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BcMettl4-Mediated DNA Adenine N(6)-Methylation Is Critical for Virulence of Botrytis cinerea

DNA adenine N(6)-methylation (6mA) plays a critical role in various biological functions, but its occurrence and functions in filamentous plant pathogens are largely unexplored. Botrytis cinerea is an important pathogenic fungus worldwide. A systematic analysis of 6mA in B. cinerea was performed in...

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Autores principales: Miao, Zhengang, Wang, Guangyuan, Shen, Heng, Wang, Xue, Gabriel, Dean W., Liang, Wenxing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9279130/
https://www.ncbi.nlm.nih.gov/pubmed/35847085
http://dx.doi.org/10.3389/fmicb.2022.925868
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author Miao, Zhengang
Wang, Guangyuan
Shen, Heng
Wang, Xue
Gabriel, Dean W.
Liang, Wenxing
author_facet Miao, Zhengang
Wang, Guangyuan
Shen, Heng
Wang, Xue
Gabriel, Dean W.
Liang, Wenxing
author_sort Miao, Zhengang
collection PubMed
description DNA adenine N(6)-methylation (6mA) plays a critical role in various biological functions, but its occurrence and functions in filamentous plant pathogens are largely unexplored. Botrytis cinerea is an important pathogenic fungus worldwide. A systematic analysis of 6mA in B. cinerea was performed in this study, revealing that 6mA is widely distributed in the genome of this fungus. The 2 kb regions flanking many genes, particularly the upstream promoter regions, were susceptible to methylation. The role of BcMettl4, a 6mA methyltransferase, in the virulence of B. cinerea was investigated. BcMETTL4 disruption and point mutations of its catalytic motif “DPPW” both resulted in significant 6mA reduction in the genomic DNA and in reduced virulence of B. cinerea. RNA-Seq analysis revealed a total of 13 downregulated genes in the disruption mutant ΔBcMettl4 in which methylation occurred at the promoter sites. These were involved in oxidoreduction, secretory pathways, autophagy and carbohydrate metabolism. Two of these genes, BcFDH and BcMFS2, were independently disrupted. Knockout of BcFDH led to reduced sclerotium formation, while disruption of BcMFS2 resulted in dramatically decreased conidium formation and pathogenicity. These observations indicated that 6mA provides potential epigenetic markers in B. cinerea and that BcMettl4 regulates virulence in this important plant pathogen.
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spelling pubmed-92791302022-07-15 BcMettl4-Mediated DNA Adenine N(6)-Methylation Is Critical for Virulence of Botrytis cinerea Miao, Zhengang Wang, Guangyuan Shen, Heng Wang, Xue Gabriel, Dean W. Liang, Wenxing Front Microbiol Microbiology DNA adenine N(6)-methylation (6mA) plays a critical role in various biological functions, but its occurrence and functions in filamentous plant pathogens are largely unexplored. Botrytis cinerea is an important pathogenic fungus worldwide. A systematic analysis of 6mA in B. cinerea was performed in this study, revealing that 6mA is widely distributed in the genome of this fungus. The 2 kb regions flanking many genes, particularly the upstream promoter regions, were susceptible to methylation. The role of BcMettl4, a 6mA methyltransferase, in the virulence of B. cinerea was investigated. BcMETTL4 disruption and point mutations of its catalytic motif “DPPW” both resulted in significant 6mA reduction in the genomic DNA and in reduced virulence of B. cinerea. RNA-Seq analysis revealed a total of 13 downregulated genes in the disruption mutant ΔBcMettl4 in which methylation occurred at the promoter sites. These were involved in oxidoreduction, secretory pathways, autophagy and carbohydrate metabolism. Two of these genes, BcFDH and BcMFS2, were independently disrupted. Knockout of BcFDH led to reduced sclerotium formation, while disruption of BcMFS2 resulted in dramatically decreased conidium formation and pathogenicity. These observations indicated that 6mA provides potential epigenetic markers in B. cinerea and that BcMettl4 regulates virulence in this important plant pathogen. Frontiers Media S.A. 2022-06-30 /pmc/articles/PMC9279130/ /pubmed/35847085 http://dx.doi.org/10.3389/fmicb.2022.925868 Text en Copyright © 2022 Miao, Wang, Shen, Wang, Gabriel and Liang. 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
Miao, Zhengang
Wang, Guangyuan
Shen, Heng
Wang, Xue
Gabriel, Dean W.
Liang, Wenxing
BcMettl4-Mediated DNA Adenine N(6)-Methylation Is Critical for Virulence of Botrytis cinerea
title BcMettl4-Mediated DNA Adenine N(6)-Methylation Is Critical for Virulence of Botrytis cinerea
title_full BcMettl4-Mediated DNA Adenine N(6)-Methylation Is Critical for Virulence of Botrytis cinerea
title_fullStr BcMettl4-Mediated DNA Adenine N(6)-Methylation Is Critical for Virulence of Botrytis cinerea
title_full_unstemmed BcMettl4-Mediated DNA Adenine N(6)-Methylation Is Critical for Virulence of Botrytis cinerea
title_short BcMettl4-Mediated DNA Adenine N(6)-Methylation Is Critical for Virulence of Botrytis cinerea
title_sort bcmettl4-mediated dna adenine n(6)-methylation is critical for virulence of botrytis cinerea
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9279130/
https://www.ncbi.nlm.nih.gov/pubmed/35847085
http://dx.doi.org/10.3389/fmicb.2022.925868
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