Summary
Necrosis‐ and ethylene‐inducing peptide 1 (Nep1)‐like proteins (NLPs) constitute a superfamily of proteins toxic to dicot plants, but the molecular basis of this toxicity remains obscure.
Using quantitative trait locus (QTL) analysis we investigated the genetic variation underlying ion leakage in Arabidopsis plants elicited with MoNLP1 derived from Magnaporthe oryzae. The QTL conditioning MoNLP1 toxicity was positionally cloned and further characterized to elucidate its mode of action.
MoNLP1‐triggered cell death varied significantly across > 250 Arabidopsis accessions and three QTLs were identified conferring the observed variation. The QTL on chromosome 4 was uncovered to encode a leucine‐rich repeat (LRR)‐only protein designated as NTCD4, which shares high sequence identity with a set of nucleotide‐binding LRR proteins. NTCD4 was secreted into the apoplast and physically interacted with multiple NLPs. Apoplastic NTCD4 facilitated the oligomerization of NLP, which was closely associated with toxicity in planta. The natural genetic variation causing D3N change in NTCD4 reduced the secretion efficiency of NTCD4 and the infection of Botrytis cinerea on Arabidopsis plants.
These observations demonstrate that the plant‐derived NTCD4 is recruited by NLPs to promote toxicity via facilitating their oligomerization, which extends our understanding of a key step in the toxic mode of action of NLPs.
Plants deploy intracellular receptors to counteract pathogen effectors that suppress cell-surface receptor-mediated immunity. To what extent pathogens manipulate also immunity mediated by intracellular receptors, and how plants tackle such manipulation, remains unknown. Arabidopsis thaliana encodes three very similar ADR1 class helper NLRs (ADR1, ADR1-L1 and ADR1-L2), which play key roles in plant immunity initiated by intracellular receptors. Here, we report that Pseudomonas syringae AvrPtoB, an effector with E3 ligase activity, can suppress ADR1-L1- and ADR1-L2-mediated cell death. ADR1, however, evades such suppression by diversification of two ubiquitination sites targeted by AvrPtoB. The intracellular sensor NLR SNC1 interacts with and guards the CCR domains of ADR1-L1 and ADR-L2. Removal of ADR1-L1 and ADR1-L2 or delivery of AvrPtoB activates SNC1, which then signals through ADR1 to trigger immunity. Our work not only uncovers the long sought-after physiological function of SNC1 in pathogen defense,but also that reveals how plants can use dual strategies, sequence diversification and a multiple layered guard-guardee system, to counteract pathogen attack on core immunity functions.
The quantitative resistance gene ACCELERATED CELL DEATH 6 (ACD6), which encodes a transmembrane protein with intracellular ankyrin repeats, has been implicated in a trade-off between growth and defense among wild strains of Arabidopsis thaliana. Naturally hyperactive alleles of the ACD6-Est-1 type can lead to spontaneous activation of immune responses, although the extent of visible hyperimmunity in strains with this allele varies substantially. We have identified a natural suppressor locus, MODULATOR OF HYPERACTIVE ACD6 1 (MHA1), which codes for a small protein of ~7 kDa that attenuates activity of the ACD6-Est-1 allele. MHA1 and its paralog MHA1-LIKE (MHAL) differentially interact with specific ACD6 variants, and both MHA1 and MHAL peptides can bind to the ACD6 ankyrin repeats. MHAL also enhances accumulation of an ACD6 complex, thereby increasing activity of the ACD6 standard allele. The ACD6 ankyrin repeats are similar to those of transient receptor potential (TRP) ion channels, and several lines of evidence support that increased ACD6 activity is linked to enhanced calcium signaling. Our work highlights how the study of natural variation reveals new aspects of plant immunity.
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