Large-scale genome sequencing of mycorrhizal fungi provides insights into the early evolution of symbiotic traits
(2020) In Nature Communications 11(1).- Abstract
Mycorrhizal fungi are mutualists that play crucial roles in nutrient acquisition in terrestrial ecosystems. Mycorrhizal symbioses arose repeatedly across multiple lineages of Mucoromycotina, Ascomycota, and Basidiomycota. Considerable variation exists in the capacity of mycorrhizal fungi to acquire carbon from soil organic matter. Here, we present a combined analysis of 135 fungal genomes from 73 saprotrophic, endophytic and pathogenic species, and 62 mycorrhizal species, including 29 new mycorrhizal genomes. This study samples ecologically dominant fungal guilds for which there were previously no symbiotic genomes available, including ectomycorrhizal Russulales, Thelephorales and Cantharellales. Our analyses show that transitions from... (More)
Mycorrhizal fungi are mutualists that play crucial roles in nutrient acquisition in terrestrial ecosystems. Mycorrhizal symbioses arose repeatedly across multiple lineages of Mucoromycotina, Ascomycota, and Basidiomycota. Considerable variation exists in the capacity of mycorrhizal fungi to acquire carbon from soil organic matter. Here, we present a combined analysis of 135 fungal genomes from 73 saprotrophic, endophytic and pathogenic species, and 62 mycorrhizal species, including 29 new mycorrhizal genomes. This study samples ecologically dominant fungal guilds for which there were previously no symbiotic genomes available, including ectomycorrhizal Russulales, Thelephorales and Cantharellales. Our analyses show that transitions from saprotrophy to symbiosis involve (1) widespread losses of degrading enzymes acting on lignin and cellulose, (2) co-option of genes present in saprotrophic ancestors to fulfill new symbiotic functions, (3) diversification of novel, lineage-specific symbiosis-induced genes, (4) proliferation of transposable elements and (5) divergent genetic innovations underlying the convergent origins of the ectomycorrhizal guild.
(Less)
- author
- publishing date
- 2020-12-01
- type
- Contribution to journal
- publication status
- published
- in
- Nature Communications
- volume
- 11
- issue
- 1
- article number
- 5125
- publisher
- Nature Publishing Group
- external identifiers
-
- pmid:33046698
- scopus:85092519868
- ISSN
- 2041-1723
- DOI
- 10.1038/s41467-020-18795-w
- language
- English
- LU publication?
- no
- additional info
- Publisher Copyright: © 2020, The Author(s).
- id
- c749ee7e-faaf-47d9-a223-0ae57d5ddb76
- date added to LUP
- 2024-06-02 15:04:10
- date last changed
- 2024-08-11 20:33:31
@article{c749ee7e-faaf-47d9-a223-0ae57d5ddb76, abstract = {{<p>Mycorrhizal fungi are mutualists that play crucial roles in nutrient acquisition in terrestrial ecosystems. Mycorrhizal symbioses arose repeatedly across multiple lineages of Mucoromycotina, Ascomycota, and Basidiomycota. Considerable variation exists in the capacity of mycorrhizal fungi to acquire carbon from soil organic matter. Here, we present a combined analysis of 135 fungal genomes from 73 saprotrophic, endophytic and pathogenic species, and 62 mycorrhizal species, including 29 new mycorrhizal genomes. This study samples ecologically dominant fungal guilds for which there were previously no symbiotic genomes available, including ectomycorrhizal Russulales, Thelephorales and Cantharellales. Our analyses show that transitions from saprotrophy to symbiosis involve (1) widespread losses of degrading enzymes acting on lignin and cellulose, (2) co-option of genes present in saprotrophic ancestors to fulfill new symbiotic functions, (3) diversification of novel, lineage-specific symbiosis-induced genes, (4) proliferation of transposable elements and (5) divergent genetic innovations underlying the convergent origins of the ectomycorrhizal guild.</p>}}, author = {{Miyauchi, Shingo and Kiss, Enikő and Kuo, Alan and Drula, Elodie and Kohler, Annegret and Sánchez-García, Marisol and Morin, Emmanuelle and Andreopoulos, Bill and Barry, Kerrie W. and Bonito, Gregory and Buée, Marc and Carver, Akiko and Chen, Cindy and Cichocki, Nicolas and Clum, Alicia and Culley, David and Crous, Pedro W. and Fauchery, Laure and Girlanda, Mariangela and Hayes, Richard D. and Kéri, Zsófia and LaButti, Kurt and Lipzen, Anna and Lombard, Vincent and Magnuson, Jon and Maillard, François and Murat, Claude and Nolan, Matt and Ohm, Robin A. and Pangilinan, Jasmyn and Pereira, Maíra de Freitas and Perotto, Silvia and Peter, Martina and Pfister, Stephanie and Riley, Robert and Sitrit, Yaron and Stielow, J. Benjamin and Szöllősi, Gergely and Žifčáková, Lucia and Štursová, Martina and Spatafora, Joseph W. and Tedersoo, Leho and Vaario, Lu Min and Yamada, Akiyoshi and Yan, Mi and Wang, Pengfei and Xu, Jianping and Bruns, Tom and Baldrian, Petr and Vilgalys, Rytas and Dunand, Christophe and Henrissat, Bernard and Grigoriev, Igor V. and Hibbett, David and Nagy, László G. and Martin, Francis M.}}, issn = {{2041-1723}}, language = {{eng}}, month = {{12}}, number = {{1}}, publisher = {{Nature Publishing Group}}, series = {{Nature Communications}}, title = {{Large-scale genome sequencing of mycorrhizal fungi provides insights into the early evolution of symbiotic traits}}, url = {{http://dx.doi.org/10.1038/s41467-020-18795-w}}, doi = {{10.1038/s41467-020-18795-w}}, volume = {{11}}, year = {{2020}}, }