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A multilocus timescale for oomycete evolution estimated under three distinct molecular clock models

BACKGROUND: Molecular clock methodologies allow for the estimation of divergence times across a variety of organisms; this can be particularly useful for groups lacking robust fossil histories, such as microbial eukaryotes with few distinguishing morphological traits. Here we have used a Bayesian mo...

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Autores principales: Matari, Nahill H, Blair, Jaime E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4030286/
https://www.ncbi.nlm.nih.gov/pubmed/24884411
http://dx.doi.org/10.1186/1471-2148-14-101
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author Matari, Nahill H
Blair, Jaime E
author_facet Matari, Nahill H
Blair, Jaime E
author_sort Matari, Nahill H
collection PubMed
description BACKGROUND: Molecular clock methodologies allow for the estimation of divergence times across a variety of organisms; this can be particularly useful for groups lacking robust fossil histories, such as microbial eukaryotes with few distinguishing morphological traits. Here we have used a Bayesian molecular clock method under three distinct clock models to estimate divergence times within oomycetes, a group of fungal-like eukaryotes that are ubiquitous in the environment and include a number of devastating pathogenic species. The earliest fossil evidence for oomycetes comes from the Lower Devonian (~400 Ma), however the taxonomic affinities of these fossils are unclear. RESULTS: Complete genome sequences were used to identify orthologous proteins among oomycetes, diatoms, and a brown alga, with a focus on conserved regulators of gene expression such as DNA and histone modifiers and transcription factors. Our molecular clock estimates place the origin of oomycetes by at least the mid-Paleozoic (~430-400 Ma), with the divergence between two major lineages, the peronosporaleans and saprolegnialeans, in the early Mesozoic (~225-190 Ma). Divergence times estimated under the three clock models were similar, although only the strict and random local clock models produced reliable estimates for most parameters. CONCLUSIONS: Our molecular timescale suggests that modern pathogenic oomycetes diverged well after the origin of their respective hosts, indicating that environmental conditions or perhaps horizontal gene transfer events, rather than host availability, may have driven lineage diversification. Our findings also suggest that the last common ancestor of oomycetes possessed a full complement of eukaryotic regulatory proteins, including those involved in histone modification, RNA interference, and tRNA and rRNA methylation; interestingly no match to canonical DNA methyltransferases could be identified in the oomycete genomes studied here.
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spelling pubmed-40302862014-05-23 A multilocus timescale for oomycete evolution estimated under three distinct molecular clock models Matari, Nahill H Blair, Jaime E BMC Evol Biol Research Article BACKGROUND: Molecular clock methodologies allow for the estimation of divergence times across a variety of organisms; this can be particularly useful for groups lacking robust fossil histories, such as microbial eukaryotes with few distinguishing morphological traits. Here we have used a Bayesian molecular clock method under three distinct clock models to estimate divergence times within oomycetes, a group of fungal-like eukaryotes that are ubiquitous in the environment and include a number of devastating pathogenic species. The earliest fossil evidence for oomycetes comes from the Lower Devonian (~400 Ma), however the taxonomic affinities of these fossils are unclear. RESULTS: Complete genome sequences were used to identify orthologous proteins among oomycetes, diatoms, and a brown alga, with a focus on conserved regulators of gene expression such as DNA and histone modifiers and transcription factors. Our molecular clock estimates place the origin of oomycetes by at least the mid-Paleozoic (~430-400 Ma), with the divergence between two major lineages, the peronosporaleans and saprolegnialeans, in the early Mesozoic (~225-190 Ma). Divergence times estimated under the three clock models were similar, although only the strict and random local clock models produced reliable estimates for most parameters. CONCLUSIONS: Our molecular timescale suggests that modern pathogenic oomycetes diverged well after the origin of their respective hosts, indicating that environmental conditions or perhaps horizontal gene transfer events, rather than host availability, may have driven lineage diversification. Our findings also suggest that the last common ancestor of oomycetes possessed a full complement of eukaryotic regulatory proteins, including those involved in histone modification, RNA interference, and tRNA and rRNA methylation; interestingly no match to canonical DNA methyltransferases could be identified in the oomycete genomes studied here. BioMed Central 2014-05-12 /pmc/articles/PMC4030286/ /pubmed/24884411 http://dx.doi.org/10.1186/1471-2148-14-101 Text en Copyright © 2014 Matari and Blair; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Matari, Nahill H
Blair, Jaime E
A multilocus timescale for oomycete evolution estimated under three distinct molecular clock models
title A multilocus timescale for oomycete evolution estimated under three distinct molecular clock models
title_full A multilocus timescale for oomycete evolution estimated under three distinct molecular clock models
title_fullStr A multilocus timescale for oomycete evolution estimated under three distinct molecular clock models
title_full_unstemmed A multilocus timescale for oomycete evolution estimated under three distinct molecular clock models
title_short A multilocus timescale for oomycete evolution estimated under three distinct molecular clock models
title_sort multilocus timescale for oomycete evolution estimated under three distinct molecular clock models
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4030286/
https://www.ncbi.nlm.nih.gov/pubmed/24884411
http://dx.doi.org/10.1186/1471-2148-14-101
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