Cargando…
Methionine biosynthesis enzyme MoMet2 is required for rice blast fungus pathogenicity by promoting virulence gene expression via reducing 5mC modification
The emergence of fungicide resistance severely threatens crop production by limiting the availability and application of established fungicides. Therefore, it is urgent to identify new fungicidal targets for controlling plant diseases. Here, we characterized the function of a conserved homoserine O-...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10547190/ https://www.ncbi.nlm.nih.gov/pubmed/37733784 http://dx.doi.org/10.1371/journal.pgen.1010927 |
_version_ | 1785115008095485952 |
---|---|
author | Li, Huimin Mo, Pengcheng Zhang, Jun Xie, Zhuoer Liu, Xinyu Chen, Han Yang, Leiyun Liu, Muxing Zhang, Haifeng Wang, Ping Zhang, Zhengguang |
author_facet | Li, Huimin Mo, Pengcheng Zhang, Jun Xie, Zhuoer Liu, Xinyu Chen, Han Yang, Leiyun Liu, Muxing Zhang, Haifeng Wang, Ping Zhang, Zhengguang |
author_sort | Li, Huimin |
collection | PubMed |
description | The emergence of fungicide resistance severely threatens crop production by limiting the availability and application of established fungicides. Therefore, it is urgent to identify new fungicidal targets for controlling plant diseases. Here, we characterized the function of a conserved homoserine O-acetyltransferase (HOA) from the rice blast fungus Magnaporthe oryzae that could serve as the candidate antifungal target. Deletion of the MoMET2 and MoCYS2 genes encoding HOAs perturbed the biosynthesis of methionine and S-adenyl methionine, a methyl group donor for epigenetic modifications, and severely attenuated the development and virulence of M. oryzae. The ∆Momet2 mutant is significantly increased in 5-methylcytosine (5mC) modification that represses the expression of genes required for pathogenicity, including MoGLIK and MoCDH-CYT. We further showed that host-induced gene silencing (HIGS) targeting MoMET2 and MoCYS2 effectively controls rice blasts. Our studies revealed the importance of HOA in the development and virulence of M. oryzae, which suggests the potential feasibility of HOA as new targets for novel anti-rice blast measurements. |
format | Online Article Text |
id | pubmed-10547190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-105471902023-10-04 Methionine biosynthesis enzyme MoMet2 is required for rice blast fungus pathogenicity by promoting virulence gene expression via reducing 5mC modification Li, Huimin Mo, Pengcheng Zhang, Jun Xie, Zhuoer Liu, Xinyu Chen, Han Yang, Leiyun Liu, Muxing Zhang, Haifeng Wang, Ping Zhang, Zhengguang PLoS Genet Research Article The emergence of fungicide resistance severely threatens crop production by limiting the availability and application of established fungicides. Therefore, it is urgent to identify new fungicidal targets for controlling plant diseases. Here, we characterized the function of a conserved homoserine O-acetyltransferase (HOA) from the rice blast fungus Magnaporthe oryzae that could serve as the candidate antifungal target. Deletion of the MoMET2 and MoCYS2 genes encoding HOAs perturbed the biosynthesis of methionine and S-adenyl methionine, a methyl group donor for epigenetic modifications, and severely attenuated the development and virulence of M. oryzae. The ∆Momet2 mutant is significantly increased in 5-methylcytosine (5mC) modification that represses the expression of genes required for pathogenicity, including MoGLIK and MoCDH-CYT. We further showed that host-induced gene silencing (HIGS) targeting MoMET2 and MoCYS2 effectively controls rice blasts. Our studies revealed the importance of HOA in the development and virulence of M. oryzae, which suggests the potential feasibility of HOA as new targets for novel anti-rice blast measurements. Public Library of Science 2023-09-21 /pmc/articles/PMC10547190/ /pubmed/37733784 http://dx.doi.org/10.1371/journal.pgen.1010927 Text en © 2023 Li et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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 Li, Huimin Mo, Pengcheng Zhang, Jun Xie, Zhuoer Liu, Xinyu Chen, Han Yang, Leiyun Liu, Muxing Zhang, Haifeng Wang, Ping Zhang, Zhengguang Methionine biosynthesis enzyme MoMet2 is required for rice blast fungus pathogenicity by promoting virulence gene expression via reducing 5mC modification |
title | Methionine biosynthesis enzyme MoMet2 is required for rice blast fungus pathogenicity by promoting virulence gene expression via reducing 5mC modification |
title_full | Methionine biosynthesis enzyme MoMet2 is required for rice blast fungus pathogenicity by promoting virulence gene expression via reducing 5mC modification |
title_fullStr | Methionine biosynthesis enzyme MoMet2 is required for rice blast fungus pathogenicity by promoting virulence gene expression via reducing 5mC modification |
title_full_unstemmed | Methionine biosynthesis enzyme MoMet2 is required for rice blast fungus pathogenicity by promoting virulence gene expression via reducing 5mC modification |
title_short | Methionine biosynthesis enzyme MoMet2 is required for rice blast fungus pathogenicity by promoting virulence gene expression via reducing 5mC modification |
title_sort | methionine biosynthesis enzyme momet2 is required for rice blast fungus pathogenicity by promoting virulence gene expression via reducing 5mc modification |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10547190/ https://www.ncbi.nlm.nih.gov/pubmed/37733784 http://dx.doi.org/10.1371/journal.pgen.1010927 |
work_keys_str_mv | AT lihuimin methioninebiosynthesisenzymemomet2isrequiredforriceblastfunguspathogenicitybypromotingvirulencegeneexpressionviareducing5mcmodification AT mopengcheng methioninebiosynthesisenzymemomet2isrequiredforriceblastfunguspathogenicitybypromotingvirulencegeneexpressionviareducing5mcmodification AT zhangjun methioninebiosynthesisenzymemomet2isrequiredforriceblastfunguspathogenicitybypromotingvirulencegeneexpressionviareducing5mcmodification AT xiezhuoer methioninebiosynthesisenzymemomet2isrequiredforriceblastfunguspathogenicitybypromotingvirulencegeneexpressionviareducing5mcmodification AT liuxinyu methioninebiosynthesisenzymemomet2isrequiredforriceblastfunguspathogenicitybypromotingvirulencegeneexpressionviareducing5mcmodification AT chenhan methioninebiosynthesisenzymemomet2isrequiredforriceblastfunguspathogenicitybypromotingvirulencegeneexpressionviareducing5mcmodification AT yangleiyun methioninebiosynthesisenzymemomet2isrequiredforriceblastfunguspathogenicitybypromotingvirulencegeneexpressionviareducing5mcmodification AT liumuxing methioninebiosynthesisenzymemomet2isrequiredforriceblastfunguspathogenicitybypromotingvirulencegeneexpressionviareducing5mcmodification AT zhanghaifeng methioninebiosynthesisenzymemomet2isrequiredforriceblastfunguspathogenicitybypromotingvirulencegeneexpressionviareducing5mcmodification AT wangping methioninebiosynthesisenzymemomet2isrequiredforriceblastfunguspathogenicitybypromotingvirulencegeneexpressionviareducing5mcmodification AT zhangzhengguang methioninebiosynthesisenzymemomet2isrequiredforriceblastfunguspathogenicitybypromotingvirulencegeneexpressionviareducing5mcmodification |