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The Proteasome Acts as a Hub for Plant Immunity and Is Targeted by Pseudomonas Type III Effectors

Suayib Üstün, Arsheed Sheikh, Selena Gimenez-Ibanez, Alexandra Jones, Vardis Ntoukakis, Frederik Börnke
Suayib Üstün
Plant Metabolism Group, Leibniz Institute of Vegetable and Ornamental Crops, 14979 Großbeeren, Germany (S.Ü., F.B.);
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  • ORCID record for Suayib Üstün
  • For correspondence: suayib.ustun@slu.se v.ntoukakis@warwick.ac.uk boernke@igzev.de
Arsheed Sheikh
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Selena Gimenez-Ibanez
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Alexandra Jones
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Vardis Ntoukakis
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  • For correspondence: suayib.ustun@slu.se v.ntoukakis@warwick.ac.uk boernke@igzev.de
Frederik Börnke
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  • For correspondence: suayib.ustun@slu.se v.ntoukakis@warwick.ac.uk boernke@igzev.de

Published November 2016. DOI: https://doi.org/10.1104/pp.16.00808

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  • © 2016 American Society of Plant Biologists. All Rights Reserved.

Abstract

Recent evidence suggests that the ubiquitin-proteasome system is involved in several aspects of plant immunity and that a range of plant pathogens subvert the ubiquitin-proteasome system to enhance their virulence. Here, we show that proteasome activity is strongly induced during basal defense in Arabidopsis (Arabidopsis thaliana). Mutant lines of the proteasome subunits RPT2a and RPN12a support increased bacterial growth of virulent Pseudomonas syringae pv tomato DC3000 (Pst) and Pseudomonas syringae pv maculicola ES4326. Both proteasome subunits are required for pathogen-associated molecular pattern-triggered immunity responses. Analysis of bacterial growth after a secondary infection of systemic leaves revealed that the establishment of systemic acquired resistance (SAR) is impaired in proteasome mutants, suggesting that the proteasome also plays an important role in defense priming and SAR. In addition, we show that Pst inhibits proteasome activity in a type III secretion-dependent manner. A screen for type III effector proteins from Pst for their ability to interfere with proteasome activity revealed HopM1, HopAO1, HopA1, and HopG1 as putative proteasome inhibitors. Biochemical characterization of HopM1 by mass spectrometry indicates that HopM1 interacts with several E3 ubiquitin ligases and proteasome subunits. This supports the hypothesis that HopM1 associates with the proteasome, leading to its inhibition. Thus, the proteasome is an essential component of pathogen-associated molecular pattern-triggered immunity and SAR, which is targeted by multiple bacterial effectors.

  • Glossary

    UPS
    ubiquitin-proteasome system
    CP
    core protease
    RP
    regulatory particles
    PRR
    pattern recognition receptor
    PAMP
    pathogen-associated molecular pattern
    PTI
    PAMP-triggered immunity
    ROS
    reactive oxygen species
    ETI
    effector-triggered immunity
    HR
    hypersensitive response
    SAR
    systemic acquired resistance
    SA
    salicylic acid
    T3E
    type III effector
    Col-0
    Columbia-0
    HA
    hemagglutinin
    MS/MS
    tandem mass spectrometry
    MS
    Murashige and Skoog
    OD
    optical density
    RT
    reverse transcription
    dpi
    days post inoculation
    • Received May 16, 2016.
    • Accepted September 7, 2016.
    • Published September 9, 2016.

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    The Proteasome Acts as a Hub for Plant Immunity and Is Targeted by Pseudomonas Type III Effectors
    Suayib Üstün, Arsheed Sheikh, Selena Gimenez-Ibanez, Alexandra Jones, Vardis Ntoukakis, Frederik Börnke
    Plant Physiology Nov 2016, 172 (3) 1941-1958; DOI: 10.1104/pp.16.00808

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    The Proteasome Acts as a Hub for Plant Immunity and Is Targeted by Pseudomonas Type III Effectors
    Suayib Üstün, Arsheed Sheikh, Selena Gimenez-Ibanez, Alexandra Jones, Vardis Ntoukakis, Frederik Börnke
    Plant Physiology Nov 2016, 172 (3) 1941-1958; DOI: 10.1104/pp.16.00808
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