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Ecology Drives the Distribution of Specialized Tyrosine Metabolism Modules in Fungi
Gene clusters encoding accessory or environmentally specialized metabolic pathways likely play a significant role in the evolution of fungal genomes. Two such gene clusters encoding enzymes associated with the tyrosine metabolism pathway (KEGG #00350) have been identified in the filamentous fungus A...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914699/ https://www.ncbi.nlm.nih.gov/pubmed/24391152 http://dx.doi.org/10.1093/gbe/evt208 |
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author | Greene, George H. McGary, Kriston L. Rokas, Antonis Slot, Jason C. |
author_facet | Greene, George H. McGary, Kriston L. Rokas, Antonis Slot, Jason C. |
author_sort | Greene, George H. |
collection | PubMed |
description | Gene clusters encoding accessory or environmentally specialized metabolic pathways likely play a significant role in the evolution of fungal genomes. Two such gene clusters encoding enzymes associated with the tyrosine metabolism pathway (KEGG #00350) have been identified in the filamentous fungus Aspergillus fumigatus. The l-tyrosine degradation (TD) gene cluster encodes a functional module that facilitates breakdown of the phenolic amino acid, l-tyrosine through a homogentisate intermediate, but is also involved in the production of pyomelanin, a fungal pathogenicity factor. The gentisate catabolism (GC) gene cluster encodes a functional module likely involved in phenolic compound degradation, which may enable metabolism of biphenolic stilbenes in multiple lineages. Our investigation of the evolution of the TD and GC gene clusters in 214 fungal genomes revealed spotty distributions partially shaped by gene cluster loss and horizontal gene transfer (HGT). Specifically, a TD gene cluster shows evidence of HGT between the extremophilic, melanized fungi Exophiala dermatitidis and Baudoinia compniacensis, and a GC gene cluster shows evidence of HGT between Sordariomycete and Dothideomycete grass pathogens. These results suggest that the distribution of specialized tyrosine metabolism modules is influenced by both the ecology and phylogeny of fungal species. |
format | Online Article Text |
id | pubmed-3914699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39146992014-02-06 Ecology Drives the Distribution of Specialized Tyrosine Metabolism Modules in Fungi Greene, George H. McGary, Kriston L. Rokas, Antonis Slot, Jason C. Genome Biol Evol Research Article Gene clusters encoding accessory or environmentally specialized metabolic pathways likely play a significant role in the evolution of fungal genomes. Two such gene clusters encoding enzymes associated with the tyrosine metabolism pathway (KEGG #00350) have been identified in the filamentous fungus Aspergillus fumigatus. The l-tyrosine degradation (TD) gene cluster encodes a functional module that facilitates breakdown of the phenolic amino acid, l-tyrosine through a homogentisate intermediate, but is also involved in the production of pyomelanin, a fungal pathogenicity factor. The gentisate catabolism (GC) gene cluster encodes a functional module likely involved in phenolic compound degradation, which may enable metabolism of biphenolic stilbenes in multiple lineages. Our investigation of the evolution of the TD and GC gene clusters in 214 fungal genomes revealed spotty distributions partially shaped by gene cluster loss and horizontal gene transfer (HGT). Specifically, a TD gene cluster shows evidence of HGT between the extremophilic, melanized fungi Exophiala dermatitidis and Baudoinia compniacensis, and a GC gene cluster shows evidence of HGT between Sordariomycete and Dothideomycete grass pathogens. These results suggest that the distribution of specialized tyrosine metabolism modules is influenced by both the ecology and phylogeny of fungal species. Oxford University Press 2014-01-02 /pmc/articles/PMC3914699/ /pubmed/24391152 http://dx.doi.org/10.1093/gbe/evt208 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Greene, George H. McGary, Kriston L. Rokas, Antonis Slot, Jason C. Ecology Drives the Distribution of Specialized Tyrosine Metabolism Modules in Fungi |
title | Ecology Drives the Distribution of Specialized Tyrosine Metabolism Modules in Fungi |
title_full | Ecology Drives the Distribution of Specialized Tyrosine Metabolism Modules in Fungi |
title_fullStr | Ecology Drives the Distribution of Specialized Tyrosine Metabolism Modules in Fungi |
title_full_unstemmed | Ecology Drives the Distribution of Specialized Tyrosine Metabolism Modules in Fungi |
title_short | Ecology Drives the Distribution of Specialized Tyrosine Metabolism Modules in Fungi |
title_sort | ecology drives the distribution of specialized tyrosine metabolism modules in fungi |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914699/ https://www.ncbi.nlm.nih.gov/pubmed/24391152 http://dx.doi.org/10.1093/gbe/evt208 |
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