Abstract
Key message
The TPS5 negatively regulates ABA signaling by mediating ROS level and NR activity during seed germination and stomatal closure in Arabidopsis thaliana.
Abstract
Trehalose metabolism is important in plant growth and development and in abiotic stress response. Eleven TPS genes were identified in Arabidopsis, divided into Class I (TPS1–TPS4) and Class II (TPS5–TPS11). Although Class I has been shown to have TPS activity, the function of most members of Class II remains enigmatic. Here, we characterized the biological function of the trehalose-6-phosphate synthase TPS5 in ABA signaling in Arabidopsis. TPS5 expression was induced by ABA and abiotic stress, and expression in epidermal and guard cells was dramatically increased after ABA treatment. Loss-of-function analysis revealed that tps5 mutants (tps5-1 and tps5-cas9) are more sensitive to ABA during seed germination and ABA-mediated stomatal closure. Furthermore, the H2O2 level increased in the tps5-1 and tps5-cas9 mutants, which was consistent with the changes in the expression of RbohD and RbohF, key genes responsible for H2O2 production. Further, TPS5 knockout reduced the amounts of trehalose and other soluble carbohydrates as well as nitrate reductase (NR) activity. In vitro, trehalose and other soluble carbohydrates promoted NR activity, which was blocked by the tricarboxylic acid cycle inhibitor iodoacetic acid. Thus, this study identified that TPS5 functions as a negative regulator of ABA signaling and is involved in altering the trehalose content and NR activity.
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Introduction
Trehalose, a non-reducing disaccharide consisting of two glucose molecules linked by 1,1-glycosidic bonds, is synthesized in a two-step reaction from UDP-glucose (UDPG) and 6-phospho-glucose (G6P) by trehalose-6-phosphate synthase (TPS) and trehalose-6-phosphate phosphatase (TPP) in plants (Eastmond and Graham 2003). Although trehalose is ubiquitous in bacteria, yeast, fungi, nematodes, and insects, serving as a reserve carbohydrate and stress protection (Crowe et al. 2003; Goddijn et al. 1997), its level in plants is extremely low and it was once thought to occur only in drought-tolerant plants (Joachim et al. 1995). Following whole-genome sequencing, 11 TPSs and 10 TPPs were identified in Arabidopsis (Genome 2000; Leyman et al. 2001). The TPS proteins, carrying a TPS- and a TPP-like domain, are further divided into Class I (TPS1–TPS4) and Class II (TPS5–TPS11) based on their homology with the yeast TPS (ScTps1) and TPP (ScTps2) proteins, respectively; the TPP proteins display significant similarity to the highly conserved phosphatase box elements of ScTPS2 (Leyman et al. 2001; Ramon et al. 2009).
Class I (e.g., TPS1), which has been shown to have TPS activity in vitro, is well characterized (Blázquez et al. 1998; Gomez et al. 2010a, b). Studies have shown that the TPS1 gene is essential for normal growth, especially in flowers and buds, in embryogenesis and in ripening fruits (Eastmond et al. 2002; van Dijken et al. 2004; Wahl et al. 2013). Beyond being closely linked to growth and development in plants, TPS1 is highly expressed in guard cells and the tps1-12 mutant, which carries a weak allele of the AtTPS1 gene, has a smaller stomatal aperture than wild-type plants (Gomez et al. 2010a, b). In addition, constitutive overexpression of TPS1 reduces the sensitivity of seed germination to abscisic acid (ABA) (Avonce et al. 2004; Van Houtte et al. 2013; Vandesteene et al. 2012). These results suggest that TPS1 is also involved in ABA signaling.
Interestingly, although most of the functions of Class II TPS remain unclear, many of the Class II genes appear to be extensively regulated at the transcriptional level by abiotic stress (Baena-Gonzalez et al. 2007; Bates et al. 2012; Scheible et al. 2004; Usadel et al. 2008; Wang et al. 2003); TPS6 was reported to regulate plant architecture, epidermal pavement cell shape, and trichome branching (Chary et al. 2008); TPS5 showed stomatal function effects without a change in stomatal density (Bates et al. 2012), and appears to be involved in thermotolerance, possibly by interaction with the transcriptional co-activator MBF1c (Suzuki et al. 2008); Ramon used a set of promoter-GUS protein reporters to demonstrate that Class II proteins have a significantly different tissue-specific expression and responsiveness to carbon availability and hormones (Ramon et al. 2009). Very recently, a rice TPS (OsTPS8) was reported conferring salt stress tolerance and controlling yield-related traits in rice (Vishal et al. 2019). In summary, evidence is increasing that Class II proteins play an important role in many key processes of plant growth and abiotic stress response.
In nature, plants face many challenges from the environment. Trehalose metabolism is considered an important pathway for plants to improve stress tolerance. Trehalose is reported to be an essential virulence factor for the rice blast fungus, Magnaporthe oryzae (Foster et al. 2014). T6P, the intermediate in trehalose biosynthesis, was found to play a possible role in ABA-mediated regulation of stomatal conductance, involving covalent modifications of nitrate reductase (NR) and the sucrose nonfermenting-1-related protein kinase2.6 (SnRK2.6) (Chen et al. 2016; Emanuelle et al. 2015; Figueroa and Lunn 2016).
TPS5 expression is closely related to ABA-induced and abiotic stress. tps5 mutants (tps5-1 and tps5-cas9) are more sensitive to ABA during seed germination and ABA-mediated stomatal closure. The obvious question that arises is how TPS5 could be involved in the regulation of ABA signaling.
As a further step towards the elucidation of TPS5 exact functions in ABA signaling, the level of H2O2 and ABA-responsive genes, such as RbohD and RbohF, were analyzed. In addition, the amounts of trehalose and other soluble carbohydrates as well as NR activity in both tps5 mutants (tps5-1 and tps5-cas9) and the wild type were determined. Finally, we determined whether trehalose metabolism is directly or indirectly involved in ABA signaling. Collectively, this study will elucidate the important role of TPS5 in ABA signaling and help develop strategies to improve stress tolerance in plants for better crop production.
Materials and methods
Plant materials and growth conditions
The Arabidopsis thaliana (L.) Heynh. ‘Columbia’ and tps5 mutant (salk_144791) used in this study were purchased from the Arabidopsis Biological Resource Center (ABRC; http://www.arabidopsis.org/). Plant growth conditions and Agrobacterium tumefaciens-mediated transformation were performed as described previously (Clough and Bent 1998). The primers for identifying tps5-1 mutants were as follows: TPS5-T-F (5′-CACTCCTCAACGCTGATTTGA-3′); TPS5-T-R (5′-ATCTTGTATAAAGCTACGCGCC-3′); LBb1.3 (5′-ATTTTGCCGATTTCGAAC-3′).
Plasmid constructs
The TPS5 cDNA was amplified by RT-PCR using the primer pair TPS5-F and TPS5-R and ligated to the pMD18-T vector. For subcellular localization analysis, the TPS5 cDNA was amplified without its stop codon using the primer pair TPS5-SF and TPS5-SR, subsequently digested with BsaI, and then inserted into transient expression vector pEZS-N. The TPS5pro::GUS for histochemical analysis was constructed as follows: a 1.6-kb fragment upstream of the ATG start codon of TPS5 was amplified by PCR using the primers TPS5-GF and TPS5-GR and cloned into the pMD18-T vector, subsequently digested with Pst I and BamHI, respectively, then subcloned into the expression vector pBI101.2.
TPS5-Cas9 vectors for transgenic plants were also designed. The chimeric sgRNA for TPS5 was constructed by cloning the annealed oligos TPS5-sgF and TPS5-sgR into pBlueScript SK-sgRNA, then both the sgRNA and hSpCas9 were subcloned into the expression vector pCAMBIA1300 (Lu et al. 2017).
Stress induction and qRT-PCR analysis
The 20-day-old seedlings were subjected to various stress treatments. Drought stress was applied by removing the seedlings from the 0.5 × Murashige and Skoog (MS) medium plate and placing them on filter paper for a specified period of time; high-temperature stress was induced by transferring the seedlings from the 0.5 × MS medium into an incubator at 42 °C; 250 mM NaCl and 100 µM ABA treatments were performed as described previously (Ding et al. 2015). Total RNA was extracted with TRIzol reagent (Invitrogen) following the provider’s instructions. Two micrograms of DNA-free RNA was used for reverse transcription according to the kit instructions (Invitrogen). Quantitative RT-PCR was performed on a Quant Studio 5 Real-Time PCR Instrument (96-well 0.2-ml block). The primers for RT-PCR and qRT-PCR are shown in Supplemental Table 1.
Histochemical GUS analysis
For GUS (β-glucuronidase) staining assays, transgenic plants were selected based on kanamycin resistance. The TPS5pro activity was analyzed via histochemical staining according to slightly modified published protocols (Li et al. 2015). Briefly, TPS5pro::GUS transgenic plants were immersed in staining buffer containing 0.1 M phosphate-buffered sodium (pH 7.0), 10 mM EDTA, 2 mM potassium ferrocyanide, 0.1% (v/v) Triton X-100, 20% (v/v) methanol, 0.5 mM X-gluc, and incubated at 37 °C overnight. After staining, tissues were observed and photographed with an Olympus SZX12 microscope equipped with a camera.
Analysis of subcellular localization of TPS5
Subcellular localization of TPS5 was done according to slightly adjusted published protocols. The recombinant plasmids 35S::TPS5-EGFP and 35S::BIP-RFP (ER marker) were used to cotransfect Arabidopsis mesophyll protoplasts transiently. TPS5–EGFP fusion protein was excited at 488 nm using a laser, and the emitted fluorescence signal was collected with a band-pass filter at 490–540 nm (GFP panel). BIP-RFP marker was excited by laser emission at 561 nm, and the emitted fluorescence was collected with a band-pass filter at 592 nm (RFP panel) (Li et al. 2015).
Stomatal movement assay
Stomatal movement assays were performed as described previously (Ding et al. 2015) with slight modification. For ABA-induced stomatal closure experiments, 20-day-old rosette leaves were isolated and incubated in stomatal opening solution (OS solution) containing 10 mM KCl, 100 mM CaCl2, and 10 mM 2-morpholinoethanesulphonic acid (MES)–KOH (pH 6.1), for 30 min in the light, and then 1 μM, 5 μM, and 10 μM ABA were added, respectively. The stomatal apertures were measured after 1 h of ABA treatment. Subsequently, the epidermis was gently torn off and mesophyll cells were carefully scraped off; the epidermal layer was mounted on glass slides and observed using an Olympus microscope.
Determination of soluble carbohydrates content
Soluble carbohydrates were detected by ion chromatography (ICS 5000, Thermo Fisher Scientific) by Shanghai Sanshu Biotechnology (www.sanshubio.com). Briefly, soluble carbohydrates were extracted with an 80% ethanol solution and shaken and mixed in a 70 °C water bath. After 2 h, the EP tube was taken out; after cooling, 700 µl of sterile water was added, and the solution was centrifuged at 1200 rps for 5 min to remove the supernatant. An aliquot of 700–1000 µl of chloroform was added to the supernatant, mixed well, and centrifuged three times. The supernatant was placed in a clean EP tube for testing. After addition of 700 µl of 80% alcohol solution to the weighed sample, it was extracted in a 70 °C water bath, and shaken 3–5 times during this period.
Construction of double mutants of tps5 and tps6
First, we selected flower buds from tps5 and tps6 single mutants, labeled as parents, and carefully removed the petals and stamens. Then, the pollens of tps5 and tps6 mutants were applied to the stigma of the emasculated flowers reciprocally. Three days after pollination, the siliques were formed and elongated, which denoted successful hybridization. An F2 generation was obtained from the F1 hybrid, and F2 homozygotes were identified by their DNA and RNA levels.
DAB staining assay of rosette leaves
The accumulation of H2O2 was monitored by 3,3′-diaminobenzidine (DAB) staining (Thordal-Christensen et al. 1997). Twenty-day-old leaves grown under control conditions were treated with 100 µM ABA for 3 h and immersed in freshly prepared 1 mg/mL DAB solution, followed by vacuuming for 10 min and shaking at 180 rpm in the dark overnight. Stained leaves were fixed with a solution of 3:1:1 ethanol:acetic acid:glycerol, and then photographed (Ding et al. 2015).
Nitrate reductase (NR) activity assay
The nitrate reductase (NR) activity was measured using 20-day-old seedling tissue extracts of both tps5 mutants (tps5-1 and tps5-cas9) and the wild type. The NR Activity in plants was determined by Nitrate Reductase (NR) Assay Kit (Solarbio, Beijing, China). The absorbance of NR was measured at 520 nm (n = 9).
Results
tps5 mutants are more sensitive to ABA during seed germination
A TPS5 T-DNA insertion allele (SALK_144791) was identified from ABRC, and named tps5-1. The site where T-DNA was inserted was determined to be 1472 bp downstream of the translational start site of TPS5 (Fig. 1A). Subsequently, we created a tps5-cas9 line using targeted genome editing of the TPS5 by applying CRISPR/Cas9 technology and we found that tps5-cas9 line lost four base pairs at 771–774 bp downstream of the translational start site of TPS5 compared with wild-type(Fig. 1A). Semi-quantitative PCR analysis suggested that the tps5-1 was an effective TPS5 knockout mutant (Fig. 1B).
Under normal growth conditions, tps5-1 and tps5-cas9 did not show any morphological alterations. Then, the germination of tps5-1 and tps5-cas9 was compared with that of wild-type plants (Columbia). The germination rate (germination rate was defined by cotyledon greening) for the mutants was the same as that of the wild type on ABA-free medium. In the presence of ABA, tps5-1 and tps5-cas9 mutants showed lower cotyledon-greening percentages than wild-type plants (Fig. 2A). To quantify the effect of ABA on germination rate, we measured the cotyledon-greening percentages of tps5 mutants and the wild type at different concentrations of ABA. When the concentration of exogenous ABA was 0.2 µM, the germination rates of tps5-1, tps5-cas9 and wild type were 90.3%, 89.6% and 99%, respectively. At 0.6 µM ABA concentration, the germination rates of tps5-1 and tps5-cas9 were significantly reduced, only 35.7%, 26.3%, while the wild-type germination rate was 78.3% indicating that the mutation in TPS5 led to ABA hypersensitivity during seed germination (Fig. 2B).
TPS5 is localized to the endoplasmic reticulum (ER) of Arabidopsis protoplasts
To determine the subcellular localization of the TPS5 protein, we constructed a vector for TPS5–GFP fusion proteins whose expression was regulated by cauliflower mosaic virus (CaMV) 35S promoter (35S::TPS5-EGFP). When transiently expressed in Arabidopsis mesophyll protoplasts, the appearance of the GFP signal in the cytoplasm was reticular, similar to the distribution and appearance of the endoplasmic reticulum (ER) (Fig. 3). Arabidopsis protoplasts were then co-transformed with 35S:TPS5-GFP and 35S: Bip-RFP plasmids (a fluorescence marker for ER localization) (Lee et al. 2011). The co-localization of both TPS5-GFP and BiP-RFP was clearly detected (Fig. 3), leading to the conclusion that TPS5 was localized to the ER.
TPS5 expression is ABA- and stress-related
To investigate the expression of TPS5, 20-day-old seedlings of the wild type were treated with exogenous ABA and subjected to various abiotic stresses, including drought, salt, and heat. Quantitative RT-PCR analysis showed that ABA induced the expression of TPS5, which was increased approximately twofold at 20 min after 100 µM ABA treatment, then gradually decreased for 4 h and maintained at a level close to the control, after which a significant rise occurred to an approximately fourfold increase at 24 h (Fig. 4A). High salt and temperature stresses also significantly induced the expression of TPS5, which increased about six- to tenfold, respectively, after the treatment was applied (Fig. 4A). By contrast, TPS5 expression was mildly responsive to drought stress, changing only about one- to twofold relative to control plants (Fig. 4A). To analyze the TPS5 expression pattern in more detail, a 1.5-kb upstream DNA fragment of TPS5 was fused with a GUS gene, and the construct was introduced into Arabidopsis thaliana to generate transgenic plants. Activity of GUS during seed germination was only detected in the root (Fig. 4B, a–c). However, in the presence of ABA, GUS was expressed more strongly in the hypocotyls and cotyledons (Fig. 4B, f–h), supporting the role of TPS5 during seed germination under ABA treatment. At the rosette stage, in addition to the strong expression of GUS in the root, there is also a weak expression in the leaf veins (Fig. 4B, d). Similarly, under ABA treatment, the intensity of GUS activity increased significantly (Fig. 4B, i), and was consistent with the qRT-PCR analysis. Interestingly, the activity of GUS in epidermal cells, guard cells and vascular bundle was also significantly enhanced by ABA treatment (Fig. 4B, j, Supplemental Fig. 4), suggesting that TPS5 is involved in regulating ABA-mediated stomatal closure and the response to abiotic stress.
TPS5 is a negative regulator of ABA-mediated stomatal closure
Since TPS5 is expressed in stomata and TPS5 expression was induced by ABA and abiotic stress, we further analyzed whether TPS5 regulates ABA-dependent stomatal closure. Stomatal closure or opening in tps5-1 and tps5-cas9 plants was similar to that of the wild type in both light and dark conditions. However, a significant difference was observed under ABA treatment. The stomatal apertures in detached leaves of the tps5-1 and tps5-cas9 mutants decreased more rapidly than those of the wild type after 1–2.5 h of ABA treatment (Fig. 5A, B). Then, the water loss in leaves of tps5-1, tps5-cas9, and the wild type was analyzed, showing that leaf water loss of tps5 mutant was significantly lower than that of the wild type (Fig. 5C). Increased H2O2 levels have been reported to function as an early signaling in response to ABA signaling (Zhang et al. 2001). Therefore, ABA-mediated accumulation of ROS (reactive oxygen species) was also compared in the wild type, tps5-1, and tps5-cas9. Leaves of 20-day-old plants were treated with 0 or 100 µM ABA for 3 h, after which the leaves were incubated in DAB for 12 h. The results showed that in tps5-1, tps5-cas9, and the wild type, H2O2 levels increased in response to ABA, while the increase in tps5-1 and tps5-cas9 was significantly larger than in the wild type (Fig. 5D). Then, the transcript levels of the key genes responsible for the production of H2O2, RbohD and RbohF were examined in the wild type and in the tps5 mutants. The expression of RbohD and RbohF in mutants was higher than that in the wild type (Fig. 5E), which was consistent with the changes in the H2O2 level. Collectively, these data indicate that TPS5 negatively regulates ABA-mediated stomatal closure.
TPS5 knockout reduces the amounts of trehalose and other soluble carbohydrates
Accumulating evidence shows that trehalose metabolism plays a particularly important role in the regulation of stomatal closure (Figueroa et al. 2016; Gomez et al. 2010a, b; Van Houtte et al. 2013; Vandesteene et al. 2012). Therefore, the negative regulation of ABA signaling by TPS5 might be associated with changes in T6P levels, resulting in downstream effects such as the accumulation of trehalose and other soluble carbohydrates. Nevertheless, trehalose has also been reported to have a signaling or regulatory function (Fernandez et al. 2012; Rodriguez-Salazar et al. 2009). To verify this possibility, the amounts of T6P, trehalose, and other soluble carbohydrates in plants were measured. Unfortunately, due to the extremely low T6P content in plants, the levels of T6P have not been detected in both mutants and wild-type plants. However, under normal conditions, the accumulation of trehalose, glucose and fructose in the tps5 mutants was lower than that in the wild type, while there was no difference in sucrose levels (Fig. 6A). When treated with ABA for 12 h in the light, the trehalose, glucose and fructose contents in both wild type and mutants were significantly increased, but the increase in the wild type was more pronounced (Fig. 6B). Although inconsistent with the result that there was no catalytic activity of Class II TPS proteins (Harthill et al. 2006; Ramon et al. 2009), these results apparently implicate a possible role for TPS5 in regulating carbohydrate metabolism and in ABA signaling. Possibly, TPS5 may be involved in the regulation of trehalose metabolism through interactions with other proteins or complex formation (Ramon et al. 2009; Vishal et al. 2019).
TPS5 knockout decreases NR activity, while trehalose and other soluble carbohydrates promote NR activity in vitro
The findings that nitric oxide (NO)-mediated ABA signaling is impaired in nia1 and nia2 mutants lacking nitrate reductase (NR) activity (Chen et al. 2016), whereas TPS induction leads to activation of NR (Figueroa and Lunn 2016), suggests a possible role for the trehalose metabolism pathway in regulating ABA signaling involving changes in the activity of NR (Figueroa and Lunn 2016). In this study, NR activity was measured using 20-day-old seedling tissue extracts of both tps5 mutants (tps5-1 and tps5-cas9) and the wild type. The results showed that the NR activity in tps5-1 and tps5-cas9 was lower than that in the wild type (Fig. 6C). Then, NR activity was measured using 3-week-old seedling tissue extracts with and without T6P in vitro. NR activity in wild-type seedling extracts enhanced by T6P was observed when exogenous 1 μM T6P was added (Fig. 6D). The same effect as with T6P was observed when glucose, sucrose, trehalose and fructose were added (Fig. 6D), indicating that the change in NR activity is most correlated with the trehalose metabolic pathway. Thus, further studies are needed to understand why adding T6P and soluble sugars to seedling extracts can lead to activation of NR. NR is widely present in plants and is a key enzyme for the conversion of plant nitrate nitrogen to ammonia nitrogen. Its catalytic effect requires the presence of NADPH and H+. Therefore, it is speculated that an increase in NR activity is associated with the production of NADH and H+ by the glycolysis pathway. To further verify this possibility, we added iodoacetic acid, an inhibitor of the tricarboxylic acid cycle, to the extract and found that the addition of T6P, trehalose, glucose and sucrose no longer led to the activation of NR (Supplemental Fig. 1). This unexpected finding led to the proposal that in regulating ABA signaling, TPS5 is most likely involved in trehalose metabolism and is associated with changes in the activity of NR.
Discussion
Role of TPS5 in ABA signaling
ABA is an important regulator of stomatal closure, and several studies have found evidence of a link between trehalose metabolism and ABA signaling (Gomez et al. 2010a, b; Van Houtte et al. 2013; Vandesteene et al. 2012). The Arabidopsis TPS family has 11 TPS genes and is subdivided into 2 distinct clades, known as Class I (TPS1–TPS4) and Class II (TPS5–TPS11) (Leyman et al. 2001). In addition to the better-established roles of the gene products of Class I, the function of most of the Class II proteins remains enigmatic (Figueroa et al. 2016). In this study, we show that the TPS5 gene, which encodes a trehalose-6-phosphate synthase and has been implicated in thermotolerance (Suzuki et al. 2008), plays an important role in ABA signaling.
ABA response assays indicated that during seed germination tps5-1 and tps5-cas9 mutants are more sensitive to ABA than the wild type (Fig. 2). However, if after germination the seedlings were shifted to ABA-containing medium, the differences in the effects between tps5-1, tps5-cas9 and wild type were less apparent when the transfer occurred after more than 7 days, meaning that the role of TPS5 in the ABA signaling pathway may be particularly important during seed germination. AtTPS5 is temporally induced by salt, drought and heat treatment. However, the tps5 mutants did not show any changes in phenotype when treated with these stresses. We supposed that it is caused by functional redundancy of the TPS genes.
After 1–2.5 h of ABA treatment, the tps5-1 and tps5-cas9 mutants show enhanced stomatal closure (Fig. 5A, B). These findings are supported by the enhanced expression of tps5 in response to ABA and abiotic stresses (Fig. 4A). Under ABA stress, stronger GUS activity was observed in the hypocotyls, cotyledons and guard cells of the TPS5pro::GUS transgenic plants (Fig. 4B). Furthermore, the expression of RbohD and RbohF in response to ABA in tps5-1 and tps5-cas9 mutants increased more significantly than in the wild type (Fig. 5E). These data were consistent with the findings obtained for changes in H2O2 content (Fig. 5D), which is a key signal for regulating stomatal closure. In addition, the accumulation of trehalose, fructose and glucose in the wild type under ABA treatment was also more than that in tps5 mutants (Fig. 6A), which is consistent with the result that the tps5 gene could link sucrose signaling to guard-cell movements (Bates et al. 2012). Collectively, these results suggest that TPS5 is a negative regulator of ABA signaling in seed germination and stomatal closure.
The obvious question that arises is how TPS5 could be involved in the regulation of ABA signaling. NO has been reported to suppress ABA signaling in guard cells by S-nitrosylation of SnRK2.6 (Wang et al. 2015a, b), which plays a key role in ABA downstream signaling and belongs to the same SNF1/AMPK/SnRK superfamily of protein kinases as SnRK1. Lunn et al. speculated that T6P could participate in the ABA-mediated regulation of stomatal closure, involving covalent modifications of NR and SnRK2.6, with NO as an intermediary signal (Lunn et al. 2014). Although speculatively, this hypothesis could be tested by investigating the NR activity in tps5 mutants and the wild type and the effect of exogenous T6P on NR activity. In this study, we demonstrated that the NR activity in the tps5-1 and tps5-cas9 mutants was lower than that in the wild type (Fig. 6C), and that exogenous T6P enhanced the NR activity significantly (Fig. 6D), which is consistent with the observation of activation of NR by Tre6P by Figueroa et al. (2016), and also explains the suppression of SnRK2.6 activity after the induction of TPS (Zhang et al. 2009). However, further proof is needed to understand how rising T6P levels lead to the activation of NR (Figueroa and Lunn 2016). It is striking that exogenous trehalose, glucose, sucrose, and fructose also increase the NR activity significantly, and that this enhancement is blocked by iodoacetic acid. Iodoacetic acid is an inhibitor of the tricarboxylic acid cycle and inhibits the production of NADPH and H+. Recently, similar results were reported in rice that the levels of trehalose and other soluble sugars were also changed in tps8 mutant. Besides, the ABA sensitivity was altered when TPS8 was mutated (Vishal et al. 2019). From these findings, a model emerged that changes in trehalose content driven by the knockout of TPS5 trigger related changes in glucose and fructose, which cause reductions of NADH and H+ and decrease the activity of NR. Another possibility is that the trehalose and fructose in the guard cells are rapidly reduced in the tps5 mutant, resulting in a decrease in malate synthesis that contributes to enhancing stomatal closure. Thus, experiments to measure T6P and related metabolites (e.g., trehalose, glucose,) in guard cells should provide new insight into how trehalose metabolism affects stomatal opening and closing.
Studies have shown that TPSs possess multiple SnRK1 phosphorylation sites, and TPS5 can bind directly or indirectly to 14-3-3 proteins (Avonce et al. 2004; Harthill et al. 2006). These correlations between TPS5 and SnRK1 lead to the hypothesis that TPS5 can interact directly with SnRK2 s to modulate ABA signaling. Analysis of transcriptional levels showed that the expression of TPS5 was very similar to that of SnRK2.6 in the wild type under ABA and heat treatment (Supplemental Fig. 2), but no direct interaction between Class II TPSs and SnRK2 s has been reported so far (Emanuelle et al. 2015; Figueroa et al. 2016).
Although detailed dynamic changes in the levels of activated NR, T6P, and S-nitrosylated SnRK2.6 in guard cells are not yet known, available evidence and the well-established ABA signaling pathway (Chen et al. 2016; Ding et al. 2015; Figueroa and Lunn 2016; Wang et al. 2015a, b) suggest the following hypothetic model for a function of TPS5 as a negative regulator of ABA signaling in regulating stomatal closure and seed germination (Fig. 7). We hypothesize that ABA treatment leads to increased expression of TPS5 in seed and guard cells (Fig. 4b), causing the synthesis of T6P and triggering-related changes in trehalose, glucose, and fructose, and causing an increase in the activity of NR (Fig. 6D), resulting in the accumulation of NO (Chen et al. 2016). When NO accumulates to high levels, the SnRK2s are S-nitrosylated by NO at cysteine 137, a residue adjacent to the kinase catalytic site (Wang et al. 2015a, b), and their activation is inhibited. Since the expression pattern of TPS5 was similar to that of SnRK2.6 under ABA and abiotic stress (Supplemental Fig. 2), and TPSs possess multiple SnRKs phosphorylation sites that bind directly or indirectly to 14-3-3 proteins (Harthill et al. 2006). Another scenario could be reached, namely that ABA treatment causes very fast and strong activation of SnRK2 s in seed and guard cells, which phosphorylates many downstream effector proteins and leads to stomatal closure and the inhibition of seed germination (Wang et al. 2015a, b). The activated SnRK2 s also promote the expression of tps5 and increase the level of trehalose to activate NR, which in turn leads to the accumulation of NO and inhibits the activity of SnRK2.6. This inhibition serves as negative feedback on ABA signaling. Furthermore, when treated with ABA, not only H2O2 production was increased in tps5 mutants, but the expression of RbohD and RbohF was also promoted (Fig. 5D, E). These results demonstrate unambiguously that the negative regulation of ABA-mediated stomatal closure by TPS5 is required for phosphorylation of the NADPH oxidases RbohD and RbohF.
Seed germination and stomatal closure analysis in mutants TPS6–TPS11 provide insight into the role of Class II TPS in regulating ABA signaling
For further insight into the role of TPS5 in regulating ABA signaling, a step forward in the analysis is to elucidate the role of other members of the Class II TPS (TPS5–TPS11) family under ABA treatment. The tps6 mutant is more sensitive to ABA than the wild type during seed germination (Fig. 8), while mutants tps7–11 showed no significant differences. A similar result was observed in ABA-mediated stomatal closure (Fig. 8). Next, a tps5/tps6 double mutant was constructed, and it exhibited higher sensitivity to ABA than the tps5 and tps6 single mutants during seed germination and ABA-mediated stomatal closure (Fig. 8). Furthermore, histochemical staining analysis of TPS6 showed that GUS activity was also increased in epidermal and guard cells after ABA treatment (data not shown), which was very similar to the effect of TPS5. In summary, accumulating data suggest important roles for the Class II proteins in regulating ABA signaling and abiotic stress response. Although a detailed analysis of the expression patterns of the entire set of Class II TPS genes showed that they differ remarkably in their tissue-specific expression and responsiveness to hormones (Ramon et al. 2009), the TPS5 and TPS6 genes are likely to play similar roles in ABA signaling. In support of these results, a phylogenetic analysis of the Class II TPS family showed that Arabidopsis TPS5 and TPS6 were more closely related to each other than to TPS7–11 (Supplemental Fig. 3).
In Arabidopsis thaliana, trehalose metabolism plays an important role in regulating stomatal conductance. However, it is unknown at present how trehalose metabolism participates in ABA signaling (Figueroa and Lunn 2016). Although many of the molecular details remain to be elucidated, our results reveal an important role for TPS5 in coordinating trehalose and NR activity in the regulation of ABA signaling in plants. The genetic mechanism defined in this study may, therefore, assist in understanding the possible mechanism by which metabolic and genetic regulation is integrated in ABA signaling.
Author contribution statement
DL, LC, LT conceived and designed the experiments. LT, ZX, CL, XH, YH, SW performed the experiments. DL, LT, ZX, LC analyzed the data and wrote the paper.
Abbreviations
- ABA:
-
Abscisic acid
- ER:
-
Endoplasmic reticulum
- GFP:
-
Green fluorescent protein
- NR:
-
Nitrate reductase
- ROS:
-
Reactive oxygen species
- T6P:
-
Trehalose-6-phosphasynthetase
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Acknowledgements
We thank Jiankang Zhu for kindly providing CRISPR/cas9 vectors. This work was supported by grants of NSFC (31570316; 31371244), HNNSF (2016JJ2089), Project of Hunan Provincial Education Department (17C0974, 13C638), China Postdoctoral Science Foundation (2013M542118).
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Tian, L., Xie, Z., Lu, C. et al. The trehalose-6-phosphate synthase TPS5 negatively regulates ABA signaling in Arabidopsis thaliana. Plant Cell Rep 38, 869–882 (2019). https://doi.org/10.1007/s00299-019-02408-y
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DOI: https://doi.org/10.1007/s00299-019-02408-y