Orchestration of cellular behavior in plant organogenesis requires integration of intercellular communication and cell wall dynamics. The underlying signaling mechanisms are poorly understood. Tissue morphogenesis in Arabidopsis depends on the receptor-like kinase STRUBBELIG. Mutations in ZERZAUST were previously shown to result in a strubbelig-like mutant phenotype. Here, we report on the molecular identification and functional characterization of ZERZAUST. We show that ZERZAUST encodes a putative GPIanchored β-1,3 glucanase suggested to degrade the cell wall polymer callose. However, a combination of in vitro, cell biological and genetic experiments indicate that ZERZAUST is not involved in the regulation of callose accumulation. Nonetheless, Fourier-transformed infraredspectroscopy revealed that zerzaust mutants show defects in cell wall composition. Furthermore, the results indicate that ZERZAUST represents a mobile apoplastic protein, and that its carbohydrate-binding module family 43 domain is required for proper subcellular localization and function whereas its GPI anchor is dispensable. Our collective data reveal that the atypical β-1,3 glucanase ZERZAUST acts in a non-cell-autonomous manner and is required for cell wall organization during tissue morphogenesis.

Background: Plant cell-surface receptors sense various ligands to regulate physiological processes. Matching ligand-receptor pairs requires evidence of their direct interaction and is often a bottleneck in functional receptor studies. The S-domain-type (SD) pattern recognition receptor LORE senses medium chain-3-hydroxy fatty acids (mc-3-OH-FAs) such as 3-hydroxy decanoic acid (3-OH-C10:0) via its extracellular domain (ECD) They are perceived as signals of danger from Gram-negative bacteria and activate immune responses in Arabidopsis thaliana. LORE is found in low levels in planta and is poorly expressed in heterologous systems. Furthermore, chemical modifications of the mc-3-OH-FA ligand affect its biological activity. Taken together, this makes LORE-mc-3-OH-FA binding studies particularly challenging. Results: To investigate the LORE-mc-3-OH-FA interaction, we have developed a sensitive assay system based on protein expression in planta. The ECDs of LORE and other proteins of interest were transiently expressed as soluble, apoplastic mCherry fusion proteins in Nicotiana benthamiana and collected in apoplastic washing fluids. Protein-ligand complexes and unbound ligand were separated according to their molecular weight. In a two-step procedure, we first investigated whether the ECD-mCherry fusion protein depletes 3-OH-C10:0 from the low molecular weight fraction (step 'depletion'). Subsequently, protein-bound 3-OH-C10:0 retained in the high molecular weight fraction in the depletion step is released and detected (step 'binding'). Both the unbound and the released 3-OH-C10:0 ligand are detected by a sensitive bioassay using LORE loss- and gain-of-function Arabidopsis plants. Using the depletion-binding assay, we show that the ECD of AtLORE and its ortholog from Capsella rubella, CrubLORE, bind 3-OH-C10:0. The ECD of AtSD1-23, the closest paralog of AtLORE, and mCherry did not bind 3-OH-C10:0 and are suitable negative controls. Conclusion: The depletion-binding assay is a simple method for reliably detecting interactions between plant-expressed SD-type receptor ectodomains and mc-3-OH-FAs. It does not require special equipment or expensive consumables and is suitable for medium throughput screening. The assay is very flexible and can be easily adapted to investigate ligand interactions of other extracellular receptor domains.

Perception and processing of various internal and external signals is essential for all living organisms. Plants have an expanded and diversified repertoire of cell surface-localized receptor-like kinases (RLKs) that transduce signals across the plasma membrane. RLKs often assemble into higher-order receptor complexes with co-receptors, regulators and scaffolds to convert extracellular stimuli into cellular responses. To date, the only S-domain-RLK from Arabidopsis thaliana with a known ligand and function is AtLORE, a pattern recognition receptor that senses bacterial 3-hydroxy fatty acids of medium chain length, such as 3-hydroxy decanoic acid (3-OH-C10:0), to activate pattern-triggered immunity. Here we show that AtLORE forms receptor homomers, which is essential for 3-OH-C10:0-induced immune signaling. AtLORE homomerization is mediated by the transmembrane and extracellular domain. We show natural variation in the perception of 3-OH-C10:0 within the Brassicaceae family. Arabidopsis lyrata and Arabidopsis halleri do not respond to 3-OH-C10:0, although they possess a putative LORE orthologue. We found that LORE orthologues of these 3-OH-C10:0 nonresponsive species have defective extracellular domains that can bind the 3-OH-C10:0 ligand but lack the ability to homomerize. Our findings shed light on the activation mechanisms of AtLORE and explain natural variation of 3-OH-C10:0 perception within the Brassicaceae family.