeneous among groups of sites. Certain types of proteins, such as transmembrane proteins, are expected to exhibit such heterogeneity. A survey of genes encoding transmembrane proteins suggests that overly simplistic models could be leading to false signal for positive selection among such genes. In these cases, LiBaC-based methods offer an important addition to a "toolbox" of methods thereby helping to uncover robust evidence for the action of positive selection.

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Year:  2008        PMID: 18586695     DOI: 10.1093/molbev/msn145

Source DB:  PubMed          Journal:  Mol Biol Evol        ISSN: 0737-4038            Impact factor:   16.240


  6 in total

Review 1.  Models of coding sequence evolution.

Authors:  Wayne Delport; Konrad Scheffler; Cathal Seoighe
Journal:  Brief Bioinform       Date:  2008-10-29       Impact factor: 11.622

2.  Why do more divergent sequences produce smaller nonsynonymous/synonymous rate ratios in pairwise sequence comparisons?

Authors:  Mario Dos Reis; Ziheng Yang
Journal:  Genetics       Date:  2013-06-21       Impact factor: 4.562

3.  Inference of functional divergence among proteins when the evolutionary process is non-stationary.

Authors:  Rachael A Bay; Joseph P Bielawski
Journal:  J Mol Evol       Date:  2013-02-27       Impact factor: 2.395

4.  Maximum-likelihood model averaging to profile clustering of site types across discrete linear sequences.

Authors:  Zhang Zhang; Jeffrey P Townsend
Journal:  PLoS Comput Biol       Date:  2009-06-26       Impact factor: 4.475

5.  Trends in substitution models of molecular evolution.

Authors:  Miguel Arenas
Journal:  Front Genet       Date:  2015-10-26       Impact factor: 4.599

6.  Improved inference of site-specific positive selection under a generalized parametric codon model when there are multinucleotide mutations and multiple nonsynonymous rates.

Authors:  Katherine A Dunn; Toby Kenney; Hong Gu; Joseph P Bielawski
Journal:  BMC Evol Biol       Date:  2019-01-14       Impact factor: 3.260

  6 in total

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