- Research article
- Open Access
Comparative mitochondrial proteomic, physiological, biochemical and ultrastructural profiling reveal factors underpinning salt tolerance in tetraploid black locust (Robinia pseudoacacia L.)
- Qiuxiang Luo†1, 2,
- Mu Peng†1, 2,
- Xiuli Zhang1,
- Pei Lei1,
- Ximei Ji1,
- Wahsoon Chow1, 3,
- Fanjuan Meng1Email author and
- Guanyu Sun1Email author
© The Author(s). 2017
- Received: 23 December 2016
- Accepted: 8 August 2017
- Published: 22 August 2017
Polyploidy is an important phenomenon in plants because of its roles in agricultural and forestry production as well as in plant tolerance to environmental stresses. Tetraploid black locust (Robinia pseudoacacia L.) is a polyploid plant and a pioneer tree species due to its wide ranging adaptability to adverse environments. To evaluate the ploidy-dependent differences in leaf mitochondria between diploid and tetraploid black locust under salinity stress, we conducted comparative proteomic, physiological, biochemical and ultrastructural profiling of mitochondria from leaves.
Mitochondrial proteomic analysis was performed with 2-DE and MALDI-TOF-MS, and the ultrastructure of leaf mitochondria was observed by transmission electron microscopy. According to 2-DE analysis, 66 proteins that responded to salinity stress significantly were identified from diploid and/or tetraploid plants and classified into 9 functional categories. Assays of physiological characters indicated that tetraploids were more tolerant to salinity stress than diploids. The mitochondrial ultrastructure of diploids was damaged more severely under salinity stress than that of tetraploids.
Tetraploid black locust possessed more tolerance of, and ability to acclimate to, salinity stress than diploids, which may be attributable to the ability to maintain mitochondrial structure and to trigger different expression patterns of mitochondrial proteins during salinity stress.
- Physiological characters proteomics
- Salinity stress
- Tetraploid black locust (Robinia pseudoacacia L.)
Salinity is a major limiting factor that adversely affects plant growth and crop productivity and quality worldwide . Increased salinization may lead to a loss of 10 million ha of farming land each year . In general, salinity stress may lead to water deficits, ion toxicity, osmotic stress, membrane alterations, ionic toxicity, and free radical production of plants . Many plants exhibit slow growth or death under salinity stress. To survive this salinity stress, plants have evolved complex mechanisms based on modifications in metabolites, gene expression, and proteins . To date, many genes responding to salinity stress in plants have been identified . However, relatively little is known about the detailed physiological and molecular mechanisms underlying polyploid plants to salinity stress.
Polyploidization occurs in 75% angiosperms and 95% ferns in plants . Therefore, polyploidy is a common phenomenon in the evolution of angiosperms [7, 8], which can facilitates adaptive evolution . Polyploid plants play important roles in agricultural production due to their specific traits such as longer leaves , morphological enlargements in seeds and corolla limbs  and delayed flowering . Additionally, some polyploidy forest species also showed a lot of advantages over their diploid counterparts, including larger leaves, greater growth vigour, better timber quality and higher stress resistance [13, 14]. However, empirical data supporting this hypothesis are scarce, especially for forest species .
In addition, many polyploids are superior to diploids with respect to tolerance to environmental stresses. In recent years, many studies have been conducted on polyploid plants. However, most of these studies are focused on various crops species, such as potato (Solanum tuberosum) , maize (Zea mays L.) , cotton (Gossypium hirsutum)  and cabbage (Brassica oleracea L)  or the model plant Arabidopsis thaliana [6, 20]. However, very little is known about polyploid forest species.
Generally, polyploidy can be classified as autopolyploidy from the doubling of chromosomes of a single species and allopolyploidy from the hybrids between two species. Tetraploids are a common type among polyploids . As a polyploid plant, tetraploid black locust (Robinia pseudoacacia L.), which is native to Korea, is a preferred tree species in the timber forest due to its rapid growth and good wood texture. Generally, leaf size is double in 4× plants than 2× plant leaves. Moreover, it can be used as fine feed for domestic fowl and livestock because its fleshy leaves are rich in vitamins and minerals. Importantly, tetraploid black locust is a pioneer tree species due to its wide ranging adaptability to adverse environments such as salt, drought, cold, and infestation. Our earlier studies have shown that the mitochondria of tetraploid black locust can maintain a relatively intact ultrastructure compared with diploids under salinity stress [22, 23], which could be attributed to the nature of divergent genomes.
Proteomics is an effective method to assess the complete proteome at the tissue or organelle level to compare the effects of salinity stress is by salinity stress [24–27]. Two-dimensional polyacrylamide gel electrophoresis (2-DE) is one of the most powerful and sensitive techniques, and it has been applied to salt treatments for different plant species . Based on the 2-DE method, it has been found that salt-tolerant genotypes are associated with a more abundant energy supply, higher reactive oxygen species (ROS) scavenging and ethylene production, and stronger photosynthetic capacity than salt-sensitive genotypes under salinity stress . Nevertheless, the precise molecular mechanism underlying the role of plant mitochondria in resisting salinity stress is still unknown.
Plant mitochondria are involved in multiple metabolic and biosynthetic processes, and are especially important in the generation of adenosine triphosphate (ATP). In addition, mitochondria export organic acid intermediates for wider cellular biosynthesis and the photorespiratory pathway . Particular, mitochondria play an important role in plant survival during stress . To date, a number of studies have investigated the effects of abiotic stresses on plant mitochondria, which include salinity [31, 32], heat , drought and cold . Among these stresses, salinity is a serious threat to plant growth that significantly alters plant metabolism, development and even leads to plant death. Some reports have also shown that salinity stress has a severe negative influence on mitochondrial respiration . In fact, respiratory metabolism plays a key role in mediating plant tolerance to salinity . The relationship between mitochondrial function and salinity tolerance has been investigated in some plant species, such as wheat , barley  and Arabidopsis [33, 38]. These studies have provided a good overview of the mitochondrial response to salinity stress. However, there is relatively little information available on polyploid plants. It is necessary to gain a better knowledge of the underlying mechanisms to understand how polyploid plants perform under salinity stress.
Here, to evaluate ploidy-dependent differences in leaf mitochondria between diploid (abbreviated as 2×) and tetraploid (abbreviated as 4×) black locust under salinity stress, we isolated and purified mitochondria from leaves, and compared the effects of salinity stress on mitochondria. Finally, the physiological, ultrastructural and proteomic traits of mitochondria in leaves of 2× and 4× black locust under salinity stress were investigated, and functional implications are discussed.
Plant materials and salt treatment
All materials were introduced directly from South Korea to China by Beijing Forestry University. The 2× and 4× black locust (Robinia pseudoacacia L.) were from one germplasm. Thus, they possess the same genetic origin. Thirty uniform plants (2 years old) of 2× and 4× were planted in plastic pots (21 cm in diameter and 21 cm in depth) filled with a 2:1 (v/v) mixture of soil and sand. The experiments were carried out at Harbin Experimental Forest Farm Greenhouse of Northeast Forestry University in June 2013. Potted plants were grown in the greenhouse (day/night air temperature, 28/22 °C; photoperiod, 12 h; relative humidity, 65–85%). Plants were treated with 250 (moderate salinity stress) or 500 mM NaCl (high salinity stress) for 7 days. After 7 days of treatment, the fully expanded fresh leaf tissues (the third to fifth leaves from the shoot apex) were collected for physiological measurements and transmission electron microscopy analysis. Other additional leaves were used for mitochondria extraction. At least three independent biological experiments for each treatment were replicated.
Transmission electron microscopy
Fresh leaves about 1.5 cm2 in size were sampled, fixed immediately with 2.5% (v/v) glutaral pentanedial at 4 °C for 2 h, and washed twice in 0.1 M PBS (sodium phosphate buffer, pH 6.8) at 4 °C. Then they were post fixed in 2% osmium tetraoxide (OsO4) for 2 h, sequentially dehydrated by 50%, 70%, 90%, and 100% acetone, and embedded in Epon 812 for 2 h. Ultrathin sections (70 nm) were sliced, stained with uranyl acetate and lead citrate, and then mounted on copper grids for viewing on the H-600 IV TEM (Hitachi, Tokyo, Japan) at an accelerating voltage of 60 kV.
Leaf respiration rate was determined by a Clark-type oxygen electrode (Hansatech Instruments, Britain) . 1 cm2 leaf segments were incubated in the dark for 30 min to minimize wounding effects and light-enhanced dark respiration. They were kept in a 2 ml reaction medium containing 10 mM HEPES, 10 mM MES (pH 7.2) and 2 mM CaCl2 and then the total respiration rate was determined. The rates of SHAM-resistant respiration (Cyt pathway) and KCN-resistant respiration (alternative pathway) were measured in the presence of SHAM (200 mM) and KCN (200 mM), respectively.
Physiological and biochemical investigations
Measurements of Hydrogen peroxide (H2O2) and Malondialdehyde (MDA) contents
H2O2 was detected spectrophotometrically according to I Sergiev, V Alexieva and E Karanov . A 0.5 ml mitochondrial extraction was homogenized in 5 ml 0.1% TCA on an ice bath. After centrifuged at 12,000×g for 10 min, 1 ml supernatant was mixed with 0.5 ml potassium phosphate buffer (pH 7.5) and 1 ml 1 M potassium iodide. The absorbance of supernatant was measured at 390 nm and the concentration of H2O2 was obtained using a standard curve.
MDA content was estimated by the method of Wang et al.  with some modifications. The extract was dissolved in 5 ml 10% TCA, centrifuged at 12,000×g for 10 min and the supernatant was transferred to a 5 ml centrifuge tube, diluted with 10% TCA to 4 ml. The supernatant (1 ml) was mixed with 4 ml 20% TCA containing 0.5% (w/v) thiobarbituric acid (TBA). The mixture was heated in boiling water for 15 min and immediately cooled on ice to stop the reaction; then the mixture was centrifuged at 12,000×g for 10 min. The absorbance of the final supernatant was measured at 532 nm, 600 nm and 450 nm. The MDA concentration was calculated by means of an extinction coefficient (155 mM−1 cm−1).
Measurements of enzyme activities
Superoxide dismutase (SOD, EC 184.108.40.206) activity was measured following the method of C Beauchamp and I Fridovich . The reaction mixture contained 20 μL enzyme extract, 50 mM sodium phosphate buffer (pH 7.8), 100 μM EDTA, and 10 mM pyrogallol. Enzyme activity was detected at 420 nm by a spectrophotometer. Glutathione reductase (GR, EC 220.127.116.11) activity was determined by NADPH oxidation at 340 nm. The reaction mixture contained 10 μL enzyme extract, 100 mM potassium phosphate buffer (pH 7.8), 0.2 mM NADPH, 2 mM EDTA, and 0.5 mM glutathione. The reaction was initiated by adding NADPH at 25 °C . Ascorbate peroxidase (APX, EC 18.104.22.168) activity assay was carried out by the method of Y Nakano and K Asada . The reaction mixture contained 50 mM sodium phosphate buffer (pH 7) including 0.2 mM EDTA, 0.5 mM ascorbic acid, 50 mg BSA, and crude enzyme extract. The reaction was started by adding H2O2 at a final concentration of 0.1 mM. Cytochrome c oxidase (COX, EC 22.214.171.124) was determined according to the method of M Neuburger, EP Journet, R Bligny, JP Carde and R Douce . Dehydroascorbate reductase (DHAR, EC 126.96.36.199) was measured following AsC formation at 265 nm in the reaction solution containing 0.5 mM DHA, 5 mM reduced glutathione (GSH) . Monodehydroascorbate reductase (MDHAR, EC 188.8.131.52) activity was determined as NADH oxidation at 340 nm. The reaction mixture contained 0.2 mM NADH, 1 mM AsC, and 1 unit of AsC oxidase .
Measurements of ascorbate (AsA) and GSH contents
AsA content was determined following MY Law, SA Charles and B Halliwell  with some modifications. The reaction mixture included 0.2 ml protein extract, 0.5 ml phosphate buffer (150 mM, pH 7.4), and 0.2 ml double distilled water. Then 0.4 ml α′-dipyridyl in 70% ethyl alcohol and 0.2 ml FeCl3 (3%) were added to the reaction solution. The mixtures were incubated at 40 °C for about 40 min. After centrifugation at 12,000×g for 10 min, the clear supernatant was collected and the change in absorbance at 525 nm was monitored.
The determination of GSH was carried out following the method of G Ellman . The absorbance of reduced chromogen and 5,5′-Dithiobis (2-nitrobenzoic acid) (DTNB) was measured at 412 nm and GSH concentration was determined.
Two-dimensional gel electrophoresis
Isolation of mitochondria and estimation of mitochondrial protein
For isolation and purification of mitochondria from leaves, we used a method of  with slight modifications. All extraction procedures were carried out between 0 and 4 °C. Leaf tissue (30 g) was ground with pre-refrigerated pestle and mortar in 200 ml grinding media containing 50 mM HEPES (pH 7.5), 5 mM hexanoic acid, 0.3% BSA (w/v), 0.3 M sucrose, 10 mM β-mercaptoethanol, 20 mM EDTA, 30 mM Na-ascorbate and 1% (w/v) PVP. After that the homogenates were squeezed through a 40 × 40 μm mesh nylon cloth and centrifuged at 4000×g for 10 min. The supernatant was centrifuged at 20,000×g for 10 min. The precipitate was suspended and washed twice in wash medium buffer A (20 mM HEPES, 330 mM sorbic alcohol, 10 mM NaCl,2 mM EDTA, 5 mM Na-ascorbate) and centrifuged at 10,000×g for 15 min. After centrifugation the precipitate was suspended in washing medium. The suspension was then loaded onto a sucrose gradient consisting of 3 ml: 8 ml: 6 ml: 6 ml, bottom to top, of 57%, 45%, 37% and 25% sucrose. The mixture was centrifuged for 1 h at 40,000×g and mitochondria were present as an opaque band at the 37%/45% interface. Then the mitochondrial band was collected, washed and centrifuged at 20,000×g for 15 min in medium buffer A.
Mitochondrial proteins were extracted by adding 0.7 ml of 10% acetone to a tube and then stored at 20 °C for 12 h. Then samples were centrifuged at 25,000×g for 15 min. The precipitate was washed with 80% and 100% cold acetone, respectively and centrifuged for 30 min. After centrifugation, the precipitate was vacuum dried. The dried powder was dissolved in an IEF buffer containing 7 mM urea, 2 mM urea, 40 μM dithiothreitol (DTT), 0.2% pharmalytes (pH 4–7) and 4% 3-[(3-cholamidopropyl)-dimethylammonio]-1-propane sulfonate (CHAPS). The protein solution was stored at −80 °C until use. Mitochondrial protein concentration was determined by the method of MM Bradford .
To estimate protein contaminant in our mitochondrial isolation, a specific antibody against chloroplast RbcL was used to assess mitochondria contamination because this organelle is the common contaminant of chloroplast protein preparations. Additionally, the signals from antibodies against AOX recognized proteins from the both mitochondrial protein fractions and the total protein extracts, were used to estimate the purity of the mitochondria fractions.
Gel electrophoresis and gel staining
400 μg protein samples were rehydrated in 250 μl protein rehydration solution and used for isoelectric focusing (IEF). Subsequently, the IPG strips (13 cm, pH 4–7) were incubated for 12 h at room temperature. The operation was followed a procedure consisting of 30 V for 14 h, 100 V for 1 h, 500 V for 1 h, 1000 V for 1 h, 8000 V for 1 h and 8000 V for 5 h. After IEF, gels were equilibrated in 10 ml equilibration buffer containing 6 M urea, 50 μM Tris-HCl (pH 8.8), 2% (w/v) SDS, 30% glycerol and 1% (w/v) dithiothreitol (DTT) for 15 min with 2.5% iodoacetamide instead of DTT for 15 min. The SDS-PAGE in the second dimension electrophoresis was conducted using 12.5% (w/v) polyacrylamide gel. After electrophoresis, the gels were stained with a coomassie brilliant blue R-250 solution containing 25% methanol, 8% acetic acid and 0.1% (w/v) CBB until protein spots were clearly visible.
Gel image analysis and Matrix-Assisted Time of Flight Mass Spectroscopy (MALDI-TOF-MS) analysis
Gel images were scanned using an ImageScanner III (GE Healthcare, Bio-Sciences, Uppsala, Sweden). Images were analyzed with ImageMaster 2D Platinum 7.0 software (Amersham Biosciences, Piscataway, NJ, USA, 2011). The average volume percent values were calculated from three technical replicates to represent the final volume percent values of each biological replicate. The experimental molecular weight (Mw) and isoelectric point (pI) of the protein spots were determined by 2-DE standards and interpolation of missing values on the IPG strips. Spots were quantified based on total density of the gels by the percentage volume. Significantly different spots, which were determined as p < 0.05 and a change of more than 2.5-fold in abundance, were considered to be differentially accumulated proteins, and they had to be consistently present in three replications.
Selected protein spots were excised, washed with 50% (v/v) acetonitrile in 0.1 M NH4HCO3, and dried at room temperature. Proteins were reduced with 1 mM DTT and 2 mM NH4HCO3 at 55 °C for 1 h and alkylated with 55 mM iodoacetamide in 25 mM NH4HCO3 in the dark at room temperature for 45 min. The gel pieces were thoroughly washed with 25 mM NH4HCO3, 50% ACN, 100% ACN, and dried. The proteins were digested in 10 ml modified trypsin (Promega, Madison, WI, USA) solution (1 ng/ml in 25 mM ammonium bicarbonate) during an overnight incubation at 37 °C. Digests were immediately spotted onto 600 mm anchorchips (Bruker Daltonics, Bremen, Germany). Spotting was achieved by pipetting 1 ml analyte onto the MALDI target plate in duplicate and then adding 0.05 ml of 20 mg/ml α-CHCA in 0.1% TFA/33% (v/v) ACN, which contained 2 mM ammonium phosphate. All samples were analyzed in the positive-ion reflection mode on a TOF Ultraflex II mass spectrometer (Bruker Daltonics, Billerica, United states). Each acquired mass spectra (m/z range 700–4000, resolution 15,000–20,000) was processed using FlexAnalysis v2.4 software (Bruker Daltonics, Bremen, Germeny, 2004). Proteins were identified with Mascot software (http://www.matrixscience.com) based on the mass signals to search for proteins in the SwissProt, NCBInr, and MSDB databases. In addition, we also combined with knowledge from literature, 9 functional categories were obtained by blasting against the NCBInr, Swissprot and UniProt database (http://www.ebi.uniprot.org). And the gene-ontology based on the functional annotation using DAVID web-server and KEGG pathway was carried out.
Statistical analyses were performed with SPSS 17.0 software (SPSS Inc., Chicago, IL, USA, 2009). All parameters are presented as mean ± standard error (SD) and were obtained from at least three replicates and analyzed using Duncan’s multiple range test or Student’s t-test. A p-value <0.05 was considered significant.
Western blot analysis
To confirm the proteomic data, western blot analysis was carried out with equal amount of mitochondria protein including three specific antibodies (ATP synthase β subnunit (spot 220, ASB), Heat Shock Protein 60 (spot 149, HSP) and β-actin (Agrisera, Sweden)). Western blot analysis was carried out by the method of  with minor modification. In brief, equal amount of mitochondria protein of black locust leaves (2× and 4×) were resolved on 10% SDS-PAGE and transferred onto nitrocellulose membrane (GE Healthcare, UK). The membranes were blocked with TBST buffer (10 mM Tris-HCl, pH 7.5, 150 mM NaCl, 0.05% Tween 20) containing 5% milk overnight and then incubated with specific antibodies (Agrisera, Sweden) in TBST over night, including ATP synthase β subnunit (ASB), Heat Shock Protein 60 (spot 149, HSP) and β-actin. After washing 3 times, the membrane was incubated with goat-anti-rabbit IgG secondary antibody conjugated to HRP (KPL, USA) diluted 1:10,000 in TBST for 1 h. Proteins were detected with enhanced chemiluminescence (ECL) reagents (Agrisera, Sweden). Western blot analysis experiments were repeated at least three times, and the representative data are shown.
Quantitative real time PCR
To investigate the relationship between the transcriptional and translational levels of salinity stress related genes, we employed qRT-PCR for 12 genes selected based on the proteomics results (Additional file 1: Table S1). Total RNA was isolated using a plant RNA extraction kit (Bioteke, China) and cDNA was synthesized from 1 μg of the total RNA with PrimeScript Reverse Transcriptase (Takara, Japan) according to the manufacturer’s instructions. Specific primer pairs for the selected genes were designed by comparing the nucleotide sequence of conserved region using BioEdit, Premier 5.0 and Oligo 6.0 (Additional file 2: Table S2). The qRT-PCR was performed using the SYBR Green Realtime PCR Master Mix (Toyobo, Japan) with Lightlycler480 (Roche, USA), based on semi-quantitative reverse transcription PCR (RT-PCR) results (Additional file 2: Table S2). The expression levels of the β-actin were used as an internal control (reference gene). Relative expression of the target genes was calculated using the comparative Ct method.
Statistical analyses were performed with SPSS 17.0 software (SPSS Inc. Chicago, IL, USA, 2009). All parameters are presented as mean ± standard error and were obtained from at least three replicates. Parameters were analyzed using Duncan’s multiple range test or Student’s t-test. A p-value <0.05 was considered significant.
Effect of salt treatment on leaf growth and ultrastructure
Effect of salt treatment on respiration rate
Effect of NaCl treatment on the respiration rates in leaves of diploid (2×) and tetraploid (2×) R. pseudoacacia
Vt (nmol O2 g−1 FW s−1)
Cytochrome pathway respiration
V Cyt (nmol O2 g−1 FW s−1)
Alternative pathway respiration
V Alt (nmol O2 g−1 FW s−1)
2.62 ± 0.025a
0.94 ± 0.035a
0.45 ± 0.050a
5.98 ± 0.200b
2.33 ± 0.162b
2.24 ± 0.146b
9.97 ± 0.510c
3.00 ± 0.265b
3.88 ± 0.278c
3.49 ± 0.125a
0.88 ± 0.036a
0.77 ± 0.074a
9.67 ± 0.495b
2.80 ± 0.127b
4.23 ± 0.104b
13.59 ± 0.121c
4.80 ± 0.210c
5.34 ± 0.056b
Effects of salt treatment on H2O2 and MDA levels
Effects of salt treatment on anti-oxidative enzyme activity and the AsA and GSH levels
Assessment of leaf mitochondria purity
Analysis of protein expression changes under salinity stress
Functional classification of salinity stress-responsive proteins
Transcriptional expression of salinity stress-responsive genes
Confirmation of the proteomic data
Physiological and biochemical characteristics and salt tolerance
The response of plants to salinity stress depends on the plant species and the severity of the salinity stress. In the present study, we investigated the responses of two black locust (R. pseudoacacia) species to salinity stress. The responses in leaf growth and physiological and biochemical characteristics to salinity stress were similar in the two species. In addition, some reports in Populus showed that vegetative growth traits, net photosynthetic rate (Pn), relative chlorophyll content index (CCI), leaf area (LA), and whole-leaf photosynthetic efficiency (PEw) in polyploidy Populus were significantly higher than those in diploids, indicating that certain polyploid Populus groups had greater advantages in these respects . Polyploid Acacia senegal also showed faster growth than their diploids , though, the reasons remain unclear. The relative effects of ploidy on mitochondrias between polyploid and diploid have not been systematically examined.
Salinity stress significantly inhibited leaf growth, damaged mitochondrial ultrastructure, increased MDA contents and respiration rates, and, at the same time, induced changes in antioxidant enzyme activities in the mitochondria of 2× and 4× leaves. In particular, H2O2 content was higher in 4× leaves in all conditions compared to that of 2× leaves (Fig. 3a) and was not changed with increase salinity stress, while, the H2O2 content in 2× leaves increased with salinity stress, especially in extreme conditions (500 mM NaCl). This may be because there is higher native H2O2 content in 4× leaves. Salinity stress did not appear to harm 4× leaves in our study. Accordingly, salinity stress induced no change in H2O2 content in 4× leaves, suggesting that 4× plants may be more tolerant to salinity stress than 2× plants. These results were also in accordance with the morphological data of 2× and 4× leaves under salinity stress (Fig. 1). To prevent cellular damage, H2O2 (a by-product of SOD activity) must be H2O through processing by APX, POD, and CAT, which regulate H2O2 levels in plants. In general, under salinity stress plants may generate abundant H2O2, a toxic species leading to lipid peroxidation and electrolyte leakage [53, 54]. However, some studies have shown that H2O2 may act as an effective signal molecule during stress responses to induce gene expression of antioxidant enzymes related to stress tolerance [55, 56]. This may be the reason we found increased H2O2 levels in the mitochondria of 2× leaves, especially under 500 mM NaCl (Fig. 3a). Increased accumulation of H2O2 has also been reported in isolated organelles after exposure to environmental stress [57, 58]. The increase in H2O2 in mitochondria after salt treatment indicated that their H2O2-detoxifying capacity did not match their generation of H2O2, as observed in chloroplasts of 2× leaves (data not shown). Similar results have also been reported in some previous studies . In general, to control the level of H2O2 under stress conditions, plant mitochondria contain several enzymes that scavenge H2O2 and its precursor O2 −, such as SOD, APX and GR . The major H2O2 detoxification route is the ascorbate-glutathione cycle, which involves the antioxidant AsA, GSH, MDHAR, DHAR and GR in mitochondria . In plants, AsA and GSH are crucial for biotic and abiotic stress tolerance . Salinity stress can lead to osmotic stress, resulting in a higher accumulation of SOD, and the level of SOD accumulation is related to the level of salt tolerance , because SOD dismutates O2 − to H2O2 and O2. In the present study, NaCl treatment with 500 mM NaCl induced significant increases in SOD and APX activities in 4× mitochondria, while both enzyme activities were depressed in 2× mitochondria (Fig. 4c), demonstrating the marked improvement of salt tolerance in 4× plants. This increased ability to dismutate O2 − and detoxify H2O2 probably played a predominant role in the greater salinity tolerance of 4× mitochondria. Additionally, although 4× mitochondria had much lower MDHAR activity in the 0 mM and 250 mM NaCl treatments in comparison with 2× mitochondria, 4× mitochondria showed a similarly high MDHAR activity at 500 mM NaCl (Fig. 4f). This demonstrates that 4× mitochondria could acclimate to very high salinity. Concerning antioxidants, salt treatment caused a significant increase of AsA and GSH levels in 2× and 4× mitochondria (Fig. 5), but the absolute contents were greater in 4× mitochondria than in 2× mitochondria (Fig. 5) in each treatment, indicating that 4× mitochondria possessed more tolerance of, and greater ability to acclimate to, salinity stress.
Environmental stresses such as chilling, salinity stress and drought can cause visible injuries to plant mitochondria. In our previous study we observed that salinity stress resulted in plant mitochondrial damage , similar results were also observed in the present study (Fig. 2). Based on differences in mitochondrial ultrastructure between 2× and 4× samples under salinity stress, we found that 4× mitochondria showed more adaptability and tolerance to salinity stress compared with 2× mitochondria.
Salinity stress can bring about damage to mitochondrial membranes to plants, as assessed by lipid peroxidation (Fig. 3d). To escape or repair membrane damage caused by salinity stress, increased levels of antioxidants for maintaining membrane integrity can effectively inhibit lipid peroxidation, which can be measured by the level of MDA an indicator of membrane damage. In this study, MDA levels increased with the aggravation of salinity stress in both 2× and 4× mitochondria during the 7 days of stress, but the absolute content was greater in 2× than in 4× mitochondria (Fig. 3d), which suggests that 4× mitochondria could adjust to salinity stress more effectively than 2× mitochondria. APX, a component of the ascorbate-glutathione pathway, plays a key role in scavenging H2O2 [62, 63]. Lower levels of MDA (an end product of lipid perocidation) are associated with higher APX activity in salt tolerant tomato , rice  and sugar beet  plants, which was consistent with our results.
In this study, we also found that COX activity significantly changed in both 2× and 4× mitochondria after 250 mM NaCl treatment, which suggested that COX played an important role in the tolerance of plants to salinity stress. Generally, COX has been considered a mitochondrial marker enzyme, participating in an important pathway that is primarily used for ATP generation from ADP and inorganic P (Pi) through oxidative phosphorylation. Additionally, the activity of the COX pathway accounts for most of the respiratory O2 uptake and mitochondrial electron flux in plants, such that higher COX activity allows greater maximum electron flux . Our results indicated that COX activity in 4× mitochondria was slightly higher than in 2× mitochondria after NaCl treatment (Fig. 4c), consistent with their difference in salt tolerance.
Leaf respiration rate increased under salinity stress in both species, reflecting the energetic demands of ion exclusion. Interestingly, 4× leaves showed a higher respiration rate compared to 2× leaves (Table 1). Although the relationship between growth and respiration rate is complex, perhaps high respiration rates under salinity stress could involve judicious allocation of stored carbon reserves to alleviate salinity stress . For example, a higher respiration rate could contribute more to ion exclusion, since more energy can be produced by a higher respiration rate . However, there are some exceptions . Therefore, based on previous studies, there was no clear expectation of a respiratory rate response in relation to whole-plant salinity tolerance. However, our results obtained with 2× and 4× leaves add weight to the idea that increased respiration could enhance whole-plant salinity tolerance.
By analyzing changes in physiological and biochemical characteristics, we have uncovered some of the factors responsible for the greater salt tolerance of 4× leaves compared to in 2× leaves. Thus far, there are very strong links between mitochondrial antioxidant defences and whole-plant salinity tolerance, which were further measured using proteomic analysis to detect changes in defence-related mitochondrial proteins.
Differentially expressed proteins spots in mitochondria of mesophyll cells of diploid (2×) and tetraploid (4×) R. pseudoacacia using 2D–Gel Analysis under 0, 250 mM and 500 mM NaCl treatment
Relative V% ±Seh
Oxidative phosphorylation (OXPHOS) system
(complex I) 75kDa subunit
NADH dehydrogenase (complex I)
iron-sulfur protein 1
putative NADH dehydrogenase (complex I)
NAD+ binding site
family protein (complex I)
Arabidopsis lyrata L. subsp
Cytochrome c reductase (complex III)
Mitochondrial processing peptidase
ATP synthase (complex V)
ATP synthase (complex V)
ATP synthase (complex V)
ATP synthase (complex V)
ATP synthase (complex V)
ATP synthase (complex V)
ATP synthase (complex V)
ATP synthase (complex V)
ATP synthase (complex V)
Cell division protein ftsH
ATP1 gene product
Chromosome segregation ATPases
Transcription, translation; DNA-binding proteins
pentatricopeptide repeat-containing protein
Ankyrin repeat domain-containing protein
Elongation factor G
ATP-dependent RNA helicase
zinc ion binding protein
Calcium-binding EF-hand family protein
kinesin heavy chain
50S ribosomal protein L21, mitochondrial
ribosomal protein S8
DNA binding protein, putative
pentatricopeptide repeat-containing protein
Chaperones and protein processing
Heat shock protein
Heat shock protein
A1 cistron-splicing factor AAR2
mitochondrial substrate carrier
Volvox carteri f. nagariensis
eukaryotic translation initiation factor 2c
Pyruvate decarboxylation and citric acid cycle
putative alcohol dehydrogenase
P-loop containing nucleoside triphosphate hydrolases superfamily protein
fucosyltransferase CAZy family GT37-like protein
Defense, stress, detoxification
1,3-β-glucan synthase subunit
BZIP transcription factor
disease resistance RPP8-like protein 3-like
Musa acuminata var. zebrina
Ribulose 1,5-bisphosphate carboxylase
Ribulose-1,5-bisphosphate carboxylase/oxygenase large subunit
Ribulose bisphosphate carboxylase large chain
Ribulose bisphosphate carboxylase large chain
Ribulose-1,5-bisphosphate carboxylase/oxygenase large subunit
Number of protein spots significantly changed under different NaCl stress
No significantly changed spots
Not detected spots
Newly detected spots
250 mM Vs 0 mM
500 mM Vs 0 mM
500 mM Vs 250 mM
250 mM Vs 0 mM
500 mM Vs 0 mM
500 mM Vs 250 mM
Oxidative phosphorylation (OXPHOS) related proteins
Oxidative phosphorylation is an important metabolic pathway in which mitochondria produce ATP using energy released by the oxidation of nutrients. In this study, 16 protein spots involved in OXPHOS were identified in both 2× and 4× mitochondria after salt treatment. In 4× mitochondria, four proteins (spots 34, 53, 88 and 190) were observed to increase in response to 250 mM and 500 mM NaCl treatment. Up-regulation of oxidative phosphorylation related proteins can ensure adequate ATP for other metabolic processes under salinity stress , which is partly supported by our findings. For example, an increased abundance of metabolism-related proteins involved in glutamine metabolism (spots 113 and 119) and alanine metabolism (spot 86) in 4× mitochondria is listed in Table 2. Glutamine synthase, GS (EC 184.108.40.206), is a particularly important enzyme for nitrogen metabolism. Nitrogen, a key element for plant growth and reproduction, is an essential building block of nucleic acids and proteins . Leaf GS activity is known to be increased by salinity stress in cashew leaves . Similarly, GS showed different levels in leaves of wheat (Triticum aestivum) seedlings exposed to different salinity . In the present study, the increase of GS may contribute to the accumulation of nitrogen, promoting the synthesis of nucleic acids and proteins and, thereby, increased plant growth. In accordance with our results, JAG Silveira, RDA Viégas, IMAD Rocha, RDA Moreira and JTA Oliveira  and CO Silva-Ortega, AE Ochoa-Alfaro, JA Reyes-Agüero, GA Aguado-Santacruz and JF Jiménez-Bremont  observed that salinity stress increased GS activity. Clearly, these results indicate that GS plays important roles in response to salinity stress.
In contrast to the case of 4× mitochondria, oxidative-phosphorylation-related proteins such as NADH dehydrogenase (complex I, spot 178), NAD+ binding site (spot 230), COX (complex III, spot 215) and ATP synthase (complex V, spots 209, 211 and 220) in 2× mitochondria showed a significant reduction under NaCl stress. In plants, these four proteins are essential for mitochondrial electron transport. The mitochondrial electron transport chain (ETC) is a major site of ROS production; excessive ROS can lead to oxidative stress . When proteins involved in mitochondrial electron transport are down-regulated during biotic or abiotic stress, ROS production may be enhanced to a level where mitochondria may be damaged by oxidative stress . In this study, we found that SOD, APX, MDHAR and GR all increased to cope with oxidative stress in 4× plants under salinity stress. By contrast, increased ROS production associated with down-regulation of OXPHOS-related proteins in 2× plants was not counteracted by a sufficient increase in anti-oxidative enzyme activities.
Transcription, translation and DNA-binding proteins
According to previous studies, DNA-transcription, translation and binding proteins with low abundance in plant mitochondria have been poorly represented . In our study, there were 12 proteins in the transcription, translation and DNA-binding proteins category (Table 2). Two pentatricopeptide repeat (PPR) proteins were identified: spots 33 and 343. Even with only two identified PPR proteins, there were clear differences between 2× and 4× mitochondria. PPR proteins decreased in abundance with increasing concentrations of NaCl in 4× mitochondria, while the opposite change occurred in 2× mitochondria. PPRs are involved in RNA metabolism and post-transcriptional regulation in plant organelles . Though extensive studies have been performed on PPRs, their functions remain largely unknown . In 2× mitochondria after salt treatment, elongation factor, ribosomal protein and a series of binding proteins were also identified. To our knowledge, these proteins are involved in plant salinity stress signalling [80–82]. Most of these proteins (spots 298, 299, 315, 350 and 317) reached maximal levels after 250 mM NaCl treatment, and were down-regulated to lower levels after 500 mM NaCl treatment. These results indicate that 2× plants were capable of coping with relatively low salt conditions by enhancing protein expression, but were unable to just to higher salinity due to signalling inhibition.
Chaperones and protein processing
In this study, one contrasting result observed was the clear induction of heat shock protein 70 (HSP70) in 4× mitochondria after NaCl treatment, whereas no clear induction was observed in salt-stressed 2× mitochondria (spot 282). This induction is consistent with many reports highlighting relationships between HSP70 and plant programmed cell death (PCD) [83, 84] and HSP70 induction under environmental stresses in plants [33, 85]. Interestingly, we also observed an increase in one small heat shock protein (spot 149) in salt-treated 2× mitochondria. This was not unexpected considering that 2× black locust is known to possess some level of salt tolerance. A protein disulfide-isomerase (spot 201), which acts as a protein-folding catalyse that interacts with nascent polypeptides to catalyse the formation, isomerisation, and reduction or oxidation of disulfide bonds was down-regulated after NaCl treatment of 2× leaves. Protein disulfide-isomerase (PDI) is known to be induced under cold, salt and abscisic acid (ABA) stresses . In addition, in 2× plants, the A1 cistron-splicing factor AAR2, which is involved in splicing pre-mRNA of the a1 cistron and other genes that are important for cell growth appeared to decrease in abundance after 500 mM NaCl treatment. Taken together, these results indicate possible inhibitory effects of salinity stress on protein processing in 2× mitochondria.
Salinity stress can induce the production of ROS, which may cause damage to plant cells and also act as secondary messengers . To regulate ROS level, many defence proteins are induced during plant responses to biotic or abiotic stresses . However, their response mechanisms are not well known. In the present study, five defence-related proteins including BZIP transcription factor (spot 186), disease resistance RPP8-like protein 3-like (spot 329), L-ascorbate peroxidase (spot 203) and lectin (spot 217) were found to be differentially regulated after salt treatment. In 4× mitochondria, the L-ascorbate peroxidase protein was down-regulated, which requires further investigation since APX activity itself was increased. In 4× mitochondria, lectin levels were increased by salinity stress. The differential expression of defence-related proteins may help to enhance the tolerance of 4× mitochondria to salinity stress and decrease the risk of damage. Disease resistance RPP8-like protein 3-like (spot 329) belongs to the disease resistance NB-LRR family, and it may play a crucial role in maintaining redox homeostasis under various stresses [89, 90]. Our results show that disease resistance RPP8-like protein 3-like was expressed at lower levels in salt-stressed 2× mitochondria. The down-regulation of this RPP8-like protein may be associated with susceptibility of 2× plants to salinity stress. Our results also imply different response mechanisms in the defence system in different ploidy groups during acclimation to salinity stress.
Membrane transport and citric acid cycle
The main family of proteins in mitochondrial stress response is the mitochondrial substrate carrier protein family (MCF) . In our study, only one MCF protein (spot 39) was found and it was down-regulated in 4× mitochondria after salinity stress. However, no MCF proteins were detected in 2× mitochondria. These results suggest that tolerant plants can respond quickly under salinity stress.
One protein (spot 265) related to the citric acid cycle was detected in both 2× and 4× mitochondria after NaCl treatment. However, spot 265 increased with salinity in 4× mitochondria, while it was significantly down-regulated in 2× mitochondria under increasing concentrations of NaCl.
Proteins of unknown function
A total of 13 proteins were identified as proteins of unknown function. Among these proteins, only one (spot 281) was induced in both 2× and 4× mitochondria after NaCl treatment. The accumulation of this protein suggested that this protein may be of particular importance in protecting plants from damage caused by salinity stress. In 4× mitochondria, three unknown proteins (spots 30, 112 and 221) increased in expression after salt treatment, but spots 129, 183 and 228 decreased in expression after salt treatment. We proposed that these unknown proteins might act as signalling molecules, although there is a great difference in their abundance. In 2× mitochondria, two proteins (spots 163 and 154) were induced only under 500 mM NaCl treatment. These findings suggest that we should pay attention to function of these proteins in plant tolerance to salt in a future study. In addition, no Arabidopsis orthologues of these unknown proteins have been identified in databases (Table 2). Nevertheless, our results indicate conservation of a number of unknown functional proteins from other plant species, thereby providing a clue for identification of novel mitochondrial functions in plants .
In addition to the functional mitochondrial proteins identified above, 5 miscellaneous proteins were detected by MS analysis (spots 246, 258, 264, 307 and 312 in Table 2). Slight contamination of the mitochondrial fraction by chloroplast proteins was visible under all purification conditions, because of the high degree of overlap between mitochondria and chloroplasts based on their density and size [93, 94]. Thus, the isolated mitochondria may be non-specifically mixed with chloroplast proteins. The methods for extraction and purification of mitochondrial protein from plant leaves remain to be improved.
To correlate the levels of the identified salinity stress response-related proteins with their gene expression changes, qRT-PCR was employed to analyse the transcription levels of 12 genes (Additional file 2: Table S2). Six of the expressed mRNA levels them showed similar trends to their protein expression pattern under salinity stress (Fig. 10). This consistency suggested that these proteins may be initially regulated at the transcriptional level after salt treatment and/or they might induce related signal transduction pathways to resist salinity stress. In contrast, four genes showed different or reversed trends when comparing mRNA levels and protein expression (Fig. 11). This inconsistency between the protein and transcription levels could be due to post-translational processing or post-transcriptional regulation (47, 48). On the other hand, the parallel and independent changes between protein and mRNA levels for these four genes might reflect the complex regulatory mechanisms of plants responding to salinity stress. This inconsistency has also been found by some previous studies (49, 50, 51). Unfortunately, two genes, NUO (spot. 34) and RPP8 (spot. 329) had no PCR results.
In addition, four genes showed different or reverse trends with their protein expression (Fig. 11). These four genes have effective positive role in regulating the tolerance of salinity stress. For example, NADH dehydrogenase, complex I (spot. 178) located in the inner mitochondrial membrane can contain type II NDH that by pass complex I and supply electrons to the ubiquinone pool . Generally, a stimulation of O2 •− generation dependent on NADH-and succinate has been reported in plants under salinity, with a higher increase insensitive cultivars than in tolerant plants . In particular, three subunits of the ATP synthase CF1, α (spot. 213), β and γ were affected by salt treatment in many plants . Currently, there is growing evidence that the ATP synthase is also a target for a damaging effect caused by salt stress . This change can protect the plant from further damage . Another protein, lectins (spot. 217) residing in the nucleocytoplasmic compartment are known to be implicated in biotic and abiotic stress responses . As part of the plant’s immune system, lectins can also act as immune receptors and/or defense proteins . Additionally, as a molecular chaperone, elongation factor G (EF-Tu protein, spot 175) can protect other proteins from thermal aggregation and degradation, which plays a role in the elongation phase of protein biosynthesis and has been studied in several plants in response to abiotic stress, such as extreme salinity, temperatures and drought [101, 102].
To date, there have been few reports concerning the relationship between mitochondrial function and salt tolerance. To gain a comprehensive physiological and biochemical and proteomic understanding of mitochondrial salinity tolerance in 2× and 4× R. pseudoacacia, we compared physiological and comparative proteomic traits of mitochondria in leaves of 2× and 4× after salinity stress. Unlike 4× mitochondria, 2× mitochondria showed significant stress symptoms in saline condition, resulting in wilting leaves, high MDA and H2O2 levels, decreased leaf respiration rate and inefficient defence systems involving antioxidant enzymes and antioxidants. In addition, defence-related proteins, metabolism-related proteins, heat shock proteins, membrane transport proteins and citric acid cycle-related proteins in 4× leaves were also induced by high salinity. These up-regulated proteins implied that defence, metabolism, ROS scavenging and protein transport may work cooperatively to maintain mitochondrial homeostasis in 4× under salinity stress. Accordingly, it can be reasonably expected that salt tolerance mechanisms in 4× are sophisticated. In contrast, the identification of salt-responsive proteins in 4× that were different from those in 2× (e.g., processing, binding and oxidative-phosphorylation-related proteins) (Additional file 1: Table S1; Additional file 2: Table S2) may provide new insights into the molecular mechanisms of resistance to salinity stress.
This study was supported by the Fundamental Research Funds for the Central Universities (No. 2572016EAJ4; 2572015DA03; 2572017AA23), the National Natural Science Foundation of China (31170568).
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FM conceived and designed the experiments; QL, MP, XZ, QW, WC performed the experiments and analyzed the data; FM wrote the paper. PL and XJ performed the western blot experiments. All authors read and approved the final manuscript.
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- Hu M, Shi Z, Zhang Z, Zhang Y, Li H. Effects of exogenous glucose on seed germination and antioxidant capacity in wheat seedings under salt stress. Plant Growth Regul. 2012;68:177–88.View ArticleGoogle Scholar
- Nelson DE, Rammesmayer G, Bohnert HJ. Regulation of cell-specific inositol metabolism and transport in plant salinity tolerance. Plant Cell. 1998;10(5):753–64.PubMedPubMed CentralGoogle Scholar
- Takahashi S, Murata N. How do environmental stresses accelerate photoinhibition? Trends Plant Sci. 2008;13(4):178–82.View ArticlePubMedGoogle Scholar
- Taji T, Seki M, Satou M, Sakura T, Kobayashi M, Ishiyama K, Narusaka Y, Narusaka M, Zh J, Shinozaki K. Comparative genomics in salt tolerance between Arabidopsis and Arabidopsis-Related halophyte salt cress using Arabidopsis microarray. Plant Physiol. 2004;135(3):1697–709.View ArticlePubMedPubMed CentralGoogle Scholar
- Inan G, Zhang Q, Li P, Wang Z, Cao Z, Zhang H, Zhang C, Quist TM, Goodwin SM, Zhu J. Salt cress. A halophyte and cryophyte Arabidopsis relative model system and its applicability to molecular genetic analyses of growth and development of extremophiles. Plant Physiol. 2004;135(3):1718–37.View ArticlePubMedPubMed CentralGoogle Scholar
- Li X, Yu E, Fan C, Zhang C, Fu T, Zhou Y. Developmental, cytological and transcriptional analysis of autotetraploid Arabidopsis. Planta. 2012;236(2):579–96.View ArticlePubMedGoogle Scholar
- Adams KL, Wendel JF. Polyploidy and genome evolution in plants. Curr Opin Plant Biol. 2005;8(2):135–41.View ArticlePubMedGoogle Scholar
- Datta AK, Mandal A, Das D, Gupta S, Saha A, Paul R, Sengupta S, Halder S, Biswas S. Polyploidy in Angiosperms: Genetic Insight to the Phenomenon. Proc Natl Acad Sci India. 2016;86(3):1–10.Google Scholar
- Soltis DE, Bell CD, Kim S, Soltis PS. Origin and early evolution of angiosperms. Ann N Y Acad Sci. 2008;1133(1):3.View ArticlePubMedGoogle Scholar
- Sugiyama SI. Polyploidy and cellular mechanisms changing leaf size: comparison of diploid and autotetraploid populations in two species of Lolium. Ann Bot. 2005;96(5):931–8.View ArticlePubMedPubMed CentralGoogle Scholar
- Anssour S. Phenotypic, genetic and genomic consequences of natural and synthetic polyploidization of Nicotiana attenuata and Nicotiana obtusifolia. Ann Bot. 2009;103(8):1207–17.View ArticlePubMedPubMed CentralGoogle Scholar
- Yao H, Kato A, Mooney B, Birchler JA. Phenotypic and gene expression analyses of a ploidy series of maize inbred Oh43. Plant Mol Biol. 2011;75(3):237–251(215).View ArticlePubMedGoogle Scholar
- Guo L, Xu W, Zhang Y, Zhang J, Wei Z. Inducing triploids and tetraploids with high temperatures in Populus sect. Tacamahaca. Plant Cell Rep. 2017;36(2):313.View ArticlePubMedGoogle Scholar
- Liao T, Cheng S, Zhu X, Min Y, Kang X. Effects of triploid status on growth, photosynthesis, and leaf area in Populus. Trees. 2016;30(4):1137–47.View ArticleGoogle Scholar
- Diallo AM, Nielsen LR, Kjær ED, Petersen KK, Ræbild A. Polyploidy can Confer Superiority to West Africanacacia senegal(L.) Willd. Trees. Front Plant Sci. 2016;7(346).Google Scholar
- Hijmans RJ, Gavrilenko T, Stephenson S, Bamberg J, Salas A, Spooner DM. Geographical And Environmental Range Expansion Through Polyploidy In Wild Potatoes (Solanum Section Petota). Glob Ecol Biogeogr. 2007;16(4):485–95.View ArticleGoogle Scholar
- Riddle NC, Jiang H, An L, Doerge R, Birchler JA. Gene expression analysis at the intersection of ploidy and hybridity in maize. Theor Appl Genet. 2010;120(2):341–53.View ArticlePubMedGoogle Scholar
- Li C, Wang C, Dong N, Wang X, Zhao H, Converse R, Xia Z, Wang R, Wang Q. QTL detection for node of first fruiting branch and its height in upland cotton (Gossypium hirsutum L.). Euphytica. 2012;188(3):441–51.View ArticleGoogle Scholar
- Albertin W, Brabant P, Catrice O, Eber F, Jenczewski E, Chèvre AM, Thiellement H. Autopolyploidy in cabbage (Brassica oleracea L.) does not alter significantly the proteomes of green tissues. Proteomics. 2005;5(8):2131–9.View ArticlePubMedGoogle Scholar
- Zheng Y, Haage K, Streit VE, Gierl A, Ruiz RAT. A large number of tetraploid Arabidopsis thaliana lines, generated by a rapid strategy, reveal high stability of neo-tetraploids during consecutive generations. Theor Appl Genet. 2009;118(6):1107–19.View ArticleGoogle Scholar
- Comai L. The advantages and disadvantages of being polyploid. Nat Rev Genet. 2005;6(11):836–46.View ArticlePubMedGoogle Scholar
- Meng F, Wang J, Huang F. Ultrastructure of mesophyll cells in two Robinia pseudoacacia hybrids under NaCl stress. J Beijing Forestry Univ. 2010;32:97–102.Google Scholar
- Wang Z, Wang M, Liu L, Meng F. Physiological and Proteomic Responses of Diploid and Tetraploid Black Locust (Robinia pseudoacacia L.) Subjected to Salt Stress. Int J Mol Sci. 2013;14(10):20299–325.View ArticlePubMedPubMed CentralGoogle Scholar
- Rai S, Agrawal C, Shrivastava AK, Singh PK, Rai L. Comparative proteomics unveils cross species variations in Anabaena under salt stress. J Proteome. 2014;98:254–70.View ArticleGoogle Scholar
- Ma H, Song L, Shu Y, Wang S, Niu J, Wang Z, Yu T, Gu W, Ma H. Comparative proteomic analysis of seedling leaves of different salt tolerant soybean genotypes. J Proteome. 2012;75(5):1529–46.View ArticleGoogle Scholar
- Qiao G, Zhang X, Jiang J, Liu M, Han X, Yang H, Zhuo R. Comparative Proteomic Analysis of Responses to Salt Stress in Chinese Willow (Salix matsudana Koidz). Plant Mol Biol Report. 2014;32(4):814–27.View ArticleGoogle Scholar
- Wang L, Pan D, Li J, Tan F, Hoffmann-Benning S, Liang W, Chen W. Proteomic analysis of changes in the Kandelia candel chloroplast proteins reveals pathways associated with salt tolerance. Plant Sci. 2015;231:159–72.View ArticlePubMedGoogle Scholar
- Yin Y, Yang R, Han Y, Gu Z. Comparative proteomic and physiological analyses reveal the protective effect of exogenous calcium on the germinating soybean response to salt stress. J Proteome. 2015;113:110–26.View ArticleGoogle Scholar
- Millar JK, James R, Christie S, Porteous DJ. Disrupted in schizophrenia 1 (DISC1): subcellular targeting and induction of ring mitochondria. Mol Cell Neurosci. 2005;30(4):477–84.View ArticlePubMedGoogle Scholar
- Millar AH, Whelan J, Soole KL, Day DA. Organization and regulation of mitochondrial respiration in plants. Annu Rev Plant Biol. 2011;62:79–104.View ArticlePubMedGoogle Scholar
- Hernández JA, Corpas FJ, Gómez M, Río LA, Sevilla F. Salt-induced oxidative stress mediated by activated oxygen species in pea leaf mitochondria. Physiol Plant. 1993;89(1):103–10.View ArticleGoogle Scholar
- Jiménez A, Sevilla F. Evidence for the Presence of the Ascorbate-Glutathione Cycle in Mitochondria and Peroxisomes of Pea Leaves. Plant Physiol. 1997;114(1):275–84.View ArticlePubMedPubMed CentralGoogle Scholar
- Wang W, Vinocur B, Shoseyov O, Altman A. Role of plant heat-shock proteins and molecular chaperones in the abiotic stress response. Trends Plant Sci. 2004;9(5):244–52.View ArticlePubMedGoogle Scholar
- Byeong-Ha L, Hojoung L, Liming X, Jian-Kang Z. A Mitochondrial Complex I Defect Impairs Cold-Regulated Nuclear Gene Expression. Plant Cell. 2002;14(6):1235–51.View ArticleGoogle Scholar
- Jolivet Y, ., Pireaux JC, Dizengremel P,. Changes in Properties of Barley Leaf Mitochondria Isolated from NaCl-Treated Plants. Plant Physiol 1990, 94(2):641-646.View ArticlePubMedPubMed CentralGoogle Scholar
- Widodo PJH, Newbigin E, Tester M, Bacic A, Roessner U. Metabolic Responses To Salt Stress Of Barley (Hordeum Vulgare L.) Cultivars, Sahara And Clipper, Which Differ In Salinity Tolerance. J Exp Bot. 2009;60(14):4089–103.View ArticlePubMedPubMed CentralGoogle Scholar
- Jacoby RP, Taylor NL, Millar AH. The role of mitochondrial respiration in salinity tolerance. Trends Plant Sci. 2011;16(11):614–23.View ArticlePubMedGoogle Scholar
- Smith CA, Melino VJ, Sweetman C, Soole KL. Manipulation of alternative oxidase can influence salt tolerance in Arabidopsis thaliana. Physiol Plant. 2009;137(4):459–72.View ArticlePubMedGoogle Scholar
- Tomaz T, Bagard M, Pracharoenwattana I, Lindén P, Lee CP, Carroll AJ, Ströher E, Smith SM, Gardeström P, Millar AH. Mitochondrial malate dehydrogenase lowers leaf respiration and alters photorespiration and plant growth in Arabidopsis. Plant Physiol. 2010;154(3):1143–57.View ArticlePubMedPubMed CentralGoogle Scholar
- Sergiev I, Alexieva V, Karanov E. Effect of spermine, atrazine and combination between them on some endogenous protective systems and stress markers in plants. C R Acad Bulg Sci. 1997;51(3):121–4.Google Scholar
- Beauchamp C, Fridovich I. Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Anal Biochem. 1971;44(1):276–87.View ArticlePubMedGoogle Scholar
- Carlberg I, Mannervik B. Purification and characterization of the flavoenzyme glutathione reductase from rat liver. J Biol Chem. 1975;250(14):5475–80.PubMedGoogle Scholar
- Nakano Y, Asada K. Hydrogen Peroxide is Scavenged by Ascorbate-specific Peroxidase in Spinach Chloroplasts. Plant Cell Physiol. 1981;22(5):867–80.Google Scholar
- Neuburger M, Journet EP, Bligny R, Carde JP, Douce R. Purification of plant mitochondria by isopycnic centrifugation in density gradients of Percoll. Arch Biochem Biophys. 1982;217(1):312–23.View ArticlePubMedGoogle Scholar
- Dalton DA, Russell SA, Hanus FJ, Pascoe GA, Evans HJ. Enzymatic reactions of ascorbate and glutathione that prevent peroxide damage in soybean root nodules. Proc Natl Acad Sci. 1986;83(11):3811–5.View ArticlePubMedPubMed CentralGoogle Scholar
- Hossain MA, Asada K. Inactivation of Ascorbate Peroxidase in Spinach Chloroplasts on Dark Addition of Hydrogen Peroxide: Its Protection by Ascorbate. Plant Cell Physiol. 1984;25(7):1285–95.Google Scholar
- Law MY, Charles SA, Halliwell B. Glutathione and ascorbic acid in spinach (Spinacia oleracea) chloroplasts. The effect of hydrogen peroxide and of Paraquat. Biochem J. 1983;210:899–903.View ArticlePubMedPubMed CentralGoogle Scholar
- Ellman G. Tissue sulfhydryl groups. J Pharm Pharmaceut Sci. 1959;4(4):206–7.Google Scholar
- Taivassalo T, Hepple RT, Picard M, Gouspillou G. Mitochondria: isolation, structure and function. J Physiol. 2011;589(18):4413–21.View ArticlePubMedPubMed CentralGoogle Scholar
- Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976;72(72):248–54.View ArticlePubMedGoogle Scholar
- Wang L, Liang W, Xing J, Tan F, Chen Y, Huang L, Cheng CL, Chen W. Dynamics of chloroplast proteome in salt-stressed mangrove Kandelia candel (L.) Druce. J Proteome Res. 2013;12(11):5124–36.View ArticlePubMedGoogle Scholar
- Meng F, Luo Q, Wang Q, Zhang X, Qi Z, Xu F, Xue L, Yuan C, Chow WS, Sun G. Physiological and proteomic responses to salt stress in chloroplasts of diploid and tetraploid black locust (Robinia pseudoacacia L.). Sci Rep. 2016;6:23098.View ArticlePubMedPubMed CentralGoogle Scholar
- Apse MP, Blumwald E. Engineering salt tolerance in plants. Curr Opin Biotechnol. 2002;13(2):146–50.View ArticlePubMedGoogle Scholar
- Sun Y. Free radicals, antioxidant enzymes, and carcinogenesis. Free Radic Biol Med. 1990;8(6):583–99.View ArticlePubMedGoogle Scholar
- Gechev TS, Hille J. Hydrogen peroxide as a signal controlling plant programmed cell death. J Cell Biol. 2005;168(1):17–20.View ArticlePubMedPubMed CentralGoogle Scholar
- Shafi A, Chauhan R, Gill T, Swarnkar MK, Sreenivasulu Y, Kumar S, Kumar N, Shankar R, Ahuja PS, Singh AK. Expression of SOD and APX genes positively regulates secondary cell wall biosynthesis and promotes plant growth and yield in Arabidopsis under salt stress. Plant Mol Biol. 2015;87(6):615–31.View ArticlePubMedGoogle Scholar
- Asada K. Ascorbate peroxidase – a hydrogen peroxide-scavenging enzyme in plants. Physiol Plant. 1992;85(2):235–241(237).View ArticleGoogle Scholar
- Zhou W, Eudes F, Laroche A. Identification of differentially regulated proteins in response to a compatible interaction between the pathogen Fusarium graminearum and its host, Triticum aestivum. Proteomics. 2006;6:4599–609.View ArticlePubMedGoogle Scholar
- Taylor NL, Tan YF, Jacoby RP, Millar AH. Abiotic Environmental Stress Induced Changes In The Arabidopsis Thaliana Chloroplast, Mitochondria And Peroxisome Proteomes. J Proteome. 2009;72(3):367–78.View ArticleGoogle Scholar
- Wang Z, Fan G, Dong Y, Zhai X, Deng M, Zhao Z, Liu W, Cao Y. Implications of polyploidy events on the phenotype, microstructure, and proteome of Paulownia australis. Plos One. 2017;12(3):e0172633.Google Scholar
- Shang G, Li Y, Hong Z, Liu C, He S, Liu Q. Transgenic sweetpotato plants expressing an LOS 5 gene are tolerant to salt stress. Plant Cell Tissue Org Cult. 2011;107(2):205.View ArticleGoogle Scholar
- Foyer CH, Noctor G. Oxidant and antioxidant signalling in plants: a re-evaluation of the concept of oxidative stress in a physiological context. Plant Cell Environ. 2005;28(8):1056–71.View ArticleGoogle Scholar
- Hernández JA, Almansa MS. Short-term effects of salt stress on antioxidant systems and leaf water relations of pea leaves. Physiol Plant. 2002;115(2):251.View ArticlePubMedGoogle Scholar
- Shalata A, Tal M. The effect of salt stress on lipid peroxidation and antioxidants in the leaf of the cultivated tomato and its wild salt-tolerant relative Lycopersicon pennellii. Physiol Plant. 2010;104(2):169–74.View ArticleGoogle Scholar
- Demiral T, Türkan İ. Comparative lipid peroxidation, antioxidant defense systems and proline content in roots of two rice cultivars differing in salt tolerance. Environ Exp Bot. 2005;53(3):247–57.View ArticleGoogle Scholar
- Bor M, Özdemir F, Türkan I. The effect of salt stress on lipid peroxidation and antioxidants in leaves of sugar beet Beta vulgaris L. and wild beet Beta maritima L. Plant Sci. 2003;164(1):77–84.View ArticleGoogle Scholar
- Zagdańska B. Respiratory energy demand for protein turnover and ion transport in wheat leaves upon water deficit. Physiol Plant. 1995;95(3):428–36.View ArticleGoogle Scholar
- Yeo AR. Salinity resistance: Physiologies and prices. Physiol Plant. 1983;58:214–22.View ArticleGoogle Scholar
- Feng L, Lin T, Uranishi H, Gu W, Xu Y. Functional analysis of the roles of posttranslational modifications at the p53 C terminus in regulating p53 stability and activity. Mol Cell Biol. 2005;25(13):5389–95.View ArticlePubMedPubMed CentralGoogle Scholar
- Gomes M, Hamer R, Reinert G, Deane CM. Mutual information and variants for protein domain-domain contact prediction. BMC Res Notes. 2012;5(1):472.View ArticlePubMedPubMed CentralGoogle Scholar
- Zhu W, Miao Q, Sun D, Yang G, Wu C, Huang J, Zheng C. The Mitochondrial Phosphate Transporters Modulate Plant Responses to Salt Stress via Affecting ATP and Gibberellin Metabolism in Arabidopsis thaliana. PLoS One. 2012;7(8):e43530.View ArticlePubMedPubMed CentralGoogle Scholar
- Bernard SM, Habash DZ. The importance of cytosolic glutamine synthetase in nitrogen assimilation and recycling. New Phytol. 2009;182(3):608–20.View ArticlePubMedGoogle Scholar
- Silveira JAG, Viégas RDA, Rocha IMAD, Moreira RDA, Oliveira JTA. Proline accumulation and glutamine synthetase activity are increased by salt-induced proteolysis in cashew leaves. J Plant Physiol. 2003;160(2):115–123(119).View ArticlePubMedGoogle Scholar
- Wang ZQ, Yuan YZ, Ou JQ, Lin QH, Zhang CF. Glutamine synthetase and glutamate dehydrogenase contribute differentially to proline accumulation in leaves of wheat (Triticum aestivum) seedlings exposed to different salinity. J Plant Physiol. 2007;164:695–701.View ArticlePubMedGoogle Scholar
- Silva-Ortega CO, Ochoa-Alfaro AE, Reyes-Agüero JA, Aguado-Santacruz GA, Jiménez-Bremont JF. Salt stress increases the expression of p5cs gene and induces proline accumulation in cactus pear. Plant Physiol Biochem. 2008;46(1):82–92.View ArticlePubMedGoogle Scholar
- Møller IM. Plant mitochondria and oxidative stress: electron transport, NADPH turnover, and metabolism of reactive oxygen species. Annu Rev Plant Physiol Plant Mol Biol. 2001;52(4):561–91.View ArticlePubMedGoogle Scholar
- Heazlewood JL, Tonti-Filippini JS, Gout AM, Day DA, Whelan J, Millar AH. Experimental analysis of the Arabidopsis mitochondrial proteome highlights signaling and regulatory components, provides assessment of targeting prediction programs, and indicates plant-specific mitochondrial proteins. The Plant Cell 16. Plant Cell. 2004;16(1):241–56.View ArticlePubMedPubMed CentralGoogle Scholar
- Pusnik M. Pentatricopeptide repeat proteins in Trypanosoma brucei function in mitochondrial ribosomes. Mol Cell Biol. 2007;27(19):6876–88.View ArticlePubMedPubMed CentralGoogle Scholar
- Laluk K, Abuqamar S, Mengiste T. The Arabidopsis Mitochondria-Localized Pentatricopeptide Repeat Protein PGN Functions in Defense against Necrotrophic Fungi and Abiotic Stress Tolerance. Plant Physiol. 2011;156(4):2053–68.View ArticlePubMedPubMed CentralGoogle Scholar
- Kawasaki S, ., Borchert C, ., Deyholos M, ., Wang H, ., Brazille S, ., Kawai K, ., Galbraith D,., Bohnert HJ: Gene expression profiles during the initial phase of salt stress in rice. Plant Cell 2001, 13(4):889-905.View ArticlePubMedPubMed CentralGoogle Scholar
- Kim J, Kim HY. Functional analysis of a calcium-binding transcription factor involved in plant salt stress signaling. FEBS Lett. 2006;580(22):5251–6.View ArticlePubMedGoogle Scholar
- Yehuda G, Slava R, Rodolfo G, Doron S, Natalia S, Zvia K, Dudy BZ. Desiccation and zinc binding induce transition of tomato abscisic acid stress ripening 1, a water stress- and salt stress-regulated plant-specific protein, from unfolded to folded state. Plant Physiol. 2007;143(2):617–28.Google Scholar
- Tsunezuka H, Fujiwara M, Kawasaki T, Shimamoto K. Proteome analysis of programmed cell death and defense signaling using the rice lesion mimic mutant cdr2. Mol Plant-Microbe Interact. 2005;18(1):52–9.View ArticlePubMedGoogle Scholar
- Chen X, Wang Y, Li J, Jiang A, Cheng Y, Wei Z. Mitochondrial proteome during salt stress-induced programmed cell death in rice. Plant Physiol Biochem. 2009;47(5):407–15.View ArticlePubMedGoogle Scholar
- Alexander H, Daniela B, Enrico S, Klaus-Dieter S. Crosstalk between Hsp90 and Hsp70 chaperones and heat stress transcription factors in tomato. Plant Cell. 2011;23(2):741–55.View ArticleGoogle Scholar
- Liu Y-H, Wang X-T, Shi Y-S, Huang Y-Q, Song Y-C, Wang T-Y. Expression and Characterization of a Protein Disulfide Isomerases in Maize (Zea Mays L.). Chin J Biochem Mol Biol. 2009;25:229–34.View ArticleGoogle Scholar
- Foyer CH, Descourvières P, Kunert KJ. Protection against oxygen radicals: an important defence mechanism studied in transgenic plants. Plant Cell Environ. 1994;17(5):507–23.View ArticleGoogle Scholar
- Xiao X, Yang F, Zhang S, Korpelainen H, Li C. Physiological and proteomic responses of two contrasting Populus cathayana populations to drought stress. Physiol Plant. 2009;136:150–68.View ArticlePubMedGoogle Scholar
- Guo Y, Fitz J, Schneeberger K, Ossowski S, Cao J, Weigel D. Genome-wide comparison of nucleotide-binding site-leucine-rich repeat-encoding genes in Arabidopsis. Plant Physiol. 2011;157(2):757–69.Google Scholar
- Fossdal CG, Yaqoob N, Krokene P, Kvaalen H, Solheim H, Yakovlev IA. Local and systemic changes in expression of resistance genes, nb-lrr genes and their putative microRNAs in norway spruce after wounding and inoculation with the pathogen ceratocystis polonica. BMC Plant Biol. 2012;12:105.View ArticlePubMedPubMed CentralGoogle Scholar
- Aken OV, Zhang B, Carrie C, Uggalla V, Paynter E, Giraud E, Whelan J. Defining the Mitochondrial Stress Response in Arabidopsis thaliana. Mol Plant. 2009;2(6):1310–24.View ArticlePubMedGoogle Scholar
- Huang S, Taylor NL, Narsai R, Eubel H, Whelan J, Millar AH. Experimental Analysis of the Rice Mitochondrial Proteome, Its Biogenesis, and Heterogeneity. Plant Physiol. 2009;149(2):719–34.View ArticlePubMedPubMed CentralGoogle Scholar
- Kruft V, Eubel H, Jänsch L, Werhahn W, Braun HP. Proteomic approach to identify novel mitochondrial proteins in Arabidopsis. Plant Physiol. 2001;127(4):1694–710.View ArticlePubMedPubMed CentralGoogle Scholar
- Lee CP, Eubel H, O'Toole N, Millar AH: Combining proteomics of root and shoot mitochondria and transcript analysis to define constitutive and variable components in plant mitochondria. Phytochemistry 2011, 72(10):1092–1108.Google Scholar
- Lázaro JJ, Jiménez A, Camejo D, Iglesiasbaena I, Martí MDC, Lázaropayo A, Barrancomedina S, Sevilla F. Dissecting the integrative antioxidant and redox systems in plant mitochondria. Effect of stress and S-nitrosylation. Front Plant Sci. 2013;4(21):3187–204.Google Scholar
- Pastore D, Trono D, Laus MN, Di Fonzo N, Flagella Z. Possible plant mitochondria involvement in cell adaptation to drought stress. A case study: durum wheat mitochondria. J Exp Bot. 2007;58(2):195.View ArticlePubMedGoogle Scholar
- Zörb C, Herbst R, Forreiter C, Schubert S. Short-term effects of salt exposure on the maize chloroplast protein pattern. Proteomics. 2009;9(17):4209–20.View ArticlePubMedGoogle Scholar
- Mahler H, Wuennenberg P Fau - Linder M, Linder M Fau - Przybyla D, Przybyla D Fau - Zoerb C, Zoerb C Fau - Landgraf F, Landgraf F Fau - Forreiter C, Forreiter C. Singlet oxygen affects the activity of the thylakoid ATP synthase and has a strong impact on its gamma subunit. (0032–0935 (Print)).Google Scholar
- Van HS, Smagghe G, Van Damme EJ. Overexpression ofNictaba-Like Lectin Genes fromGlycine maxConfers Tolerance towardPseudomonas syringaeInfection, Aphid Infestation and Salt Stress in TransgenicArabidopsisPlants. Front Plant Sci. 2016;7Google Scholar
- Lannoo N, Damme EJMV. Lectin domains at the frontiers of plant defense. Front Plant Sci. 2014;5(5):397.PubMedPubMed CentralGoogle Scholar
- Rodziewicz P, Swarcewicz B, Chmielewska K, Wojakowska A, Stobiecki M. Influence of abiotic stresses on plant proteome and metabolome changes. Acta Physiol Plant. 2014;36(1):1–19.View ArticleGoogle Scholar
- Rao D, Momcilovic I, Kobayashi S, Callegari E, Ristic Z. Chaperone activity of recombinant maize chloroplast protein synthesis elongation factor, EF-Tu. FEBS J. 2004;271(18):3684.View ArticleGoogle Scholar