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Effects of MeJA on Arabidopsis metabolome under endogenous JA deficiency

Scientific Reports volume 6, Article number: 37674 (2016) | Download Citation

Abstract

Jasmonates (JAs) play important roles in plant growth, development and defense. Comprehensive metabolomics profiling of plants under JA treatment provides insights into the interaction and regulation network of plant hormones. Here we applied high resolution mass spectrometry based metabolomics approach on Arabidopsis wild type and JA synthesis deficiency mutant opr3. The effects of exogenous MeJA treatment on the metabolites of opr3 were investigated. More than 10000 ion signals were detected and more than 2000 signals showed significant variation in different genotypes and treatment groups. Multivariate statistic analyses (PCA and PLS-DA) were performed and a differential compound library containing 174 metabolites with high resolution precursor ion-product ions pairs was obtained. Classification and pathway analysis of 109 identified compounds in this library showed that glucosinolates and tryptophan metabolism, amino acids and small peptides metabolism, lipid metabolism, especially fatty acyls metabolism, were impacted by endogenous JA deficiency and exogenous MeJA treatment. These results were further verified by quantitative reverse transcription PCR (RT-qPCR) analysis of 21 related genes involved in the metabolism of glucosinolates, tryptophan and α-linolenic acid pathways. The results would greatly enhance our understanding of the biological functions of JA.

Introduction

Metabolomics utilizes high-throughput methods, such as high resolution mass spectrometry and nuclear magnetic resonance to obtain comprehensive information of metabolites in a given biological system1. UPLC-HRMS has been regarded as one of the most promising tools for metabolic profiling with improved accuracy and resolution2,3,4. Metabolomics have been widely used in biology study, especially in the field of biomedical research5,6,7. Plant metabolomics combined with other biology approaches were used to investigate gene function and biological processes. Large scale metabolomics profiling of plant materials can identify compounds involved in key metabolic pathways for plant growth and stress response, reveal correlation/interaction between metabolites from distinct metabolic pathways and construct a metabolite regulatory network. Chen et al. investigated the effects of drought stress on rice metabolome using MS2T based approach and found possible regulation coordination of abscisic acid (ABA) with serotonin derivatives and polyamine conjugates8. This study also found some C-glycosylated flavones as potential biomarkers for discrimination between two rice subspecies. Metabolomics was also used to illustrate the contrasting effects of metabolites on herbivore resistance in leaves and roots of maize upon attack by herbivores9.

Jasmonate acid (JA) is an important phytohormone, it regulates a wide variety of developmental processes and mediates the response to various environmental stresses in higher plants. JA plays essential roles in seed germination, flowering and fruit development, leaf abscission and senescence10,11. JA also regulates plant stress response such as insects, fungal pathogens, UV radiation, ozone and other biotic or abiotic stresses12,13,14,15,16,17. The biosynthesis of JA starts with the conversion of linolenate to 12-oxo-phytodienoate (OPDA) in the chloroplast. OPDA is then transported into peroxisome where it is reduced by OPDA reductase18 through three cycles of β-oxidation19 to produce JA. JA can be reversibly esterified by JMT (JA-methyl transferase) to MeJA20 and can be conjugated to amino acids by JAR121 in cytoplasm. Exogenous stimuli induce rapid accumulation of JA in plants and subsequently induce the expression of a number of JA regulated genes.

Mutants in JA synthesis and signaling pathways were used to study the mechanism of JA synthesis as well as the roles of JA in plants22,23,24. These studies focused on phenotypic and molecular features, while at the metabolites level, only a few metabolites such as OPC:8, OPDA, JA, MeJA and JA-Ile25,26,27 were quantified. This is far from enough, as plant metabolites are end products of genes regulation that reflect the real physiological condition within the plant. It has already been demonstrated that plant secondary metabolites, especially plant hormones have an intricate interaction network. Environmental stresses or the application of exogenous hormones can trigger a cascade of responses of different types of plant hormones28,29,30. Comprehensive profiling of plant metabolites of various mutants or under different physiological/stress conditions can provide a perspective view of the plant and provide insights into the interaction and regulation network of plant metabolites.

Most mutants defective in JA synthesis, reception or signaling, such as aos, dad1, opr3, coi1, myb21 and myb21 myb24, are male-sterile due to defects in late stamen development22,23,24,31. This phenotype can be rescued efficiently by exogenous MeJA application in JA-deficit mutant opr3. The opr3 mutant, defective in OPR3 expression, shows dwarf and male-sterile phenotype with insufficient anther filaments elongation, unseasonal anther locule dehiscence and inefficient pollen maturation32. OPR3 encodes OPDA Reductase 3 (OPR3), the key enzyme catalyzing the conversion of OPDA to OPC-8:0 in JA biosynthesis. There are other OPR enzymes in Arabidopsis (OPR1 and OPR2) but the efficiency is not up to the level of OPR326. OPR3 co-localizes with the enzymes of β-oxidation in peroxisomes, which catalyze the final steps in the formation of JA33. In opr3 mutant, OPR3 transcript and JA synthesis were absent in both reproductive and vegetative tissues, but resistance to fungal infection and insect attack retained. Wound induced genes previously known to be JA-dependent were still induced in opr3 plants, thus, other octadecanoid-derived molecular(s) may be effective for defense in plants in the absence of JA27. Although the core signaling transduction pathway and functions of JA are clarified, unsolved questions remain. How does exogenous MeJA restore the function of endogenous JA? Whether endogenous JA can be replaced by exogenous MeJA? How does JA regulate plant metabolites and crosstalk with other plant hormones? Comprehensive profiling of metabolites involved in JA functions and the establishment of plant hormones interaction network is essential for a better understanding of plant defense mechanism.

In the present study, we performed high throughput metabolic profiling to investigate the effects of JAs on Arabidopsis. The metabolomes of Arabidopsis wild type and opr3 were compared to study the effect of endogenous JA deficiency due to OPR3 mutation. In addition, opr3 plants treated with MeJA at various time points were used to study the effects of exogenous MeJA on plants. The knowledge about differential metabolites identified in wild type, opr3 and MeJA-treated opr3 plants helps us understand the functions of JA integrally and dynamically. We obtained a list of hundreds of non-redundant metabolites that exhibited significant variations. The biological functions and metabolic pathways of 109 annotated metabolites were examined. The expressions of 21 genes involved in the annotated metabolic pathways were validated by RT-qPCR. The results would greatly enhance our understanding of the biological functions of JA.

Results

Optimization of the extraction methods

Plant metabolites have diverse chemical and physical properties. In order to achieve maximum recovery of the metabolites, the sample extraction procedure needs to be optimized. The extract solvents, the ratio between sample and extract solvent, the duration and temperature of extraction all need to be considered34. Aqueous (water) and organic (MeOH/ACN) solvents were used in sequential at various sample/solution ratios to extract metabolites of different polarity (Supplementary Table S1).

With all extraction methods, a strong peak corresponding to polar compounds can be observed as the flow-through peak in the TIC (total ion chromatogram). When the sample to extract solvent ratio was 1:3 (W/V), that peak was the most intensive peak, while peaks corresponding to non-polar and mid-polar compounds showed very weak signal. A small improvement in TIC was observed after increasing the volume of extract solvent. The signal increased significantly after concentrating the extract solution by vacuum concentrator, while there exhibited no obvious difference between ultrasound and heating for extraction (Supplementary Fig. S1).

The numbers of detected peaks (intensity threshold, 5 × 106) were compared between different extraction methods. The peak number increased significantly after changing the ratio of sample to solvent from 1:3 to 1:15 (Supplementary Fig. S2, p = 4.10 × 10−7). Similarly, significant increase in peak number was observed after concentrating the sample by vacuum concentrator (p = 5.57 × 10−6). There was no significant change in the number of detected peaks between ultrasound and heating (p = 0.273). But, extraction method C had more peaks with higher intensities than extraction method D (Supplementary Fig. S2, insert, p = 0.00254). So, solvent extraction combined with ultrasound and vacuum concentration detected the highest number of peaks and was used for subsequent sample extraction. As shown in Supplementary Fig. S1, no contamination was introduced by this method.

Data preprocessing and statistical analysis

Extracts from Arabidopsis wild type, opr3 and opr3 plants treated with MeJA at various time points were analyzed with UPLC-HRMS using a C18 column in the positive ion mode. TIC from different genotypes and treatments were very similar visually, with a few exceptions at retention time 4.51 and 8.23 min (Supplementary Fig. S3). Raw MS data were analyzed with SIEVE software to extract mass spectrometric features, 12016 ion signals were detected (above the 5 × 105 peak intensity threshold). Most of the detected peaks (77.8%) have a coefficient of variation (CVs) equal or less than 20% in 10 replicates (Supplementary Fig. S4).

Principal component analysis (PCA) and hierarchical cluster analysis (HCA) of the 12016 ion signals were performed to reveal intrinsic difference within the signals (Fig. 1a,b and c). Both statistical methods revealed similar relationship between different genotype and treatment groups. PCA score plot showed that the two genotypes were mainly separated along PC1 (50.9%), while PC2 (18.0%) represented difference between opr3 after MeJA treatments. The long distance along PC1 between wild type and opr3 plants indicated there are major differences in the metabolome between these two genotypes. The opr3 migrated gradually along both PC1 and PC2 in the PCA score plot after MeJA treatment. After 8 h, opr3 moved from the forth quadrant to the second quadrant on the score plot, indicating MeJA treatment can greatly alter the composition of opr3 metabolome. The relative position between wild type and MeJA treated opr3 (8 h after treatment) indicated exogenous MeJA can bring some features back to a level comparable to the wild type, while at the same time, the content of other features changed in the opposite direction to that of wild type. HCA revealed that the samples were separated into two major clusters (Fig. 1c). The first cluster included opr3, opr3 treated with MeJA for 1 h, the second cluster included wild type and opr3 treated with MeJA for 4 and 8 h. Such phenomenon implied that exogenous application of MeJA may rescue at least part of the features disturbed by OPR3 deficiency in a time dependent manner.

Figure 1: Statistical analysis of normalized dataset.
Figure 1

(a) Score Plot, (b) Loading Plot of Principal component analysis (PCA) and (c) Hierarchical cluster analysis (HCA) using all of the 12016 ion signals. (d) S-plot of orthogonal partial least squares discriminant analysis (OPLS-DA) of wild type and opr3 leaf extracts. Compounds with a p value less than 0.05 and fold change higher than 2 are highlighted in red.

Orthogonal partial least squares discriminant analysis (OPLS-DA) was carried out to highlight differential features between genotypes wild type and opr3 (Fig. 1d). With filter conditions: CV < 20%, p value < 0.05 and fold change >2, we obtained a matrix containing 754 non-redundant differential mass spectrometric features as putative biomarkers, which were highlighted in red in the S-plot. Features affected by MeJA treatment in opr3 mutant were screened similarly and 1475 differential features were obtained.

Identification, classification and pathway analysis of differential compounds

JA regulates plant growth, development and reproduction as well as stress responses. Thus, a wide range of metabolites can be affected by OPR3 deficiency or MeJA treatment in opr3 plants. Further analysis was then focused on metabolites that showed significant variations between different genotype and treatment groups (p < 0.05 and fold change >2). Metabolite identification was performed with the help of accurate mass measurement of molecular ions and fragment ions with high resolution. Accurate mass, isotopic pattern and MS/MS spectra were searched against metabolite databases and theoretical fragmentations. It’s impossible to realize thorough and comprehensive metabolite identification due to the diversity of plant metabolites and the incompleteness of metabolite databases. Thus, we established a differential compound library containing 174 compounds with high signal intensity and signal to noise ratio (Supplementary Information Spreadsheet 1). The spreadsheet contains m/z, peak intensity, mass error, isotope similarity, MS/MS fragment ions and method used for metabolite identification. These compounds were affected either by the absence of endogenous JA or the application of exogenous MeJA. Accurate and high resolution precursor-product ions pairs combined with reproducible retention time in this library will help identification of the metabolites in the future.

Within the 174 differential metabolites, 109 compounds were identified (Supplementary Table S2). Metabolite identifications can be classified as level II according to MSI criteria based upon their spectral similarities with public/commercial spectral libraries35. These compounds included aliphatic and aromatic compounds, amino acids and peptides, carbohydrates and carbohydrate conjugates, organic acids and derivatives and lipids. Heat map analysis of the differential metabolites revealed 5 clusters (Fig. 2). The sequence numbers in Fig. 2 were corresponding to Supplementary Table S2. Cluster II contained almost all of the amino acids and small peptides. Several isothiocyanates, lipids and other compounds were also found in this cluster. These metabolites have higher abundances in opr3 than in wild type, MeJA treatment down-regulated some of the metabolites. Cluster V contained mainly lipids with a few other compounds. The abundances of these metabolites declined dramatically with endogenous JA deficiency, which can be rescued by exogenous MeJA treatment. Metabolites in these two clusters had opposite variation trends and may be the basis of remedy of endogenous JA deficiency by exogenous MeJA. Cluster III contained lipids and isothiocyanates while cluster IV contained aromatic compounds, glucosinolates and lipids. Metabolites in these two clusters had comparable abundances in wild type and opr3 plants, but dramatic changes were induced by the application of exogenous MeJA, resulting in either down-regulation (cluster III) or up-regulation (cluster IV) of the metabolites. So, these metabolites are regulated by exogenous MeJA application but not by endogenous JA deficiency. In summary, the functions of endogenous JA can be compensated partially, but not completely by exogenous MeJA at the metabolic level in a time-dependent manner, and endogenous JA cannot be completely replaced by exogenous MeJA.

Figure 2: Heat map analysis of the identified compound revealed 5 clusters according to their variation trends.
Figure 2

The sequence numbers were corresponding to Supplementary Table S2.

Pathway analysis was performed using MetaboAnalyst 3.0, which uses high-quality KEGG metabolic pathways as the backend knowledgebase36,37. Peak intensities of the identified compounds were normalized by sum, log transformed, Pareto scaled and factored into the pathway analysis (Supplementary Fig. S5). Ten most relevant metabolic pathways were identified by pathway enrichment and pathway topology analysis (Fig. 3 and Supplementary Table S3). Identified pathways include: arginine and proline metabolism, aminoacyl-tRNA biosynthesis, alpha-linolenic acid metabolism, tryptophan metabolism, glucosinolate biosynthesis, biosynthesis of unsaturated fatty acids, alanine, aspartate and glutamate metabolism, purine metabolism, pyrimidine metabolism and nitrogen metabolism.

Figure 3: Result of pathway analysis.
Figure 3

The p values were calculated from the enrichment analysis while the pathway impact values were calculated from pathway topology analysis.

Glucosinolates and tryptophan metabolism affected by OPR3 deficiency and MeJA treatment

Glucosinolates are important secondary metabolites mainly found in the Brassicaceae family. There are about 40 glucosinolates identified in Arabidopsis, mainly derived from methionine and tryptophan38. Glucosinolates can be hydrolyzed into isothiocyanates in the presence of myrosinase in response to abiotic stresses. Isothiocyanates are important for both plant defense and human nutrition39. We found several methionine derived aliphatic glucosinolates and related metabolites. Among them, 5 exhibited decreased levels in opr3 and no restoration was observed after MeJA treatment, 5 showed increased levels in opr3 and slightly declined after MeJA treatment (Fig. 4a).

Figure 4: Glucosinolates and tryptophan metabolism affected by OPR3 deficiency and MeJA treatment.
Figure 4

(a) Methionine derived glucosinolates metabolism, (b) tryptophan metabolism were influenced by OPR3 deficiency and MeJA treatment. Differential metabolites detected are labeled in red, fold changes compared to opr3 were displayed in the boxes.

1-Isothiocyanato-4-methylsulfinylbutane, 4-isothiocyanato-1-butene, 1-isothiocyanato-5-(methylsulfinyl) pentane, 5-isothiocyanato-1-pentene and 1-isothiocyanato-6-(methylsulfinyl) hexane have significantly lower abundances in opr3. MeJA treatment resulted in further decrease of these compounds during the first 4 h of treatment and slight recovery was observed after 8 h (Fig. 4a). 1-Isothiocyanato-4-methylsulfinylbutane, a natural product derived from aliphatic glucosinolates, reduces damage by herbivores and inhibits growth of non-host pseudomonas bacteria in Arabidopsis40. 4-isothiocyanato-1-butene and 5-isothiocyanato-1-pentene display potent antibacterial activity against A. hydrophila41. 1-isothiocyanato-5-(methylsulfinyl)pentane is a 1-isothiocyanato-4-methylsulfinylbutane analog which exhibits potent anti-inflammatory properties42. The variation of these metabolites implied that the antibacterial activity and insect resistant of plant might be impaired in the opr3 mutant which can’t be mitigated by exogenous MeJA treatment.

Metabolite variation patterns similar to methionine (increased levels in opr3 and slightly declined after MeJA treatment, Fig. 4a) were observed with 3-methylsulfinylpropyl isothiocyanate, 1-isothiocyanato-7-(methylsulfinyl)heptanes, 8-Methylthiooctyl glucosinolate, 1-isothiocyanato-8-(methylsulfinyl)octane and 1-isothiocyanato-9-(methylsulfinyl)nonane (Fig. 4a). Guo et al. found that 1-isothiocyanato-8-(methylsulfinyl)octane could inhibit germination of lettuce seeds and affects growth of roots of lettuce seedlings43. The increased levels of these isothiocyanates in opr3 implied that plant growth may be inhibited in response to the deficiency of endogenous JA. This is consistent with the dwarf phenotype of opr3. Endogenous JA deficiency-induced isothiocyanates accumulations were slightly relieved by MeJA treatment in a time dependent manner. This must be associated with the function recovery in opr3 by exogenous MeJA. Almost all aliphatic isothiocyanates detected showed no significant difference after MeJA treatment (Fig. 4a). Ku et al. found that exogenous MeJA treatment increases glucosinolate biosynthesis in Kale leaf tissue44. So, the hydrolysis of glucosinolates may be not significantly influenced by exogenous MeJA in 8 h in opr3.

The lack of endogenous JA can reduce the content of certain isothiocyanates, while at the same time; it can increase the content of other isothiocyanates. The application of exogenous MeJA, on the other hand, generally resulted in slightly decreased isothiocyanates content. This phenomenon indicated that some adverse impacts from endogenous JA deficiency may be alleviated by exogenous MeJA application. In addition to antibacterial activity and insect resistance, isothiocyanates also act as heat tolerance enhancers in plant45. Khokon et al. found that exogenous allyl isothiocyanates (AITCs) induce stomatal closure accompanied and mediated by the production of ROS and NO46. This process requires MeJA priming and AITC signaling shares some components with JA signaling. In conclusion, there are close associations between glucosinolates metabolism and JA in plant growth and stress response.

Tryptophan metabolism was also impacted by endogenous JA deficiency and exogenous MeJA treatment. Tryptophan is the metabolic precursor of many important secondary metabolites. Serotonin and indoleacetic acid (IAA) are two major secondary metabolites derived from tryptophan metabolism pathway. They are essential for plant growth and development, plant morphogenesis, pathogen defense, plant-insect interactions and other stress responses47,48. The content of tryptophan remained relatively stable between different genotype and treatment groups. 5-Hydroxyindoleacetaldehyde and 5-Hydroxyindoleacetylglycine, metabolites of serotonin, showed higher abundances in opr3 plants (Fig. 4b). The synthesis and metabolism of serotonin may be activated by endogenous JA deficiency. MeJA treatment resulted in reduction of them during the first 4 h. Their concentrations rose again to the levels of untreated mutant after 8 h. Such phenomenon indicated MeJA has antagonistic effect on serotonin metabolism. Tryptophan-dependent IAA synthesis contains four different pathways and we found three differential metabolites in them. For indolylmethyl-desulfoglucosinolate and 3-indoleacetonitrile, the variation between wide type and opr3 samples was small. Exogenous application of MeJA resulted in dramatic increase of these two metabolites after 4 h of treatment, consistent with the fact that these two metabolites are at the downstream of the metabolism pathway, a series of reactions are involved which may result in slow response of the metabolite. For indoleacetaldehyde, higher intensity was found in opr3 plants, and MeJA treatment resulted in decreased intensities. This variation pattern was similar to methionine and related glucosinolates. The opposite variation trends between indoleacetaldehyde and indoleacetonitrile after MeJA treatment under nearly constant level of tryptophan indicated that plants have redundant pathways for IAA synthesis and the application of MeJA can affect the synthesis of IAA by different pathways. It was found that IAA decreased significantly while serotonin increased significantly under various stress conditions in rice49. Our finding showed constant tryptophan content between different genotype and treatment groups and antagonistic variation between different tryptophan metabolism pathways after MeJA treatments in opr3 plants. Taken together, we suggest a negative correlation between tryptophan derived IAA and serotonin synthesis. The activation of serotonin synthesis in opr3 may result in inhibition of IAA synthesis, which is consistent with the dwarf phenotype of opr3 mutant. Serotonin involves in almost all aspects of plant growth, development and stress defense50. The activation of serotonin synthesis and metabolism may be used to help regulate plant growth and stress response to make up the lack of endogenous JA in opr3 plants.

Lipid metabolism affected by OPR3 deficiency and MeJA treatment

Lipid metabolism, especially fatty acyls metabolism, was impacted extensively by endogenous JA deficiency and exogenous MeJA treatment. We found 45 lipids that covered five lipid subcategories based on lipid classification system of LIPID MAPS, including, fatty acyls (23), prenol lipids (13), sterol lipids (7), sphingolipids (1) and glycerophospholipids (1) (Supplementary Information Spreadsheet 1).

In plants, fatty acyles and their derivatives are recognized as signaling molecules to control various biological processes including, cell membrane construction, intracellular signal transduction, protein modification51. They can significantly impact gene expression and metabolism in plant-microbe and plant-herbivore interactions52. α-linolenic acid, colnelenic acid and 13(S)-HOT, three key components of α-linolenic acid metabolism, showed decreased levels in opr3 and increased levels after MeJA treatment. Linolenic acid, a stress signal by itself 53, is one of the major unsaturated fatty acids in plants. Under stress conditions, it can be released into the plastid. This is the initial step of unsaturated fatty acid metabolism. Catalyzed by lipoxygenase, linolenic acid can produce a series of bioactive compounds, such as JA, MeJA, and 12-OPDA. The higher abundances of linolenic acid and their metabolites (except JA) in wild type indicated that plant keep a certain amount of “raw material” in reserve for the synthesis of JA when needed. In opr3, such reserve was greatly reduced (75% reduction in signal intensities), application of exogenous MeJA can alleviate the situation in a time dependent manner. The content of colnelenic acid and 13(S)-HOT can reach levels of the wild type after applying MeJA for 8 h, indicating exogenous MeJA can trigger its synthesis pathway by itself, but the lack of OPDA reductase in opr3 routed linolenic acid metabolism to pathways other than JA synthesis, as indicated by the high intensities of 13(S)-HOT and colnelenic acid in MeJA treated opr3 (Fig. 5). This finding suggested that JA is regulated in plant in a close-loop circuit. It has been reported that overexpression of fatty acid desaturase increased level of linolenic acid, accompanied by increase of drought resistance, salt54 and chill tolerance55. These findings suggested opr3 have weaker resistance towards abiotic stress due to decreased content of linolenic acid. But, such deficiency can be made up by exogenous MeJA application. This is consistent with the result of Vijayan et al., exogenous MeJA can protect mutants deficient in JA synthesis from pathogen infection and strengthen disease resistance of plants56. In addition to the fatty acyles mentioned above, we have found other fatty acyles negatively regulated by OPR3 deficiency and positively regulated by MeJA treatment (Supplementary Fig. S6). Their variation patterns were similar to that of α-linolenic acid.

Figure 5: alpha-linolenic acid metabolism was influenced by OPR3 deficiency and MeJA treatment.
Figure 5

Differential metabolites detected are labeled in red, fold changes compared to opr3 were displayed in the boxes.

JA is also involved in the metabolism of several prenol lipids and sterol lipids (Supplementary Fig. S7). Two types of variation pattern were observed. For 4, 5-Dihydrovomifoliol, 3-Methyl-alpha-ionyl acetate, 5-Hydroxy-p-mentha-6, 8-dien-2-one and (1beta, 2beta, 5beta)-p-Menth-3-ene-1,2,5-triol, comparable intensities were observed in wild type, opr3 and opr3 treated with MeJA for 1 h. opr3 plants treated with MeJA for 4 and 8 h showed significantly reduction of these compounds (Supplementary Fig. S7). Other prenol and sterol lipids showed variation patterns similar to that of α-linolenic acid.

Amino acids and small peptides

As shown in Figs 2 and 3 and Supplementary Information Spreadsheet 1, there are other metabolites and pathways influenced by endogenous and exogenous JA. Amino acids and small peptides are among them (Supplementary Fig. S8). L-glutamine and proline, two essential amino acids, showed increased content in opr3. After MeJA treatment, these two amino acids showed slightly different trends of variation. The content of proline increased initially and then dropped suddenly after 8 h. While for L-glutamine, the decrease occurred at 4 h after treatment. Glutamine involves in plant ammonia assimilation and provides nitrogen for amino acid synthesis. The increased level of glutamine in opr3 indicates enhanced nitrogen uptake of plants in the absence of JA. This situation is alleviated by exogenous MeJA. Proline metabolism has roles in cellular redox buffering, energy transfer, programmed cell death, osmotic balance regulation and plant pathogen interactions57. The increased level of proline in opr3 indicates an increased level of resistance in the mutant, and application of MeJA further enhanced such situation until 8 h after treatment when the concentration of JA in plant started to decrease (Fig. 5). These findings suggest there are associations between proline and JA in plant growth and stress response.

It is noteworthy that many dipeptides, tripeptides and amino acid metabolites were induced by OPR3 deficiency, they showed higher intensities in opr3 than in the wild type. This situation remained after exogenous MeJA treatment (Supplementary Fig. S8). Protein contents were measured by Bradford assay and no obvious difference was observed between WT and opr3 (Supplementary Fig. S9). Thus, the increased content of small peptide was not induced by large scale degradation of proteins in opr3. Small peptides may act as bioactive or signaling molecules. They have antioxidant, antihypertensive, anticarcinogenic, antimicrobial, and immunomodulatory activities in animals58. Here, we found many small peptides (especially dipeptides) that showed significant variation in the absence of endogenous JA, these small peptides may act as signaling molecules in plants and collaborate with JA in plants growth and stress regulation. Further study is needed to elucidate the role of small peptides in plant stress defense.

Quantitative analysis of expression of glucosinolates, tryptophan and α-linolenic acid metabolism related genes

To further verify our observation from metabolomics experiments, we examined the expression of 21 genes in MeJA-treated leaves of opr3, untreated leaves of opr3 and wild type Arabidopsis by RT-qPCR. These genes were selected based on their functions in the specific metabolic pathways identified in this study (glucosinolates, tryptophan and α-linolenic acid).

BCAT4, encoding branched-chain aminotransferase 4, catalyzes the initial step of aliphatic glucosinolate biosynthesis from methionine. The chain-elongated methionines are converted by MAM1 and MAM3 and further metabolized by CYP79F1 to produce aldoximes. TGG1 and TGG2 specifically expressed in aerial part of the plants and encode myrosinase, which catalyses the hydrolysis of glucosinolates to form isothiocyanates. The expression levels of these genes (except TGG2) were lower in opr3 than in wild type and this deficiency can be relieved by MeJA treatment in a time dependent manner (Fig. 6). Thus, RT-qPCR results confirmed that the biosynthesis and hydrolysis of aliphatic glucosinolates were negatively regulated by endogenous JA deficiency and positively regulated by exogenous MeJA treatment. This indicated that plant resistance to bacteria and insects may be impaired in the absence of endogenous JA and this impairment may be rescued by exogenous MeJA. Notably, almost all aliphatic isothiocyanates detected showed slow decrease in content after MeJA treatment according to our metabolomics data, while the expression of TGG1 and TGG2 decreased initially after MeJA treatment in opr3 then increased after 8 h of treatment. Taken together, we can conclude that for the hydrolysis of aliphatic glucosinolates, the change of gene expression may has not been passed to the metabolites level even after 8 h of MeJA treatment.

Figure 6: Gene expression analysis by RT-qPCR.
Figure 6

21 genes were selected based on their functions in specific metabolic pathways (glucosinolates, tryptophan and α-linolenic acid). Data represent mean ± SD from three biological and three technical replicates. Superscript letter indicates the result of ANOVA test (p < 0.05).

UGT74B1 (encodes a UDP-glucosyl transferase) and SOT16 (encodes a desulfo-glucosinolate sulfotransferase) are critical genes involved in indolic glucosinolate biosynthesis from tryptophan. There were no significant differences in their expressions between wild type and opr3. In contrast, MeJA treatment induced significant increases of their expressions in opr3 (Fig. 6). Similar variation trend was observed for their metabolic intermediate indolylmethyl-desulfoglucosinolate in this pathway (Fig. 4b). For tryptophan-dependent auxin biosynthesis, indole-3-aldoxime is converted by CYP79B2 and CYP79B3 and further catalyzed by CYP71A13 to produce indole-3-acetonitrile. Subsequently, three nitrilases (NIT1, NIT2 and NIT3) catalyse the terminal activation step in IAA biosynthesis. The lack of endogenous JA resulted in slight down-regulation of the expression of these genes, while application of exogenous MeJA resulted in significant up-regulation of these genes, suggesting JA has a positive correlation with tryptophan-dependent auxin biosynthesis (Fig. 6).

AOS (allene oxide synthase), AOCs (allene oxide cyclase1, 2, 3 and 4) and OPR3 are key genes involved in the synthesis of JA. The upstream genes, AOS and AOCs, showed comparable expression levels in wild type and opr3. MeJA treatment resulted in significant increases of these genes in opr3 (Fig. 6). OPR3 was not expressed in opr3 in any conditions as expected. The downstream gene involved in JA biosynthesis/signaling included JAZ10 (jasmonate-zim-domain protein 10), which regulates JA signaling pathway. The expression of this gene showed extremely low levels in wild type and non-treated opr3. The transcript level of JAZ10 increased significantly and quickly after MeJA treatment, indicating JAZ10 is actively involved in response to JA stimulus.

Most of these genes showed lower level of expression in opr3, indicating endogenous JA is required for their proper expression. Most of the genes also showed late response upon MeJA treatment in opr3. The highest level of expression was observed at 8 h after MeJA treatment, indicating a series of action is needed to initiate expression of these genes.

Discussion

High resolution mass spectrometry based metabolomics approach was used as a discovery tool to identify metabolites actively involved in JA synthesis and signaling in Arabidopsis. Multivariate statistic analyses revealed that there is significant difference between the metabolomes of Arabidopsis wild type and JA synthesis deficient mutant opr3. The application of exogenous MeJA can partially amend such difference in a time-dependent manner. Classification and pathway analysis of differential metabolites indicated that glucosinolates and tryptophan metabolism, amino acids and small peptides metabolism, lipid metabolism, especially fatty acyls metabolism were affected by endogenous JA deficiency and exogenous MeJA treatment.

Some isothiocyanates involved in plant resistance showed lower abundances in opr3 than wild type, thus plant’s bacterial and insect resistance capability might be impaired by endogenous JA deficiency. No significant restorations were observed after MeJA treatment in opr3. But gene expression analysis revealed that the biosynthesis and hydrolysis of aliphatic glucosinolates related genes were down-regulated by endogenous JA deficiency and up-regulated by exogenous MeJA treatment. We suggest that plant resistance to bacteria and insects was impaired in the absence of endogenous JA and this impairment can be rescued by exogenous MeJA. Isothiocyanates that inhibit plant growth showed higher abundances in opr3, indicating plant growth may be inhibited in response to JA deficiency and the inhibition can be relieved by MeJA treatment. As a category of essential bioactive substances for plant defense, multiple glucosinolates and their hydrolysis products were influenced differentially by endogenous JA deficiency. This complex regulation may be due to diversity of their biological activities and their synthetic pathways.

The synthesis of serotonin was activated in opr3, indicating plants have other means of stress defense in the absence of endogenous JA. Similar trends of metabolites and genes involved in tryptophan-dependent auxin biosynthesis were observed, which indicated that this pathway was influenced by endogenous JA deficiency and exogenous MeJA treatment. α-linolenic acid metabolism was activated by MeJA treatments as evidenced by both metabolomics and gene expression analyses, supporting a positive feedback regulation of JA synthesis pathway. Many lipid metabolites showed variation patterns similar to that of α-linolenic acid, suggesting JA interacts with other lipids synergistically. We also found many small peptides regulated by JA, they may act as signaling molecules, further study is needed to elucidate their biological functions.

JAs are of great importance in plant growth, development and stress responses. Previous studies on JAs were principally focused on plant’s phenotypic and molecular aspects and lacked overall understanding of plant metabolites. In this study, we combined metabolomics and gene expression analyses to obtain comprehensive profiling of metabolites involved in JA functions and synthesis. The results provided a perspective view of the interaction and regulation network of plant metabolites regulated by JA, as well as a better understanding of interaction network of plant hormones and the mechanism of plant resistance.

Methods

Plant materials and MeJA treatment

Arabidopsis thaliana wild type Wassileskija (Ws) and mutant opr3 were used in the experiment. The seeds were sown on 1/2 Murashige and Skoog medium after disinfection by 2% NaClO and 70% ethanol and vernalized at 4 °C for 3 days. The seedlings were transferred to pots after 10 days and cultivated in climate chamber (22 °C; 8/16 h light/dark cycle, 65% r. h.).

MeJA, Tween-20 (Sigma Aldrich) and deionized water (Millipore, Milford, MA, USA) were used to prepare 0.03% MeJA solution. The MeJA solution was sprayed on plant leaves after a vegetative growth period of approximately 28 days. The leaves were collected at different time points after treatment (0 h, 1 h, 4 h and 8 h), immediately frozen in liquid nitrogen and ground to fine powder. The powders were stored at −80 °C until analysis.

Metabolite extraction

10 biological replicates were prepared for each genotype and treatment group. For each sample, 100 mg plant leaf powder was weighted and transferred to a 1.5 mL centrifuge tube. 750 μL water was added and the tube was placed in an ultrasonic cleaner (KunShan, China) for 30 min. After centrifugation (Centrifuge 5417 R, Eppendorf) at 15000 rpm for 10 min, the supernatant was transferred to another tube and 750 μL MeOH-ACN (1:1, v/v) was added, followed by sonication and centrifugation. The supernatants were combined and 400 μL of the mixture was dried using a vacuum concentrator (Concentrator plus, Eppendorf). The dried samples were redissolved in aliquots of 80 μL MeOH-H2O (1:1, v/v), filtered through a 0.1 μm membrane and transferred to sample vials for LC-MS analysis. Total protein was extracted by Phenol method and quantified by Bradford assay59. Three biological replicates were performed.

UPLC-MS analysis

The plant extracts were analyzed using an UPLC-HRMS system (UPLC, ACQUITY UPLC H-Class Bio, Waters; MS, Q-Exactive, Thermo Scientific) equipped with a heated electrospray ionization (HESI) source. UPLC separation was performed on a BEH C18 column (2.1 × 100 mm, 1.7 μm, Waters) at a flow rate of 0.3 mL min−1. HPLC grade solvents and additives were from Fisher Scientific (ThermoFisher Scientific, NJ, USA). The gradient program using 0.1% FA in water (phase A) and 0.1% FA in ACN (phase B) was applied as follows: 95% A at 0 min to 55% A at 7 min, 5% A at 10 min and held for 4 min, then returned to initial condition. The column temperature was 35 °C and the injection volume was 5 μL.

MS analysis was performed in the positive ion mode. The instrument was calibrated using external standard before analysis to ensure mass accuracy of better than 3 ppm throughout the experiment. The HESI source parameters were as follows: Spray voltage at 3.5 kV, Capillary temperature at 320 °C, Sheath gas flow rate at 30 arb. units, Aux gas flow rate at 10 arb. units, Sweep gas flow rate at 5 arb. units, Heater temperature at 350 °C, S-lens RF level at 55. Full MS scan (m/z 70–1000) with resolution of 70 000 was used. 3 scans can be obtained per second, which provides sufficient data points for quantification. MS2 scan used normalized collision energy of 35 V, an isolation window of 0.8 m/z and a mass resolution of 35 000.

Metabolomics data processing

Peak alignment, background subtraction and component extraction of the raw data were achieved by SIEVE 2.1 software (Thermo Scientific). Component extraction was performed between retention time 0.5 and 16 min with intensity threshold at 500 000, minimum scan at 9 and signal to noise ratio at 10. Principal component analysis (PCA), hierarchical cluster analysis (HCA), orthogonal partial least squares discriminant analysis (OPLS-DA) were performed using SIMCA-P 13 software (Umetrics) after data were scaled to Pareto variance. Statistical analyses of the quantitative data were performed using EXCEL and SAS. Compounds with CV < 20%, fold change >2 and p < 0.05 were picked for further identification.

Identification of differential compounds was achieved with the help of accurate mass measurement of molecular ions and fragment ions with high resolution. Accurate mass of molecular ions was searched against compound database (METLIN, KEGG, PlantCyc, AraCyc, HMDB, LIPID MAPS, MassBank, PubChem and MeSH) with mass accuracy at 5 ppm to generate a list of candidate chemical formulas. Isotopic pattern of the molecular ions helped to determine the probable formulas. MS/MS spectra database match was used to match the fragment ion spectra to the candidate compounds. MS/MS spectra were also compared with theoretical fragmentation pattern with mass accuracy at 10 ppm using Progenesis QI 2.0 (Waters). Metabolite identifications can be classified as level II based upon their spectral similarities with public/commercial spectral libraries in accordance with the MSI guidelines35.

Cluster analysis of identified differential compounds was achieved using Cluster 3.0 and TreeView. Pathway analysis was performed using MetaboAnalyst 3.0 (http://www.metaboanalyst.ca/MetaboAnalyst/faces/Secure/upload/PathUploadView.xhtml) and Pathway and Compound Databases (Plant Metabolic Netwok, MetaCyc, KEGG pathway) in TAIR (http://www.arabidopsis.org/portals/metabolome/metabolomedatabase.jsp).

Gene expression analysis

Total RNA was extracted using TRIzol reagent (Invitrogen, USA) according to manufacturer’s instructions. RNA concentration and purity were determined using a Nanodrop ND-1000 spectrophotometer (Nanodrop Technologies, Rockland, DE, USA), and RNA integrity was checked by 1% (w/v) agarose gel electrophoresis (data not shown). Genomic DNA elimination and first-strand cDNA synthesis were performed with a FastQuant RT Kit (Tiangen Biotech, Beijing, China) using 1.5 μg of total RNA. Three independent biological replicates for each sample were performed in this procedure.

RT-qPCR was performed using SYBR Premix Ex Taq (TaKaRa, Dalian, China) on a 7500 Fast Real-Time PCR System (Applied Biosystems, USA). Three technical replicates for each biological replicate were performed in the same qPCR run. The qPCR reaction system mix was prepared according to manufacturer’s instructions and subjected to an initial denaturation step of 95 °C/30 s, followed by 40 cycles of 95 °C/3 s, 60 °C/30 s. Finally, a melting curve was generated by increasing temperature from 65 to 95 °C in order to verify specificity of the amplification product. Gene-specific primers (a single peak in qPCR melting curve products) used were listed in Supplementary Table S4 and ACTIN was used as control. Relative expression values of all genes were calculated with the formula 2−∆∆Ct using the cycle threshold (Ct) values and verified using One Way ANOVA (P < 0.05).

Additional Information

How to cite this article: Cao, J. et al. Effects of MeJA on Arabidopsis metabolome under endogenous JA deficiency. Sci. Rep. 6, 37674; doi: 10.1038/srep37674 (2016).

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References

  1. 1.

    & Analytical strategies in metabonomics. J. Proteome Res. 6, 443–458 (2007).

  2. 2.

    et al. Metabolomics in cerebrospinal fluid of patients with amyotrophic lateral sclerosis: an untargeted approach via high-resolution mass spectrometry. J. Proteome Res. 12, 3746–3754 (2013).

  3. 3.

    et al. Developing urinary metabolomic signatures as early bladder cancer diagnostic markers. Omics-a Journal of Integrative Biology 19, 1–11 (2015).

  4. 4.

    , , , & Untargeted metabolomics from biological sources using ultraperformance liquid chromatography-high resolution mass spectrometry (UPLC-HRMS). Jove-Journal of Visualized Experiments 75, e50433 (2013).

  5. 5.

    & Lipidomics in situ: insights into plant lipid metabolism from high resolution spatial maps of metabolites. Prog. Lipid Res. 54, 32–52 (2014).

  6. 6.

    et al. Metabolomic profiles delineate potential role for sarcosine in prostate cancer progression. Nature 457, 910–914 (2009).

  7. 7.

    et al. Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease. Nature 472, 57–63 (2011).

  8. 8.

    et al. A novel integrated method for large-scale detection, identification, and quantification of widely targeted metabolites: application in the study of rice metabolomics. Mol. Plant 6, 1769–1780 (2013).

  9. 9.

    et al. Metabolomics reveals herbivore-induced metabolites of resistance and susceptibility in maize leaves and roots. Plant, Cell Environ. 36, 621–639 (2013).

  10. 10.

    et al. The tomato homolog of CORONATINE-INSENSITIVE1 is required for the maternal control of seed maturation, jasmonate-signaled defense responses, and glandular trichome development. Plant Cell 16, 126–143 (2004).

  11. 11.

    & Jasmonates and octadecanoids: signals in plant stress responses and development. Prog. Nucleic Acid Res. Mol. Biol. 72, 165–221 (2002).

  12. 12.

    et al. Ultraviolet-B-induced stress and changes in gene expression in Arabidopsis thaliana: role of signalling pathways controlled by jasmonic acid, ethylene and reactive oxygen species. Plant, Cell Environ. 22, 1413–1423 (1999).

  13. 13.

    , , , & Jasmonate is essential for insect defense in Arabidopsis. Proc. Natl. Acad. Sci. USA 94, 5473–5477 (1997).

  14. 14.

    et al. Ozone-sensitive Arabidopsis rcd1 mutant reveals opposite roles for ethylene and jasmonate signaling pathways in regulating superoxide-dependent cell death. Plant Cell 12, 1849–1862 (2000).

  15. 15.

    & Jasmonate and salicylate as global signals for defense gene expression. Curr. Opin. Plant Biol. 1, 404–411 (1998).

  16. 16.

    , & Jasmonate signaling mutants of Arabidopsis are susceptible to the soil fungus Pythium irregulare. Plant J. 15, 747–754 (1998).

  17. 17.

    & Transport of [2-14C]jasmonic acid from leaves to roots mimics wound-induced changes in endogenous jasmonic acid pools in Nicotiana sylvestris. Planta 203, 436–441 (1997).

  18. 18.

    & Biosynthesis of jasmonic acid by several plant-species. Plant Physiol. 75, 458–461 (1984).

  19. 19.

    et al. Role of beta-oxidation in jasmonate biosynthesis and systemic wound signaling in tomato. Plant Cell 17, 971–986 (2005).

  20. 20.

    et al. Jasmonic acid carboxyl methyltransferase: a key enzyme for jasmonate-regulated plant responses. Proc. Natl. Acad. Sci. USA 98, 4788–4793 (2001).

  21. 21.

    & The oxylipin signal jasmonic acid is activated by an enzyme that conjugates it to isoleucine in Arabidopsis. Plant Cell 16, 2117–2127 (2004).

  22. 22.

    , , & Arabidopsis mutants selected for resistance to the phytotoxin coronatine are male-sterile, insensitive to methyl jasmonate, and resistant to a bacterial pathogen. Plant Cell 6, 751–759 (1994).

  23. 23.

    , , , & The DEFECTIVE IN ANTHER DEHISCENCE1 gene encodes a novel phospholipase A1 catalyzing the initial step of jasmonic acid biosynthesis, which synchronizes pollen maturation, anther dehiscence, and flower opening in Arabidopsis. Plant Cell 13, 2191–2209 (2001).

  24. 24.

    et al. A knock-out mutation in allene oxide synthase results in male sterility and defective wound signal transduction in Arabidopsis due to a block in jasmonic acid biosynthesis. Plant J. 31, 1–12 (2002).

  25. 25.

    et al. Silencing of OPR3 in tomato reveals the role of OPDA in callose deposition during the activation of defense responses against Botrytis cinerea. Plant J. 81, 304–315 (2015).

  26. 26.

    , , , & 12-oxophytodienoate reductase 3 (OPR3) is the isoenzyme involved in jasmonate biosynthesis. Planta 210, 979–984 (2000).

  27. 27.

    , , , & Plant defense in the absence of jasmonic acid: the role of cyclopentenones. Proc. Natl. Acad. Sci. USA 98, 12837–12842 (2001).

  28. 28.

    et al. Systems analysis of plant functional, transcriptional, physical interaction, and metabolic networks. Plant Cell 24, 3859–3875 (2012).

  29. 29.

    et al. Salicylate-mediated suppression of jasmonate-responsive gene expression in Arabidopsis is targeted downstream of the jasmonate biosynthesis pathway. Planta 232, 1423–1432 (2010).

  30. 30.

    & Developing a model of plant hormone interactions. Plant Signaling Behav. 6, 494–500 (2011).

  31. 31.

    et al. The Arabidopsis DELAYED DEHISCENCE1 gene encodes an enzyme in the jasmonic acid synthesis pathway. Plant Cell 12, 1041–1061 (2000).

  32. 32.

    & The Arabidopsis male-sterile mutant, opr3, lacks the 12-oxophytodienoic acid reductase required for jasmonate synthesis. Proc. Natl. Acad. Sci. USA 97, 10625–10630 (2000).

  33. 33.

    et al. Characterization and cDNA-microarray expression analysis of 12-oxophytodienoate reductases reveals differential roles for octadecanoid biosynthesis in the local versus the systemic wound response. Plant J. 32, 585–601 (2002).

  34. 34.

    & Sample preparation for plant metabolomics. Phytochem. Anal. 21, 4–13 (2010).

  35. 35.

    et al. Proposed minimum reporting standards for chemical analysis. Metabolomics 3, 211–221 (2007).

  36. 36.

    , , , & MetaboAnalyst 2.0-a comprehensive server for metabolomic data analysis. Nucleic Acids Res. 40, W127–W133 (2012).

  37. 37.

    , , & MetaboAnalyst: a web server for metabolomic data analysis and interpretation. Nucleic Acids Res. 37, W652–W660 (2009).

  38. 38.

    , & Comparative quantitative trait loci mapping of aliphatic, indolic and benzylic glucosinolate production in Arabidopsis thaliana leaves and seeds. Genetics 159, 359–370 (2001).

  39. 39.

    et al. Arabidopsis glucosyltransferase UGT74B1 functions in glucosinolate biosynthesis and auxin homeostasis. Plant J. 40, 893–908 (2004).

  40. 40.

    et al. Pseudomonas sax genes overcome aliphatic isothiocyanate-mediated non-host resistance in Arabidopsis. Science 331, 1185–1188 (2011).

  41. 41.

    , & Evaluation of antibacterial activity of 3-butenyl, 4-pentenyl, 2-phenylethyl, and benzyl isothiocyanate in Brassica vegetables. J. Food Sci. 75, M412–M416 (2010).

  42. 42.

    et al. Berteroin present in cruciferous vegetables exerts potent anti-inflammatory properties in murine macrophages and mouse skin. Int. J. Mol. Sci. 15, 20686–20705 (2014).

  43. 43.

    , , & Liquid chromatography-tandem mass spectrometric assay for the determination of CTN986 and its deglycosylation products in the rat brain dialysate. Chem J. Chinese U. 30, 1528–1532 (2009).

  44. 44.

    , & Exogenous methyl jasmonate treatment increases glucosinolate biosynthesis and quinone reductase activity in kale leaf tissue. PLoS ONE 9, e103407 (2014).

  45. 45.

    , & Administration of isothiocyanates enhances heat tolerance in Arabidopsis thaliana. Plant Growth Regul. 69, 71–77 (2013).

  46. 46.

    et al. Allyl isothiocyanate (AITC) induces stomatal closure in Arabidopsis. Plant, Cell Environ. 34, 1900–1906 (2011).

  47. 47.

    Auxin: a major regulator of organogenesis. C. R. Biol. 333, 290–296 (2010).

  48. 48.

    Auxin and monocot development. Cold Spring Harbor Perspect. Biol. 2, a001479 (2010).

  49. 49.

    The regulation of serotonin biosynthesis under abiotic stresses. Master thesis, HuaZhong Agricultural University (2014).

  50. 50.

    , & Phytoserotonin: a review. Plant Signaling Behav. 6, 800–809 (2011).

  51. 51.

    et al. Arachidonic Acid: An evolutionarily conserved signaling molecule modulates plant stress signaling networks. Plant Cell 22, 3193–3205 (2010).

  52. 52.

    Fatty acid unsaturation, mobilization, and regulation in the response of plants to stress. Biotechnol. Lett. 30, 967–977 (2008).

  53. 53.

    Impact of phyto-oxylipins in plant defense. Trends Plant Sci. 7, 315–321 (2002).

  54. 54.

    et al. Modulated fatty acid desaturation via overexpression of two distinct omega-3 desaturases differentially alters tolerance to various abiotic stresses in transgenic tobacco cells and plants. Plant J. 44, 361–371 (2005).

  55. 55.

    et al. Overexpression of endoplasmic reticulum omega-3 fatty acid desaturase gene improves chilling tolerance in tomato. Plant Physiol. Biochem. 47, 1102–1112 (2009).

  56. 56.

    , , , & A role for jasmonate in pathogen defense of Arabidopsis. Proc. Natl. Acad. Sci. USA 95, 7209–7214 (1998).

  57. 57.

    & Proline metabolism and its implications for plant-environment interaction. The Arabidopsis book 8, e0140 (2010).

  58. 58.

    & Research progress in structure-activity relationship of bioactive peptides. J. Med. Food 18, 147–156 (2015).

  59. 59.

    , & Plant Proteomics: Methods and Protocols (ed. ) 8–11 (Science Press. 2013).

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Acknowledgements

We would thank Dr. Yan He (Professor, College of Agriculture and Biotechnology, China Agricultural University) and Dr. Yan Guo (Professor, College of Biological Sciences, China Agricultural University) for reading the manuscript and providing thoughtful insights. This work was supported by National Science Foundation of China (31170343) and the Chinese Universities Scientific Fund (NCET-11-0484).

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Affiliations

  1. State Key Laboratory of Plant Physiology and Biochemistry, College of Biological Sciences, China Agricultural University, Beijing, 100193, China

    • Jingjing Cao
    • , Jian Chen
    •  & Zhen Li
  2. College of Resources and Environmental Sciences, China Agricultural University, Beijing, 100193, China

    • Mengya Li
    •  & Pei Liu

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Contributions

J.C., P.L. and Z.L. designed the experiments and wrote the manuscript; J.C. performed lab work, data acquisition and data analysis; J.C. assisted in performing RT-qPCR experiment; P.L. and M.L. contributed to the discussion and reviewed the manuscript. All authors read and approved the final manuscript.

Competing interests

The authors declare no competing financial interests.

Corresponding author

Correspondence to Zhen Li.

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