1. Introduction
With continuous changes in the ecological environment, the area of saline-alkali land worldwide is increasing every year, becoming a global, burning issue [1]. Secondary salinization caused by the excessive use of fertilizers and irrational soil cultivation seriously affects the growth, development, yield, and quality of crops [2,3]. Salt stress affects water absorption, leading to cell dehydration and osmotic stress [4]. The excessive accumulation of salt ions caused by water transpiration triggers ionic stress in plant cells, which affects plant morphology and physiological and biochemical processes and ultimately limits plant growth and development [5]. High salinity also affects plant photosynthesis by regulating gene expression and stomatal closure, ultimately leading to a reduction in crop productivity due to decreased carbon dioxide absorption [6].
mRNA sequencing (mRNA-seq) based on transcriptome profiling has become an efficient, routine technology for the signaling pathway analysis of transcriptional regulation in plant responses to salt stress [7]. Under salt stress, many defense-related genes are activated by transcriptional reprogramming in plants, a process in which transcription factors play vital roles [8,9]. Apetala2/ethylene-responsive factor (AP2/ERF) is a major plant-specific family of transcription factors comprised of four main functional domains: the nuclear localization signal region, DNA-binding domain, transcriptional regulatory domain, and oligomerization site [10]. AP2/ERF transcription factor superfamily members have one or more typical AP2/ERF domains composed of 60–70 highly conserved amino acids that recognize and bind DNA [11]. According to sequence similarity and the number of AP2/ERF domains, the AP2/ERF transcription factor superfamily is divided into three main families: AP2, ERF, and RAV (related to ABI3/VP1). AP2 family members contain two conserved AP2 domains, RAV family members harbor an AP2 domain and a B3 domain, and ERF family members have an AP2 domain and a WLG motif [12]. The ERF transcription factor family can be divided into two subfamilies: dehydration-responsive element-binding protein (DREB) and ERF [13]. The sequences of the AP2/ERF-conserved domains are relatively similar, and they differ in the type of cis-elements within the target gene promoter bound by subtribe members of the AP2/ERF transcription factor [14,15]. DREB proteins recognize and bind to the drought-responsive cis-element harboring the A/GCCGAC core sequence [16], while ERF proteins bind to the GCC box (AGCCGCC) cis-element [17]. ERF transcription factors are mostly involved in ethylene and abscisic acid (ABA) signaling pathways and function in plant responses to salt [18,19,20], cold [21,22,23], heat [24,25], drought [26,27,28,29], and pathogen attacks [30,31,32]. These transcription factors regulate the expression of the downstream stress-response genes by binding to specific cis-elements within the promoters [33,34]. However, the roles and mechanisms of most ERF transcription factors in eggplant responses to salt stress remain largely unknown.
Abscisic acid (ABA) acts as a phytohormone and plays a vital role in plant responses to abiotic stress including salt and drought stress [35,36,37]. Salt or drought stress can cause the endogenous plant ABA level to rise by 40-fold [38]. The activation of ABA biosynthetic enzymes plays a vital role in the plant against salt and drought stresses. During ABA biosynthesis, 9-cis-epoxycarotenoid dioxygenases (NCEDs) can catalyze 9-cis-epoxycarotenoids, the cleavage of 9-cis-epoxycarotenoids, to xanthoxin [39]. In Arabidopsis thaliana, NCED3 acts as a key regulation factor in ABA biosynthesis in plant responses to water deficit and salt stress [40,41]. The transcription factor NGATHA1 can regulate the NCED3 expression level in the Arabidopsis thaliana response to salt stress [42].
Eggplant is an agriculturally vital solanaceous vegetable cultivated worldwide [43]. Salt stress critically affects eggplant yield; however, the mechanisms underlying the salt stress response of eggplant remain unclear. In this study, we aimed to investigate the response mechanisms of eggplant to salt stress and identify the key genes involved in eggplant responses to salt stress. We performed an RNA sequencing assay to screen the differentially expressed genes (DEGs) in the eggplant roots under salt stress and identified the different metabolic pathways involved in eggplant responses to salt stress by gene ontology (GO) annotation and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis. We selected and characterized an AP2/ERF transcription factor family member, SmERF1, which acts as a positive regulator of the eggplant response to salt stress.
2. Results
2.1. Sequencing Data Summary and DEGs Analysis
Transcriptional assays in the eggplant inbred line ML41 were performed to screen potential target genes involved in the response to salt stress. The roots of ML41 treated with 150 mM NaCl solution were harvested at 0 and 24 h post-treatment for mRNA-seq analysis [7]. Illumina high-throughput sequencing yielded 281.9 million clean reads, corresponding to an average of 47 million sequence reads per sample. Approximately 91.53% of the paired-end clean reads were aligned to the Solanum melongena reference genome (
2.2. GO Analysis of DEGs
The functional classification of the DEGs induced by salt treatment was investigated using GO enrichment analysis. The top 20 enriched GO terms included biological processes, molecular functions, and cellular components (Figure 2). The upregulated DEGs were significantly assigned to 127 pathways in biological processes, 82 pathways in molecular functions, and 67 pathways in cellular components; the downregulated DEGs were assigned to 215 pathways related to biological processes, 96 pathways in molecular functions, and 34 pathways in cellular components (Table S2).
Within biological processes, upregulated DEGs were significantly enriched in 127 pathways, including the response to oxygen-containing compounds (GO:1901700) related to ABA responsiveness [46], the response to acid chemicals (GO:0001101) such as pyruvic acid, which is related to the process of ABA biosynthesis [47], and the response to water (GO:0009415) (Table S2). This indicated the role of ABA in plant responses to salt treatment and suggested that the expression of the genes upregulated by salt may involve in these pathways.
2.3. KEGG Analysis of DEGs
KEGG analyses were conducted to further understand the function of the DEGs associated with the salt response. The 14 up-enrichment pathways and 18 down-enrichment pathways were enriched by salt stress treatment in eggplant roots, respectively (Table S3). The up-regulated genes were significantly enriched in the categories “plant-pathogen interaction” and “plant hormone signal transduction” (Figure 3a), whereas the down-regulated genes were enriched for the categories “metabolic pathways”, “biosynthesis of secondary metabolites”, “starch and sucrose metabolism”, and “pentose and glucuronate interconversions” (Figure 3b). These results indicated that salt stress induces multiple biological processes in eggplants at the whole-genome level.
The results of the KEGG analyses showed that salt stress treatment upregulates the transcript expression levels of genes related to plant–pathogen interaction and plant hormone signal transduction (Figure 3a). Therefore, we selected eight plant–pathogen interaction-related genes (Table S4), namely, SmMAPKKK1, SmWRKY20, SmRIN1, SmERF1, SmHSP90-5, SmCNGC17, SmCDPK11, and SmCDPK32, and five ABA signal transduction-related genes (Table S4), including the environmental stress-inducible protein TAS14 (SmTAS14), a late embryogenesis abundant protein family member Dehydrin 1 (SmDHN1) [48], Dehydrin Xero 1 (SmDHNX1), which is regulated by ABA signaling [49], abscisic acid 8′-hydroxylase 3 (SmABA8′HO3) [25], and glutathione S-transferase U10 (SmGSTU10), to detect their transcript expression levels in eggplant roots under salt stress by a quantitative real-time PCR (qPCR) assay. Four biological replications (one plant root as a biological repeat) were used for the detection of above-mentioned genes’ transcript expression levels treated with salt stress at 0, 3, 6, 12, 24, and 48 h post treatment. The transcript expression levels of these genes were significantly upregulated by the salt stress treatment (Figure 4), which is consistent with the mRNA-seq data. Similarly, salt stress significantly upregulated the transcript expression levels of the salt stress defense-related marker genes 9-cis-epoxycarotenoid dioxygenase 1 (SmNCED1) and SmNCED2 [40,50] (Figure 5).
2.4. Sequence Analysis of SmERF1
The KEGG analysis showed that SmERF1 belongs to the plant–pathogen interaction pathway, and its relative transcript expression level was significantly upregulated by salt stress treatment. The fold of the transcript expression level of SmERF1 up-regulated at 48 h post-salt stress treatment was higher than the other seven selected genes. This suggests that SmERF1 may play a role in eggplant responses to salt stress or pathogen attacks. To verify the function of SmERF1 in the eggplant response to salt stress, we first analyzed the sequence of SmERF1. The full-length open reading frame (ORF) sequence of SmERF1 was obtained by searching the Eggplant Genome Database (
2.5. Subcellular Localization of SmERF1
We analyzed the subcellular localization of SmERF1 in the epidermal cells of N. benthamiana leaves. The full-length ORF of SmERF1 was cloned into the destination vector pBinGFP2 to generate the recombinant vector pBinGFP2-SmERF1 (35S:SmERF1-GFP); the empty vector pBinGFP2 (35S:GFP) was used as a control (Figure S2a). Cells of the Agrobacterium tumefaciens strain GV3101 carrying 35S:SmERF1-GFP (containing a GFP tag), 35S:H2B-RFP (containing a red fluorescence protein tag and acting as a marker of nuclear localization), or 35S:GFP constructs were cultivated in liquid Luria–Bertani (LB) medium overnight, and the bacterial fluid was infiltrated into N. benthamiana leaves. Green and red fluorescence signals in the epidermal cells of N. benthamiana leaves were detected at 48 h post-infiltration. Both green fluorescence signals of 35S:SmERF1-GFP and red fluorescence signals of 35S:H2B-RFP were observed in the nuclei, whereas the green fluorescence signals of 35S:GFP appeared throughout the cell (Figure S2b).
2.6. Transcriptional Activation Activity Analysis
Accumulating evidence has demonstrated that ERF transcription factors play a vital role in plant responses to biotic or abiotic stresses by activating the expression of downstream target genes [31,52,53,54,55]. To investigate the SmERF1 activity in transcriptional activation, we performed a transcriptional activation activity assay using the yeast GAL4 system. The full-length ORF of SmERF1 was cloned into the bait vector pGBKT7 to generate the recombinant vector pGBKT7-SmERF1 (Figure 6a). Yeast cells (AH109) containing the pGBKT7-SmERF1 construct and those with pGBKT7 formed colonies on the solid yeast peptone dextrose adenine (YPDA) medium lacking tryptophan (Trp). We further inoculated the yeast cells with pGBKT7-SmERF1 or pGBKT7 on a solid YPDA medium containing X-α-Gal but lacking both Trp and histidine (His). The yeast cells carrying pGBKT7-SmERF1 constructs grew well and formed blue bacterial colonies. In contrast, the yeast cells carrying the pGBKT7 vector did not survive on the solid YPDA medium supplemented with X-α-Gal and lacking Trp and His (Figure 6b), suggesting that SmERF1 has transcriptional activation activity.
2.7. SmERF1 Silencing Enhanced the Susceptibility of Eggplant to Salt Stress
For the silencing of SmERF1, Agrobacterium tumefaciens GV3101 cells transformed with the pTRV1 vector were mixed with the cells carrying pTRV2:SmERF1, pTRV2:00, or pTRV2:SmPDS constructs, and the bacterial fluid was infiltrated into the cotyledon of 2–4 leaf-stage eggplant seedlings. When photobleaching occurred in the eggplant plant leaves infiltrated with Agrobacterium tumefaciens GV3101 cells contenting TRV:SmPDS constructs, four biological repeats (one plant root as a biological repeat) of the control (TRV:00) or SmERF1-silenced (TRV:SmERF1) plants were used to detect the silencing efficiency of SmERF1 using qPCR in the conditions of salt stress treatment. The relative transcript expression levels of SmERF1 in SmERF1-silenced (TRV:SmERF1) eggplant roots were significantly reduced by approximately 85% compared with those in the control plants (Figure 7a). The TRV:SmERF1 and TRV:00 plants were treated with 150 mM NaCl solution to assess their tolerance to salt stress. The TRV:SmERF1 plants displayed more serious wilt symptoms and lower survival rates than the TRV:00 plants at 2 days post-treatment (Figure 7b,c). Compared with the control plants, SmERF1 silencing significantly reduced the relative transcript expression levels of the defense-related marker genes SmNCED1, SmNCED2, SmDHN1, and SmDHNX1, which were respectively reduced by approximately 81%, 86%, 93%, and 92%, in SmERF1-silenced eggplant roots (Figure 7d). We also monitored the enzyme activity of superoxide dismutase (SOD) and catalase (CAT), as well as the content of H2O2 and proline, and four biological repeats at each time point were used to detect the above-mentioned physiological indexes and found that SmERF1 silencing significantly reduced the accumulation of H2O2 and proline and the activity of SOD and CAT compared to the control plants in the 150 mM NaCl solution treatment (Figure 7e). These data suggest that SmERF1 acts as a positive regulator of eggplant responses to salt stress.
2.8. The Transient Overexpression of SmERF1 Triggers Cell Death in Eggplant Leaves
The analysis of the mRNA-seq data revealed that SmERF1 belongs to the plant immune response pathway. To investigate the role of SmERF1 in the eggplant immune response, we transiently overexpressed 35S:SmERF1-GFP or 35S:00 (empty vector, EV) in eggplant leaves. We first detected the expression of SmERF1 in eggplant leaves (four biological repeats) 48 h post-infiltration by a qPCR assay, thus confirming its successful expression (Figure 8a). In addition, the transient overexpression of SmERF1 accumulated more H2O2, as indicated by the diaminobenzidine (DAB) staining and the darker trypan blue staining of the eggplant leaves with 35S:SmERF1 transient overexpression compared to the leaves with EV transient overexpression at 3 days post-infiltration (Figure 8b). These data indicate that SmERF1 may function in the eggplant immune response.
3. Discussion
Salt stress is one of the most important abiotic stressors in eggplants. It reduces the yield and quality of eggplant by affecting physiological and biochemical processes such as water transport, cell osmotic pressure, and photosynthesis [4,5]. A better understanding of the underlying molecular mechanisms of eggplant response to salt stress will aid the breeding of varieties with improved salt tolerance. Through the mRNA-seq assay, we identified the DEGs in eggplant roots treated with salt stress and investigated the markedly enriched biological processes and pathways by GO and KEGG analyses. Accumulating evidence has demonstrated that AP2/ERF transcription factors play a vital role in plant resistance to salt stress [56,57,58,59]. An AP2/ERF transcription factor superfamily member, SmERF1, belonging to the plant–pathogen interaction pathway, was selected and was confirmed to act as a positive regulator in eggplant responses to salt stress.
SmERF1 (711 bp) encoded a 26 kDa protein and shared the highest sequence identity (86%) and the closest affinity with Solanum tuberosum ERF1 (Figure S1a,c). The promoter of SmERF1 harbored stress− or pathogen-responsive cis−elements, suggesting that SmERF1 may play a role in eggplant responses to biotic or abiotic stresses (Figure S1d). Our data showed that the transcript expression level of SmERF1 in eggplant roots was markedly upregulated by salt stress treatment (Figure 4a). SmERF1 localizes to the nucleus and activates the transcriptional activation (Figure 6 and Figure S2). In the VIGS assay, SmERF1 silencing significantly enhanced the susceptibility of the plants to salt stress (Figure 7b) and down−regulated the transcript expression levels of the salt stress defense−related marker genes SmNCED1 [40,50], SmNCED2, SmDHN1 [48], and SmDHNX1 (Figure 7d). These genes contribute to the plant’s response to salt stress via the ABA signaling pathway, which is accompanied by a reduction in SOD and CAT enzyme activity and an increase in H2O2 and proline content (Figure 7e). These data indicate that SmERF1 positively regulates eggplant responses to salt stress and is closely related to ABA signaling networks. However, it remains unknown how SmERF1 affects the transcript expression levels of the above-mentioned salt stress defense-related marker genes. One possible explanation is that SmERF1 binds to the dehydration-responsive element (DRE) core cis-element within the SmDHN1 promoter, regulating eggplant tolerance to salt stress (Figure 7d and Figure 9). KEGG analyses revealed that SmERF1 belongs to the plant–pathogen interaction pathway (Table S3), and intense cell death was triggered in eggplant leaves by the transient overexpression of SmERF1 (Figure 8b). The AP2/ERF transcription factors CaAP2/ERF064 and CaAIL1 can trigger reactive oxygen species (ROS) burst, leading to intense cell death in pepper and N. benthamiana leaves, as they mediate the immunity of these species [60,61]. Therefore, it can be speculated that SmERF1 positively regulates the plant immune response by mediating ROS signaling networks. In conclusion, our data suggest that SmERF1 acts as a positive regulator of salt stress in eggplants.
4. Materials and Methods
4.1. Plant Material and Salt Treatment
The seeds of the inbred eggplant line ML41 were germinated by wrapping them in moistened gauze and incubating them at 25 °C for 1 week. For mRNA-seq analysis, the roots of 4–6 leaf-stage seedlings with a uniform size were soaked in Hoagland nutrient solution, and the seedlings were grown at 25 °C under a 16 h light/8 h dark photoperiod with 800 μmol m−2 s−2 illumination. For the virus-induced gene silencing and subcellular localization assay, the ML41 and N. benthamiana seedlings were grown in plastic flowerpots filled with sterilized soil in an illumination incubator at 25 °C under a 16 h light/8 h dark photoperiod with 800 μmol m−2 s−2 illumination.
For the salt treatment, the roots of 4–6 leaf-stage eggplant seedlings were soaked in 150 mM NaCl solution for 24 h; ddH2O treatment served as a control. Three different samples were used as biological replicates for the salt treatment. The eggplant roots were washed with ddH2O, frozen in liquid nitrogen, and stored at −80 °C for mRNA-seq analysis.
4.2. Total RNA Extraction, cDNA Library Construction, and Illumina Sequencing
The total RNA was extracted from the NaCl-treated and ddH2O-treated roots of eggplant seedlings using a FastPure Plant Total RNA Isolation Kit (Vazyme, Nanjing, China), according to the manufacturer’s instructions. RNA purity and concentration were examined using a NanoDrop 2000 spectrophotometer (Thermo Fisher Scientific, Waltham, MA, USA), and RNA integrity and quantity were measured using an Agilent 2100/4200 system (Agilent Technologies, Santa Clara, CA, USA).
cDNA sequencing libraries were constructed using a TruSeq RNA Sample Preparation kit (Illumina, San Diego, CA, USA), following the manufacturer’s instructions. mRNA was purified from the total RNA using poly-T and then fragmented into 300–350 bp fragments. First-strand cDNA was reverse-transcribed using fragmented RNA and dNTPs, and second-strand cDNA was synthesized subsequently. The sequencing adaptors were ligated to cDNA, and the library fragments were purified. The template was enriched by PCR, and the PCR product was purified to obtain the final library.
Paired-end reads of 150 bp were generated by sequencing on an Illumina HiSeq 2000 system after library preparation and the pooling of different samples.
4.3. mRNA-Seq Read Processing and Assembly
Raw data (raw reads) in FASTQ format were generated using an Illumina HiSeq X-ten genome analyzer. Fast Q was used to analyze the raw reads and assess the base quality [62]. Clean data (clean reads) were obtained by removing the reads harboring adaptor sequences and low-quality reads with more than 20% nucleotides with Qphred ≤ 5. The Q20, Q30, and GC contents of the clean data were calculated, and the SILVA database (
4.4. Sequencing Data Processing and Analysis
The fragments per kilobase per million mapped reads (FPKM) value was used to assess the transcript expression levels of the genes. The FPKM value was measured using EdgeR to identify DEGs [63]. Genes with a |log2 (Fold Change)| > 1 & a q value < 0.05 were assigned as significantly differently expressed. Hierarchical cluster analysis was performed on the DEGs by using the heatmap package in R language. To investigate the biological function of the DEGs, the pathways enriched under salt stress treatment were identified using GO and KEGG analyses, as described previously [64,65]. The q value < 0.05 was assigned as significant enrichment.
4.5. Vector Construction
For the subcellular localization and transcriptional activation of SmERF1, the full-length ORF of SmERF1 was amplified by PCR and cloned into the destination vector pBinGFP2 or pGBKT7 using a ClonExpress II One Step Cloning Kit (Vazyme), according to the manufacturer’s instructions.
For the VIGS assay, a specific 300 bp DNA fragment from the SmERF1 full-length ORF was amplified and cloned into the entry vector pDONR207 by a BP recombination reaction and then transferred into the destination vector pTRV2 by LR recombination, according to the manufacturer’s instructions.
4.6. Agrobacterium tumefaciens Cultivation and Infiltration and Subcellular Localization Analysis of SmERF1
The recombinant vector pBinGFP2-SmERF1 was transformed into competent cells of the Agrobacterium tumefaciens strain GV3101. Positive GV3101 cells carrying 35S:SmERF1-GFP, 35S:GFP, or 35S:H2B-RFP constructs were cultivated in liquid LB medium containing 50 mg/mL kanamycin and 50 mg/mL rifampicin at 28 °C and 200 rpm overnight. The bacterial culture was centrifuged at 28 °C and 6000 rpm for 10 min and resuspended in an infiltration medium (10 mM MES, 10 mM MgCl2, 200 mM acetosyringone, pH = 5.4) to adjust the OD600 to 0.8. The bacterial fluid of GV3101 cells harboring 35S:H2B-RFP constructs was mixed with cells carrying 35S:SmERF1-GFP or 35S:GFP constructs at a 1:1 ratio. The mixed bacterial fluid was infiltrated into the leaves of N. benthamiana using a disposable sterile syringe without a needle. Fluorescence signals were observed using a laser scanning confocal microscope (TCS SP8; Leica Microsystems, Wetzlar, Germany).
4.7. VIGS Assay
The VIGS assay was performed as previously described [66]. The function of SmERF1 in eggplant responses to salt stress was verified by conducting a VIGS assay. A specific 300 bp DNA fragment from the full-length ORF of SmERF1 was amplified by PCR, cloned into the entry vector pDONR207, and transferred into the destination vector pTRV2. Agrobacterium tumefaciens GV3101 cells carrying the pTRV1 vector were mixed with cells containing pTRV2:SmERF1, pTRV2:00, or pTRV2:SmPDS constructs at a 1:1 ratio. The mixtures were slowly incubated at 28 °C and 60 rpm for 3 h and injected into the cotyledon of 2–4 leaf-stage eggplant seedlings. The infiltrated seedlings were placed at 25 °C without light for 24 h and then transferred to an illumination incubator at 25 °C under a 16 h light/8 h dark photoperiod.
4.8. qPCR Assay
The qPCR assay was performed as previously described to analyze the transcript expression levels of the selected genes [66,67], and four biological repeats were used to detect the transcript expression levels of the target genes. The primer pairs used in this study are listed in Supplementary Table S5.
4.9. Physiological Index Measurement
The contents of proline and H2O2 and the enzyme activities of CAT and SOD were measured as previously described [68].
4.10. Histochemical Staining
Histochemical staining with DAB and trypan blue was performed as previously described [69].
5. Conclusions
In this study, we obtained the DEGs in the roots of eggplant plants treated with salt stress and investigated the biological processes and pathways significantly enriched by salt stress treatment. Eight genes related to the plant–pathogen interaction pathway and five genes associated with the ABA signal transduction pathway were selected, and the transcript expression levels of these genes were notably upregulated in the eggplant roots treated with salt stress. We further confirmed the positive function of SmERF1, which belongs to the plant–pathogen interaction pathway, in eggplant responses to salt stress and found that the transient overexpression of SmERF1 triggered intense cell death in eggplant leaves. These results indicate that SmERF1 acts as a positive regulator of salt stress in eggplant. In summary, our study provides the first report on the role of the ERF transcription factor in eggplant responses to salt stress and will help to further elucidate the mechanisms of SmERF1-regulated stress responses in eggplant. The results presented here lay the foundation for the effective genetic improvement of salt stress tolerance in eggplant.
L.S. and X.Y. designed the research. L.S. and E.Z. conducted the experiments. L.S. and X.Y. analyzed the data and wrote the manuscript. L.S. and R.L. revised the manuscript. All authors have read and agreed to the published version of the manuscript.
Not applicable.
Not applicable.
Not applicable.
The authors declare no conflict of interest.
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Enlarge this image.Figure 1. Spatiotemporal gene expression patterns under salt stress treatment. (a) Principal component analysis (PCA) of the samples at 0 and 24 h post−treatment based on the normalized expression levels of differentially expressed genes (DEGs). (b) Volcano plot of the differential expression levels of up-regulated and down−regulated DEGs in eggplant roots under salt stress. (c) Heat map of correlations between the transcript expression levels of DEGs in eggplant roots treated with salt stress. FPKM values were used for the hierarchical cluster analysis after the normalization of FPKM values with Z-score.
Enlarge this image.Figure 2. Functional classification of DEGs in eggplant roots under salt stress based on gene ontology (GO) analysis. GO analysis of up-regulated (a) and down-regulated (b) DEGs of the top 20 terms of biological processes (BP), molecular functions (MF), and cellular components (CC).
Enlarge this image.Figure 3. KEGG analysis of DEGs in eggplant roots under salt stress. KEGG analysis of the significantly up-regulated (a) and down-regulated (b) DEGs of the enriched pathways.
Enlarge this image.Figure 4. Transcript expression levels of genes associated with the plant–pathogen interaction pathway (a) and the ABA signal transduction pathway (b) in eggplant roots under salt stress detected by a qPCR assay. Data are means ± standard deviation from four biological replicates. Different capital letters between samples denote significant differences according to one-way ANOVA and Tukey’s test (p < 0.01).
Enlarge this image.Figure 5. Analysis of the relative transcript expression levels of marker genes related to salt stress responses in eggplant roots under salt stress inferred by a qPCR assay. Data are means ± standard deviation from four biological replicates. Different capital letters between samples denote significant differences according to one-way ANOVA and Tukey’s test (p < 0.01).
Enlarge this image.Figure 6. Transcriptional activation activity assay of SmERF1 using the yeast GAL4 system. (a) Diagram of pGBKY7 and the recombinant pGBKT7-SmERF1 vector. (b) Growth of yeast cells transformed with the pGBKT7 empty vector or recombinant pGBKT7−SmERF1 on a medium supplemented with X−α−Gal but lacking His and Trp. Blue color indicates the activation of the transcriptional activity. BD, binding domain.
Enlarge this image.Figure 7. Effects of SmERF1 silencing on eggplant responses to salt stress (TRV:SmERF1, SmERF1-silenced; TRV:00, control). (a) Silencing efficiency of SmERF1 in plants under a salt stress base on a qPCR assay. (b) Phenotype of SmERF1-silenced and control plants challenged with salt stress at 2 days post-treatment. (c) Survival frequencies of SmERF1-silenced and control plants subjected to salt stress at 2 days post-treatment. (d) Relative transcript expression levels of the salt stress defense-related marker genes SmCNGC1, SmCNGC2, SmDHNX1, and SmDHN1 in SmERF1-silenced and control plants under salt stress at 48 h post-treatment. (e) Proline and H2O2 content and catalase (CAT) and superoxide dismutase (SOD) activity in SmERF1-silenced and control plant roots under salt stress at 48 h post-treatment. In (a,c–e), data are the means ± standard deviation from four biological replicates. Different capital letters between samples denote significant differences according to the one-way ANOVA test (p < 0.01).
Enlarge this image.Figure 8. Transient overexpression of SmERF1 in eggplant leaves. (a) qPCR-based detection of SmERF1 transcript expression levels in leaves with transiently overexpressed SmERF1 and the empty vector (EV) at 48 h post-infiltration. (b) DAB and trypan blue staining of leaves infiltrated with Agrobacterium tumefaciens GV3101 cells transformed with 35S:SmERF1-GFP or 35S:GFP constructs at 3 days post-infiltration. Data are the means ± standard deviation from four biological replicates. Different capital letters between samples denote significant differences according to Student’s test (p < 0.01).
Supplementary Materials
The following supporting information can be downloaded at:
References
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