The Arabidopsis AtUNC-93 Acts as a Positive Regulator of Abiotic Stress Tolerance and Plant Growth via Modulation of ABA Signaling and K+ Homeostasis

Potassium (K⁺) is one of the essential macronutrients required for plant growth and development, and the maintenance of cellular K⁺ homeostasis is important for plants to adapt to abiotic stresses and growth. However, the mechanism involved has not been understood clearly. In this study, we demonstrated that AtUNC-93 plays a crucial role in this process under the control of abscisic acid (ABA). AtUNC-93 was localized to the plasma membrane and mainly expressed in the vascular tissues in Arabidopsis thaliana. The atunc-93 mutants showed typical K⁺-deficient symptoms under low-K⁺ conditions. The K⁺ contents of atunc-93 mutants were significantly reduced in shoots but not in roots under either low-K⁺ or normal conditions compared with wild type plants, whereas the AtUNC-93-overexpressing lines still maintained relatively higher K⁺ contents in shoots under low-K⁺ conditions, suggesting that AtUNC-93 positively regulates K⁺ translocation from roots to shoots. The atunc-93 plants exhibited dwarf phenotypes due to reduced cell expansion, while AtUNC-93-overexpressing plants had larger bodies because of increased cell expansion. After abiotic stress and ABA treatments, the atunc-93 mutants was more sensitive to salt, drought, osmotic, heat stress and ABA than wild type plants, while the AtUNC-93-overexpressing lines showed enhanced tolerance to these stresses and insensitive phenotype to ABA. Furthermore, alterations in the AtUNC-93 expression changed expression of many ABA-responsive and stress-related genes. Our findings reveal that AtUNC-93 functions as a positive regulator of abiotic stress tolerance and plant growth by maintaining K⁺ homeostasis through ABA signaling pathway in Arabidopsis.

Introduction

Plants have developed a wide range of adaptive mechanisms to control growth and development under various abiotic stresses. The regulation of ion flux, including ion influx and efflux, in maintaining an appropriate level of ion homeostasis plays an essential role in improving plant adaptation to abiotic stresses, particularly salt stress. Salt injury to plants is mainly caused by Na⁺ toxicity. Plant cells depend on Na⁺ exclusion and sequestration to avoid Na⁺ toxicity (Osakabe et al., 2014). The SOS pathway is known to regulate plant salt stress tolerance by Na⁺ exclusion. The Na⁺/H⁺ antiporter SOS1, regulated by the SOS2-SOS3 complex, is involved in Na⁺ efflux from cytosol to the extracellular environment across the plasma membrane to maintain a low concentration of Na⁺ in cells (Qiu et al., 2002; Zhu, 2003). The CBL10-CIPK24 complex may predominantly function in Na⁺ sequestration into the vacuole in plant shoots (Kim et al., 2007; Quan et al., 2007). In addition, an increasing number of reports demonstrate that cytosolic potassium (K⁺) retention and maintenance of K⁺/Na⁺ homeostasis is important for plants to adapt to and tolerate salt stress. The endophytic fungus Piriformospora indica promotes Arabidopsis growth by maintaining K⁺/Na⁺ homeostasis under salt stress conditions (Abdelaziz et al., 2017). Jatropha curcas adapts to salt stress which is related to transport and selectivity of K⁺ and K⁺/Na⁺ homeostasis (Silva et al., 2015). Arbuscular mycorrhizal symbiosis alleviates salt stress in black locust through K⁺/Na⁺ homeostasis (Chen et al., 2017). Therefore, the maintenance of K⁺/Na⁺ homeostasis is one of the important mechanisms which plants use to increase their adaptation to abiotic stresses. K⁺ is not only essential for stress responses, but also functions as an important role in cell expansion regulated by turgor pressure. The K⁺ transport systems triple mutants, kup268 and kup68 gork, exhibited enhanced cell expansion and significantly decreased drought tolerance in Arabidopsis, suggesting that these K⁺ transporters act as key factors in K⁺ homeostasis in both drought stress responses and cell growth (Osakabe et al., 2013). The Na⁺/H⁺ antiporters NHX5 and NHX6 play important roles in cellular K⁺/Na⁺ homeostasis as the nhx56 double knockout mutant reduced Arabidopsis tolerance to salt tress and salinity stress and exhibited suppressed growth, with smaller and fewer cells (Bassil et al., 2011).

The phytohormone abscisic acid (ABA) plays a pivotal role in stress tolerance, and growth and development (Finkelstein et al., 2002; Weiner et al., 2010). In ABA signaling pathway, the PYR/PYL/RCAR receptor proteins can disrupt the interaction between the SnRK2s and PP2Cs in the presence of ABA, thus preventing the PP2Cs-mediated dephosphorylation of the SnRK2s and resulting in the activation of the SnRK2s. The relieved SnRK2s (SnRK2.2/2.3/2.6) can then phosphorylate ABFs to activate ABA-responsive genes (Ma et al., 2009; Park et al., 2009). Recent studies have reported that ABA signaling can control membrane transport systems in response to drought and salt stresses by maintaining ion homeostasis in plant (Osakabe et al., 2014). The K⁺ transporter KUP6 can be phosphorylated by SnRK2.6, a key component of ABA signaling, suggesting that KUP6 plays an important role in K⁺ homeostasis mediated by ABA signaling (Osakabe et al., 2013). An outward anion channel SLAC1 is directly activated by SnRK2.6 that is involved in stomatal closure regulated by ABA signaling (Lee et al., 2009). BdCIPK31, a calcineurin B-like protein-interacting protein kinase in Brachypodium distachyon, plays a positive role in regulating drought and salt stress tolerance by maintaining K⁺/Na⁺ homeostasis through ABA signaling pathway (Luo et al., 2017).

The UNC-93 in Caenorhabditis elegans was identified to be a component of a multi-subunit K⁺ channel complex that coordinates muscle contraction, and it may be a regulatory subunit of this channel (de la Cruz et al., 2003). But there is no functional report so far regarding UNC-93 domain protein in plants. In this study, we demonstrate that AtUNC-93, a novel UNC-93 domain protein, regulates K⁺ translocation from roots to shoots in Arabidopsis thaliana, and plays a critical role in abiotic stress tolerance and plant growth by maintaining K⁺ homeostasis through ABA-dependent signal transduction pathways.

Materials and Methods

Plant Materials and Growth Conditions

Arabidopsis thaliana ecotype Columbia was used in this study. The T-DNA insertion mutants, including atunc-93-1 (CS879007) and atunc-93-2 (SALK_010430C) (Columbia-0 background), were obtained from the Arabidopsis Biological Resource Center (ABRC). Homozygous individuals were isolated in the F2 progeny by PCR genotyping. The expression levels of the mutant genes were confirmed by RT-PCR. Homozygous mutants were used for experiments.

For non-sterile culture, Arabidopsis plants were grown in potting soil mixture (rich soil: vermiculite = 1:1, v/v) and kept in growth chambers at 22°C with illumination at 120 μmol m^-2 s^-1 for a 16 h daily light period. The relative humidity was approximate 65% (± 5%). For sterile culture, seeds were surface sterilized and placed on 1/2 Murashige and Skoog (MS) medium containing 3% (w/v) sucrose and 2.5g L^-1 phytagel and kept in growth chambers as described above after 3 days of vernalization in darkness at 4°C.

Vector Constructions and Arabidopsis Transformation

For generation of AtUNC-93-overexpressing lines, the construct was generated by cloning the coding sequence of AtUNC-93 into the pCAMBIA1301-Multi (modified from pCAMBIA1301) vector under the control of the cauliflower mosaic virus 35S promoter (Xiang et al., 2013). The construct was transformed into wild type Arabidopsis. For generation of complementation lines of atunc-93 mutants, the 35S:AtUNC-93 construct was transformed into atunc-93-1 and atunc-93-2, respectively. Arabidopsis transformation with Agrobacterium tumefaciens strain GV3101 was performed by the floral-dip method (Clough and Bent, 1998). Analyses of transgenic lines were performed on homozygous T3 progeny plants.

Growth Assays and Stress Treatments

To observe atunc-93 mutants and transgenic plants growth phenotypes under normal conditions grown in soil, plant growth was monitored and photographed at the indicated times in figure legends. To investigate the stem cell size, the plant stems were sliced into the paraffin sections after 6 weeks growth in soil and observed by inverted microscopy. For measurement of hypocotyl and root length, the seedlings grown on 1/2 MS medium in the light for 7 days or darkness for 10 days in the vertical position were photographed. The hypocotyl and primary root lengths of seedlings were measured using a ruler. The dry weight of seedling roots and shoots was measured after 14 days of growth on 1/2 MS medium. Forty plants of each line were analyzed in independent experiments, and all experiments were repeated three times.

For NaCl or mannitol treatments, 4-day-old seedlings were transferred to 1/2 MS medium supplemented with different concentrations of NaCl or mannitol. Results were documented photographically after 14 or 20 days of treatment. For heat stress, 4-day-old seedlings grown on 1/2 MS medium plates were exposed to one of the following heat treatments: 45°C for 1 to 3 h; 38°C for 90 min, followed by 45°C for 2 to 4 h; or 38°C for 90 min, followed by 2 h of recovery at 22°C and then 2 to 4 h at 45°C. For cold stress, 4-day-old seedlings were incubated at 4°C for 10 days. After heat or cold treatments, the plates were returned to 22°C, and viability was assessed daily for 7 days. For drought stress, potted seedlings were grown under normal watering conditions for 14 days and then stressed by completely depriving them of irrigation for 16 days (normal drought stress) or 19 days (severe drought stress). The plants were rewatered when significant differences in wilting were observed and survival was assessed at 2 days after rewatering. For ABA treatments, seeds were germinated on the ABA-free medium after 48 h stratification and transferred to 1/2 MS medium supplemented with different concentrations (0, 1, 3, 5, and 10 μM) of ABA in the vertical position. Seedling growth was investigated at 7 days after transfer, and the length of primary roots was measured. Several independent experiments were performed in this study to obtain statistically significant data.

For water loss measurement, rosette leaves were detached from 6-week-old plants, weighed immediately, and then placed on the laboratory bench. Weight loss of the detached leaves was monitored at the designated time periods. Water loss rate was expressed as the percentage of initial fresh weight. Three leaves per plant were excised, and ten plants of each genotype and transgenic line were tested in independent experiments repeated at least three times.

GUS Assays

To analyze the histological expression patterns of AtUNC-93 in Arabidopsis, the 2100 bp fragment before the ATG codon of AtUNC-93 was cloned from wild type Arabidopsis. The AtUNC-93 promoter fragment was fused in front of the GUS coding sequence in pCAMBIA1305 vector. This construct was confirmed by sequencing and introduced into wild type Arabidopsis plants by using A. tumefaciens-mediated transformation. The T3 homozygous transgenic plants of ProAtUNC-93:GUS were stained by submersion in staining solution at 37°C until sufficient staining developed as described previously (Jefferson et al., 1987). Then the chlorophyll in green tissues was cleared by 75% (v/v) ethanol. Images were taken under a stereomicroscope.

Subcellular Localization Analysis

For generation of AtUNC-93-GFP fusion protein, the coding sequence of AtUNC-93 was fused with GFP in the pBI121-GFP vector. The construct confirmed by sequencing and empty vector were transformed into A. tumefaciens strain GV3101 and then transiently transferred to onion (Allium cepa) epidermal cells mediated by A. tumefaciens. The fluorescence of GFP in the transformed onion epidermal cells was imaged using a confocal laser scanning microscope (Leica sp5) after the onion epidermal cells were incubated at 25°C for 16 h.

Real-Time PCR and RT-PCR

To check the expression level of AtUNC-93 gene under abiotic stress and ABA treatments, 14-day-old Arabidopsis plants were transferred from normal 1/2 MS medium to medium containing 150 mM NaCl, 200 mM mannitol or 3 μM ABA, respectively. For heat and cold stress, 14-day-old seedlings were transferred to a growth chamber at 38 or 4°C. Samples were taken after treatment for 0, 1, 5, 10, and 24 h separately. To detect the transcript levels of AtUNC-93 in different tissues, tissue samples of roots, stems, rosette leaves, stem leaves, flowers, and siliques were collected from 6-week-old Arabidopsis plants. Seedlings were obtained from 14-day-old seedlings grown on normal 1/2 MS medium. To test the expression levels of stress-related and ABA-responsive genes, 14-day-old seedlings were treated with NaCl, mannitol or ABA as described above for 5 h. For drought stress, 14-day-old seedlings grown in soil spots were exposed to water deficit stress by not watering them for 2 weeks. Relative expression of K⁺ channel genes was analyzed in RNA samples of 14-day-old seedlings grown on normal 1/2 MS medium.

For real-time PCR assay, total RNA was extracted using the Trizol reagent (Invitrogen) according to the manufacturer’s protocol, and then treated with DNase I (TaKaRa) to eliminate genomic DNA. cDNA was synthesized from treated RNA using SuperScript II reverse transcriptase (Invitrogen). Real-time PCR was performed using SYBR Premix Ex Taq (TaKaRa) on an ABI 7300 real-time PCR system (Applied Biosystems) according to the manufacturer’s instructions. The PCR thermal cycles were as follows: 95°C for 30 s, followed by 40 cycles at 95°C for 5 s and 60°C for 31 s. Relative quantitative results were calculated by normalization to ACTIN2. Three replications were performed for each sample. All experiments were repeated three times.

For RT-PCR assay, total RNA was isolated from the atunc-93 mutants, complementation lines and wild type plants, and then, the expression of AtUNC-93 was determined by RT-PCR. The Arabidopsis ACTIN2 gene was used as an internal control.

The primers used in this experiment were listed in Supplementary Table S1.

Low-K⁺ Stress Treatment and Ion Content Measurement

For low-K⁺ (LK) stress treatment, the K⁺ concentration in the LK medium was 100 μM throughout this study. The LK medium was made by modification of MS medium as described previously (Xu et al., 2006). For the post-germination growth assay on LK medium, 4-day-old seedlings were transferred from MS medium to LK or MS medium, and the low-K⁺ phenotype was observed at 10 days after transfer. For seed germination on LK medium, Arabidopsis seeds were germinated directly on MS, LK, or LK/LNH (low-K⁺ and low-NH₄⁺) medium for 4 days. The LK/LNH medium was modified from LK medium. Briefly, 28.6 mM NH₄NO₃ was removed, and others were unchanged. The actual and final K⁺ concentration in LK/LNH medium was 100 μM, and NH₄⁺ concentration was 1.25 mM.

For K⁺ and Na⁺ content measurements, 4-day-old Arabidopsis seedlings were transferred from MS medium to LK or MS medium and treated for 10 days. The root and shoot tissues were harvested separately and dried at 80°C for 48 h. The dry weight was measured as an indicator of biomass. Samples were powdered and digested with perchloric acid and nitric acid (1:4) solution. After complete digestion, the acid solution was adjusted to 10 mL with double-distilled water. K⁺ and Na⁺ concentrations of the samples were measured by atomic absorption spectrophotometry. Sixty plants of each line were used for each experiment. All experiments were replicated at least three times.

Results

Protein Structure of AtUNC-93

Arabidopsis gene At3g09470 encodes a protein containing a UNC-93 domain and was named AtUNC-93, based on orthology to UNC-93 in Caenorhabditis elegans (de la Cruz et al., 2003). No other homologs were found in Arabidopsis. AtUNC-93 appears to be an integral membrane protein possessing ten transmembrane-spanning domains of the deduced AtUNC-93 protein¹. A Protein BLAST search against the National Center for Biotechnology Information protein database revealed that AtUNC-93 shared high similarity with other UNC-93 orthologs from various species (Supplementary Figure S1). Phylogenetic analysis of the UNC-93 sequences of 18 species indicated that these UNC-93 orthologs were classified from plants and animals separately, and the plants were clustered into two clades, dicotyledons and monocotyledons (Supplementary Figure S2). The strict conservation of these UNC-93 orthologs indicates that they likely play evolutionary conserved roles and have extremely important physiological functions in the different species.

Expression Pattern and Subcellular Localization of AtUNC-93

Two-week-old seedlings of wild type Arabidopsis were treated with various abiotic stresses and ABA to investigate the expression of AtUNC-93. Real-time PCR analysis revealed that AtUNC-93 expression was significantly induced by heat stress and ABA treatment. By contrast, AtUNC-93 was only mildly responsive to high salinity and osmotic stress, increasing by ∼2-fold relative to unstressed plants, and was almost not affected by cold stress (Figure 1A). The up-regulation of AtUNC-93 expression by abiotic stresses prompted us to examine its promoter sequence (2,000 bp upstream from the transcription start site) by searching the promoter sequence against the new PLACE database (Higo et al., 1999). The results revealed that the promoter contains many putative stress response-related cis-elements (Figure 1B), which may be important reason of AtUNC-93 responding to abiotic stresses.

FIGURE 1

FIGURE 1. Expression pattern and subcellular localization of AtUNC-93. (A) Expression levels of AtUNC-93 under abiotic stress and ABA treatments. (B) Distribution of major stress-related cis-elements in the promoter region of AtUNC-93. (C) Expression levels of AtUNC-93 expression in different tissues as indicated. (D) Expression pattern of AtUNC-93 determined in ProAtUNC-93:GUS transgenic Arabidopsis plants. The GUS staining of primary root (i), primary root tip (ii), leaf (iii), hypocotyl (iv), stem (v), flower (vi), and silique (vii). (E) Subcellular localization analysis of AtUNC-93-GFP in onion epidermic cells. The expression of GFP alone was used as controls. Bars = 50 μm. Data in (A,C) represent the means ± standard error (SE) (n = 3), 3 independent experiments.

We also investigated AtUNC-93 spatial expression patterns in Arabidopsis by real-time PCR. The transcript of AtUNC-93 was widely detected in all organs tested. AtUNC-93 expression in the roots and seedlings was very high, but was extremely low in siliques (Figure 1C). To gain more insight into the expression patterns of AtUNC-93, transgenic Arabidopsis plants expressing β-glucuronidase gene (GUS) under control of AtUNC-93 promoter were generated. GUS activity was strongly detected in the roots, hypocotyls and leaf veins. However, almost no GUS signals were detected in siliques, petals and mesophyll cells (Figure 1D). In root tissues, strong GUS staining could be observed in mature root, while the expression was absent in the primary root tip. In shoot tissues, GUS activity was not obviously found in stem, but the expression level of AtUNC-93 in stem by real-time PCR testing is similar to that in leaf, probably because AtUNC-93 mainly expressed in vascular bundles but not in stem epidermal cells. The results demonstrate that AtUNC-93 is preferentially expressed in the vascular tissues of roots, stems and leaves.

The subcellular localization of AtUNC-93 was tested using an AtUNC-93-GFP fusion protein. Transient expression of this fusion protein was examined under confocal microscopy in onion (Allium cepa) epidermic cells. AtUNC-93–GFP fluorescence was observed only in the plasma membrane (PM), whereby GFP fluorescence was observed ubiquitously (Figure 1E). Thus, we concluded that AtUNC-93 localized to the PM.

AtUNC-93 Enhanced Abiotic Stress Tolerance

The AtUNC-93 T-DNA insertion mutants, atunc-93-1 and atunc-93-2, were used to reveal the function of AtUNC-93. The T-DNA insertion sites of atunc-93-1 and atunc-93-2 are located in the sixth intron and the eighth exon of AtUNC-93 gene, respectively (Figure 2A), which were confirmed by PCR analysis and sequencing the amplified fragments (Figure 2B). Reverse transcription (RT)-PCR analysis showed that AtUNC-93 expression was abolished in these two homozygous atunc-93 mutants (Figure 2C). We observed that the atunc-93-1 and atunc-93-2 plants grown under standard growth conditions showed retarded growth and no other obvious phenotypic difference compared with the wild type. But under salt stress conditions, the cotyledons of most atunc-93-1 and atunc-93-2 seedlings were bleached with 100 mM NaCl treatment, whereas only few wild type seedlings were impaired (Figures 2D,E). Even under the treatment of 150 mM NaCl, all atunc-93-1 and atunc-93-2 seedlings were completely dead, but about 30% of wild type seedlings still survived (Figures 2D,E). These results showed that disruption of AtUNC-93 resulted in decreased salt stress tolerance at seedling stage. To further reveal the role of AtUNC-93 in response to salt stress, AtUNC-93-overexpressing lines were generated, and the expression levels of AtUNC-93 in these lines were much higher than in the wild type (Figure 2F). After 125 mM NaCl treatment for 14 days, the survival rate of wild type plants fell to about 58%, whereas nearly 100% of AtUNC-93-overexpressing seedlings were alive (Figures 2G,H). These results suggested that overexpression of AtUNC-93 significantly enhanced salt tolerance of transgenic lines at seedling stage and three independent overexpression lines showed similar results. Data of the independent overexpression line OE1 and OE2 are shown in afterward analysis. To directly discern salt tolerance differences of atunc-93 mutants and overexpression lines, all materials were tested in the same plate. This finding was consistent with the fact that atunc-93 mutants were more susceptible to salt stress, whereas the overexpression lines improved salt tolerance (Supplementary Figures S3A,C). The complementation lines showed the wild type salt tolerance inclination (Supplementary Figures S4B,D), indicating that the hypersensitivity to salt stress of atunc-93 mutants is due to the loss of function of AtUNC-93.

FIGURE 2

FIGURE 2. Phenotype tests of wild type, atunc-93 and AtUNC-93-overexpressing seedlings under salt stress. (A) Schematic structure of AtUNC-93 and the positions of the T-DNA insertion of atunc-93-1 and atunc-93-2. The boxes indicate exons, and the lines represent introns and untranslated regions. (B) Genomic identification of atunc-93-1 and atunc-93-2. LP, left primer; RP, right primer; LB1 and LBb1.3, the T-DNA left border primer. WT is the wild type. (C) Reverse transcription (RT)-PCR verification of AtUNC-93 expression in atunc-93 mutants. (D,E) Phenotype (D) and the survival rates (E) of atunc-93 mutant seedlings and the wild type grown on 1/2 MS medium containing 100, 125, and 150 mM NaCl for 14 days, respectively. (F) Real-time PCR verification of AtUNC-93 in 35S:AtUNC-93 transgenic lines (OE1, OE2, and OE3). (G,H) Phenotype (G) and the survival rates (H) of AtUNC-93-overexpressing lines and the wild type grown on 1/2 MS medium containing 100 and 125 mM NaCl for 14 days, respectively. Data in (E,F,H) represent the means ± SE (n = 3). The student’s t-test (^∗∗P < 0.01) was used to analyze statistical significance compared with the wild type.

Salt-tolerant role of AtUNC-93 led us to check the tolerance to other abiotic stresses. For drought stress, two-week-old seedlings grown on soil pots were subjected to drought stress by stopping watering. Sixteen days later atunc-93-1 and atunc-93-2 plants showed severe wilting and chlorosis, and wild type plants showed weak chlorosis, whereas no obvious damage was observed in the AtUNC-93-overexpressing plants (Figure 3A). More severe wilting symptoms were observed in nearly all plants as the drought stress was prolonged for 3 days again (Figure 3A). After rewatering for 2 days, about 80% wild type plants were able to survive and continued to grow. By contrast, all of atunc-93-1 and atunc-93-2 plants did not recover from the stress and died. Almost all of the AtUNC-93-overexpressing plants were survived and showed more vigorous growth than the wild type (Figures 3A,B). Moreover, the water loss from detached leaves was increased in the atunc-93 mutant plants compared with the wild type, while the AtUNC-93-overexpressing plants reduced water loss (Figure 3C). These results indicated that AtUNC-93 may function as a positive regulator in response to drought stress. Osmotic stress treatments were also performed at seedling stage. The atunc-93 mutant plants became chlorotic and died under the treatment with mannitol (Supplementary Figures S3B,D). In contrast, the wild type and AtUNC-93-overexpressing plants still remained more green leaves and higher survival rates, and AtUNC-93-overexpressing plants grew better than wild type plants after mannitol treatment (Supplementary Figures S3B,D). The complementation lines of atunc-93-1 and atunc-93-2 mutants rescued sensitive phenotype of these mutant seedlings to osmotic stress (Supplementary Figures S4C,E).

FIGURE 3

FIGURE 3. Wild type, atunc-93 and AtUNC-93-overexpressing seedlings under drought stress and ABA treatment. (A) Phenotype comparison of wild type, atunc-93 and AtUNC-93-overexpressing seedlings under drought stress. Two-week-old seedlings were grown for 16 or 19 days without irrigation, and then were rewatered for 2 days. Irrigated seedlings were used as controls. The experiments were repeated three times, with similar results. (B) The survival rates of various plant materials were determined as the number of visible green plants after rehydration. (C) Quantitative determination of water loss of detached leaves. (D) Seedlings grown in medium lacking or supplemented with ABA for 7 days. (E) Relative root length of seedlings based on panel (D). Forty plants of each line were used for each experiment. Data in (B,C,E) are shown as means ± SE (n = 3), 3 independent experiments. Student’s t-test (^∗P < 0.05 and ^∗∗P < 0.01) was used to analyze statistical significance compared with the wild type.

Thermotolerance of atunc-93 mutants and AtUNC-93-overexpressing plants was further investigated. First, we tested them for basal thermotolerance at 45°C. The atunc-93 mutant plants showed more severe inhibition in shoot growth when directly exposed to 45°C for 2 h (Supplementary Figure S5A). Next, we measured the acquired thermotolerance using two strategies. One was that seedlings were acclimated for 2 h at 38°C and immediately subjected to 45°C. After 3 h treatment at 45°C, atunc-93-1 and atunc-93-2 plants were severely injured, but wild type plants showed no observable symptoms. When plants were continuously subjected to 45°C for 4 h, atunc-93-1 and atunc-93-2 plants nearly completely died, but half of wild type plants survived (Supplementary Figure S5A). The other strategy was that seedlings were recovered for 2 h at the normal temperature (22°C) between acclimation (38°C) and lethal treatment (45°C). When lethal heat treatment was imposed for 4 h in this strategy, atunc-93-1 and atunc-93-2 plants suffered severe damage, but wild type plants survived, which is similar to the result after 3 h of lethal heat treatment without recovery period (Supplementary Figure S5A). The two strategies in heat treatment were manifested that recovery period between acclimation and lethal treatment can retard heat-damage. In all thermotolerance assays, atunc-93 mutants decreased the basal and acquired thermotolerance, but no differences were observed between AtUNC-93-overexpressing plants and the wile type. The atunc-93 mutants, AtUNC-93-overexpressing lines and the wild type were also tested for chilling-tolerance at seedling stage, but no significant difference was observed (Supplementary Figure S5B).

The atunc-93 Mutants Are Hypersensitive to ABA

Abscisic acid is an important hormone for abiotic stress in plants (Finkelstein et al., 2002). Most experimental evidences were provided for the involvement of bZIP transcription factors and ion channels in regulation of abiotic stress tolerance by ABA signaling (Diaz et al., 2016; Zong et al., 2016). In this experiment, atunc-93-1 and atunc-93-2 plants showed ABA hypersensitive phenotypes in ABA-induced post-germination growth inhibition. The root growth of atunc-93-1 and atunc-93-2 was more severely inhibited as the ABA concentration increased. The relative root length (the root length in the ABA treatment to that in the ABA-free medium) of atunc-93-1 and atunc-93-2 was significantly decreased to 32 and 24% under the treatment with 10 μM ABA, respectively (Figures 3D,E). The AtUNC-93-overexpressing plants exhibited high relative root length (89 and 85%) compared with the wild type (69%) after treatment with 10 μM ABA (Figures 3D,E). These results suggested that disruption of AtUNC-93 in plants generated hypersensitivity to ABA, while overexpression of AtUNC-93 in plants resulted in decreased sensitivity to ABA.

The Expression of Stress-Related and ABA-Responsive Genes Is Affected by the Transcript Level of AtUNC-93

Many studies have reports that plant tolerance to abiotic stress is involved in the transcription regulation of a number of stress-related genes (Yamaguchi-Shinozaki and Shinozaki, 2006; Shi et al., 2017). Then we analyzed expression levels of some stress-related genes, such as RD29A, RD22, DREB2A, COR15A, and COR47, under stress conditions. All these genes were induced by various abiotic stresses in wild type plants (Figure 4). Moreover, the expression levels of these genes were significantly lower in atunc-93 mutants and higher in AtUNC-93-overexpressing plants than in the wild type under stress conditions (Figure 4). These results suggested that expression level changes of the stress-related genes in atunc-93 mutants and AtUNC-93-overexpressing plants under stress conditions may contribute to the significant difference of stress tolerance.

FIGURE 4

FIGURE 4. Expression of the stress-related genes in atunc-93 mutants and AtUNC-93-overexpressing lines under stress conditions. The expression levels of RD29A, RD22, DREB2A, COR15A, and COR47 were determined by using real-time PCR under NaCl, drought and mannitol treatments. Seedlings before stress treatments were used as controls. Each data bar represents the mean ± SE (n = 3).

Next, the ABA hypersensitivity of atunc-93 mutants prompted us to check the expression of ABA-responsive genes in atunc-93 mutants and AtUNC-93-overexpressing plants. Under normal growth conditions, the expression levels of the core component genes of ABA signaling pathway, including PYR1, ABI1, ABI2, SnRK2.3, and ABF4, were apparently down-regulated in the atunc-93 mutants compared with the wild type (Figure 5). However, the negative regulator genes, ABI1 and ABI2, were significantly up-regulated by exogenous ABA application in the atunc-93 mutants compared with the wild type (Figure 5). Meanwhile, the expressions of positive regulators (SnRK2.3, SnRK2.6, and ABF4) were also up-regulated by exogenous ABA, but the up-regulation level was strongly suppressed in the atunc-93 mutants (Figure 5). This result demonstrated that the expressions of ABI1, ABI2, SnRK2.3, SnRK2.6, and ABF4 are modulated by AtUNC-93. It is noteworthy that, the expression of PYR1 was not changed by ABA in the atunc-93 mutants, but was significantly down-regulated in the wild type and decreased to the transcript level in the atunc-93 mutants after ABA treatment (Figure 5), suggesting that the transcript of PYR1 is also regulated by AtUNC-93. The expression of these genes was also tested in the AtUNC-93-overexpressing lines, but no significant difference was observed between the AtUNC-93-overexpressing lines and the wild type under the treatment with or without ABA (Figure 5). In addition, the expression levels of DREB1A and DREB2A were significantly lower in the atunc-93 mutants and higher in the AtUNC-93-overexpressing lines than those in the wild type with ABA treatment (Supplementary Figure S6). MYB2 expression was markedly repressed in the atunc-93 mutants without ABA treatment (Supplementary Figure S6). However, the expression levels of other ABA-responsive genes in this study were not changed much in the atunc-93 mutants and the AtUNC-93-overexpressing lines compared with the wild type, though some differences were still detected.

FIGURE 5

FIGURE 5. Expression of the core component genes in ABA signaling pathway in atunc-93 mutants and AtUNC-93-overexpressing lines. Relative expression of PYR1, ABI1, ABI2, SnRK2.3, SnRK2.6, and ABF4 was analyzed by using real-time PCR under the treatments with or without ABA. Data represent the means ± SE (n = 3).

AtUNC-93 Positively Controlled Plant Growth

When grown in soil, atunc-93-1 and atunc-93-2 plants showed dwarf phenotypes compared with wild type plants, especially for atunc-93-2, while AtUNC-93-overexpressing plants exhibited larger bodies than wild type plants (Figures 6A,C). Along with plants growth and development, the difference significance of growth phenotypes increased gradually. The differences of leaves size (Figure 6B) and plants height (Figure 6D) among all lines were in accord with phenotypes. Previous studies have shown that cell expansion plays an essential role in plant growth (Zonia and Munnik, 2007; Osakabe et al., 2013). Then we observed that the stem cells from 6-week-old plants were smaller in atunc-93-1 and atunc-93-2, larger in AtUNC-93-overexpressing plants, than in the wild type (Figures 6E,F). These observations implied that the phenotype differences of atunc-93 mutants and the AtUNC-93-overexpressing plants were resulted from alterations of cell expansion.

FIGURE 6

FIGURE 6. Plant growth phenotypes of the wild type, atunc-93 mutants and AtUNC-93-overexpressing plants. (A) 14-day-old seedlings grown in soil pots. Bars = 5 mm. (B) Rosette leaves of 21-day-old seedlings. Bars = 10 mm. (C,D) Phenotype (C) and plant height (D) of 6-week-old plants. Bars = 30 mm. (E,F) Stem cells comparison (E) and cell areas (F) of 6-week-old plants. Bars = 100 μm. Relative cell areas were calculated from the microscope image data using ImageJ. (G) RT-PCR verification of AtUNC-93 expression levels in the wild type, atunc-93-2 and complementation lines (COM1 and COM2). (H,I) Phenotype comparison (H) and rosette leaves (I) of the wild type, atunc-93-2 and complementation plants grown in soil pots for 6 weeks. Data in (D,F) are shown as means ± SD (n = 30), thirty plants or cells were tested. Student’s t-test (^∗P < 0.05 and ^∗∗P < 0.01) was used to analyze statistical significance compared with the wild type.

We also observed that the length of roots and hypocotyls of atunc-93-1 and atunc-93-2 was significantly shorter than that of the wild type (Supplementary Figures S7A–C). Interestingly, atunc-93-1 had longer hypocotyls but shorter roots than those of atunc-93-2. Meanwhile AtUNC-93-overexpressing lines showed a little longer hypocotyls and roots compared with the wild type (Supplementary Figures S7A–C). Especially AtUNC-93-overexpressing plants showed more root biomass than that in wild type plants when grown for 2 weeks (Supplementary Figure S7E), which suggested that AtUNC-93-overexpressing plants exhibited rapid growth phenotype due to its extensive root system.

To further confirm the role of AtUNC-93 involved in plant growth, we observed the growth phenotype and leaf size in the complementation lines of atunc-93-2. It had been shown that the complementation lines rescued the inhibited growth phenotype of atunc-93-2 (Figures 6H,I). Thus, atunc-93 mutants showed dwarf phenotypes were caused by disruption of the AtUNC-93 gene.

AtUNC-93 Regulates K⁺ Accumulation in Arabidopsis Shoots

UNC-93 was defined as a regulatory protein of the SUP-9 two-pore K⁺ channel in Caenorhabditis elegans and conserved among Caenorhabditis elegans, humans and Arabidopsis thaliana (Levin and Horvitz, 1992; de la Cruz et al., 2003), suggesting that UNC-93-like regulatory proteins represent a conserved mechanism for the regulation of K⁺ transport. This finding led us to hypothesize that AtUNC-93 may also regulate K⁺ uptake and/or translocation in Arabidopsis. To verify this hypothesis, phenotype observation and K⁺ content measurements of atunc-93 mutants, AtUNC-93-overexpressing lines and the wild type under normal (MS medium, 20 mM K⁺) and low-K⁺ (LK medium, 100 μM K⁺) growth conditions were performed. The leaves of atunc-93-1 and atunc-93-2 became chlorotic, and their growth was suppressed significantly under low-K⁺ conditions (Figure 7A). The phenotypes of leaf chlorosis and inhibition of growth are taken as typical symptoms under K⁺-deficient conditions (Xu et al., 2006). The low-K⁺ sensitive phenotypes of atunc-93 mutants were also found below 500 μM external K⁺ concentrations. But along with the external K⁺ concentrations rising, the sensitive phenotypes of atunc-93 mutants disappeared gradually (Supplementary Figure S8A). In addition, we also tested the seed germination under low-K⁺ conditions. Because the presence of millimolar NH₄⁺ is necessary for low-K⁺ sensitive phenotype of plants at germination stage (Hirsch et al., 1998; Spalding et al., 1999), we planted the seeds directly in medium supplemented with various concentrations of K⁺ and NH₄⁺. After incubated for 4 days, the atunc-93 mutants exhibited no significant difference from the wild type under low-K⁺ (100 μM K⁺, 30 mM NH₄⁺) conditions (Figure 7B). Under low-K⁺ and low-NH₄⁺ (100 μM K⁺, 1.25 mM NH₄⁺) conditions, atunc-93-1 and atunc-93-2 showed brown cotyledons, inhibited primary root growth and stimulated root hair elongation, which were typical K⁺-deficient symptoms (Jung et al., 2009; Tsay et al., 2011). But these were not detected in AtUNC-93-overexpressing lines and wild type plants. These results indicated that atunc-93 mutants displayed hypersensitivity to low-K⁺ stress in both seed germination and post-germination growth.

FIGURE 7

FIGURE 7. Phenotype tests and K⁺ content measurements of the wild type, atunc-93 mutants and AtUNC-93-overexpressing lines under low-K⁺ conditions. (A) Phenotype of various materials after being transferred to MS or LK medium for 10 days. MS indicates Murashige and Skoog medium (20 mM K⁺, 20 mM NH₄⁺). LK indicates modified MS medium containing low-K⁺ concentration (100 μM K⁺, 30 mM NH₄⁺). (B) Phenotype comparison of various materials after the seeds germinated directly on MS, LK or LK/LNH medium for 4 days. MS and LK indicate as shown in (A). LK/LNH indicates modified MS medium containing low-K⁺ and low-NH₄⁺ concentration (100 μM K⁺, 1.25 mM NH₄⁺). (C,D) Dry weight (C) and K⁺ content (D) of various plant materials as indicated under MS and LK conditions. Data are shown as means ± SE (n = 3). Student’s t-test (^∗P < 0.05) was used to analyze statistical significance compared with the wild type.

To quantify K⁺-dependent plant growth, the biomass measurements were determined. The atunc-93-1 and atunc-93-2 seedlings showed less dry weight of roots and shoots under low-K⁺ conditions than those under normal growth conditions, which were in agreement with their grow phenotype (Figure 7C). In addition, the dry weight of roots of AtUNC-93-overexpressing lines was remarkably higher than that of wild type plants under normal growth conditions, but was not significantly different from that of wild type plants under low-K⁺ conditions (Figure 7C), which further demonstrated that overexpression of AtUNC-93 gene may promote root growth in Arabidopsis under normal growth conditions.

The shoot K⁺ content of atunc-93-1 and atunc-93-2 was much lower than that of the AtUNC-93-overexpressing lines and wild type plants after cultured on both MS and LK medium (Figure 7D). The AtUNC-93-overexpressing lines showed significantly higher K⁺ content in shoots compared with the wild type under low-K⁺ conditions, but no significant difference was observed under the normal growth conditions (Figure 7D). Additionally, there was no significant difference in root K⁺ content among the all tested materials under either normal or low-K⁺ conditions (Figure 7D). In the meantime, we also detected Na⁺ contents. The results of Na⁺ content measurement indicated that all tested materials had similar Na⁺ contents (Supplementary Figure S9A). The K⁺/Na⁺ ratios were significantly lower for the shoots of atunc-93 mutants compared with the AtUNC-93-overexpressing lines and wild type plants under both normal and low-K⁺ conditions. The AtUNC-93-overexpressing lines exhibited higher K⁺/Na⁺ ratios for the shoots compared with the wild type under low-K⁺ conditions (Supplementary Figure S9B). All of these results suggested that AtUNC-93 gene in Arabidopsis may play a crucial role in translocating K⁺ from roots to shoots. This may explain the K⁺-deficient symptoms of atunc-93 mutants under low-K⁺ stress. To investigate whether AtUNC-93 participates in the regulation of K⁺ transport in Arabidopsis by changing the transcript levels of K⁺ channels, the expression of 15 K⁺ channel genes were detected. Whereas no significant difference was tested among all the materials (Supplementary Figure S8B), indicating that the regulation of K⁺ transport by AtUNC-93 may not occur at the transcriptional alteration of K⁺ channels. AtUNC-93 plays an important role in the regulation of K⁺ transport in Arabidopsis. K⁺ homeostasis is a key factor for plant in response to abiotic stresses and growth. Then, these results together suggest that AtUNC-93 regulates abiotic stress tolerance and growth by maintaining K⁺ homeostasis in Arabidopsis.

Discussion

K⁺ is one of the principal nutrient elements for plant growth and development. Many reports have shown that the mutants of K⁺ channels or regulators exhibit leaf chlorosis, inhibition of growth and lower K⁺ contents under low-K⁺ conditions, which are K⁺-deficient symptoms (Xu et al., 2006; Li et al., 2017; Wang and Wu, 2017). In this study, the atunc-93 mutants showed significant LK-sensitive phenotype at both germination and post-germination stages and lower K⁺ contents in shoots compared with the wild type, while no obvious difference of the root K⁺ content was observed (Figure 7). It is suggested that AtUNC-93 participates in the response to K⁺ deficiency and is involved in the root-to-shoot K⁺ translocation. The outward-rectifying K⁺ channel SKOR is localized in root stelar tissues and contributes to K⁺ translocation from roots to shoots (Gaymard et al., 1998). The expression of AtUNC-93 was detected mainly in the vascular tissues (Figure 1D), suggesting that AtUNC-93 may have the similar role as SKOR in K⁺ translocation toward the shoots. This regulation of K⁺ translocation from roots to shoots was recently reported in Arabidopsis by transporter NRT1.5 and in rice by outward Shaker K⁺ channel OsK5.2 (Li et al., 2017; Nguyen et al., 2017). However, the AtUNC-93-overexpressing plants did not show significant phenotype differences compared with wild type plants (Figures 7A,B). Only the shoot K⁺ contents of the AtUNC-93-overexpressing plants were much higher than those of wild type plants under low-K⁺ conditions (Figure 7D). The possible reason is that the expression levels of AtUNC-93 in the wild type are sufficient to maintain K⁺ homeostasis in plant cells under normal growth conditions so that no significant difference of the shoot K⁺ contents was detected between the AtUNC-93-overexpressing plants and the wild type. But under low-K⁺ conditions, more amounts of AtUNC-93 are needed to promote the K⁺ translocation from roots to shoots. The similar result has also been reported for CBL10, which is involved in K⁺ homeostasis by negatively regulating AKT1 activity in Arabidopsis. The CBL10-overexpressing lines showed a phenotype as sensitive as that of the akt1 mutant under low-K⁺ conditions, while the cbl10 mutant did not show significant phenotype differences compared with wild type plants (Ren et al., 2013). AtUNC-93 is identified to be a member of major facilitator superfamily (MFS), which is a large and diverse group of secondary transporters. The main function of MFS proteins is to facilitate the transport across cytoplasmic or internal membranes of a variety of substrates including ions, nucleosides, amino acids, and so on (Marchler-Bauer, 2015). The MFS transporter ZIFL2 promotes cellular K⁺ efflux in the root and regulates K⁺ translocation from roots to shoots in Arabidopsis under conditions of high K⁺ external supply (Remy et al., 2015).

The maintenance of cellular K⁺ homeostasis will contribute to improving plant tolerance to abiotic stresses. Recent studies reported that two K⁺ channels OsAKT1 and OsTPKb play pivotal roles in osmotic and drought stress tolerance by maintaining cellular K⁺ homeostasis (Ahmad et al., 2016a,b). In this study, AtUNC-93 was induced by salt, osmotic and heat stress (Figure 1A). Overexpression of AtUNC-93 in Arabidopsis significantly enhanced salt, drought and heat tolerance during seedling development, while disruption of AtUNC-93 resulted in lower stress tolerance (Figures 2, 3 and Supplementary Figures S3–5). This finding suggests that AtUNC-93 may play a critical role in stress tolerance by maintaining K⁺ homeostasis in plants. K⁺, as osmotically active substance, can regulate cell turgor pressure, which facilitates cell expansion and leads to plant growth (Wang and Wu, 2013). KUP6 acts as a key factor in K⁺ homeostasis and negatively regulates turgor-dependent growth (Osakabe et al., 2013). Our study reveals that the atunc-93 mutant plants exhibited dwarf phenotypes, while AtUNC-93-overexpressing transgenic plants had large plant bodies (Figure 6 and Supplementary Figure S7). The changes of vegetative growth resulted from the alteration of cell expansion, suggesting that AtUNC-93 positively modulate turgor-dependent growth through cellular K⁺ homeostasis.

Abscisic acid is produced rapidly in response to abiotic stress and plays a crucial role in the modulation of stress responses. AtHSPR, a heat shock protein-related, is involved in salt and drought stress tolerance in Arabidopsis by maintaining K⁺ /Na⁺ homeostasis in ABA-dependent pathways (Yang et al., 2015). In this study, the expression of AtUNC-93 was up-regulated by ABA treatment (Figure 1A). On the other hand, AtUNC-93 also regulated the expression of a set of ABA-responsive genes (Figure 5 and Supplementary Figure S6). Under no exogenous ABA conditions, the expression levels of PYR1, ABI1, ABI2, SnRK2.3, and ABF4 were apparently down-regulated in the atunc-93 mutants compared with the wild type. The transcript abundance of ABA receptor gene PYR1 in the atunc-93 mutants under no exogenous ABA conditions was similar to that in the wild type under ABA treatment (Figure 5), suggesting that atunc-93 mutants under normal conditions has same physiological responses of the wild type under ABA treatment. But with the exogenous ABA treatment, the ABA signaling negative regulator-encoding genes, ABI1 and ABI2, were strongly induced, and positive regulator-encoding genes, SnRK2.3, SnRK2.6, and ABF4, were obviously repressed in the atunc-93 mutants compared with the wild type (Figure 5). These results demonstrate that AtUNC-93 functions as a negative regulator in the ABA signaling pathway of the PYR/PYL/RCARs-PP2Cs-SnRK2s regulatory module (Fujii et al., 2009), and regulates PYR1, ABI1, ABI2, SnRK2.3, SnRK2.6, and ABF4 expression. In the phenotype tests, atunc-93 mutants showed the strongest ABA hypersensitive phenotypes in post-germination growth, while the AtUNC-93-overexpressing plants were ABA-insensitive in terms of root growth (Figure 3D). It is also indicated that AtUNC-93 is a negative regulator in ABA signaling. The atunc-93 mutants both increased the sensitivity to ABA and decreased salt, drought, and heat stress tolerance during seedling development. Meanwhile, the AtUNC-93-overexpressing plants displayed ABA-insensitive phenotypes as well as enhanced tolerance to salt, drought, and heat stress. Considering ABA can mediate diverse aspects of physiological responses to environmental stresses such as salt, drought, heat, and cold stress (Finkelstein et al., 2002), AtUNC-93 may be a major player in mediating ABA-dependent pathways for conferring stress tolerance.

Conclusion

In conclusion, AtUNC-93 promotes K⁺ translocation from roots to shoots in Arabidopsis and positively regulates salt, drought and heat stress tolerance and turgor-dependent growth. These stresses tolerance and plant growth are involved in maintaining K⁺ homeostasis through ABA-dependent signal transduction pathways. AtUNC-93 provides a novel important component to examine the ABA-dependent regulatory networks in stress responses and plant growth.

Author Contributions

XC conceived the study. JX performed all the experiments, analyzed the data and wrote the manuscript. XyZ, XwZ, AL, and YP participated in the experiment. XC, YX, and MY reviewed and edited the manuscript. All authors read and approved the manuscript for final submission.

Funding

This work was supported by the National Natural Science Foundation of China (No. 30870206), the Research Foundation of Education Bureau of Hunan Province, China (No. 14C0453), Southern Regional Collaborative Innovation Center for Grain and Oil Crops in China, Hunan Agricultural University and Program for Innovative Research Team in University (IRT1239).

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2018.00718/full#supplementary-material

Footnotes

1. ^ http://www.cbs.dtu.dk/services/TMHMM-2.0/

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