Attenuation of pattern recognition receptor signaling is mediated by a MAP kinase kinase kinase

Publication date

2016

Authors

Mithoe, S.C.ISNI 0000000387772160
Ludwig, Christina
Pel, M.J.C.ISNI 0000000419438416
Cucinotta, Mara
Casartelli, Alberto
Mbengue, Malick
Sklenar, Jan
Derbyshire, Paul
Robatzek, Silke
Pieterse, Corné M.J.ORCID 0000-0002-5473-4646ISNI 0000000357875345

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Article
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Abstract

Pattern recognition receptors (PRRs) play a key role in plant and animal innate immunity. PRR binding of their cognate ligand triggers a signaling network and activates an immune response. Activation of PRR signaling must be controlled prior to ligand binding to prevent spurious signaling and immune activation. Flagellin perception in Arabidopsis through FLAGELLIN-SENSITIVE 2 (FLS2) induces the activation of mitogen-activated protein kinases (MAPKs) and immunity. However, the precise molecular mechanism that connects activated FLS2 to downstream MAPK cascades remains unknown. Here, we report the identification of a differentially phosphorylated MAP kinase kinase kinase that also interacts with FLS2. Using targeted proteomics and functional analysis, we show that MKKK7 negatively regulates flagellin-triggered signaling and basal immunity and this requires phosphorylation of MKKK7 on specific serine residues. MKKK7 attenuates MPK6 activity and defense gene expression. Moreover, MKKK7 suppresses the reactive oxygen species burst downstream of FLS2, suggesting that MKKK7-mediated attenuation of FLS2 signaling occurs through direct modulation of the FLS2 complex.

Keywords

Arabidopsis, Innate immunity, Phosphorylation, Signaling, Targeted proteomics, Taverne, Genetics, Molecular Biology, Biochemistry

Citation

Mithoe, S C, Ludwig, C, Pel, M J C, Cucinotta, M, Casartelli, A, Mbengue, M, Sklenar, J, Derbyshire, P, Robatzek, S, Pieterse, C M J, Aebersold, R & Menke, F L H 2016, 'Attenuation of pattern recognition receptor signaling is mediated by a MAP kinase kinase kinase', EMBO Reports, vol. 17, pp. 441-454. https://doi.org/10.15252/embr.201540806