4.7 Article

Phylogenomic incongruence in Ceratocystis: a clue to speciation?

期刊

BMC GENOMICS
卷 21, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12864-020-6772-0

关键词

Ceratocystis; Incongruence; Hybridisation; Phylogenomics

资金

  1. South African National Research Foundation (NRF)
  2. University of Pretoria Research Development Programme
  3. South African Department of Science and Technology (DST)/NRF Centre of Excellence in Tree Health Biotechnology (CTHB) at the Forestry and Agricultural Biotechnology Institute (FABI)
  4. University of Pretoria, Genomics Research Institute (GRI)
  5. South African DST-NRF SARChI Chair in Fungal Genomics

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Background The taxonomic history of Ceratocystis, a genus in the Ceratocystidaceae, has been beset with questions and debate. This is due to many of the commonly used species recognition concepts (e.g., morphological and biological species concepts) providing different bases for interpretation of taxonomic boundaries. Species delineation in Ceratocystis primarily relied on genealogical concordance phylogenetic species recognition (GCPSR) using multiple standard molecular markers. Results Questions have arisen regarding the utility of these markers e.g., ITS, BT and TEF1-alpha due to evidence of intragenomic variation in the ITS, as well as genealogical incongruence, especially for isolates residing in a group referred to as the Latin-American clade (LAC) of the species. This study applied a phylogenomics approach to investigate the extent of phylogenetic incongruence in Ceratocystis. Phylogenomic analyses of a total of 1121 shared BUSCO genes revealed widespread incongruence within Ceratocystis, particularly within the LAC, which was typified by three equally represented topologies. Comparative analyses of the individual gene trees revealed evolutionary patterns indicative of hybridization. The maximum likelihood phylogenetic tree generated from the concatenated dataset comprised of 1069 shared BUSCO genes provided improved phylogenetic resolution suggesting the need for multiple gene markers in the phylogeny of Ceratocystis. Conclusion The incongruence observed among single gene phylogenies in this study call into question the utility of single or a few molecular markers for species delineation. Although this study provides evidence of interspecific hybridization, the role of hybridization as the source of discordance will require further research because the results could also be explained by high levels of shared ancestral polymorphism in this recently diverged lineage. This study also highlights the utility of BUSCO genes as a set of multiple orthologous genes for phylogenomic studies.

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