Cargando…
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...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
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 |
_version_ | 1784746327231430656 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9279130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT miaozhengang bcmettl4mediateddnaadeninen6methylationiscriticalforvirulenceofbotrytiscinerea AT wangguangyuan bcmettl4mediateddnaadeninen6methylationiscriticalforvirulenceofbotrytiscinerea AT shenheng bcmettl4mediateddnaadeninen6methylationiscriticalforvirulenceofbotrytiscinerea AT wangxue bcmettl4mediateddnaadeninen6methylationiscriticalforvirulenceofbotrytiscinerea AT gabrieldeanw bcmettl4mediateddnaadeninen6methylationiscriticalforvirulenceofbotrytiscinerea AT liangwenxing bcmettl4mediateddnaadeninen6methylationiscriticalforvirulenceofbotrytiscinerea |