Covarion processes allow changes in evolutionary rates at sites along the branches of a phylogenetic tree. Covarion-like evolution is increasingly recognized as an important mode of protein evolution. Several recent reports suggest that maximum likelihood estimation employing covarion models may support different optimal topologies than estimation using standard rates-across-sites (RAS) models. However, it remains to be demonstrated that ignoring covarion evolution will generally result in topological misestimation. In this study we performed analytical and theoretical studies of limiting distances under the covarion model and four-taxon tree simulations to investigate the extent to which the covarion process impacts on phylogenetic estimation. In particular, we assessed the limits of an RAS model-based maximum likelihood method to recover the phylogenies when the sequence data were simulated under the covarion processes. We find that, when ignored, covarion processes can induce systematic errors in phylogeny reconstruction. Surprisingly, when sequences are evolved under a covarion process but an RAS model is used for estimation, we find that a long branch repel bias occurs.
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http://dx.doi.org/10.1007/s00239-007-9062-4 | DOI Listing |
Syst Biol
October 2024
Department of Biological Sciences and Museum of Natural Science, Louisiana State University, Baton Rouge, LA 70803, USA.
J Evol Biol
December 2024
Department of Zoology, University of Otago, Dunedin, New Zealand.
Many hypotheses in the field of phylogenetic comparative biology involve specific changes in the rate or process of trait evolution. This is particularly true of approaches designed to connect macroevolutionary pattern to microevolutionary process. We present a method to test whether the rate of evolution of a discrete character has changed in one or more clades, lineages, or time periods.
View Article and Find Full Text PDFSyst Biol
January 2021
Department of Biostatistics, Jonathan and Karin Fielding School of Public Health, University of California, Los Angeles, CA 90095, USA.
Markov models of character substitution on phylogenies form the foundation of phylogenetic inference frameworks. Early models made the simplifying assumption that the substitution process is homogeneous over time and across sites in the molecular sequence alignment. While standard practice adopts extensions that accommodate heterogeneity of substitution rates across sites, heterogeneity in the process over time in a site-specific manner remains frequently overlooked.
View Article and Find Full Text PDFPLoS One
December 2013
Unit of Typing and Genetics of Mycobacteria, Laboratory of Molecular Microbiology, Vaccinology, and Biotechnology Development, Institut Pasteur de Tunis, Tunis, Tunisia.
Background: PE and PE_PGRS are two mycobateria-restricted multigene families encoding membrane associated and secreted proteins that have expanded mainly in the pathogenic species, notably the Mycobacterium tuberculosis complex (MTBC). Several lines of evidence attribute to PE and PE_PGRS genes critical roles in mycobacterial pathogenicity. To get more insight into the nature of these genes, we sought to address their evolutionary trajectories in the group of smooth tubercle bacilli (STB), the putative ancestor of the clonal MTBC.
View Article and Find Full Text PDFPLoS One
April 2011
CNRS UMR 6214-INSERM 771, Faculté de Médecine, Angers, France.
Class A G-protein-coupled receptors (GPCRs) constitute the largest family of transmembrane receptors in the human genome. Understanding the mechanisms which drove the evolution of such a large family would help understand the specificity of each GPCR sub-family with applications to drug design. To gain evolutionary information on class A GPCRs, we explored their sequence space by metric multidimensional scaling analysis (MDS).
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