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Histone Methylation Is Required for Virulence, Conidiation, and Multi-Stress Resistance of Alternaria alternata
Histone methylation, which is critical for transcriptional regulation and various biological processes in eukaryotes, is a reversible dynamic process regulated by histone methyltransferases (HMTs) and histone demethylases (HDMs). This study determined the function of 5 HMTs (AaDot1, AaHMT1, AaHnrnp,...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245015/ https://www.ncbi.nlm.nih.gov/pubmed/35783406 http://dx.doi.org/10.3389/fmicb.2022.924476 |
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author | Meng, Shuai Huang, Suya Liu, Jinhua Gai, Yunpeng Li, Min Duan, Shuo Zhang, Shuting Sun, Xuepeng Yang, Qi Wang, Yuchun Xu, Kai Ma, Haijie |
author_facet | Meng, Shuai Huang, Suya Liu, Jinhua Gai, Yunpeng Li, Min Duan, Shuo Zhang, Shuting Sun, Xuepeng Yang, Qi Wang, Yuchun Xu, Kai Ma, Haijie |
author_sort | Meng, Shuai |
collection | PubMed |
description | Histone methylation, which is critical for transcriptional regulation and various biological processes in eukaryotes, is a reversible dynamic process regulated by histone methyltransferases (HMTs) and histone demethylases (HDMs). This study determined the function of 5 HMTs (AaDot1, AaHMT1, AaHnrnp, AaSet1, and AaSet2) and 1 HDMs (AaGhd2) in the phytopathogenic fungus Alternaria alternata by analyzing targeted gene deletion mutants. The vegetative growth, conidiation, and pathogenicity of ∆AaSet1 and ∆AaSet2 were severely inhibited indicating that AaSet1 and AaSet2 play critical roles in cell development in A. alternata. Multiple stresses analysis revealed that both AaSet1 and AaSet2 were involved in the adaptation to cell wall interference agents and osmotic stress. Meanwhile, ∆AaSet1 and ∆AaSet2 displayed serious vegetative growth defects in sole carbon source medium, indicating that AaSet1 and AaSet2 play an important role in carbon source utilization. In addition, ∆AaSet2 colony displayed white in color, while the wild-type colony was dark brown, indicating AaSet2 is an essential gene for melanin biosynthesis in A. alternata. AaSet2 was required for the resistance to oxidative stress. On the other hand, all of ∆AaDot1, ∆AaHMT1, and ∆AaGhd2 mutants displayed wild-type phenotype in vegetative growth, multi-stress resistance, pathogenicity, carbon source utilization, and melanin biosynthesis. To explore the regulatory mechanism of AaSet1 and AaSet2, RNA-seq of these mutants and wild-type strain was performed. Phenotypes mentioned above correlated well with the differentially expressed genes in ∆AaSet1 and ∆AaSet2 according to the KEGG and GO enrichment results. Overall, our study provides genetic evidence that defines the central role of HMTs and HDMs in the pathological and biological functions of A. alternata. |
format | Online Article Text |
id | pubmed-9245015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92450152022-07-01 Histone Methylation Is Required for Virulence, Conidiation, and Multi-Stress Resistance of Alternaria alternata Meng, Shuai Huang, Suya Liu, Jinhua Gai, Yunpeng Li, Min Duan, Shuo Zhang, Shuting Sun, Xuepeng Yang, Qi Wang, Yuchun Xu, Kai Ma, Haijie Front Microbiol Microbiology Histone methylation, which is critical for transcriptional regulation and various biological processes in eukaryotes, is a reversible dynamic process regulated by histone methyltransferases (HMTs) and histone demethylases (HDMs). This study determined the function of 5 HMTs (AaDot1, AaHMT1, AaHnrnp, AaSet1, and AaSet2) and 1 HDMs (AaGhd2) in the phytopathogenic fungus Alternaria alternata by analyzing targeted gene deletion mutants. The vegetative growth, conidiation, and pathogenicity of ∆AaSet1 and ∆AaSet2 were severely inhibited indicating that AaSet1 and AaSet2 play critical roles in cell development in A. alternata. Multiple stresses analysis revealed that both AaSet1 and AaSet2 were involved in the adaptation to cell wall interference agents and osmotic stress. Meanwhile, ∆AaSet1 and ∆AaSet2 displayed serious vegetative growth defects in sole carbon source medium, indicating that AaSet1 and AaSet2 play an important role in carbon source utilization. In addition, ∆AaSet2 colony displayed white in color, while the wild-type colony was dark brown, indicating AaSet2 is an essential gene for melanin biosynthesis in A. alternata. AaSet2 was required for the resistance to oxidative stress. On the other hand, all of ∆AaDot1, ∆AaHMT1, and ∆AaGhd2 mutants displayed wild-type phenotype in vegetative growth, multi-stress resistance, pathogenicity, carbon source utilization, and melanin biosynthesis. To explore the regulatory mechanism of AaSet1 and AaSet2, RNA-seq of these mutants and wild-type strain was performed. Phenotypes mentioned above correlated well with the differentially expressed genes in ∆AaSet1 and ∆AaSet2 according to the KEGG and GO enrichment results. Overall, our study provides genetic evidence that defines the central role of HMTs and HDMs in the pathological and biological functions of A. alternata. Frontiers Media S.A. 2022-06-16 /pmc/articles/PMC9245015/ /pubmed/35783406 http://dx.doi.org/10.3389/fmicb.2022.924476 Text en Copyright © 2022 Meng, Huang, Liu, Gai, Li, Duan, Zhang, Sun, Yang, Wang, Xu and Ma. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Meng, Shuai Huang, Suya Liu, Jinhua Gai, Yunpeng Li, Min Duan, Shuo Zhang, Shuting Sun, Xuepeng Yang, Qi Wang, Yuchun Xu, Kai Ma, Haijie Histone Methylation Is Required for Virulence, Conidiation, and Multi-Stress Resistance of Alternaria alternata |
title | Histone Methylation Is Required for Virulence, Conidiation, and Multi-Stress Resistance of Alternaria alternata |
title_full | Histone Methylation Is Required for Virulence, Conidiation, and Multi-Stress Resistance of Alternaria alternata |
title_fullStr | Histone Methylation Is Required for Virulence, Conidiation, and Multi-Stress Resistance of Alternaria alternata |
title_full_unstemmed | Histone Methylation Is Required for Virulence, Conidiation, and Multi-Stress Resistance of Alternaria alternata |
title_short | Histone Methylation Is Required for Virulence, Conidiation, and Multi-Stress Resistance of Alternaria alternata |
title_sort | histone methylation is required for virulence, conidiation, and multi-stress resistance of alternaria alternata |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245015/ https://www.ncbi.nlm.nih.gov/pubmed/35783406 http://dx.doi.org/10.3389/fmicb.2022.924476 |
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