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Inferring clocks when lacking rocks: the variable rates of molecular evolution in bacteria

BACKGROUND: Because bacteria do not have a robust fossil record, attempts to infer the timing of events in their evolutionary history requires comparisons of molecular sequences. This use of molecular clocks is based on the assumptions that substitution rates for homologous genes or sites are fairly...

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Autores principales: Kuo, Chih-Horng, Ochman, Howard
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2760517/
https://www.ncbi.nlm.nih.gov/pubmed/19788732
http://dx.doi.org/10.1186/1745-6150-4-35
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author Kuo, Chih-Horng
Ochman, Howard
author_facet Kuo, Chih-Horng
Ochman, Howard
author_sort Kuo, Chih-Horng
collection PubMed
description BACKGROUND: Because bacteria do not have a robust fossil record, attempts to infer the timing of events in their evolutionary history requires comparisons of molecular sequences. This use of molecular clocks is based on the assumptions that substitution rates for homologous genes or sites are fairly constant through time and across taxa. Violation of these conditions can lead to erroneous inferences and result in estimates that are off by orders of magnitude. In this study, we examine the consistency of substitution rates among a set of conserved genes in diverse bacterial lineages, and address the questions regarding the validity of molecular dating. RESULTS: By examining the evolution of 16S rRNA gene in obligate endosymbionts, which can be calibrated by the fossil record of their hosts, we found that the rates are consistent within a clade but varied widely across different bacterial lineages. Genome-wide estimates of nonsynonymous and synonymous substitutions suggest that these two measures are highly variable in their rates across bacterial taxa. Genetic drift plays a fundamental role in determining the accumulation of substitutions in 16S rRNA genes and at nonsynonymous sites. Moreover, divergence estimates based on a set of universally conserved protein-coding genes also exhibit low correspondence to those based on 16S rRNA genes. CONCLUSION: Our results document a wide range of substitution rates across genes and bacterial taxa. This high level of variation cautions against the assumption of a universal molecular clock for inferring divergence times in bacteria. However, by applying relative-rate tests to homologous genes, it is possible to derive reliable local clocks that can be used to calibrate bacterial evolution. REVIEWERS: This article was reviewed by Adam Eyre-Walker, Simonetta Gribaldo and Tal Pupko (nominated by Dan Graur).
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spelling pubmed-27605172009-10-13 Inferring clocks when lacking rocks: the variable rates of molecular evolution in bacteria Kuo, Chih-Horng Ochman, Howard Biol Direct Research BACKGROUND: Because bacteria do not have a robust fossil record, attempts to infer the timing of events in their evolutionary history requires comparisons of molecular sequences. This use of molecular clocks is based on the assumptions that substitution rates for homologous genes or sites are fairly constant through time and across taxa. Violation of these conditions can lead to erroneous inferences and result in estimates that are off by orders of magnitude. In this study, we examine the consistency of substitution rates among a set of conserved genes in diverse bacterial lineages, and address the questions regarding the validity of molecular dating. RESULTS: By examining the evolution of 16S rRNA gene in obligate endosymbionts, which can be calibrated by the fossil record of their hosts, we found that the rates are consistent within a clade but varied widely across different bacterial lineages. Genome-wide estimates of nonsynonymous and synonymous substitutions suggest that these two measures are highly variable in their rates across bacterial taxa. Genetic drift plays a fundamental role in determining the accumulation of substitutions in 16S rRNA genes and at nonsynonymous sites. Moreover, divergence estimates based on a set of universally conserved protein-coding genes also exhibit low correspondence to those based on 16S rRNA genes. CONCLUSION: Our results document a wide range of substitution rates across genes and bacterial taxa. This high level of variation cautions against the assumption of a universal molecular clock for inferring divergence times in bacteria. However, by applying relative-rate tests to homologous genes, it is possible to derive reliable local clocks that can be used to calibrate bacterial evolution. REVIEWERS: This article was reviewed by Adam Eyre-Walker, Simonetta Gribaldo and Tal Pupko (nominated by Dan Graur). BioMed Central 2009-09-29 /pmc/articles/PMC2760517/ /pubmed/19788732 http://dx.doi.org/10.1186/1745-6150-4-35 Text en Copyright © 2009 Kuo and Ochman; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Kuo, Chih-Horng
Ochman, Howard
Inferring clocks when lacking rocks: the variable rates of molecular evolution in bacteria
title Inferring clocks when lacking rocks: the variable rates of molecular evolution in bacteria
title_full Inferring clocks when lacking rocks: the variable rates of molecular evolution in bacteria
title_fullStr Inferring clocks when lacking rocks: the variable rates of molecular evolution in bacteria
title_full_unstemmed Inferring clocks when lacking rocks: the variable rates of molecular evolution in bacteria
title_short Inferring clocks when lacking rocks: the variable rates of molecular evolution in bacteria
title_sort inferring clocks when lacking rocks: the variable rates of molecular evolution in bacteria
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2760517/
https://www.ncbi.nlm.nih.gov/pubmed/19788732
http://dx.doi.org/10.1186/1745-6150-4-35
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