Identification of the Cytosolic Glucose-6-Phosphate Dehydrogenase Gene from Strawberry Involved in Cold Stress Response

Abstract

Glucose-6-phosphate dehydrogenase (G6PDH) plays an important role in plant stress responses. Here, five FaG6PDH sequences were obtained in strawberry, designated as FaG6PDH-CY, FaG6PDH-P1, FaG6PDH-P1.1, FaG6PDH-P2 and FaG6PDH-P0, which were divided into cytosolic (CY) and plastidic (P) isoforms based on the bioinformatic analysis. The respective FaG6PDH genes had distinct expression patterns in all tissues and at different stages of fruit development. Notably, FaG6PDH-CY was the most highly expressed gene among five FaG6PDH members, indicating it encoded the major G6PDH isoform throughout the plant. FaG6PDH positively regulated cold tolerance in strawberry. Inhibition of its activity gave rise to greater cold-induced injury in plant. The FaG6PDH-CY transcript had a significant increase under cold stress, similar to the G6PDH enzyme activity, suggesting a principal participant in response to cold stress. Further study showed that the low-temperature responsiveness (LTR) element in FaG6PDH-CY promoter can promote the gene expression when plant encountered cold stimuli. Besides, FaG6PDH-CY was involved in regulating cold-induced activation of antioxidant enzyme genes (FaSOD, FaCAT, FaAPX and FaGR) and RBOH-dependent ROS generation. The elevated FaG6PDH-CY enhanced ROS-scavenging capability of antioxidant enzymes to suppress ROS excessive accumulation and relieved the oxidative damage, eventually improving the strawberry resistance to cold stress.

1. Introduction

The oxidative pentose phosphate pathway (OPPP) generates nicotinamide adenine dinucleotide phosphate (NADPH) for reductive biosynthesis of metabolic products including fatty acids and amino acids, as well as many intermediary metabolites such as ribulose-5-phosphate for nucleotide synthesis and erythrose-4-phosphate for aromatic amino acids production, which plays an important role in plant life cycle [1].

Glucose-6-phosphate dehydrogenase (G6PDH, EC1.1.1.49) is well-known as the first and rate-limiting enzyme of OPPP that catalyzes the conversion of glucose-6-phosphate to 6-phosphogluconolactone and exists widely in animals, plants and prokaryotes [1]. According to their subcellular localization in plant, G6PDHs are divided into cytosolic and plastidic isoforms [2,3]. Cytosolic isoform (Cy-G6PDH) accounts for the major part of total activity of the enzyme in plant cells and generally shows a low sensitivity to reducing power, and its amino acid sequence lacks a transit peptide at the N-end [4,5,6]. Differences in the specific antibodies, biochemical characteristics and gene expression pattern represent a further point for the discrimination of the plastidic isoforms. Two compartmented isoforms in plastids have been defined as P1-G6PDH (also known as chloroplastic G6PDH) that seems to be exclusively found in green tissues, and P2-G6PDH (also known as plastidic G6PDH) that is mainly detected in roots and heterotrophic tissues. P2-G6PDH was less sensitive to NADPH feedback inhibition than P1-G6PDH [7,8]. Subsequently, the basic plastidic but catalytically inactive P0-G6PDH is identified and it can help P1-G6PDH enter peroxisomes [9,10].

In addition to its involvement in plant growth and development, the critical functions of G6PDHs in stress-response mechanisms have been widely documented, such as drought [11], salt [12], cold [13], heat [14], heavy metals [15], nutrient deficiency [16] and disease [17]. In response to various stress, plants have evolved efficient enzymatic and non-enzymatic antioxidative defense systems to suppress accumulation of reactive oxygen species (ROS). G6PDHs provide NADPH for the antioxidant system to protect cells from oxidative damage and maintain cellular homeostasis, thereby enhancing stress resistance in plants [18]. It has been found that overexpression of cytosolic PsG6PDH gene from Populus suaveolens improves tobacco cold tolerance by supplying sustainable levels of NADPH for SOD and POD scavenging reactions [13]. Additionally, G6PDHs play a central role in the control of output of GSH from its oxidative form (GSSG) by utilizing NADPH, which contribute to enhance ascorbate-glutathione (AsA–GSH) cycle rate and maintain H₂O₂ homeostasis under salt stress [19].

Although a major involvement of G6PDHs in stress responses has been widely proven in several plants, little is known about actual biological function of it in fruit trees. Strawberry is a model fruit crop in Rosaceae genomics research and also has high economic and nutritional value. However, strawberry is often subjected to extreme sporadic chilling injury in the short term in early spring and winter as a result of inadequate insulation measures, which causes enormous economic loss. Thus, the goal of the present paper is to investigate the G6PDHs specific role in response to cold stress, which contributes to strawberry breeding for cold resistance.

2. Results

2.1. Cloning and Characterization of G6PDH Genes in Strawberry

Five FaG6PDH gene sequences, respectively referred to as FaG6PDH-CY, FaG6PDH-P1, FaG6PDH-P1.1, FaG6PDH-P2 and FaG6PDH-P0 were isolated from strawberry (Table S1). The analysis of physicochemical properties showed that the open reading frame (ORF) length of FaG6PDHs ranged from 1542 to 1881bp and deduced proteins had 513 to 626 amino acid residues. The protein molecular weight (MW) and theoretical pI varied from 58.5 to 70.8kDa, 5.93 to 8.57, respectively. All FaG6PDH proteins had no signal peptide and transmembrane helix. Besides, FaG6PDH-CY had no transit peptide (Table S2), which can be also confirmed from the multiple sequence alignment that plastidic isoforms were much longer than the FaG6PDH-CY at the N-terminal. Clearly, FaG6PDHs were highly conservative and contained typical domains of the G6PDH family including Rossman fold, substrate-binding site and NADP⁺ binding site (Figure S1). In addition, G6PDHs in strawberry were divided into cytosolic (CY) and plastidic (P1, P2 and P0) types as other species in the phylogenetic tree (Figure 1).

2.2. Expression Profile of FaG6PDHs in Different Tissues and during the Fruit Development

FaG6PDHs constitutively expressed among different tissues, but they displayed variable expression patterns (Figure 2). FaG6PDH-CY was the most highly expressed gene among five FaG6PDH members and had the highest expression level in root. FaG6PDH-P1 expressed more highly in leaf, root and flower than stem and fruit. FaG6PDH-P1.1 transcript kept low-abundance in almost all tissues except flower. FaG6PDH-P2 had the highest transcript abundance in root, followed by old leaf, and had lowest expression level in stem. FaG6PDH-P0 had a relatively significant transcript accumulation in flower and stem (Figure 2A). Clearly, FaG6PDH-CY expression was remarkably higher than other genes during the fruit development, especially at initial red and small green stages. FaG6PDH-P1 and FaG6PDH-P1.1 displayed very low transcript abundance at all stages of fruit development. FaG6PDH-P2 showed the similar expression pattern to FaG6PDH-P0, a relatively higher expression level only at small green and initial red stages (Figure 2B).

2.3. Effect of FaG6PDH Enzyme Activity on Related Physiological Indexes in Response to Cold Stress

The enzymatic assay showed that the FaG6PDH activity significantly increased under cold stress. Using glucosamine (GLUCM, a G6PDH inhibitor) to modulate the FaG6PDH activity, a significant decrease in the FaG6PDH activity was achieved in the control and cold stress (Figure 3A). After the FaG6PDH activity was inhibited, superoxide dismutase (SOD) activity notably decreased, and peroxidase (POD) activity had no significant change, and catalase (CAT) activity evidently decreased only in cold stress (Figure 3D–F). Inhibition of FaG6PDH activity with GLUCM treatment did not affect proline, soluble protein and soluble sugar contents, although these osmoregulation substances were induced by cold stress (Figure 3G–I). Additionally, the malondialdehyde (MDA) content and electrolyte leakage were notably upregulated using GLUCM when strawberry was exposed to cold stress, indicating that plant cell membrane was damaged more seriously when FaG6PDH activity was suppressed under cold stress (Figure 3B,C).

2.4. Identification of FaG6PDH Genes Related to Cold Stress

In order to investigate the sensitivity of five FaG6PDH genes to the cold stimuli, transcript abundances of them were detected during the short-term response to cold stress. FaG6PDH-CY transcript rapidly accumulated after 3 h cold exposure, and then had a fluctuated trend, and subsequently kept rising and reached the maximum value after 24 h cold de-acclimation. FaG6PDH-P2 expression level reached the peak value after 12 h cold treatment, but then gradually decreased and eventually had no difference from that without cold stress. FaG6PDH-P1, FaG6PDH-P1.1 and FaG6PDH-P0 almost had no dramatic change during the whole process, suggesting that they were not sensitive to cold stress. Overall, FaG6PDH-CY probably played an important role in cold tolerance for its significant response to cold stress (Figure 4).

2.5. Isolation and Cold Stress-Induced Activity Analysis of FaG6PDH-CY Promoter

1015 bp 5′ flanking sequence of FaG6PDH-CY upstream of the ATG start codon from strawberry genomic DNA was isolated. The sequence analysis showed that FaG6PDH-CY promoter contained the common cis-acting elements (TATA-box and CAAT-box) and light responsive (Box 4, GT1-motif and P-box), hormone-related (CGTCA-motif, GARE-motif, P-box, TGA-box, TGACG-motif), and stress-related (ARE and LTR) cis-acting regulatory elements (Table S3). The existence of element LTR indicated that FaG6PDH-CY was involved in low-temperature responsiveness. Hence, two 5′-deletion fragments of FaG6PDH-CY promoter with LTR (FaG6PDHpro-C) or without LTR (FaG6PDHpro-D) were fused to the GUS reporter gene and transferred into tobacco to test the promoter activities under cold stress. As shown in Figure 5, there was a significant increase in the inducible GUS activity of tobacco leaves harboring LTR promoter under cold stress, whereas no significant changes were observed under the normal condition when compared with the control promoter, which indicated that LTR element in FaG6PDH-CY promoter can promote high expression of downstream target genes when plant encountered cold signal.

2.6. Effect of FaG6PDH-CY Transient Expression on Strawberries in Response to Cold Stress

FaG6PDH-CY was transiently expressed in strawberry fruits by overexpressing and silencing strategies to explore its function in response to cold stress (Figures S2 and S3). The DAB and NBT staining showed that cold stress promoted H₂O₂ and O₂^- accumulation (Figure 6A and Figure 7A). FaG6PDH-CY overexpression had less H₂O₂ and O₂^- content than the control under cold stress (Figure 6A), whereas FaG6PDH-CY silencing had the opposite effect (Figure 7A). MDA content was significantly reduced in FaG6PDH-CY overexpressing fruits compared to the empty vector under cold treatment (Figure 6B), but there were no significant differences between FaG6PDH-CY silencing and the control (Figure 7B). In addition, FaG6PDH-CY overexpression significantly increased FaSOD, FaCAT, FaAPX, FaGR and FaRBOHD expression levels in response to cold stress (Figure 6C–K), whereas FaG6PDH-CY silencing significantly reduced FaSOD, FaCAT, FaAPX and FaCOR47 expression levels (Figure 7C–K). These data indicated that alteration of FaG6PDH-CY expression affected strawberry cold tolerance.

3. Discussion

OPPP is a pivotal source of reducing power and biosynthetic precursors in plants. G6PDH as the key enzyme in the OPPP controls NADPH production and carbon flow, which plays an important role in plant growth, development, and stress responses [20,21,22]. Genes encoding G6PDH, a small gene family have been identified in several plants including potato [5], wheat [23], Arabidopsis [9], barley [24], tomato [11], rubber tree [25] and soybean [26]. Based on the presence of transit peptide, six FaG6PDHs in our study were divided into cytosolic and plastidic two types (Figure 1, Figure S1 and Table S2), which was in accord with previous reports [9,27]. Different G6PDH isoforms distribute in tissue-specific manner. The cytosolic G6PDHs are widespread in all tissues and especially have a high expression in sink tissues, whereas plastidic P1-G6PDHs are predominantly expressed in green tissues and P2-G6PDHs abundance is considerably higher in roots [7,9]. Here, FaG6PDH-CY was most abundantly expressed in different tissues and at different fruit developmental stages (Figure 2A,B), indicating that it encoded the major G6PDH isoform throughout the plant and played an important role in various biological processes. It has been reported that cytosolic G6PDHs account for approximately 80% of the total activity of G6PDH in plant tissues [4,28]. FaG6PDH-P1 and FaG6PDH-P2 respectively showed highest transcript level in leaves and roots (Figure 2A), consistent with the expression patterns of their orthologues in Arabidopsis, tobacco and rubber tree [9,25,29]. The maximum values of FaG6PDH-P1.1 and FaG6PDH-P0 were detected in flower (Figure 2A). Additionally, FaG6PDH-P1 and FaG6PDH-P1.1 were detectable but their abundances were considerably lower compared with other isoforms during fruit development (Figure 2B). Differential expression of FaG6PDHs in distinct tissues suggested that they were probably multifarious players in plant growth and development.

G6PDH activity could be induced by diverse (a)biotic-stress related elicitors. It plays a vital role in maintaining redox balance and protecting cells from oxidative damage by providing the antioxidative defense system with the reducing power [17,30]. FaG6PDH activity was dramatically induced after strawberry was subjected to cold stress, accompanied by significant increasing of SOD, POD, CAT, proline, soluble protein, soluble sugar, MDA and electrolyte leakage. However, activities of antioxidant enzymes decreased, and more MDA and electrolyte leakage produced, when FaG6PDH activity was inhibited by GLUCM, indicating plant suffered greater injury caused by cold stress. This result demonstrated that FaG6PDH positively regulated cold tolerance in strawberry (Figure 3). G6PDH has been shown to respond to various oxidative stresses at the levels of enzyme activity and gene expression [31,32]. Meanwhile, the subcellular location of G6PDH seemed to have certain impacts on their stress responses [26,33]. Quantitative real-time PCR analyzed the expression profile of FaG6PDH gene family under cold stress. The result showed that cytosolic FaG6PDH-CY expression was significantly upregulated like its enzymatic activity and the plastidic FaG6PDHs had no dramatic change, implying a major role of FaG6PDH-CY in response to cold stress (Figure 3 and Figure 4). Gene expression is mainly controlled by cis-acting elements in the promoter region that determines many biological process and stress responses [34]. The 1015 bp fragment of FaG6PDH-CY promoter contained a putative LTR cis-element (Table S3), indicating that the expression of this gene might be regulated by low temperature, which was confirmed by the cold-inducible increases of GUS activity in the promoter construct containing LTR element (Figure 5).

To further understand the role of FaG6PDH-CY gene in cold-stress response, its functionality has been evaluated by transient expression assays. The burst out of ROS is one of the common phenomena in plant in response to different biotic and abiotic stresses [35]. In our study, cold stress promoted ROS production (Figure 6A and Figure 7A). It has been reported that cytosolic G6PDHs participate in the modulation of cellular redox states by supplying NADPH [26,36]. We found that the levels of ROS were obviously lower in FaG6PDH-CY overexpression than control under cold stress, and the cellular membrane damage in cold-exposed overexpression strawberry was less severe as manifested by the notable decrease in MDA content (Figure 6B). These evidences showed that FaG6PDH-CY overexpression could inhibit the cold-induced ROS accumulation, and consequently alleviate the membrane lipid peroxidation and confer cold tolerance. On the contrary, silencing FaG6PDH-CY enhanced ROS generation under cold stress, but it did not significantly trigger cellular membrane damage (Figure 7A,B), which probably resulted from incomplete silencing of FaG6PDH-CY or indicated that FaG6PDH-CY would be an indirect factor in the development of cold tolerance. SOD, CAT, POD, and those enzymes (APX, DHAR, MDAR and GR) implicated in the ascorbate-glutathione (AsA–GSH) cycle are important ROS scavengers, with NADPH required as a reducing agent in these scavenging reactions [37,38]. Exposure to cold stress, FaG6PDH-CY overexpression significantly up-regulated FaSOD and FaCAT expression levels (Figure 6C,D), whereas FaG6PDH-CY silencing significantly down-regulated their expression levels (Figure 7C,D), which was consistent with change of enzymatic activity (Figure 3D,F). Besides, FaG6PDH-CY modulated AsA–GSH pathway to resist cold stress by predominantly affecting FaAPX and FaGR transcript levels (Figure 6F,I and Figure 7F,I), in agreement with the research in salt-induced cy-G6PD gene function in Arabidopsis [39]. Cold-responsive gene COR47 was reported to involve the strawberry cold acclimation [40]. However, our data suggested that it was not regulated by FaG6PDH-CY expression under cold stress (Figure 6J and Figure 7J). NADPH oxidases, also named respiratory burst oxidase homologues (RBOHs), require NADPH to generate the superoxide anion (O₂^-), subsequently ending with the secondary production of other ROS such as hydrogen peroxide (H₂O₂) [41]. Our previous study demonstrated that RBOHD was important in response to cold stress in strawberry [42]. As shown in Figure 6K and Figure 7K, the expression of FaRBOHD was markedly increased under cold treatment, and significantly higher in overexpressing FaG6PDH-CY than that in control. In contrast, FaRBOHD expression level was reduced in silencing FaG6PDH-CY compared to control. These results indicated that FaG6PDH-CY was involved in RBOH-dependent ROS production in cold-stressed strawberry. Taken together, function of FaG6PDH-CY in response to cold stress is achieved through FaSOD, FaCAT, FaAPX, FaGR and FaRBOHD. On the basis of our above results and previous reports, we propose the model shown in Figure 8. In cold stress, FaG6PDH-CY was induced and produced more NADPH for a defense response, which enhanced antioxidant ability that contributed to scavenge excessive ROS generated by NADPH oxidase, and eventually alleviated the cold-induced oxidative damages.

4. Materials and Methods

4.1. Plant Materials and Treatments

Strawberries (Fragaria×ananassa cv. Benihoppe) are grown in a simple greenhouse at Chengdu campus of Sichuan Agricultural University (30°42’N, 103°51´E) with the routine management. Strawberry root, stem, young leaf, old leaf, flower and fruit (small green, big green, de-green, white, initial red and full red) were collected for tissue- and stage-specific transcript analysis of G6PDH genes. Potted strawberry plantlets with vigorous and uniform growth status were selected for the cold treatments. One set of plantlets was treated with 100 mM glucosamine (GLUCM, a G6PDH inhibitor) by spraying evenly over the whole leaf. Another set of plantlets as control was treated with distilled water. Half of the above treated plantlets were kept at room temperature, and the others were put into 0 °C environment. Leaves were collected after 24 h. In addition, some potted strawberries were directly subjected to cold stress at 0 °C, followed by sampling at 0, 3, 6, 12, 24 and 48 h after treatment. Subsequently, plants were taken out to de-acclimate at room temperature for 24 h. Nicotiana benthamiana seeds were sowed in the soil (peat, perlite and vermiculite, 2:1:1 in volume ratio) and cultured in the growth room (23 ± 2 °C, 16 h light/8 h dark, 6000 l×). The strawberry fruits for transient expression were harvested from a local farm at Shuangliu County, Sichuan Province (southwest China).

4.2. Determination of G6PDH, SOD, CAT and POD Activities

The extract was prepared for G6PDH activity and assayed using the commercial kits purchased from SuZhou Keming Bioengineer Company (SuZhou, China), following the manufacturer’s instruction. G6PDH can reduce NADP⁺ to NAPDH in OPPP reaction. The G6PDH activity was measured by increasing rate of NAPDH at 340 nm. One unit (U) of enzyme activity was defined as the amount of enzyme that produced 1 nmol of NAPDH per milligram of protein in 1 min. A total of 0.2 g samples was homogenized in 10 mL ice-cold potassium phosphate buffer (50 mM, pH 7.8) and then centrifuged at 8000 r/min for 20 min at 4 °C. The supernatant was prepared for assay of SOD, CAT and POD activities. All of them were measured according to the protocols described by Xiong (2003) [43]. SOD activity was detected by monitoring its ability to inhibit the photochemical reduction of NBT. CAT activity was determined using potassium permanganate titration. POD activity was evaluated with guaiacol colorimetric method.

4.3. Electrolyte Leakage and MDA Content Assay

Electrolyte leakage and MDA content were assayed based on the methods described by Xiong (2003) [43]. Leaves were washed and immersed in de-ionized water for 2 h at 25 °C. The conductivity in the solution was measured (C1). Samples were then incubated in boiling water for 1 h and cooled down to the room temperature before the ultimate conductivity was measured (C2). Relative electrolyte leakage was expressed as the ratio C1/C2. A total of 0.3 g samples was homogenized in 8 mL of 10% (w/v) trichloroacetic acid (TCA). The homogenate was centrifuged at 5000 r/min for 10 min. MDA content in the supernatant was determined using the thiobarbituric acid method.

4.4. Proline, Soluble Sugar and Soluble Protein Content Determination

Finely ground leaf tissue (0.2 g) was suspended in 5 mL of 3% sulphosalicylic acid and then centrifuged at 5000 r/min for 10 min. The proline content in the solution was determined by acid ninhydrin method [43]. A total of 0.5 g samples was ground and added into 8 mL distilled water. The homogenate was centrifuged at 5000 r/min for 10 min. The supernatant was used for soluble sugar and soluble protein determination. The content of soluble sugar was measured using anthrone colorimetric method and the soluble protein was quantified by Coomassie brilliant blue G-250 [43].

4.5. RNA Extraction, First-Strand cDNA Synthesis and Genomic DNA Isolation

Total RNA and genomic DNA were isolated from tissue samples according to the protocols described by Chen et al. (2012) [44]. After quantity and quality evaluation, 1 µg of total RNA was reversely transcribed into the first-strand cDNA using PrimeScript^TM RT Reagent Kit with gDNA Eraser (Perfect Real Time) (Takara, Japan) according to the manufacturer’s instructions.

4.6. Cloning and Bioinformatic Analysis of G6PDH Genes

Five strawberry G6PDH sequences were downloaded using Arabidopsis G6PDHs as query probes to BLAST search against GDR (Genome Database for Rosaceae) and NCBI (National Center for Biotechnology Information) databases. Except for FaG6PDH-CY (KC433888), FaG6PDH-P1 (KC433889), FaG6PDH-P2 (JQ260862.1) submitted to NCBI in our previous study, another two members FaG6PDH-P1.1 and FaG6PDH-P0 were cloned using primers (FaG6PDH-P1.1: 5′-GTCTACACGATTTAGCCGACATGG-3′, 5′-GCTTACACCTGACAATGGATGAGTG-3′; FaG6PDH-P0: 5′-AAGATCTTAGACCTGAACAGGGA-3′, 5′-AGAGTAGCCGTTGTACCTCACAA-3′). Subsequently, all strawberry G6PDHs were performed bioinformatic analysis using ExPASy-ProtParam for physicochemical parameter computation, TargetP 2.0 and ProtComp 9.0 for N-terminal transit peptide (TP) prediction, SignalP 4.1 for signal peptide (SignalP) prediction, TMHMM 2.0 for transmembrane helix (TMH) prediction, DNAMAN for multiple sequence alignment, ClustalX and MEGA for phylogenetic tree construction. Additionally, to obtain the FaG6PDH-CY promoter, approximately 1000 bp upstream sequence flanking start codon was amplified with specific primers (5′-CTGCTTGACTTGGTGCTGAAAAC-3′ and 5′-CCTTCCTGAGCTGTTGCGC-3′) using genomic DNA. Putative cis-acting elements of FaG6PDH-CY promoter were identified by PlantCare online tool.

4.7. Quantitative Real-Time PCR

qRT-PCR was conducted using SYBR Green Premix Ex Taq ^TM (Takara, Japan) on the CFX96 real-time PCR system (Bio-Rad, Hercules, CA, USA). The 20 μL reaction mixture included 10 μL SYBR Premix, 0.8 μL each primer (0.4 μM), 1.5 μL cDNA template and 6.9 μL ddH₂O. Reaction protocol was set as follows: 95 °C for 3 min, followed by 40 cycles of 95 °C for 10 s, 55 °C for 30 s and 72 °C for 15 s. After that, melting curve was inserted to verify specificity of primer amplification. The relative expression level was calculated with the 2 ^−△△Ct method. Primers designed for the target and internal control genes were listed in Table S4.

4.8. Vector Construction

For functional validation of FaG6PDH-CY promoter in response to cold stimuli, two 5′-deletion fragments of the promoter, 393 bp FaG6PDHpro-C with LTR element and 323 bp FaG6PDHpro-D without LTR element were amplified with primers (FaG6PDHpro-C: 5′-CCAAGCTTCCGAAATTCGATCGCGCTCT-3′, 5′-GCTCTAGACCTTCCTGAGCTGTTGCGCA-3′; FaG6PDHpro-D: 5′-CCAAGCTTTTCGATCGCGCTCTGCTCAAT-3′, 5′-GCTCTAGACCTTCCTGAGCTGTTGCGCA-3′). The obtained amplicons were used to replace the CaMV 35S promoter in pBI121 vector with help of HindⅠⅠⅠ and XbaⅠ (Figure S4). FaG6PDHpro-C:: GUS and FaG6PDHpro-D:: GUS plasmids were prepared for tobacco transient transformation assay. For overexpression, the coding sequence of FaG6PDH-CY gene was amplified with primers (oFaG6PDH-CY: 5′-GGGGTACCGAGCTACGTAGTTGCGCAACAG-3′, 5′-GCTCTAGAACACACAATACCGCACTC-3′) and cloned into the modified pCAMBIA1301 vector driven by CaMV 35S promoter using restriction enzymes KpnⅠ and XbaⅠ. For virus-induced gene silencing (VIGS), the tobacco rattle virus RNA1 (pTRV1) and tobacco rattle virus RNA2 (pTRV2) vectors were applied. A 680 bp fragment specifically targeting FaG6PDH-CY gene was amplified with primers (vFaG6PDH-CY: 5′-GGGGTACCATATCTTATCCAAGGAGCTTCCTCCA-3′, 5′-GCTCTAGATCGTCGTTAATTGGAAGTACCGATT-3′) and then subcloned into pTRV2 with KpnⅠ and XbaⅠ.

4.9. Transient Expression and Cold-Resistance Assay in Tobacco Leaves and Strawberry Fruits

Agrobacterium-mediated transient expression assays were performed. All recombinant and empty vectors were introduced into the agrobacterium strain GV3101 by freeze-thaw method. The pelleted cells were resuspended in infiltration medium (10 mM MgCl_2, 10 mM MES pH 5.6, 200 μM AS). The agrobacterium suspensions (OD600 = 0.4) harboring FaG6PDHpro-C:: GUS and FaG6PDHpro-D:: GUS vectors were respectively injected into the abaxial surfaces of the leaves of 30 day-old tobaccos using a 1 mL needleless syringe. After 24 h cultivation in dark, the transgenic tobacco plants were transferred to 4 °C and kept for 48 h. The cell suspensions containing pCAMBIA1301-G6PDH-CY and pCAMBIA1301-35SN were respectively diluted to OD600  =  0.8–1.0 using infiltration medium. In addition, the OD600 of TRV1, TRV2 and pTRV2-G6PDH-CY cultures were regulated to 1.6–2.0. Subsequently, Equal volumes of TRV1 and TRV2/ TRV2-G6PDH-CY cultures were mixed together. Transient overexpression and VIGS by infiltration of corresponding construct into strawberry fruits followed the procedures described by Chen et al. (2018) [45]. The treated strawberries were cultured in dark for 12 h, and then subjected to 4 °C treatment. The overexpressing samples were harvest after 5 days and VIGS fruits were collected after 6 days.

4.10. Histochemical Staining and Activity Assays for GUS

Round leaf discs with a diameter of 1 cm were punched from the treated tobacco leaves using a hole puncher and then stained by a GUS staining kit (Solarbio, Beijing). A total of 0.2 g treated samples was homogenized in 1.8 mL ice-cold potassium phosphate buffer (50 mM, pH 7.8) and then centrifuged at 8000 r/min for 20 min at 4 °C. The aqueous (upper) phase was analyzed by ELISA kit (Mlbio, Shanghai) for GUS activity.

4.11. DAB and NBT Staining

The treated fruits were cut into discs with a razor blade and immersed them in 0.1% (w/v) DAB or 0.1% (w/v) NBT staining solution for detection of H₂O₂ or O₂^-, respectively. The tubes were wrapped with aluminum foil and kept into the 80 r/min shaker at 25 °C for 4–6 h. Then, samples were put into absolute ethanol and heated in a boiling water-bath for 20 min or more (intermittent refreshing of absolute ethanol) for proper visualization of the staining. After that, the residual alcohol on fruit surface was removed by absorbent paper. The change in fruit color was observed and photographed.

4.12. Statistical Analyses

All data presented here are mean± standard error of at least three independent biological replicates. The statistical significance of the difference was evaluated by Data Processing System (DPS) using Duncan’s multiple range test at p < 0.05.