Functional Analysis of Pepper F-box Protein CaDIF1 and Its Interacting Partner CaDIS1: Modulation of ABA Signaling and Drought Stress Response.

Plant adaptive responses to environmental stress are coordinated by inhibition of plant growth and development. Abscisic acid (ABA) is a major phytohormone that regulates the stress response, and its sensitivity determines stress tolerance levels. In this study, we report the identification and functional role of a novel F-box protein, CaDIF1 (Capsicum annuum Drought-Induced F-box Protein 1). The expression of CaDIF1 in pepper leaves was induced by ABA, drought, H2O2, and NaCl treatments. In comparison with wild-type pepper plants, CaDIF1-silenced pepper plants exhibited a drought-sensitive phenotype, whereas CaDIF1-overexpressing (OX) plants exhibited ABA-sensitive and drought-tolerant phenotypes. Using a yeast two-hybrid assay, we identified CaDIS1 (C. annuum DIF1-Interacting SKP 1), which interacts with CaDIF1 in the cytoplasm and nucleus. Consistent with CaDIF1-silenced pepper plants, CaDIS1-silenced pepper plants displayed ABA insensitivity and reduced drought tolerance, and these were characterized by larger stomatal apertures and greater transpirational water loss. Taken together, our results indicate that CaDIF1 and its interacting partner CaDIS1 synergistically regulate the ABA-dependent defence signaling response to drought stress.

Introduction

Plants are sessile organisms; hence, they have evolved defence mechanisms to adapt to abiotic stresses, such as drought, high salinity, and extreme temperatures. When plants encounter drought stress, they modify their cellular processes to trigger the defence response, including abscisic acid (ABA) biosynthesis and reprogramming of gene expression (Lee and Luan, 2012; Lim et al., 2015a). The plant hormone ABA plays a critical role in numerous aspects of cellular processes, including plant growth, development, and adaptation to abiotic stress (Cutler et al., 2010; Lim et al., 2015a). ABA modulates defence responses to drought stress through stress-responsive gene expression, regulations of stomatal opening/closing, and root hydraulic conductivity (Sirichandra et al., 2009; Lim et al., 2015b). Under stress conditions, a large number of genes are upregulated in vegetative tissues and several plant hormones are associated with modulation of stress-related gene expression. ABA also modulates numerous genes compared with other major plant hormones (Goda et al., 2008; Mizuno and Yamashino, 2008). The induction of ABA-regulated genes, including transcription factors and E3 ligases, plays a key role in conferring enhanced stress tolerance and protecting plants from drought stress.

Protein degradation process through the ubiquitin/26S proteasome (UPS) pathway is an important mechanism involved in regulating defence responses to biotic and abiotic stresses because of its ability to rapidly remove unnecessary intracellular proteins (Lim et al., 2017). Ubiquitination is a type of post-translational modification found in eukaryotic cells, and it involves the sequential action of three key enzymes—ubiquitin-activating enzyme (E1), ubiquitin-conjugating enzyme (E2), and ubiquitin ligase (E3) (Ciechanover and Schwartz, 1998). Initially, E1 activates ubiquitin in an ATP-dependent manner and transfers activated ubiquitin to E2. Finally, ubiquitin is attached to the target protein—this process is facilitated by E3 ligase. Polyubiquitinated target proteins are degraded by the 26S proteasome system. In this process, E3 ligase defines substrate specificity and recruits target proteins. More than 1400 E3 ligases have been identified in the Arabidopsis genome (Vierstra, 2009; Sadanandom et al., 2012). E3 ligases are classified into two types based on their subunit compositions and are subsequently divided according to distinct functional motifs. The RING (really interesting new gene), PUB (plant U-box), and HECT (homology to E6-AP C-terminus) E3 ligases consist of a single subunit, whereas the SCF [Skp (S-phase kinase-associated protein)/cullin/F-box] and CUL4-DDB1 (CULLIN4-damaged-specific DNA binding protein1) ligases consist of a multi-subunit (Stone et al., 2005; Pazhouhandeh et al., 2011; Irigoyen et al., 2014; Seo et al., 2014).

The SCF complex is composed of Skp1, CULLIN1, a RING finger protein Rbx1/Hrt/Roc1, and F-box protein (Deshaies, 1999; Kipreos and Pagano, 2000). Among these, the F-box protein determines and delivers target protein to the complex, because F-box is associated with protein–protein interaction (Kipreos and Pagano, 2000; Koops et al., 2011). The Arabidopsis genome encodes 694 F-box proteins that are components of the SCF complex (Gagne et al., 2002). The SCF complex comprises the largest family of E3 ubiquitin ligases, and these ligases are associated with many processes involving signal transductions, including biotic and abiotic stress responses. Recently, overexpression of GmSK1 conferred enhanced tolerance to high salinity and drought stress (Chen et al., 2018). SCF type E3 ligase RIFP1 negatively regulates ABA signaling and drought stress response by involvement of ubiquitination and degradation of RCAR3 ABA receptor at the nucleus (Li et al., 2016). Moreover, CRL4 type E3 ligase complex was found to degrade nuclear ABA receptor PYL8 (Irigoyen et al., 2014). The biological role of SCF type E3 ligases in defence response to drought stress through the ABA-signaling pathway has been largely investigated in several monocot and dicot plants; however, their exact role remains unclear.

To gain further insight into the molecular process of drought stress response, we isolated the F-box protein CaDIF1 gene and the expression level of CaDIF1 was induced in response to abiotic stress applications. Based on these expression levels of CaDIF1 gene, we examined the biological roles in responses to ABA and drought stress treatments by using virus-induced gene-silenced pepper and overexpressed (OX) Arabidopsis thaliana plants. To better investigate the further biological role of CaDIF1, we performed a yeast two-hybrid analysis to identify CaDIS1, which form a complex with CaDIF1. Consistent with CaDIF1-silenced pepper plants, CaDIS1-silenced pepper plants showed ABA signaling-mediated drought-sensitive phenotype. This study suggests that CaDIF1 and CaDIS1 function together as positive modulators of ABA signaling and the drought stress response.

Results

Identification of the CaDIF1 Gene and Amino Acid Sequence Analysis of the CaDIF1 Protein

To isolate a drought stress inducible gene, we performed RNA-seq assay and identified the pepper CaDIF1 gene from drought stress applied pepper leaves (Lim and Lee, 2016). The CaDIF1 consists of 282 amino acid, which are encoded by an 849 bp coding region ( ). The isoelectric point and molecular mass of CaDIF1 protein was 8.03 and 31,548 Da, respectively. The putative CaDIF1 protein contains highly conserved F-box and EID1-Like Protein (ELP) domains, including amino acid residues 30–86 and 125-252, respectively ( ). The amino acid sequence analysis of CaDIF1 by multiple alignment ( ) and phylogenetic tree analysis ( ) revealed that this protein has high homology with F-box proteins from other plant species ( ). In particular, CaDIF1 shares 50.3–77.0% identities and 67.1–85.1% similarities with other F-box proteins.

Figure 1

Homology of the pepper CaDIF1 (Capsicum annuum Drought-Induced F-box protein 1) protein. (A) Alignment of the deduced amino acid sequences of CaDIF1 with its homologous proteins was performed using ClustalW2. Identical and similar amino acid residues are shaded according to the percentage identity in ClustalW2. Sequences include CaDIF1 (accession no. XP_016553423.1), Solanum lycopersicum (accession no. XP_004247146.1), Nicotiana tomentosiformis (accession no. XP_009606180.1), Gossypium arboretum (accession no. XP_017614523.1), and Arabidopsis thaliana (accession no. NP_567137.1). The red box indicates the F-box like protein domain; the blue box indicates the ELP (EID1-Like Protein) domain. (B) Phylogenetic tree analysis of the CaDIF1 protein. BLAST search was performed using deduced amino acid sequences of CaDIF1, and sequences with the highest similarity were gathered from each plant species. Multiple sequence alignment was performed using Clustal Omega (http://www.ebi.ac.uk/Tools/msa/clustalo/) with default settings. The phylogenetic tree was drawn using the neighbour-joining method with MEGA software (version 7.0) (Kumar et al., 2016). Bootstrap values were calculated from 1000 bootstrap replications and were indicated at each branch point. Scale bar indicates genetic distance.

Induction of the CaDIF1 Gene and Subcellular Localization of the CaDIF1 Protein

The CaDIF1 gene was identified in drought stress-treated pepper plants; therefore, we investigated whether the expression level of CaDIF1 was increased by drought, ABA, H2O2, and NaCl treatments ( ). First, we investigated the expression level of CaDIF1 transcripts in pepper leaves at different time points after drought stress treatment. The CaDIF1 transcripts dramatically induced at all times measured. ABA is known to function as a key modulator in the defence response to water deficit condition (Jakab et al., 2005). To examine whether ABA is also associated with CaDIF1 expression, we treated pepper plants with ABA and monitored accumulation of CaDIF1 transcripts. The CaDIF1 transcripts were strongly accumulated after ABA treatment. H2O2 functions as a signal component in ABA-mediated stomatal closure (Zhang et al., 2001); hence, we determined the expression level of CaDIF1 after H2O2 treatment. The induction of CaDIF1 transcripts were detected at 2 h after treatment and gradually increased until 24 h. High salinity treatment induced weak accumulation of CaDIF1 transcripts.

Figure 2

Expression of the CaDIF1 gene and localization of the CaDIF1 protein. (A) Induction of CaDIF1 in pepper leaves at various time points after treatment with drought, 100 μM abscisic acid (ABA), H2O2 (100 μM), and NaCl (200 mM). The pepper Actin1 gene was used as an internal control. Data represent the mean ± standard error of five independent biological replicates. Asterisks indicate significant differences between 0 h and other times (Student’s t-test; P 0.05). (B) Subcellular localization of the CaDIF1 protein using transient expression of the green fluorescent protein (GFP) fusion protein in Nicotiana benthamiana cells. The 35S:CaDIF1-GFP construct was expressed using agroinfiltration of N. benthamiana leaves and observed under a confocal laser-scanning microscope. 4′,6-Diamidino-2-phenylindole (DAPI) staining was used as a marker for the nucleus. White bar = 10 μm.

To determine the subcellular localization of CaDIF1 protein in the plant cell, GFP-tagged CaDIF1 fusion protein was transiently expressed in the epidermal cells of Nicotiana benthamiana. GFP signals were generated in the nucleus ( ). We also detected that the blue signals localized to the nucleus overlapped with the GFP signals by using diamidino-2-phenylindole (DAPI) staining. These results suggest that the CaDIF1 has a functional role in the nucleus.

ABA Hyposensitivity and Enhanced Drought Sensitivity of CaDIF1-Silenced Pepper Plants

CaDIF1 was induced by drought and ABA treatment; therefore, we postulated that this gene is involved in drought response and ABA signaling. To confirm this prediction, we conducted phenotypic analysis using loss-of function and gain-of function mutants by virus-induced gene silencing (VIGS) in pepper and generating transgenic Arabidopsis plants, respectively. We monitored CaDIF1 silencing by measurement of CaDIF1 transcripts in control (TRV2:00) and CaDIF1-knock down pepper (TRV2:CaDIF1) plants. The accumulation of CaDIF1 transcripts was low in the CaDIF1-knock down pepper leaves compared with control leaves ( ). We subjected control and CaDIF1-knock down pepper plants to drought stress and compared their phenotypes ( ). We withheld water (11 days; middle panel) and resupply water (2 days; right panel) and assessed growth status in both plants. After treatment of drought stress and re-watering, leaf wilting phenotypes were more appeared in CaDIF1-knock down pepper plants than in control plants. The survival ratios of CaDIF1-knock down pepper plants (19.3%) were much lower than control pepper plants (71.8%) ( ). Previous studies suggested that water retention capacity is associated with drought tolerance; hence, the drought-sensitive phenotype of CaDIF1-knock down pepper plants is probably caused by altered water retention capacity. To asses this prediction, we monitored the fresh weight of leaves detached from control and CaDIF1-knock down pepper plants ( ). The leaf fresh weight of CaDIF1-knock down pepper plants was low compared with that of control plants. To examine whether the difference in water retention capacity was derived from a variation of ABA sensitivity, we measured leaf temperatures ( ). Leaf temperature shows the strength of water evaporation by transpiration, with a low left temperature reflecting high level of transpiration (Park et al., 2015). In the ABA untreated condition, leaf temperatures were not significantly different between control pepper and CaDIF1-knock down pepper plants ( ). However, after ABA treatment, the leaf temperatures of CaDIF1-knock down pepper plants were significantly low compared with control pepper plants. Consistent with leaf temperatures, the stomatal apertures were significantly larger in CaDIF1-silenced pepper plants than in control plants ( ). These results indicate that the increased transpirational water loss in CaDIF1-knock down pepper plants, which leads to reduced drought tolerance, is derived from ABA hyposensitivity.

Figure 3

Reduced tolerance of CaDIF1-silenced pepper plants to drought stress. (A) Drought susceptibility of CaDIF1-silenced pepper plants. Four-week-old TRV2:CaDIF1 and TRV2:00 pepper plants were subjected to drought stress by withholding watering for 11 days. Representative images were taken before (left) and after (middle) drought stress and 2 days after re-watering (right). (B) The survival rate was measured by counting the number of plants with green and rehydrated leaves 2 days after re-watering. Data represent the mean ± standard error of three independent biological replicates, each evaluating 30 plants. (C) Transpirational water loss from the leaves of empty vector control and CaDIF1-silenced pepper plants at various times after detachment of leaves. Data represent the mean ± standard deviation of three independent biological replicates. (D and E) Leaf temperatures of empty vector control and CaDIF1-silenced pepper plants after treatment with 100 μM ABA. Representative thermographic images were taken 6 h after treatment (D) and the mean leaf temperature was measured using 10 plants of each line (E). Data represent the mean ± SD of three independent biological replicates. (F and G) Stomatal apertures in empty vector control and CaDIF1-silenced pepper plants after ABA treatment. Representative images were taken under a microscope (F) and the stomatal apertures were measured (G). Leaf peels were harvested from 2-week-old pepper plants and incubated in stomatal opening solution containing 10 μM ABA; the stomatal apertures were then measured under a microscope. Representative images were taken before (left) and 2.5 h after (right) ABA treatment. Data represent the mean ± standard error of three independent biological replicates, each evaluating 20 plants. Asterisks indicate significant differences between the control and the CaDIF1-silenced pepper plants (Student’s t-test; P 0.05).

Enhanced ABA Sensitivity of CaDIF1-OX Plants

To further investigate the in vivo function of CaDIF1, we generated transgenic Arabidopsis plants, exhibiting overexpression of the CaDIF1 gene. A real-time transcription PCR (RT-PCR) assay revealed that the accumulation of CaDIF1 transcripts was high in CaDIF1-OX plants, but not detected in the wild-type plants ( ); hence, CaDIF1-OX plants were used in our subsequent phenotypic analysis. Under normal growth conditions, we observed no phenotypic differences between the wild-type and CaDIF1-OX plants ( and ). To investigate whether altered expression of CaDIF1 affects the ABA response, we examined germination rate, primary root growth, and seedling establishment in the presence and absence of ABA ( ). CaDIF1-OX seeds were germinated on MS medium supplemented with 0.0 and 1.0 µM ABA. In the presence of ABA, the germination rate of CaDIF1-OX seeds at 2 days after sowing was significantly lower than that of wild-type seeds ( ). We measured the primary root lengths in wild-type and CaDIF1-OX plants at 8 days after sowing ( ). In the absence of ABA, the root lengths did not differ significantly between wild-type and transgenic plants; however, in the presence of 1.0 µM ABA, the roots of CaDIF1-OX plants were significantly shorter than those of wild-type plants ( ). Consistent with root growth, seedling establishment of CaDIF1-OX plants was significantly lower than that of wild-type plants ( ). These data suggest that altered CaDIF1 expression affects ABA response in germination and post-germination stages.

Figure 4

Enhanced sensitivity of CaDIF1-OX transgenic Arabidopsis lines to ABA. (A) Germination rates of CaDIF1-OX mutants and wild-type (WT) plants on 0.5× Murashige and Skoog (MS) medium supplemented with 1.0 μM ABA. (B and C) Primary root elongation of WT and transgenic lines exposed to ABA. Representative images were taken (B) and the root length of each plant was measured 8 days after sowing (C). Data represent the mean ± standard error of three independent biological replicates, each evaluating 25 seeds. Asterisks indicate significant differences between WT and transgenic lines (Student’s t-test; P 0.05). (D and E) Seedling development of CaDIF1-OX mutants and WT plants exposed to ABA. Representative images were taken 7 days after plating (D) and the number of seedlings in each line with expanded cotyledons was recorded (E). Data represent the mean ± standard error of four independent biological replicates, each evaluating 25 seeds. Asterisks indicate significant differences between WT and transgenic lines. (Student’s t-test; P 0.05).

Figure 5

Enhanced tolerance of CaDIF1-OX transgenic Arabidopsis lines to drought stress. (A) Drought tolerance of CaDIF1-OX transgenic plants. Three-week-old WT and transgenic plants were subjected to drought stress by withholding watering for 14 days and re-watering for 1 day. (B) Survival rates of plants after re-watering. Data represent the mean ± standard error of three independent biological replicates, each evaluating 30 plants. (C) Transpirational water loss from the leaves of WT and transgenic plants at various time points after leaf detachment. Data represent the mean ± standard error of three independent biological replicates, each evaluating 50 leaves. (D and E) Stomatal apertures in WT and CaDIF1-OX plants treated with ABA. Leaf peels were harvested from 3-week-old plants of each line and incubated in stomatal opening solution containing 10 or 20 μM ABA. Representative images were taken under a microscope (D) and stomatal apertures were measured (E). Data represent the mean ± standard error of three independent biological replicates. (F and G) Representative thermographic images of CaDIF1-OX transgenic Arabidopsis lines and WT plants 6 h after treatment with 100 μM ABA (F); the mean leaf temperatures of the three largest leaves were measured using 10 plants of each line (G). Data represent the mean ± SD of three independent biological replicates. Asterisks indicate significant differences between WT and transgenic lines (Student’s t-test; P 0.05).

Enhanced Drought Tolerance of CaDIF1-OX Plants

CaDIF1 was markedly induced by drought stress treatment ( ), and CaDIF1-knock down pepper plants showed an altered phenotype to drought stress ( ). Hence, we examined the in vivo role of CaDIF1 in response to drought stress ( ). First, we investigated the drought phenotype of CaDIF1-OX plants by withholding water for 14 days and then re-watering for 1 day ( ). Under well-watered conditions, we were not able to observe any phenotypic differences between CaDIF1-OX plants and wild-type plants ( , upper panel). However, under conditions of drought stress, CaDIF1-OX plants exhibited a less wilted phenotype than wild-type plants ( , middle panel). Furthermore, upon re-watering, the CaDIF1-OX plants resumed their growth rapidly compared with the wild-type plants ( , lower panel). At 1 day after re-watering, the survival ratio of CaDIF1-OX plants was 51.8–54.2%, whereas only 18.8% of wild-type plants resumed their growth ( ).

To find why CaDIF1-OX plants had drought tolerance phenotype, we measured the transpirational water loss, leaf temperature, stomatal aperture, and stress-related gene expressions. We monitored transpirational water loss by measuring the fresh weights of detached rosette leaves ( ). We found that the transpirational water loss was significantly lower in CaDIF1-OX plants than in the wild-type plants, suggesting that the enhanced drought tolerance of CaDIF1-OX plants was derived from a reduced transpiration rate. To determine whether low transpirational water loss in CaDIF1-OX plants was caused by increased ABA sensitivity, we measured stomatal aperture and leaf temperature after treatment with various concentrations of ABA. First, we estimated significant differences in stomatal pore sizes between wild-type and CaDIF1-OX plants after ABA treatment ( ). ABA treatment triggered a reduction in the stomatal aperture in wild-type and CaDIF1-OX plants; however, transgenic plants displayed smaller stomatal apertures than wild-type plants. These results indicate that low transpirational water loss in CaDIF1-OX plants was derived from enhanced ABA sensitivity, especially in the stomata. Next, we measured the leaf temperatures of wild-type and CaDIF1-OX plants. Consistent with the stomatal aperture, CaDIF1-OX plants exhibited significantly higher leaf temperatures than wild-type plants ( ).

In a previous studies, drought sensitivity and tolerance is related with the transcripts accumulation of stress-related genes, and that increased or decreased drought tolerance are related with altered expression of these genes (Cheong et al., 2007; Joo et al., 2019). Hence, we performed quantitative RT-PCR analysis of stress-related genes, including NCED3, DREB2A, RAB18, RD20, RD29A, and RD29B, and group A 2C type protein phosphatases (PP2Cs), such as ABI1, ABI2, and HAB1 ( ). The transcripts accumulation of stress-related genes were significantly high in CaDIF1-OX plants compared with wild-type plants. However, the expression level of 2C type protein phosphatases are not different between both plants. Collectively, these data indicate that enhanced expression of CaDIF1 increases drought tolerance by reducing stomatal pore size and enhancing stress-related gene expression.

Figure 6

Drought-inducible genes in CaDIF1-OX plants. Quantitative reverse transcription PCR analysis was performed on the detached leaves of plants exposed to drought stress at 3 h after detachment. The relative expression levels (∆∆CT) of each gene were normalized to the geometric mean of Actin8 as an internal control gene. Data represent the mean ± standard error of three independent biological replicates. Asterisks indicate significant differences between WT and transgenic lines (Student’s t-test; P 0.05).

CaDIF1 Interacts With CaDIS1

To determine whether CaDIF1 is a component of SCF1 type E3 ligase complex, we performed Y2H assay using five pepper SKP proteins as prey and CaDIF1 as bait ( ). Yeast cell transformed with CaDIF1 and XP_016539969.1 grew on selective media, indicating that XP_016539969.1 interacts with CaDIF1 in yeast cells. We performed further analysis by designating XP_016539969.1 as CaDIS1 (Capsicum annuum DIF1-Interacting SKP 1). To confirm the interaction and localization of CaDIF1 and CaDIS1 in vivo, a bimolecular fluorescence complementation (BiFC) assay was performed ( ). The yellow fluorescence derived from co-expression of CaDIF1:VYNE with CaDIS1:CYCE localized constitutive strong nuclear and cytosolic localization. Consistent with these data, an in vitro pull-down assay verified that CaDIF1 interacts directly with CaDIS1 ( ). Taken together, these data demonstrate that CaDIF1 is able to interact with CaDIS1.

Figure 7

Interaction of CaDIF1 with CaDIS1. (A) Identification of the CaDIF1-interacting partner CaDIS1 (C. annuum DIF1-Interacting SKP 1). Yeast strain AH109 was transformed with pGBKT7-CaDIF1 as bait and pGADT7-CaSKPs as prey. Interaction was indicated by growth on selective medium (SC-Ade-His-Leu-Trp; right); growth on SC-Leu-Trp was used as a control (left). (B) Bimolecular fluorescence complementation (BiFC) assay of interactions between CaDIF1 and CaDIS1. CaDIF1-VYNE was co-expressed with CaDIS1-CYCE in the leaves of N. benthamiana. White bar = 10 μm. (C) Pull-down assay of interaction between CaDIF1 and CaDIS1.

The CaDIS1 protein consists of 156 amino acids and have a conserved SKP1-like protein domain (including 4–106 amino acid residues) ( ). Protein sequence assays showed that CaDIS1 has high homology with SKP1 proteins from other plants ( ). Because the CaDIS1 is able to interact with CaDIF1, CaDIS1 plays a role as a positive regulator in ABA and drought signaling, we determined whether the transcripts accumulation of CaDIS1 is induced by ABA or abiotic stress treatments. Drought treatment induced CaDIS1 expression; however, unlike the expression patterns of CaDIF1, the CaDIS1 transcripts did not accumulate more strongly after treatment with ABA, H2O2, or high salinity ( ). When the fusion proteins of CaDIS1-GFP was expressed in the N. benthamiana epidermal cells, this protein was also localized to the nucleus, and cytoplasm ( ).

Reduced Drought Tolerance of CaDIS1-Silenced Pepper Plants

CaDIF1-knock down pepper plants displayed a sensitive phenotype to drought stress ( ); therefore, we also postulated that CaDIS1 is involved in the defence signaling to drought stress. To confirm this prediction, we conducted phenotypic analysis by VIGS assay in pepper plants ( ). We examined CaDIS1 knock down by RT-PCR assay of control (TRV2:00) and CaDIS1-knock down pepper (TRV2:CaDIS1) plants. The CaDIS1 transcripts were lowly accumulated in the CaDIS1-knock down pepper leaves compared with the control leaves ( ). To subject drought treatment to control and CaDIS1-knock down pepper plants, we withheld water for 11 days and re-watering for 2 days ( ). In comparison with control plants, CaDIS1-knock down pepper plants showed a wilted phenotype after drought stress and showed reduced drought tolerance after re-watering. The survival ratio of CaDIS1-knock down pepper plants was 36.9%, while the survival ratio of control pepper was approximately 48.7% ( ). Next, the transpirational water loss was compared by estimating the leaf fresh weights detached from control and CaDIS1-knock down pepper plants ( ). As same with the drought-sensitive phenotype, CaDIS1-knock down pepper leaves exhibited dramatically lower fresh weight than control leaves. Next, we measured leaf temperatures and stomatal apertures in the presence and absence of ABA ( ). In the absence of ABA, we were not able to detect different leaf temperatures significantly between control pepper and CaDIS1-knock down pepper plants ( ). However, after treatment with 100 µM ABA, the leaf temperatures of CaDIS1-silenced pepper were significantly lower than those of control plants. Consistent with leaf temperatures, the stomatal apertures were significantly larger in CaDIS1-silenced pepper than in control plants. ( ). These data demonstrate that the guard cells constituting stomatal pore of CaDIS1-knock down pepper plants display ABA hyposensitivity, and altered ABA sensitivity probably lead to reduced water retention in drought stress conditions.

Figure 8

Reduced tolerance of CaDIS1-silenced pepper plants to drought stress. (A) Drought susceptibility of CaDIS1-silenced pepper plants. Four-week-old TRV2:CaDIS1 and TRV2:00 pepper plants were subjected to drought stress by withholding watering for 11 days. Representative images were taken before (left) and after (middle) drought stress and 2 days after re-watering (right). (B) The survival rate was measured by counting the number of plants with green and rehydrated leaves 2 days after re-watering. Data represent the mean ± standard deviation of three independent biological replicates. (C) Transpirational water loss from the leaves of empty vector control and CaDIS1-silenced pepper plants at various times after detachment of leaves. Data represent the mean ± standard deviation of three independent biological replicates. (D and E) Leaf temperatures of empty vector control and CaDIS1-silenced pepper plants after treatment with 100 μM ABA. Representative thermographic images were taken 6 h after treatment (D) and the mean leaf temperature was measured using 10 plants of each line (E). Data represent the mean ± SD of three independent biological replicates. (F and G) Stomatal apertures in empty vector control and CaDIS1-silenced pepper plants after ABA treatment. Representative images were taken under a microscope (F) and the stomatal apertures were measured (G) Leaf peels were harvested from 2-week-old pepper plants and incubated in stomatal opening solution containing 10 or 20 μM ABA; the stomatal apertures were then measured under a microscope. Representative images were taken before (left) and 2 h after (right) ABA treatment. Data represent the mean ± standard error of three independent biological replicates, each evaluating 20 plants. Asterisks indicate significant differences between the control and the CaDIS1-silenced pepper plants (Student’s t-test; P 0.05).

Discussion

A large number of studies have suggested that regulation of protein stability using the ubiquitin–proteasome system is crucial for transfer of ABA signaling and the drought stress response at multiple steps. Several E3 ligases, which are related to ABA signaling and the drought stress response, have been isolated (Li et al., 2016; Yu et al., 2016; Lim et al., 2017). Recent studies have reported that the stability of core ABA-signaling components—such as ABA receptors and group A PP2Cs—is modulated by different types of E3 ligases. The RING type E3 ligase RSL1 and the SCF type E3 ligase complexes RIFP1 and CRL4 interact with and ubiquitinate ABA receptors such as RCAR1, RCAR3, RCAR10, and RCAR11 (Bueso et al., 2014; Irigoyen et al., 2014; Li et al., 2016). PUB12 and PUB 13, which are U-box type E3 ligases, are involved in ubiquitination and degradation of ABI1 (Kong et al., 2015). RING type E3 ligases CaAIRF1, RGLG1, and RGLG5 are associated with stability of group A PP2Cs, including CaADIP1, CaAIPP1 PP2CA, HAB2, and ABI2 (Wu et al., 2016; Baek et al., 2017; Lim et al., 2017). In this study, we have determined that the pepper F-box protein CaDIF1—which is one of component of the SKP type E3 ligase complex—interacts with CaDIS1 and positively modulates ABA signaling and drought stress response.

Pepper plants have very low transformation efficiency; therefore, to determine the biological role of CaDIF1 and CaDIS1 in ABA signaling and response to drought stress, we subjected CaDIF1- and CaDIS1-silenced pepper plants, and CaDIF1-OX Arabidopsis plants to ABA treatment and drought stress. Under drought stress conditions, plants displayed adaptive processes, including ABA biosynthesis, which increases water retention and enhances drought tolerance by regulating transpirational water loss via stomatal opening/closure. In this condition, CaDIF1- and CaDIS1-silenced pepper plants exhibited more wilted phenotypes, and these were characterized by decreased leaf fresh weight and reduced stomatal closure ( and ). Conversely, CaDIF1-OX plants exhibited less wilted phenotypes, and these were characterized by increased water retention and enhanced stomatal closure ( ). These data indicate that regulation of stomatal apertures in CaDIF1- and CaDIS1-knock down pepper plants, and in CaDIF1-OX transgenic plants confers reduced and enhanced drought-tolerant phenotypes, respectively.

Previous studies have shown that F-box proteins are involved in a large number of cellular processes in higher plants, such as tissue development and different hormone responses (Lechner et al., 2006; Fonseca et al., 2009; Schwechheimer and Willige, 2009). SCF type E3 ubiquitin ligase complex is composed of four subunits (Lechner et al., 2006). Among these, SKP1 protein interacts with CULLIN1 and F-box proteins. Most F-box proteins contain F-box domains in the N-terminus, and these domains have high variability in their amino acid composition; therefore, to determine the cellular function of these proteins, interaction assays are necessary (Deshaies, 1999; Koops et al., 2011). The CaDIF1 protein localized predominantly in the nucleus and CaDIS1-GFP fusion protein signal also detected in the nucleus. Moreover, our BiFC assay revealed that the interaction signals of both proteins were also observed in the nucleus. These results imply that CaDIF1 and CaDIS1 function as components of the SCF type E3 ubiquitin ligase complex. CaDIF1- and CaDIS1-silenced pepper plants exhibited hyposensitivity and reduced drought tolerance, whereas CaDIF1-overexpressing Arabidopsis plants displayed contrasting phenotypes. These data indicate that CaDIF1 and CaDIS1 function as positive modulators of ABA signaling and the response to drought stress. Moreover, the target proteins of SCFCaDIF1 ubiquitin ligase may negatively regulate ABA signaling and the drought stress response.

A large number of positive modulators of ABA induce mechanisms related to defence processes—including stress-related gene expression—thereby conducting adaptation in environmental stress condition (Yamaguchi-Shinozaki and Shinozaki, 2006; Cutler et al., 2010). In the present study, we were unable to identify the target protein of SCF ubiquitin ligase, which is composed of CaDIF1 and CaDIS1. Expression levels of stress-related genes indicated that CaDIF1 may regulate expression of DREB2A, RAB18, RD20, RD29A, and RD29B directly or indirectly, and that this protein likely acts modulator of these genes in the response to drought stress. However, the accumulation of NCED3 transcripts did not differ significantly between wild-type and CaDIF1-OX plants grown under well-watered and drought stress conditions. Under stress conditions, NCED3 functions in ABA biosynthesis, which is essential for the plant defence response to stress (Nambara and Marion-Poll, 2005; Urano et al., 2009). Several studies have shown that NCED3 gene expression induces stress-related gene expression and increases endogenous ABA levels (Iuchi et al., 2001; Lim et al., 2017). These results suggest that phenotypic variations may not be caused by differences in ABA levels but may be derived from changes in the ABA-signaling process. Moreover, enhanced expression CaDIF1 did not influence the induction level of group A PP2Cs ( ), which function as negative regulators of ABA signaling. Several studies have elucidated that the ABA-signal transduction pathway—from ABA perception to defence response to environmental stress (Lee and Luan, 2012). ABA perception by ABA receptors (PYR/PYLs/RCARs) and downstream ABA-signaling modulators—including group A PP2Cs and SnRK2 type kinases—are conserved in higher plants (Klingler et al., 2010; Umezawa et al., 2010; Kim et al., 2012); hence ABA receptors and other ABA-signaling components presumably play critical roles in adaptation to stress (Gonzalez-Guzman et al., 2012; Lee and Luan, 2012; Lim et al., 2013; Ding et al., 2015). On the basis of these results, it might be speculated that altered expression of CaDIF1 is unable to influence ABA biosynthesis and events occurring upstream of ABA signaling, but does influence events related to stress-related gene expression—located downstream of PP2Cs—leading to changes in ABA sensitivity and drought tolerance. Since CaDIF1 and CaDIS1 could function as components of the SCF type E3 ubiquitin ligase complex, we also did not rule out the possibility of the CaDIF1 and CaDIS1-mediated regulation in the protein stability of NCED3, PP2Cs or upstream transcriptional regulators of the stress-related genes.

In conclusion, our studies suggest that CaDIF1 and CaDIS1 positively regulate in the drought stress response through changes in ABA sensitivity, including induction of stomatal closure and stress-related gene expression. We have elucidated the biological functions of CaDIF1 and CaDIS1 in the drought stress response; however, the precise mechanisms whereby these proteins function remain unclear. Therefore, to clarify the functions of CaDIF1 and CaDIS1 under drought stress conditions, further studies to identify the direct target proteins are required.

Materials and Methods

Plant Materials and Growth Conditions

Seeds of pepper (C. annuum L., “Nockwang”), tobacco (N. benthamiana), and A. thaliana (ecotype Col-0) were sown in a steam-sterilized compost soil mix (peat moss, perlite, and vermiculite, 5:3:2, v/v/v), sand, and loam soil (1:1:1, v/v/v). The plants were raised at 25 ± 1°C under a 16 h light/8 h dark photoperiod (130 μmol photons·m−2·s−1). Arabidopsis [wild-type (ecotype Col-0) and CaDIF1-OX] seeds were grown on MS medium containing 1% sucrose. Details of plasmid construction and transgenic plants were described below.

Virus-Induced Gene Silencing (VIGS)

VIGS analysis was performed to knockdown CaDIF1 and CaDIS1 in C. annuum (pepper) as described previously (Lim et al., 2017). A 254 bp (1–254 nucleotide sequences) fragment of the CaDIF1 or a 299 bp (2–300 nucleotide sequences) fragment of the CaDIS1 cDNA was inserted into the pTRV2 vector and introduced into Agrobacterium tumefaciens strain GV3101 via electroporation. A. tumefaciens strain GV3101 containing pTRV1, pTRV2:00, pTRV2:CaDIF1, or pTRV2:CaDIS1 was infiltrated to the fully expanded pepper cotyledons (OD600 = 0.2, each from different construct).

Generation of CaDIF1-OX Plants

Agrobacterium transformation into the A. thaliana was conducted by using the floral dip method (Clough and Bent, 1998); all mutants generated in this study were in the Col-0 background. For CaDIF1-OX, full-length cDNA sequences were integrated into the pBIN35SGFP binary vector. For selection of overexpressing plants, we used 25 μg·ml−1 phosphinothricin.

ABA, Drought, NaCl, and H2O2 Treatments

To analyze CaDIF1 and CaDIS1 expression in pepper plants, we treated with ABA (100 μM), H2O2 (100 μM), drought, or NaCl (200 mM) as described previously (Lim et al., 2015a; Lim et al., 2015b). Pepper leaves were harvested at 0, 2, 6, 12, and 24 h after each treatment. For the determination of ABA sensitivity, we measured the seed germination rates, cotyledon development, and primary root lengths on ABA containing MS plants. For drought sensitivity analysis, we used 4-week-old pepper and 3-week-old Arabidopsis plants and subjected to drought stress by withholding water for 11 and 14 days, respectively. After re-watering for 2 days and 1 day, respectively, we calculated the survival. To determine drought sensitivity or tolerance, transpirational water loss was measured. Pepper and Arabidopsis rosette leaves were detached, and the reduced fresh weight was measured for each time points. For quantitative RT-PCR assay, 4-week-old CaDIF1-OX transgenic Arabidopsis plants were subjected to drought stress. All the experiments were conducted three times.

Measurements of Stomatal Apertures and Thermal Imaging

Leaf temperatures and stomatal apertures were measured as described previously (Lim and Lee, 2016). Briefly, A. thaliana and pepper leaf peels were floated in buffer with 10 μM CaCl2, 10 mM MES–KOH (pH 6.15), and 50 mM KCl, in day condition. After incubation for 3 h, stomata begins to close by replacing the buffer with 10 and 20 μM of ABA. Then after 2.5, 100 stomata apertures per 10 leaves were measured under a Nikon Eclipse 80i microscope. To analyze the thermal imaging, we used full expanded first and second leaves of pepper plants and Arabidopsis were treated with 100 μM ABA. For measurement of leaf temperatures, we used infrared camera (T420; FLIR) equipped with FLIR ver 5.2 software. All the experiments were conducted three times.

Transient CaDIF1-GFP and CaDIS1-GFP Fusion Proteins Expression in N. Benthamiana

To investigate subcellular localization and BiFC assay of CaDIF1 and CaDIS1, we used the open reading frame of CaDIF1, CaDIS1, and pBIN35SGFP, Pro-35S:VYNE, and Pro-35S:CYCE vectors, which express the proteins driven by the 35S promoter. The different constructs were introduced into the A. tumefaciens strain GV3101 and selected by 50 μg·ml−1 kanamycin. These cells were combined with the silencing suppressor p19 and introduced into the N. benthamiana epidermal cells by using agroinfiltration method. At 3 days after infiltration, leaf discs were cut, and the lower epidermal cells were examined under a confocal microscope (510 UV/Vis Meta; Zeiss) equipped with LSM Image Browser software.

Yeast-Two Hybrid Assay

Yeast-two hybrid (Y2H) assays were performed as described previously (Lim et al., 2017). The cDNA fragments of CaDIF1 or CaDIS1 were subcloned into the pGBKT7 or pGADT7 vectors, respectively, and co-transformed into yeast strain AH109 using the lithium acetate-mediated transformation method (Ito et al., 1983). To evaluate the interaction between bait and prey proteins, transformant candidates were selected on SC-Leu-Trp medium. Next, 10-fold serial dilutions were prepared from each yeast cell culture (OD600 = 0.5), and 5 μl of each sample was spotted onto SC-Leu-Trp medium or SC-Ade-His-Leu-Trp medium. Yeast colonies were incubated at 30°C for 5 days.

Expression of the MBP-CaDIS1 and GST‐CaDIF1 Recombinant Proteins in Bacterial Cells and Pull‐Down Assay

For expression of the maltose‐binding protein (MBP) and glutathione‐S‐transferase (GST) recombinant proteins, the pMAL‐c2X (New England Biolabs) and pGEX‐4T‐3 (GE Healthcare) vectors were respectively used. Each vector, harboring the full‐length cDNA sequence of CaDIS or CaDIF1, was introduced into Escherichia coli strain BL21 cells. The fusion proteins were induced and purified according to the manufacturer’s instructions.

For the pull‐down assay, 5 μg of GST or GST‐CaDIF1 were incubated with 5 μg of MBP or MBP‐CaDIS1 for 2 h at 4°C on constant rocking in 0.5 ml of binding buffer (20 mM Tris–HCl, pH 7.5, 200 mM NaCl, 1 mM EDTA, 0.5% Tween‐20) containing GST resin. After boiling at 97°C for 5 min, eluted proteins were analyzed using SDS‐PAGE, followed by western blotting and immunodetection with anti‐MBP and anti‐GST antibodies.

Data Availability Statement

All datasets generated for this study are included in the article/ .

Author Contributions

JL and CWL performed the experiments and analyzed the results. SCL designed the experiments and wrote the manuscript.

Conflict of Interest

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.