Plants are sessile and rely on hormonal cues for response against stresses. Jasmonic acid (JA) and its methylated form, methyl JA (MeJA) are among the critical hormones for such defense roles and plant adaptation. JAs are known to be induced by wounding, insects and pathogen attack, UV radiation, drought and other stresses (Dar et al., 2015). Their elicitation further invokes various cellular and molecular signalling, influencing protein expression and metabolite production to cope with stress.
Persicaria minor [syn. Polygonum minus], also known as kesum in Malaysia, is widely used as an ingredient in local cuisine due to its pungent smell. It is also used for aromatherapy and dandruff treatment (Azlim Almey et al., 2010). Several studies have reported antioxidant, antiviral, antimicrobial and anticancer activities in P. minor extracts (Vikram et al., 2014). Our previous results showed increase in P. minor leaf volatile metabolites under heat stress (Goh et al., 2016) and MeJA elicitation (Rahnamaie-Tajadod et al., 2017). Transcriptome profiling indicated the activation of defense genes involving phenylpropanoid pathway upon MeJA elicitation (Rahnamaie-Tajadod et al., 2017). However, as transcripts may be subjected to post-translational modifications, understanding MeJA signalling at the proteome level will enable key regulatory proteins involved to be identified.
Several studies have been conducted to elucidate the proteome dynamics upon MeJA elicitation in plants. However, these studies are mainly performed using Arabidopsis (Alvarez, Zhu & Chen, 2009; Chen et al., 2011), rice (Rakwal & Komatsu, 2000), as well as hairy root cultures of Silybum marianum (Gharechahi et al., 2013). To the best of our knowledge, no study at the proteome level of an herbal plant species such as P. minor has been reported on the effects of MeJA elicitation. In this study, the SWATH-MS approach was taken to quantify the proteome of control and MeJA-treated leaf samples.
SWATH-MS analysis is an emerging label-free technique in proteomics which has revolutionized many proteome research. SWATH-MS analysis is capable of profiling any given proteome quantitatively with better coverage than a traditional shotgun proteomics (which mostly relies on data-dependent acquisition) (Gillet et al., 2012). Several studies using this approach have successfully profiled proteomes from human (Bourassa et al., 2015; Chang et al., 2015), animals (Li et al., 2016; Perez-Patiño et al., 2016), microbes (Loke et al., 2016b) and plants (Zhang et al., 2016; Zhu et al., 2016). SWATH-MS proteomics is also known to be a far more sensitive, reproducible and accurate than the Western blotting alone (Gillet et al., 2012; Picotti & Aebersold, 2012). Hence, the use of SWATH-MS analysis is suited for the profiling of proteins in our non-model herbal plant.
This study aims to profile the proteome of P. minor leaf using SWATH-MS analysis to study the effects of MeJA treatment. As this herb is a non-model organism, a previously reported de novo transcriptome library (Loke et al., 2016a; Rahnamaie-Tajadod et al., 2017) was used as a reference protein sequence database, allowing a comprehensive protein profiling and identification. Furthermore, this proteome study complemented the reported transcriptome data set, allowing statistical correlation to be performed comparing their differential expression upon MeJA induced signaling. Proteins found to have significantly different abundance between control and treated samples were discussed in relation to MeJA regulation and stress physiology.
Material & Methods
P. minor plants were treated and prepared as per Rahnamaie-Tajadod et al. (2017). The same leaf samples were utilized for both transcriptomics (Rahnamaie-Tajadod et al., 2017) and proteomics studies (this report). Total proteins were extracted from three biological replicates of control and MeJA-treated pooled leaf samples (24 h after treatment). Each biological replicate was extracted three times as three technical replicates. Overall experimental design is illustrated in Fig. 1.
Total protein extraction
Samples (100 mg) were ground in liquid nitrogen before solubilizing in 1 mL TRI-reagent for 5 min followed by 200 µL chloroform for 15 min at room temperature (RT). Samples were then centrifuged at 2,000× g for 15 min at 4 °C and the supernatant discarded. The obtained pellets were dissolved in 300 µL 100% ethanol and incubated for 3 min at RT before centrifuged at 2,000× g for 5 min at 4 °C. The supernatants were transferred into new tubes before three times (v/v) 100% acetone were added, inverted for 15 s and incubated for 10 min at RT. Samples were then centrifuged for 12,000× g for 10 min at 4 °C and the supernatant was removed. Pellets were washed with 1 mL 0.3 M guanidine hydrochloride in 95% ethanol and 2.5% glycerol and incubated for 10 min at RT before centrifuged at 8,000× g for 5 min at RT. Resulting supernatants were discarded and the washing step was repeated twice. Then, 2.5% glycerol in absolute ethanol was added and incubated for 10 min at RT and samples were centrifuged at 8,000× g for 5 min at 4 °C. Supernatants were discarded and the pellets were dried for 10 min at RT and stored in −80 °C until required. Samples were then sent for proteomics analysis at the Australian Proteome Analysis Facility (APAF), Sydney.
The protein pellets were first solubilized in 1% sodium deoxycholate with 100 mM triethyl ammonium bicarbonate (TEAB) and agitated with five short pulses using ultrasonic probes. Samples were then heated to 95 °C for 5 min before centrifuged at 12,000× g for 5 min. Each sample was reduced with dithiothreitol (pH 9, 5 mM for 1 hr at 68 °C), then alkylated with iodoacetamide (pH 9, 12.5 mM for 1 hr at RT) and digested with trypsin overnight at 37 °C. Peptides were recovered from each sample using solid phase extraction with OMIX C18 (100 µL) tips and the eluate was dried using a vacuum concentrator. Dried peptides were resolubilized in 40 µL 2% acetonitrile and 0.1% formic acid prior to SWATH-MS analysis.
All samples were analyzed using a TripleTOF 5600 mass spectrometer (SCIEX, Foster City, CA, USA) coupled to an Eksigent NanoLC-Ultra 2Dplus system (Eksigent Technologies, Dublin, CA, USA). Peptides were desalted using a 3.5 cm peptide trap (packed with 2.7 µm, Halo C18 solid core, 100 µm × 3.5 cm) using 2% acetonitrile (0.1% formic acid) at a flow rate of 2 µL per minute for 10 min. After desalting, the trap was switched in-line with a 20 cm C18 column (packed with 2.7 µm, Halo C18 solid core, 100 µm × 20 cm). Peptides were eluted from the column at 50 °C using a linear gradient from 95:5 mobile phase A/mobile phase B to 60:40 mobile phase A/mobile phase B (mobile phase A: 0.1% v/v formic acid; mobile phase B: 80% v/v ACN containing 0.1% v/v formic acid) over 80 min at a flow rate of 400 nL/min. All peptide separation steps were carried out at 50 °C using a column oven. The LC eluent was subjected to positive ion nanoflow analysis using an ion spray voltage, heater interface temperature, curtain gas flow and nebulizing gas flow of 2.5 kV, 150 °C, 25 and 30, respectively for the TripleTOF 5600.
Information-dependent acquisition (IDA) experiments were conducted on each biological replicate (controls and treated) using a survey scan (350–1,500 Da) of 250 millisec (ms) followed by 20 MS/MS product ion scans (350–1,500 Da) at an accumulation time of 100 ms. Product ion scans were collected for ions with a 2+ to 5+ charge-state and an ion intensity threshold of 150 counts per second (cps). Rolling collision energy (CE) was used during the IDA runs with maximum allowed CE of 80 V. SWATH experiments were conducted on each biological and technical replicate (controls and treated) using a TOF MS scan (350–1,500 Da) of 40 ms followed by 60 TOF MS/MS product ion scans in 12.5 Da windows from 400–1,150 Da each at an accumulation time of 50 ms. The collision energy was set using the CE curve (CE = 0.05 *m/z + 4) and utilised a collision energy spread of 10eV for each variable window.
Protein identification and PeakView analysis
Proteins were identified using the Paragon search algorithm in ProteinPilot Version 22.214.171.124 (AB SCIEX, Foster City, CA, USA). A spectral library was constructed by combining searches for each of the 3 biological replicates for control and treated samples using the P. minor in-house transcriptome database (Loke et al., 2016a; Rahnamaie-Tajadod et al., 2017).
All SWATH files and the ProteinPilot spectral library were imported into PeakView (version 126.96.36.19957; AB SCIEX, Foster City, CA, USA). Protein level quantitation from SWATH data was performed using an extraction window of 10 min, an extracted ion chromatogram width of 10 ppm, and the following peptide filter settings: 25 peptides per protein, six transitions per peptide, 99% peptide confidence, and a 1% False Discovery Rate threshold. The mass spectrometry proteomics data was deposited to the ProteomeXchange Consortium via the PRIDE (Vizcaíno et al., 2016) partner repository with the dataset identifier PXD005749. The ProteinPilot software analysis computes the local and global False Discovery Rate (FDR) for spectral (Table S1), unique peptide (Table S2) and protein (Table S3) levels data. The peak areas for all identified proteins were incorporated in Table S4.
All statistical analysis was performed using protein level data from PeakView and Perseus version 188.8.131.52. Peak areas were log-transformed and median-normalised to generate a normal data distribution. The data was further subjected to the principal component analysis and clustering. One technical replicate of the treated sample (T3 replicate 1) was removed from subsequent analyses for being an outlier (Aizat et al., 2018). Subsequently, the data was then normalized using z-score and clustering was performed to visualize the differences between samples via heatmap and principle component analysis (Fig. 2).
Three statistical analyses were performed to determine the differentially expressed proteins (Table S5). Firstly, a t-test was done to compare control and treated samples by considering all replicates (both biological and technical) as independent samples. Secondly, a t-test using average values of biological replicates was performed. Thirdly, the data was analyzed using a linear mixed effect model (LME) by considering a technical replicate random effect and a treatment fixed effect. Significantly differentially expressed proteins have p < 0.05 for all the three statistical analyses, as well as normalized fold change (FC.norm) of control over treated samples greater than 1.5 (significantly upregulated proteins) or lesser than 0.67 (significantly downregulated proteins). Comparative analysis between the proteome FC.norm and transcriptome log2 fold change (logFC) was performed using Pearson product moment correlation coefficient and the significance at p-value <0.001 was determined using a regression analysis in Microsoft Excel 2010 (Table S6).
Identified proteins were cross-referenced with transcriptome annotations as reported by Rahnamaie-Tajadod et al. (2017) for functional identification. The annotations were performed using Trinotate annotation pipeline (Loke et al., 2016a). The Blast2GO program (https://www.blast2go.com/) was also used to annotate proteins based on cellular component, molecular function and biological process (Fig. S1). This data was then graphically presented using the WEGO program (http://wego.genomics.org.cn/cgi-bin/wego/index.pl). Furthermore, pathway enrichment tool called KOBAS (http://kobas.cbi.pku.edu.cn/) was used to highlight the most enriched biological pathways in our dataset.
SWATH-MS proteomics analysis was performed to profile proteins quantitatively from P. minor leaf samples, which were elicited with MeJA and compared to control without treatment (Fig. 1). ProteinPilot analysis successfully identified 6,249 distinct peptides using 1% global FDR threshold (Fig. S2). Subsequently, 751 proteins were identified (Table S5 ) and they were further clustered according to either control or treated (Fig. 2). Further analysis using Blast2GO has assigned these proteins with 841 Gene Ontology (GO) terms. These terms are categorized into three different functional classifications: “cellular component”, “molecular function” and “biological process” (Fig. 3). Most protein assignments in the “cellular component” belong to “cell” (506 proteins, 67.4%), “cell part” (499, 66.4%), “organelle” (387 proteins, 51.5%) and “organelle part” (264 proteins, 35.2%). Meanwhile, “catalytic” (378 proteins, 50.3%), “binding” (354 proteins, 47.1%), “structural molecule” (45 proteins, 6.0%) and “antioxidant” (30 proteins, 4.0%) encompass the majority of the GO terms in the “molecular function”. In the “biological process” classification, the highest percentages of GO terms fall under “metabolic process” (480 proteins, 63.9%), “cellular process” (438 proteins, 58.3%), “response to stimulus” (118 proteins, 15.7%) and “biological regulation” (60 proteins, 8.0%) (Fig. 3). Most of these GO matches possessed significant E-value of 1 ×10−180 (Fig. S1A), sequence similarity distribution of more than 70% (Fig. S1B) as well as top hit species distribution to “other” species followed by beet (Beta vulgaris) and spinach (Spinacia oleracea) (Fig. S1C).
Furthermore, pathway enrichment analysis using KOBAS revealed that the top most enriched biological pathways in our proteome dataset were metabolism (corrected p-value of 1.79E–130), metabolic pathways (corrected p-value of 3.66E–85), carbon metabolism (corrected p-value of 3.66E–79), metabolism of proteins (corrected p-value of 8.00E–49) as well as metabolism of amino acids and derivatives (corrected p-value of 1.51E–47) (Table 1).
|Term||Database||Input number||Background number||p-value||Corrected p-value|
|All identified proteins|
|Metabolic pathways||KEGG pathway||133||1,243||6.83E−88||3.66E−85|
|Carbon metabolism||KEGG pathway||65||113||1.02E−81||3.66E−79|
|Metabolism of proteins||Reactome||101||1,378||2.99E−51||8.00E−49|
|Metabolism of amino acids and derivatives||Reactome||60||339||7.04E−50||1.51E−47|
|Protein ID||Mean C||Mean T||FC.norm||Protein name||UniProt accession #||Organism|
|Significantly up-regulated proteins upon MeJA treatment|
|cds.c56865_g2_i9—m.103397||376,975.69||1,737,837.61||6.87||Proteinase inhibitor||P82381||Linum usitatissimum|
|cds.c56865_g2_i6—m.103394||1,555,104.16||5,873,182.80||5.58||Proteinase inhibitor||P82381||Linum usitatissimum|
|cds.c56865_g2_i3—m.103392||1,473,435.88||4,406,842.71||4.44||Proteinase inhibitor||P82381||Linum usitatissimum|
|cds.c56865_g2_i7—m.103395||2,574,250.57||3,654,504.10||2.08||Proteinase inhibitor||P82381||Linum usitatissimum|
|cds.c55935_g2_i2—m.93522||175,025.05||668,494.17||5.37||Peroxidase 12||Q96520||Arabidopsis thaliana|
|cds.c55935_g2_i6—m.93526||1,385,492.12||1,962,003.60||2.09||Peroxidase 12||Q96520||Arabidopsis thaliana|
|cds.c51696_g2_i3—m.56033||2,223,906.61||3,067,324.59||2.03||Peroxidase 12||Q96520||Arabidopsis thaliana|
|cds.c55509_g2_i1—m.89283||2,093,087.19||2,810,777.22||2.00||Peroxidase 12||Q96520||Arabidopsis thaliana|
|cds.c48482_g2_i8—m.34843||1,360,455.24||1,524,257.70||1.63||Peroxidase 51||Q9SZE7||Arabidopsis thaliana|
|cds.c48482_g4_i2—m.34836||1,137,963.39||1,243,194.77||1.58||Peroxidase 51||Q9SZE7||Arabidopsis thaliana|
|cds.c44085_g1_i1—m.17116||98,123.59||103,360.01||1.57||Thioredoxin O1||O64764||Arabidopsis thaliana|
|cds.c54051_g1_i9—m.75181||4449.63||15,270.92||5.28||Carbonic anhydrase 2||P42737||Arabidopsis thaliana|
|cds.c54084_g3_i17—m.75490||73,270.41||130,253.17||2.59||Serine carboxypeptidase-like 18;||Q9C7Z9||Arabidopsis thaliana|
|cds.c56708_g2_i3—m.101695||158,802.63||22,1382.40||2.06||Serine carboxypeptidase-like 17||Q9C7D6||Arabidopsis thaliana|
|cds.c56645_g8_i5—m.101004||305,355.00||317,549.28||1.54||Aspartic proteinase A1||O65390||Arabidopsis thaliana|
|cds.c55798_g3_i4—m.92174||46,335.46||80,368.30||2.27||Linoleate 13S-lipoxygenase 2-1||O24370||Solanum tuberosum|
|cds.c48157_g2_i2—m.33078||44,999.96||62,352.04||2.03||GDSL esterase/lipase||Q9LY84||Arabidopsis thaliana|
|cds.c48582_g2_i1—m.35349||54,305.20||58,084.49||1.59||Chorismate mutase 1||P42738||Arabidopsis thaliana|
|Aromatic compound biosynthesis|
|cds.c56987_g1_i3—m.104679||303,398.86||329,336.50||1.54||Enone oxidoreductase||K4BW79||Solanum lycopersicum|
|cds.c50257_g2_i3—m.45689||2,777.00||3,317.73||1.86||Beta-hexosaminidase 1||A7WM73||Arabidopsis thaliana|
|cds.c51882_g2_i1—m.57255||5,854,784.07||7,322,486.75||1.84||Bark storage protein A (BSPA)||Q07469||Populus deltoides|
|cds.c46849_g1_i2—m.26698||245,864.94||294,842.61||1.83||MFP1 (Matrix Attachment Region binding filament-like protein) attachment factor 1 (MAF1)||Q9M7N6||Solanum lycopersicum|
|cds.c45380_g1_i1—m.20949||441,316.13||47,1058.03||1.62||Ubiquitin-conjugating enzyme E2 variant 1D||Q9SVD7||Arabidopsis thaliana|
|cds.c55178_g1_i9—m.85889||166,317.71||177,336.50||1.57||Endonuclease 4||F4JJL0||Arabidopsis thaliana|
|Cell wall degradation|
|cds.c57837_g2_i2—m.114445||64,963.22||76,742.82||1.70||α-L-arabinofuranosidase 1 (ARAF1)||Q9SG80||Arabidopsis thaliana|
|cds.c52258_g2_i5—m.60154||4,321,984.23||4,568,443.02||1.55||FO synthase||Q5YQD7||Nocardia farcinica|
|cds.c42560_g3_i2—m.13863||413,951.96||426,939.66||1.54||Uncharacterized protein||Q9ZUX4||Arabidopsis thaliana|
|Significantly down-regulated proteins upon MeJA treatment|
|cds.c49616_g1_i1—m.41564||3,013,895.02||1,408,517.22||0.66||Elongation factor-Tu||P46280||Glycine max|
|cds.c44545_g1_i1—m.18392||168,891.20||54,051.02||0.44||Probable deoxyhypusine synthase||Q9YE72||Aeropyrum pernix|
|cds.c56271_g1_i1—m.97063||585,856.87||265,127.66||0.66||ATP-dependent zinc metalloprotease FTSH 8||Q8W585||Arabidopsis thaliana|
|cds.c54200_g1_i2—m.76520||2,163,792.92||954,822.57||0.65||Protein translocon at the inner envelope membrane of chloroplasts (TIC) 62||Q8SKU2||Pisum sativum|
|cds.c52014_g2_i2—m.58176||585,776.63||254,375.22||0.61||chloroplast stem-loop binding protein of 41 kDa b||Q9SA52||Arabidopsis thaliana|
|cds.c52536_g1_i1—m.62408||577,417.30||176,611.11||0.48||Rhodanese-like domain-containing protein 4||Q9M158||Arabidopsis thaliana|
|cds.c54808_g4_i1—m.82256||742,278.68||228,493.84||0.45||ATP-dependent zinc metalloprotease FTSH 1||Q5Z974||Oryza sativa|
|cds.c49073_g3_i3—m.38259||748,656.47||194,635.44||0.38||Glycerate dehydrogenase||P13443||Cucumis sativus|
|cds.c57862_g3_i2—m.114731||199,431.98||85,355.50||0.65||Pescadillo homolog||A4RLI4||Magnaporthe oryzae|
|cds.c53365_g2_i1—m.69332||383,685.96||148,936.95||0.54||Tubulin beta-2 chain||Q40106||Lupinus albus|
|cds.c37568_g1_i1—m.8344||102,097.61||37,178.92||0.53||Transcription factor GATA-6||P43693||Gallus gallus|
Among these identified proteins, 40 proteins were found to be differentially expressed between control and MeJA treated samples (Table 2) with a cut-off value of greater than 1.5-fold or lesser than 0.67-fold differences. Furthermore, these differentially expressed proteins must satisfy three statistical tests at p-value <0.05 as detailed in the Material and Methods section. These stringent selection criteria were employed to be selective in our discussion as well as to minimize false positive results. This is also important for our subsequent correlation analysis with the transcriptome data set.
Twenty-eight proteins were upregulated upon the treatment and these proteins were involved in various biochemical pathways and cellular processes. Four proteinase inhibitors increased between 2.08 to 6.87-folds upon the treatment whereas several peroxidases (four peroxidase 12 and two peroxidase 51) were upregulated between 1.58 to 5.37-folds. Thioredoxin O1 which is involved in the redox processes similarly as the peroxidases was also upregulated (1.57-fold). Another three proteins were proteases (serine caboxypeptidase-like 18, serine caboxypeptidase-like 17 and aspartic proteinase A1). Three other proteins were involved in DNA binding or processing such as MFP1 (Matrix Attachment Region binding filament-like protein) attachment factor 1 (MAF1), ubiquitin-conjugating enzyme E2 variant 1D and endonuclease 4 with fold changes between 1.57 to 1.83. Furthermore, other proteins involved in lipid metabolism (linoleate 13S-lipoxygenase 2-1 and GDSL esterase/lipase) as well as phenolic biosynthesis (flavanone-3-hydroxylase and chorismate mutase 1) and aromatic compound biosynthesis (enone oxidoreductase) were also differentially regulated, with 1.54 to 2.27-fold increase upon MeJA treatment. The treatment also caused the upregulation of proteins involved in photosynthesis (carbonic anhydrase 2, 5.28-fold), protein glycosylation (beta-hexominidase 1, 1.86-fold), nitrogen storage (bark storage protein A (BSPA), 1.84-fold), cell wall degradation (α-L-arabinofuranosidase 1, 1.7-fold), cofactor biosynthesis (FO synthase, 1.55-fold) as well as an uncharacterized protein (1.54-fold).
Twelve proteins were found to be significantly downregulated upon the MeJA treatment (Table 2). Proteins mainly involved in photosynthesis (ATP-dependent zinc metalloprotease FTSH 8, protein translocon at the inner envelope membrane of chloroplasts (TIC) 62, chloroplast stem-loop binding protein of 41 kDa b, rhodanese-like domain-containing protein 4, ATP-dependent zinc metalloprotease FTSH 1 and glycerate dehydrogenase) were downregulated by 0.38 to 0.66-folds. Whereas the expression of proteins involved in protein synthesis/modification (elongation factor-Tu and probable deoxyhypusine synthase) as well as rRNA processing (Pescadillo homolog) were also reduced by 0.44 to 0.66-folds. Moreover, other proteins involved in structural organisation (tubulin beta-2 chain, 0.54-fold), a transcription factor (transcription factor GATA-6, 0.53-fold) as well as an unknown protein (0.6-fold) were also significantly downregulated.
All identified proteins were also compared with their transcript abundance from a previous transcriptomics report (Rahnamaie-Tajadod et al., 2017). Statistical correlation analysis between these proteome and transcriptome data sets suggests a weak correlation with Pearson’s r(738) = 0.341, p < 0.001 (Fig. 4A). However, a significantly positive correlation was observed for the 40 differentially expressed proteins with their corresponding transcripts (r(38) = 0.787, p < 0.001) (Fig. 4B). Among them, 28 significantly upregulated proteins also showed a strongly positive correlation (r(26) = 0.677, p < 0.001) (Fig. 4C) and the remaining downregulated proteins were weakly correlated (r(10) = 0.147, not significant) with their cognate transcript levels (Fig. 4D).
Proteomics study relies heavily on the protein sequence database which is often lacking in non-model species such as herbs including P. minor. The use of integrative proteomics and transcriptomics approaches (Fig. 1) allow a comprehensive study on this herb which successfully identified 751 proteins from the SWATH-MS analysis. MeJA elicitation also has been known to trigger various responses and this is further substantiated by current findings that a rather high percentage (15.7%) of identified proteins was assigned to the “response to stimulus” GO term (Fig. 3). Furthermore, “cellular process”, “metabolic process” and “biological regulation” terms were also having the most protein assignment (Fig. 3), suggesting that biochemical processes might be actively regulated in the proteome of P. minor in response to MeJA. Evidently, the differentially expressed proteins (Table 2) further indicate that several key biological pathways were modulated, including stress response mechanism, lipid metabolism, secondary metabolite production, apoptosis, photosynthesis as well as the regulation of protein synthesis and structural proteins.
MeJA triggers proteins related to stress response mechanism, lipid metabolism and secondary metabolite production
Several proteins related to defense and stress responses were differentially regulated upon the MeJA elicitation. For example, four proteinase inhibitors were significantly upregulated. These proteins were shown to be activated by similar elicitation in tomato, alfalfa, tobacco (Bolter & Jongsma, 1995; Farmer & Ryan, 1992) and maize (Zhang et al., 2015), mimicking a wounding response. These proteinase inhibitors are important for plant defense responses, capable of disrupting digestive system of insects to deter them from feeding on the plants (Sharma, 2015). Furthermore, an enzyme responsible for protein glycosylation, beta-hexominidase has also been implicated in plant defense against insects as it is shown to possess chitinase activity (Strasser et al., 2007). Another wound inducible protein with potential chitinase activity is BSPA (Meuriot et al., 2004). This protein was also implicated in nitrogen storage (Meuriot et al., 2004), yet its upregulation together with beta-hexominidase after MeJA treatment may imply the activation of a defense mechanism against such stress signal.
Stresses such as wounding also caused plants to generate reactive oxygen species (ROS). ROS may attack cellular proteins and enzymes causing aberrant modifications to their structural integrity and functions (Ray, Huang & Tsuji, 2012). Therefore, the presence of proteases during stress conditions are crucial for protein homeostasis. Our proteomics study revealed significant upregulation of a few proteases such as serine carboxypeptide-like 17, serine carboxypeptide-like 18 and aspartic proteinase A1 upon MeJA treatment. Consistent with our report, these proteins were also stimulated upon injury and MeJA treatment in other plant species such as tomato and rice (Feng & Xue, 2006; Moura, Bergey & Ryan, 2001).
Given that ROS are damaging to the plant cells, their homeostasis through redox-related enzymes such as peroxidases and thioredoxin are important for cellular integrity and biochemical processes (Zhang et al., 2015). In this study, several peroxidases (four peroxidases 12 and two peroxidases 51) and one thioredoxin (thioredoxin O1) were upregulated upon exogenous application of MeJA, suggesting their involvement in stress response. Peroxidases were also involved in lignin and suberin polymerization (Singh, Rastogi & Dwivedi, 2010), perhaps providing extracellular structural strength during an attack. Another upregulated protein, FO synthase which catalyses the coenzyme FO (7,8-didemethyl-8-hydroxy-5-deazariboflavin) may also be involved in this redox-related process (Grochowski, Xu & White, 2009) upon MeJA elicitation.
Furthermore, lipid metabolism may also be induced by exogenous MeJA application. Two lipolytic enzymes, linoleate 13S-lipoxygenase 2-1 and GDSL esterase/lipase were upregulated more than 2-fold upon the treatment. Interestingly, linoleate 13S-lipoxygenase 2-1 is the first enzyme in the α-linolenic acid metabolic pathway producing jasmonate (Luge et al., 2014). Proteomics study of Nicotiana occidentalis infected with phytoplasma, a pathogenic bacterium also revealed significant increase in both linoleate 13S-lipoxygenase 2-1 enzyme and jasmonate level (Luge et al., 2014). This suggests that the enzyme regulates positive feedbacks of jasmonate production during an injury response or stress. Furthermore, GER1 gene (GDSL containing enzyme rice 1) containing a GDSL motif was responsible for the light regulated JA response (Riemann et al., 2007), suggesting that the GDSL esterase/lipase could also be part of the defense mechanism mediated by jasmonate (Chepyshko et al., 2012).
Application of MeJA has also been known to induce secondary metabolite production including phenolic compounds such as flavonoids (Petrussa et al., 2013). Enzymes involved in this phenolic pathway, chorismate mutase and flavanone-3-hydroxylase (Tohge et al., 2013) were significantly upregulated in the MeJA treated herbs. Phenolics increase is associated with defense mechanism, owing to its antimicrobial activity to curb attacks from microbes during an injury response (Petrussa et al., 2013). Another secondary metabolite biosynthetic protein, enone oxidoreductase is involved in the production of furaneol, an aromatic volatile compound found in fruit such as pineapple and strawberry (Eshghi, Jamali & Rowshan, 2014; Klein et al., 2007). P. minor has been shown to increase both flavonoid and volatile organic compounds upon high temperature treatment (Goh et al., 2016), and this study further implies that MeJA elicitation could also exhibit similar response.
MeJA treatment induced apoptosis related proteins and downregulated photosynthetic proteins
Significant stresses on plants including biotic and abiotic factors may induce cellular apoptosis which can be characterized by hallmark events such as DNA degradation (Kacprzyk, Daly & McCabe, 2011; Reape & McCabe, 2008). In this study, a protein potentially involved in this event, endonuclease 4 (Triques et al., 2007) was significantly upregulated in MeJA treated samples. In a tobacco plant infected with a tobacco mosaic virus, nucleases activities were induced to degrade DNA (Mittler, Simon & Lam, 1997). This is perhaps as a means of recycling building blocks of the DNA during programmed cell death after pathogen invasion or stress signals (Reape & McCabe, 2008). Interestingly, ubiquitin-conjugating enzyme E2 variant 1D protein involved in the DNA damage tolerance (Wen et al., 2008) was also upregulated, suggesting DNA repair mechanism might be activated almost simultaneously upon DNA degradation. Despite such repair, the increase of endonuclease 4 as early as 24 h after MeJA treatment can be detrimental to the plant. Our study indicates that MeJA signal may induce apoptotic events such as leaf decoloration (due to chlorophyll breakdown) and yellowing towards our P. minor plants after 3 to 5 days upon treatment (Rahnamaie-Tajadod et al., 2017). This further suggests that photosynthesis and chloroplast integrity might be affected by the MeJA elicitation.
Congruently, several proteins involved in photosynthesis and/or chloroplast components such as ATP-dependent zinc metalloprotease FTSH 1 and 8, rhodanese-like domain containing protein 4, glycerate dehydrogenase, chloroplast stem-loop binding protein of 41 kDa b as well as protein TIC62 were significantly downregulated in P. minor leaf treated with MeJA. This suggests that in response to stress, plants reduced energy expensive processes such as photosynthesis, saving the energy for its defense mechanism (Attaran et al., 2014). In other species such as rice (Rakwal & Komatsu, 2000) and Arabidopsis (Chen et al., 2011), some photosynthetic proteins such as ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCO) were also reduced upon JA and MeJA treatment, respectively. This implies similar downregulation response towards photosynthesis upon exposure to stress signals in various plants. Interestingly, the level of carbonic anhydrase 2 involved in photosynthesis was significantly increased (more than 5-fold) in our P. minor treated samples. Carbonic anhydrase was known to be involved in salt stress adaptation and JA treatment caused its upregulation (Walia et al., 2007). MeJA signals might upregulate its expression in this study, but the main reason why such photosynthetic protein increased after the stress signals remains to be investigated.
Another protein found to be upregulated upon MeJA elicitation was MAF1. It is a nuclear structural protein responsible for the attachment of chromatin to the nuclear matrix, with other interacting partners (Gindullis, Peffer & Meier, 1999). MAF1 has also been shown to be significantly increased in drought-induced wheat (Bazargani et al., 2011), suggesting its potential role in chromatin reorganization during stress. Interestingly, another characteristic event for apoptosis is chromatin condensation (Reape & McCabe, 2008), but whether MAF1 also involved in this process requires further study.
MeJA negatively regulates protein synthesis and structural proteins
Proteins involved in the synthesis and modification of proteins such as elongation factor-Tu (EF-Tu) (Fu, Momčilović & Prasad, 2012) and probable deoxyhypusine synthase (Park et al., 2010) respectively, were decreased upon MeJA elicitation (Table 2). Furthermore, a protein related to rRNA processing, Pescadillo homolog protein (Zografidis et al., 2014) as well as a transcription factor GATA-6 were also downregulated. This implies that protein synthesis was switched off during an injury response induced by MeJA. This further supports plant strategy for energy conservation during an attack or stress signals, to cater for defense and recovery.
MeJA induction may also influence plant growth and cell wall structure. In this study, a structural protein, tubulin beta-2 chain was downregulated whereas a cell wall remodelling protein, α-L-arabinofuranosidase 1 (ARAF1) was upregulated. Beta-tubulin, a component of microtubules in cells is mainly involved in plant cell division, elongation and cell wall structure formation (Yakovleva, Egorova & Tarchevsky, 2013). Tubulin has also been shown to be downregulated, along with plant growth impediment in rice (Cho et al., 2007) and pea (Yakovleva, Egorova & Tarchevsky, 2013) upon JA or MeJA elicitation, respectively. Furthermore, ARAF1 is associated with polysaccharide degradation in plant cell wall (Minic et al., 2004), suggesting its upregulation upon stress signal may contribute to cell wall modification. This further supports that growth-related processes are suppressed in plant treated with MeJA, as would be expected in a stress condition, perhaps in response to the apoptosis discussed earlier.
Two unknown proteins were also found to be either upregulated or downregulated, respectively upon MeJA treatment (Table 2). As such, these proteins may be associated with stress conditions, yet further investigation are needed to characterize their functions and roles in this P. minor herbs.
Correlation analysis between proteome and transcriptome data reveals the existence of post-transcriptional and post-translational regulation
In the previous transcriptome study, several candidate genes involved in jasmonate biosynthesis and signaling were validated using quantitative Real Time-PCR (qRT-PCR) (Rahnamaie-Tajadod et al., 2017). The results showed a considerably good correlation (R2 = 0.82) between the RNAseq and qRT-PCR data. In this study, we have extended such analysis to compare both the transcriptome and currently obtained proteome data. As this plant is considered as a non-model organism, we have used the transcriptome non-redundant sequences as our reference sequence database for protein identification (proteomics informed by transcriptomics approach) and as such comparative analysis is important to illuminate complementing or contrasting trends between the different molecular levels, proteins and transcripts. Other plant proteomics studies have only utilised qRT-PCR for complementing their protein expression levels such as in Botrytis infected kiwifruit (Liu et al., 2018), virus infected rice (Yu et al., 2017) and rapeseed varieties (Wang et al., 2018). The comparison between both proteome and transcriptome as performed in this report will allow even wider comparative analysis of the expression profiles between these two omics studies.
Our result suggests that the majority of both proteome and transcriptome expression levels do not correlate as measured by Pearson’s r = 0.341 (Fig. 4A), differences that can be attributed to the existence of post-transcriptional regulation. Such regulation is common in eukaryotic organisms as shown previously in the omics studies of plant nematodes (Zhou et al., 2016) and the stress treatments of Arabidopsis (Lan, Li & Schmidt, 2012; Liang et al., 2016; Marmiroli et al., 2015). Interestingly, a comparison between significantly expressed proteins and their corresponding transcripts were positively well-correlated (r = 0.787) (Fig. 4B). Such significant correlation may have been mostly attributed by the proteins that were upregulated (r = 0.677) (Fig. 4C) rather than the downregulated proteins (r = 0.147) (Fig. 4D). These contrasting correlations were similarly observed in phosphate deficient Arabidopsis (Lan, Li & Schmidt, 2012), speculating that stresses may specifically induce protein degradation post-translationally while not affecting transcript levels. This may serve as an advantage to the plant, as further de novo transcription is not needed if the stress is released (Lan, Li & Schmidt, 2012). Another possibility is that transcript and protein downregulation may have different timing such that their monitoring at a specific time point is not possible (Lan, Li & Schmidt, 2012). However, further experimentation is needed to account for these notions.
In conclusion, this is the first proteomics study on this non-model herbal species, P. minor particularly using an advance proteomics platform called SWATH-MS, enriched with a previously reported transcriptome database for protein identification. This has enabled us to profile a comprehensive proteome coverage of 751 proteins, and forty were found differentially expressed. The modulated levels of these proteins suggest that the hormone invoked defense and recovery response but suppressed proteins involved in growth and development. Correlation analysis between our proteome study and previously reported transcriptome analysis suggests that post-transcriptional and post-translational regulation may have existed to regulate certain groups of proteins.
Basic bioinformatics obtained through Blast2GO analysis which include E-value distribution, sequence similarity distribution and top-hit species distribution
Distinct peptide level False Discovery Rate (FDR) analysis using ProteinPilot software
The raw data for the peak areas of 751 identified proteins from Persicaria minor
Three biological replicates for both control (C1, C2 and C3) and treated (T1, T2 and T3) samples as well as three technical replicates (rep 1, rep 2 and rep 3) for each biological replicate were run using SWATH-MS analysis.
The statistical analyses performed for the 751 identified proteins from Persicaria minor
Mean peak areas (three biological replicates) for control (Mean C) and treated (Mean T) samples were generated from SWATH-MS proteomics analysis.