Cargando…
BcRPD3-Mediated Histone Deacetylation Is Involved in Growth and Pathogenicity of Botrytis cinerea
Histone deacetylase activity plays an important role in transcriptional repression. Botrytis cinerea is an important necrotrophic fungal pathogen distributed worldwide and parasites a wide range of hosts. However, the molecular mechanisms of how B. cinerea regulates growth and host infection remain...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403187/ https://www.ncbi.nlm.nih.gov/pubmed/32849432 http://dx.doi.org/10.3389/fmicb.2020.01832 |
_version_ | 1783566901188755456 |
---|---|
author | Zhang, Ning Yang, Zhenzhou Zhang, Zhonghua Liang, Wenxing |
author_facet | Zhang, Ning Yang, Zhenzhou Zhang, Zhonghua Liang, Wenxing |
author_sort | Zhang, Ning |
collection | PubMed |
description | Histone deacetylase activity plays an important role in transcriptional repression. Botrytis cinerea is an important necrotrophic fungal pathogen distributed worldwide and parasites a wide range of hosts. However, the molecular mechanisms of how B. cinerea regulates growth and host infection remain largely unknown. Here, the function of BcRPD3, a histone deacetylase of B. cinerea, was investigated. Overexpression of the BcRPD3 gene resulted in significantly decreased acetylation levels of histone H3 and H4. The BcRPD3 overexpression strains showed slightly delayed vegetative growth, dramatically impaired infection structure formation, oxidative stress response, and virulence. RNA-Seq analysis revealed that enzymatic activity related genes, including 9 genes reported to function as virulence factors, were downregulated in BcRPD3 overexpression strain. Chromatin immunoprecipitation followed by qPCR confirmed the enrichment of BcRPD3 and H3Kac at the promoter regions of these nine genes. These observations indicated that BcRPD3 regulated the transcription of enzymatic activity related genes by controlling the acetylation level of histones, thereby affecting the vegetative growth, infection structure formation, oxidative stress response, and virulence of B. cinerea. |
format | Online Article Text |
id | pubmed-7403187 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74031872020-08-25 BcRPD3-Mediated Histone Deacetylation Is Involved in Growth and Pathogenicity of Botrytis cinerea Zhang, Ning Yang, Zhenzhou Zhang, Zhonghua Liang, Wenxing Front Microbiol Microbiology Histone deacetylase activity plays an important role in transcriptional repression. Botrytis cinerea is an important necrotrophic fungal pathogen distributed worldwide and parasites a wide range of hosts. However, the molecular mechanisms of how B. cinerea regulates growth and host infection remain largely unknown. Here, the function of BcRPD3, a histone deacetylase of B. cinerea, was investigated. Overexpression of the BcRPD3 gene resulted in significantly decreased acetylation levels of histone H3 and H4. The BcRPD3 overexpression strains showed slightly delayed vegetative growth, dramatically impaired infection structure formation, oxidative stress response, and virulence. RNA-Seq analysis revealed that enzymatic activity related genes, including 9 genes reported to function as virulence factors, were downregulated in BcRPD3 overexpression strain. Chromatin immunoprecipitation followed by qPCR confirmed the enrichment of BcRPD3 and H3Kac at the promoter regions of these nine genes. These observations indicated that BcRPD3 regulated the transcription of enzymatic activity related genes by controlling the acetylation level of histones, thereby affecting the vegetative growth, infection structure formation, oxidative stress response, and virulence of B. cinerea. Frontiers Media S.A. 2020-07-29 /pmc/articles/PMC7403187/ /pubmed/32849432 http://dx.doi.org/10.3389/fmicb.2020.01832 Text en Copyright © 2020 Zhang, Yang, Zhang and Liang. http://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 Zhang, Ning Yang, Zhenzhou Zhang, Zhonghua Liang, Wenxing BcRPD3-Mediated Histone Deacetylation Is Involved in Growth and Pathogenicity of Botrytis cinerea |
title | BcRPD3-Mediated Histone Deacetylation Is Involved in Growth and Pathogenicity of Botrytis cinerea |
title_full | BcRPD3-Mediated Histone Deacetylation Is Involved in Growth and Pathogenicity of Botrytis cinerea |
title_fullStr | BcRPD3-Mediated Histone Deacetylation Is Involved in Growth and Pathogenicity of Botrytis cinerea |
title_full_unstemmed | BcRPD3-Mediated Histone Deacetylation Is Involved in Growth and Pathogenicity of Botrytis cinerea |
title_short | BcRPD3-Mediated Histone Deacetylation Is Involved in Growth and Pathogenicity of Botrytis cinerea |
title_sort | bcrpd3-mediated histone deacetylation is involved in growth and pathogenicity of botrytis cinerea |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403187/ https://www.ncbi.nlm.nih.gov/pubmed/32849432 http://dx.doi.org/10.3389/fmicb.2020.01832 |
work_keys_str_mv | AT zhangning bcrpd3mediatedhistonedeacetylationisinvolvedingrowthandpathogenicityofbotrytiscinerea AT yangzhenzhou bcrpd3mediatedhistonedeacetylationisinvolvedingrowthandpathogenicityofbotrytiscinerea AT zhangzhonghua bcrpd3mediatedhistonedeacetylationisinvolvedingrowthandpathogenicityofbotrytiscinerea AT liangwenxing bcrpd3mediatedhistonedeacetylationisinvolvedingrowthandpathogenicityofbotrytiscinerea |