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PLoS Pathog. 2019 Jul 3;15(7):e1007900. doi: 10.1371/journal.ppat.1007900. eCollection 2019 Jul.

Perturbations of the ZED1 pseudokinase activate plant immunity.

Author information

1
Department of Cell and Systems Biology, University of Toronto, Toronto, Ontario, Canada.
2
Centre for the Analysis of Genome Evolution & Function, University of Toronto, Toronto, Ontario, Canada.
3
Department of Microbiology and Immunology, University of British Columbia, Vancouver, British Columbia, Canada.
4
Department of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada.

Abstract

The Pseudomonas syringae acetyltransferase HopZ1a is delivered into host cells by the type III secretion system to promote bacterial growth. However, in the model plant host Arabidopsis thaliana, HopZ1a activity results in an effector-triggered immune response (ETI) that limits bacterial proliferation. HopZ1a-triggered immunity requires the nucleotide-binding, leucine-rich repeat domain (NLR) protein, ZAR1, and the pseudokinase, ZED1. Here we demonstrate that HopZ1a can acetylate members of a family of 'receptor-like cytoplasmic kinases' (RLCK family VII; also known as PBS1-like kinases, or PBLs) and promote their interaction with ZED1 and ZAR1 to form a ZAR1-ZED1-PBL ternary complex. Interactions between ZED1 and PBL kinases are determined by the pseudokinase features of ZED1, and mutants designed to restore ZED1 kinase motifs can (1) bind to PBLs, (2) recruit ZAR1, and (3) trigger ZAR1-dependent immunity in planta, all independently of HopZ1a. A ZED1 mutant that mimics acetylation by HopZ1a also triggers immunity in planta, providing evidence that effector-induced perturbations of ZED1 also activate ZAR1. Overall, our results suggest that interactions between these two RLCK families are promoted by perturbations of structural features that distinguish active from inactive kinase domain conformations. We propose that effector-induced interactions between ZED1/ZRK pseudokinases (RLCK family XII) and PBL kinases (RLCK family VII) provide a sensitive mechanism for detecting perturbations of either kinase family to activate ZAR1-mediated ETI.

PMID:
31269090
PMCID:
PMC6634424
DOI:
10.1371/journal.ppat.1007900
[Indexed for MEDLINE]
Free PMC Article

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