Re-targeting of a plant defense protease by a cyst nematode effector.
Animals
Arabidopsis
/ enzymology
Arabidopsis Proteins
/ genetics
Beta vulgaris
/ parasitology
Cell Nucleus
/ metabolism
Cell Wall
/ metabolism
Cysteine Proteases
/ genetics
Cytoplasm
/ metabolism
Female
Helminth Proteins
/ genetics
Host-Parasite Interactions
Plant Diseases
/ immunology
Plant Immunity
Protein Transport
Two-Hybrid System Techniques
Tylenchoidea
/ physiology
Vacuoles
/ metabolism
defense
effector
nematode
plant-pathogen interaction
protease
re-localization
Journal
The Plant journal : for cell and molecular biology
ISSN: 1365-313X
Titre abrégé: Plant J
Pays: England
ID NLM: 9207397
Informations de publication
Date de publication:
06 2019
06 2019
Historique:
received:
23
03
2018
revised:
08
02
2019
accepted:
15
02
2019
pubmed:
26
2
2019
medline:
9
4
2020
entrez:
26
2
2019
Statut:
ppublish
Résumé
Plants mount defense responses during pathogen attacks, and robust host defense suppression by pathogen effector proteins is essential for infection success. 4E02 is an effector of the sugar beet cyst nematode Heterodera schachtii. Arabidopsis thaliana lines expressing the effector-coding sequence showed altered expression levels of defense response genes, as well as higher susceptibility to both the biotroph H. schachtii and the necrotroph Botrytis cinerea, indicating a potential suppression of defenses by 4E02. Yeast two-hybrid analyses showed that 4E02 targets A. thaliana vacuolar papain-like cysteine protease (PLCP) 'Responsive to Dehydration 21A' (RD21A), which has been shown to function in the plant defense response. Activity-based protein profiling analyses documented that the in planta presence of 4E02 does not impede enzymatic activity of RD21A. Instead, 4E02 mediates a re-localization of this protease from the vacuole to the nucleus and cytoplasm, which is likely to prevent the protease from performing its defense function and at the same time, brings it in contact with novel substrates. Yeast two-hybrid analyses showed that RD21A interacts with multiple host proteins including enzymes involved in defense responses as well as carbohydrate metabolism. In support of a role in carbohydrate metabolism of RD21A after its effector-mediated re-localization, we observed cell wall compositional changes in 4E02 expressing A. thaliana lines. Collectively, our study shows that 4E02 removes RD21A from its defense-inducing pathway and repurposes this enzyme by targeting the active protease to different cell compartments.
Substances chimiques
Arabidopsis Proteins
0
Helminth Proteins
0
Cysteine Proteases
EC 3.4.-
RD21 protein, Arabidopsis
EC 3.4.-
Banques de données
GENBANK
['DC3000', 'AF473826', 'AT4G08500', 'AT3G52430', 'AT3G48090']
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
1000-1014Informations de copyright
© 2019 The Authors The Plant Journal © 2019 John Wiley & Sons Ltd.