Cargando…

Comparative Proteomic Analysis of Plasma Membrane Proteins in Rice Leaves Reveals a Vesicle Trafficking Network in Plant Immunity That Is Provoked by Blast Fungi

Rice blast, caused by Magnaporthe oryzae, is one of the most devastating diseases in rice and can affect rice production worldwide. Rice plasma membrane (PM) proteins are crucial for rapidly and precisely establishing a defense response in plant immunity when rice and blast fungi interact. However,...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Zhi, Li, Meng, Zhang, He, Yu, Yao, Ma, Lu, Wang, Wei, Fan, Yunxin, Huang, Ning, Wang, Xinying, Liu, Kunquan, Dong, Shinan, Tang, Haijuan, Wang, Jianfei, Zhang, Hongsheng, Bao, Yongmei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9083198/
https://www.ncbi.nlm.nih.gov/pubmed/35548300
http://dx.doi.org/10.3389/fpls.2022.853195
_version_ 1784703371824857088
author Zhao, Zhi
Li, Meng
Zhang, He
Yu, Yao
Ma, Lu
Wang, Wei
Fan, Yunxin
Huang, Ning
Wang, Xinying
Liu, Kunquan
Dong, Shinan
Tang, Haijuan
Wang, Jianfei
Zhang, Hongsheng
Bao, Yongmei
author_facet Zhao, Zhi
Li, Meng
Zhang, He
Yu, Yao
Ma, Lu
Wang, Wei
Fan, Yunxin
Huang, Ning
Wang, Xinying
Liu, Kunquan
Dong, Shinan
Tang, Haijuan
Wang, Jianfei
Zhang, Hongsheng
Bao, Yongmei
author_sort Zhao, Zhi
collection PubMed
description Rice blast, caused by Magnaporthe oryzae, is one of the most devastating diseases in rice and can affect rice production worldwide. Rice plasma membrane (PM) proteins are crucial for rapidly and precisely establishing a defense response in plant immunity when rice and blast fungi interact. However, the plant-immunity-associated vesicle trafficking network mediated by PM proteins is poorly understood. In this study, to explore changes in PM proteins during M. oryzae infection, the PM proteome was analyzed via iTRAQ in the resistant rice landrace Heikezijing. A total of 831 differentially expressed proteins (DEPs) were identified, including 434 upregulated and 397 downregulated DEPs. In functional analyses, DEPs associated with vesicle trafficking were significantly enriched, including the “transport” term in a Gene Ontology enrichment analysis, the endocytosis and phagosome pathways in a Encyclopedia of Genes and Genomes analysis, and vesicle-associated proteins identified via a protein–protein interaction network analysis. OsNPSN13, a novel plant-specific soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) 13 protein, was identified as an upregulated DEP, and transgenic plants overexpressing this gene showed enhanced blast resistance, while transgenic knockdown plants were more susceptible than wild-type plants. The changes in abundance and putative functions of 20 DEPs revealed a possible vesicle trafficking network in the M. oryzae-rice interaction. A comparative proteomic analysis of plasma membrane proteins in rice leaves revealed a plant-immunity-associated vesicle trafficking network that is provoked by blast fungi; these results provide new insights into rice resistance responses against rice blast fungi.
format Online
Article
Text
id pubmed-9083198
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-90831982022-05-10 Comparative Proteomic Analysis of Plasma Membrane Proteins in Rice Leaves Reveals a Vesicle Trafficking Network in Plant Immunity That Is Provoked by Blast Fungi Zhao, Zhi Li, Meng Zhang, He Yu, Yao Ma, Lu Wang, Wei Fan, Yunxin Huang, Ning Wang, Xinying Liu, Kunquan Dong, Shinan Tang, Haijuan Wang, Jianfei Zhang, Hongsheng Bao, Yongmei Front Plant Sci Plant Science Rice blast, caused by Magnaporthe oryzae, is one of the most devastating diseases in rice and can affect rice production worldwide. Rice plasma membrane (PM) proteins are crucial for rapidly and precisely establishing a defense response in plant immunity when rice and blast fungi interact. However, the plant-immunity-associated vesicle trafficking network mediated by PM proteins is poorly understood. In this study, to explore changes in PM proteins during M. oryzae infection, the PM proteome was analyzed via iTRAQ in the resistant rice landrace Heikezijing. A total of 831 differentially expressed proteins (DEPs) were identified, including 434 upregulated and 397 downregulated DEPs. In functional analyses, DEPs associated with vesicle trafficking were significantly enriched, including the “transport” term in a Gene Ontology enrichment analysis, the endocytosis and phagosome pathways in a Encyclopedia of Genes and Genomes analysis, and vesicle-associated proteins identified via a protein–protein interaction network analysis. OsNPSN13, a novel plant-specific soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) 13 protein, was identified as an upregulated DEP, and transgenic plants overexpressing this gene showed enhanced blast resistance, while transgenic knockdown plants were more susceptible than wild-type plants. The changes in abundance and putative functions of 20 DEPs revealed a possible vesicle trafficking network in the M. oryzae-rice interaction. A comparative proteomic analysis of plasma membrane proteins in rice leaves revealed a plant-immunity-associated vesicle trafficking network that is provoked by blast fungi; these results provide new insights into rice resistance responses against rice blast fungi. Frontiers Media S.A. 2022-04-25 /pmc/articles/PMC9083198/ /pubmed/35548300 http://dx.doi.org/10.3389/fpls.2022.853195 Text en Copyright © 2022 Zhao, Li, Zhang, Yu, Ma, Wang, Fan, Huang, Wang, Liu, Dong, Tang, Wang, Zhang and Bao. 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 Plant Science
Zhao, Zhi
Li, Meng
Zhang, He
Yu, Yao
Ma, Lu
Wang, Wei
Fan, Yunxin
Huang, Ning
Wang, Xinying
Liu, Kunquan
Dong, Shinan
Tang, Haijuan
Wang, Jianfei
Zhang, Hongsheng
Bao, Yongmei
Comparative Proteomic Analysis of Plasma Membrane Proteins in Rice Leaves Reveals a Vesicle Trafficking Network in Plant Immunity That Is Provoked by Blast Fungi
title Comparative Proteomic Analysis of Plasma Membrane Proteins in Rice Leaves Reveals a Vesicle Trafficking Network in Plant Immunity That Is Provoked by Blast Fungi
title_full Comparative Proteomic Analysis of Plasma Membrane Proteins in Rice Leaves Reveals a Vesicle Trafficking Network in Plant Immunity That Is Provoked by Blast Fungi
title_fullStr Comparative Proteomic Analysis of Plasma Membrane Proteins in Rice Leaves Reveals a Vesicle Trafficking Network in Plant Immunity That Is Provoked by Blast Fungi
title_full_unstemmed Comparative Proteomic Analysis of Plasma Membrane Proteins in Rice Leaves Reveals a Vesicle Trafficking Network in Plant Immunity That Is Provoked by Blast Fungi
title_short Comparative Proteomic Analysis of Plasma Membrane Proteins in Rice Leaves Reveals a Vesicle Trafficking Network in Plant Immunity That Is Provoked by Blast Fungi
title_sort comparative proteomic analysis of plasma membrane proteins in rice leaves reveals a vesicle trafficking network in plant immunity that is provoked by blast fungi
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9083198/
https://www.ncbi.nlm.nih.gov/pubmed/35548300
http://dx.doi.org/10.3389/fpls.2022.853195
work_keys_str_mv AT zhaozhi comparativeproteomicanalysisofplasmamembraneproteinsinriceleavesrevealsavesicletraffickingnetworkinplantimmunitythatisprovokedbyblastfungi
AT limeng comparativeproteomicanalysisofplasmamembraneproteinsinriceleavesrevealsavesicletraffickingnetworkinplantimmunitythatisprovokedbyblastfungi
AT zhanghe comparativeproteomicanalysisofplasmamembraneproteinsinriceleavesrevealsavesicletraffickingnetworkinplantimmunitythatisprovokedbyblastfungi
AT yuyao comparativeproteomicanalysisofplasmamembraneproteinsinriceleavesrevealsavesicletraffickingnetworkinplantimmunitythatisprovokedbyblastfungi
AT malu comparativeproteomicanalysisofplasmamembraneproteinsinriceleavesrevealsavesicletraffickingnetworkinplantimmunitythatisprovokedbyblastfungi
AT wangwei comparativeproteomicanalysisofplasmamembraneproteinsinriceleavesrevealsavesicletraffickingnetworkinplantimmunitythatisprovokedbyblastfungi
AT fanyunxin comparativeproteomicanalysisofplasmamembraneproteinsinriceleavesrevealsavesicletraffickingnetworkinplantimmunitythatisprovokedbyblastfungi
AT huangning comparativeproteomicanalysisofplasmamembraneproteinsinriceleavesrevealsavesicletraffickingnetworkinplantimmunitythatisprovokedbyblastfungi
AT wangxinying comparativeproteomicanalysisofplasmamembraneproteinsinriceleavesrevealsavesicletraffickingnetworkinplantimmunitythatisprovokedbyblastfungi
AT liukunquan comparativeproteomicanalysisofplasmamembraneproteinsinriceleavesrevealsavesicletraffickingnetworkinplantimmunitythatisprovokedbyblastfungi
AT dongshinan comparativeproteomicanalysisofplasmamembraneproteinsinriceleavesrevealsavesicletraffickingnetworkinplantimmunitythatisprovokedbyblastfungi
AT tanghaijuan comparativeproteomicanalysisofplasmamembraneproteinsinriceleavesrevealsavesicletraffickingnetworkinplantimmunitythatisprovokedbyblastfungi
AT wangjianfei comparativeproteomicanalysisofplasmamembraneproteinsinriceleavesrevealsavesicletraffickingnetworkinplantimmunitythatisprovokedbyblastfungi
AT zhanghongsheng comparativeproteomicanalysisofplasmamembraneproteinsinriceleavesrevealsavesicletraffickingnetworkinplantimmunitythatisprovokedbyblastfungi
AT baoyongmei comparativeproteomicanalysisofplasmamembraneproteinsinriceleavesrevealsavesicletraffickingnetworkinplantimmunitythatisprovokedbyblastfungi