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Duplication of a Pks gene cluster and subsequent functional diversification facilitate environmental adaptation in Metarhizium species

The ecological importance of the duplication and diversification of gene clusters that synthesize secondary metabolites in fungi remains poorly understood. Here, we demonstrated that the duplication and subsequent diversification of a gene cluster produced two polyketide synthase gene clusters in th...

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Autores principales: Zeng, Guohong, Zhang, Peng, Zhang, Qiangqiang, Zhao, Hong, Li, Zixin, Zhang, Xing, Wang, Chengshu, Yin, Wen-Bing, Fang, Weiguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6042797/
https://www.ncbi.nlm.nih.gov/pubmed/29958281
http://dx.doi.org/10.1371/journal.pgen.1007472
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author Zeng, Guohong
Zhang, Peng
Zhang, Qiangqiang
Zhao, Hong
Li, Zixin
Zhang, Xing
Wang, Chengshu
Yin, Wen-Bing
Fang, Weiguo
author_facet Zeng, Guohong
Zhang, Peng
Zhang, Qiangqiang
Zhao, Hong
Li, Zixin
Zhang, Xing
Wang, Chengshu
Yin, Wen-Bing
Fang, Weiguo
author_sort Zeng, Guohong
collection PubMed
description The ecological importance of the duplication and diversification of gene clusters that synthesize secondary metabolites in fungi remains poorly understood. Here, we demonstrated that the duplication and subsequent diversification of a gene cluster produced two polyketide synthase gene clusters in the cosmopolitan fungal genus Metarhizium. Diversification occurred in the promoter regions and the exon-intron structures of the two Pks paralogs (Pks1 and Pks2). These two Pks genes have distinct expression patterns, with Pks1 highly expressed during conidiation and Pks2 highly expressed during infection. Different upstream signaling pathways were found to regulate the two Pks genes. Pks1 is positively regulated by Hog1-MAPK, Slt2-MAPK and Mr-OPY2, while Pks2 is positively regulated by Fus3-MAPK and negatively regulated by Mr-OPY2. Pks1 and Pks2 have been subjected to positive selection and synthesize different secondary metabolites. PKS1 is involved in synthesis of an anthraquinone derivative, and contributes to conidial pigmentation, which plays an important role in fungal tolerance to UV radiation and extreme temperatures. Disruption of the Pks2 gene delayed formation of infectious structures and increased the time taken to kill insects, indicating that Pks2 contributes to pathogenesis. Thus, the duplication of a Pks gene cluster and its subsequent functional diversification has increased the adaptive flexibility of Metarhizium species.
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spelling pubmed-60427972018-07-26 Duplication of a Pks gene cluster and subsequent functional diversification facilitate environmental adaptation in Metarhizium species Zeng, Guohong Zhang, Peng Zhang, Qiangqiang Zhao, Hong Li, Zixin Zhang, Xing Wang, Chengshu Yin, Wen-Bing Fang, Weiguo PLoS Genet Research Article The ecological importance of the duplication and diversification of gene clusters that synthesize secondary metabolites in fungi remains poorly understood. Here, we demonstrated that the duplication and subsequent diversification of a gene cluster produced two polyketide synthase gene clusters in the cosmopolitan fungal genus Metarhizium. Diversification occurred in the promoter regions and the exon-intron structures of the two Pks paralogs (Pks1 and Pks2). These two Pks genes have distinct expression patterns, with Pks1 highly expressed during conidiation and Pks2 highly expressed during infection. Different upstream signaling pathways were found to regulate the two Pks genes. Pks1 is positively regulated by Hog1-MAPK, Slt2-MAPK and Mr-OPY2, while Pks2 is positively regulated by Fus3-MAPK and negatively regulated by Mr-OPY2. Pks1 and Pks2 have been subjected to positive selection and synthesize different secondary metabolites. PKS1 is involved in synthesis of an anthraquinone derivative, and contributes to conidial pigmentation, which plays an important role in fungal tolerance to UV radiation and extreme temperatures. Disruption of the Pks2 gene delayed formation of infectious structures and increased the time taken to kill insects, indicating that Pks2 contributes to pathogenesis. Thus, the duplication of a Pks gene cluster and its subsequent functional diversification has increased the adaptive flexibility of Metarhizium species. Public Library of Science 2018-06-29 /pmc/articles/PMC6042797/ /pubmed/29958281 http://dx.doi.org/10.1371/journal.pgen.1007472 Text en © 2018 Zeng et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Zeng, Guohong
Zhang, Peng
Zhang, Qiangqiang
Zhao, Hong
Li, Zixin
Zhang, Xing
Wang, Chengshu
Yin, Wen-Bing
Fang, Weiguo
Duplication of a Pks gene cluster and subsequent functional diversification facilitate environmental adaptation in Metarhizium species
title Duplication of a Pks gene cluster and subsequent functional diversification facilitate environmental adaptation in Metarhizium species
title_full Duplication of a Pks gene cluster and subsequent functional diversification facilitate environmental adaptation in Metarhizium species
title_fullStr Duplication of a Pks gene cluster and subsequent functional diversification facilitate environmental adaptation in Metarhizium species
title_full_unstemmed Duplication of a Pks gene cluster and subsequent functional diversification facilitate environmental adaptation in Metarhizium species
title_short Duplication of a Pks gene cluster and subsequent functional diversification facilitate environmental adaptation in Metarhizium species
title_sort duplication of a pks gene cluster and subsequent functional diversification facilitate environmental adaptation in metarhizium species
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6042797/
https://www.ncbi.nlm.nih.gov/pubmed/29958281
http://dx.doi.org/10.1371/journal.pgen.1007472
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