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A Small Horizontally Transferred Gene Cluster Contributes to the Sporulation of Alternaria alternata
Horizontal gene transfer (HGT) has been identified as an important source of genomic innovation in fungi. However, how HGT drove the evolution of Alternaria alternata, a necrotrophic fungus which can be ubiquitously isolated from soil and various plants and decaying plant materials is largely known....
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916707/ https://www.ncbi.nlm.nih.gov/pubmed/31764979 http://dx.doi.org/10.1093/gbe/evz257 |
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author | Wang, Mingshuang Fu, Huilan Ruan, Ruoxin |
author_facet | Wang, Mingshuang Fu, Huilan Ruan, Ruoxin |
author_sort | Wang, Mingshuang |
collection | PubMed |
description | Horizontal gene transfer (HGT) has been identified as an important source of genomic innovation in fungi. However, how HGT drove the evolution of Alternaria alternata, a necrotrophic fungus which can be ubiquitously isolated from soil and various plants and decaying plant materials is largely known. In this study, we identified 12 protein-encoding genes that are likely acquired from lineages outside Pezizomycotina. Phylogenetic trees and approximately unbiased comparative topology tests strongly supported the evolutionary origin of these genes. According to their predicted functions, these HGT candidates are involved in nitrogen and carbohydrate metabolism. Especially, five genes of them were likely transferred as a physically linked cluster from Tremellales (Basidiomycota). Functionally knocking out the five-gene cluster in an A. alternata isolate causing citrus brown spot resulted in an 80% decrease in asexual spore production in the deletion mutant. We further knocked out each of these five genes in this cluster and the resultant single-gene deletion mutants exhibited a various degree of reduction in spore production. Except for conidiation, functions of these genes associated with vegetative growth, stress tolerance, and virulence are very limited. Our results provide new evidence that HGT has played important roles over the course of the evolution of filamentous fungi. |
format | Online Article Text |
id | pubmed-6916707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-69167072019-12-19 A Small Horizontally Transferred Gene Cluster Contributes to the Sporulation of Alternaria alternata Wang, Mingshuang Fu, Huilan Ruan, Ruoxin Genome Biol Evol Research Article Horizontal gene transfer (HGT) has been identified as an important source of genomic innovation in fungi. However, how HGT drove the evolution of Alternaria alternata, a necrotrophic fungus which can be ubiquitously isolated from soil and various plants and decaying plant materials is largely known. In this study, we identified 12 protein-encoding genes that are likely acquired from lineages outside Pezizomycotina. Phylogenetic trees and approximately unbiased comparative topology tests strongly supported the evolutionary origin of these genes. According to their predicted functions, these HGT candidates are involved in nitrogen and carbohydrate metabolism. Especially, five genes of them were likely transferred as a physically linked cluster from Tremellales (Basidiomycota). Functionally knocking out the five-gene cluster in an A. alternata isolate causing citrus brown spot resulted in an 80% decrease in asexual spore production in the deletion mutant. We further knocked out each of these five genes in this cluster and the resultant single-gene deletion mutants exhibited a various degree of reduction in spore production. Except for conidiation, functions of these genes associated with vegetative growth, stress tolerance, and virulence are very limited. Our results provide new evidence that HGT has played important roles over the course of the evolution of filamentous fungi. Oxford University Press 2019-11-25 /pmc/articles/PMC6916707/ /pubmed/31764979 http://dx.doi.org/10.1093/gbe/evz257 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Article Wang, Mingshuang Fu, Huilan Ruan, Ruoxin A Small Horizontally Transferred Gene Cluster Contributes to the Sporulation of Alternaria alternata |
title | A Small Horizontally Transferred Gene Cluster Contributes to the Sporulation of Alternaria alternata |
title_full | A Small Horizontally Transferred Gene Cluster Contributes to the Sporulation of Alternaria alternata |
title_fullStr | A Small Horizontally Transferred Gene Cluster Contributes to the Sporulation of Alternaria alternata |
title_full_unstemmed | A Small Horizontally Transferred Gene Cluster Contributes to the Sporulation of Alternaria alternata |
title_short | A Small Horizontally Transferred Gene Cluster Contributes to the Sporulation of Alternaria alternata |
title_sort | small horizontally transferred gene cluster contributes to the sporulation of alternaria alternata |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916707/ https://www.ncbi.nlm.nih.gov/pubmed/31764979 http://dx.doi.org/10.1093/gbe/evz257 |
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