Cargando…

Rhizobacterial volatiles and photosynthesis‐related signals coordinate MYB72 expression in Arabidopsis roots during onset of induced systemic resistance and iron‐deficiency responses

In Arabidopsis roots, the transcription factor MYB72 plays a dual role in the onset of rhizobacteria‐induced systemic resistance (ISR) and plant survival under conditions of limited iron availability. Previously, it was shown that MYB72 coordinates the expression of a gene module that promotes synth...

Descripción completa

Detalles Bibliográficos
Autores principales: Zamioudis, Christos, Korteland, Jolanda, Van Pelt, Johan A., van Hamersveld, Muriël, Dombrowski, Nina, Bai, Yang, Hanson, Johannes, Van Verk, Marcel C., Ling, Hong‐Qing, Schulze‐Lefert, Paul, Pieterse, Corné M.J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5019235/
https://www.ncbi.nlm.nih.gov/pubmed/26307542
http://dx.doi.org/10.1111/tpj.12995
_version_ 1782453020652470272
author Zamioudis, Christos
Korteland, Jolanda
Van Pelt, Johan A.
van Hamersveld, Muriël
Dombrowski, Nina
Bai, Yang
Hanson, Johannes
Van Verk, Marcel C.
Ling, Hong‐Qing
Schulze‐Lefert, Paul
Pieterse, Corné M.J.
author_facet Zamioudis, Christos
Korteland, Jolanda
Van Pelt, Johan A.
van Hamersveld, Muriël
Dombrowski, Nina
Bai, Yang
Hanson, Johannes
Van Verk, Marcel C.
Ling, Hong‐Qing
Schulze‐Lefert, Paul
Pieterse, Corné M.J.
author_sort Zamioudis, Christos
collection PubMed
description In Arabidopsis roots, the transcription factor MYB72 plays a dual role in the onset of rhizobacteria‐induced systemic resistance (ISR) and plant survival under conditions of limited iron availability. Previously, it was shown that MYB72 coordinates the expression of a gene module that promotes synthesis and excretion of iron‐mobilizing phenolic compounds in the rhizosphere, a process that is involved in both iron acquisition and ISR signaling. Here, we show that volatile organic compounds (VOCs) from ISR‐inducing Pseudomonas bacteria are important elicitors of MYB72. In response to VOC treatment, MYB72 is co‐expressed with the iron uptake‐related genes FERRIC REDUCTION OXIDASE 2 (FRO2) and IRON‐REGULATED TRANSPORTER 1 (IRT1) in a manner that is dependent on FER‐LIKE IRON DEFICIENCY TRANSCRIPTION FACTOR (FIT), indicating that MYB72 is an intrinsic part of the plant's iron‐acquisition response that is typically activated upon iron starvation. However, VOC ‐induced MYB72 expression is activated independently of iron availability in the root vicinity. Moreover, rhizobacterial VOC‐mediated induction of MYB72 requires photosynthesis‐related signals, while iron deficiency in the rhizosphere activates MYB72 in the absence of shoot‐derived signals. Together, these results show that the ISR‐ and iron acquisition‐related transcription factor MYB72 in Arabidopsis roots is activated by rhizobacterial volatiles and photosynthesis‐related signals, and enhances the iron‐acquisition capacity of roots independently of the iron availability in the rhizosphere. This work highlights the role of MYB72 in plant processes by which root microbiota simultaneously stimulate systemic immunity and activate the iron‐uptake machinery in their host plants.
format Online
Article
Text
id pubmed-5019235
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-50192352016-09-23 Rhizobacterial volatiles and photosynthesis‐related signals coordinate MYB72 expression in Arabidopsis roots during onset of induced systemic resistance and iron‐deficiency responses Zamioudis, Christos Korteland, Jolanda Van Pelt, Johan A. van Hamersveld, Muriël Dombrowski, Nina Bai, Yang Hanson, Johannes Van Verk, Marcel C. Ling, Hong‐Qing Schulze‐Lefert, Paul Pieterse, Corné M.J. Plant J Original Articles In Arabidopsis roots, the transcription factor MYB72 plays a dual role in the onset of rhizobacteria‐induced systemic resistance (ISR) and plant survival under conditions of limited iron availability. Previously, it was shown that MYB72 coordinates the expression of a gene module that promotes synthesis and excretion of iron‐mobilizing phenolic compounds in the rhizosphere, a process that is involved in both iron acquisition and ISR signaling. Here, we show that volatile organic compounds (VOCs) from ISR‐inducing Pseudomonas bacteria are important elicitors of MYB72. In response to VOC treatment, MYB72 is co‐expressed with the iron uptake‐related genes FERRIC REDUCTION OXIDASE 2 (FRO2) and IRON‐REGULATED TRANSPORTER 1 (IRT1) in a manner that is dependent on FER‐LIKE IRON DEFICIENCY TRANSCRIPTION FACTOR (FIT), indicating that MYB72 is an intrinsic part of the plant's iron‐acquisition response that is typically activated upon iron starvation. However, VOC ‐induced MYB72 expression is activated independently of iron availability in the root vicinity. Moreover, rhizobacterial VOC‐mediated induction of MYB72 requires photosynthesis‐related signals, while iron deficiency in the rhizosphere activates MYB72 in the absence of shoot‐derived signals. Together, these results show that the ISR‐ and iron acquisition‐related transcription factor MYB72 in Arabidopsis roots is activated by rhizobacterial volatiles and photosynthesis‐related signals, and enhances the iron‐acquisition capacity of roots independently of the iron availability in the rhizosphere. This work highlights the role of MYB72 in plant processes by which root microbiota simultaneously stimulate systemic immunity and activate the iron‐uptake machinery in their host plants. John Wiley and Sons Inc. 2015-10-08 2015-10 /pmc/articles/PMC5019235/ /pubmed/26307542 http://dx.doi.org/10.1111/tpj.12995 Text en © 2015 The Authors The Plant Journal published by Society for Experimental Biology and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Zamioudis, Christos
Korteland, Jolanda
Van Pelt, Johan A.
van Hamersveld, Muriël
Dombrowski, Nina
Bai, Yang
Hanson, Johannes
Van Verk, Marcel C.
Ling, Hong‐Qing
Schulze‐Lefert, Paul
Pieterse, Corné M.J.
Rhizobacterial volatiles and photosynthesis‐related signals coordinate MYB72 expression in Arabidopsis roots during onset of induced systemic resistance and iron‐deficiency responses
title Rhizobacterial volatiles and photosynthesis‐related signals coordinate MYB72 expression in Arabidopsis roots during onset of induced systemic resistance and iron‐deficiency responses
title_full Rhizobacterial volatiles and photosynthesis‐related signals coordinate MYB72 expression in Arabidopsis roots during onset of induced systemic resistance and iron‐deficiency responses
title_fullStr Rhizobacterial volatiles and photosynthesis‐related signals coordinate MYB72 expression in Arabidopsis roots during onset of induced systemic resistance and iron‐deficiency responses
title_full_unstemmed Rhizobacterial volatiles and photosynthesis‐related signals coordinate MYB72 expression in Arabidopsis roots during onset of induced systemic resistance and iron‐deficiency responses
title_short Rhizobacterial volatiles and photosynthesis‐related signals coordinate MYB72 expression in Arabidopsis roots during onset of induced systemic resistance and iron‐deficiency responses
title_sort rhizobacterial volatiles and photosynthesis‐related signals coordinate myb72 expression in arabidopsis roots during onset of induced systemic resistance and iron‐deficiency responses
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5019235/
https://www.ncbi.nlm.nih.gov/pubmed/26307542
http://dx.doi.org/10.1111/tpj.12995
work_keys_str_mv AT zamioudischristos rhizobacterialvolatilesandphotosynthesisrelatedsignalscoordinatemyb72expressioninarabidopsisrootsduringonsetofinducedsystemicresistanceandirondeficiencyresponses
AT kortelandjolanda rhizobacterialvolatilesandphotosynthesisrelatedsignalscoordinatemyb72expressioninarabidopsisrootsduringonsetofinducedsystemicresistanceandirondeficiencyresponses
AT vanpeltjohana rhizobacterialvolatilesandphotosynthesisrelatedsignalscoordinatemyb72expressioninarabidopsisrootsduringonsetofinducedsystemicresistanceandirondeficiencyresponses
AT vanhamersveldmuriel rhizobacterialvolatilesandphotosynthesisrelatedsignalscoordinatemyb72expressioninarabidopsisrootsduringonsetofinducedsystemicresistanceandirondeficiencyresponses
AT dombrowskinina rhizobacterialvolatilesandphotosynthesisrelatedsignalscoordinatemyb72expressioninarabidopsisrootsduringonsetofinducedsystemicresistanceandirondeficiencyresponses
AT baiyang rhizobacterialvolatilesandphotosynthesisrelatedsignalscoordinatemyb72expressioninarabidopsisrootsduringonsetofinducedsystemicresistanceandirondeficiencyresponses
AT hansonjohannes rhizobacterialvolatilesandphotosynthesisrelatedsignalscoordinatemyb72expressioninarabidopsisrootsduringonsetofinducedsystemicresistanceandirondeficiencyresponses
AT vanverkmarcelc rhizobacterialvolatilesandphotosynthesisrelatedsignalscoordinatemyb72expressioninarabidopsisrootsduringonsetofinducedsystemicresistanceandirondeficiencyresponses
AT linghongqing rhizobacterialvolatilesandphotosynthesisrelatedsignalscoordinatemyb72expressioninarabidopsisrootsduringonsetofinducedsystemicresistanceandirondeficiencyresponses
AT schulzelefertpaul rhizobacterialvolatilesandphotosynthesisrelatedsignalscoordinatemyb72expressioninarabidopsisrootsduringonsetofinducedsystemicresistanceandirondeficiencyresponses
AT pietersecornemj rhizobacterialvolatilesandphotosynthesisrelatedsignalscoordinatemyb72expressioninarabidopsisrootsduringonsetofinducedsystemicresistanceandirondeficiencyresponses