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Link to original content: http://www.ncbi.nlm.nih.gov/pubmed/10760278
Phylogeny of seed plants based on all three genomic compartments: extant gymnosperms are monophyletic and Gnetales' closest relatives are conifers - PubMed Skip to main page content
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. 2000 Apr 11;97(8):4092-7.
doi: 10.1073/pnas.97.8.4092.

Phylogeny of seed plants based on all three genomic compartments: extant gymnosperms are monophyletic and Gnetales' closest relatives are conifers

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Phylogeny of seed plants based on all three genomic compartments: extant gymnosperms are monophyletic and Gnetales' closest relatives are conifers

L M Bowe et al. Proc Natl Acad Sci U S A. .

Abstract

Efforts to resolve Darwin's "abominable mystery"-the origin of angiosperms-have led to the conclusion that Gnetales and various fossil groups are sister to angiosperms, forming the "anthophytes." Morphological homologies, however, are difficult to interpret, and molecular data have not provided clear resolution of relationships among major groups of seed plants. We introduce two sequence data sets from slowly evolving mitochondrial genes, cox1 and atpA, which unambiguously reject the anthophyte hypothesis, favoring instead a close relationship between Gnetales and conifers. Parsimony- and likelihood-based analyses of plastid rbcL and nuclear 18S rDNA alone and with cox1 and atpA also strongly support a gnetophyte-conifer grouping. Surprisingly, three of four genes (all but nuclear rDNA) and combined three-genome analyses also suggest or strongly support Gnetales as derived conifers, sister to Pinaceae. Analyses with outgroups screened to avoid long branches consistently identify all gymnosperms as a monophyletic sister group to angiosperms. Combined three- and four-gene rooted analyses resolve the branching order for the remaining major groups-cycads separate from other gymnosperms first, followed by Ginkgo and then (Gnetales + Pinaceae) sister to a monophyletic group with all other conifer families. The molecular phylogeny strongly conflicts with current interpretations of seed plant morphology, and implies that many similarities between gnetophytes and angiosperms, such as "flower-like" reproductive structures and double fertilization, were independently derived, whereas other characters could emerge as synapomorphies for an expanded conifer group including Gnetales. An initial angiosperm-gymnosperm split implies a long stem lineage preceding the explosive Mesozoic radiation of flowering plants and suggests that angiosperm origins and homologies should be sought among extinct seed plant groups.

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Figures

Figure 1
Figure 1
Molecular phylogenies of seed plants are inconsistent with the anthophyte hypothesis (= gnetophytes + angiosperms) and instead support a close Gnetales–conifer relationship. Unrooted phylograms of seed plant DNA sequences found with paup* (heuristic search algorithm, ML) by using Macintosh G3 computers. ML bootstrap percentages on the basis of 100 replicates are also shown on key branches with data and tree characteristics as follows: (A) mitochondrial cox1: 27 taxa, 1,324 (aligned total) and 325 (parsimony informative) bases; -ln likelihood = 6,196.7314; ti/tv = 1.165; inv sites = 0.261; gamma = 0.698. (B) plastid rbcL: 26 taxa, 1,329 and 365 bases; -ln likelihood = 8292.7942; ti/tv = 3.03; inv sites = 0.52; gamma = 1.3. (C) nuclear 18S rDNA, 27 taxa, 1,715 and 224 bases; -ln likelihood = 6,694.0414; ti/tv = 2.26, inv sites = 0.6199, gamma = 0.624.
Figure 2
Figure 2
Alternative phylogenetic analyses of four genes by using ML, MP, and NJ. Analyses are unrooted, with arrows indicating position of root in additional rooted analyses (see text for details). BS above 50% for each analysis are given on internal branches. Taxa and tree characteristics are as Fig. 1, except long-branch taxa (Ephedra, Podocarpus, Phyllocladus) are excluded for cox1. Additional tree characteristics for each analysis: for cox1: 23 taxa, ML: -ln likelihood = 4827.7315 (ti/tv = 1.464, inv sites = 0.335, gamma = 0.758); MP: 1 tree at 502 steps, CI = 0.707, RI = 0.850; NJ: min. evol. score = 0.5217; for atpA: 16 taxa, 1,283 and 228 bases; ML: -ln likelihood = 5,118.0457 (ti/tv = 1.783, inv sites = 0.542, gamma = 3.911); MP = 1 tree at 639 steps; CI = 0.655, RI = 0.767; NJ: min. evol. score = 0.8169; for rbcL: 26 taxa, MP: 3 trees at 1,329 steps; CI = 0.438, RI = 0.637; NJ: min. evol. score = see text; for 18S: 27 taxa, MP: 2 trees at 780 steps, CI = 0.499, RI = 0.717; NJ: min. evol. = see text.
Figure 3
Figure 3
Rooted seed-plant phylogenies by using three-genome combined data from (A) cox1, rbcL, and 18S rDNA, and (B) including atpA. Identical topologies were obtained by using ML, MP (except arrangement of angiosperms, where Nymphaea is basal in three-gene MP), and NJ analyses, rooted or unrooted, with or without long-branch Ephedra. (A) ML/MP bootstraps are shown. Twenty-eight taxa; 4,367 and 1,025 bases; ML: –ln likelihood = 24,645.044 (ti/tv = 2.137, inv sites = 0.427, gamma = 0.685); MP: 3 trees at 3,583 steps (CI = 0.49; RI = 0.67). ML/MP bootstraps also given for two key nodes (in brackets) after deletion of long-branch Ephedra. (B) ML/MP bootstraps shown for atpA alone (Left) and all four genes (Right). For atpA (17 taxa, 1,283 and 244 bases): ML: -ln likelihood = 5,678.420 (ti/tv = 1.774, inv sites = 0.431, gamma = 1.836; MP: 1 tree at 777 steps (CI = 0.621; RI = 0.723). For all 4 genes (5,650 and 920 bases): ML: -ln likelihood = 23,323.1563 (ti/tv = 2.224, inv sites = 0.508, gamma = 0.938); MP: 1 tree at 3,044 steps, CI = 0.549, RI = 0.641.

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