The full-length phylogenetic tree from 1551 ribosomal sequences of chitinous fungi, Fungi.

A data set with 1551 fungal sequences of the small subunit ribosomal RNA has been analysed phylogenetically. Four animal sequences were used to root the tree. The parsimony ratchet algorithm in combination with tree fusion was used to find most parsimonious trees and the parsimony jackknifing method was used to establish support frequencies. The full-length consensus tree, of the most parsimonious trees, is published and jackknife frequencies above 50% are plotted on the consensus tree at supported nodes. Until recently attempts to find the most parsimonious trees for large data sets were impractical, given current computational limitations. The parsimony ratchet in combination with tree fusion was found to be a very efficient method of rapid parsimony analysis of this large data set. Parsimony jackknifing is a very fast and efficient method for establishing group support. The results show that the Glomeromycota are the sister group to a monophyletic Dikaryomycota. The majority of the species in the Glomeromycota/Dikaryomycota group have a symbiotic lifestyle--a possible synapomorphy for a group 'Symbiomycota'. This would suggest that symbiosis between fungi and green plants evolved prior to the colonization of land by plants and not as a result of the colonization process. The Basidiomycotina and the Ascomycotina are both supported as monophyletic. The Urediniomycetes is the sister group to the rest of the Basidiomycotina successively followed in a grade by Ustilaginomycetes, Tremellomycetes, Dacrymycetales, Ceratobasidiales and Homobasidiomycetes each supported as monophyletic except the Homobasidiomycetes which are left unsupported. The ascomycete node begins with a polytomy consisting of the Pneumocystidomycetes, Schizosaccharomycetes, unsupported group with the Taphrinomycetes and Neolectales, and finally an unnamed, monophyletic and supported group including the Saccharomycetes and Euascomycetes. Within the Euascomycetes the inoperculate euascomycetes (Inoperculata) are supported as monophyletic excluding the Orbiliomycetes which are included in an unsupported operculate, pezizalean sister group together with Helvellaceae, Morchellaceae, Tuberaceae and others. Geoglossum is the sister group to the rest of the inoperculate euascomycetes. The Sordariomycetes, Dothideomycetes, Chaetothyriomycetes and Eurotiomycetes are each highly supported as monophyletic. The Leotiomycetes and the Lecanoromycetes both appear in the consensus of the most parsimonious trees but neither taxon receives any jackknife support.

[1]  O. Eriksson,et al.  Outline of Ascomycota : 2003 , 2003 .

[2]  A. Tehler Morphological data, molecular data, and total evidence in phylogenetic analysis , 1995 .

[3]  J. Farris,et al.  Simultaneous parsimony jackknife analysis of 2538rbcL DNA sequences reveals support for major clades of green plants, land plants, seed plants and flowering plants , 1998, Plant Systematics and Evolution.

[4]  Changbao Wu,et al.  Jackknife, Bootstrap and Other Resampling Methods in Regression Analysis , 1986 .

[5]  H. Clémençon Die Strukturen der Basidiosporenwand und des Apikulus, und deren Beziehung zur Exogenisation der Spore , 1977 .

[6]  S. Stickel,et al.  Monophyletic origins of the metazoa: an evolutionary link with fungi , 1993, Science.

[7]  D. Bhattacharya,et al.  Widespread occurrence of spliceosomal introns in the rDNA genes of ascomycetes. , 2000, Molecular biology and evolution.

[8]  Ernst A. Bessey Morphology and taxonomy of fungi , 1950 .

[9]  S. Damberger,et al.  Nuclear-encoded rDNA group I introns: origin and phylogenetic relationships of insertion site lineages in the green algae. , 1996, Molecular biology and evolution.

[10]  M. Berbee,et al.  Fungal Molecular Evolution: Gene Trees and Geologic Time , 2001 .

[11]  J. Hafellner Problems in Lecanorales Systematics , 1994 .

[12]  J. Farris,et al.  Support, Ribosomal Sequences and the Phylogeny Of The Eukaryotes , 1998, Cladistics : the international journal of the Willi Hennig Society.

[13]  J. Felsenstein CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP , 1985, Evolution; international journal of organic evolution.

[14]  Yves Van de Peer,et al.  The European database on small subunit ribosomal RNA , 2002, Nucleic Acids Res..

[15]  J. Farris,et al.  Phylogenetic analyses of the fungi based on large rDNA data sets. , 2000 .

[16]  Thomas D. Bruns,et al.  Fungal Molecular Systematics , 1991 .

[17]  P. Goloboff Analyzing Large Data Sets in Reasonable Times: Solutions for Composite Optima , 1999, Cladistics : the international journal of the Willi Hennig Society.

[18]  A. Tehler,et al.  Multiple origins of lichen symbioses in fungi suggested by SSU rDNA phylogeny. , 1995, Science.

[19]  J. W. Taylor,et al.  Phylogeny of Discomycetes and early radiations of the apothecial Ascomycotina inferred from SSU rDNA sequence data. , 1995, Experimental mycology.

[20]  David L. Hawksworth,et al.  Ascomycete systematics : problems and perspectives in the nineties , 1995 .

[21]  H. Vogel Distribution of Lysine Pathways Among Fungi: Evolutionary Implications , 1964, The American Naturalist.

[22]  S. Hedges,et al.  Molecular Evidence for the Early Colonization of Land by Fungi and Plants , 2001, Science.

[23]  A. Tehler,et al.  A Cladistic Outline of the Eumycota , 1988, Cladistics : the international journal of the Willi Hennig Society.

[24]  P. DePriest Small subunit rDNA variation in a population of lichen fungi due to optional group-I introns. , 1993, Gene.

[25]  David L. Hawksworth,et al.  Ainsworth & Bisby's Dictionary of the Fungi , 1972 .

[26]  D. Moore,et al.  Evolutionary Biology of the Fungi , 1989 .

[27]  Daniel Schwarzott,et al.  A new fungal phylum, the Glomeromycota: phylogeny and evolution * * Dedicated to Manfred Kluge (Tech , 2001 .

[28]  D. Hawksworth,et al.  Always deposit vouchers , 2000 .

[29]  J. Farris,et al.  PARSIMONY JACKKNIFING OUTPERFORMS NEIGHBOR‐JOINING , 1996, Cladistics : the international journal of the Willi Hennig Society.

[30]  W. Doolittle,et al.  Microsporidia are related to Fungi: evidence from the largest subunit of RNA polymerase II and other proteins. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[31]  D. Bhattacharya,et al.  Vertical Evolution and Intragenic Spread of Lichen-Fungal Group I Introns , 2002, Journal of Molecular Evolution.

[32]  D. McLaughlin Ultrastructure and Cytochemistry of Basidial and Basidiospore Development , 1982 .

[33]  D. Redecker,et al.  Glomalean fungi from the Ordovician. , 2000, Science.

[34]  F. Kauff,et al.  Phylogeny of the Gyalectales and Ostropales (Ascomycota, Fungi): among and within order relationships based on nuclear ribosomal RNA small and large subunits. , 2002, Molecular phylogenetics and evolution.

[35]  A. Tehler,et al.  β-tubulin, ITS and group I intron sequences challenge the species pair concept in Physcia aipolia and P. caesia , 2001 .

[36]  David L. Hawksworth,et al.  The fungal dimension of biodiversity: magnitude, significance, and conservation , 1991 .

[37]  M. Källersjö,et al.  Variable sizes of introns in the SSU rDNA in three species of Roccella (Arthoniales, Euascomycetes) , 1999, Current Genetics.

[38]  J. Sugiyama,et al.  Are Microsporidia really related to Fungi?: a reappraisal based on additional gene sequences from basal fungi , 2002 .

[39]  A. Crespo,et al.  Terminal-sequence conservation identifies spliceosomal introns in ascomycete 18S RNA genes. , 2000, Molecular biology and evolution.

[40]  K. Nixon,et al.  The Parsimony Ratchet, a New Method for Rapid Parsimony Analysis , 1999, Cladistics : the international journal of the Willi Hennig Society.