Overexpression of the CaTIP1-1 pepper gene in tobacco enhances resistance to osmotic stresses.

Both the gene expression and activity of water channel protein can control transmembrane water movement. We have reported the overexpression of CaTIP1-1, which caused a decrease in chilling tolerance in transgenic plants by increasing the size of the stomatal pore. CaTIP1-1 expression was strongly induced by salt and mannitol stresses in pepper (Capsicum annuum). However, its biochemical and physiological functions are still unknown in transgenic tobacco. In this study, transient expression of CaTIP1-1-GFP in tobacco suspension cells revealed that the protein was localized in the tonoplast. CaTIP1-1 overexpressed in radicle exhibited vigorous growth under high salt and mannitol treatments more than wild-type plants. The overexpression of CaTIP1-1 pepper gene in tobacco enhanced the antioxidant enzyme activities and increased transcription levels of reactive oxygen species-related gene expression under osmotic stresses. Moreover, the viability of transgenic tobacco cells was higher than the wild-type after exposure to stress. The pepper plants with silenced CaTIP1-1 in P70 decreased tolerance to salt and osmotic stresses using the detached leaf method. We concluded that the CaTIP1-1 gene plays an important role in response to osmotic stresses in tobacco.

1. Introduction

Water is an essential part of life. Water transport in plants is significantly controlled through integral membrane channel proteins, called aquaporins, which belong to the major intrinsic proteins (MIPs) of a multigene family [1]. Water management is mediated by aquaporins in vascular plants, which is required in different physiological processes [2]. Abiotic stresses, including osmotic stresses (drought and salt stress) and low temperature, can enhance water loss in plants [3,4,5,6,7]. Plants under osmotic stress have lower germination, stunted growth, reduced root function, a slower growth rate and lower yield and, ultimately, die [3,8].

Unlike animals or microbes, plants are known to express a larger number of aquaporins [9,10]. Based on the sequence homology and subcellular localization, the MIP gene family in plants is classified into seven evolutionarily different subfamilies, including the plasma membrane intrinsic proteins (PIPs), the tonoplast intrinsic proteins (TIPs), the nodulin-26-like intrinsic proteins (NIPs), the small basic intrinsic proteins (SIPs), the GlpF-like intrinsic proteins (GIPs), the hybrid intrinsic proteins (HIPs) and the uncategorized X intrinsic proteins (XIPs) [11]. Subcellular localization of TIPs was observed at the tonoplast or plasma membrane [12]. The tonoplast membrane is highly permeable to water. The expression of GhTIP1-1 is involved in response to low temperatures, which gradually increased in cotyledons under cold stress [13]. The importance of aquaporins in abiotic stresses has been demonstrated through genetic engineering, including reverse genetics and overexpression tools [7,14,15,16,17,18]. The osmotic water permeability coefficient was increased in the Arabidopsis leaf mesophyll (transient gene expression). Overexpressing the SlTIP2-2 gene also enhanced the relative transpiration compared to the control under water stress [14]. Conversely, PIP1b overexpression tobacco plants required more water consumption to maintain a normal phenotype [19]. Two alternative mechanisms have been developed to explain the performance of aquaporins in transgenic plants under water stress [20]. The overexpression of the plasma membrane intrinsic protein (PIP) subfamily in tobacco increased drought or salt tolerance by enhancing the antioxidant system [21,22,23]. It is necessary to address the function of aquaporins involved in the regulation of osmotic stress [24].

There are certain limitations in the genetic transformation of Capsicum biotechnology due to the low efficiency of pepper’s regeneration ability [25]. The virus-induced gene-silencing (VIGS) method is an effective tool to study gene functions in different tissues [26,27]. In our previous study, we found that overexpression of CaTIP1-1 (CaAQP, Accession No. GU116569) decreased chilling tolerance in transgenic tobacco plants by increasing the stomatal aperture. The expression patterns of CaTIP1-1 were different between low temperature and osmotic stress in pepper seedlings [7]. However, the role of CaTIP1-1 in pepper plants under low temperature and osmotic stress is unclear. In this study, we reported the subcellular localization of CaTIP1-1 and determined antioxidant enzyme activities related to gene expression during abiotic stresses. The present study revealed that overexpression of the CaTIP1-1 pepper gene conferred tolerance to osmotic stresses in plants, which is correlated to increasing antioxidant enzyme activities and cell viability under stresses. Finally, we have used CaTIP1-1 gene silencing as a VIGS tool to analyze the function in pepper under osmotic stresses.

2. Results and Discussion

2.1. Subcellular Localization of CaTIP1-1

Overexpressed GFP and GFP-fused CaTIP1-1 (CaTIP1-1-GFP) were reinserted into the vector pVBG2307. Suspension-cultured cells of tobacco were plasmolysed in 0.8 M mannitol for 15 min and compared with the control. In order to investigate the subcellular localization of CaTIP1-1 in treated and control cells, a fluorescent image was taken with a fluorescent microscope (BX51; Olympus, Tokyo, Japan) and a 50-W mercury lamp. The results in Figure 1A2,B2, showed that pVBG2307-GFP protein was expressed in the cell membrane and nucleus in the case of the control treatment, while the protein of treated cells was expressed in cell nucleus, cytoplasm and plasma membrane. It is clear from Figure 1A4,B4 that the subcellular localization of pVBG2307-CaTIP1-1-GFP was expressed inside the cell in the case of treated cells, and there was no expression in the cell wall; while, in the control treatment, the expression was inside the cell. These results suggest that CaTIP1-1 was localized in the tonoplasts.

Figure 1

Subcellular localization of CaTIP1-1. A fluorescent image was taken with a fluorescent microscope (BX51; Olympus) and a 50-W mercury lamp. (A) Control (untreated) suspension-cultured cells of tobacco and (B) suspension-cultured cells of tobacco were plasmolysed in 0.8 M mannitol for 15 min. The arrow indicates the nucleus; (A1,A3,B1,B3) image taken by a fluorescent microscope (bright light); (A2,A4,B2,B4) image taken by a fluorescent microscope (GFP filter).

2.2. Radicle Growth of CaTIP1-1-Overexpressing Tobacco Plants

Tobacco plants were transformed with a full-length sequence of the CaTIP1-1 pepper gene driven by the constitutive CaMV 35S promoter. Two lines (T2-1-3 and T4-2-5) were selected for further analysis. Both the transgenic and WT plants have similar radicle growth under normal growth conditions (Figure 2A,B). All transgenic seedlings treated with 0.15 M NaCl showed normal root and cotyledon growth, which was the same as the salt-free medium. While the radicle length of the WT seedlings decreased by 26.5% when compared to the transgenic plants (Figure 2A,B). After 7 days when exposed to the higher mannitol concentration, the transgenic plant seedlings’ growth quantity was two-fold more than that of the WT seedlings (Figure 2A,B).

Figure 2

Seedling growth of WT and transgenic lines of T3 tobacco plants subjected to osmotic stress. (A) Germinated seedlings with radicles of similar length were cultured in half-strength MS medium supplemented with 0.15 M NaCl or 0.4 M mannitol or control, and photographs were taken after 7 days of incubation; the scale bar represents 1.0 cm; (B) Results are the mean ± standard error (SE), replicated thrice. * indicates significant differences when compared with the control at a p value <0.05.

2.3. Analysis of Relative Water Content (RWC), Relative Electrolyte Leakage (REL), Malondialdehyde (MDA) and Antioxidant Enzyme Activities

The T3 tobacco seedlings were subjected to osmotic stresses. Under these conditions, in the WT tobacco leaves, wilting became evident after 12 h, which was earlier than that of the transgenic plants (Figure 3A). To investigate the transcription levels of CaTIP1-1, transgenic lines were obtained and confirmed by PCR analysis using genomic DNA (data not shown); the expression was firstly detected in the WT and transgenic plants (Figure 3B) and then evaluated by qRT-PCR under the osmotic stresses. The differences between the WT and transgenic plants related to the relative water content (RWC), relative electrolyte leakage (REL), malondialdehyde (MDA) and antioxidant enzyme activities were measured at various times (data for after 12 h only included). The MDA content was higher in the WT plants than in the transgenic lines after exposure to the osmotic stresses (Figure 4). After 12 h of osmotic stress, the WT displayed a greater increase in REL than transgenic plants. Both lines of transgenic plants gave similar REL values, which were close to that in WT before the stress treatments (Figure 4). The RWC displayed non-significant differences in the treatments (Figure 4).

Figure 3

Phenotype analysis and expressions of CaTIP1-1 in WT and transgenic plants. (A) Phenotype analysis of WT and T3 transgenic plants (T2-1-3 and T4-2-5 are independent transgenic lines) that were subjected to salt (0.15 M NaCl) or mannitol (0.25 M) stress for 12 h. The scale bar represents 3.0 cm; (B) Expressions of CaTIP1-1 in WT and transgenic plants (T2-1-3 and T4-2-5 are independent transgenic lines) under normal growth conditions by semi-quantitative PCR. PCR was performed for 28 or 30 cycles for different genes.

Figure 4

Physiological analysis of WT and CaTIP1-1-overexpressing transgenic lines under normal conditions and osmotic stress. Changes in relative water content (RWC), relative electrolyte leakage (REL) and malondialdehyde (MDA) were measured in the leaves of WT and CaTIP1-1-overexpressing transgenic lines (T2-1-3 and T4-2-5, which are independent transgenic lines) under normal conditions or osmotic stresses (0.15 M NaCl or 0.25 M mannitol for 12 h). The results are the mean ± standard error (SE), replicated thrice. * indicates significant difference when compared with the control at a p value <0.05.

The activities of three antioxidant enzymes (CAT, SOD and POD) were assessed in leaves during the different stages of osmotic stress. Under normal growth conditions, the stresses had minimal effects on the SOD activities from the transgenic plants, except for the line of T4-2-5 that increased 39.23% from 88.64 to 123.42 U/gFW/min (0.25 M mannitol stress). In addition, the transgenic lines had greatly improved CAT and POD activities under the osmotic stresses (Figure 5).

Figure 5

SOD, catalase (CAT) and peroxiredoxin (POD) were detected in the leaves of the transgenic lines (T2-1-3 and T4-2-5) and WT at 12 h after osmotic stress. Results are the mean ± standard error (SE), replicated thrice. * indicates significant differences when compared with the control at a p value <0.05.

2.4. Cell Viability under Osmotic Stresses

The treatments with 0.1 M NaCl and 0.1 M mannitol significantly decreased the viability of the tobacco suspension cells (76.51% and 55.9%, respectively) for 6 h (Figure 6). However, the same concentration of mannitol caused a slight increase in the death rate (T) at 48 h compared to the control at 6 h. The cell death rate was higher in salt stress than mannitol stress. Overexpression of CaTIP1-1 led to a marked decrease in the cell death rate under osmotic stress. It was also clear that the cell viability percent in transgenic plants was higher than wild-type plants.

Figure 6

Cell death was determined by fluorescein diacetate (FDA) staining in the tobacco cell suspension induced by 0.1 M mannitol or NaCl for 6, 24 and 48 h. Results are the mean ± standard error (SE), replicated thrice. * indicates significant differences compared with the control at a p value <0.05.

2.5. ROS-Related Genes Expression under Osmotic Stresses in Transgenic Tobacco

Under osmotic stress conditions, the transcription level of CaTIP1-1 remained higher in the transgenic (T) plants than in WT (Figure 7). Furthermore, under osmotic stress, the transcription levels of CaTIP1-1, NtCAT, NtSOD and NtPOD were assessed in the two transgenic lines. The two lines showed similar results; therefore, only one line is presented (Figure 7). The transcription levels of NtCAT, NtSOD and NtPOD were downregulated when the WT plants were subjected to osmotic stress for 48 h (Figure 7A,C). A rapid accumulation of the NtSOD transcript in transgenic plants was observed within 2 h (2.1-fold); it peaked at 24 h (13.1-fold) and reached a normal level (1.4-fold) 48 h after mannitol treatment. The transcription levels of NtPOD were higher in the transgenic plants than the WT plants.

Figure 7

Quantitative RT-PCR was used to assess the transcript levels of CaTIP1-1, NtCAT, NtSOD and NtPOD in the leaves of the transgenic lines and the wild-type. The relative fold differences in the mRNA levels were calculated using the 2−∆∆ formula with NtL25 as the internal control. Bars with different lower case letters in each group were significantly different, as determined using Duncan’s multiple range test (p < 0.05). S indicates 0.15 M NaCl stress ((A) wild-type and (C) transgenic plants); M means 0.25 M mannitol stress ((B) wild-type and (D) transgenic plants).

2.6. Leaf Discs Phenotype of Gene-Silenced Pepper in Response to Osmotic Stresses

When the positive control (inoculated with TRV2:CaPDS) showed a large bleaching symptom, young leaves of CaTIP1-1-silenced plants and the negative control (inoculated with TRV2) were collected to detect the silencing effect. Compared to the negative control, the CaTIP1-1 silencing rate reached nearly 75% (Figure 8A). Leaf discs (0.5 cm in diameter) were obtained from the young leaves with a rate of more than 50% gene silencing to perform osmosis stress. The CaTIP1-1-silenced materials led to quick chlorophyll degradation after 48 h (Figure 8B).

Figure 8

CaTIP1-1 expression level of gene-silenced pepper plants. (A) The expression of CaTIP1-1 in gene-silenced pepper (TRV2:CaTIP1-1) cv P70 and control plants (TRV2:00) were tested at 45 days after inoculation; (B) leaf discs phenotypes (0.5 cm in diameter) of the gene-silenced plants in response to 0.1 M salt stress and 0.3 M mannitol stress after 48 h.

2.7. Discussion

TIPs’ subcellular localization has been performed by immunofluorescence and the transient or stable expression of fluorescent protein fusions [28]. The tobacco suspension cell technique is suitable to observe the localization of modified GFPs with various signals in different compartments in a vacuolar-sorting system [29,30]. Based on its amino acid sequence, CaTIP1-1 is predicted to be a TIP and to be aligned together with the 35 AQPs of Arabidopsis [31]. In the current results, the CaTIP1-1-GFP protein was investigated in the central vacuole of the suspension cells using the transient expression system [32]. The massive amount of TIPs can facilitate water movement across the cells, which might favor the growth of transgenic plants under normal conditions. However, CaTIP1-1 overexpression showed no significant effect on the transgenic plants without stress. These results suggest that environmental stimuli regulated the expression of CaTIP1-1 and PgTIP at different levels [16]. Arabidopsis mutant lines attip1-1 and attip1-2 are alive and showed no lethal phenotype [33]. The pepper plants with silenced CaTIP1-1 in P70 decreased in their tolerance to salt and mannitol stresses.

It has been shown previously that CaTIP1-1 has a negative role in chilling stress. This also indicated that the mechanisms of overexpression of CaTIP1-1 decreased the water use efficiency due to stomatal aperture changes when exposed to low temperatures [7]. The expression analysis of the CaTIP1-1 gene showed upregulation at a low salt and mannitol concentration in pepper seedlings [7]. Osmotic stress significantly increased the CaTIP1-1 gene expression in transgenic plants, which showed higher RWC. It is unclear whether the beneficial effects are related to water transport or have a well-established role in the membranes that have been damaged by oxidative stress, which in this role caused less electrolyte leakage.

Plants commonly accumulate reactive oxygen species (ROS) in response to environmental stresses [34], and ROS accumulation during stress greatly depends on the balance between ROS production and ROS scavenging [35]. The present study considered the possible regulation role of ROS-scavenging enzymes, including superoxide dismutase (SOD), catalase (CAT) and peroxiredoxin (POD). The current results indicated that the ROS-scavenging enzymes’ activities were increased in both WT and transgenic plants when exposed to osmotic stress. Controlling the ROS balance was shown to be important for abiotic and biotic stresses tolerance, such as drought, salinity stress and Phytophthora capsici infection, in transgenic plants or tolerant cultivars [36]. In addition, the higher activities of CAT and POD during stress may be responsible for reducing the damage of transgenic plants. At the same time, our results indicated that the transcription of CaTIP1-1 increased after 12 h. Macroarray experiments revealed PIP2 and TIP1 homology that showed 20% to 40% decreases in abundance 6 h after treatment [3]. These mechanisms may act in concert with the overexpression of CaTIP1-1 in tobacco seedlings.

Generally, plant growth and root development stages are sensitive to osmotic stress. The radicles of transgenic plants were more tolerant to osmotic stresses than those of WT plants. The present data also showed that the transgenic tobacco seedlings exhibited less damage, which means that the overexpression of CaTIP1-1 in plants makes them more tolerant to osmotic stresses. The WT plants wilted within 12 h of treatment with 0.15 M NaCl or 0.25 M mannitol. The transcription levels of CaTIP1-1 showed high levels in the transgenic plants after 6 h. The expression levels of CaTIP1-1 may be related to the tolerance to osmotic stresses. The complex expression patterns of aquaporins in plants have been determined by different groups under various environmental conditions [9,14,37]. In the current study, the transgenic plants preserved the RWC at a constant level. It is possible that CaTIP1-1 overexpression influences the activities of other endogenous aquaporins, which positively regulates the response to the stress [37]. Further research is needed to completely understand the expression of other endogenous aquaporins under osmotic stress. MDA and REL are important indicators of cell membrane injury. Osmotic stress significantly increased the MDA and REL in the WT, which suggested that the WT plants suffered more damage than the transgenic plants. The cell death rate also displayed similar results.

3. Experimental Section

3.1. Plant Materials, Cell Culture and Seedling Treatment

Tobacco (Nicotiana tabacum) cv Bairihong was used for gene transformation according to the leaf disc method; T3 transgenic tobacco plants were used for all experiments, and the seedlings were selected and incubated as previously described [7]. Callus cultures and subcultures were maintained on the same medium [38]. The cell suspension cultures of tobacco were cultured in liquid MS medium supplemented with 0.2 mg/L 2,4-dichlrophenoxyacetic acid and 3% sucrose on a rotary shaker. Cells were transferred to fresh medium every week. For the suspension of cultured cells during osmotic stress treatments, fresh cells were transferred to medium containing a high concentration of salt (0.1 M NaCl) or mannitol (0.1 M mannitol). Both wild-type (WT) and transgenic tobacco germinated seeds were exposed to osmotic stresses (0.15 M NaCl or 0.4 M mannitol), and their growth rate was measured. For osmotic and salt stress treatments, ten-week old tobacco seedlings were cultured with 1/2-strength Hoagland’s nutrient solution [39] and then treated with 0.15 M NaCl and 0.25 M mannitol, respectively. Control seedlings were grown in a growth chamber at 25 °C under fluorescent lighting (14 h light/10 h dark cycle, 200 µmol/m2/s, 70% relative humidity). Leaves from stress-treated plants were collected at 0, 2, 6, 12, 24 and 48-h intervals after treatment and immediately frozen in liquid nitrogen, then kept at −80 °C for RNA isolation.

3.2. Subcellular Localization of CaTIP1-1 Protein

The full length of the CaTIP1-1 pepper gene coding region was cloned into a pVBG2307 vector [40]. Under the control of a CaMV 35S promoter and fused in the 3' region with the green fluorescence protein (GFP) gene, pVBG2307-CaTIP1-1-GFP was produced. The specific gene primers are presented in Table 1. The plasmids of pVBG2307-GFP (used as the control) and pVBG2307-CaTIP1-1-GFP were transformed into tobacco cell suspension culture using Agrobacterium tumefaciens by the co-cultivation method [32]. The CaTIP1-1 protein was localized subcellularly using a fluorescent microscope. Plasmolysed cells were examined with a fluorescent microscope (BX51; Olympus) using a 50-W mercury lamp. Suspension-cultured cells of tobacco were plasmolysed in 0.8 M mannitol for 15 min [27].

Table 1

Primers used in this investigation.

Primers	Primer Sequence (5'→3')	Explanation
CaTIP1-1	F1: CGATGGCGTCACTACTCCTCR1: TGATGTACAGAAGTCCCCTG	RT-PCR
	a F: GCCTCTTCAGTTTGGTTGTAGGCb R: CGGGCACCGAAAGTAACAGCAG	VIGS Vector construct
	a F2: GCATGCCGATCCGCCAAATTGb R2: CGGAAAATCTCCTCCACTTGGGATTTGC	Subcellular localization
GFP	F: GTAAGGGAGAAGAACTTTTCACTGR: TGTGGTCTCTCTTTTCGTTGG
NtCAT	F: GTATTGCTTGAGGATTACCATTTR: CTTGACAGCAAACCCACG	RT-PCR
NtSOD	F: CTCCTACCGTCGCCAAATR: GCCCAACCAAGAGAACCC
NtPOD	F: GCTGTTCGACGAGTTGTTAACAGR: CTCTGGCTGAGTTGTTGTTGG
NtL25	F: CCTAAAGTATCCCCTCACCACAGR: CTTTCTTCGTCCCATCAGGC
CaUbi3	F: TGTCCATCTGCTCTCTGTTGR: CACCCCAAGCACAATAAGAC

a Black frames indicate that the primers of CaTIP1-1F and CaTIP1-1F2 carried the XbaI enzyme site; b black frames indicate that the primers of CaTIP1-1R and CaTIP1-1R2 carried the KpnI enzyme site.

3.3. RWC, REL, MDA and Antioxidant Enzyme Assays in the Transgenic Tobacco Plants

Leaves from stress-treated plants were collected 12 h after the stress treatment, and the relative water content (RWC) and relative electrolyte leakage (REL) were measured according to the method of Yin et al. [7]. The level of lipid peroxidation was measured in terms of malondialdehyde (MDA) and antioxidative enzymes, followed the procedure of Guo et al. [41].

3.4. RNA Isolation and Quantitative Real-Time PCR Analysis

Reverse transcription was performed using the Primescript™ first strand cDNA Synthesis Kit (TaKaRa, Dalian, China). Quantitative real-time PCR (qRT-PCR) was performed according to the method of Guo et al. [41], and semi-quantitative PCR was carried out as described by Yin et al. [7]. The L25 ribosomal protein (NtL25, Accession No. L18908) was used as a tobacco reference gene [42]. The ubiquitin-conjugating protein (CaUbi3, Accession No. AY486137) was used as a pepper reference gene [43]. The specific gene primers used, including NtCAT (Accession No. HF564632), NtSOD (Accession No. AB093097) and NtPOD (Accession No. AB178953), are presented in Table 1. The relative fold difference in mRNA levels was calculated using the 2−∆∆ formula with NtL25 as the internal control [22].

3.5. Determination of Viability of Tobacco Suspension Cells under Osmotic Stresses

Suspension cells of T3 transgenic tobacco (Nicotiana tabacum) cv Bairihong and WT were placed in the culture media amended with 0.1 M NaCl or 0.1 M mannitol to induce salt or osmotic stresses. Control cells were cultured on the same media without adding NaCl or mannitol. Cells were stained with fluorescein diacetate (FDA) (AAT Bioquest, Sunnyvale, CA, USA) to estimate cell viability after stress exposure [44]. Dimethyl sulfoxide (Sigma Aldrich, Saint Louis, MO, USA) was selected as the permeabilizing agent for FDA staining. FDA-stained cells were examined with a fluorescent microscope (BX51; Olympus) using a 50-W mercury lamp. For each sample, at least 200 cells were counted in each treatment.

3.6. VIGS Assay of CaTIP1-1 in Pepper Plants

The TRV-based VIGS system was used for gene silencing, as described previously [26]. To generate the CaTIP1-1/TRV2 construct, a 325-bp fragment of the CaTIP1-1 gene was PCR amplified from pepper. The resulting product was cloned into the TRV2 vector using the double digested method with enzymes of XbaI and KpnI. Agrobacterium tumefaciens strain GV3101 harboring pTRV1 was respectively mixed with pTRV2 (as the negative control), TRV2-CaPDS (as the positive control) or TRV2-CaTIP1-1 at a 1:1 ratio. The mixtures were inoculated into pepper cv P70 at the fully-expanded cotyledons stage. After injection, all of the seedlings were placed at 18 °C and 60% relative humidity for 2 days and then moved to a growth chamber according to the protocol [26]. The gene-silenced leaves discs were used for 0.1 M salt or 0.3 M mannitol stress.

3.7. Statistical Analysis

Statistical analysis was performed using the Statistical Analysis System software (SAS 8.2, North Carolina State University, Cary, NC, USA), and the means were compared using Duncan’s multiple range test, taking p < 0.05 as a significant difference. Values were expressed as the mean ± standard error (SE). All experiments were performed and analyzed separately with three biological replicates.

4. Conclusions

In conclusion, the overexpression of CaTIP1-1 pepper gene increased the tolerance in tobacco to osmotic stresses during the seedling stage. The CaTIP1-1-transgenic plants showed higher cell viability and antioxidant enzyme activities under osmotic stress compared to the wild-type cells. After exposure to osmotic stresses, in the transgenic plants, there was a rapid accumulation of antioxidant enzyme-related gene transcripts. CaTIP1-1-silenced pepper led to quick chlorophyll degradation. We conclude that the overexpression of CaTIP1-1 pepper gene in tobacco increased osmotic stress tolerance by contributing to the ROS balance.