Literature DB >> 19328858

Repeated evolution of closed fruiting bodies is linked to ascoma development in the largest group of lichenized fungi (Lecanoromycetes, Ascomycota).

Imke Schmitt1, Ruth Del Prado, Martin Grube, H Thorsten Lumbsch.   

Abstract

Fruiting bodies are responsible for the effective dispersal of meiospores in ascomycetes. Different fruiting body types include open (apothecia) or closed (perithecia, cleistothecia) forms, which have traditionally been used as key paradigms for ascomycete classification. Molecular phylogenies show that most fruiting body types have multiple phylogenetic origins within the phylum, and are not suitable for the circumscription of classes. One exception are perithecia that are restricted in non-lichenized fungi to the monophyletic class Sordariomycetes. However, lichenized fungi with perithecioid fruiting bodies were found to belong to three other classes unrelated to Sordariomycetes. One of these is Lecanoromycetes, which includes the bulk of lichenized fungi. To understand the evolution of perithecioid fruiting bodies in the mostly apotheciate Lecanoromycetes, we assembled a combined data set of nuclear and mitochondrial ribosomal, and RPB1 DNA sequences, and traced the evolution of two morphological characters (fruiting body type and fruiting body development). We reconstructed ancestral character states using maximum likelihood and Bayesian methods. Additionally, we tested for correlation of character changes in a combined Bayesian/maximum likelihood framework. The results suggest that perithecia have evolved in unrelated groups of lichen-forming fungi. Within Lecanoromycetes they have evolved independently several times from apotheciate ancestors. Further, our analyses support a correlation between the type of fruiting body and the type of ascoma ontogeny. The evolution of angiocarpous ascoma development in Lecanoromycetes is a pre-adaptation for the repeated gain of perithecia. This finding is consistent with the hypothesis of a neotenic origin of perithecioid fruiting bodies in Lecanoromycetes.

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Year:  2009        PMID: 19328858     DOI: 10.1016/j.ympev.2009.03.017

Source DB:  PubMed          Journal:  Mol Phylogenet Evol        ISSN: 1055-7903            Impact factor:   4.286


  6 in total

1.  Fertile Prototaxites taiti: a basal ascomycete with inoperculate, polysporous asci lacking croziers.

Authors:  Rosmarie Honegger; Dianne Edwards; Lindsey Axe; Christine Strullu-Derrien
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2018-02-05       Impact factor: 6.237

2.  Apothecial Ancestry, Evolution, and Re-Evolution in Thelebolales (Leotiomycetes, Fungi).

Authors:  Luis Quijada; Neven Matočec; Ivana Kušan; Joey B Tanney; Peter R Johnston; Armin Mešić; Donald H Pfister
Journal:  Biology (Basel)       Date:  2022-04-11

3.  Understanding phenotypical character evolution in parmelioid lichenized fungi (Parmeliaceae, Ascomycota).

Authors:  Pradeep K Divakar; Frank Kauff; Ana Crespo; Steven D Leavitt; H Thorsten Lumbsch
Journal:  PLoS One       Date:  2013-11-29       Impact factor: 3.240

4.  Circumscription of the genus Lepra, a recently resurrected genus to accommodate the "Variolaria"-group of Pertusaria sensu lato (Pertusariales, Ascomycota).

Authors:  Xinli Wei; Imke Schmitt; Brendan Hodkinson; Adam Flakus; Martin Kukwa; Pradeep K Divakar; Paul M Kirika; Jürgen Otte; Anjuli Meiser; H Thorsten Lumbsch
Journal:  PLoS One       Date:  2017-07-11       Impact factor: 3.240

5.  Phylogenetic placement within Lecanoromycetes of lichenicolous fungi associated with Cladonia and some other genera.

Authors:  R Pino-Bodas; M P Zhurbenko; S Stenroos
Journal:  Persoonia       Date:  2017-06-28       Impact factor: 11.051

6.  A Molecular Phylogeny of the Lichen Genus Lecidella Focusing on Species from Mainland China.

Authors:  Xin Zhao; Lu Lu Zhang; Zun Tian Zhao; Wei Cheng Wang; Steven D Leavitt; Helge Thorsten Lumbsch
Journal:  PLoS One       Date:  2015-09-28       Impact factor: 3.240

  6 in total

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