Over-expression of chrysanthemum CmDREB6 enhanced tolerance of chrysanthemum to heat stress.

BACKGROUND: Chrysanthemum is among the top ten traditional flowers in China, and one of the four major cut flowers in the world, but the growth of chrysanthemum is severely restricted by high temperatures which retard growth and cause defects in flowers. DREB (dehydration-responsive element-binding) transcription factors play important roles in the response to abiotic and biotic stresses. However, whether the DREB A-6 subgroup is involved in heat tolerance has not been reported conclusively. RESULT: In the present study, CmDREB6 was cloned from chrysanthemum (Chrysanthemum morifolium) 'Jinba'. CmDREB6, containing a typical AP2/ERF domain, was classed into the DREB A-6 subgroup and shared highest homology with Cichorium intybus L. CiDREB6 (73%). CmDREB6 was expressed at its highest levels in the leaf. The CmDREB6 protein localized to the nucleus. Based on the yeast one hybrid assay, CmDREB6 showed transcription activation activity in yeast, and the transcriptional activation domain was located in the 3 'end ranging from 230 to 289 amino acids residues. CmDREB6 overexpression enhanced the tolerance of chrysanthemum to heat. The survival rate of two transgenic lines was as high as 85%, 50%, respectively, in contrast to 3.8% of wild-type (WT). Over-expression of CmDREB6 promoted the expression of CmHsfA4, CmHSP90, and the active oxygen scavenging genes CmSOD and CmCAT.
CONCLUSION: In this study, DREB A-6 subgroup gene CmDREB6 was cloned from chrysanthemum 'Jinba'. Overexpression of CmDREB6 enhanced heat tolerance of chrysanthemum by regulating genes involved in the heat shock response and ROS homeogenesis.

Background

Plants face various abiotic stresses, among which heat stress has become one of the main factors affecting crop growth, quality and yield. High temperatures hamper plant photosynthesis, causing cell membrane damage, cell aging and death [1]. Heat stress can also affect enzymatic activities, which in turn have a negative impact on plant growth and metabolism.

Plants and other organisms have both an inherent ability to survive exposure to temperatures above the optimal for growth (basal thermotolerance) and an ability to acquire tolerance to otherwise lethal heat stress (acquired thermotolerance), where acquired tolerance depends on the activation of a number of transcription factors [2]. DREB transcription factors belong to a subfamily of the AP2/EREBP transcription factors family, whose conserved AP2/EREBP (ethylene-responsive element binding proteins) domain plays a key role in the binding of DREB transcription factors to cis-acting elements of DREB. The DREB group is divided into 6 subgroups (A-1 to A-6), and the A-1 and A-2 subgroups contain DREB1s and DREB2s genes, respectively. In Arabidopsis, these two types of genes are involved in low temperature, drought and high salt stress responses [3]. Overexpression of AtDREB1A was found to enhance tolerance of chrysanthemum to heat [4]. However, whether the DREB A-6 subgroup is involved in heat tolerance has not been reported conclusively.

Generally, when the temperature is higher than an ambient temperature of 10–15 °C, plants will generate a heat shock response (HSR) quickly, within a few hours, in order to tolerate the otherwise lethal temperature [5]. The HSR is mediated at the transcriptional level by cis-acting sequences called heat shock elements (HSEs) that are present in multiple copies upstream of the heat shock protein (HSP) genes [6]. The heat shock factor (HSF) plays an important role in the regulation of the expression of HSP genes in plants. When the plants are subjected to heat stimulation, a HSF can specifically bind to a HSE, thus activating the HSP gene expression in vivo. The rapid accumulation of heat shock proteins in the plant helps the folding, stabilization and assembling of proteins, thus improving the tolerance of plants to high temperature [7].

Chrysanthemum is among the top ten traditional flowers in China, and one of the four major cut flowers in the world. However, the growth of chrysanthemum is severely restricted by high temperatures which retard growth and cause defects in flowers [8]. In this study, we cloned CmDREB6, a member of the DREB family of the A-6 subgroup, from chrysanthemum ‘Jinba’ and further analyzed its expression profiles and transactivation activities. We successfully generated CmDREB6 overexpressing chrysanthemum lines and elucidated its regulatory roles in heat stress tolerance of chrysanthemum, thus shading a new light on the roles of the A-6 group DREB in abiotic stress tolerance.

Results

Cloning and phylogenetic analysis of CmDREB6 from chrysanthemum

We cloned a 1,028 bp CmDREB6 fragment from chrysanthemum. The largest open reading frame was 936 bp encoding a polypeptide of 311 amino acid residues (Additional file 1). The molecular weight of the putative protein was about 34.36 KDa, and the theoretical isoelectric point was 6.72. Phylogenic analysis of CmDREB6 and DREB members from other species showed that CmDREB6 is classified into the DREB A-6 subgroup, and is most closely related to CiDREB6 from Cichorium intybus (Fig. 1a), displaying 73% similarity to CiDREB6. The amino acid alignment showed that CmDREB6 contains one typical AP2/ERF domain which includes 1 α-helices and 3 β-sheet with the 14th valine and 19th leucine conserved in the DREB A-6 subgroup (Fig. 1b).

Fig. 1

Phylogenetic analysis and alignment of the deduced amino acid sequences of the DREB peptide sequences. a The phylogenic relationship of CmDREB6 and 39 members from other species of CvDREB2A(ABR23508.1), CiDREB2(AHJ08574.1), HaDREB2(AAS82861.1), GmDREB2A(AFU35563.1), DREB2A(BAA33794.1), OsDREB2A(AAN02487.2), FaDREB2(AAR11157.1), SiDREB2(ADM73511.1), SbDREB2A(AEI69362.1), PeDREB2L(ABV03750.1), WDREB2(BAD97369.1), ZmDREB2A(BAE96012.1), PgDREB2A(AAV90624.1), ZmDBF(AAM80486.1), CiDREB6(AHJ08575.1), RAP2–4(NP_177931.1), ABI4(AAC39489.1), ZmABI4(AAM95247.1), RAP2–1(NP_564496.1), RAP2–10(NP_195408.1), GhDBP1(AAO43165.1), CiDREN5(AHJ08576.1), TINY(AAC29139.1), GmTINY(ACP40513.1), ZmDBF2(AAM80485.1), CiDREB1A(AHI59150.1), DgDREB1B(ABD90467.1), DgDREB1A(ABD90468.1), CiDREB1B(AHI59151.1), CaDREB(AAR88363.1), MtDREB1C(ABB72792.1), HvCBF1(AAL84170.1), ZmDBP4(ACO72995.1), HvCBF2(AAM13419.1), OsDREB1B(AAN02488.1), HvCBF3(ACC63520.1), ZmDREB1A(AAN76804.1), OsDREB1A(AEW67332.1), LpCBF3(AAX57275.1). b Alignment of the deduced amino acid sequences of A-6 subgroup of CmDREB6 and CiDREB6(AHJ08575.1), ZmDBF(AAM80486.1), RAP2–4(NP_1777931.1). The red line represents the conserved DNA-binding domain (AP2/ERF domain), the blue line represents two motifs of M1 and M2, 3 green box, 1 orange box and ▲ respectively represent 3 β-sheets, 1 α-helix and V14, L19

Subcellular localization of CmDREB6

The pMDC43-GFP-CmDREB6 construct and empty vector pMDC43-GFP was transformed into onion epidermal cells via particle bombardment. GFP fluorescence of the control vector was evenly distributed throughout the observed onion epidermal cells (Fig. 2). In contrast, GFP fluorescence in the pMDC43-GFP-CmDREB6 fusion protein was observed only in the nucleus of the onion epidermal cells (Fig. 2), indicating that CmDREB6 localized to the nucleus in vivo.

Fig. 2

Subcellular localization of CmDREB6. Subcellular localization of transiently expressed CmDREB6 products in onion epidermal cells. The upper row shows the control 35S::GFP signal, and the lower row shows the signal of the 35S::GFP-CmDREB6 transgenes. The left panel shows bright field images, the middle one green fluorescence signals detected at 488 nm and the right one the merged Green Fluorescent Protein (GFP) and bright field images. Bar: 50 μm

Transactivation ability of CmDREB6 and its transcriptional activation domain analysis

The pGBKT7-CmDREB6 and the control plasmids were introduced into the yeast strain Y2H gold. The results showed that the yeast strain containing the recombinant plasmid pGBKT7-CmDREB6 was able to grow on SD / -Trp single-deficient medium, indicating that the recombinant plasmid was successfully transferred into the yeast strain Y2H gold; then the grown yeast was transferred to double-deficient medium SD / -His-Ade. The recombinant plasmid pGBKT7-CmDREB6 grew normally, while the negative control strain containing the pGBKT7 plasmid did not grow on SD / -His-Ade, with the positive control pCL1 growing normally (Fig. 3a). The pGBKT7-CmDREB6 colony on the double-defective plate supplemented with X-α-Gal turned blue (Fig. 3a), suggesting that pGBKT7-CmDREB6 possessed transcriptional activation abilities.

Fig. 3

Transcriptional activity assay of CmDREB6 protein and the analysis of transactivation activity domain of CmDREB6, (a): pGBKT7-CmDREB6; (b): distributed model; (c): transactivation activity domain analysis

To analyze the transcriptional activation domain of CmDREB6, the recombinant plasmid pGBKT7-CmDREB6 (1–311 amino acid, full length), the truncated fragment constructs of pGBKT7-CmDREB6 (1–290), pGBKT7-CmDREB6 (1–229), pGBKT7-CmDREB6 (1–189), and the pGBKT7 empty vector were subjected to yeast one hybrid assays. It was found that the yeast strains containing recombinant plasmids pGBKT7-CmDREB6 (1–229) and pGBKT7-CmDREB6 (1–189) could not grow normally, but pGBKT7-CmDREB6 (1–311) and pGBKT7-CmDREB6 (1–290) grew normally. The negative control strain containing the pGBKT7 empty plasmid did not grow on the SD / -His-Ade plate, but the positive control pCL1 grew normally (Fig. 3b). The results showed that the transcriptional activation domain of CmDREB6 was located in the 230–290 amino acid at the C terminal.

Tissue specific expression profiles and expression patterns of CmDREB6 in response to heat stress

RNA from root, stem, leaf and flower of chrysanthemum was extracted for analysis of the relative expression levels of CmDREB6 in different tissues. The expression levels of CmDREB6 was highest in leaves, followed by those in stem, flower and root in turn. The expression levels of CmDREB6 in stem, leaves and flower was 1.6, 5.2 and 1.1 folds higher respectively than in the root (Fig. 4a). The expression levels of CmDREB6 at 8 h, 12 h and 24 h after heat stress were 1.8, 2.6 and 1.2 folds higher than those at 0 h (before heat stress), respectively (Fig. 4b).

Fig. 4

Expression patterns of CmDREB6 in different organs and after 40 °C treatment. a Relative expression leveal of CmDREB6 in root, stem, leaf and flower of chrysanthemum. The expression of CmDREB6 was determined through qRT-PCR analysis. The expression level of CmDREB6 in root was set to 1, the error bars indicate the SE from three replicate samples. Asterisks indicate significant differences in expression levels of CmDREB6 in stem, leaf and flower compared with that in root. * represents significance at p < 0.05, ** represents significance at p < 0.01. b Relative expression leveal of CmDREB6 after 40 °C treatment. The expression of CmDREB6 was determined through qRT-PCR analysis. The expression level of CmDREB6 in WT was set to 1, the error bars indicate the SE from three replicate samples. Asterisks indicate significant differences in expression level of CmDREB6 under heat stress compared with WT at 0 h, 1 h, 3 h and 24 h, respectively, * represents significance at p < 0.05, ** represents significance at p < 0.01

CmDREB6 overexpression enhanced the tolerance of chrysanthemum to heat stress

Putative transgenic plants were verified by PCR amplification of hygromycin resistant gene. The expected bands with a fragment size of Ca. 750 bp were present in five putative transgenic lines, but not in WT plants (Fig. 5a; Additional file 2). The expression levels of CmDREB6 plants in overexpressing lines were higher than those of WT ‘Jinba’; two overexpressing lines with higher expression levels of CmDREB6, ox-8 and ox-15, were selected for further heat stress tolerance assays (Fig. 5b). The results showed that WT plants wilted severely, and all the leaves of WT plants became wilted, shrunk and drooped, and especially the top leaves of WT were severely burned after 24 h heat-shock. In contrast, ox-8 and ox-15 lines displayed minor wilting, and most leaves remained green (Fig. 5c). After one-week recovery growth, almost all WT plants were scorched, and only one out of 26 plants survived with very weak growth, and the survival rate of WT plants was 3.8%, whereas the survival rate of ox-8 and ox-15 was 85% and 50%, respectively (Fig. 5c), indicating that CmDREB6 conferred heat stress tolerance to chrysanthemum.

Fig. 5

Analysis of phenotype and survival rate of two transgenic chrysanthemum and WT chrysanthemum. a PCR identification results of CmDREB6 in the putative transgenic ‘Jinba’ by Hyg primers; M, 2000 Maker; 8, 9, 10, 11, 15 represents putative transgenic lines; 21 represents WT. b Relative expression level of CmDREB6 in five putative transgenic lines; The expression of CmDREB6 was determined through qRT-PCR analysis. The expression level of CmDREB6 in WT was set to 1, the error bars indicate the SE from three replicate samples. Asterisks indicate significant differences in CmDREB6 expression levels in putative transgenic lines compared with that in WT. * represents significance at p < 0.05, ** represents significance at p < 0.01. c The phenotype and survival rate of two transgenic chrysanthemum and WT plants under heat stress

CmDREB6 over-expression induced the expression of CmHsfA4, CmHSP90 and antioxidant enzymes encoding genes CmSOD and CmCAT

To dissect the pathways that lead to improved heat stress tolerance in chrysanthemum by overexpressing CmDREB6, the expression levels of CmHsfA4, CmHSP90, CmSOD and CmCAT were quantified in chrysanthemum under heat stress. Expression of CmHsfA4 was enhanced by heat shock treatment in both WT and ox lines plants, the expression levels of CmHsfA4 in ox-8, ox-15 plants were always higher than those in WT (Fig. 6a). The expression of CmHSP90 increased in response to heat stress, the expression level of CmHSP90 in both ox-8 and ox-15 plants remained higher than that of WT during heat stress (Fig. 6b). CmDREB6 overexpression promoted expression of the reactive oxygen scavenging genes CmSOD and CmCAT in ox-8 and ox-15 plants; the expression levels of these two genes were higher than those in WT plants under heat stress (Fig. 6c, d).

Fig. 6

Relative expression levels of CmHsfA4, CmHSP90, CmSOD and CmCAT. a Relative expression levels of CmHsfA4; b Relative expression levels of CmHsp90; c Relative expression levels of CmSOD; d Relative expression levels of CmCAT. The expression of these genes was determined via qRT-PCR analysis. The expression level of CmDREB6 in WT at 0 h was set to 1, the error bars indicate the SE from three replicate samples. Asterisks indicate significant differences in gene expression levels in CmDREB6 overexpression lines compared with WT. * represents significance at p < 0.05, ** represents significance at p < 0.01

Discussion

Chrysanthemum CmDREB6 over-expression conferred heat tolerance

Members of the A-6 DREB family have been isolated from several species, and their roles in stress responses and development have been characterized. CiDREB6 was mainly induced under intense heat and drought, but not by low temperature and high salt [9]. One of the eight members of the Arabidopsis DREB A-6 subgroup, ERF055, was expressed in the roots, stems, leaves, flowers and pods of Arabidopsis, with the highest expression levels in the pods; it has been verified that ERF055 gene in Arabidopsis is involved in the development of embryo and postembryonic development [10]. The AP2/ERF transcription factor WIND1 (WOUND INDUCED DEDIFFERENTIATION 1), which belongs to the A-6 DREB subgroup, promotes cell dedifferentiation in Arabidopsis, and induces callus formation in rapeseed, tomato, and tobacco [11]. Other members of the A-6 subgroup were successively isolated in different species. For example, in Jatropha curcas L., expression of JcDREB was induced by cold, salt and drought stress, but not by ABA (Abscisic acid), and overexpression of JcDREB in Arabidopsis enhances salt tolerance and freezing tolerance [12]. GhDBP2 was expressed at high levels in the leaves of Gossypium hirsutum, and was strongly induced by drought, high salt, low temperature and ABA [13]. In Nicotiana tabacum, overexpressing the Suaeda salsa SsDREB, a member of A-6 subgroup, tolerance to salt and drought increased, as well as the growth rate, chlorophyll content and photosynthetic rate, protein level and soluble sugar content compared to WT plants [14]. The expression of MsDREB6.2 from Malus sieversii Roem is strongly induced by drought and salinity stress, and is expressed at high levels in roots. Overexpression of MsDREB6.2 resulted in cytokinin-deficient developmental phenotypes by enhancing MdCKX4a expression and enhanced drought tolerance in transgenic apple plants [15]. These data indicate that DREB transcription factors could be used to improve the tolerance of plants to abiotic stress, and different DREB transcription factors have different members and species specificity [16]. In this study, the expression of the DREB A-6 subgroup member CmDREB6 was highest in leaves, and was induced by high temperatures, suggesting that CmDREB6 may play a role in response to heat stress. In agreement with heat inducible expression, CmDREB6-overexpressed chrysanthemum enhanced the tolerance to heat (Fig. 5), suggesting that CmDREB6 confers heat tolerance.

CmDREB6 enhanced heat tolerance of chrysanthemum by upregulating the expression of CmHsfA4 and CmHSP90

HSFs (Heat shock factors) play important roles in the response to heat stress [17]. HsfA3 acts as a thermo-stable regulator under the control of the DREB2A pathway, is downstream of the DREB2A stress-modulating mechanism, and regulates the expression of many heat-inducible genes [18]. More evidence showed that DREB2A activates the HsfA3 and subsequently regulates the expression of HSP genes involved in the early phases of the HSR, and DREB2C transactivates DRE-dependent transcription of HsfA3 inducing the expression of the downstream gene HSPs, thereby enhancing thermotolerance in the late phases of HSR [19, 20]. Recent studies have shown that HsfA2 and HsfA3 function in the same heat regulation pathway, and HsfA2 plays a dominant role over HsfA3 [21]. HsfA4 is a potent activator of heat stress gene expression [22]. However, the regulation of HsfA4 by DREB has not been reported previously. In the present study, induction of CmHsfA4 was observed in CmDREB6 overexpressed plants either in non-stressed or heat stressed plants (Fig. 6), suggesting the DREB A-6 subfamily member CmDREB6, might enhance heat tolerance in chrysanthemum by activating the expression of CmHsfA4. However, whether CmDREB6 binds to the promoter of CmHsfA4 directly remains to be determined.

HSPs are important molecular chaperones, widely mediating stress signals [23]. In the absence of stress, HSP and HSF exist together as molecular chaperones. After a heat shock reaction, plants produce large amounts of toxic proteins, and HSPs are released from HSFs and then bind to toxin proteins [24]. Many HSP proteins are known to act as molecular chaperones for the protection of thermo-labile proteins against heat-induced denaturation in plant cells [25-27]. In this study, expression of CmHSP90 was induced in CmDREB6 overexpressing plants, which might protect chrysanthemum from heat induced damage. Members of the HsfA subclass A4 have been shown to serve as transcriptional activators for HSP genes [19, 28, 29]. Whether induction of CmHsfA4 in CmDREB6 overexpressing plants upregulates the expression of CmHSP70 and CmHSP90 remains to be elucidated. The MsHSFA4 gene in Medicago sativa was not expressed under non-stress conditions but its expression was induced by heat shock, similarly to AtHSFA4a expression [30].

CmDREB6 enhanced heat tolerance of chrysanthemum by regulating ROS homogenesis

Heat stress may induce the generation and reactions of activated oxygen species (ROS) including singlet oxygen (1O2), superoxide radical (O2−), hydrogen peroxide (H2O2) and hydroxyl radical (OH−) [31]. ROS causes the autocatalytic peroxidation of membrane lipids and pigments, thus leading to the loss of membrane semi-permeability and modifying its functions [1]. In response, plants will then produce antioxidant enzymes, such as superoxide dismutase (SOD), catalase (CAT) to mitigate the damage to the cell membrane and improve heat resistance [1]. HSP90 was found to be involved in the regulation of HsfA2 expression in response to oxidative stress, where the heat shock response promotes expression of SOD, while the active oxygen scavenging gene CAT expression was not significantly altered [24]. Overexpression of HsfA4A could prevent oxidative damage in Arabidopsis and enhance tolerance not only to salt but also to osmotic stress, paraquat, H2O2 and anoxia [32]. The ThDREB from Tamarix hispida could effectively improve tolerance to salt and drought stress by enhancing the antioxidase activity that keeps ROS accumulation at low levels, thus facilitating scavenging [33]. Ectopic expression of EgDREB1 from Elaeis guineensis enhanced expression of tomato peroxidase (LePOD), ascorbate peroxidase (LeAPX), catalase (LeCAT), superoxide dismutase (LeSOD), heat shock protein 70 (LeHSP70) in tomato seedlings under PEG treatment and cold stress [34]. The AtDREB1B transgenic plants generally displayed lower levels of malondialdehyde (MDA) but higher levels of superoxide dismutase (SOD), catalase (CAT), and peroxidase (POD) activities than the WT under drought stress [35]. Similarly, CmDREB6 overexpression could promote the expression of ROS pathway related genes CmSOD and CmCAT in chrysanthemum, suggesting that CmDREB6 enhances heat tolerance of chrysanthemum by regulating ROS homeostasis.

In addition, over accumulation of stress-related transcription regulators could be detrimental to growth and is not deemed preferable [36, 37]. In this study, growth retardation was observed in the CmDREB6 ox-15 line with highest expression levels of CmDREB6. Compared to the WT plants, the tolerance of ox-15 line to heat stress and the activation of the expression of downstream genes are not as obvious as those of the ox-8 line, suggesting that over accumulation of CmDREB6 retarded growth might affect tolerance to heat stress.

Conclusions

The expression of the DREB A-6 subgroup member CmDREB6 was induced by high temperatures. And CmDREB6-overexpressed chrysanthemum enhanced the tolerance to heat, suggesting that CmDREB6 confers heat tolerance. Induction of CmHsfA4 was observed in CmDREB6 overexpressed, and CmHSP90 was induced in CmDREB6 overexpressing plants, which might protect chrysanthemum from heat induced damage. CmDREB6 overexpression could promote the expression of ROS pathway related gene CmSOD and CmCAT in chrysanthemum, suggesting that CmDREB6 enhances heat tolerance of chrysanthemum by regulating ROS homeostasis.

Methods

Plant materials and growth conditions

Cuttings of the chrysanthemum variety ‘Jinba’ were obtained from the Chrysanthemum Germplasm Resource Preserving Center (Nanjing Agricultural University, Nanjing, China). The cuttings were potted into a 1:2 (v/v) mixture of garden soil and vermiculite, and were maintained in a greenhouse with a relative humidity of 80%, light intensity 100 μmol·m− 2·s− 1 and a 16 h/8 h (light/dark) photoperiod, with day and night temperatures of 23 °C and 18 °C, respectively.

Isolation and sequence analysis of CmDREB6

Total RNA was isolated from chrysanthemum leaves using the RNAiso reagent (Takara, Tokyo Japan) and following the manufacturer’s protocol. A 1 μg aliquot of the resulting RNA treated with RNase-free DNase I was included as the template for 1st strand cDNA synthesis, using Super Script III reverse transcriptase (Invitrogen, Carlsbad, CA, USA). The CmDREB6 open reading frame (ORF) was amplified using CmDREB6-F/R primers (Additional file 3). The PCR product purified using a Biospin Gel Extraction kit (Bio Flux, Hangzhou, China) was introduced into pMD19-T (Takara) for sequencing. The CmDREB6 sequence was aligned with its homologs using the DNAMANV6 software [38], and a phylogenic tree was generated using MEGA5.0 software based on the neighbor-joining method and 1,000 bootstrap replicates. The polypeptides sequences of other DREB members from other species were obtained from the NCBI website (https://www.ncbi.nlm.nih.gov).

Tissues specific expression patterns of CmDREB6 and its expression profiles in response to heat stress

Roots, stems and leaves were harvested from four-week old chrysanthemum plants to characterize the tissue specific expression profile of CmDREB6 transcription. The heat stress experiment (40 °C) was conducted as previously described [39]. The second leaf (counted from the shoot apex) at 0 h, 4 h, 8 h, 12 h and 24 h after heat stress, respectively, was sampled for RNA isolation. 1st strand cDNA was transcribed as previously described. Transcript abundance was detected by quantitative real time PCR (qPCR) using SYBR® Premix Ex Taq™ II (Tli RNaseH Plus) (Takara) and the primer pair CmDREB6-RT-F/R (Additional file 3). The primer pair CmEF1α-F/R (Additional file 3) was used to amplify the reference gene CmEF1α. Fold changes were calculated using the 2−ΔΔCt method [40]. Each experiment included three biological replicates.

Sub-cellular localization and transcriptional activation assay of CmDREB6

The CmDREB6 ORF was amplified using a Phusion® High Fidelity PCR Kit (New England Biolabs, Ipswich, MA, USA) with the primer pair CmDREB6-Nde-F/-BamH-R (Additional file 3). The resulting amplification was digested by NdeI/BamHI, and then ligated into pENTR™1A (Invitrogen) to form the construct pENTR™1A-CmDREB6.

For the subcellular assay, CmDREB6 was further inserted into the destination vector pMDC43 or pDEST-GBKT7 via LR reaction. The pMDC43-GFP-CmDREB6 construct and the empty pMDC43 vector were introduced into onion epidermal cells via particle bombardment (PDS-1000; Bio-Rad). Transformed cells were held for 16 h on Murashige and Skoog (MS) medium in the dark, and then GFP (Green fluorescent protein) florescence was observed under a confocal laser scanning microscope.

For the transcriptional activation assay, CmDREB6 was inserted into the destination vector pDEST-GBKT7 via LR reaction. The pDEST-GBKT7 vector with different segments of CmDREB6 (1–311, 1–189, 1–229, 1–290 amino acid) was constructed to screen the transactivation region of the protein. Clones were sequenced to verify the inserts were correct. The recombinant plasmids pGBKT7-CmDREB6 or pGBKT7 empty vector (negative control) or pCL1 (positive control) were transformed into a Y2H gold yeast strain, then plated on SD / -Trp plates and cultured at 30 °C for 3 days. Yeast colonies were then transferred to medium SD / -His-Ade and cultured in the dark at 30 °C for 3 days. The growth of yeast was observed and photographed.

Regeneration of CmDREB6 overexpressing chrysanthemum plants

To identify the function of CmDREB6, the vector of pMDC43-GFP-CmDREB6 driven by 35S promoter was introduced into chrysanthemum ‘Jinba’ by Agrobacterium-mediated leaf disc infection [41]. Putative transgenic plants were verified by PCR analysis using Hyg (hygromycin) F/R primers, and over-expression of CmDREB6 in transgenic plants was detected via qPCR using primers CmDREB6-RT-F/R.

Heat stress tolerance assay for CmDREB6 overexpressing chrysanthemum plants

Over-expression lines and WT plants were planted in the same batch (soil: vermiculite; 1: 1, v/v). For the heat tolerance assay, chrysanthemum seedlings at the 6–8 leaves stage were exposed to 45 °C for 24 h; heat stressed plants were then transferred to 22 °C and left to recover for one-week [4]. Phenotypic changes before and after heat treatment respectively were documented, and survival rates were calculated.

Gene expression profiles in CmDREB6 overexpressing chrysanthemum plants

To further dissect the mechanisms involved in CmDREB6 regulated heat tolerance in chrysanthemum, the third leaves (counted from the shoot apex) of heat stressed chrysanthemum and WT plants were sampled at 0 h, 1 h, 3 h, 24 h after exposure to heat treatment. Total RNA isolation and cDNA were prepared as detailed above. Expression levels of the heat stress-related genes CmHsfA4 (CmHsfA4 F/R), CmHSP90 (CmHSP90 F/R) and antioxidant enzymes encoding genes of CmSOD (CmSOD F/R) and CmCAT (CmCAT F/R) were quantified. All the primers used are listed in Additional file 3.

Statistical analysis

Results are expressed as mean ± standard error. Statistical significance was determined by SPSS 19.0 amongst the means of WT and transgenic plants, and a one-way analysis of variance using LSD (least significant diferrence) multiple range test was employed to identify treatment means that differed statistically.

Text S1. The amino acid sequence of CmDREB6 under accession No. MG199593. (DOC 22 kb)

Figure S1. The electrophoresis analysis of PCR products of hygromycin resistant gene HptII in the putative CmDREB6 transgenic ‘Jinba’. (TIF 59 kb)

Table S1. The sequence of primers used in this research. (DOC 24 kb)