Molecular cloning, overexpression, and characterization of autophosphorylation in calcium-dependent protein kinase 1 (CDPK1) from Cicer arietinum

In plants, calcium-dependent protein kinases (CDPKs) are key intermediates in calcium-mediated signaling that couple changes in Ca²⁺ levels to a specific response. In the present study, we report the high-level soluble expression of calcium-dependent protein kinase1 from Cicer arietinum (CaCDPK1) in Escherichia coli. The expression of soluble CaCDPK1 was temperature dependent with a yield of 3–4 mg/l of bacterial culture. CaCDPK1 expressed as histidine-tag fusion protein was purified using Ni–NTA affinity chromatography till homogeneity. The recombinant CaCDPK1 protein exhibited both calcium-dependent autophosphorylation and substrate phosphorylation activities with a V _max and K _m value of 13.2 nmol/min/mg and 34.3 μM, respectively, for histone III-S as substrate. Maximum autophosphorylation was seen only in the presence of calcium. Optimum temperature for autophosphorylation was found to be 37 °C. The recombinant protein showed optimum pH range of 6–9. The role of autophosphorylation in substrate phosphorylation was investigated using histone III-S as exogenous substrate. Our results show that autophosphorylation happens before substrate phosphorylation and it happens via intra-molecular mechanism as the activity linearly depends on enzyme concentrations. Autophosphorylation enhances the kinase activity and reduces the lag phase of activation, and CaCDPK1 can utilize both ATP and GTP as phosphodonor but ATP is preferred than GTP.     

14-3-3 proteins activate a plant calcium-dependent protein kinase (CDPK)

Plants and protozoa contain a unique family of calcium-dependent protein kinases (CDPKs) which are defined by the presence of a carboxyl-terminal calmodulin-like regulatory domain. We present biochemical evidence indicating that at least one member of this kinase family can be stimulated by 14-3-3 proteins. Isoform CPK-1 from the model plant Arabidopsis thaliana was expressed as a fusion protein in E. coli and purified. The calcium-dependent activity of this recombinant CPK-1 was shown to be stimulated almost twofold by three different 14-3-3 isoforms with 50% activation around 200 nM. 14-3-3 proteins bound to the purified CPK-1, as shown by binding assays in which either the 14-3-3 or CPK-1 were immobilized on a matrix. Both the 14-3-3 binding and activation of CPK-1 were specifically disrupted by a known 14-3-3 binding peptide LSQRQRSTpSTPNVHMV (IC₅₀=30 μM). These results raise the question of whether 14-3-3 can modulate the activity of CDPK signal transduction pathways in plants.     

Membrane localization of a rice calcium-dependent protein kinase (CDPK) is mediated by myristoylation and palmitoylation

Calcium-dependent protein kinases (CDPKs), the most abundant serine/threonine kinases in plants, are found in various subcellular localizations, which suggests that this family of kinases may be involved in multiple signal transduction pathways. A complete analysis to try to understand the molecular basis of the presence of CDPKs in various localizations in the cell has not been accomplished yet. It has been suggested that myristoylation may be responsible for membrane association of CDPKs. In this study, we used a rice CDPK, OSCPK2, which has a consensus sequence for myristoylation at the N-terminus, to address this question. We expressed wild-type OSCPK2 and various mutants in different heterologous systems to investigate the factors that affect its membrane association. The results show that OSCPK2 is myristoylated and palmitoylated and targeted to the membrane fraction. Both modifications are required, myristoylation being essential for membrane localization and palmitoylation for its full association. The fact that palmitoylation is a reversible modification may provide a mechanism for regulation of the subcellular localization. OSCPK2 is the first CDPK shown to be targeted to membranes by an src homology domain 4 (SH4) located at the N-terminus of the molecule.     

A calcium-dependent protein kinase regulates Plasmodium ookinete access to the midgut epithelial cell

Plasmodium parasites are fertilized in the mosquito midgut and develop into motile zygotes, called ookinetes, which invade the midgut epithelium. Here we show that a calcium-dependent protein kinase, CDPK3, of the rodent malarial parasite (Plasmodium berghei) is produced in the ookinete stage and has a critical role in parasite transmission to the mosquito vector. Targeted disruption of the CDPK3 gene decreased ookinete ability to infect the mosquito midgut by nearly two orders of magnitude. Electron microscopic analyses demonstrated that the disruptant ookinetes could not access midgut epithelial cells by traversing the layer covering the cell surface. An in vitro migration assay showed that these ookinetes lack the ability to migrate through an artificial gel, suggesting that this defect caused their failure to access the epithelium. In vitro migration assays also suggested that this motility is induced in the wild type by mobilization of intracellular stored calcium. These results indicate that a signalling pathway involving calcium and CDPK3 regulates ookinete penetration of the layer covering the midgut epithelium. Because humans do not possess CDPK family proteins, CDPK3 is a good target for blocking malarial transmission to the mosquito vector.     

Structure of the regulatory apparatus of a calcium-dependent protein kinase (CDPK): a novel mode of calmodulin-target recognition

Calcium-dependent protein kinases (CDPKs) are a class of calcium-binding sensory proteins that are found in plants and certain protozoa, including the causative agent of malaria, Plasmodium falciparum. CDPKs have diverse regulatory functions, including involvement in the triggering of the lytic cycle of malarial infection. CDPKs contain an autoinhibitory junction (J) region whose calcium-dependent interaction with the tethered regulatory calmodulin-like domain (CaM-LD) activates the catalytic kinase domain. We report here the X-ray crystal structure of the J-CaM-LD region of CDPK from Arabidopsis thaliana (AtCPK1), determined to 2.0 A resolution using multiple-wavelength anomalous dispersion (MAD). The structure reveals a symmetric dimer of calcium-bound J-CaM-LD with domain-swap interactions, in which the J region of one protomer interacts extensively with the carboxy-terminal EF-hand domain (C-lobe) of the partner protomer. However, as the J-CaM-LD is monomeric in solution, the activated monomer was modelled to account for the intra-molecular recognition of the two domains. While the J-CaM-LD segment mimics certain aspects of target motif recognition by CaM other features are specific to CDPKs, in particular the combination of the strong interaction between the N and C-lobes of the CaM-LD and the exclusive use of only the C-lobe in the recognition of the covalently tethered target region. Combined with our previous observations showing that there is likely to be strong interactions between this tethered J region and the CaM-LD even at basal Ca(2+) concentrations, the new structural data indicate that the response to calcium of CDPKs is clearly unique among the CaM family.     

OsCDPK13, a calcium-dependent protein kinase gene from rice,is induced in response to cold and gibberellin

Ca²⁺-dependent protein kinases (CDPKs) (EC 2.7.1.37) are the predominant Ca²⁺-regulated serine/threonine protein kinase in plants and their genes are encoded by a multigene family. CDPKs are important components in signal transduction, but the precise role of each individual CDPK is still largely unknown. A CDPK gene designated as OsCDPK13 was cloned from rice seedlings and it showed a high level of sequence similarities to rice and other plant CDPK genes. OsCDPK13 contains all conserved regions found in CDPKs. It was a single copy gene and was highly expressed in root and leaf sheath tissues of rice seedlings. OsCDPK13 expression was increased in leaf sheath segments treated with gibberellin or subjected to cold stress. The results in this investigation, together with our previous studies, suggest that OsCDPK13 may be an important signaling component in rice seedlings under cold stress condition and in response to gibberellin.     

The calcium-dependent protein kinase CPK28 negatively regulates the BIK1-mediated PAMP-induced calcium burst

Plants are protected from microbial infection by a robust immune system. Two of the earliest responses mediated by surface-localized immune receptors include an increase in cytosolic calcium (Ca²⁺) and a burst of apoplastic reactive oxygen species (ROS). The Arabidopsis plasma membrane-associated cytoplasmic kinase BIK1 is an immediate convergent substrate of multiple surface-localized immune receptors that is genetically required for the PAMP-induced Ca²⁺ burst and directly regulates ROS production catalyzed by the NADPH oxidase RBOHD. We recently demonstrated that Arabidopsis plants maintain an optimal level of BIK1 through a process of continuous degradation regulated by the Ca²⁺-dependent protein kinase CPK28. cpk28 mutants accumulate more BIK1 protein and display enhanced immune signaling, while plants over-expressing CPK28 accumulate less BIK1 protein and display impaired immune signaling. Here, we show that CPK28 additionally contributes to the PAMP-induced Ca²⁺ burst, supporting its role as a negative regulator of BIK1.     

Resistance gene-dependent activation of a calcium-dependent protein kinase in the plant defense response

In the Cf-9/Avr9 gene-for-gene interaction, the Cf-9 resistance gene from tomato confers resistance to the fungal pathogen Cladosporium fulvum, which expresses the corresponding pathogen-derived avirulence product Avr9. To understand R gene function and dissect the signaling mechanisms involved in the induction of plant defenses, we studied Cf-9/Avr9-dependent activation of protein kinases in transgenic Cf9 tobacco cell cultures. Using a modified in-gel kinase assay with histone as substrate, we identified a membrane-bound, calcium-dependent protein kinase (CDPK) that showed a shift in electrophoretic mobility from 68 to 70 kD within 5 min after Avr9 elicitor was added. This transition from the nonelicited to the elicited CDPK form was caused by a phosphorylation event and was verified when antibodies to CDPK were used for protein gel blot analysis. In addition, the interconversion of the corresponding CDPK forms could be induced in vitro in both directions by treatment with either phosphatase or ATP. In vitro protein kinase activity toward syntide-2 or histone with membrane extracts or gel-purified enzyme was dependent on Ca(2)+ content and was compromised by the calmodulin antagonist N-(6-aminohexyl)-5-chloro-1-naphthalenesulfonamide (W-7) but not by its inactive isoform N-(6-aminohexyl)-1-naphthalenesulfonamide. In these assays, the CDPK activity in elicited samples, reflecting predominantly the phosphorylated 70-kD CDPK form, was greater than in nonelicited samples. Thus, Avr9/Cf-9-dependent phosphorylation and subsequent transition from the nonelicited to the elicited form correlate with the activation of a CDPK isoform after in vivo stimulation. Because that transition was not inhibited by W-7, the in vivo CDPK activation probably is not the result of autophosphorylation. Studies with pharmacological inhibitors indicated that the identified CDPK is independent of or is located upstream from a signaling pathway that is required for the Avr9-induced active oxygen species.     

Biotic and abiotic stress responses through calcium-dependent protein kinase (CDPK) signaling in wheat (Triticum aestivum L.)

Calcium-dependent protein kinases (CDPKs) sense the calcium concentration changes in plant cells and play important roles in signaling pathways for disease resistance and various stress responses as indicated by emerging evidences. Among the 20 wheat CDPK genes studied, 10 were found to respond to drought, salinity and ABA treatments. Consistent with previous observations, one CDPK gene was shown to respond to multiple abiotic stresses in wheat suggesting that CDPKs could be converging points for multiple signaling pathways. Among the 12 wheat CDPK genes that were responsive to Blumeria graminis tritici (Bgt) infection or the treatment of hydrogen peroxide (H₂O₂), eight also responded to abiotic stresses, suggesting a cross-talk between biotic and abiotic stress signaling pathways. Phylogenetic analysis indicated that some of these genes were closely related to CDPKs from other species, whose functions have been partially studied, suggesting similar functions wheat CDPK genes. Combining the up-to-date knowledge of CDPK functions and our observations, a model was developed to project the possible roles of wheat CDPK genes in the signaling of biotic and abiotic stress responses.Key words: CDPK, calcium, kinase, stress response, disease resistance, signal transduction, wheatSessile plants have developed sophisticated signaling pathways to deal with dramatic environmental changes that may affect their normal growth, such as pathogen attack, drought, and cold. Calcium is a universal secondary messenger that responds to these stimuli. The fluctuation in cytosolic Ca²⁺ levels can be sensed by calcium-dependent protein kinases (CDPKs), which will modify the phosphorylation status of substrate proteins.^1–3 Accumulating evidence indicate that CDPKs mediate biotic and abiotic stress signaling pathways.^4–7 For example, overexpression of the rice CDPK gene OsCDPK7 provides cold, salt, and drought tolerance for the transgenic rice plants, demonstrating the potential of CDPK engineering to generate stress tolerance enhanced crops.^8,9In wheat, 10 out of 14 CDPK genes appeared to respond to abiotic stresses including drought, NaCl, as well as ABA stimulus (Fig. 1A).¹⁰ Five CDPKs (TaCPK4, 6, 9, 10 and 18) were particularly interesting since they could respond to at least two of the three treatments, among which the expression level of TaCPK9 was enhanced under all three treatments suggesting that TaCPK9 is the point where multiple signaling pathways cross. In wheat, TaCPK4 responded to both ABA treatment and NaCl stress (Fig. 1A). Interestingly, its best Arabidopsis homologs AtCPK4 and AtCPK11, as suggested by a Neighbor-Joining phylogenetic analysis (Fig. 1B), have been postulated as two important positive regulators in CDPK/calcium-mediated ABA signaling pathways.¹¹ Such a correlation strongly supports the idea that TaCPK4 is a good candidate in wheat for ABA signaling. Figure 1A also shows that one wheat CDPK gene could respond to multiple abiotic stresses suggesting that CDPKs are converging points for multiple signaling pathways. On the other hand, multiple CDPKs were involved in single stress response. It is however not clear how these CDPKs are organized in one signaling pathway.Open in a separate windowFigure 1The roles of wheat CDPKs in abiotic and biotic stress responses. (A) One CDPK gene responded to multiple abiotic stresses and multiple CDPKs were required for single stress response. (B) Phylogenetic relationship of wheat CDPKs with functionally studied CDPKs from barley (HvCPKs), Arabidopsis (AtCPKs), and potato (StCDPKs) that are known to be involved in ABA signaling, oxidative burst regulation and defense to powdery mildew pathogenesis. (C) A model depicting CDPK-mediated signaling pathways under biotic and abiotic treatments in wheat (see text for details). Dotted lines with a question mark indicate unknown intermediate steps.Regarding the roles of CDPKs in defense reactions, 12 TaCPKs were found to be responsive to either Blumeria graminis tritici (Bgt) infection or H₂O₂ treatment. The response to H₂O₂ was investigated because cytosolic calcium influx and reactive oxygen species, such as H₂O₂ are known to be implicated in both plant innate immunity and abiotic stresses.^12–17 Among these CDPK genes, five responded to both treatments (Group II) whereas the ones that responded to Bgt infection (Group I) or H₂O₂ treatment (Group III) were four and three respectively. The differential expression patterns suggest different functional modes of these CDPK genes. Involvement of CDPK genes in plant defense response has been shown in multiple species.^5,7 Recently, two barley CDPK paralogs (HvCDPK3 and HvCDPK4) were found to play antagonistic roles during the early phase of powdery mildew pathogenesis.⁵ The close similarity between wheat CDPK genes (TaCPK2 and TaCPK5, Fig. 1B) with these two barley genes may suggest their potential roles in wheat powdery mildew resistance. Surprisingly, we did not detect the responsiveness of TaCPK5 to wheat Bgt infection, indicating the divergence of CDPK functions in these two members of Triticeae family. Recently, one potato (Solanum tuberosum) CDPK gene StCDPK5 has been shown to be directly involved in regulating oxidative burst via phosphorylation of the NADPH oxidase StRBOHB.¹⁸ In light of the close relationship of TaCPK2 with HvCDPK5 and StCDPK5 (Fig. 1B), we speculate that TaCPK2 could be associated with both biotic and abiotic stress response signaling pathways and therefore play multiple roles in wheat.A model was proposed in Figure 1C regarding the positions of wheat CDPK genes in signaling pathways for biotic and abiotic responses. The hypothesis depicted four different roles of wheat CDPK genes: (1) Group I genes that respond only to Bgt infection may, like potato StCDPK5, render defense response through an oxidase like NADPH oxidase that generates increased amount of H₂O₂;¹⁸ (2) At one aspect, Group II genes may participate in defense response in a manner similar to Group I genes; (3) On the other hand, since Group II genes also respond to H₂O₂ treatment directly, an auto-regulation circuit was proposed, which eventually joins the oxidase pathway; (4) Group III CDPK genes and some remaining CDPK genes are considered to be mainly involved in abiotic stress responses. The model positioned CDPKs both upstream and downstream of H₂O₂, presenting a complicated wiring of the signaling pathway network involving wheat CDPKs. Future biochemical, genetic, and transgenic analyses may help elucidate the genuineness of such a rather early model for the functions of wheat CDPK genes.