Overexpression of PgCBF3 and PgCBF7 Transcription Factors from Pomegranate Enhances Freezing Tolerance in Arabidopsis under the Promoter Activity Positively Regulated by PgICE1

Cold stress limits plant growth, development and yields, and the C-repeat binding factors (CBFs) function in the cold resistance in plants. However, how pomegranate CBF transcription factors respond to cold signal remains unclear. Considering the significantly up-regulated expression of PgCBF3 and PgCBF7 in cold-tolerant Punica granatum ‘Yudazi’ in comparison with cold-sensitive ‘Tunisia’ under 4 °C, the present study focused on the two CBF genes. PgCBF3 was localized in the nucleus, while PgCBF7 was localized in the cell membrane, cytoplasm, and nucleus, both owning transcriptional activation activity in yeast. Yeast one-hybrid and dual-luciferase reporter assay further confirmed that PgICE1 could specifically bind to and significantly enhance the activation activity of the promoters of PgCBF3 and PgCBF7. Compared with the wild-type plants, the PgCBF3 and PgCBF7 transgenic Arabidopsis thaliana lines had the higher survival rate after cold treatment; exhibited increased the contents of soluble sugar and proline, while lower electrolyte leakage, malondialdehyde content, and reactive oxygen species production, accompanying with elevated enzyme activity of catalase, peroxidase, and superoxide dismutase; and upregulated the expression of AtCOR15A, AtCOR47, AtRD29A, and AtKIN1. Collectively, PgCBFs were positively regulated by the upstream PgICE1 and mediated the downstream COR genes expression, thereby enhancing freezing tolerance.


Introduction
Among various environmental stresses, cold stress as a common abiotic stress adversely affects plant growth and development, even survivability, and significantly restricts the geographical distribution of plants and agricultural productivity [1,2]. It is estimated that the loss of 51-82% of annual crop yield was attributed to extreme cold stress globally [3]. Cold stress causes cell membrane lipid peroxidation, decreases cell membrane fluidity, impairs photosynthesis, correspondingly leading to the accumulation of electrolyte leakage, malondialdehyde (MDA), soluble sugar, and proline [2,4,5]. Furthermore, the stability of the cell membrane system is positively correlated with the cold resistance of plants [6].
Plants have developed complex biochemical and physiological mechanisms and a flexible transcriptional network regulated by a series of transcription factors to adapt to cold stress. At present, ICE (Inducer of CBF Expression)-CBF/DREB1(C-Repeat Binding Factor/DRE Binding Factor1)-COR (cold-regulated genes) is the clearest and most pivotal regulation pathway of cold adaptation at the plant transcription level [7]. ICE1, as a transcription activator of CBFs, attaches to MYC elements in the promoter of the downstream target CBF genes, thus increasing CBFs transcript [8,9]. CBFs, also known as DREB1, are critical for cold acclimation in higher plants [10], and regulate COR gene expressions via recognizing the CRT/DRE cis-element in the COR promoter under cold stress [1,11]. The

Screening and Analyzing the Candidate CBF Genes
Potential CBF proteins were identified in pomegranate genome databases by their homology with Arabidopsis. Seven PgCBF genes were distributed on two chromosomes (Chromosome 1 and Chromosome 4) in pomegranate and named according to their positions on the chromosomes in the pomegranate genome ( Figure 1a). Here, the comparison of expression patterns of CBFs from two pomegranate cultivars was investigated under 4°C by qRT-PCR method. The results indicate that the expressions of PgCBF3, PgCBF4, PgCBF6, and PgCBF7 were higher in 'Yudazi' than in 'Tunisia', especially for PgCBF3 and PgCBF7, showing significant differences. Moreover, PgCBF3 and PgCBF7 transcript abundance both peaked at 4 h after cold treatment (Figure 1b). Accordingly, the genes PgCBF3 and PgCBF7 located at Chromosome 1 and Chromosome 4 were selected as the candidate genes in this study ( Figure 1a).
As shown in Figure 1c, PgCBF3 and PgCBF7 had tissue-specificity expression in six tissues from 'Yudazi' with tissue specificity. The expression of PgCBF3 revealed to be the highest in leaves, followed by the roots, and the lowest in seeds and peel. The expression of PgCBF7 also revealed to be the highest in leaves, followed by the aril and stem, and the lowest in seeds (Figure 1c). As shown in Figure 1c, PgCBF3 and PgCBF7 had tissue-specificity expression in six tissues from 'Yudazi' with tissue specificity. The expression of PgCBF3 revealed to be the highest in leaves, followed by the roots, and the lowest in seeds and peel. The expression of PgCBF7 also revealed to be the highest in leaves, followed by the aril and stem, and the lowest in seeds (Figure 1c).

Subcellular Localization and Transcriptional Activity Analysis of PgCBF3 and PgCBF7
In order to explore the function of PgCBF3 and PgCBF7, the recombinant vectors pCAMBIA2300-35S-PgCBF3-GFP and pCAMBIA2300-35S-PgCBF7-GFP were transiently transformed into tobacco leaves. The results demonstrate that 35S::PgCBF3-GFP was located in the nucleus, 35S::PgCBF7-GFP was located in the nucleus, cell membrane, and cytoplasm, while 35S:: GFP was located in the whole cell ( Figure 3a). As shown in Figure  3b, the yeast stains harboring pGBKT7-PgCBF3 and pGBKT7-PgCBF7 both grew normally on SD/-Trp-Leu-His-Ade medium with X-α-gal and turned to blue, indicating that PgCBF3 and PgCBF7 functioned as a transcription activator in yeast.

Subcellular Localization and Transcriptional Activity Analysis of PgCBF3 and PgCBF7
In order to explore the function of PgCBF3 and PgCBF7, the recombinant vectors pCAMBIA2300-35S-PgCBF3-GFP and pCAMBIA2300-35S-PgCBF7-GFP were transiently transformed into tobacco leaves. The results demonstrate that 35S::PgCBF3-GFP was located in the nucleus, 35S::PgCBF7-GFP was located in the nucleus, cell membrane, and cytoplasm, while 35S:: GFP was located in the whole cell ( Figure 3a). As shown in Figure 3b, the yeast stains harboring pGBKT7-PgCBF3 and pGBKT7-PgCBF7 both grew normally on SD/-Trp-Leu-His-Ade medium with X-α-gal and turned to blue, indicating that PgCBF3 and PgCBF7 functioned as a transcription activator in yeast.

Validation of Activation Activity of PgICE1 on the Promoters of PgCBF3/PgCBF7
In view of the fact that a bHLH-type transcription factor AtICE1 positively regulated the expression of CBFs in the cold, PgICE1 gene was cloned from P. granatum 'Yudazi', and its protein sequence showed a higher homology with ICE1 proteins from other species, sharing 49.81% of amino acid identity with AtICE1 ( Figure S2a), and clustered into the same clade with EgICE1 and SoICE1 (Syzygium oleosum) ( Figure S2b).
In order to explore the relationship of PgICE1 on PgCBF3 and PgCBF7 promoters, the promoter sequences of PgCBF3 (1991 bp) and PgCBF7 (2000 bp) from P. granatum 'Yudazi' were analyzed ( Figure S3). Using PlantCARE, some cis-acting elements were found in the promoters of PgCBF3 and PgCBF7, both including LTR (cis-acting element involved in low-temperature responsiveness), MYC recognition sequences which ICE1 specifically binds to, along with ABRE and MBS ( Figure S3). In addition, the PgICE1 expression was also induced by low temperature, significantly higher in cold-tolerant cultivar 'Yudazi' than in cold-sensitive cultivar 'Tunisia', especially at 12 h after cold treatment (Figure 4a), which demonstrated that PgICE1 as well as PgCBF3 and PgCBF7 all expressed at a higher level in 'Yudazi' under low temperature.   low-temperature responsiveness), MYC recognition sequences which ICE1 specifically binds to, along with ABRE and MBS ( Figure S3). In addition, the PgICE1 expression was also induced by low temperature, significantly higher in cold-tolerant cultivar 'Yudazi' than in cold-sensitive cultivar 'Tunisia', especially at 12 h after cold treatment (Figure 4a), which demonstrated that PgICE1 as well as PgCBF3 and PgCBF7 all expressed at a higher level in 'Yudazi' under low temperature. Different letters present significant differences (p < 0.05), and ** presents significant differences (p < 0.01).
The binding of PgICE1 to the promoters of PgCBF3 and PgCBF7 were verified by yeast one-hybrid technology, indicating that PgICE1 induced the activity of the promoters of PgCBF3 and PgCBF7, respectively ( Figure 4b). Furthermore, PgICE1 had a stronger The binding of PgICE1 to the promoters of PgCBF3 and PgCBF7 were verified by yeast one-hybrid technology, indicating that PgICE1 induced the activity of the promoters of PgCBF3 and PgCBF7, respectively ( Figure 4b). Furthermore, PgICE1 had a stronger activation effect on the promoter sequences of the promoters of PgCBF3 and PgCBF7, based on the dual-LUC reporter assay (Figure 4c,d).

Overexpression of PgCBF3/PgCBF7 Enhanced Freezing Tolerance in A. thaliana
To further explore the potential function of PgCBFs in plants, the overexpression vectors were transformed into A. thaliana. After PCR validation, three transgenic PgCBF3-OE lines and two transgenic PgCBF7-OE lines were obtained (Figure 5a,b). We found that the survival rate of PgCBF3-OE plants and PgCBF7-OE plants reached 80.9% and 79.2%, respectively, which is higher than 45.5% in the wild-type plants at 1 h after −2 • C treatment (Figure 5c-f). Moreover, we examined whether the freezing tolerance of the transgenic PgCBF3 and PgCBF7 plants was regulated by CBF genes under both NA and CA conditions. The results demonstrated that chlorophyll fluorescence was weaker in the leaves from the CA and NA groups than in the controls (Figure 6a). Additionally, the Fv/Fm values reduced after CA and NA treatment, but was higher in the transgenic PgCBF3 and PgCBF7 plants than in the wild-type plants (Figure 6b). Collectively, PgCBF3 and PgCBF7 genes may improve the freezing tolerance in the transgenic A. thaliana plants.
( Figure 5c-f). Moreover, we examined whether the freezing tolerance of the transgenic PgCBF3 and PgCBF7 plants was regulated by CBF genes under both NA and CA conditions. The results demonstrated that chlorophyll fluorescence was weaker in the leaves from the CA and NA groups than in the controls (Figure 6a). Additionally, the Fv/Fm values reduced after CA and NA treatment, but was higher in the transgenic PgCBF3 and PgCBF7 plants than in the wild-type plants (Figure 6b). Collectively, PgCBF3 and PgCBF7 genes may improve the freezing tolerance in the transgenic A. thaliana plants.  Subsequently, the physiological and biochemical indices were investigated between wild-type and transgenic plants under freezing stress, including the accumulation of ROS, O 2-, and H 2 O 2 . As shown in Figure 6c,d, the DAB and NBT staining revealed that a lighter color appeared in transgenic and wild-type Arabidopsis plants before freezing treatment, without obvious difference. However, after CA and NA treatments, more brown or blue plaques distributed on the leaves from the wild-type ones, suggesting that less ROS accumulation presented in the transgenic lines than the wild-type plants under freezing stress. Furthermore, electrolyte leakage and MDA content were also lower in the transgenic plants than in wild-type plants after CA and NA treatments (Figure 6e,f). These results suggested that the heterologous expression of PgCBF3 and PgCBF7 in A. thaliana protected the integrity of cell membrane and reduced oxidation damage, which is beneficial for freezing tolerance.
Generally, proline and soluble sugars are considered important compatible solutes in response to cold treatment. In the current study, the contents of proline and soluble sugars were significantly higher in PgCBF3-OE and PgCBF7-OE lines than in wild-type plants after −6 • C treatment (Figure 7a,b). The enzyme activities of SOD, POD, and CAT are also used to evaluate the freezing tolerance. It was found that they significantly accumulated in transgenic plants (PgCBF3-OE and PgCBF7-OE lines) after −6 • C treatment (Figure 7c-e). Furthermore, qRT-PCR analysis supported the finding, as the expression of AtCOR15A, AtCOR47, AtRD29A, and AtKIN1 were all higher in the PgCBF3-OE and PgCBF7-OE lines than in the wild-type plants after cold treatment (Figure 8). In conclusion, our findings demonstrated that the overexpression of PgCBF3 and PgCBF7 in A. thaliana enhances cold tolerance, which was likely via the increasing expression of four cold-responsive genes. Subsequently, the physiological and biochemical indices were investigated between wild-type and transgenic plants under freezing stress, including the accumulation of ROS, O 2-, and H2O2. As shown in Figure 6c,d, the DAB and NBT staining revealed that a lighter color appeared in transgenic and wild-type Arabidopsis plants before freezing treatment,   (Figure 7c-e). Furthermore, qRT-PCR analysis supported the finding, as the expression of AtCOR15A, AtCOR47, AtRD29A, and AtKIN1 were all higher in the PgCBF3-OE and PgCBF7-OE lines than in the wild-type plants after cold treatment (Figure 8). In conclusion, our findings demonstrated that the overexpression of PgCBF3 and PgCBF7 in A. thaliana enhances cold tolerance, which was likely via the increasing expression of four cold-responsive genes.

Discussion
For perennial fruit trees, the cold tolerance is a determinant factor for survival, especially in fall and late winter, when even young plants are more sensitive to low temperatures. The prominent role of CBF transcription factor genes in response to cold stress also attracted many researchers' attention. Plum blossom CBFs were higher in high

Discussion
For perennial fruit trees, the cold tolerance is a determinant factor for survival, especially in fall and late winter, when even young plants are more sensitive to low temperatures. The prominent role of CBF transcription factor genes in response to cold stress also attracted many researchers' attention. Plum blossom CBFs were higher in high cold resistance variety than in low cold resistance variety [18]. Meanwhile, three longan DlCBF genes exhibited differences in their expression and function [20]. Therefore, a cold-sensitive 'Tunisia' and a cold-tolerance 'Yudazi' were selected to screen potential CBF genes. The expression profiles of seven pomegranate CBF genes in the two pomegranate cultivars produced a satisfied result that PgCBF3 and PgCBF7 were significantly up-regulated expression in 'Yudazi' at 4 • C (Figure 1), then provided a significant theoretical basis for further study of the two CBF genes. Additionally, the tissue-specific expression of PgCBF3 and PgCBF7 revealed to be the highest in leaves, in agreement with the higher expression of DlCBF1 and DlCBF2 in longan young leaves [20]. Sequence analysis showed that PgCBF3 and PgCBF7 shared a high homology with B. platyphylla CBF3 and E. globulus CBF3, respectively. Furthermore, subcellular localization analysis revealed that PgCBF3 was located on the nucleus while PgCBF7 was located on the nucleus, cytoplasm, and cell membrane, and both PgCBF3 and PgCBF7 had a transcriptional activation function (Figure 3), similar to the previous results of tea CBF1-6 proteins [19] and longan DlCBF1, DlCBF2, and DlCBF3 [20].
Transcription factors are largely responsible for the selectivity in gene regulation; therefore, gene expression is mainly regulated at the transcriptional level, dependent on diverse cis-acting elements in the promoter [40,41]. CBF gene expression is modulated at the transcriptional level by various transcription factors via recognizing different ciselements, including ICE1 [9,42], ICE2 [42,43], brassinazole-resistant 1 (BZR1) [44], pseudo response regulators (PRRs) [45], ethylene-insensitive 3 (EIN3) [46], etc. To explore the possible mechanisms for the two pomegranate CBFs, their upstream sequences were cloned. Our findings show that the promoters of PgCBF3 and PgCBF7 contained the LTR element and MYC recognition site which was necessary for ICE binding under cold stress (Supplementary Figure S3). Furthermore, yeast one-hybrid and Dual-LUC assay proved that PgICE1 positively regulated the expression of PgCBF3 and PgCBF7 genes by combining with the promoters (Figure 4), which was consistent with the result that ICE binds to the MYC cis-acting element in the CBF promoter and activates the expression of CBFs [3,9,47]. Collectively, PgICE1 could bind to the promoters of PgCBF3 and PgCBF7, likely via the MYC recognition sequences.
Seen as transcription factors possess unique characteristics and modes of action, the overexpression strategy has been particularly effective in revealing transcription factor function [40]. Some evidence has also indicated that the heterologous expression of CBF genes from peach [26], longan [20], and sweet cherry [25] increased cold tolerance in apple and Arabidopsis plants. For −2 • C treatment, the ectopic expression of PgCBF3 and PgCBF7 in Arabidopsis improved the freezing tolerance significantly by higher survival rate and less phenotype damage, as seen from similar results in previous studies [19,48]. Moreover, the higher expression of AtCOR15A, AtCOR47, AtKIN1, and AtRD29A were presented in the PgCBF3-OE and PgCBF7-OE transgenic lines under 4 • C treatment, suggesting that PgCBF3/7 up-regulated the expression of these target genes and increased the tolerance against low temperature damage. Although the protein sequences of PgCBF3 and PgCBF7 had no high similarity with Arabidopsis CBF3 (46.15% and 53.85%), and were not clustered into the same group with AtCBF1-4, PgCBF3, and PgCBF7, they played an important role in COR genes expression, which was attributed to COR genes expression regulated by ICE-CBF/DREB1 cascade under cold stress [20,28,49,50].
In addition, low temperature causes multiple biochemical and physiological changes. MDA accumulation and electrolyte leakage are widely used to evaluate membrane integrity [51,52]. In the PgCBF3-OE and PgCBF7-OE transgenic lines, the contents of electrolyte leakage and MDA both rose after CA and NA treatments, but lowered in the wild-type Arabidopsis plants, especially exhibiting a significant difference of MDA content with the wild-type plants. ROS production is investigated to assess the stress tolerance in response to cold stress in plants [20,52,53]. In the current study, after CA and NA treatments, ROS accumulation increased in both the transgenic lines and wild-type plants, but was strikingly lower than the wild-type plants, which was consistent with the rapidly accumulated ROS for cold acclimation [54]. Meanwhile, the ectopic expression of two Asian pear PpyCBFs and three longan DlCBFs also resulted in lower ROS accumulation [20,53]. Consequently, we detected the activity of POD, SOD, and CAT in pomegranate, responsible for the elimination of ROS in plant cells [54,55]. The findings demonstrated that higher activity of the three major ROS scavenging enzymes (CAT, SOD, and POD) existed in the transgenic lines PgCBF3-OE and PgCBF7-OE, compared with wild-type plants after −6 • C treatment, which partially accounted for less ROS accumulation in the transgenic lines. In conclusion, it was noted that the transgenic PgCBF3 and PgCBF7 lines acquired increased cold tolerance due to minor oxidation damage in cells and relatively stabilizing cell membranes via activating the antioxidant enzymes activity in a more robust manner. Besides, the higher concentration of soluble sugar and proline in transgenic lines greatly contributes to rising the tolerance against cold stress, which was stated in the overexpression of Arabidopsis CBF3 [30].

Plant Materials and Growth Conditions
P. granatum vs. 'Yudazi' and 'Tunisia' plants were grown in the fruit tree experimental station of the College of Horticulture, Henan Agricultural University, Zhengzhou, China. 'Yudazi' has a strong tolerance to low temperature, while 'Tunisia' has a weak tolerance to low temperature [39]. Cuttings from 'Yudazi' and 'Tunisia' were rooted and grown in a growth chamber at 22 • C and 75% of relative moisture with a 16/8 light/dark photoperiod. Additionally, Arabidopsis thaliana seedlings (ecotype Columbia, Col-0) and N. benthamiana seedlings were grown under the same conditions.

Cold-Tolerance Assays
The healthy 30-day-old pomegranate cuttings and the 3-week-old A. thaliana plants were transferred into a growth chamber at 4 • C for cold treatment. The leaves were collected at 0, 2,4,8,12,24,48, and 72 h after cold treatment and immediately frozen in liquid nitrogen.
Freezing tolerance assays were conducted as described by Hu et al. [56], with some modifications. The 10-day-old Arabidopsis seedlings were maintained for 1 h in a growth chamber at −2 • C, and transferred to 22 • C. The survival rates were measured visually after 24 h. Three-week-old Arabidopsis plants were divided into two groups, one group (cold-acclimated, CA) was set at 4 • C for 7 days, and −7 • C for 8 h, while the other group (non-acclimated, NA) was placed at −6 • C for 8 h.

RNA Extraction and Quantitative RT-PCR (qRT-PCR) Analysis
The total RNA was extracted from pomegranate and Arabidopsis using the Plant Total RNA Isolation Kit (Shanghai Sangon Biotech Co., Ltd., Shanghai, China), and the cDNA was synthesized using HiScript III RT SuperMix for qPCR (+gDNA wiper) (Nanjing Vazyme Biotech Co., Ltd., Nanjing, China). qRT-PCR was carried out using ChamQ Universal SYBR qPCR Master Mix (Nanjing Vazyme Biotech Co., Ltd., Nanjing, China) on ABI 7500 PCR instrument (Applied Biosystems, Foster, CA, USA). The PgActin (LOC116200207) and AtActin (AT3G18780) genes were used as an internal reference. All the primers used were listed in Supplementary Table S1.
Pomegranate genome annotation information, genome sequences, and protein sequences were obtained from the pomegranate genome database (Table S2) [57]. The coding sequences of 7 pomegranate CBF candidate genes were obtained using TBtools v.1.09876 and NCBI website (https://www.ncbi.nlm.nih.gov/) with BLAST search. Sequences of the other plant CBF proteins were retrieved using BLAST search in NCBI database (https://blast.ncbi.nlm.nih.gov/Blast.cgi, accessed on 17 March 2022). The amino acid sequence alignment was performed using DNAMAN software. A phylogenetic tree was constructed with the neighbor-joining method by MEGA6.0.

Chlorophyll Fluorescence Detection
The Arabidopsis plants at low temperature were imaged by a SPAD-502 chlorophyll (Chl) meter (Minolta, Tokyo, Japan), and SPAD values were recorded. The maximum quantum efficiency of PSII efficiency (Fv/Fm) was assessed using FluorCam7 Chl fluorescence imaging (Photon Systems Instruments, Brno, Czech Republic) and LI-6400 portable photosynthesis measurement system (LI-COR Inc., Lincoln, NE, USA) [60].

Recombination Vectors Construction and Transgenic Plants Generation
To generate the overexpression transgenic plants, the open reading frame (ORF) sequences of PgCBF3 and PgCBF7 (containing KpnI and BamHI digestion sites) driven by the CaMV 35S promoter were cloned into the pCAMBIA2300-GFP vector, generating the vectors pCAMBIA2300-35S-PgCBF3/PgCBF7-GFP. The recombinant vectors were introduced into A. thaliana (ecotype Columbia, Col-0) via Agrobacterium tumefaciens strain GV3101 using inflorescence infection method [61].

Determination of Electrolyte Leakage, MDA and Proline Content, and Enzyme Activity
The electrolyte leakage was evaluated according to the method described by Nanjo et al. [62]. MDA content (µmol kg −1 fresh weight) was measured by thiobarbituric acid method using MDA-2-Y Kit (Suzhou Comin Biotechnology Co. Ltd., Suzhou China). The enzyme activity of catalase (CAT) and superoxide dismutase (SOD) were determined using CAT-2-W Kit and SOD-2-Y Kit and (Suzhou Comin Biotechnology Co. Ltd., China), respectively. Soluble sugar content was measured using KT-1-Y Kit (Suzhou Comin Biotechnology Co. Ltd., China). The proline content was assessed using Proline (PRO) Content Assay Kit BC02905 (Beijing Solarbio Science & Technology Co., Ltd., Beijing, China). Peroxidase (POD) activity was determined according to the method described previously [63].

Determination of Electrolyte Leakage, MDA and Proline Content, and Enzyme Activity
The A. tumefaciens strain GV3101 with recombinant vectors pCAMBIA2300-35S-PgCBF3-GFP and pCAMBIA2300-35S-PgCBF7-GFP were infiltrated into tobacco leaves, the empty vector as the control. After 72 h, GFP fluorescence was observed by a confocal laser microscopy (Carl Zeiss, Jena, Germany).

Transcriptional Activation Activity Analysis
The ORF sequences of PgCBF3 and PgCBF7 were cloned into pGBKT7. According to the procedure of Yeastmaker TM Yeast transformation system 2 (Clontech, Takara, Kusatsu, Japan), the recombinants of pGBKT7-PgCBF3 and pGBKT7-PgCBF7 were transformed into the yeast strains Y2HGold stain, which were screened on SD/-Trp-Leu-His-Ade/X-α-Gal medium. The yeast with pGADT7-T + pGBKT7-Lam was used as the negative control and with pGADT7-T + pGBKT7-p53 as the positive control.

Extraction of Genomic DNA and the Cloning of the Promoters
DNA extraction from pomegranate leaves was performed using the EZ-10 Spin Column Plant Genomic DNA Purification Kit (Shanghai Sangon Biotech Co., Ltd., China). The purified DNA was used for the promoter amplification of PgCBF3/PgCBF7 genes. The promoter sequences were analyzed using PLACE (https://www.dna.affrc.go.jp/PLACE/ ?action=newplace, accessed on 8 January 2007) and PlantCARE (http://bioinformatics.psb. ugent.be/webtools/plantcare/html/).

Yeast One-Hybrid Assay
The promoter fragments of PgCBF3 and PgCBF7 genes were inserted into the pLacZi vector, while the ORF of PgICE1 was cloned into the pB42AD vector. After co-transformation pPgCBF3/7-pLacZi and PgICE1-pB42AD in EGY48 yeast strains, yeast cells grown on SD-Trp/Ura media were suspended in sterile water and then placed on SC-Trp/Ura/X-Gal media for culturing at 28 • C for 12-24 h.

Dual-Luciferase (Dual-LUC) Reporter Assay
The ORF sequence of PgICE1 was cloned into the pSAK277 vector, which acted as the effector, and the promoters of PgCBF3 and PgCBF7 were cloned into the pGREENII0800-LUC, which acted as the reporter. All constructs were individually transformed into Agrobacterium GV3101 stain and expressed transiently in tobacco leaves by A. tumefaciensmediated infiltration. After culturing for 3 days, the ratio of enzyme activities of firefly luciferase (LUC) and renilla luciferase (REN) was measured using Dual Luciferase Reporter Gene Assay Kit (Vazyme Biotech Co., Ltd., Nanjing, China).

Statistical Analysis
The mean values and standard deviation (SD) were obtained for at least three repetitions. Statistical analysis was performed using SPSS Statistics v.20. Significant difference was evaluated using one-sided paired t test (p < 0.05).

Conclusions
Two CBFs (PgCBF3 and PgCBF7) were identified from a cold-tolerant pomegranate cultivar. The overexpression of PgCBF3 and PgCBF7 led to enhanced cold tolerance in transgenic Arabidopsis plants under cold stress, as revealed by the increased concentration of proline and soluble sugar, as well as the decreased electrolyte leakage, MDA content, and ROS accumulation, the latter being associated with higher ROS scavenging by enzymes activity (CAT, SOD, and POD). Importantly, the signaling response to cold stress was elucidated in pomegranate, namely, PgICE1 activated the promoter activity of PgCBF3 and PgCBF7 via MYC recognition site and sped up the PgCBF3 and PgCBF7 transcripts. Moreover, the two pomegranate CBFs may mediate the expression of the downstream Arabidopsis COR genes in transgenic plants in response to cold stress. Taken together, PgCBF3 and PgCBF7 conferred higher cold tolerance in Arabidopsis, which provided new insights for enhancing cold tolerance using genetic engineering in perennial fruit trees.