ArticleBMC evolutionary biology2014
A multilocus timescale for oomycete evolution estimated under three distinct molecular clock models.
Article in BMC evolutionary biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.
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33 citing papers in PubMed, 68 citations in OpenAlex.
- Oomycete plant pathogens: biology, pathogenesis and emerging control strategies.Nature reviews. Microbiology · 2026Review
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- Specific Transcriptional Regulation Controls Plant Organ-Specific Infection by the Oomycete Pathogen Phytophthora sojae.Molecular plant pathology · 2024Article
- 1.63-billion-year-old multicellular eukaryotes from the Chuanlinggou Formation in North China.Science advances · 2024Article
- Evolutionary dynamics of plastomes in coscinodiscophycean diatoms revealed by comparative genomics.Frontiers in microbiology · 2023Article
- Review
- Comparative Analysis of Bacillariophyceae Chloroplast Genomes Uncovers Extensive Genome Rearrangements Associated with Speciation.International journal of environmental research and public health · 2022Article
- Phytophthora: an ancient, historic, biologically and structurally cohesive and evolutionarily successful generic concept in need of preservation.IMA fungus · 2022Article
- Comparative Analyses of Complete Peronosporaceae (Oomycota) Mitogenome Sequences-Insights into Structural Evolution and Phylogeny.Genome biology and evolution · 2022Article
- A whole genome duplication drives the genome evolution of Phytophthora betacei, a closely related species to Phytophthora infestans.BMC genomics · 2021Article
- Genome Analysis ofPlants (Basel, Switzerland) · 2021Article
- Predicting Lifestyle from Positive Selection Data and Genome Properties in Oomycetes.Pathogens (Basel, Switzerland) · 2021Article
- The Destructive Tree PathogenJournal of fungi (Basel, Switzerland) · 2021Article
- Phylogenetic analyses suggest centipede venom arsenals were repeatedly stocked by horizontal gene transfer.Nature communications · 2021Article
- Diverse Trajectories Drive the Expression of a Giant Virus in the Oomycete Plant PathogenFrontiers in microbiology · 2021Article
- Comparative Analysis of Chloroplast Genomes of SevenFrontiers in microbiology · 2021Article
- Article
- Polycystic Kidney Disease Ryanodine Receptor Domain (PKDRR) Proteins in Oomycetes.Pathogens (Basel, Switzerland) · 2020Article
- Independent Whole-Genome Duplications Define the Architecture of the Genomes of the Devastating West African Cacao Black Pod PathogenG3 (Bethesda, Md.) · 2020Article
- Article
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2 authors at 1 institution in 1 country.
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Abstract
backgroundMolecular 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.
resultsComplete 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.
conclusionsOur 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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