Evolution of gilled mushrooms and puffballs inferred from ribosomal DNA sequences.

Homobasidiomycete fungi display many complex fruiting body morphologies, including mushrooms and puffballs, but their anatomical simplicity has confounded efforts to understand the evolution of these forms. We performed a comprehensive phylogenetic analysis of homobasidiomycetes, using sequences from nuclear and mitochondrial ribosomal DNA, with an emphasis on understanding evolutionary relationships of gilled mushrooms and puffballs. Parsimony-based optimization of character states on our phylogenetic trees suggested that strikingly similar gilled mushrooms evolved at least six times, from morphologically diverse precursors. Approximately 87% of gilled mushrooms are in a single lineage, which we call the "euagarics." Recently discovered 90 million-year-old fossil mushrooms are probably euagarics, suggesting that (i) the origin of this clade must have occurred no later than the mid-Cretaceous and (ii) the gilled mushroom morphology has been maintained in certain lineages for tens of millions of years. Puffballs and other forms with enclosed spore-bearing structures (Gasteromycetes) evolved at least four times. Derivation of Gasteromycetes from forms with exposed spore-bearing structures (Hymenomycetes) is correlated with repeated loss of forcible spore discharge (ballistospory). Diverse fruiting body forms and spore dispersal mechanisms have evolved among Gasteromycetes. Nevertheless, it appears that Hymenomycetes have never been secondarily derived from Gasteromycetes, which suggests that the loss of ballistospory has constrained evolution in these lineages.

[1]  M. Donoghue,et al.  Cretaceous mushrooms in amber , 1995, Nature.

[2]  R. Singer The Agaricales in modern taxonomy , 1949 .

[3]  G. R. Bisby,et al.  A Dictionary of the Fungi , 1943, Nature.

[4]  M. Donoghue,et al.  Fossil mushrooms from Miocene and Cretaceous ambers and the evolution of Homobasidiomycetes. , 1997, American journal of botany.

[5]  J. Palmer,et al.  Accelerated evolution of a false-truffle from a mushroom ancestor , 1989, Nature.

[6]  D. Hibbett,et al.  Phylogenetic evidence for horizontal transmission of group I introns in the nuclear ribosomal DNA of mushroom-forming fungi. , 1996, Molecular biology and evolution.

[7]  D. Hibbett,et al.  Sporocarp ontogeny in Panus (Basidiomycotina): evolution and classification , 1993 .

[8]  T. Mcclean,et al.  Persistence of basidiospores and sclerotia of ectomycorrhizal fungi and Morchella in soil , 1994 .

[9]  H. Thiers The secotioid syndrome , 1984 .

[10]  D. Savile,et al.  Fungal Spores: Their Liberation and Dispersal , 1973 .

[11]  R. Vilgalys,et al.  Phylogenetic relationships among coprinoid taxa and allies based on data from restriction site mapping of nuclear rDNA , 1994 .

[12]  G. Baura,et al.  Gastrosuillus laricinus is a recent derivative of Suillus grevillei : molecular evidence , 1992 .

[13]  T. Bruns,et al.  Amplification and sequencing of DNA from fungal herbarium specimens. , 1990 .

[14]  G. Mueller,et al.  DNA data provide evidence on the evolutionary relationships between mushrooms and false truffles , 1994 .

[15]  C. Ingold,et al.  Ballistospore discharge in Itersonilia perplexans , 1984 .

[16]  John W. Taylor,et al.  Higher taxa of basidiomycetes: an 18S rRNA gene perspective , 1993 .

[17]  T. Szaro,et al.  Rate and mode differences between nuclear and mitochondrial small-subunit rRNA genes in mushrooms. , 1992, Molecular biology and evolution.

[18]  D. Hibbett,et al.  The secotioid form of Lentinus tigrinus: genetics and development of a fungal morphological innovation , 1994 .

[19]  D. Hibbett,et al.  Phylogenetic Relationships of Lentinus (Basidiomycotina) Inferred from Molecular and Morphological Characters , 1993 .