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Innovation and constraint leading to complex multicellularity in the Ascomycota
The advent of complex multicellularity (CM) was a pivotal event in the evolution of animals, plants and fungi. In the fungal Ascomycota, CM is based on hyphal filaments and arose in the Pezizomycotina. The genus Neolecta defines an enigma: phylogenetically placed in a related group containing mostly...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5309816/ https://www.ncbi.nlm.nih.gov/pubmed/28176784 http://dx.doi.org/10.1038/ncomms14444 |
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author | Nguyen, Tu Anh Cissé, Ousmane H. Yun Wong, Jie Zheng, Peng Hewitt, David Nowrousian, Minou Stajich, Jason E. Jedd, Gregory |
author_facet | Nguyen, Tu Anh Cissé, Ousmane H. Yun Wong, Jie Zheng, Peng Hewitt, David Nowrousian, Minou Stajich, Jason E. Jedd, Gregory |
author_sort | Nguyen, Tu Anh |
collection | PubMed |
description | The advent of complex multicellularity (CM) was a pivotal event in the evolution of animals, plants and fungi. In the fungal Ascomycota, CM is based on hyphal filaments and arose in the Pezizomycotina. The genus Neolecta defines an enigma: phylogenetically placed in a related group containing mostly yeasts, Neolecta nevertheless possesses Pezizomycotina-like CM. Here we sequence the Neolecta irregularis genome and identify CM-associated functions by searching for genes conserved in Neolecta and the Pezizomycotina, which are absent or divergent in budding or fission yeasts. This group of 1,050 genes is enriched for functions related to diverse endomembrane systems and their organization. Remarkably, most show evidence for divergence in both yeasts. Using functional genomics, we identify new genes involved in fungal complexification. Together, these data show that rudimentary multicellularity is deeply rooted in the Ascomycota. Extensive parallel gene divergence during simplification and constraint leading to CM suggest a deterministic process where shared modes of cellular organization select for similarly configured organelle- and transport-related machineries. |
format | Online Article Text |
id | pubmed-5309816 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53098162017-02-27 Innovation and constraint leading to complex multicellularity in the Ascomycota Nguyen, Tu Anh Cissé, Ousmane H. Yun Wong, Jie Zheng, Peng Hewitt, David Nowrousian, Minou Stajich, Jason E. Jedd, Gregory Nat Commun Article The advent of complex multicellularity (CM) was a pivotal event in the evolution of animals, plants and fungi. In the fungal Ascomycota, CM is based on hyphal filaments and arose in the Pezizomycotina. The genus Neolecta defines an enigma: phylogenetically placed in a related group containing mostly yeasts, Neolecta nevertheless possesses Pezizomycotina-like CM. Here we sequence the Neolecta irregularis genome and identify CM-associated functions by searching for genes conserved in Neolecta and the Pezizomycotina, which are absent or divergent in budding or fission yeasts. This group of 1,050 genes is enriched for functions related to diverse endomembrane systems and their organization. Remarkably, most show evidence for divergence in both yeasts. Using functional genomics, we identify new genes involved in fungal complexification. Together, these data show that rudimentary multicellularity is deeply rooted in the Ascomycota. Extensive parallel gene divergence during simplification and constraint leading to CM suggest a deterministic process where shared modes of cellular organization select for similarly configured organelle- and transport-related machineries. Nature Publishing Group 2017-02-08 /pmc/articles/PMC5309816/ /pubmed/28176784 http://dx.doi.org/10.1038/ncomms14444 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Nguyen, Tu Anh Cissé, Ousmane H. Yun Wong, Jie Zheng, Peng Hewitt, David Nowrousian, Minou Stajich, Jason E. Jedd, Gregory Innovation and constraint leading to complex multicellularity in the Ascomycota |
title | Innovation and constraint leading to complex multicellularity in the Ascomycota |
title_full | Innovation and constraint leading to complex multicellularity in the Ascomycota |
title_fullStr | Innovation and constraint leading to complex multicellularity in the Ascomycota |
title_full_unstemmed | Innovation and constraint leading to complex multicellularity in the Ascomycota |
title_short | Innovation and constraint leading to complex multicellularity in the Ascomycota |
title_sort | innovation and constraint leading to complex multicellularity in the ascomycota |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5309816/ https://www.ncbi.nlm.nih.gov/pubmed/28176784 http://dx.doi.org/10.1038/ncomms14444 |
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