In plants leucine-rich repeat receptor kinases (LRR-RKs) located at the plasma membrane play a pivotal role in the perception of extracellular signals. For two of these LRR-RKs, the brassinosteroid receptor BRI1 and the flagellin receptor FLS2, interaction with the LRR receptor-like kinase BAK1 (BRI1-associated receptor kinase 1) was shown to be required for signal transduction. Here we report that FLS2⅐BAK1 heteromerization occurs almost instantaneously after perception of the ligand, the flagellin-derived peptide flg22. Flg22 can induce formation of a stable FLS2⅐BAK1 complex in microsomal membrane preparations in vitro, and the kinase inhibitor K-252a does not prevent complex formation. A kinase dead version of BAK1 associates with FLS2 in a flg22-dependent manner but does not restore responsiveness to flg22 in cells of bak1 plants, demonstrating that kinase activity of BAK1 is essential for FLS2 signaling. Furthermore, using in vivo phospholabeling, we are able to detect de novo phosphorylation of both FLS2 and BAK1 within 15 s of stimulation with flg22. Similarly, brassinolide induces BAK1 phosphorylation within seconds. Other triggers of plant defense, such as bacterial EF-Tu and the endogenous AtPep1 likewise induce rapid formation of heterocomplexes consisting of de novo phosphorylated BAK1 and proteins representing the ligand-specific binding receptors EF-Tu receptor and Pep1 receptor 1, respectively. Thus, we propose that several LRR-RKs form tight complexes with BAK1 almost instantaneously after ligand binding and that the subsequent phosphorylation events are key initial steps in signal transduction.One of the central themes in cell biology is the sensing of extracellular chemical signals through cell surface receptors: How does the event of receptor-ligand interaction on the outside of the cell activate a signal transduction chain in the inside of the cell? In higher plants, the most prominent class of membrane receptors is formed by proteins with intracellular serine/ threonine-type protein kinases. These receptors account for ϳ2.5-4% of all proteins encoded by the genome of a plant (1). Despite their importance, there is still little experimental evidence on the molecular activation mechanisms of plant transmembrane receptor kinases. Current models are based on the precedent of animal receptor tyrosine kinases where ligand binding causes receptor tyrosine kinases to form homo-or hetero-oligomers, followed by transphosphorylation (2). In the case of the epidermal growth factor receptor, these phosphorylation events occur within 60 s of receptor activation (3).The best studied plant transmembrane receptor kinase is BRI1, the receptor for the brassinosteroid growth hormones (4). BRI1 is one of the 224 members of LRR-RKs 2 in Arabidopsis (5). Upon ligand binding BRI1 interacts with a second LRR receptor-like kinase named BAK1 (6, 7). Two further well characterized plant LRR-RKs are the flagellin receptor FLS2 (flagellin sensing 2) (8) and the EF-Tu receptor (EFR) (9). FLS2 perceives a generally conser...
In illuminated chloroplasts, one mechanism involved in reduction-oxidation (redox) homeostasis is the malate-oxaloacetate (OAA) shuttle. Excess electrons from photosynthetic electron transport in the form of nicotinamide adenine dinucleotide phosphate, reduced are used by NADP-dependent malate dehydrogenase (MDH) to reduce OAA to malate, thus regenerating the electron acceptor NADP. NADP-MDH is a strictly redox-regulated, light-activated enzyme that is inactive in the dark. In the dark or in nonphotosynthetic tissues, the malate-OAA shuttle was proposed to be mediated by the constitutively active plastidial NADspecific MDH isoform (pdNAD-MDH), but evidence is scarce. Here, we reveal the critical role of pdNAD-MDH in Arabidopsis (Arabidopsis thaliana) plants. A pdnad-mdh null mutation is embryo lethal. Plants with reduced pdNAD-MDH levels by means of artificial microRNA (miR-mdh-1) are viable, but dark metabolism is altered as reflected by increased nighttime malate, starch, and glutathione levels and a reduced respiration rate. In addition, miR-mdh-1 plants exhibit strong pleiotropic effects, including dwarfism, reductions in chlorophyll levels, photosynthetic rate, and daytime carbohydrate levels, and disordered chloroplast ultrastructure, particularly in developing leaves, compared with the wild type. pdNAD-MDH deficiency in miR-mdh-1 can be functionally complemented by expression of a microRNA-insensitive pdNAD-MDH but not NADP-MDH, confirming distinct roles for NAD-and NADP-linked redox homeostasis.
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