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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...

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Autores principales: Greene, George H., McGary, Kriston L., Rokas, Antonis, Slot, Jason C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
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.
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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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