WRKY Transcriptional Factor IlWRKY70 from Iris laevigata Enhances Drought and Salinity Tolerances in Nicotiana tabacum

Drought and high salinity greatly affect plant growth and development. WRKY transcription factors play a key role in plant tolerance to abiotic stress, but the functions of WRKYs in the ornamental monocotyledon Iris laevigata remain largely unexplored. In this study, we cloned IlWRKY70 and found that it is a Group III WRKY localized in the nucleus. The expression of IlWRKY70 was induced by NaCl and PEG-6000, which reached peaks (4.38 and 5.65 times) after 3 h and 1 h, respectively. The exogenous overexpression of IlWRKY70 in N. tabacum significantly improved the resistance under NaCl and drought treatments, as evidenced by higher germination rates, longer root lengths, and increased fresh weights compared to those of control plants. In addition, transgenic seedlings showed significantly reduced wilting, higher photosynthetic performance, higher Fv/Fm and chlorophyll content, and lower stomatal conductance. Moreover, transgenic lines showed higher antioxidant enzymatic activities, lower reactive oxygen species (ROS), and lower malondialdehyde contents. Accordingly, we also found higher expressions of antioxidant defense genes, including SOD, CAT, and POD, in transgenic lines compared to controls under salt and drought stresses. Thus, IlWRKY70 enhances the abilities of salt and drought tolerances in plants, at least partially, via ROS regulation and can be used for breeding I. laevigata possessing enhanced salt and drought resistances.


Introduction
Salt and drought stresses are among the most prevalent abiotic stresses in the plant kingdom [1].Recent years have witnessed notable shifts in climate dynamics, resulting in altered rainfall patterns, thereby exacerbating land desertification [2] and salinization [3] trends.It is noteworthy that both salt and drought conditions predominantly induce osmotic stress in plants.Beyond water-scarcity-induced drought, salt-induced osmotic pressure also engenders water deficits in plants, compounded by the direct toxicity of salt ions [4].Therefore, it is very important to screen and study plant salt-and droughtresistance genes, clarify the mechanisms of plant salt and drought resistances, and use genetic engineering to quickly create various salt-and drought-resistant plants to solve practical problems.I. laevigata is a perennial cold-resistant herb of the Iris genus.Its flowers are blue and purple, large and colorful, and tall and beautiful, with a long flowering period.It grows mostly in wetlands and swamps and has high ornamental value.The characteristic of I. laevigata's moisture preference and the increasing salinization of urban land severely limit the promotion and application of I. laevigata outside of wetlands.Therefore, exploring genes that regulate both salt and drought resistances in plants and creating I. laevigata varieties which can possess drought and salt resistances through genetic engineering can greatly expand the application scenarios of I. laevigata, which is of great significance for enriching cold landscapes.
Numerous studies have demonstrated that plants subjected to abiotic stress transmit stress signals to stress-response transcription factors (TFs) via signal transduction pathways, regulating downstream resistance-related genes to combat adverse environmental damage.Notably, transcription-factor families, such as bZIP, bHLH, WRKY, and MYB, are involved in plant responses to abiotic stress [5][6][7][8].Among them, the WRKY family is one of the largest transcription-factor families unique to plants, and the WRKY protein has a fast response to adverse environments [9], playing a key role in the tolerance of various plants to abiotic stress.For example, LlWRKY22 promotes the heat tolerance of lilies through the self-activation and activation of LlDREB2B [10], PyWRKY75 enhances the cadmium stress tolerance of poplar trees [11], GmWRKY21 of soybeans enhances the tolerance of arabidopsis to aluminum stress [12], while WRKY8 of tomatoes can promote plant stress resistance under drought and salt stresses [13].
All WRKY proteins derive their nomenclature from the presence of conserved WRKY domains (WDs), which are characterized by the medium to high conservation of the WRKYGQK motif and C2H2 or C2HC zinc finger motifs.These zinc finger motifs play a pivotal role in binding specifically to the W-box structure within the target genes, thereby orchestrating the regulation of diverse target genes [9,14].The WRKY family, classified based on the number of conserved WRKY domains and the type of zinc finger structure, comprises four distinct groups [15].The WD of Group I has two C2H2 zinc finger structural motifs, the WD of Group II has one C2H2 zinc finger structural motif, the WD of Group III has one C2HC zinc finger structural motif, and the WD of Group IV lacks a zinc finger structural motif [9].It is widely believed that Group I is the ancestral group, with Group II evolving subsequently through the loss of one WRKY domain.The emergence of Group III can be attributed to a mutation in the C-terminal zinc finger of Group II.Research indicates that Group III evolved relatively late in the evolutionary timeline of terrestrial plants and is unique to higher plants [16,17].
Although the functional role of WRKY genes has primarily been explored in crops [9], the utilization of WRKY genes in ornamental flowers, particularly within the monocotyledonous plant I. laevigata, has been relatively unexplored.One notable member of the Group III WRKY transcription factors is WRKY70, which has garnered attention in recent years for its ability to confer drought tolerance, salt tolerance, and disease resistance in plants [18][19][20][21][22].However, the role of WRKY70 in drought and salt tolerances has only been studied in dicotyledons, and WRKY70 from different sources may have opposite effects on drought or salt tolerance.WRKY70 from a special group of monocot plants has not been reported.I. laevigata is a poorly understood but magnificent monocotyledon ornamental plant with no reported genes; and as a hygrophyte, it is necessary to open the study of drought-and salt-stress-resistance genes.
In the context of this study, we have successfully cloned the WRKY70 gene from I. laevigata, which demonstrates inducible expression in response to salt and drought stress conditions.The overexpression of IlWRKY70 has been shown to significantly enhance salt and drought tolerances in transgenic tobacco seeds and seedlings.This discovery positions IlWRKY70 as a promising candidate gene for improving drought and salt resistances not only in I. laevigata but also in other iris species, with potential implications for the advancement of ornamental horticulture.It also provides a basis for further study on the function of WRKY70 in other monocot plants.

IlWRKY70 Gene Cloning and Phylogenetic Tree Analysis
The 900 bp IlWRKY70 gene, which encodes 299 amino acids, was cloned from I. laevigata cDNA through PCR amplification.ProtParam analysis revealed that the IlWRKY70 protein has a molecular weight of 32.866 kDa, a theoretical isoelectric point of 5.01, total numbers of negatively charged residues (Asp + Glu) of 42 and positively charged residues (Arg + Lys) of 30, and an instability index (II) of 49.34, indicating it is an unstable protein.
According to ProtScale analysis, the highest hydrophilicity score for the IlWRKY70 protein was at amino acid position 157 (−2.656), while its highest hydrophobicity score was at position 233 (1.667).The number and scores of hydrophilic amino acids in the peptide chain were higher than those for hydrophobic ones, suggesting that the IlWRKY70 protein is hydrophilic.By constructing the WRKY70 phylogenetic tree with other species, IlWRKY70 was the most homologous to the WRKY70 protein of Asparagus officinalis in the monocotyledon plant (Figure 1B).Through protein sequence alignment (Figure 1A), the highly conserved domain WRKYGQK [9] in the WRKY family was also identified in the IlWRKY70 protein sequence, and the assumed C2HC zinc finger structure of C-X7-C-X23-H-X-C was identified in this domain.

IlWRKY70 Gene Cloning and Phylogenetic Tree Analysis
The 900 bp IlWRKY70 gene, which encodes 299 amino acids, was cloned from I. laevigata cDNA through PCR amplification.ProtParam analysis revealed that the IlWRKY70 protein has a molecular weight of 32.866 kDa, a theoretical isoelectric point of 5.01, total numbers of negatively charged residues (Asp + Glu) of 42 and positively charged residues (Arg + Lys) of 30, and an instability index (II) of 49.34, indicating it is an unstable protein.According to ProtScale analysis, the highest hydrophilicity score for the IlWRKY70 protein was at amino acid position 157 (−2.656), while its highest hydrophobicity score was at position 233 (1.667).The number and scores of hydrophilic amino acids in the peptide chain were higher than those for hydrophobic ones, suggesting that the IlWRKY70 protein is hydrophilic.By constructing the WRKY70 phylogenetic tree with other species, IlWRKY70 was the most homologous to the WRKY70 protein of Asparagus officinalis in the monocotyledon plant (Figure 1B).Through protein sequence alignment (Figure 1A), the highly conserved domain WRKYGQK [9] in the WRKY family was also identified in the IlWRKY70 protein sequence, and the assumed C2HC zinc finger structure of C-X7-C-X23-H-X-C was identified in this domain.

Expression of IlWRKY70 in I. laevigata
The expression of IlWRKY70 was examined in the roots, tubers, and leaves of I. laevigata, and the results showed that the expression level of IlWRKY70 in leaves was significantly higher than those in roots and tubers (Figure 2A).The expression of IlWRKY70 increased significantly after treatment (Figure 2B,C) and reached the peak values (4.38 times) after 3 h of salt treatment and (5.65 times) after 1 h of drought-stress treatment.

Expression of IlWRKY70 in I. laevigata
The expression of IlWRKY70 was examined in the roots, tubers, and leaves of I. laevigata, and the results showed that the expression level of IlWRKY70 in leaves was significantly higher than those in roots and tubers (Figure 2A).The expression of IlWRKY70 increased significantly after treatment (Figure 2B,C) and reached the peak values (4.38 times) after 3 h of salt treatment and (5.65 times) after 1 h of drought-stress treatment.

Subcellular Localization of IlWRKY70
To determine the subcellular localization of the IlWRKY70 protein, the pCAMBIA1300:IlWRKY70-GFP plasmid vector was constructed and transiently transformed into onion epidermal cells.With the help of fluorescence microscopy, DAPI staining showed the location of the nucleus.The fluorescence signal of the empty vector pCAMBIA1300-GFP protein was present in both the cytoplasm and the nucleus, while the fluorescence signal of the IlWRKY70 protein was only localized in the nucleus (Figure 3).

Subcellular Localization of IlWRKY70
To determine the subcellular localization of the IlWRKY70 protein, the pCAMBIA1300: IlWRKY70-GFP plasmid vector was constructed and transiently transformed into onion epidermal cells.With the help of fluorescence microscopy, DAPI staining showed the location of the nucleus.The fluorescence signal of the empty vector pCAMBIA1300-GFP protein was present in both the cytoplasm and the nucleus, while the fluorescence signal of the IlWRKY70 protein was only localized in the nucleus (Figure 3).

Subcellular Localization of IlWRKY70
To determine the subcellular localization of the IlWRKY70 protein, the pCAMBIA1300:IlWRKY70-GFP plasmid vector was constructed and transiently transformed into onion epidermal cells.With the help of fluorescence microscopy, DAPI staining showed the location of the nucleus.The fluorescence signal of the empty vector pCAMBIA1300-GFP protein was present in both the cytoplasm and the nucleus, while the fluorescence signal of the IlWRKY70 protein was only localized in the nucleus (Figure 3).

Establishment of Transgenic Tobacco Lines Overexpressing IlWRKY70
The ORF sequence of IlWRKY70 was successfully cloned into the pCAMBIA1300: IlWRKY70-GFP plasmid vector through homologous recombination (Figure 4A,B).Ten T0 transgenic tobacco lines were successfully transformed using Agrobacterium tumefaciensmediated leaf disc transformation (Figure 4C).The positive inbred progenies were screened with hygromycin B and identified by PCR until the T3 generation.After that, three positive lines were randomly selected and named as overexpression line 1 (The abbreviation is OE-1, and the others are similar), OE-2, and OE-3 positive seedlings for subsequent experiments.RT-qPCR analysis showed that the IlWRKY70 gene was highly expressed in OE-1, OE-2, and OE-3 compared to the wild type (WT) (Figure 4D).

Establishment of Transgenic Tobacco Lines Overexpressing IlWRKY70
The ORF sequence of IlWRKY70 was successfully cloned into the pCAMBIA1300:IlWRKY70-GFP plasmid vector through homologous recombination (Figure 4A,B).Ten T0 transgenic tobacco lines were successfully transformed using Agrobacterium tumefaciens-mediated leaf disc transformation (Figure 4C).The positive inbred progenies were screened with hygromycin B and identified by PCR until the T3 generation.After that, three positive lines were randomly selected and named as overexpression line 1 (The abbreviation is OE-1, and the others are similar), OE-2, and OE-3 positive seedlings for subsequent experiments.RT-qPCR analysis showed that the IlWRKY70 gene was highly expressed in OE-1, OE-2, and OE-3 compared to the wild type (WT) (Figure 4D).

Physiological Indexes of Overexpressed N. tabacum Seeds
To explore the effect of the exogenous IlWRKY70 expression on salt and drought stresses, the tobacco seeds of the OE-1, OE-2, and OE-3 lines overexpressing IlWRKY70 at the T3 generation were treated with salt stress or drought stress for 15 days, with WT and EV seeds as controls (Figure 5A-H).Under MS medium conditions, all the tobacco seeds germinated normally and grew well after 15 days (Figure 5E), indicating that there was no significant difference between transgenic plants, empty vector, and wild type under normal conditions.However, after three gradient treatments of salt stress (NaCl concentrations of 100, 150, and 200 mM) and drought stress (mannitol concentrations of 100, 200, and 300 mM), the seed germination rate (Figure 5I,L), total root length (Figure 5J,M), and fresh weight (Figure 5K,N) of the OE-1, OE-2, and OE-3 transgenic lines were significantly higher than those of the WT and EV lines (p < 0.05), and there was no significant difference between the WT and EV lines (p > 0.05).

Physiological Indexes of Overexpressed N. tabacum Seeds
To explore the effect of the exogenous IlWRKY70 expression on salt and drought stresses, the tobacco seeds of the OE-1, OE-2, and OE-3 lines overexpressing IlWRKY70 at the T3 generation were treated with salt stress or drought stress for 15 days, with WT and EV seeds as controls (Figure 5A-H).Under MS medium conditions, all the tobacco seeds germinated normally and grew well after 15 days (Figure 5E), indicating that there was no significant difference between transgenic plants, empty vector, and wild type under normal conditions.However, after three gradient treatments of salt stress (NaCl concentrations of 100, 150, and 200 mM) and drought stress (mannitol concentrations of 100, 200, and 300 mM), the seed germination rate (Figure 5I,L), total root length (Figure 5J,M), and fresh weight (Figure 5K,N) of the OE-1, OE-2, and OE-3 transgenic lines were significantly higher than those of the WT and EV lines (p < 0.05), and there was no significant difference between the WT and EV lines (p > 0.05).

Physiological Indices of Overexpressed N. tabacum Seedlings
The transgenic tobacco seedlings were subjected to natural drought and salt stresses (NaCl concentration of 300 mM) to assess the resistance level.Under normal growth conditions, CK, EV, OE-1, OE-2, and OE-3 exhibited similar growth patterns with no significant differences among the five lines (Figure 6A).However, on the seventh day of salt stress, WT and EV showed lower leaf growth rates compared to the transgenic lines and displayed evident wilting symptoms.At day 14, the transgenic lines demonstrated significantly higher leaf growth rates and plant heights than the WT and EV lines, whereas WT and EV plants wilted, with yellowing signs on the lower leaves along with a slower overall growth rate (Figure 6B).Similarly, on the seventh day of drought stress, both WT and EV plants exhibited obvious wilting symptoms.At day 14, although WT and EV plants exhibited clear wilting throughout their foliage, transgenic plants displayed noticeable wilting on the lower leaves but only slight wilting on the upper leaves along with significantly greater heights compared to those WT and EV plants (Figure 6C).
Plants use H 2 O and CO 2 to produce organic matter through photosynthesis and maintain their growth.The net photosynthetic rate, total chlorophyll content, Fv/Fm, stomatal conductance, and intercellular CO 2 content are common indicators reflecting the level of a plant's photosynthetic capacity.Higher values of these indicators tend to represent higher photosynthetic capacities of plants.The transpiration rate can reflect the water demand of the plant, and the faster the transpiration rate, the lower the water demand of the plant.To explore the photosynthetic capacity and growth status of transgenic tobacco under salt and drought stresses, the above six indicators were measured.The results showed that at day 0 of the salt stress, there was no significant difference among all the six indexes (Figure 7A-F).With increasing salt stress time, the total chlorophyll content showed an increasing trend (Figure 7B), but the net photosynthetic rate, Fv/Fm, stomatal conductance, intercellular CO 2 content, and transpiration rate (Figure 7A,C-F) showed a decreasing trend.At 7 and 14 days, the net photosynthetic rate, total chlorophyll content, and Fv/Fm of the three IlWRKY70 overexpressing tobacco lines were significantly higher than those of the WT and EV lines (p < 0.05), and the stomatal conductance, intercellular CO 2 content, and transpiration rate were significantly lower than those of the control lines (p > 0.05).Similarly, at day 0 of the drought stress, there was no significant difference (Figure 7G-L) in the six indexes of all the strains (p > 0.05).With the extension of the stress time, the total chlorophyll showed an increasing trend (Figure 7H), while the net photosynthetic rate, Fv/Fm, stomatal conductance, intercellular CO 2 content, and transpiration rate (Figure 7G,I-L) showed a decreasing trend, indicating that the photosynthetic capacity of the plants was severely limited under the drought stress.With increasing drought time, the net photosynthetic rate, stomatal conductance, and plant transpiration rate decreased rapidly; all reached very low levels at 14 days; and the plants were severely short of water.The net photosynthetic rate, total chlorophyll content, and Fv/Fm of the IlWRKY70 overexpressed tobacco lines were significantly higher than those of the WT and EV lines at 7 and 14 days, while the stomatal conductance, intercellular CO 2 content, and transpiration rate were significantly lower than those of the control lines.These results indicated that under salt stress and drought stress, IlWRKY70 alleviated the decrease in photosynthetic efficiency by increasing or maintaining the total chlorophyll content, and increased the plants' water resistance under osmotic stress by closing the stomata to retain water.
Plants under abiotic stress often suffer from oxidative stress and produce excessive oxygen free radicals (ROS), which cause damage to plants.ROS and lipids undergo peroxidation, ultimately producing the cytotoxic substance malondialdehyde (MDA), which endangers plant growth.Superoxide anions (O − 2 ) and H 2 O 2 are the main ROS substances [13].Superoxide dismutase (SOD), catalase (CAT), and peroxidase (POD) are the main enzymes in the plant antioxidant system, effectively removing H 2 O 2 and other substances produced by stress [23].To explore the resistance levels of tobacco overexpressing IlWRKY70 under salt stress and drought stress, the WT and EV lines were selected as controls to detect the SOD, CAT, and POD enzymatic activities and the contents of MDA, O − 2 , and H 2 O 2 in tobacco leaves at 0, 7, and 14 days.The leaves were stained with NBT and DAB to show the accumulation of O − 2 and H 2 O 2 in the leaves, respectively.
The transgenic tobacco seedlings were subjected to natural drought and salt stresses (NaCl concentration of 300 mM) to assess the resistance level.Under normal growth conditions, CK, EV, OE-1, OE-2, and OE-3 exhibited similar growth patterns with no significant differences among the five lines (Figure 6A).However, on the seventh day of salt stress, WT and EV showed lower leaf growth rates compared to the transgenic lines and displayed evident wilting symptoms.At day 14, the transgenic lines demonstrated significantly higher leaf growth rates and plant heights than the WT and EV lines, whereas WT and EV plants wilted, with yellowing signs on the lower leaves along with a slower overall growth rate (Figure 6B).Similarly, on the seventh day of drought stress, both WT and EV plants exhibited obvious wilting symptoms.At day 14, although WT and EV plants exhibited clear wilting throughout their foliage, transgenic plants displayed noticeable wilting on the lower leaves but only slight wilting on the upper leaves along with significantly greater heights compared to those WT and EV plants (Figure 6C).The results showed that there was no significant difference in the contents of MDA, O − 2 , and H 2 O 2 among all the plants at day 0 of the salt stress (Figure 8A-C).With the number of stress days increases, the contents of these three components showed an upward trend, indicating that the plants were gradually subjected to enhanced oxidative stress damage.The contents of MDA, O − 2 , and H 2 O 2 in the three lines overexpressing IlWRKY70 on days 7 and 14 were significantly lower than those in WT and EV (p < 0.05).Similarly, the contents of MDA, O − 2 , and H 2 O 2 in all the lines were not significantly different on day 0 of the drought stress (Figure 8G-I).However, the levels of these substances increased in all the lines on days 7 and 14 under drought stress conditions.The contents of the three substances in the overexpressed tobacco were significantly lower than those in the WT and EV lines (p < 0.05).The NBT and DAB staining results also visually demonstrated that the IlWRKY70 overexpressed tobacco accumulated less O − 2 and H 2 O 2 under salt and drought stresses than the WT and EV plants (Figure 8M-P).The results showed that the enzymatic activities of SOD, CAT, and POD were almost the same at day 0 of the salt stress (Figure 8D-F).However, with the number of stress days increases, the enzymatic activities of SOD, CAT, and POD in the OE-1, OE-2, and OE-3 lines were significantly higher than those in the WT and EV lines on days 7 and 14 (p < 0.05).Consistently, under drought stress, there was no significant difference in the three enzymatic activities at the initial stage of the stress (Figure 8J-L), but with the number of stress days increases, the three enzymatic activities of the OE-1, OE-2, and OE-3 lines at 7 and 14 days were significantly higher than those of the WT and EV lines (p < 0.05).These results indicated that the tobacco overexpressing IlWRKY70 had a stronger ability to remove ROS and accumulate fewer harmful substances under salt and drought stresses than the control and could better cope with salt and drought stresses.The results showed that there was no significant difference in the contents of MDA, O , and H2O2 among all the plants at day 0 of the salt stress (Figure 8A-C).With the number of stress days increases, the contents of these three components showed an upward trend, indicating that the plants were gradually subjected to enhanced oxidative 0.05).Consistently, under drought stress, there was no significant difference in the three enzymatic activities at the initial stage of the stress (Figure 8J-L), but with the number of stress days increases, the three enzymatic activities of the OE-1, OE-2, and OE-3 lines at 7 and 14 days were significantly higher than those of the WT and EV lines (p < 0.05).These results indicated that the tobacco overexpressing IlWRKY70 had a stronger ability to remove ROS and accumulate fewer harmful substances under salt and drought stresses than the control and could better cope with salt and drought stresses.

The Effect of the Overexpressed IlWRKY70 on the Expression Levels of Stress-Related Genes NtSOD, NtCAT, and NtPOD under Salt Stress and Drought Stress
RT-qPCR was used to analyze the changes in the expression levels of stress-responsive genes after overexpressing IlWRKY70 in tobacco.After 7 and 14 days of salt stress (NaCl concentration of 300 mM) and natural drought stress, the expression levels of the NtSOD, NtCAT, and NtPOD genes in the overexpressed IlWRKY70 tobacco were significantly higher than those in the WT and EV lines (Figure 9), indicating that IlWRKY70 could directly or indirectly regulate the expression of downstream stress-responsive genes.
RT-qPCR was used to analyze the changes in the expression levels of stressresponsive genes after overexpressing IlWRKY70 in tobacco.After 7 and 14 days of salt stress (NaCl concentration of 300 mM) and natural drought stress, the expression levels of the NtSOD, NtCAT, and NtPOD genes in the overexpressed IlWRKY70 tobacco were significantly higher than those in the WT and EV lines (Figure 9), indicating that IlWRKY70 could directly or indirectly regulate the expression of downstream stressresponsive genes.

Discussion
An increasing number of studies has shown that WRKY transcription factors play a crucial role in plants' responses to biotic or abiotic stress.Recent studies have shown that different genes within the WRKY family play an important role in improving plants' resistances to disease [24,25], salt [26], and drought [27].However, studies on the resistance functions of these WRKY genes have mostly concentrated on crop plants [13,28]

Discussion
An increasing number of studies has shown that WRKY transcription factors play a crucial role in plants' responses to biotic or abiotic stress.Recent studies have shown that different genes within the WRKY family play an important role in improving plants' resistances to disease [24,25], salt [26], and drought [27].However, studies on the resistance functions of these WRKY genes have mostly concentrated on crop plants [13,28] and have rarely been explored in ornamental flowers, especially in the monocotyledonous plant I. laevigata.
This study cloned and identified the WRKY70 gene of I. laevigata, which has the highest homology with the WRKY70 protein of Asparagus officinalis in monocotyledonous plants.IlWRKY70 has a classic WRKY domain and a C2HC zinc finger structure, belonging to the Group III WRKY family.IlWRKY70 is in the nucleus, consistent with the reported localization of its homologous genes, indicating its ability to act as a transcription factor.WRKY70 has been confirmed to be involved in plant drought and salt stress responses.However, in early studies, WRKY70 was considered as a negative regulatory factor for salt and drought stresses.In Populus simonii × P. nigra, there are many cis-acting elements in the PsnWRKY70 promoter that respond to biotic and abiotic stresses, and PsnWRKY70 has self-regulation ability.Under salt stress, the expression of PsnWRKY70 is downregulated in both wild and overexpressing poplar trees.Poplar plants that inhibit PsnWRKY70 have stronger salt resistance [21].Through research in arabidopsis, the WRKY70 single mutant and the WRKY70 and WRKY54 double mutants have better drought resistance, which may be achieved by regulating leaf stomatal closure [22].However, in the WRKY70 and WRKY54 double mutants, the expression of 58 response genes to osmotic stress was strongly suppressed, and the proline content in the plant was significantly reduced.WRKY70 may not only be a negative regulatory factor of abiotic stress but also has the potential to enhance osmotic stress.In recent years, this hypothesis has been confirmed because the WRKY70 gene of Myrothamnus flabellifolius is significantly upregulated in the early dehydration stage, and the introduction of WRKY70 to arabidopsis can significantly improve the salt and drought resistances of arabidopsis [19].Meanwhile, in this study, the significant expression patterns of IlWRKY70 under salt and drought stresses also indicate that it may play a key role in regulating the response of I. laevigata to salt and drought stresses.
In abiotic stress environments, the ability of seeds to germinate and grow normally is a prerequisite for plants to reproduce and survive in harsh environments.Plant roots are highly sensitive to salt and drought stresses [1], and the root length can indicate the underground growth status and resistance level of plants [29][30][31].Transgenic lines treated with NaCl stresses at different gradients (0, 100, 150, and 200 mM) for 15 days and drought stresses at different gradients (mannitol concentrations of 0, 100, 200, and 300 mM) for 15 days showed higher germination rates, longer total root lengths, and higher fresh weights.This indicates that the overexpression of IlWRKY70 improves the salt and drought resistances of transgenic tobacco seeds to a certain extent.
Plants provide the organic matter necessary for their own growth through photosynthesis, which is one of the most critical biological processes for plant survival [32].In addition, salt and drought stresses cause plants to lose water owing to high osmotic pressure; this, in turn, leads to stomatal closure, reducing the intercellular CO 2 content and blocking the supply of raw materials for plant photosynthesis [32,33].The PSII primary light-energy-conversion efficiency (Fv/Fm) is commonly used to represent the maximum photosynthetic capacity of plants [34].The tobacco seedlings overexpressed with IlWRKY70 exhibited better growth statuses, higher net photosynthetic rates, higher chlorophyll contents, and higher PSII primary light-energy-conversion efficiencies under both salt and drought stresses.And overexpressing IlWRKY70 tobacco plants have a lower stomatal conductance, lower intercellular CO 2 content, and lower transpiration rate.This may be due to the smaller stomatal openings of transgenic plants under drought and salt stresses, reducing water evaporation and gas exchange and increasing the plant's water retention capacity.This finding aligns with the research by Sun and Xiang et al., who demonstrated that the overexpression of WRKY70 does not affect the degree of stomatal opening in plants under regular conditions.However, it has been shown that WRKY70 overexpression can decrease the degree of stomatal opening during drought stress.[18,19].The research results indicate that IlWRKY70 can maintain more chlorophyll content to cope with salt and drought stresses and may reduce the degree of plant stomatal opening to maintain the water content of plants during the stress process.However, further research is needed on how IlWRKY70 maintains or produces chlorophyll content and how it participates in plant stomatal regulation.
Plants produce a large amount of ROS substances, such as superoxide anions and H 2 O 2 , under various abiotic stresses [35].ROS can damage plant cell membranes and produce toxins, such as MDA, that harm plant growth [36,37].To prevent the excessive accumulation of ROS under stress, plant cells have evolved antioxidant mechanisms, such as enzymatic systems, including common antioxidant enzymes, such as SOD, CAT, and POD [23,38,39].Tobacco seedlings overexpressing IlWRKY70 exhibit less accumulation of MDA, superoxide anions, and H 2 O 2 under salt and drought stresses while also exhibiting higher SOD, CAT, and POD enzymatic activities.Compared with the control plants, the transgenic tobacco possessed expression levels of genes related to ROS clearance under salt and drought stresses that were significantly increased, indicating that IlWRKY70 may enhance the plant's ability to scavenge ROS by increasing the expression of genes related to plant antioxidant enzyme systems in response to salt and drought stresses.
In terms of the responses of WRKY70 to salt and drought stresses, previous studies have focused on WRKY70 derived from dicot plants and found that WRKY70 derived from different plants may have different effects on salt and drought stresses.IlWRKY70 is the first WRKY70 gene to be extracted from a monocotyledon ornamental plant species and demonstrated to be involved in the response of I. laevigata to drought and salt stresses.Although our indirect validation of IlWRKY70's positive effect on drought and salt stresses only in tobacco has some limitations due to the lack of a genetic transformation system in the monocotyledon I. laevigata, it has pioneered the broadening of the range of sources of WRKY70 research and is a good foundation for further research on drought and salt tolerance mechanisms in monocot plants.In the future, it is expected that IlWRKY70 will be used or WRKY70 will be obtained from very drought-and salt-tolerant I. lactea and I. halophila to improve the drought resistance of irises that grow in humid environments, such as I. ensata, and to improve the drought tolerances of varieties of I. ensata var.hortensis through crossbreeding.Of course, the resistance breeding of many famous monocot ornamental plants, may has a new foothold.

Plant Materials and Growth Conditions
I. laevigata plants were cultivated in the nursery at Northeast Forestry University's College of Landscape Sciences.Onions for subcellular localization studies were procured from Carrefour Supermarket, while N. tabacum (ordinary tobacco) seeds were provided by the research group's laboratory.The tobacco seeds were sterilized with 75% alcohol (LIRCON, Dezhou, China) on a sterile platform for 1 min, rinsed three times with sterile water, sterilized with 2% NaClO (XiLONG, Shenzhen, China) for 10 min, rinsed five times with sterile water, and then planted in MS sterile medium (Hope Bio-Technology, Qingdao, China).The plants were incubated at 25 • C with a photoperiod of 14 h of light and 10 h of darkness, and the plants could be used for infection when they bore 4-6 true leaves.

Treatment of I. laevigata under Salt Stress and Drought Stress
To further verify whether IlWRKY70 is involved in the responses of I. laevigata to drought and salt stresses, one-year-old I. laevigata plants with consistent growth were selected for water culture for seven days.They were treated with NaCl at a concentration of 150 mM and PEG-6000 at a concentration of 20%.The real-time expression level of IlWRKY70 in the leaves was detected after 0, 1, 3, 6, 12, and 24 h.

IlWRKY70 Gene Cloning and Phylogenetic Tree Analysis
The total RNA was extracted from the roots of I. laevigata using the Plant RNA Kit (OMEGA).The integrity of the total RNA was assessed through agarose gel electrophoresis, and high-quality RNA was subsequently reverse-transcribed into complementary DNA (cDNA) using the Primer Script TM RT Reagent Kit (TaKaRa, Beijing, China).In accordance with the sequence previously annotated as WRKY70 (designated as IlWRKY70) in the root transcriptome of I. laevigata in our prior research, cloning primers were designed using Primer Premier 5.The obtained primer sequences were as follows: 5 -ATGGAAGGTACCAAAACTGG-3 and 5 -ATAGAGAGTTCCTCCTTGATTGTAATC-3 .The sequences were cloned using the KOD-Plus-Neo Kit (ToYoBo, Shanghai, China), with an annealing temperature set at 56 • C. Subsequently, the cloned sequences were inserted into the Cloning vector pEASY ® -Blunt Zero Cloning Kit (TransGen, Beijing, China) and transformed into Escherichia coli DH5α (WEIDI).WRKY70 protein sequences from various species were downloaded from the National Center for Biotechnology Information (NCBI) website (https://www.ncbi.nlm.nih.gov/,accessed on 20 July 2022).Multiple sequence alignment was conducted using DNAMAN (Version 5.2.2), and phylogenetic analysis was carried out using MEGA 5.0 (Version 10.1.8).To analyze the physicochemical properties of IlWRKY70, the ExPASy website's ProtParam tools (https://web.expasy.org/protparam/,accessed on 20 July 2022) and ProtScale tools (https://web.expasy.org/protscale/,accessed on 20 July 2022) were employed.The experimental procedures followed the instructions provided with the respective kits, and the primers were synthesized by RuiBiotech Inc. (China, Harbin, China)

Expression Vector Construction
The pCAMBIA1300:IlWRKY70-GFP carrier was constructed for heterologous expression by homologous recombination.In the first step, SnapGene (version 4.2.4) was used to design homologous recombination primers based on the target fragment and the plant vector sequence, and the SalI and BamHI restriction sites were inserted.In the second step, the following homologous recombination primers for IlWRKY70 were used: 5 -TTGATACATATGCCCGTCGACATGGAAGGTACCAAAACTGG-3 and 5 -CCCTTGCTCACCATGGATCCATAGAGAGTTCCTCCTTGAT-3 , underscores represent homology arms.With positive plasmid cloning as the template, the target fragment with the homology arm was amplified using a KOD-Plus-Neo Kit (ToYoBo, Shanghai, China), and the annealing temperature was 63 • C. Next, SalI and BamHI enzymes (TaKaRa, Beijing, China) were selected for the linearization of the plant vector, and the linearized product was recombined with the homology arm amplification product using ClonEx-pressII One-Step Cloning Kit (Vazyme, Nanjing, China).The recombinant pCAMBIA1300-IlWRKY70-GFP was transformed into E. coli DH5α (WEIDI, Shanghai, China) for sequencing and preservation.Finally, the positive pCAMBIA1300-IlWRKY70-GFP plasmid obtained by sequencing was transferred into A. tumefaciens GV3101 (WEIDI, Shanghai, China) for subsequent infection experiments.The experimental methods were according to the instructions for the use of each kit.Primer synthesis and sequencing services were provided by RuiBiotech Inc. (Harbin, China)

Subcellular Localization
Using the gene gun (PDS-1000) method [40], the pCAMBIA1300:IlWRKY70-GFP and empty-vector pCAMBIA1300:GFP plasmids were transiently transformed into onion epidermal cells, and the nuclei were stained with DAPI dye [41].After 24 h of incubation in MS medium at 25 • C in the dark, the GFP expression in cells was observed using a fluorescence microscope (Leica) excited at 395 nm and DAPI nuclear localization dyestuff excited at 358 nm.

Establishment of Transgenic Lines
Agrobacterium GV3101 strains harboring the pCAMBIA1300:IlWRKY70-GFP plasmid and the empty-vector pCAMBIA1300-GFP plasmid were activated, and transgenic lines were generated through the leaf-disc method mediated by A. tumefaciens [42].Plant genomic DNA from the transformed plants served as a template and was extracted using the plant genomic DNA extraction kit (TianGen, Beijing, China).PCR-positive plants were identified using IlWRKY70 homologous-arm recombinant primers, as described in the previous vector construction step.T0 generation plants were selected on an MS medium supplemented with 25 mg/L Hygromycin B and confirmed via PCR.Subsequently, seeds from inbred lines were meticulously chosen in successive generations until the T3 generation.Three transgenic lines (named OE-1, OE-2, and OE-3) and one empty-vector line (EV) were randomly selected for further experiments.

Treatment of Transgenic N. tabacum under Salt Stress and Drought Stress
To investigate the salt and drought tolerances of IlWRKY70-overexpressing tobacco lines in comparison with control lines, the seeds and seedlings of the transgenic plants were treated with salt and drought stresses, respectively, and the stress conditions were set according to related studies [19,43].During the seed-stress treatment, wild tobacco seeds and T3 seeds from transgenic and empty-vector lines were sown on MS media containing varying concentrations of NaCl (0, 100, 150, and 200 mM) and mannitol (0, 100, 200, and 300 mM).These seeds were placed in an environment at a temperature of 26 • C, subjected to 16 h of light and 8 h of dark cycles for a duration of 15 days, and then monitored for any observable phenotypic changes.The samples designated for the total root length measurements were sown in square Petri dishes under identical stress conditions and were oriented vertically to ensure vertical root growth, facilitating the convenient measurement of the total root length [42].In the seedling-stress treatment, the wild-type, transgenic, and empty-vector positive plants were first grown for 30 days at 28 • C and a relative humidity of 75% under 16 h of light and 8 h of darkness, and the cultivation medium comprised peat soil, perlite, and vermiculite mixed in a 3:1:1 ratio.Subsequently, plants in the same growth stage were selected for either salt-stress or drought-stress treatments.For the salt-stress treatment, a 100 mL solution of NaCl at a concentration of 300 mM was applied to the cultivation substrate every three days.As for the drought treatment, it involved in subjecting the plants to natural drought conditions for a span of 14 days.Phenotypic observations and physiological data measurements were conducted on days 0, 7, and 14.

Phenotypic Observation and Physiological Data Measurement of Transgenic Plants under Salt and Drought Stresses
To ensure the accuracy of the data, three plants were selected from each line of each treatment gradient for measurements which were repeated three times.After 15 days of treatment, the germination rate, total root length, and fresh weight of the seeds under the stress treatments were observed and recorded.Total root length data were obtained using a root scanner (Epson Expression 11000XL, Epson, Beijing, China).For the seedlings under the stress treatments, data were measured at 0, 7, and 14 days of their stress cycle.The net photosynthetic rate, stomatal conductance, intercellular CO 2 concentration, and transpiration rate of the plants were measured using a portable photosynthesis meter (LI-6400, ecotek, Beijing, China).The total chlorophyll content was measured using acetone extraction [44].The second fully expanded leaf of the upper part of the plant was selected, and the leaves were cut off after being treated with tin foil for 30 min in the dark.The chlorophyll fluorescence data were measured using a portable modulated chlorophyll fluorometer (PAM-2500, WALZ, Effeltrich, Germany) [42].The content of malondialdehyde (MDA), the activity of superoxide dismutase (SOD), and the activity of peroxidase (POD) were determined according to the research method of Wang [43].The catalase (CAT) activity was measured using the catalase assay kit G0105F (Grace Biotechnology, Shanghai, China), and the hydrogen peroxide content was measured using the hydrogen peroxide assay kit G0112F (Grace Biotechnology, Shanghai, China).The superoxide anion content was measured with the use of the superoxide anion kit G0116F (Grace Biotechnology, Shanghai, China) according to the method provided in the instructions of the kit.The stressed tobacco leaves were cut into leaf discs with a diameter of 1.5 cm, referring to the method of Wang [43], and p-nitro-blue tetrazolium chloride (NBT) and 3,3 -diaminobenzidine tetrahydrochloride (DAB) stainings were used to detect the contents of superoxide anions and hydrogen peroxide in the leaves, respectively.The expression patterns of IlWRKY70 in different parts of I. laevigata were measured from roots, tubers, and leaves of normal growth, and the responses of IlWRKY70 in I. laevigata were measured at 0, 1, 3, 6, 12, and 24 h after salt and drought stresses.Tobacco leaves with a positive overexpression of IlWRKY70 at 30 days of growth were used to measure the expression of IlWRKY70.The expression levels of stress-response genes (NtSOD, Nt-CAT, and NtPOD) were measured in WT, EV, and three overexpressed IlWRKY70 lines of tobacco leaves at 0, 7, and 14 days of NaCl and drought stresses.The method of the total RNA extraction and reverse transcription to cDNA is the same as the method of the total RNA extraction and reverse transcription above.The IlPP2A and NtTUBA genes are the internal reference genes of I. laevigata and tobacco, respectively.Real-time quantitative PCR was performed using the SYBR Green I method.The specific experimental procedures were followed according to the instructions of the UltraSYBR Mixture (CWBIO, Beijing, China).The results were calculated as 2 −∆∆CT .The quantitative primers were as follows: IlPP2A, 5 -TCGCATCAAGACAGGAGAAG-3 and 5 -GGGAATGAGAAGGGAAGAAT-3 ; NtTUBA, 5 -CTCCTATGCTCCTGTCATTTC-3 and 5 -GGCGAGGATCACACTTAAC-3 ; IlWRKY70, 5 -CGCAACTCGGGGCAATATTG-3 and 5 -CACTGCTGACTACGTCCTCG-3 ; NtSOD, 5 -CTCCTACCGTCGCCAAAT-3 and 5 -GCCCAACCAAGAGAACCC-3 ; NtPOD, 5 -CCTCAGCTTCAAGCATTATGTCCA-3 and 5 -ACCTTTGTAGAAGCATCGGTCCAC-3 ; NtCAT, 5 -AGGTACCGCTCATTCACACC-3 and 5 -AAGCAAGCTTTTGACCCAGA-3 .

Statistical Analyses
Excel (Version 2021) was used for data recording and statistic analysis.The least significant difference method was used to test the data in the confidence interval (p < 0.05), data analysis was performed using SPSS (Version 26), and Origin (Version 2021) was used for drawing graphs.

Conclusions
In summary, IlWRKY70 plays a significant role in the responses of I. laevigata to salt and drought stresses.The overexpressionof IlWRKY70 can strengthen the abilities of tobacco seeds and seedlings to resist salt stress and drought stress; enhance the seed germination rate, total root length, and fresh weight; relatively raise the level of photosynthesis in seedlings under salt stress and drought stress; reduce the plant's stomatal conductance to preserve the plant's moisture contents; and enhance the antioxidant enzyme system, which makes tobacco more resistant to salt and drought stresses.This study provides insight into important functional genes for salt-and drought-tolerance breeding in iris plants, laying the foundation for revealing the salt-and drought-tolerance mechanisms of I. laevigata.

Figure 1 .
Figure 1.Sequence analysis and phylogenetic tree analysis of IlWRKY70.(A) Evolutionary tree of IlWRKY70 and other plant WRKY70.The red box is the highly conserved domain "WRKYGQK" of the WRKY family.The pink background color represents >75% similarity.The black background color represents 100% agreement.The red triangle indicates WRKY's zinc finger structure.(B) Evolutionary tree of IlWRKY70 and its homologs.Black dots indicate IlWRKY70 protein from I. laevigata.

Figure 1 .
Figure 1.Sequence analysis and phylogenetic tree analysis of IlWRKY70.(A) Evolutionary tree of IlWRKY70 and other plant WRKY70.The red box is the highly conserved domain "WRKYGQK" of the WRKY family.The pink background color represents >75% similarity.The black background color represents 100% agreement.The red triangle indicates WRKY's zinc finger structure.(B) Evolutionary tree of IlWRKY70 and its homologs.Black dots indicate IlWRKY70 protein from I. laevigata.

Figure 2 .
Figure 2. Expression analysis of IlWRKY70.(A) Expression analysis of IlWRKY70 in roots, tubers, and leaves of I. laevigata.(B) Expression analysis of IlWRKY70 in response to NaCl stress at different times.(C) Expression analysis of IlWRKY70 in response to PEG-6000 stress at different times.The different letters on the top of the bar chart are significantly different from each other (p < 0.05).

Figure 3 .
Figure 3. Subcellular localization of IlWRKY70 protein.pCAMBIA1300:GFP and pCAMBIA1300:IlWRKY70-GFP were transfected into onion epidermal cells; and after DAPI staining, they were observed by fluorescence microscopy using 395 nm excitation GFP and 358 nm excitation DAPI nuclear localization dye, respectively.From left to right, green fluorescence of GFP, blue light of DAPI nuclear localization dye, cells under bright field, and cells under superposition of GFP and bright field.The red bar represents a scale bar of 20 μm.

Figure 2 .
Figure 2. Expression analysis of IlWRKY70.(A) Expression analysis of IlWRKY70 in roots, tubers, and leaves of I. laevigata.(B) Expression analysis of IlWRKY70 in response to NaCl stress at different times.(C) Expression analysis of IlWRKY70 in response to PEG-6000 stress at different times.The different letters on the top of the bar chart are significantly different from each other (p < 0.05).

Figure 2 .
Figure 2. Expression analysis of IlWRKY70.(A) Expression analysis of IlWRKY70 in roots, tubers, and leaves of I. laevigata.(B) Expression analysis of IlWRKY70 in response to NaCl stress at different times.(C) Expression analysis of IlWRKY70 in response to PEG-6000 stress at different times.The different letters on the top of the bar chart are significantly different from each other (p < 0.05).

Figure 3 .
Figure 3. Subcellular localization of IlWRKY70 protein.pCAMBIA1300:GFP and pCAMBIA1300:IlWRKY70-GFP were transfected into onion epidermal cells; and after DAPI staining, they were observed by fluorescence microscopy using 395 nm excitation GFP and 358 nm excitation DAPI nuclear localization dye, respectively.From left to right, green fluorescence of GFP, blue light of DAPI nuclear localization dye, cells under bright field, and cells under superposition of GFP and bright field.The red bar represents a scale bar of 20 μm.

Figure 3 .
Figure 3. Subcellular localization of IlWRKY70 protein.pCAMBIA1300:GFP and pCAM-BIA1300:IlWRKY70-GFP were transfected into onion epidermal cells; and after DAPI staining, they were observed by fluorescence microscopy using 395 nm excitation GFP and 358 nm excitation DAPI nuclear localization dye, respectively.From left to right, green fluorescence of GFP, blue light of DAPI nuclear localization dye, cells under bright field, and cells under superposition of GFP and bright field.The red bar represents a scale bar of 20 µm.

Figure 4 .
Figure 4. Establishment of IlWRKY70 transgenic tobacco lines.(A) Schematic representation of the pCAMBIA1300:IlWRKY70-GFP vector construction.(B) PCR validation gel plot of the successful construction of pCAMBIA1300:IlWRKY70-GFP vector; M is marker of length 2000.The numbers 1-10 represent a positive plasmid.(C) Positive validation gel plot of IlWRKY70 transgenic T0 generation plants; M is marker of length 2000, H2O is negative control, P is pCAMBIA1300:IlWRKY70-GFP plasmid positive control, CK is WT tobacco, and 1-10 is T0 transgenic tobacco.(D) Relative expression of IlWRKY70 in three T3 transgenic tobacco lines.

Figure 4 .
Figure 4. Establishment of IlWRKY70 transgenic tobacco lines.(A) Schematic representation of the pCAMBIA1300:IlWRKY70-GFP vector construction.(B) PCR validation gel plot of the successful construction of pCAMBIA1300:IlWRKY70-GFP vector; M is marker of length 2000.The numbers 1-10 represent a positive plasmid.(C) Positive validation gel plot of IlWRKY70 transgenic T0 generation plants; M is marker of length 2000, H 2 O is negative control, P is pCAMBIA1300:IlWRKY70-GFP plasmid positive control, CK is WT tobacco, and 1-10 is T0 transgenic tobacco.(D) Relative expression of IlWRKY70 in three T3 transgenic tobacco lines.

Figure 5 .
Figure 5. Overexpression of the IlWRKY70 gene enhanced the response of tobacco seeds to salt and drought stresses.(A) Schematic diagram of tobacco seed zoning for different lines.The white horizontal line in the figure represents 2 cm.(B-D) Germination and growth of tobacco seeds from WT, EV, and OE lines after 15 days of different salt stress treatments.(E) Germination and growth of tobacco seeds from WT, EV, and OE lines after 15 days in MS medium.(F-H) Germination and growth of tobacco seeds from WT, EV, and OE lines after 15 days of different drought stress treatments.(I-K) Germination rate, total root length, and fresh weight of tobacco seeds in each line treated with different gradients of salt stress for 15 days.(L-N) Germination rate, total root length, and fresh weight of tobacco seeds in different lines treated with different gradients of drought stress for 15 days.The letters above the bar chart represent significant differences between each other, p < 0.05.

Figure 5 .
Figure 5. Overexpression of the IlWRKY70 gene enhanced the response of tobacco seeds to salt and drought stresses.(A) Schematic diagram of tobacco seed zoning for different lines.The white horizontal line in the figure represents 2 cm.(B-D) Germination and growth of tobacco seeds from WT, EV, and OE lines after 15 days of different salt stress treatments.(E) Germination and growth of tobacco seeds from WT, EV, and OE lines after 15 days in MS medium.(F-H) Germination and growth of tobacco seeds from WT, EV, and OE lines after 15 days of different drought stress treatments.(I-K) Germination rate, total root length, and fresh weight of tobacco seeds in each line treated with different gradients of salt stress for 15 days.(L-N) Germination rate, total root length, and fresh weight of tobacco seeds in different lines treated with different gradients of drought stress for 15 days.The letters above the bar chart represent significant differences between each other, p < 0.05.

Figure 6 .
Figure 6.Phenotypic changes in tobacco seedlings overexpressing the IlWRKY70 gene under salt and drought stresses.(A) Top view and elevation of the growth status of WT, EV, and OE lines of

Figure 6 .
Figure 6.Phenotypic changes in tobacco seedlings overexpressing the IlWRKY70 gene under salt and drought stresses.(A) Top view and elevation of the growth status of WT, EV, and OE lines of tobacco at 0, 7, and 14 days in the normal growth state.(B) Top view and elevation of the growth status of WT, EV, and OE lines of tobacco at 0, 7, and 14 days under NaCl stress at 300 mM.(C) Top view and elevation of the growth status of WT, EV, and OE lines of tobacco at 0, 7, and 14 days under natural drought stress.The scale bar is 20 cm.

Figure 7 .
Figure 7. Analysis of various photosynthetic and transpiration rate indexes of tobacco seedlings overexpressing IlWRKY70 under salt and drought stresses.(A-F) Net photosynthetic rate, total chlorophyll content, Fv/Fm, stomatal conductance, intercellular CO2 content, and transpiration rate of WT, EV, and OE tobacco lines at 0, 7, and 14 days under 300 mM NaCl stress.(G-L) Net photosynthetic rate, total chlorophyll content, Fv/Fm, stomatal conductance, intercellular CO2 content, and transpiration rate of WT, EV, and OE tobacco lines under natural drought stress at 0, 7, and 14 days.The letters above the bar chart represent significant differences between each other, p < 0.05.

Figure 7 .
Figure 7. Analysis of various photosynthetic and transpiration rate indexes of tobacco seedlings overexpressing IlWRKY70 under salt and drought stresses.(A-F) Net photosynthetic rate, total chlorophyll content, Fv/Fm, stomatal conductance, intercellular CO 2 content, and transpiration rate of WT, EV, and OE tobacco lines at 0, 7, and 14 days under 300 mM NaCl stress.(G-L) Net photosynthetic rate, total chlorophyll content, Fv/Fm, stomatal conductance, intercellular CO 2 content, and transpiration rate of WT, EV, and OE tobacco lines under natural drought stress at 0, 7, and 14 days.The letters above the bar chart represent significant differences between each other, p < 0.05.

Figure 8 .
Figure 8. Analysis of physiological indexes of tobacco seedlings overexpressing IlWRKY70 under salt stress and drought stress.(A-F) The contents of MDA, O , H2O2 and the activities of SOD, CAT,

Figure 8 .
Figure 8. Analysis of physiological indexes of tobacco seedlings overexpressing IlWRKY70 under salt stress and drought stress.(A-F) The contents of MDA, O − 2 , H 2 O 2 and the activities of SOD, CAT, and POD in WT, EV, and OE tobacco leaves were measured at 0, 7, and 14 days after 300 mM NaCl stress.(G-L) The contents of MDA, O − 2 , H 2 O 2 and the activities of SOD, CAT, and POD in the leaves of the WT, EV, and OE lines were measured at 0, 7, and 14 days of natural drought stress.Different letters on the bar chart represent significant differences, p < 0.05.(M,N) Plots of leaf disc staining using NBT and DAB in WT, EV, and OE lines at 0, 7, and 14 days of NaCl stress at 300 mM.(O,P) Plots of leaf disc staining using NBT and DAB in WT, EV, and OE lines at 0, 7, and 14 days of natural drought stress.Deeper NBT staining means more O − 2 accumulation, deeper DAB staining means more H 2 O 2 accumulation, and more O − 2 and H 2 O 2 accumulation means more severe plant damage.The black horizontal line in the figure represents 1.5 cm, the diameter of the leaf disc.

Figure 9 .
Figure 9. Expression analysis of genes related to salt stress and drought stress in over-expressed IlWRKY70 tobacco.(A-C) Real-time expression of NtSOD, NtCAT, and NtPOD genes in WT, EV, and OE tobacco lines at 0, 7, and 14 days of NaCl stress at 300 mM.(D-F) Real-time expression of NtSOD, NtCAT, and NtPOD genes in tobacco leaves of WT, EV, and OE lines at 0, 7, and 14 days of drought stress.Different letters on the bar chart represent significant differences, p < 0.05.

Figure 9 .
Figure 9. Expression analysis of genes related to salt stress and drought stress in over-expressed IlWRKY70 tobacco.(A-C) Real-time expression of NtSOD, NtCAT, and NtPOD genes in WT, EV, and OE tobacco lines at 0, 7, and 14 days of NaCl stress at 300 mM.(D-F) Real-time expression of NtSOD, NtCAT, and NtPOD genes in tobacco leaves of WT, EV, and OE lines at 0, 7, and 14 days of drought stress.Different letters on the bar chart represent significant differences, p < 0.05.