- Research article
- Open Access
Localization and expression of EDS5H a homologue of the SA transporter EDS5
© Parinthawong et al.; licensee BioMed Central. 2015
- Received: 17 January 2015
- Accepted: 1 May 2015
- Published: 9 June 2015
An important signal transduction pathway in plant defence depends on the accumulation of salicylic acid (SA). SA is produced in chloroplasts and the multidrug and toxin extrusion transporter ENHANCED DISEASE SUSCEPTIBILITY5 (EDS5; At4g39030) is necessary for the accumulation of SA after pathogen and abiotic stress. EDS5 is localized at the chloroplast and functions in transporting SA from the chloroplast to the cytoplasm. EDS5 has a homologue called EDS5H (EDS5 HOMOLOGUE; At2g21340) but its relationship to EDS5 has not been described and its function is not known.
EDS5H exhibits about 72 % similarity and 59 % identity to EDS5. In contrast to EDS5 that is induced after pathogen inoculation, EDS5H was constitutively expressed in all green tissues, independently of pathogen infection. Both transporters are located at the envelope of the chloroplast, the compartment of SA biosynthesis. EDS5H is not involved with the accumulation of SA after inoculation with a pathogen or exposure to UV stress. A phylogenetic analysis supports the hypothesis that EDS5H may be an H+/organic acid antiporter like EDS5.
The data based on genetic and molecular studies indicate that EDS5H despite its homology to EDS5 does not contribute to pathogen-induced SA accumulation like EDS5. EDS5H most likely transports related substances such as for example phenolic acids, but unlikely SA.
- Salicylic Acid
- NdeI Site
- Tomato DC3000
- Salicylic Acid Accumulation
- Salicylic Acid Content
The signal transduction for induced resistance to many pathogens including viruses, bacteria, fungi and oomycetes involves the phenolic compound salicylic acid (SA) [1–3]. The importance of SA for the activation of defences has been repeatedly demonstrated with a number of mutants or transgenic plants impaired in the accumulation of SA. In particular, the Arabidopsis thaliana eds5/sid1 (enhanced disease susceptibility5/salicyclic acid-deficient 2) and sid2 mutants accumulate only 10 % of the SA produced in wild-type plants after induction and exhibit increased susceptibility to Pseudomonas syringae and Hyaloperonospora parasitica and fail to express the pathogenesis-related gene PR1 . The eds5/sid1 mutation was found in a gene encoding a member of the MATE (MULTIDRUG AND TOXIN EXTRUSION) transporter family , while the sid2 mutation was found in the ISOCHORISMATE SYNTHASE1 gene (ICS1) .
The identification of ICS1 in A. thaliana, definitely demonstrated the importance of the isochorismate pathway for SA biosynthesis, similar to the pathway described in some Pseudomonas species . The ICS1 gene product was confirmed to possess ICS activity and to be targeted to the plastidic compartment . Synthesis of SA following exposure to ozone in Arabidopsis was also proposed to proceed through the activity of ICS enzymes . The involvement of isochorismate in the synthesis of SA was confirmed in transgenic tobacco plants overexpressing an ICS of Catharanthus roseus  as well as in tomato  and Nicotiana benthamina . The second ICS gene present in the Arabidopsis genome named ICS2  encodes a protein that is also localized in the chloroplast and has ICS activity . ICS2 participates in the synthesis of SA in partial redundancy with ICS1 since ics1/ics2 double mutants produce only 36 % of the SA amount found in the ics1 single mutant. The conversion from isochorismate to SA has not yet been described in plants. In Pseudomonas aeruginosa it is catalyzed by a bifunctional enzyme displaying isochorismate pyruvate-lyase and chorismate mutase activities . Thus, at the current state of knowledge, more than 95 % of SA synthesized under inductive conditions is formed in the chloroplast.
Interestingly, a recent analysis showed that EDS5 is localized at the chloroplast envelope and functions in the export of SA from the chloroplast to the cytoplasm  . It represents one of the few regulated transporters involved in the movement of a signal for induced defences.
In fact, MATE-transporters are present in almost all prokaryotes and eukaryotes and are thus one of the most conserved families in nature [15, 16]. Plants have the largest gene family of MATE-transporters with 58 genes in Arabidopsis, while prokaryotes have approximately 10 genes and mammals only 2. Plant MATE–transporters have not only been found at the plasma membrane, but also at the vacuolar membrane acting in the sequestration of toxic metabolites. For example, the MATE-transporter TT12 acts as flavonoid/H+ antiporter at the vacuole and is active in proanthocyanidin accumulation in the seed coat of Arabidopsis [17, 18]. In tobacco, the alkaloid nicotine is sequestered into the vacuole in exchange with protons by the action of NtMATE1 and NtMATE2 in the roots and by the MATE-transporter NtJAT1 in the shoots [19, 20]. These MATE-transporters may also transport other alkaloids, such as anabasine, hyoscyamine, scopolamine or berberine, but no flavonoids. Here we report a detailed characterization of EDS5H, a close homologue of the SA transporter EDS5.
Identification and characterization of EDS5H
Expression of EDS5H
Subcellular localization of EDS5H
Analysis of plants with downregulated EDS5H expression
Analysis of transgenic eds5-3 plants overexpressing EDS5H and a EDS5::EDS5H fusion protein
EDS5 and EDS5H show a very high percentage of homology at the C-terminal region containing the transmembrane spanning domains. In contrast, a small domain of approximately 60 aa that lies between the signal peptide for plastid targeting and the beginning of the transmembrane spanning domains shows little homology. In EDS5, this domain contains a hepta-peptide potentially forming a coiled-coil domain (http://embnet.vital-it.ch/software/COILS_form.html), while not in EDS5H. In order to test if the N-terminal domain confers specificity to the function of EDS5, eds5-3 plants were transformed with a CaMV35S::EDS5-EDS5H fusion that contained the plastid localization signal from EDS5 as well as the N-terminus of the mature protein. The accumulation of SA was monitored in transgenic eds5-3 plants overexpressing the EDS5::EDS5H fusion protein after their exposure to UV-light followed by a 12-h incubation time. The expression of the EDS5::EDS5H fusion protein did not result in a better rescue of the eds5-3 phenotype than the original EDS5H (Fig. 7b), but still increased the SA amount of the eds5 mutant suggesting that the resulting fusion protein still had transport activity. The fusion of the entire N-terminal domain of EDS5H to the EDS5 transporter region did not rescue SA accumulation (Fig. 7b). These results show that EDS5H does not function better in SA accumulation when the EDS5 N-terminus is present.
Potential transport function of EDS5 and EDS5H
A detailed characterization of the related MATE-transporter EDS5H was undertaken in order to obtain more information on its possible function relative to EDS5. The present studies confirm earlier results that EDS5 is only weakly expressed under non-inducing conditions and strongly after pathogen infection as reported for SA accumulation (Fig. 6a) . The homologue EDS5H is constitutively expressed in all green tissues, independently of pathogen infection (Fig. 3). The fact that the eds5-3 mutant phenotype is clearly detectable under conditions where EDS5H is strongly expressed indicates that EDS5 and EDS5H may only have partially redundant functions.
The determination of the sub-cellular localization of EDS5H by fluorescence microscopy reveals that it is localized at the plastid where most of the SA is synthesized [13, 30]. This is similar to EDS5 that was shown to localize within the chloroplast envelope and to function as a multidrug and toxin extrusion-like transporter in the export of SA from the chloroplast to the cytoplasm where it controls the innate immune response .
In order to clarify the functional relationship between EDS5 and EDS5H, T-DNA insertion mutants and RNAi lines where the EDS5H transcript was knocked out have been isolated or produced in the Col-0 or in the eds5-3 mutant background. The analysis of all these lines clearly show that EDS5H is not involved in SA accumulation after pathogen or UV-light induction (Fig. 6). Two explanations may be proposed for why the eds5-3/eds5H double mutants do not have less SA than eds5-3. Firstly, EDS5H could have a very low SA transport activity and therefore not reduce the SA content in the plastid. Secondly, the SA content that remains in the eds5-3 mutant is actually not produced in the plastid. Similarly, the single mutant ics1 or the double mutant ics1/ics2 contain a similarly low amount of SA indicating the existence of an alternative pathway for the production of SA . Also, eds5-3 lines overexpressing EDS5H contain only slightly more SA independent of whether EDS5H was equipped with the N-terminus of EDS5 or not. These studies suggest that EDS5H has no, or at best a very weak transport activity for SA and is not involved in resistance to P. syringae pv. tomato or Botrytis cinerea (unpublished data). Since EDS5H is closely related to EDS5 (Fig. 8) it is most likely involved in transporting related substances, for example other phenolic acids. The biochemical characterization of the transport activities of EDS5H will be exciting objectives for future work.
Despite its homology to EDS5, EDS5H does not contribute to pathogen-induced SA accumulation like EDS5. The phylogenetic relatedness of EDS5H with EDS5 supports a function of EDS5H in the transport of phenolic substances.
Growth conditions, bacterial inoculations and plant transformation
Arabidopsis accessions Columbia-0 (Col-0) and Wassilewskija (Ws) or transgenic plants were grown under either sterile or non-sterile conditions. Non-sterile plants were grown on a pasteurized soil mix of commercial potting soil:perlite (3:1), in a growth chamber at 22 ± 2 °C under a 12-h photoperiod. Seed dormancy was broken by stratification at 4 °C for 3 days. For sterile cultures, seeds were surface sterilized by treating for 15 min in 2.5 % (v/v) commercial bleach containing 0.05 % Triton X-100 with continuous agitation and rinsed four times with sterile distilled water. Seeds were placed on solid medium consisting of ½ MS (Murashige and Skoog basal medium, Sigma) with 1 % sucrose, 0.1 % vitamins (Murashige and Skoog, Sigma). P. syringae pv tomato with or without avrRpt2 was cultured at 28 °C and 220 rpm in Luria-Bertani medium containing 30 μg/ml rifampicin and 50 μg/ml kanamycin. Four-week-old plants were syringe-inoculated with a suspension of ~ 105 colony-forming units per ml in 10 mM MgCl2 and mock control plants with 10 mM MgCl2.
Arabidopsis was transformed by the floral dip method . A. tumefaciens strain GV3101, transformed by heat shock with the construct of interest, was grown at 28 °C in LB medium with an appropriate antibiotic. Transgenic plants were selected on ½ MS plates, containing 30 μg/ml hygromycin.
Cloning of EDS5H and sequence analysis
cDNA of EDS5H (At2g21340) was amplified from Col-0 plants using the Access RT-PCR system from Promega. The 5’ end of the cDNA was determined by RT-PCR using primers located 75 (75UpStream), and 150 (150UpStream) bp upstream of the predicted ATG on the annotated genomic sequence (for these and all other primers indicated below, see sequences in Additional file 1: Figure S1). The 3’ end of the cDNA was determined by RT-PCR using primers located 50 (50DownStream), 100 (100DownStream), 200 (200DownStream), 250 (250DownStream), and 300 (300DownStream) bp downstream of the stop codon of the annotated genomic sequence. RT-PCR products were cloned into pGEM-T Easy Vector (Promega) for sequencing.
Isolation of RNA and DNA, transcript analysis
For RNA gel blot analysis, RNA was isolated as previously described . For qPCR, RNA was isolated using the Qiagen RNA easy kit including the recommended DNAase treatment. Genomic DNA was isolated using a protocol modified from . Briefly, a leaf was extracted with buffer (0.2 M Tris–HCl pH 9.0, 0.4 M LiCl, 25 mM EDTA, 1 % SDS). The extracted tissue was centrifuged and the DNA was precipitated with isopropanol. The airdried pellet was resuspended in TE (10 mM Tris pH 8.0, 1 mM EDTA).
For RNA gel blot analysis, total RNA (10 μg) was separated in formaldehyde-agarose (1 %) gels, transferred to a Nylon membrane (Hybond-N, Amersham Biosciences, UK) and crosslinked by UV-light. Hybridization was carried out in hybridization buffer (0.5 M NaHPO4 pH 7.2, 7 % SDS, 1 mM EDTA, 1 % BSA) at 65 °C. The membrane was washed twice with 2X SSC containing 0.1 % SDS and twice with 0.2X SSC containing 0.1 % SDS at 65 °C, before exposing to X-Omat or Bio Max film (Kodak).
Isolation of mutants carrying a T-DNA in the EDS5H region
Plants carrying a T-DNA fragment in the region of exon 1 and exon 10, called eds5h-1 and eds5H-10, respectively, were screened by PCR www.biotech.wisc.edu/NewServicesAndResearch/Arabidopsis. eds5H-1 plants were isolated by using the forward primer JL-202, which is present on the left border of T-DNA region (JL-202) and the reverse primer GSP1. The homozygous line was selected by the absence of the wild-type fragment using GSP2 and GSP1 as forward and reverse primers, respectively. eds5h-10 plants were selected by using JL-202 as forward primer and GSP3 as reverse primer. A homozygous line was identified by the absence of the wild-type fragment by using GSP4 and GSP3 as forward and reverse primers, respectively.
Construction of the plasmid used for RNAi
A fragment of about 350 bp of the non-conserved region of EDS5H was amplified by RT-PCR and cloned into plasmid pHANNIBAL  in sense and anti-sense orientation. The sense strand was designed to include XhoI and KpnI as cloning sites (forward primer: E5H-sens-For; reverse primer: E5H-sens-Rev) and the anti-sense strand was designed to include BamHI and ClaI as cloning sites (forward primer: E5H-anti-For; reverse primer: E5H-anti-Rev). The construct was cloned into the binary vector pART27 using the NotI sites .
Construction of promoter:GUS and cMyc-tagged constructs
Three fragments of the promoter region of EDS5H were amplified using the High Fidelity Kit (Roche) with gene-specific primers designed to introduce EcoRI at the 5’ ends and NcoI sites at the 3’ ends of the fragments. The forward primers used for the amplification of EDS5H promoter fragments were: Pro500F, Pro1000F and Pro2000F resulting in fragments of 546 bp, 1057 and 1984 bp, respectively. The reverse primer for the EDS5H promoter fragments was ProE5H-R. The PCR fragments were cloned into the plasmid pCAMBIA 1303 (www.CAMBIA.org) from which the fragments of the promoter CaMV 35S and LacZ alpha had been removed.
The ORF of EDS5H was amplified by High-fidelity RT-PCR using the Omniscript RT-PCR system (Qiagen) and the forward primer Nco-E5H introducing a NcoI site as well the reverse primer E5H-Mycs introducing a triple cMyc-tag and the restriction sites SmaI and NdeI. The PCR fragment was cloned into pGEM-T Easy Vector (Promega) in the NcoI and NdeI sites. The clone was sequenced and the NcoI-SmaI fragment that included EDS5H::3xcMyc-tagg was then cloned into pCAMBIA 1304 (www.CAMBIA.org) from which the GUS and GFP genes had been removed.
Construction of plasmid for overexpressing of EDS5H
The cDNA of EDS5H was amplified by RT-PCR using the forward primer E5H-For and the reverse primer E5H-Rev and was sub-cloned into pGEM-T Easy Vector (Promega). The cDNA was digested with EcoRI, blunted, and cloned into pART7 . Clones were selected based on the correct orientation of the cDNA between the CaMV35S promoter and OCS terminator. The cassette of CaMV35S::EDS5H::OCS was digested with NotI and cloned into the binary vector pART27 .
Constructions of plasmids for protein domain swapping
The constructs for the peptide-swapping experiments were designed to include the triple cMyc-epitope tag (3xcMyc-tag). Therefore, a fragment of 3xcMyc-tag was amplified using the synthesized oligonucleotide E5H-Mycs as template. The PCR fragment included a NotI site at 5’-end and a SmaI and NdeI sites at 3’-end and 4 alanine residues upstream of cMyc-tag (forward primer: For-Ala-Myc; reverse primer: Rev-Myc-PCS). The 3xcMyc-tag was cloned into pGEM-T Easy vector at corresponding sites.
EDS5 and EDS5H genes were swapped at the NdeI site of EDS5 (281 bp downstream of ATG). The NdeI site was introduced into EDS5H by changing of a nucleotide T to A (336 bp downstream of ATG) that caused no change in amino acid residues. Therefore, the N-terminus of each protein was designed to include NcoI and NdeI as cloning sites. The fragments were amplified by RT-PCR using forward primer Nco-EDS5, reverse primer EDS5-Nde for EDS5, and forward primer Nco-E5H, reverse primer E5H-Nde for EDS5H. The C-terminus of each protein was designed to include NdeI and NotI as cloning sites. The fragments were amplified using forward primer Nde-eds5, reverse primer EDS5-Rev for EDS5, and forward primer Nde-e5h, reverse primer E5H-Swap-Rev for EDS5H. The swapped domains of either EDS5::EDS5H or EDS5H::EDS5 were constructed in pBluescript (Stratagene).
The constructs were placed upstream of 3xcMyc-tag with NcoI and NotI sites. The cassettes of the swapped peptide domains and 3xcMyc-tag were then cloned into pCAMBIA 1304 (www.CAMBIA.org). The GFP and GUS reporter genes of the binary vector were replaced with either EDS5::EDS5H::3xcMyc-tag or EDS5H::EDS5::3xcMyc-tag cassettes at NcoI and PmlI sites.
Immunolabelling and fluorescence microscopy
For immunolabelling, plant tissue was prepared according to the protocol described in . The PEG-embedded tissue was sectioned into 4–5 μm-thick slices and placed on poly-L-lysine-covered slides. The slides were incubated in PBS for 10 min in order to remove the PEG from the section. Each slide was blocked for free aldehyde by incubation with 0.1 M NH4Cl (in PBS) for 5 min, and washed for 5 min with PBS. The unspecific binding sites were blocked by incubation with 5 % BSA (in PBS) for 30 min. Slides were then incubated overnight with primary antibody solution (mouse anti-cMyc diluted in 5 % BSA/PBS in ratio 1:500) at 4 °C, washed three times with 0.1 % BSA (in PBS) for 10 min each, and once with 1 % BSA (in PBS) for 10 min. The secondary antibody used was goat anti-mouse-IgG conjugated with Alexa Fluor 488 or goat anti-rabbit-IgG conjugated with Alexa Fluor 568, diluted 1:500 in 5 % BSA (in PBS). Slides were placed in a humid chamber, incubated with secondary antibody for 2 h at 37 °C. After washing with PBS (4x10 min, samples were kept at 4 °C in the dark. Fluorescent signals were recorded with a BioRad MCR 1024 Kripton-Argon confocal microscope using an excitation wavelength of 488 nm with an emission filter 522 DF32, or an excitation wavelength of 568 nm with emission filters 605 DF32 and 585 EFLP.
GUS-assays and determination of SA
We would like to thank Linda Grainger and Martine Schorderet for excellent technical assistance. This work was supported by grants from the Swiss National Science Foundation to Jean-Pierre Métraux and Christiane Nawrath.
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