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Open Access

Peer-reviewed

Research Article

Arabidopsis HFR1 Is a Potential Nuclear Substrate Regulated by the Xanthomonas Type III Effector XopDXcc8004

  • Choon Meng Tan,

    Affiliations Institute of Biochemistry, National ChungHsing University, Taichung, Taiwan, Ph.D. Program in Microbial Genomics, National ChungHsing University and Academia Sinica, Taipei, Taiwan

    ⨯
  • Meng-Ying Li,

    Affiliation Institute of Biochemistry, National ChungHsing University, Taichung, Taiwan

    ⨯
  • Pei-Yun Yang,

    Affiliation Institute of Biochemistry, National ChungHsing University, Taichung, Taiwan

    ⨯
  • Shu Heng Chang,

    Affiliation Institute of Biochemistry, National ChungHsing University, Taichung, Taiwan

    ⨯
  • Yi-Ping Ho,

    Affiliation Institute of Biochemistry, National ChungHsing University, Taichung, Taiwan

    ⨯
  • Hong Lin,

    Affiliation Institute of Biochemistry, National ChungHsing University, Taichung, Taiwan

    ⨯
  • Wen-Ling Deng,

    Affiliation Department of Plant Pathology, National ChungHsing University, Taichung, Taiwan

    ⨯
  • Jun-Yi Yang

    jyang@nchu.edu.tw

    Affiliations Institute of Biochemistry, National ChungHsing University, Taichung, Taiwan, Ph.D. Program in Microbial Genomics, National ChungHsing University and Academia Sinica, Taipei, Taiwan, Institute of Biotechnology, National ChungHsing University, Taichung, Taiwan, NCHU-UCD Plant and Food Biotechnology Center, National ChungHsing University, Taichung, Taiwan, Agricultural Biotechnology Center, National ChungHsing University, Taichung, Taiwan

    ⨯

Abstract

XopDXcc8004, a type III effector of Xanthomonas campestris pv. campestris (Xcc) 8004, is considered a shorter version of the XopD, which lacks the N-terminal domain. To understand the functions of XopDXcc8004, in planta, a transgenic approach combined with inducible promoter to analyze the effects of XopDXcc8004 in Arabidopsis was done. Here, the expression of XopDXcc8004, in Arabidopsis elicited the accumulation of host defense-response genes. These molecular changes were dependent on salicylic acid and correlated with lesion-mimic phenotypes observed in XVE::XopDXcc8004 transgenic plants. Moreover, XopDXcc8004 was able to desumoylate HFR1, a basic helix-loop-helix transcription factor involved in photomorphogenesis, through SUMO protease activity. Interestingly, the hfr1-201 mutant increased the expression of host defense-response genes and displayed a resistance phenotype to Xcc8004. These data suggest that HFR1 is involved in plant innate immunity and is potentially regulated by XopDXcc8004.

Citation: Tan CM, Li M-Y, Yang P-Y, Chang SH, Ho Y-P, Lin H, et al. (2015) Arabidopsis HFR1 Is a Potential Nuclear Substrate Regulated by the Xanthomonas Type III Effector XopDXcc8004. PLoS ONE 10(2): e0117067. https://doi.org/10.1371/journal.pone.0117067

Academic Editor: Ya-Wen He, Shanghai Jiao Tong University, CHINA

Received: September 11, 2014; Accepted: December 18, 2014; Published: February 3, 2015

Copyright: © 2015 Tan et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited

Data Availability: All relevant data are within the paper and its Supporting Information files.

Funding: This work was supported by the Ministry of Science and Technology (NSC 100-2321-B- 005-007-MY3, NSC 103-2911-I-005-301, MOST 103-2321-B-005-020) and Ministry of Education (ATU plan), Taiwan. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing interests: The authors have declared that no competing interests exist.

Introduction

Post-translational modifications enable plants to rapidly modify the stability and activity of key factors that play fundamental roles in defense signaling during bacterial infections [1], [2]. Studies have shown that sumoylation, a reversible and dynamic process, appears to be essential for suppressing defense responses in non-infected plants [3]. The sumoylation machinery is composed of small ubiquitin-like modifier (SUMO)-specific E1 (SAE1/SAE2 heterodimer), E2 (SCE1), and E3 (SIZ1 and MMS21/HPY2) to make SUMO conjugates [4], [5]. Elevated accumulation of salicylic acid (SA) accompanied by localized programmed cell death in sum1sum2 and siz1mutants exhibits increased resistance to Pseudomonas syringae and suggests that sumoylation machinery is likely to contribute to systemic-acquired resistance (SAR), resulting in enhanced resistance against further pathogen attacks [6–8].

The plant immune system is a multilayered type of immune response, which contains pathogen-associated molecular pattern-triggered immunity and effector-triggered immunity [9], [10]. To overcome the complex immune system, pathogens secrete or inject a range of effectors into host cells to manipulate host cellular functions and alter host defense responses [11], [12]. Although the functions of these virulence factors remain largely unknown, an increasing body of evidence demonstrates that pathogens employ a strategy to structurally or functionally mimic host cellular activities [13], [14]. In the past years, several bacterial effectors have been found to share structural similarity with SUMO proteases. Because bacteria do not have a SUMO system, it would be interesting to understand the role of pathogen effectors employing SUMO protease activity.

Previous studies have shown that the Xanthomonas type III effector XopD possesses desumoylation activity and localizes to nuclear foci in plant cells [15–17]. The subnuclear localization of XopD suggests that XopD may target SUMO-conjugated proteins in the plant nucleus. Indeed, XopDXccB100 from the strain B100 of Xcc specifically interacts with MYB30 to suppress its activity in activating plant defense responses required for anti-Xcc immunity [16]; XopDXcv85–10 from the strain 85–10 of Xanthomonas campestris pv. vesicatoria (Xcv) specifically interacts with SIERF4 to suppress its activity in activating ethylene-induced responses, which is required for anti-Xcv immunity [18]. XopD is composed of an N-terminal domain, ERF-associated amphiphilic repression motifs, and a C-terminal SUMO protease domain [17], [19]. Although the C-terminal domain of XopD has SUMO peptidase and isopeptidase activities, lacking the functional N-terminal domain fails to suppress MYB30-mediated defense responses or desumoylation of SIERF4 [16], [18]. Thus, the N-terminus of XopD is essential for the virulence of Xanthomonas in planta. However, in the Xcc8004 strain, XopDXcc8004 was considered as a XopD without N-terminal domain [17], [19]. Although XopDXcc8004 has been shown to be able to be secreted via a hrp-dependent pathway and contains functional SUMO protease activity, the action of XopDXcc8004 in planta is still largely unknown [19].

Recently, light has been considered as an important regulator in modulating plant immunity [20], [21]. The availability and quality of light affects the plant development, as well as influences the plant defense responses. For example, a high ratio of red to far-red light enhances plant resistance to herbivorous insects [22]; a low ratio of red to far-red light reduces plant resistance to bacterial pathogens [23], [24]. Thus, mutations in the photoreceptors greatly influence plant defense responses. In this study, an inducible expression system was used to study the functions of XopDXcc8004 in transgenic Arabidopsis plants. Finally, we showed that HFR1, a basic helix-loop-helix transcription factor involved in light-signaling pathway, is a potential nuclear substrate regulated by XopDXcc8004.

Materials and Methods

Plant materials and growth conditions

Arabidopsis thaliana was grown at 21°C under a 16-h light/8-h dark photoperiod for Agrobacterium transformations, and a 12-h light/12-h dark photoperiod for Xanthomonas spp. inoculations. N. benthamiana was grown at 26°C under a 16-h light/8-h dark photoperiod for Agrobacterium transient expression assay. The Arabidopsis WT, hfr1–201 mutant, and nahG transgenic plants are in the Columbia ecotype background [6], [25].

Plasmid constructions

Xcc8004 genomic DNA was used for amplification of the XC_1213 DNA fragment encoding XopDXcc8004. An A. thaliana cDNA library was used for the amplification of the At1g02340 DNA fragment encoding HFR1. DNA fragments amplified by PCR using AccuPrime pfx DNA polymerase (Invitrogen) were subcloned into appropriate vectors by restriction site reconstructions. For the generation of Arabidopsis transgenic plants, PCR products were subcloned into the pER8 vector under the control of the XVE promoter [26]. For subcellular localization assays, PCR products were subcloned into pBA-YFP or pBA-CFP vectors under the control of the Cauliflower mosaic virus 35S promoter [27]. For yeast two-hybrid assays, PCR products were subcloned into pGADT7 and pGBKT7 vectors (Clontech) to generate AD-HFR1 and BK-XopDXcc8004 constructs. For the expression of recombinant proteins, PCR products were subcloned into pET-SUMO (Invitrogen), pMAL-c2 (New England Biolabs), or pGEX4T-1 (GE Healthcare) vectors to produce N-terminal His-SUMO-, MBP-, or GST-tagged XopDXcc8004, HFR1, or AS2 proteins. The K72A mutant of HFR1 and the C355A mutant of XopDXcc8004 were generated by QuikChange site-directed mutagenesis (Stratagene) according to the manufacturer’s instructions. For homologous recombination, the 985-bp upstream and 976-bp downstream regions of XopDXcc8004 were amplified from Xcc8004 genomic DNA and subcloned into a pK18mobsacB vector. To establish an in vitro sumoylation system, DNA fragments encoding Arabidopsis SAE1 (SAE1b), SAE2, and SCE1 were excised from the pACYCDuet-AtSAE1b-AtSAE2 and pCDFDuet-AtSUMO1(GG)-AtSCE1 plasmids [28], and subcloned into pET28a or pET29a vectors (Invitrogen) by restriction site reconstructions to produce His-tagged SAE1, SAE2, and SCE1 proteins. All plasmids were verified by DNA sequencing.

Arabidopsis transformations

To obtain Arabidopsis transgenic plants, plasmids were introduced into the Agrobacterium tumefaciens strain ABI by the freeze-thaw method [29] and then transformed into A. thaliana Col-0 using the floral-dip method [30]. Arabidopsis seeds were grown on half-strength Murashige and Skoog (1/2× MS) medium containing hygromycin (12.5 μg mL–1) and carbenicillin (100 μg mL–1) to obtain transgenic lines. Homozygous seeds were further selected and amplified for analyses.

Trypan blue staining

To characterize the lesion-mimic phenotype, Arabidopsis transgenic plants expressing XopDXcc8004 were examined by trypan blue staining [31]. Briefly, transgenic seeds were germinated on 1/2× MS medium containing DMSO or 20 μM β-estradiol. Three-week-old seedlings were stained by boiling in a solution containing 10 mL of lactic acid, 10 mL of glycerol, 10 g of phenol, and 10 mg of trypan blue (dissolved in 10 mL of distilled water), and further destained in 2.5 g mL–1 chloral hydrate solution. Images were collected with a Leica ZM75 microscope.

qRT-PCR

To measure Arabidopsis gene expression levels, total RNA was extracted by using the Trizol reagent and reverse transcribed into cDNAs using a Superscript III first-strand synthesis supermix according to the manufacturer’s instructions (Invitrogen). The qRT-PCR reactions were performed on an Eco real-time PCR system (Illumina) with the KAPA SYBR fast qPCR kit (Kapa Biosystems). Relative amounts of transcripts were normalized to the transcript level of a house keeping gene, EF1α. Experiments were repeated at least 3 times.

Recombinant protein purifications and antibody production

To produce recombinant proteins, all constructs were transformed into Escherichia coli BL21 (DE3) cells and cultured at 24°C until the optical density at 600 nm reached 0.4. Then, isopropyl β-D-1-thiogalactopyranoside was added to a final concentration of 0.2 mM and cells were further incubated overnight. After cell lysis, bacterial cell extracts were purified using appropriate resins according to the manufacturer’s instruction. For in vitro sumoylation assays, Arabidopsis SAE1, SAE2, SCE1, and AtSUMO1 (with Gly-Gly at the C-terminus) proteins were purified using Ni2+-NTA resin (Qiagen). For in vitro pull-down assays, MBP- and GST-tagged proteins were purified using an amylose resin (New England Biolabs) and glutathione-Sepharose 4B (GE Healthcare), respectively. To generate a specific antibody against XopDXcc8004, the His-SUMO-XopDXcc8004 protein was purified using a Ni2+-NTA resin and cleaved with Ubl-specific protease 1 (Ulp1) to remove the His-SUMO tag. After cleavage, proteins were purified by using a Sephacryl S-200 HR gel filtration column (GE Healthcare) to obtain the XopDXcc8004 protein alone. Finally, a rabbit polyclonal antibody raised against XopDXcc8004 was obtained by affinity purification using a polyvinylidene difluoride membrane as a coupling matrix [32].

Bacterial strains and inoculations

The Xcc8004 ΔXopD mutant strain was obtained using the sacB system [33]. Plasmid for homologous recombination was introduced into Xcc8004, and deletion mutant was verified by PCR. For bacterial inoculations, Xcc8004 spp. were cultured in nutrient broth supplemented with yeast extract (3 g of beef extract, 5 g of peptone, and 3 g of yeast extract in 1 liter of water) at 28°C. Four- to five-week-old Arabidopsis plants were used for bacterial growth assays. For XVE::XopDXcc8004 transgenic plants, leaves were infiltrated with a bacterial suspension (2 × 106 CFU mL–1) by using a syringe at 24 h after plants had been sprayed with 20 μM β-estradiol. After inoculation, plants were kept at 21°C in a growth chamber, and bacterial populations in leaves were determined at indicated time intervals using agar plates of nutrient broth supplemented with yeast extract containing rifampin (50 μg mL–1). Experiments were repeated at least 3 times.

Yeast two-hybrid assays

AD-HFR1 and BK-XopDXcc8004 constructs were transformed into the yeast strain AH109 by using the lithium acetate/single-stranded carrier DNA/polyethylene glycol method [34]. First, yeast cells were grown on synthetic-defined minimal yeast medium lacking leucine and tryptophan (Clontech) to maintain plasmids. Transformed colonies were further plated on synthetic-defined minimal yeast medium lacking leucine, tryptophan, and histidine (Clontech) to test the interaction between XopDXcc8004 and HFR1.

Subcellular localization assays

To examine the subcellular localization of HFR1-CFP and XopDXcc8004-YFP, agroinfiltration was performed [35]. Briefly, A. tumefaciens stains carrying the 35S::HFR1-CFP or 35S::XopDXcc8004-YFP plasmid were inoculated into N. benthamiana leaves. Fluorescence signals were observed by confocal laser scanning microscopy at 36 h after agroinfiltration, and images were collected with the Olympus Fluoview FV1000 system.

In vitro pull-down assays

GST pull-down experiments were performed by inoculating 2 μg of GST alone or GST-tagged proteins with 2 μg of MBP alone or MBP-tagged proteins in binding buffer (50 mM Tris-HCl at pH 7.5, 100 mM NaCl, 0.25% Triton X-100, 35 mM β-mercaptoethanol) for 2 h at room temperature. Next, 25 μL of glutathione-Sepharose 4B (GE Healthcare) were added, and samples were further incubated for 1 h at room temperature. After extensive wash, pulled down proteins were eluted with 2.5× sample buffer and separated on a 10% sodium dodecyl sulfate-polyacrylamide gel. Western blotting was performed using an anti-MBP antibody to detect MBP-tagged proteins (Amersham). The chemiluminescence signals generated by the ECL reagent were further examined with the ImageQuant LAS4000 mini (GE Healthcare).

In vitro sumoylation assays

In vitro sumoylation was performed using purified recombinant proteins in a reaction buffer (50 mM Tris-HCl, pH7.4, 100 mM NaCl, 4 mM ATP, 10 mM MgCl2, 4 mM DTT) in a total volume of 30 μL. After incubation for 2 h at 30°C, the reaction mixtures were separated on 10% sodium dodecyl sulfate-polyacrylamide gels. MBP-HFR1 and sumoylated MBP-HFR1 were detected by western blotting using an anti-MBP antibody. The chemiluminescence signals generated by the ECL reagent were further examined with the ImageQuant LAS4000 mini (GE Healthcare).

RNA-Seq analysis

To identify differentially expressed genes in XVE::XopDXcc8004transgenic plants upon β-estradiol treatment, next-generation sequencing was done on the Hiseq 2000 (Illumina) using total RNA samples extracted with the RNeasy plant mini kit (Qiagen). For transcriptome analysis, sequence reads were aligned using CLC bio and gene expression levels were normalized as reads per kilobase of exon model per million mapped reads. Finally, the differentially expressed genes were identified by DEseq [36].

Primers

Primer sequences for plasmid constructions and qRT-PCR analyses are listed in S1 Table.

Results

Expression of XopDXcc8004 elicits a SA-mediated defense response in Arabidopsis

XopDXcc8004 from the Xcc strain 8004 is a shorter version of XopD, which lacks the N-terminal domain (Fig. 1A). To characterize the functions of XopDXcc8004 in plant cells, Arabidopsis transgenic plants carrying an inducible XVE::XopDXcc8004 transgene were generated. Here, a lesion-mimic phenotype associated with localized, necrotic spots was observed in XVE::XopDXcc8004 transgenic plants after β-estradiol (inducer) treatment (Fig. 1B, C). Further examination using trypan blue staining confirmed that lesion-mimics were formed because of cell death (Figs. 1B, S1), whereas transgenic plants harboring empty vector (XVE) did not show cell death phenotype upon β-estradiol treatment (S2 Fig.).

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Figure 1. Salicylic acid-dependent defense responses were elicited by the expression of XopDXcc8004 in Arabidopsis.

(a) Schematic representation of XopD proteins. (b) Morphological examination and trypan blue staining of two-week-old leaves of Arabidopsis XVE::XopDXcc8004 transgenic plants. Lesion-mimic phenotypes were indicated by arrows. Scale bar: 1 mm. (c) Translated products of XopDXcc8004 and XopDXcc8004(C355A) were examined by western blotting using a specific antibody against XopDXcc8004. Anti-tubulin was used for loading control. (d) The expression levels of genes involved in the SA-mediated defense signaling network were examined by qRT-PCR and normalized to EF1α. The relative expression levels of each gene in the DMSO control were set at 1.

https://doi.org/10.1371/journal.pone.0117067.g001

To examine whether XopDXcc8004 can trigger a SA-mediated defense response which may contribute to the hypersensitive cell death, genes involved in the SA-mediated defense-signaling network [37] were selected for quantitative reverse transcription-polymerase chain reaction (qRT-PCR) validation. Compared with dimethyl sulfoxide (DMSO) control treatment, genes involved in defense response (AIG1 and DOX1), SA biosynthesis (EDS5 and SID2), SA accumulation and downstream signaling (WIN3, PAD4 and WRKY70), as well as SA-standard marker genes (PR1, PR2 and PR5) were highly elevated in XVE::XopDXcc8004 transgenic plants after β-estradiol treatment (Figs. 1D, S1). By contrast, no significant difference was observed in XVE (vector only) transgenic plants (S2 Fig.). Next, we transfected XVE::XopDXcc8004 into an Arabidopsis transgenic line overexpressing bacterial salicylate hydroxylase (nahG). With the expression of nahG, the cell death phenotype and SA response-related genes induced by XopDXcc8004 were all inhibited by nahG (Figs. 1D, S3). These results suggest that XopDXcc8004 elicits a SA-dependent defense response which may contribute to the lesion-mimic phenotype observed in XVE::XopDXcc8004 transgenic plants.

To investigate the genome-wide expression profile of mRNAs in response to the expression of XopDXcc8004 in Arabidopsis, the total RNA from XVE::XopDXcc8004 transgenic seedlings upon DMSO and β-estradiol treatments were extracted for a comparative transcriptome analysis. In summary, a total of 23.1 million reads mapped to the Arabidopsis genome were generated after quality trim and a total of 103 differentially expressed genes with p < 0.001 were identified using the DESeq method (S2 and S3 Tables). Among them, 85 genes were upregulated and 18 genes were downregulated after β-estradiol treatment. Functional annotations on the 85 up-regulated genes revealed that a total of 25 genes associated with defense responses including the SA-mediated response were highly induced by XopDXcc8004 (Table 1).

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Table 1. Annotation of the differentially expressed genes (p < 0.001) involved in plant defense responses.

https://doi.org/10.1371/journal.pone.0117067.t001

Suppression of Xcc8004 growth by XopDXcc8004

Because the lesion-mimic phenotype accompanied by the up-regulation of SA response-related genes in XopDXcc8004-transgenic plants resembles the hypersensitive response (HR) in pathogen infection, we hypothesize that the expression of XopDXcc8004 in Arabidopsis may result in enhanced resistance against bacterial pathogens. In order to examine the effect of XopDXcc8004 on the resistance of Arabidopsis, multiplication of the Xcc8004 strain on XVE::XopDXcc8004 transgenic plants was tested after β-estradiol treatment. Compared with XVE transgenic plants, multiplication of the Xcc8004 strain was suppressed by the expression of XopDXcc8004 in planta at 5 days post inoculation (dpi) (Fig. 2A).

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Figure 2. XopDXcc8004 suppresses the virulence of the Xcc8004.

(a) Bacterial growth of the Xcc8004 strain in Arabidopsis transgenic plants. DMSO or β-estradiol was applied 24 h before bacterial inoculation. Hand-infiltrated leaves were collected at the indicated times for measuring the in planta growth of bacterial populations. (b) Bacterial growth of Xcc8004 spp. in Arabidopsis plants were measured to examine the effects of XopDXcc8004 on the virulence of Xcc8004. Statistically significant differences were determined using one-way ANOVA (* indicates p < 0.05).

https://doi.org/10.1371/journal.pone.0117067.g002

We further generated a xopD null mutant by homologous recombination to validate the function of XopDXcc8004 in suppressing the virulence of Xcc8004. Here, Arabidopsis WT leaves inoculated with Xcc8004 ΔXopD strain exhibited a higher titer of bacteria at 5 dpi than those inoculated with the Xcc8004 strain (Fig. 2B). This phenotype was able to be complemented when Xcc8004 ΔXopD strain was transformed with a broad host plasmid (pBBR1) expressing XopDXcc8004 (Fig. 2B). Taken together, these results suggest that XopDXcc8004 acts as a negative factor in suppressing the growth of Xcc8004.

XopDXcc8004-eliciting defense responses are mainly dependent on the SUMO protease activity

To examine whether the SUMO protease activity of XopDXcc8004 is required for eliciting the plant immunity, XVE::XopDXcc8004(C355A) transgenic plants were generated, in which mutation of the conserved cysteine (C355A) in XopDXcc8004 was not able to hydrolyse the SUMO substrates. Compared with XVE::XopDXcc8004 transgenic plants, no hypersensitive cell death was observed in XVE::XopDXcc8004(C355A) transgenic plants after β-estradiol treatment (Figs. 1B, 3A, S4). Further investigation of the gene expression involved in defense responses revealed that the C355A mutation largely suppressed the ability of XopDXcc8004 in eliciting the expression of SA response-related genes in Arabidopsis (Figs. 3B, S4). Next, we transformed Xcc8004 ΔXopD strain with a broad host plasmid to express XopDXcc8004(C355A). However, Arabidopsis WT leaves inoculated with Xcc8004 ΔXopD/XopDXcc8004(C355A) strain still exhibited a higher titer of bacteria at 5 dpi as well as those inoculated with Xcc8004 ΔXopD strain (Fig. 2B). These results suggest that the SUMO protease activity of XopDXcc8004 is required for eliciting a SA-mediated defense response in Arabidopsis and suppressing the virulence of Xcc8004.

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Figure 3. XopDXcc8004(C355A) loses the activity for activating plant immunity.

(a) Morphological examination and trypan blue staining of two-week-old leaves of Arabidopsis XVE::XopDXcc8004(C355A) transgenic plants. Scale bar: 1 mm. (b) The expression levels of genes involved in the SA-mediated defense signaling network were examined by qRT-PCR and normalized to EF1α. The relative expression levels of each gene in the DMSO control were set at 1.

https://doi.org/10.1371/journal.pone.0117067.g003

XopDXcc8004 interacts with Arabidopsis HFR1

Unexpectedly, a long hypocotyl phenotype associated with the lesion-mimic phenotype was observed with the expression of XopDXcc8004 in Arabidopsis (Fig. 4A). Compared with XVE transgenic plants, the hypocotyl length of XVE::XopDXcc8004 seedlings reached to 4.5 mm at 14 days after germination in medium containing β-estradiol (Figs. 4B, S5). We noted that the long hypocotyl phenotype elicited by the expression of XopDXcc8004 similar to those observed in siz1–2 carrying a partially functional SIZ1phd [38]. SIZ1phd contains a C134Y mutation in the zinc finger motif required for the SUMO E3 ligase activity of SIZ1. Cheong et al. found that expression of SIZ1phd in the siz1–2 mutant created a light-dependent long hypocotyl phenotype. Therefore, we investigated whether light signaling components were potential substrates of XopDXcc8004. Here, several key components involved in the light signaling pathway including HY5, LAF1, Fin219, PAT3, SPA1, and HFR1were analyzed for their interaction with XopDXcc8004 using the yeast two-hybrid assay. Among them, HFR1, a basic helix-loop-helix transcription factor, showed a positive interaction with XopDXcc8004 in selection medium lacking tryptophan/leucine/histidine (Fig. 5A).

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Figure 4. Expression of XopDXcc8004 induces a long hypocotyl phenotype in Arabidopsis.

(a) Phenotypes of 12-day-old Arabidopsis transgenic plants carrying a XopDXcc8004 gene driven by the inducible XVE promoter. Scale bars: 8 mm. (b) Average hypocotyl lengths of seedlings grown on medium containing DMSO or 20 μM β-estradiol. Statistically significant differences were determined using one-way ANOVA (** indicates p < 0.005).

https://doi.org/10.1371/journal.pone.0117067.g004

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Figure 5. XopDXcc8004 interacts with HFR1.

(a) Investigation of the interaction between HFR1 and XopDXcc8004 by yeast two-hybrid analysis. Yeast strains transformed with two plasmids (prey and bait) were plated onto synthetic-defined (SD) minimal medium lacking tryptophan/leucine or tryptophan/leucine/histidine. (b) Nicotiana benthamiana leaves were co-infiltrated with agrobacterium carrying 35S::XopDXcc8004-YFP and 35S::HFR1-CFP. Fluorescence and differential interference contrast (DIC) images were obtained by confocal laser scanning microscopy. 35S::YFP and 35S::CFP were used for control. Scale bars: 15 μm. (c) Investigation of the interaction between HFR1 and XopDXcc8004 by using pull-down assays. Briefly, 2 μg of GST or GST fusion proteins were used to pull down 2 μg of MBP or MBP fusion proteins, and an anti-MBP antibody was used to detect the associated proteins by western blotting (the left panel). The right panels present the input proteins examined by anti-MBP or anti-GST antibodies. The asterisk indicates the protein signal of MBP-HFR1.

https://doi.org/10.1371/journal.pone.0117067.g005

Next, we investigated whether XopDXcc8004 can colocalize with HFR1 in plant cells. HFR1 has been shown to localize to nucleus in subnuclear foci [27], whereas XopDXcc8004 was localized to the nucleus in a homogeneous pattern [17]. If XopDXcc8004 can interact with HFR1, the coexpression of HFR1 may cause the relocalization of XopDXcc8004 to HFR1-containing nuclear foci. Here, we coexpressed XopDXcc8004-yellow fluorescence protein (YFP) and HFR1-cyan fluorescent protein (CFP) in Nicotiana benthamiana cells using agroinfiltration and found that XopDXcc8004-YFP was colocalized with HFR1-CFP in nuclear foci (Fig. 5B). To further examine whether XopDXcc8004 can directly interact with HFR1 in vitro, a pull-down assay was performed with purified recombinant proteins. Fig. 5C shows that maltose-binding protein (MBP)-HFR1 was specifically pulled down by glutathione S-transferase (GST)-XopDXcc8004 but not by GST alone. By contrast, no signal was observed when the negative control proteins MBP and MBP-AS2 were used in the assay (Fig. 5C).

To examine whether the long hypocotyl phenotype observed in XVE::XopDXcc8004 seedlings is dependent on the SUMO protease activity of XopDXcc8004, we investigated the phenotype of XVE::XopDXcc8004(C355A) transgenic plants. However, a long hypocotyl phenotype was also observed in XVE::XopDXcc8004(C355A) seedlings (S5 Fig.). This result suggests that the long hypocotyl phenotype caused by XopD Xcc8004 is not simply due to the SUMO protease activity.

K72 in HFR1 is desumoylated by XopDXcc8004 in vitro

Because XopDXcc8004 has been shown to possess SUMO protease activity [16], [17], the interaction between XopDXcc8004 and HFR1 prompted us to examine whether HFR1 can be modified with SUMO and further desumoylated by XopDXcc8004. Here, the examination of the deduced amino acid sequence of HFR1 revealed a probable sumoylation site at lysine 72 (K72) in the consensus motif ΨKxE/D (where Ψ is a large and hydrophobic amino acid and x is any amino acid) (Fig. 6A). To address whether HFR1can be modified with SUMO, an in vitro sumoylation assay was performed with Arabidopsis SAE1/SAE2 (SUMO-activating E1), SCE1 (SUMO-conjugating E2), AtSUMO1, and MBP-HFR1. Fig. 6B shows that a clear mobility shift of MBP-HFR1was detected after incubation with the components of the Arabidopsis sumoylation cascade, and the shift was in a molecular mass consistent with mono-SUMO modification. Compared with MBP-HFR1, no mobility shift was detected for MBP-HFR1(K72A) in the in vitro sumoylation system (Fig. 6B). These results indicate that the K72 of HFR1 is the principal site for SUMO conjugation. Next, we examined whether the sumoylated HFR1 can be desumoylated by XopDXcc8004. Fig. 6C shows that no sumoylated MBP-HFR1 was detected when XopDXcc8004, but not the catalytic mutant XopDXcc8004(C355A), was present in the in vitro sumoylation reaction. These results indicate that XopDXcc8004 catalyzes the SUMO hydrolysis from the K72 of HFR1.

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Figure 6. K72 in HFR1 is desumoylated by XopDXcc8004 in vitro.

(a) The deduced amino acid sequence of HFR1 from 65 to 80 a.a. The arrow indicates a putative sumoylation site at K72 of the consensus motif ΨKxE/D of HFR1. (b) An in vitro sumoylation system was established by using purified recombinant proteins, including Arabidopsis SAE1, SAE2, SCE1, and AtSUMO1. MBP-HFR1 or MBP-HFR1(K72A) were used as potential substrates for sumoylation and detected with an anti-MBP antibody. (c) Together with SAE1, SAE2, SCE1, AtSUMO1, and MBP-HFR1, XopDXcc8004 was added to the reaction mixture to investigate the sumoylation of HFR1. XopDXcc8004(C355A), a SUMO protease mutant, was used as control. Asterisks indicate sumoylated MBP-HFR1 proteins. Arrowheads indicate unmodified MBP-HFR1 proteins. Signals below the unmodified MBP-HFR1 proteins were degraded products of purified MBP-HFR1 proteins.

https://doi.org/10.1371/journal.pone.0117067.g006

hfr1–201 increases resistance to Xcc8004

Based on the interaction between HFR1and XopDXcc8004, we propose that HFR1 may play a role in the plant immune response. To this end, we monitored the expression levels of genes involved in the SA-mediated defense-signaling network in hfr1–201 mutants and WT plants. Irrespective of treatment with or without 2 mM SA, we found that the levels of PR2, WRKY70, WIN3, EDS5, AIG1, PUB54, WRKY18, PR1, and WRKY51 transcripts are higher in the hfr1–201 mutant than in WT plants (Fig. 7A). We further investigated the growth of Xcc8004 WT and ΔXopD mutant strains in the hfr1–201 mutant. Compared with WT plants, multiplication of Xcc8004 and Xcc8004 ΔXopD strains was suppressed in the hfr1–201 mutant (Fig. 7B). These results suggest that HFR1 is required for modulating the defense response in Arabidopsis, and the loss-of-function mutant in the HFR1 increases resistance to Xcc8004 spp.

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Figure 7. hfr1–201 increases plant immunity against Xcc8004 spp.

(a) Arabidopsis WT and hfr1–201 mutant plants treated with (8 hr) or without (0 hr) 2 mM SA were collected for total RNA extraction. The expression levels of genes involved in the SA-mediated defense signaling network were examined by qRT-PCR and normalized to EF1α. The relative expression levels of each gene in the WT plants without SA treatment were set at 1. (b) Bacterial growth in Arabidopsis WT and hfr1–201 mutant plants were measured to examine the effects of HFR1 on the resistance of Arabidopsis against Xcc8004 spp. Hand-infiltrated leaves were collected at the indicated times for measuring the in planta growth of bacterial populations. Statistically significant differences were determined using one-way ANOVA (* indicates p < 0.05).

https://doi.org/10.1371/journal.pone.0117067.g007

Discussion

XopD is composed of an N-terminal domain, ERF-associated amphiphilic repression motifs, and a C-terminal SUMO protease domain. In XopDXcv85–10 and XopDXccB100, the N-terminal domain has been suggested to play a role in specifying substrate recognition and modulating SUMO protease activity [16], [18]. However, XopDXcc8004 was considered as a shorter version of XopD that does not contain an N-terminal domain [17], [19]. Using a transgenic approach, we found that possessing a C-terminal SUMO protease domain, the XopDXcc8004-overexpressing transgenic plants showed morphological and molecular phenotypes similar to those of the mutants defective in the sumoylation machinery. In Arabidopsis, mutants defective in the sumoylation machinery, e.g., siz1 and sum1sum2 mutants, display localized programmed cell death and elevated accumulation of SA, which contribute to the enhanced resistance against bacterial attacks [6], [7]. In this study, we showed that the expression of XopDXcc8004 in Arabidopsis elicited a lesion-mimic phenotype associated with increased expression of disease-response genes (Fig. 1B). Moreover, the multiplication of the Xcc8004 strain was suppressed in XopDXcc8004-overexpressing transgenic plants (Fig. 2A), and Xcc8004 ΔXopD displayed a higher bacterial growth rate than Xcc8004 (Fig. 2B). Different from XopDXcv and XopDXccB100, which contain a complete N-terminal domain and are successful in suppressing anti-Xcv and anti-XccB100 immunities [16], [18], XopDXcc8004 induced host defense responses to inhibit Xcc8004 growth. Although it is still unknown how the N-terminal domain modulates the SUMO protease activity of XopD, it is clear that impairment in the N-terminal domain of XopD not only loses the ability to suppress host immunity, but also elicits host defense responses.

Based on the results that the catalytic mutant XopDXcc8004(C355A) was not able to elicit HR and plant immunity (Fig. 3A, B), we suggest that the activity of XopDXcc8004 in eliciting host defense responses is mainly dependent on the SUMO protease activity. Yet, the substrates of XopDXcc8004 functioning in plant defense responses remain largely unknown. Nevertheless, we identified that HFR1 was a potential nuclear substrate of XopDXcc8004 and could be modified by sumoylation (Figs. 5, 6). With the in vitro assay, we found that the sumoylated-residue K72 within the consensus sumoylation motif of HFR1 was desumoylated by XopDXcc8004 through the SUMO protease activity (Fig. 6B, C). Although the direct impact of SUMO protease activity of XopDXcc8004 on the function of HFR1 remains unknown, we observed that the loss-of-function mutation in HFR1 gene accelerated SA-mediated responses and increased the resistance against Xcc8004 (Fig. 7A, B). These results clearly indicate that HFR1 plays a role in repression of defense responses in plants.

HFR1 is an important regulator involved in photomorphogenesis and regulated by ubiquitin-mediated degradation through the coat protein complex I [27], [39], [40]. Because the highly unstable character of HFR1 [41], it is a technical challenge to provide a tight connection between XopDXcc8004 and HFR1 during infection. Thus, further experiments are required to demonstrate the function of sumoylation on the manipulation of the activity of HFR1. Sumoylation has been shown to play a role in mediating the transcriptional repression activity of many transcription factors [42–46]. Therefore, we do not exclude the possibility that the repression activity of HFR1 on defense responses requires a modification of SUMO. In fact, our data only explain a possible mechanism for XopDXcc8004-triggered host defense responses, and we do not exclude the possibility that XopDXcc8004 may have several targets in plants. Thus, we still observed a higher growth rate of Xcc8004 even in the hfr1–201 mutant (Fig. 7B).

Recently, Tan et al. (2014) reported that XopDXcc8004 triggers plant disease tolerance by targeting DELLA proteins [47]. In their study, they did not observe the significant difference in bacterial titers between Xcc8004 and Xcc8004 ΔXopD. This difference may be depending on the different experimental conditions used in our study. Here, a syringe infiltration method and a higher titer of bacterial suspension (2 × 106 CFU mL–1) were used. Nevertheless, our findings are not in conflict with the fact that XopDXcc8004 may act as a virulence-controlling factor by interfering with plant defense responses.

Recent studies on plant-pathogen interaction have provided new insights into fundamental cellular processes in plants [48], [49]. In this study, we identified a dual role of HFR1 in development and immunity. This finding indicates that HFR1 is required for the fine-tuning of the immune response, as well as contributes to our knowledge of the crosstalk between the light-signaling pathway and immune response.

Supporting Information

S1 Fig. Salicylic acid-dependent defense responses were elicited by the expression of XopDXcc8004 in Arabidopsis.

(a) Trypan blue staining of two-week-old leaves of Arabidopsis XVE::XopDXcc8004 transgenic plants. Scale bar: 1 mm. (b) Translated products of XopDXcc8004 were examined by western blotting using a specific antibody against XopDXcc8004 and indicated by an arrow. Rubisco large subunit (RBCL) stained with coomassie brilliant blue served as a loading control. (c) The expression levels of genes involved in the SA-mediated defense signaling network were examined by qRT-PCR and normalized to EF1α. The relative expression levels of each gene in the DMSO control were set at 1.

https://doi.org/10.1371/journal.pone.0117067.s001

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S2 Fig. Transgenic plants harboring empty vector (XVE) did not show cell death phenotype upon β-estradiol treatment and elicited defense responses.

(a) Trypan blue staining of two-week-old leaves of Arabidopsis XVE transgenic plants. Scale bar: 1 mm. (b) Expression levels of genes involved in the SA-mediated defense signaling network were examined by qRT-PCR and normalized to EF1α. The relative expression levels of each gene in the DMSO control were set at 1.

https://doi.org/10.1371/journal.pone.0117067.s002

(TIF)

S3 Fig. Salicylic acid-dependent defense responses elicited by the expression of XopDXcc8004 were inhibited by nahG.

(a) Trypan blue staining of two-week-old leaves of Arabidopsis XVE::XopDXcc8004 / nahG transgenic plants. Scale bar: 1 mm. (b) Translated products of XopDXcc8004 were examined by western blotting using a specific antibody against XopDXcc8004 and indicated by an arrow. Rubisco large subunit (RBCL) stained with coomassie brilliant blue served as a loading control. (c) The expression levels of genes involved in the SA-mediated defense signaling network were examined by qRT-PCR and normalized to EF1α. The relative expression levels of each gene in the DMSO control were set at 1.

https://doi.org/10.1371/journal.pone.0117067.s003

(TIF)

S4 Fig. XopDXcc8004(C355A) loses the activity for activating plant immunity.

(a) Morphological examination and trypan blue staining of two-week-old leaves of Arabidopsis XVE::XopDXcc8004(C355A) transgenic plants. Scale bar: 1 mm. (b) Translated products of XopDXcc8004(C355A) were examined by western blotting using a specific antibody against XopDXcc8004 and indicated by an arrow. Rubisco large subunit (RBCL) stained with coomassie brilliant blue served as a loading control. (c) The expression levels of genes involved in the SA-mediated defense signaling network were examined by qRT-PCR and normalized to EF1α. The relative expression levels of each gene in the DMSO control were set at 1.

https://doi.org/10.1371/journal.pone.0117067.s004

(TIF)

S5 Fig. Expression of XopDXcc8004 induces a long hypocotyl phenotype in Arabidopsis.

(a, b) Average hypocotyl lengths of seedlings grown on medium containing DMSO (grey bars) and 20 μM β-estradiol (black bars). Statistically significant differences were determined using one-way ANOVA (** indicates p < 0.005).

https://doi.org/10.1371/journal.pone.0117067.s005

(TIF)

S1 Table. Primer sequences for plasmid constructions and qRT-PCR.

https://doi.org/10.1371/journal.pone.0117067.s006

(XLS)

S2 Table. Reads counting (mapped read sequence statistic) for Illumina sequencing data.

https://doi.org/10.1371/journal.pone.0117067.s007

(XLS)

S3 Table. Differentially expressed genes with p < 0.001.

Identification genes that were differentially expressed in Arabidopsis after XopDXcc8004 were induced by β-estradiol.

https://doi.org/10.1371/journal.pone.0117067.s008

(XLS)

Acknowledgments

We thank M. Dow (National University of Ireland, Cork, Ireland) for the X. campestris pv. campestris 8004 strain; K. Tanaka (Kwansei Gakuin University, Sanda, Japan) for the in vivo sumoylation system; K. Miura (University of Tsukuba, Tukuba, Japan) and D.-J. Yun (Gyeongsang National University, Jinju, Korea) for the Arabidopsis nahG transgenic line.

Author Contributions

Conceived and designed the experiments: CMT JYY. Performed the experiments: CMT MYL PYY SHC YPH HL JYY. Analyzed the data: CMT JYY. Contributed reagents/materials/analysis tools: WLD. Wrote the paper: JYY.

References

  1. 1. Stulemeijer IJ, Joosten MH (2008) Post-translational modification of host proteins in pathogen-triggered defence signalling in plants. Mol Plant Pathol 9: 545–560. pmid:18705867
  2. 2. Ribet D, Cossart P (2010) Post-translational modifications in host cells during bacterial infection. FEBS Lett 584: 2748–2758. pmid:20493189
  3. 3. van den Burg HA, Takken FL (2010) SUMO-, MAPK-, and resistance protein-signaling converge at transcription complexes that regulate plant innate immunity. Plant Signal Behav 5: 1597–1601. pmid:21150289
  4. 4. Colby T, Matthäi A, Boeckelmann A, Stuible HP (2006) SUMO-conjugating and SUMO-deconjugating enzymes from Arabidopsis. Plant Physiol 142: 318–332. pmid:16920872
  5. 5. Park H, Kim WY, Park H, Lee S, Bohnert H, et al. (2011) SUMO and SUMOylation in plants. Mol Cells 32: 305–316. pmid:21912873
  6. 6. Lee J, Nam J, Park HC, Na G, Miura K, et al. (2007) Salicylic acid-mediated innate immunity in Arabidopsis is regulated by SIZ1 SUMO E3 ligase. Plant J 49: 79–90. pmid:17163880
  7. 7. van den Burg HA, Kini RK, Schuurink RC, Takken FL (2010) Arabidopsis small ubiquitin-like modifier paralogs have distinct functions in development and defense. Plant Cell 22: 1998–2016. pmid:20525853
  8. 8. Park BS, Song JT, Seo HS (2011) Arabidopsis nitrate reductase activity is stimulated by the E3 SUMO ligase AtSIZ1. Nat Commun 2: 400. pmid:21772271
  9. 9. Göhre V, Robatzek S (2008) Breaking the barriers: microbial effector molecules subvert plant immunity. Annu Rev Phytopathol 46: 189–215. pmid:18422429
  10. 10. Dodds PN, Rathjen JP (2010) Plant immunity: towards an integrated view of plant–pathogen interactions. Nat Rev Genet 11: 539–548. pmid:20585331
  11. 11. Grant SR, Fisher EJ, Chang JH, Mole BM, Dangl JL (2006) Subterfuge and manipulation: type III effector proteins of phytopathogenic bacteria. Annu Rev Microbiol 60: 425–449. pmid:16753033
  12. 12. Lee AHY, Middleton MA, Guttman DS, Desveaux D (2013) Phytopathogen type III effectors as probes of biological systems. Microb Biotechnol 6: 230–240. pmid:23433088
  13. 13. Hotson A, Mudgett MB (2004) Cysteine proteases in phytopathogenic bacteria: identification of plant targets and activation of innate immunity. Curr Opin Plant Biol 7: 384–390. pmid:15231260
  14. 14. Desveaux D, Singer AU, Dangl JL (2006) Type III effector proteins: doppelgangers of bacterial virulence. Curr Opin Plant Biol 9: 376–382. pmid:16713730
  15. 15. Hotson A, Chosed R, Shu H, Orth K, Mudgett MB (2003) Xanthomonas type III effector XopD targets SUMO-conjugated proteins in planta. Mol Microbiol 50: 377–389. pmid:14617166
  16. 16. Canonne J, Marino D, Jauneau A, Pouzet C, Brière C, et al. (2011) The Xanthomonas type III effector XopD targets the Arabidopsis transcription factor MYB30 to suppress plant defense. Plant Cell 23: 3498–3511. pmid:21917550
  17. 17. Kim JG, Taylor KW, Mudgett MB (2011) Comparative analysis of the XopD type III secretion (T3S) effector family in plant pathogenic bacteria. Mol Plant Pathol 12: 715–730. pmid:21726373
  18. 18. Kim JG, Stork W, Mudgett MB (2013) Xanthomonas type III effector XopD desumoylates tomato transcription factor SlERF4 to suppress ethylene responses and promote pathogen growth. Cell Host Microbe 13: 143–154. pmid:23414755
  19. 19. Canonne J, Marino D, Noël LD, Arechaga I, Pichereaux C, et al. (2010) Detection and functional characterization of a 215 amino acid N-terminal extension in the Xanthomonas type III effector XopD. PLoS ONE 5: e15773. pmid:21203472
  20. 20. Ballare CL, Mazza CA, Austin AT, Pierik R (2012) Canopy light and plant health. Plant Physiol 160: 145–155. pmid:22802612
  21. 21. Kangasjärvi S, Neukermans J, Li S, Aro EM, Noctor G (2012) Photosynthesis, photorespiration, and light signalling in defence responses. J Exp Bot 63: 1619–1636. pmid:22282535
  22. 22. Moreno JE, Tao Y, Chory J, Ballaré CL (2009) Ecological modulation of plant defense via phytochrome control of jasmonate sensitivity. Proc Natl Acad Sci USA 106: 4935–4940. pmid:19251652
  23. 23. Genoud T, Buchala AJ, Chua NH, Métraux JP (2002) Phytochrome signalling modulates the SA-perceptive pathway in Arabidopsis. Plant J 31: 87–95. pmid:12100485
  24. 24. Faigón-Soverna A, Harmon FG, Storani L, Karayekov E, Staneloni RJ, et al. (2006) A constitutive shade-avoidance mutant implicates TIR-NBS-LRR proteins in Arabidopsis photomorphogenic development. Plant Cell 18: 2919–2928. pmid:17114357
  25. 25. Kim YM, Woo JC, Song PS, Soh MS (2002) HFR1, a phytochrome A-signalling component, acts in a separate pathway from HY5, downstream of COP1 in Arabidopsis thaliana. Plant J 30: 711–719. pmid:12061902
  26. 26. Zuo J, Niu QW, Chua NH (2000) An estrogen receptor-based transactivator XVE mediates highly inducible gene expression in transgenic plants. Plant J 24: 265–273. pmid:11069700
  27. 27. Jang IC, Yang JY, Seo HS, Chua NH (2005) HFR1 is targeted by COP1 E3 ligase for post-translational proteolysis during phytochrome A signaling. Genes Dev 19: 593–602. pmid:15741320
  28. 28. Okada S, Nagabuchi M, Takamura Y, Nakagawa T, Shinmyozu K, et al. (2009) Reconstitution of Arabidopsis thaliana SUMO pathways in E. coli: functional evaluation of SUMO machinery proteins and mapping of SUMOylation sites by mass spectrometry. Plant Cell Physiol 50: 1049–1061. pmid:19376783
  29. 29. Wise A, Liu Z, Binns A (2006) Three methods for the introduction of foreign DNA into Agrobacterium. Methods Mol Biol 343: 43–53. pmid:16988332
  30. 30. Clough SJ, Bent AF (1998) Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. Plant J 16: 735–743. pmid:10069079
  31. 31. Ho YP, Tan CM, Li MY, Lin H, Deng WL, et al. (2012) The AvrB_AvrC domain of AvrXccC of Xanthomonas campestris pv. campestris is required to elicit plant defense responses and manipulate ABA homeostasis. Mol Plant-Microbe Interact 26: 419–430.
  32. 32. Nishino H, Ishibashi T, Nakamura H (1994) Preparation method of highly-purified antibodies from antisera by using polyvinylidene difluoride membrane. Application to fatty acid binding protein in rat liver. Biochem Mol Biol Int 34: 409–417. pmid:7849652
  33. 33. Schäfer A, Tauch A, Jäger W, Kalinowski J, Thierbach G, et al. (1994) Small mobilizable multi-purpose cloning vectors derived from the Escherichia coli plasmids pK18 and pK19: selection of defined deletions in the chromosome of Corynebacterium glutamicum. Gene 145: 69–73. pmid:8045426
  34. 34. Daniel Gietz R, Woods RA (2002) Transformation of yeast by lithium acetate/single-stranded carrier DNA/polyethylene glycol method. Methods Enzymol 350: 87–96. pmid:12073338
  35. 35. Vaghchhipawala Z, Rojas C, Senthil-Kumar M, Mysore K (2011) Agroinoculation and agroinfiltration: simple tools for complex gene function analyses. Methods Mol Biol 678: 65–76. pmid:20931373
  36. 36. Anders S, Huber W (2010) Differential expression analysis for sequence count data. Genome Bio 11: R106.
  37. 37. Lu H (2009) Dissection of salicylic acid-mediated defense signaling networks. Plant Signal Behav 4: 713–717. pmid:19820324
  38. 38. Cheong MS, Park HC, Hong MJ, Lee J, Choi W, et al. (2009) Specific domain structures control abscisic acid-, salicylic acid-, and stress-mediated SIZ1 phenotypes. Plant Physiol 151: 1930–1942. pmid:19837819
  39. 39. Duek PD, Elmer MV, van Oosten VR, Fankhauser C (2004) The degradation of HFR1, a putative bHLH class transcription factor involved in light signaling, is regulated by phosphorylation and requires COP1. Curr Biology 14: 2296–2301.
  40. 40. Yang J, Lin R, Sullivan J, Hoecker U, Liu B, et al. (2005) Light regulates COP1-mediated degradation of HFR1, a transcription factor essential for light signaling in Arabidopsis. Plant Cell 17: 804–821. pmid:15705947
  41. 41. Jang IC, Niu QW, Deng S, Zhao P, Chua NH (2012) Enhancing protein stability with retained biological function in transgenic plants. Plant J 72: 345–354. pmid:22631228
  42. 42. Perdomo J, Verger A, Turner J, Crossley M (2005) Role for SUMO modification in facilitating transcriptional repression by BKLF. Mol Cell Biol 25: 1549–1559. pmid:15684403
  43. 43. Lin DY, Huang YS, Jeng JC, Kuo HY, Chang CC, et al.(2006) Role of SUMO-interacting motif in Daxx SUMO modification, subnuclear localization, and repression of sumoylated transcription factors. Mol Cell 24: 341–354. pmid:17081986
  44. 44. Wang Y, Rao VK, Kok WK, Roy DN, Sethi S, et al. (2012) SUMO modification of Stra13 is required for repression of cyclin D1 expression and cellular growth arrest. PLoS ONE 7: e43137. pmid:22905217
  45. 45. Kim M, Chen Z, Shim M, Lee M, Kim J, et al. (2013) SUMO modification of NZFP mediates transcriptional repression through TBP binding. Mol Cell 35: 70–78.
  46. 46. Rohira AD, Chen CY, Allen JR, Johnson DL (2013) Covalent SUMO modification of Maf1 controls RNA polymerase III-dependent transcription repression. J Biol Chem 288: 19288–19295. pmid:23673667
  47. 47. Tan L, Rong W, Luo H, Chen Y, He C (2014) The Xanthomonas campestris effector protein XopDXcc8004 triggers plant disease tolerance by targeting DELLA proteins. New Phytol 204: 595–608. pmid:25040905
  48. 48. Deslandes L, Rivas S (2012) Catch me if you can: bacterial effectors and plant targets. Trends Plant Sci 17: 644–655. pmid:22796464
  49. 49. Xin XF, He SY (2013) Pseudomonas syringae pv. tomato DC3000: a model pathogen for probing disease susceptibility and hormone signaling in plants. Annu Rev Phytopathol 51: 473–498. pmid:23725467