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. 2018 Feb 1;7(2):1-11.
doi: 10.1093/gigascience/gix116.

Large-scale phylogenomic analysis resolves a backbone phylogeny in ferns

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Large-scale phylogenomic analysis resolves a backbone phylogeny in ferns

Hui Shen et al. Gigascience. .

Abstract

Background: Ferns, originated about 360 million years ago, are the sister group of seed plants. Despite the remarkable progress in our understanding of fern phylogeny, with conflicting molecular evidence and different morphological interpretations, relationships among major fern lineages remain controversial.

Results: With the aim to obtain a robust fern phylogeny, we carried out a large-scale phylogenomic analysis using high-quality transcriptome sequencing data, which covered 69 fern species from 38 families and 11 orders. Both coalescent-based and concatenation-based methods were applied to both nucleotide and amino acid sequences in species tree estimation. The resulting topologies are largely congruent with each other, except for the placement of Angiopteris fokiensis, Cheiropleuria bicuspis, Diplaziopsis brunoniana, Matteuccia struthiopteris, Elaphoglossum mcclurei, and Tectaria subpedata.

Conclusions: Our result confirmed that Equisetales is sister to the rest of ferns, and Dennstaedtiaceae is sister to eupolypods. Moreover, our result strongly supported some relationships different from the current view of fern phylogeny, including that Marattiaceae may be sister to the monophyletic clade of Psilotaceae and Ophioglossaceae; that Gleicheniaceae and Hymenophyllaceae form a monophyletic clade sister to Dipteridaceae; and that Aspleniaceae is sister to the rest of the groups in eupolypods II. These results were interpreted with morphological traits, especially sporangia characters, and a new evolutionary route of sporangial annulus in ferns was suggested. This backbone phylogeny in ferns sets a foundation for further studies in biology and evolution in ferns, and therefore in plants.

Keywords: evolution; monilophytes; phylogenomic; sporangium; transcriptome.

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Figures

Figure 1:
Figure 1:
Topologies (a-f) adapted from published results [5, 12–14, 26, 34]. Branches with support <75% were shown using dotted lines, and taxa that differ in their phylogeny locations were shown in different colors.
Figure 2:
Figure 2:
A working flow diagram showing the major processes of data production and analysis in this study. Three major processes are de novo transcriptome assembly, 1-to-1 orthologs prediction, and phylogenetic analysis. The rectangles represent the main results, and the ellipses represent the main methods and analysis.
Figure 3:
Figure 3:
Phylogeny of ferns reconstructed by coalescent-based method using nucleotide sequence with divergence times calculated. Support values for the main phylogeny (A) calculated from Matrix 1/Matrix 2 are listed as percentages. *Indicates 100%/100%. Representative leave(s), sporangium, and the corresponding lineage are labeled with a same number. Simplified topology (B) shows the main linages as in Fig. 1. Species in phylogeny (A) and the corresponding lineage in topology (B) are shown in the same color.
Figure 4:
Figure 4:
Reconstruction of the evolutionary history of sporangial annulus in ferns. Sampled species with 7 types of sporangial annulus are shown in different colours. For each ancient node, percentage of character state of sporangial annulus is shown.

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