Response of an aspartic protease gene OsAP77 to fungal, bacterial and viral infections in rice
© Alam et al.; licensee springer. 2014
Received: 8 December 2013
Accepted: 13 May 2014
Published: 27 August 2014
Aspartic protease (APs) plays important roles in plant growth, development and biotic and abiotic stresses. We previously reported that the expression of a rice AP gene (OsAP77, Os10g0537800) was induced by probenazole (PBZ), a chemical inducer of disease resistance. In this study we examined some characteristics of this gene in response to fungal, bacterial and viral pathogens.
To elucidate the spatial and temporal expression of OsAP77, the chimeric gene was constructed carrying the structural gene encoding β-glucuronidase (GUS) driven by the OsAP77 promoter. This construct was introduced into rice and the transgenic lines were tested to analyze gene expression by fungal, bacterial and viral infections. Inoculation with Magnaporthe oryzae or Xanthomonas oryzae pv. oryzae revealed the enhanced GUS activities in vascular tissues surrounding the symptom sites by each pathogen. Moreover, GUS activity also increased after inoculation with Cucumber mosaic virus (CMV). Transgenic plants immersed in a solution containing salicylic acid (SA), isonicotinic acid (INA), hydrogen peroxide (H2O2) or abscisic acid (ABA) showed an increased level of GUS activity exclusively in vascular tissues. RT-PCR analysis showed that OsAP77 was induced not only by infection with these pathogens, but also after treatment with SA, INA, H2O2 or ABA. A knockout mutant line of OsAP77 by the insertion of Tos17 after inoculation with M. oryzae, X. oryzae pv. oryzae or CMV showed an enhanced susceptibility compared to wild type.
These results suggest that the expression of OsAP77 is induced by pathogen infection and defense related signaling molecules in a vascular tissue specific manner and that this gene has a positive role of defense response against fungal, bacterial and viral infections.
KeywordsAspartic protease Rice Magnaprthe oryzae Xanthomonas oryzae pv. oryzae Cucumber mosaic virus Tos17 mutant Probenazole Salicylic acid Hydrogen peroxide Abscisic acidv
Probenazole (PBZ) is a well-known chemical inducer of plant disease resistance (Watanabe et al. ) and has been used to protect rice from blast disease for more than three decades in Japan. A previous study was carried out to elucidate the gene expression profiles of PBZ-treated rice plants (Shimono et al. ). Aspartic protease 77 (OsAP77, Os10g0537800, accession number AK061277) is a PBZ-inducible gene. Shimono et al. () found that OsAP77 induced by 10 fold with the microarray analysis after PBZ treatment (S02370) although it was under the detection level by northern blot analysis. OsAP77, Os10g39260.1, is composed of 395 amino acids (aas) and has a conserved domain of aspartic peptidase (49–390 aas).
Aspartic proteases (APs) are widely distributed in all living organisms, constituting one of the four super families of proteolytic enzymes (Rawlings and Barrett ). APs are expressed in different plant organs, such as seed, grain, tuber, leaf, flower, petal, root and pollen, as well as in the digestive fluids of carnivorous plants (Chen et al. ). Plant APs play versatile roles in protein processing and degradation in different plant organs, as well as in plant senescence, stress response, programmed cell death and reproduction (Simoes and Faro ). Xia et al. () reported that CDR1 (At5g33340) in Arabidopsis encodes an AP with a function in bacterial disease resistance. More recently the overexpression of the rice ortholog (OsCDR1/OsAP5, Os01g08330) has been reported to induce resistance against fungal and bacterial infections in Arabidopsis and rice (Prasad et al. ). Chen et al. () identified the total number of 96 AP genes in rice and showed the expression data for most of them. However, those of both OsCDR1/OsAP5 and OsAP77 were not shown in their list because it includes only OsAPs of which the expression was detectable in their test. Both APs have signal peptide and a protease motif but are different in active sites: presence/absence in OsCDR1/OsAP77, respectively (Chen et al. ).
Plants are exposed regularly to various environmental stresses including biotic stress caused by a wide range of plant pathogens, such as fungi, bacteria and viruses. However, to our knowledge, there is no report of OsAP77 in response to plant pathogens. Because of the expression of OsAP77 was induced by PBZ (Shimono et al. ), it would be reasonable to expect that the OsAP77 gene is involved in plant defense against pathogens. As a first step to elucidate the role of OsAP77 gene in disease defense its promoter was analyzed using β-glucuronidase (GUS) reporter gene system. Transgenic rice plants expressing GUS under the control of OsAP77 promoter were generated and used to analyze the spatial patterns of GUS expression in those plants post fungal, bacterial or viral infection and by treatments with some defense related signaling molecules. Treatments include: 1) infection with blast fungus (Magnaporthe oryzae), leaf blight bacterium (Xanthomonas oryzae pv. oryzae) or Cucumber mosaic virus (CMV) and 2) treatment with salicylic acid (SA), isonicotinic acid (INA), hydrogen peroxide (H2O2) and abscisic acid (ABA). These molecules have previously been used for analysis of abiotic stress (Liu et al. ).
An endogenous retrotransposon Tos17 has been revealed to be an efficient tool for the functional analysis of rice genes (Hirochika ). The rice mutant lines with the insertion of Tos17 have become a potent tool for practical use in the systematic analysis of gene function (Kumar and Hirochika ). We used OsAP77 mutant line disrupted by the insertion of Tos17 for examining the effect of knockout of OsAP77. In this paper we present the GUS activity in vascular tissues of the leaves and the induced expression of OsAP77 by M. oryzae, X. oryzae pv. oryzae, and several signaling molecules and an enhanced susceptibility of OsAP77 knockout mutant line to the pathogens.
Characterization of putative cis-acting elements in the 5′-flanking region of OsAP77
PCR primers used in this study
PCR analysis and GUS staining for selection of transgenic lines
Analysis of OsAP77::GUS -transgenic rice plants by genomic PCR and GUS staining
Plants tested (T2 generation)
Plants stained blue
Expression of GUS in leaves and roots in 4 week-old plants
To analyze the tissue-specific expression driven by the OsAP77 promoter, GUS expression was examined in the leaves and roots of 4 week-old transgenic T3 plants (Additional file 3). The plants were maintained in the growth chamber. In mature plants at the 1-month-old stage, GUS activity was found in the vascular tissue, but not in mesophyll cells, epidermal cells or guard cells (Additional file 3). These findings show that the promoter is responsible for the precise transcriptional regulation that determines the tissue-specific of the gene in the leaves and roots.
Induction of OsAP77 gene expression by probenazole (PBZ)
To confirm whether OsAP77 is induced in leaves by PBZ, 12-day-old rice plants were treated with PBZ and GUS gene expression was examined. OsAP77::GUS expression increased gradually, reached a plateau at 3–5 days and decreased after PBZ treatment. GUS expression was observed only in vascular tissues (Additional file 4).
Expression of OsAP77 under biotic stress
OsAP77::GUS expression levels appeared to increase in response to X. oryzae pv. oryzae and wounding with symptoms (Figure 2C and D), which was confirmed by in vitro assay of GUS activity (Additional file 5B), suggesting that the expression of OsAP77 has roles in the defense response to bacterial leaf blight (BLB). Increased GUS activity was detected around the BLB symptom sites as well as the wounding sites (Figure 2C). As shown in Figure 2C, GUS activity was restricted to the vascular tissues around the wounded area, but not in the mesophyll cells, guard cells, epidermal cells and vascular tissues in the BLB and wounded areas. These findings indicate that OsAP77::GUS expression is induced specifically in the vascular tissues in the vicinity of the BLB at this stage of growth.
Expression of OsAP77 in response to defense related signaling molecules
RT-PCR analysis of OsAP77 expression by pathogen infections and defense related signaling molecules
Enhanced susceptibility to M oryzae, X oryzae pv oryzae or CMV infection in OsAP77 knockout mutant plants
In this paper we analyzed the special expression pattern of OsAP77 using GUS reporter gene and the function in defense response using its knockout mutant rice. We previously reported that OsAP77 was PBZ inducible by the microarray analysis (Shimono et al. ). We postulated that this gene might be involved in the defense response against pathogens because PBZ is a chemical inducer of disease resistance (Watanabe et al. ). We took approaches first to analyze OsAP77 gene expression. Thus we produced the transgenic rice carrying GUS reporter gene under the control of OsAP77 promoter (Figure 1A) and then examined it under various conditions.
In the mature leaves of 1-month-old plants, OsAP77::GUS was expressed in the vascular tissues, but not in other tissues (Additional file 3B), which is why it was under the detection level by northern blot analysis, but was expressed 10-folds higher by microarray analysis after PBZ treatment (Shimono et al. ). In the roots, OsAP77::GUS expression was restricted to the vascular tissues of the primary and lateral roots (maturation zone). The plant vascular system includes phloem tissues that transport organic materials and xylem cells that transport water and soil derived nutrients. The detection of cis-elements of promoters distinct for vascular tissues may provide a functional approach to illuminate these mechanisms (Yin et al. ). The GATA motifs, ASL box (GCATC) and box-II (CCCCT) are present in many promoter regions and described as vascular tissue-specific elements (Yin et al. ; Hatton et al. ). These cis-acting regulatory elements responding to vascular tissue specific expression (VTREs) were also found in the 5′-flanking region of OsAP77. Therefore, OsAP77::GUS may be involved in regulating vascular development and function in roots and leaves (Additional file 1 and Additional file 2).
Since OsAP77 can be induced by PBZ, SA, INA, H2O2 or ABA, which play important roles in signal defense responses, it is expected that OsAP77 is also responsive to pathogen infection. The expression of OsAP77::GUS was examined under biotic stresses, such as fungal, bacterial or viral infection. It was found that expression of OsAP77::GUS as well as OsAP77 was induced with the fungus, M. oryzae, and the bacterium, X. oryzae pv. oryzae (Figure 2A,B and C). In response to wounding stress, OsAP77::GUS exhibited expression patterns parallel to but a little weaker than those induced by M. oryzae or X. oryzae pv. oryzae infection (Figure 2A,B and C). Wounding caused extensive changes in the synthesis of defense proteins, leading to localized resistance at the site of the lesion (McConn et al. ). These observations support the hypothesis that the differential expression of OsAP77::GUS indicates the presence of different defense mechanisms in a tissue- and organ-specific manner.
We previously found that CMV-SRO could infect rice without any significant symptoms (Chen et al. ). CMV-SRO is a pseudorecombinant containing CMV-SR RNA1 and 2 and CMV-O RNA3 (Hanada and Tochihara ). Here we present that CMV infection caused the induction of OsAP77::GUS expression (Figure 3A). Since in rice there are few virus species which are easy to inoculate manually, this CMV isolate may be very important in studying molecular interaction between rice and viruses as a model system.
Plant hormones such as ABA, JA, ethylene and SA are essential components of different signaling pathways involved in plant defense (Hu et al. ; Vicent and Plasencia ). The expression pattern of OsAP77 was analyzed after pathogen infections and the treatment by some defense related signaling molecules. We found that OsAP77 can be induced by SA, INA, H2O2 or ABA but not by MeJA (Figure 4 and Figure 5). SA plays an important role against pathogens, some insect pests and abiotic stress, while JA does mostly for the defense against insect pests and some pathogens (Vicent and Plasencia ; War et al. ). SA and JA/ET defense pathways interact antagonistically, but emerging records suggest a more complex signaling network inducing both positive and negative interactions (Loake and Grant ). In our study, SA, not MeJA could mediate the up-regulation of OsAP77::GUS and endogenous OsAP77 in rice. Thus this gene may participate in SA pathway in rice. It seems unlikely that the induction of OsAP77::GUS expression by pathogen infections is caused by an increased level of SA by pathogen. Although there are some data of this gene in response to six plant hormones including ABA and JA (http://ricexpro.dna.affrc.go.jp/GGEP/), however, it is not clear which plant hormone(s) induced the gene expression. Besides that, there is no data available on vascular tissue specific expression of this gene in rice leaves. There are also no expression data of this gene in the comprehensive list by Chen et al. (). Our data is the first to clearly show the induced expression of this gene in vascular tissues of leaves by pathogen infections and defense related signaling molecules.
Reactive oxygen species (ROS) play a main role in crosstalk between biotic and abiotic stress responses (Fujita et al. ). Plants produce antioxidants and ROS-scavenging enzymes to control the damage made by harmful molecules (Apel and Hirt ). Pathogen spreading is inhibited by hypersensitive response and cell death requiring coordinated down regulation of ROS-scavenging mechanisms (Apel and Hirt ). H2O2 is thought to be produced through membrane-bound NADPH oxidases on pathogen infection or wounding, then diffuses into cells and activates various plant defenses (Apel and Hirt ). Furthermore, ROS production is required for ABA-driven stomatal closure, which is closely related to stomatal penetration resistance (Robert-Seilaniantz et al. ). ABA largely regulated abiotic stress, while defense against different biotic stress is specified by antagonism between the SA and JA/ethylene signalling pathways. ABA acts both synergistically and antagonistically with biotic stress signalling, creating a complex network of interacting pathways with cross-talk at different levels (Fujita et al. ; Yasuda et al. ). In our study, H2O2 was found to induce OsAP77 expression. However, in our observation SA and ABA both can up-regulated expression of OsAP77::GUS and OsAP77.
The experiments with the knockout mutant line of OsAP77 showed that the most severe symptoms by M. oryzae and X. oryzae pv. oryzae was observed in OsAP77 (−/−) compared to those in OsAP77 (+/+) (Figure 6). These results showed that OsAP77 participates in the defense reaction against M. oryzae and X. oryzae pv. oryzae. In the OsAP77 mutant line, Tos17 is inserted in the upstream region (−560) of OsAP77. This is the case where the insertion of Tos17 in the upstream of a gene caused the repression of downstream gene expression.
It is not known how OsAP77 functions for pathogen infections in vascular tissues. Arabidopsis CDR1 which was up-regulated by SA, has a signal peptide (1–25 aas) from the N-terminal portion, is extracellular AP and accumulates in the intercellular fluid (Xia et al. ). Actually OsAP77 is postulated to have a signal peptide 1–20 aas based on the method of Signal PHMM. The role of CDR1 in defense is suggested to degrade its target proteins/peptides for generation of an extracellular peptide elicitor, which may function as a mobile signal for defense response (Xia et al. ). From this point of view, most plausible scenario for the vascular tissue expression of OsAP77 may be that OsAP77 accumulates in the extracellular space, sieve-tubes, where host proteins may be present, and functions as protease for processing possible target proteins/peptides into a signal peptide(s). Then this signal molecule may spread through sieve tube to activate host defense response systemically. It remains to determine whether OsAP77 are accumulated in sieve tubes and what are the proteins/peptides targeted for degradation by OsAP77.
Chen et al. () reported 96 rice AP genes in rice genome and their expression data in different tissues and under various conditions. However, it includes no expression data on OsAP77 and others including OsCDR1/OsAP5 because their data was from OsAPs, of which the gene expression was detectable in their test (Chen et al. ). OsAP77 is similar to OsCDR1/OsAP5 in that both have signal peptide at the N terminus and protease dmotif and only difference is the presence/absence of active sites in that motif for OsCDR1/OsAP5 and OsAP77, respectively (Chen et al. ). OsCDR1/OsAP5 would be also expressed in vascular tissues because it has signal peptide as OsAP77 does. Bi et al. () reported three rice APs, OsAsp1, OsAsp2 and OsAsp3. OsAsp1 were most abundantly present in early embryo. OsAsp2 appeared in leaf, callus and immature seeds while OsAsp3 did in leaf, stem and phloem. However they never mentioned any functional involvement in the response to biotic stress. OsAP77::GUS was expressed mainly in pollen, vascular tissue of leaf and root meristem (Additional file 3). Thus it would be possible that OsAP77 has any other function. Recently OsAP25 and OsAP37 have been reported to be involved in programmed cell death for development of embryo (Niu et al. ).
To our knowledge, this is the first report on the expression of OsAP77 induced by fungal, bacterial and viral infections as well as after the treatment with SA, INA, H2O2, ABA or wounding and the involvement of this gene in defense reaction. The data from our study implicate the importance of comparative analysis in identifying the expression of OsAP77::GUS in each tissue and cell type as well as in response to different stresses in order to understand the complexity underlying multiple signaling systems. From this point of view, it is significant and relevant to characterize the transgenic rice over-expressing the OsAP77.
To conclude, this study has shown the role of OsAP77 in defense response to fungal, bacterial and viral infections.
Plasmid constructs and rice transformation
To generate OsAP77::GUS chimeric gene, which contains the GUS reporter gene under the control of the 5′-flanking region of OsAP77, the OsAP77 promoter region was isolated using a pair of gene-specific primers designated AP77 pro-5′ and AP77 pro-3′ (Table 1) that carry the extra sequences for Sbf I and Xba I recognition sites, respectively. The OsAP77 promoter fragment was amplified by PCR with a DNA polymerase (KOD -Plus-, Toyobo, Osaka, Japan), and the genomic DNA from (O. sativa cv. Nipponbare) as a template. The fragment with the accurate sequence for OsAP77 promoter was then digested with Sbf I and Xba I and cloned into to a binary vector pSMAHdN627-M2GUS (Hakata et al. ) treated with the same restriction enzymes followed by dephosphorylation (Figure 1). The resulting construct was introduced into Agrobacterium tumefaciens strain EHA101 (Hood et al. ) and used to transform rice (O. sativa cv. Nipponbare) as described in Toki et al. (). Putative transformants were selected on a series of selection media supplemented with 30 mg/L hygromycin B (hyg). The integration of the expression cassettes in the plant genome was confirmed by PCR using primers (Table 1) directed against the OsAP77 promoter (AP77 pro-5′ and AP77 pro-3′) and GUS region (∆GUS-5′ and ∆GUS-3′). T1, T2, and T3 progenies were used in the subsequent observation, and analyses. The PlantCARE database (http://bioinformatics.psb.ugent.be/webtools/plantcare/html/) was used for the silico identification of the putative cis-acting elements in the 5′-flanking region.
Wild type rice (O. sativa cv. Nipponbare) and the transgenic lines were used in this study. OsAP77 mutant line (NC2562) was obtained from National Institute of Agrobiological Sciences (NIAS, https://tos.nias.affrc.go.jp/~miyao/pub/tos17/). The mutant line by the insertion of Tos17 was selected based on the nucleotide sequence of OsAP77 as a query as described previously (Chen et al. ) and grown in a growth chamber under the conditions at 25°C, 14/8 hr light and dark. In this mutant line Tos17 is inserted in the upstream region at −560 of OsAP77. Asominori and Sensyo, which are resistant to X. oryzae pv. oryzae and M. oryzae respectively, were gifted by Drs. H. Ochiai and M. Mori at NIAS, respectively. Rice seeds on the MS agar medium with/without hygromycin (30 μg/ml) were incubated in a Petri dish at 27°C under a daily cycle of 16 h continuous light and 8 h dark. One week later the seedlings were transferred to small plastic boxes containing commercial soil for rice cultivation (Iseki, Matsuyama, Japan) and placed in growth chambers where the temperature ranged between 23 and 26°C under 16 h daylight and 8 h dark conditions. Approximately three weeks later the plants were transferred to buckets containing the soil in the growth chambers.
Histochemical GUS-staining assay
Histochemical GUS staining was performed as previously described by Jefferson (). For testing the expression level of GUS in leaves, fully expanded 4th leaf of each seedling at four-leaf stage was used. Flowers, seeds and roots were directly placed in a 1.5 ml microtube. When fungal or bacterial infection occurred, the infected areas of leaves were cut out after the disease symptoms appeared. The samples were then briefly subjected to vacuum infiltration and kept at 37°C overnight. The samples were treated with fresh 70% ethanol several times, if necessary, until the plant tissues were mostly decolored. Some of the samples were cut into 30-μm thick cross-sections using a microtome (Retoratome REM-710, Yamato Kohki Industrial, Asaka, Saitama, Japan) and observed under a microscope (Labphoto-2, Nikon, Tokyo, Japan). Samples were collected from three transgenic plants (T3 progenies of 2A) for each line and only the representative one was shown in Figure.
DNA extraction and PCR amplification
DNA was extracted from rice leaves by cetyltrimethyl ammonium bromide-based (CTAB-based) extraction procedure (Doyle and Doyle ). Quantity and purity of DNA was measured using a spectrophotometer (GeneSpec I, Hitachi High-Technologies Corporation, Tokyo, Japan). Integration of the expression cassette in the transgenic genome was confirmed by PCR with a pair of primers directed against the OsAP77 promoter (AP77 pro-5′ and AP77 pro-3′) and GUS-coding region (∆GUS-5′ and ∆GUS-3′) (Table 1). Genomic DNA (100 ng) from each transgenic line was used as template. pBI221 vector (Jefferson ) was used as a template DNA for positive control with the GUS-specific primers (Table 1). The PCR reaction was for 2 min of 94°C preheating, followed by a 30 cycle amplification program (1 min at 94°C for denaturation, 1 min at 58°C for annealing, and 1 min at 72°C for extension) and a final extension at 72°C for 5 min. The PCR products were analyzed by electrophoresis on a 1.0% agarose gel followed by staining with ethidium bromide.
Strains of blast fungus M. oryzae, virulent race 001, virMo (MAFF #238988) and avirulent race 102.0, avrMo (MAFF #238991), were obtained from NIAS Genebank, (http://www.gene.affrc.go.jp/index_en.php). The fungal culture and fungal inoculation of rice were carried out essentially as described previously (Shimono et al. ) with slight modifications. A disk of M. oryzae was put in the centre of an oatmeal agar medium and incubated in darkness in a growth chamber at 25°C for 15 days. For spore induction, the M. oryzae culture was kept under the continuous illumination for 2–5 days. The spores were used at the concentration of 2 × 105 conidia/ml (Shimono et al. ). Detached rice leaves were wounded using needles and a droplet of conidia suspension (2 × 105 conidia/ml) containing 0.05% Tween 20 was applied to the leaf covering the wounded portion (Wang et al. ). The inoculated leaves were incubated under high humid conditions in darkness for 24 h and then transferred to the dark growth chamber at 25°C. Under such conditions, lesions were induced on the leaves. At 0, 1, 3, 5 and 7 days after inoculation, the leaf samples were used for GUS staining as well as for total RNA extraction followed by RT-PCR analysis.
A suspension (500 μl) of X. oryzae pv. oryzae strain 001 (MAFF #311018, NIAS Gene Bank) was spread on a peptone agar medium and then cultured in darkness in chamber at 28°C for 48 h. The bacteria were collected by adding sterilized ultrapure water and the concentration of bacteria was adjusted to 0.3 OD at 600 nm. For inoculation of rice with X. oryzae pv. oryzae, rice leaves were wounded with a needle and the wounded regions were immersed in the bacterial suspension. Additionally, a bacterial suspension (20 μl) containing 0.05% Tween 20 was placed the wounded regions of the leaf surfaces. After inoculation, the samples were kept in a growth chamber at 28°C. After 5 days, 50% of the leaf area was covered with bacterial leaf blight symptoms. The samples were then used for GUS staining and RT-PCR.
Quantitative assay of GUS activity
GUS activity was measured by observing cleavage of the β-glucuronidase substrate 4-methylumbelliferyl β-D-glucuronide (MUG) (Sigma, USA; Jefferson ; Gallagher ). Samples (100 mg) of mock, AvrMo, VirMo and VirXoo infected leaves at different pti were frozen in liquid nitrogen and homogenized for 15 sec. GUS extraction buffer [100 mM potassium phosphate pH 7.8, 1 mM EDTA, 1% Triton X-100, 10% glycerol] (1 ml) was added and mixed by vortex for 10 sec. Centrifuge at 14000 rpm for 10 min at room temperature and the supernatant for each sample (600 μl) was collected and kept on ice for use in MUG assays and for protein quantification. Sample extract (10 μl) was mixed with 400 μl assay buffer (GUS extraction buffer containing 3.2 mM MUG) and incubated in a dark at 37°C. After 60 minutes 590 μl stop buffer (200 mM sodium carbonate) was transferred to the tube. Fluorescence was measured on a RF-1500 Spectrofluorophotometer (Shimadzu Co. Ltd., Kyoto, Japan) at 465 nm when excited at 355 nm. Protein concentrations were determined by the method described by Bradford ().
Data were subjected to software package used for statistical analysis (SPSS version 16, 2007) and significant differences between individual means established using a Student’s t test. Differences at the 5% level were considered significant and denoted by asterisk among different groups.
Purified CMV-SRO strain (MAFF #104016, NIAS GeneBank) was used as an inoculum because this isolate had been found to infect rice plants (Chen et al. ). The 4th leaves of the 4-week-old seedlings were inoculated with a suspension of virus (10 μg/ml in 10 mM sodium phosphate buffer, pH 7.0) after spreading of Carborundum (600 mesh, Nacalai Tesque Co. Ltd., Kyoto, Japan) on their adaxial surfaces. The leaves were collected from the inoculated plants up to 7 days after inoculation and total RNA extraction followed by RT-PCR analysis using a pair of primers CMV-R3-cDNA-F-5′ and CMV-R3-cDNA-R-3′ (Table 1). PCR program was at 94°C for 2 min, followed by 30 or 35 cycles of amplification (94°C for 45 s, 60°C for 45 s and 72°C for 45 s) followed by the final extension at 72°C for 5 min.
Treatments by defense related signaling molecules
Twelve-day-old rice seedlings were submerged in water containing 1.0 g/l Oryzemate (24% granules of PBZ) (Meji Seika Pharma, Tokyo, Japan). After 7 days of treatment with Oryzemate, the youngest leaf was used for GUS staining (Shimono et al. ). Rice seedlings at 4-leaf stage were dipped in 3 ml each of solutions containing 10 mM SA, 5 mM INA, 20 mM H2O2, 10 mM ABA 10 mM MeJA and incubated for 72 h in the growth chamber following the procedure of Mitsuhara et al. () with a slight modification. SA was dissolved in sterilized water, while INA was first dissolved in dimethyl sulfoxide (DMSO) and then diluted appropriately with ultrapure water. H2O2, ABA and MeJA were first dissolved in 99.5% ethanol and then diluted appropriately with ultrapure water, respectively.
Extraction of total RNA and expression analysis
Total RNA was extracted from flowers, panicles, leaf blades, leaf sheaths and roots of rice plants using TRI reagents kit (Molecular Research Center, Cincinnati, Oh, USA) according to the supplier’s protocol with some modifications. RT-PCR was performed using RNAs isolated from the above-mentioned tissues. Total RNA was treated with RNase-free DNase I (Takara Bio, Ohtsu, Japan) for 30 min at 37°C to remove genomic DNA, and then the cDNA was synthesized from 1 μg of total RNA by using RevertAid reverse transcriptase (Thermo Fisher Scientific, Waltham, MA, USA). A pair of primers, OsAP-5′ and OsAP-3′ (Table 1), was used to amplify a cDNA fragment of OsAP77. The amplification was performed at 94°C for 5 min, followed by 30 cycles of amplification (94°C for 1 min, 60°C for 1 min, and 72°C for 72 s). Actin transcript was used as internal standard using primers: Actin-5′ and Actin-3′ (Table 1). The RT-PCR experiments were done at least three times.
Abscisic acid responsive elements
Bacterial leaf blight
Cucumber mosaic virus
Vascular tissue-responsive elements
Wounding- and pathogen-responsive elements
The authors are grateful to Drs. I. Mitsuhara, M. Mori and H. Ochiai for the seeds of transgenic rice carrying GUS driven by 35S promoter of cauliflower mosaic virus, Sensyo and Asominori, respectively. They also thank M. Kajikawa, S. Ando and Dr. N. Endo-Higashi for their technical assistance on plasmid construction and production of transgenic rice plants. They are also grateful for D. Murphy for English correction. This work was supported by the Program for Promotion of Basic and Applied Researches in Bio-oriented Industry (BRAIN), the Ministry of Education, Culture, Sports and Technology of Japan [Grant-in-Aid for Scientific Research for Scientific Research (C), No. 22119010] to MN and by grants from the Ministry of Agriculture, Forestry and Fisheries of Japan (Rice Genome Project to MN; Green Technology Project EF-1001 and EF-1004 to HI).
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