Ectopic Expression of the Coleus R2R3 MYB-Type Proanthocyanidin Regulator Gene SsMYB3 Alters the Flower Color in Transgenic Tobacco

Qinlong Zhu; Shunzhao Sui; Xinghua Lei; Zhongfang Yang; Kun Lu; Guangde Liu; Yao-Guang Liu; Mingyang Li

doi:10.1371/journal.pone.0139392

Abstract

Proanthocyanidins (PAs) play an important role in plant disease defense and have beneficial effects on human health. We isolated and characterized a novel R2R3 MYB-type PA-regulator SsMYB3 from a well-known ornamental plant, coleus (Solenostemon scutellarioides), to study the molecular regulation of PAs and to engineer PAs biosynthesis. The expression level of SsMYB3 was correlated with condensed tannins contents in various coleus tissues and was induced by wounding and light. A complementation test in the Arabidopsis tt2 mutant showed that SsMYB3 could restore the PA-deficient seed coat phenotype and activated expression of the PA-specific gene ANR and two related genes, DFR and ANS. In yeast two-hybrid assays, SsMYB3 interacted with the Arabidopsis AtTT8 and AtTTG1 to reform the ternary transcriptional complex, and also interacted with two tobacco bHLH proteins (NtAn1a and NtJAF13-1) and a WD40 protein, NtAn11-1. Ectopic overexpression of SsMYB3 in transgenic tobacco led to almost-white flowers by greatly reducing anthocyanin levels and enhancing accumulation of condensed tannins. This overexpression of SsMYB3 upregulated the key PA genes (NtLAR and NtANR) and late anthocyanin structural genes (NtDFR and NtANS), but downregulated the expression of the final anthocyanin gene NtUFGT. The formative SsMYB3-complex represses anthocyanin accumulation by directly suppressing the expression of the final anthocyanin structural gene NtUFGT, through competitive inhibition or destabilization of the endogenous NtAn2-complex formation. These results suggested that SsMYB3 may form a transcription activation complex to regulate PA biosynthesis in the Arabidopsis tt2 mutant and transgenic tobacco. Our findings suggest that SsMYB3 is involved in the regulation of PA biosynthesis in coleus and has the potential as a molecular tool for manipulating biosynthesis of PAs in fruits and other crops using metabolic engineering.

Citation: Zhu Q, Sui S, Lei X, Yang Z, Lu K, Liu G, et al. (2015) Ectopic Expression of the Coleus R2R3 MYB-Type Proanthocyanidin Regulator Gene SsMYB3 Alters the Flower Color in Transgenic Tobacco. PLoS ONE 10(10): e0139392. https://doi.org/10.1371/journal.pone.0139392

Editor: Yuepeng Han, Wuhan Botanical Garden of Chinese Academy of Sciences, CHINA

Received: June 16, 2015; Accepted: September 11, 2015; Published: October 8, 2015

Copyright: © 2015 Zhu et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited

Data Availability: All relevant data are within the paper and its Supporting Information files.

Funding: This work was supported by grants from the China Postdoctoral Science Foundation (20070420787), the National High Technology Research and Development Program (‘863’ Program) of China (2007AA10Z184), and the National Natural Science Foundation of China (31000698). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing interests: The authors have declared that no competing interests exist.

Introduction

Proanthocyanidins (PAs), also called condensed tannins (CTs), result from condensation of flavan-3-ols, and belong to one of the main classes of polyphenolic compounds synthesized via the flavonoid biosynthetic pathway [1]. PAs are widely present in the plant kingdom, in fruits, seeds, flowers, leaves, and bark, and play an important role in defense against plant diseases and herbivores [2]. PAs contribute to the quality and health benefits of many important plant products, such as fruit and wine [3]. As powerful antioxidants, PAs can provide multiple beneficial effects for human health, including enhanced immunity and protection against free radical-mediated injury and cardiovascular diseases [4, 5]. For these reasons, it is important to further understand the molecular regulation and metabolic engineering of PAs to improve the nutrient and health values of important crops and fruits. As a branch of the flavonoid pathway, PA biosynthesis shares almost all structural genes with anthocyanin biosynthesis, except for the last catalytic steps (Fig 1).

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Fig 1. Schematic diagram of the flavonoid biosynthesis pathway, including main branches of anthocyanins, PAs, and flavonols.

PAL, phenylalanine ammonia lyase; CHS, chalcone synthase; CHI, chalcone isomerase; F3H, flavonone 3-hydroxylase; DFR, dihydroflavonol reductase; FLS, flavonol synthase; ANS, anthocyanin synthase; LAR, leucoanthocyanidin reductase; ANR, anthocyanidin reductase; UFGT, UDP-glucose: flavonoid 3-O-glucosyltransferase. Asterisks indicate key structural enzymes in PA biosynthesis.

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Synthesis of PAs begins with the generation of flavan-3-ol units (e.g., catechin and epicatechin); two key structural genes and one R2R3 MYB-type regulatory gene involved in PAs biosynthesis have been identified. The key enzymes are leucoanthocyanidin reductase (LAR, EC 1.17.1.3) and anthocyanidin reductase (ANR, EC 1.3.1.77), which convert leucocyanidin and cyanidin to catechin and epicatechin, respectively. The molecular and biochemical functions of the genes encoding these enzymes have been identified in several plant species, for example, LARs in apple [5], legume[6], grapevine (Vitis vinifera)[3, 7], and Medicago truncatula [8]; and ANRs in Arabidopsis[9], grapevine [3, 7], tea [10], apple [11], and soybean [12]. In flavonoid biosynthesis, the transcriptional activities of the key enzymes are controlled by R2R3 MYB transcription factors (TFs) combined with bHLH and WD40 proteins that form a MYB-bHLH-WD40 (MBW) transcriptional activation complex in which the MYBs play a crucial role [1, 13–15]. To date, functional characterization of the MYBs involved in the production of PAs has been reported in Arabidopsis (AtTT2) [16], grapevine (VvMYBPA1 and VvMYBPA2) [17, 18], Lotus japonicus (LjTT2a/b/c) [19], persimmon (DkMYB2 and DkMYB4) [20, 21], poplar (PtMYB134) [22], and Medicago truncatula (MtPAR) [23]. For example, in Arabidopsis, the MBW transcription complex of PA regulation is composed of three TRANSPARENT TESTA (TT) genes: AtTT2 (AtMYB123), AtTT8 (AtbHLH042), and AtTTG1 (WD40-repeat protein) [16, 24]. The AtANR transcripts could not be detected in the tt2 mutant, and PAs cannot accumulate in the seed coat. In grapevines, VvMYBPA1 and VvMYBPA2 regulate PA synthesis during fruit development and significantly activate VvLAR1, VvANR, and several flavonoid structural genes [17, 18]. In persimmon fruits, DkMYB4 regulates the expression of DkANR and has little influence on DkLAR, but DkMYB2 can directly activate both of these key genes, which are induced by wound stress [20, 21].

Ectopic overexpression of the key enzyme-encoding genes of the PA pathway has been utilized to engineer CT biosynthesis in tobacco. However, there are few reports on the use of the MYB-type PA-regulation method. Although ectopic expression of ANRs from Arabidopsis [9], grapevine [7], and Medicago truncatula [11], led to loss of anthocyanins and accumulation of CTs, overexpression of MtLAR did not increase the content of CTs in transgenic tobacco flowers [8]. These results indicate the limitations and uncertainty of the single key enzyme strategy. In contrast, MYBs are more suitable for engineering CT biosynthesis because of their regulation of multiple structural genes. Therefore, isolation and utilization of novel MYBs involved in the PA pathway will provide valuable insights into the molecular regulation and metabolic engineering of PA biosynthesis in plants.

Coleus, Solenostemon scutellarioides (L.) Codd, is a well-known ornamental plant with colorful foliage and is a popular houseplant worldwide [24, 25]. Because it is rich in secondary metabolites (e.g., rosmarinic acid and flavonoids), coleus is used as a medical plant in countries such as India, Indonesia, and Mexico [26]. Rosmarinic acid is an ester of caffeic acid involved in plant defense and antioxidant activities. The biosynthesis pathway and related genes for rosmarinic acid have been characterized in coleus [27, 28]. However, few studies have reported on the key structural and regulatory genes involved in the flavonoid pathway (especially in biosynthesis of PAs and anthocyanins) in coleus. Therefore, isolation and characterization of these regulatory genes, such as MYBs, will be necessary for understanding the molecular regulation of biosynthesis of PAs or anthocyanins in this species.

In this study, we isolated and characterized a regulatory gene in coleus, SsMYB3, which encodes an R2R3 MYB TF. The expression level of SsMYB3 is correlated with CT content in various tissues of coleus and is induced by wounding and light. A complementation test of this TF gene in the Arabidopsis tt2 mutant shows that SsMYB3 could restore the PA-deficient seed coat phenotype. Ectopic overexpression of SsMYB3 leads to a large reduction in anthocyanin level and enhanced accumulation of CTs in transgenic tobacco flowers. These results suggest that SsMYB3 is a functional PA regulator and may be a useful molecular tool for metabolic engineering of PA biosynthesis in plants.

Materials and Methods

Plant materials, stress treatments, and isolation of total RNA

The red-leaved coleus variety ‘Red Trailing Queen’ was grown in a greenhouse under natural light conditions at 25°C. Wild-type and T1 transgenic tobacco (Nicotiana tabacum W38) plants were grown under the same conditions. The Arabidopsis tt2 mutant was purchased from ABRC (Arabidopsis Biological Resource Center, OH, USA) and was used for complementation analysis.

Three stress treatments were performed for gene-expression studies. In a dark experiment, coleus seedlings were cultured in the dark and leaves were collected at 0, 1, 8, 24, and 48 h after treatment. After 2 weeks continuous culture under dim light (200 lux), leaves of the coleus seedlings were exposed to high light intensity (25,000 lux) and collected at 0, 0.5, 1, 2, and 8 h after lighting. For wounding treatments with reference to [22], the edges of coleus leaves were crushed with pliers. All the required samples were immediately frozen in liquid nitrogen and stored at –80°C until analysis.

Total RNA was isolated from frozen samples using a W6711 Total RNA Extraction Kit (Watson, China) or Trizol reagent (Invitrogen, USA) according to the manufacturer’s instructions, followed by incubation with RNase-free DNase I (Takara, Dalian, China).

Cloning of the full-length SsMYB3 gene

First-strand cDNA was synthesized from 1 μg of DNase-treated RNA with an M-MLV reverse transcriptase kit (Promega, USA) in a total volume of 20 μL, using oligo (dT) 15 primer. The numerous fragments encoding parts of the R2R3 MYB domains were obtained from young red coleus leaves using degenerate oligonucleotide primer PCR. The degenerate primers, FdMYB and RdMYB, were designed according to the conserved regions of the coleus R2R3 MYBs involved in flavonoid biosynthesis.

One cDNA clone, SsMYB3, showed high similarity to other known flavonoid regulators and was selected to isolate the full-length cDNA sequence using RACE PCR (GeneRacer Kit, Invitrogen, USA). The full-length cDNA and DNA was then amplified with two specific primers, FMYB3 and RMYB3, in a total volume of 50 μL with the following protocol: 94°C for 4 min; 35 cycles of 94°C for 30 s; 56°C for 30 s; and 72°C for 2 min; followed by a final extension of 72°C for 5 min. All amplified products were purified, subcloned, and sequenced. The primers used for the degenerate PCR, RACE PCR, and the full-length amplification of the SsMYB3 gene are listed in S1 Table.

Sequence analysis and construction of expression vector

Molecular characterizations and multiple sequence alignments of SsMYB3 were analyzed using the Vector NTI 10.0 software package (Invitrogen, USA). For phylogenetic analysis, several full-length amino acid sequences of R2R3 MYBs involved in regulation of flavonoid metabolism were selected for alignment using the ClustalX 1.8 program with default parameters, and the tree was constructed using the neighbor-joining method in the MEGA 5.0 package [29].

The modified plant binary vector pCAMBIA2301G was constructed by inserting an expression cassette with CaMV 35S promoter, multiple cloning sites (XbaI, BamHI, SmaI, KpnI, and SacI) and NOS terminator into the EcoRI and HindIII sites of pCAMBIA2301; the PCR product of SsMYB3 cDNA with XbaI and SmaI sites was then subcloned into the same sites of pCAMBIA2301G. The resulting vector, pCAMBIA2301G-SsMYB3, containing a plant-selectable marker NPTII gene conferring kanamycin resistance, was sequenced and then transferred into Agrobacterium tumefaciens strain LBA4404 by the freeze-thaw method [30].

Arabidopsis complementation analysis

The Arabidopsis tt2 mutant lacking PA biosynthesis in the seed coat was transformed with A. tumefaciens strain LBA4404 containing the binary construct pCAMBIA2301G-SsMYB3 by floral dipping [31]. Harvested seeds were selected on MS medium containing 3% (v/v) sucrose and with 100 mg/L kanamycin. For phenotypic analysis of CT accumulation in the seed coat, T₁ seeds were stained with dimethylaminocinnaldehyde reagent (DMACA, Sigma) according to a previous report [32].

Transformation of tobacco plants

The Agrobacterium strain LBA4404 containing the binary vector was incubated in liquid YEB medium supplemented with 200 mmol/L acetone-syringone at 28°C. The Agrobacterium was co-cultivated with leaf discs from N. tabacum cv.W38 until OD₆₀₀ reached 0.5–0.6, and the transformation method according to a previous report [33]. Transformed plants were grown on MS medium containing 100 mg/L kanamycin under a 16-h photoperiod at 25°C. Finally, transgenic tobacco plants were identified by PCR amplification of the NPTII and SsMYB3 genes of kanamycin-resistant plantlets.

Yeast two-hybrid analysis

To detect proteins that may interact with SsMYB3 in Arabidopsis and tobacco, yeast two-hybrid (Y2H) assays were performed, using the Matchmaker™ Gold Y2H System (Clontech, USA). For the Y2H experiments, the full-length coding sequence of SsMYB3 was ligated into the pGADT7 (activation domain, AD) and pGBKT7 (binding domain, BD) vectors. The full-length cDNAs of AtTT2, AtTTG1, and NtAn11-1 (WD40), and the coding sequences of MYB-interaction regions of AtTT8 (aa1-204), NtAn1a (aa1-195), or NtJAF13-1 (aa1-203) were ligated into the pGBKT7 (BD) vector using previous method [34]. The AD and BD fusion vectors were co-transformed into the Saccharomyces cerevisiae strain Y2HGold using the lithium-acetate method as described in the Clontech yeast protocol handbook. Co-transformed colonies were first selected on SD medium lacking leucine and tryptophan (SD-Leu–Trp), and were then screened for growth on quadruple-selection SD medium lacking adenine, histidine, leucine, and tryptophan (SD-Ade–His–Leu–Trp).

Expression analysis of RT-PCR and quantitative real-time PCR (qPCR)

Isolation of total RNA from different plant materials and synthesis of first-strand cDNA was performed as described above.

Expression of the SsMYB3 gene and several key flavonoid genes in SsMYB3-overexpressing Arabidopsis immature siliques and tobacco flowers were determined by RT-PCR using the following program: 94°C (4 min); 18–22 cycles of 94°C (30 s), 58°C (30 s), and 72°C (30 s); and 72°C (5 min). All primers used for RT-PCR are listed in S2 Table. The transcript levels of the SsMYB3 gene in different coleus tissues and in leaves subjected to the different treatments were measured by qPCR. The coleus actin gene SsACT was used as an internal control to normalize gene expression. The results were calculated as differences in cycle threshold (Ct) between SsMYB3 and actin genes (2^-ΔCt). The expression of the structural genes of anthocyanin and PA pathways was measured by qPCR using RNA isolated from the SsMYB3-overexpressing tobacco flowers. The tobacco GAPDH gene was used as an endogenous control to normalize gene expression. The results were analyzed using the comparative Ct method and quantified relative to the wild type (2^-ΔΔCt).

All qPCR assays were performed using SYBR Green Master Mix reagent (TaKaRa, Dalian, China) using a BioRad IQ5 real-time PCR detection system, following thermal cycling conditions recommended by the manufacturer. All PCR reactions were performed in triplicate and repeated twice. The primer sequences for qPCR are listed in S3 Table.

Measurement of anthocyanin and condensed tannins

Quantification of anthocyanin was performed as described by Rabino et al. [35, 36] with some modifications. Briefly, fresh flowers of SsMYB3-overexpressing tobacco were ground in liquid nitrogen and placed into 5 mL extraction buffer (1% HCl in methanol) overnight in the dark at 4°C. After centrifugation, 1 mL of extract was diluted with1 mL of water, 2 mL of chloroform was added to remove chlorophyll, and the mixture was centrifuged for 10 min at 12,000 × g. Absorption of the aqueous phase was measured spectrophotometrically at 530 and 650 nm. The anthocyanin content was quantified as (A530–0.25 × A650) g^-1 fresh weight (FW). The experiment was repeated three times for each transgenic plant.

The amount of soluble CTs from leaves of coleus or wild-type and transgenic tobacco flowers was determined by the vanillin-HCl method as reported previously [37, 38]. Leaves or flowers were ground in liquid nitrogen, extracted with 10 mL of methanol, and shaken for 20 min following centrifugation. One milliliter of supernatant was incubated with 5 mL vanillin-HCl reagent (0.5% vanillin solution in methanol containing 4% HCl [v/v]) for 30 min at 30°C. The reaction solution was determined at 500 nm using a UV-VIS spectrophotometer (Shimadzu, Japan). The mean CT content was obtained from three replicate measurements of each plant material.

Results and Discussion

Isolation and characterization of SsMYB3 gene

On the basis of the conserved sequences of R2R3 MYBs from ZmP (U57002), AtMYB12 (AEC10843), AtPAP1 (ABB03879), PhAN2 (AF146702), and GmYB10 (AJ554700), we designed degenerate PCR primers to amplify an approximately 200-bp fragment using cDNA from coleus leaves as a template. Following subcloning and sequencing of the PCR product, nine different DNA fragments were obtained from 20 independent clones. One of which, named SsMYB3, had similarity with the conserved region of MYBs related to flavonoid synthesis. According to this partial sequence, the complete cDNA sequence of the SsMYB3 gene was determined by 5′- and 3′-RACE PCR. Then, the genomic sequence of SsMYB3 was amplified and sequenced (S1 Fig).The GenBank accession numbers of the sequences are EF522163 and EF522164, respectively.

The full-length cDNA sequence was 826 bp in size, containing a 747-bp ORF; the corresponding genomic sequence was 931 bp and consisted of two exons and a 105-bp intron with a standard GT/AG splicing site (S2 Fig). SsMYB3 encoded a 248 amino acid protein with predicted molecular mass of 27 kDa and calculated isoelectric point of 10.42. Using the NCBI conserved domain search program (http://www.ncbi.nlm.nih.gov/Structure/cdd/wrpsb.cgi), an N-terminal R2R3 repeat corresponding to the DNA-binding (MYB) domain was detected in the deduced amino acid sequence of SsMYB3 (Fig 2A). Similar to related MYBs, the bHLH motif [D/E]Lx₂[R/K]x₃Lx₆Lx₃R that interacts with bHLH proteins was identified in the highly conserved N-terminal R2R3 region of SsMYB3 (Fig 2A). Despite the fact that C-terminal regions of MYBs are highly variable, a novel, possibly conserved motif, K[I/V]x₂PKPx₁Rx₂S[I/L], was found only in SsMYB3 and in two other members of PA-clade 1 (Fig 2A) by alignment with MYBs of known function that regulate PA biosynthesis, using Vector NTI 10.0 software. At the same time, the C-terminal conserved motif in AtTT2, VI[R/P]TKAx₁RC[S/T] [16], was found only in members of PA-clade 2. The MYB domain and full-length sequence of SsMYB3 were most closely related to the grapevine PA-synthesis regulator VvMYBPA1, with 83% and 60% identical amino acid residues, respectively.

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Fig 2. Comparison of SsMYB3 with other functional R2R3-MYB TFs.

(A) Full-length protein sequence alignments of the MYBs by Vector NTI 10.0 software. The R2 and R3 domains are shown; the bHLH motif [D/E]Lx₂[R/K]x₃Lx₆Lx₃R and two possible PA specifically conserved motifs, K[I/V]x₂PKPx₁Rx₂S[I/L] and VI[R/P]TKAx₁RC[S/T], are indicated in the green and blue box, respectively. (B) Phylogenetic tree analysis depicts SsMYB3 belonging to PA-clade 1. The tree was constructed from the ClustalX 1.8 alignment using the neighbor-joining method in the MEGA 5.0 program. Scale bar represents 0.1 substitutions per site, and numbers next to nodes are bootstrap values from 1,000 replicates (only values >50% are shown). SsMYB3 and other known functional PA-biosynthesis regulators are divided into two subclades (PA-clades 1 and 2) with different genomic structures indicated in gray background. MYB proteins with known functions and MYB subgroups (G03, G05, G07, G20, N08, and N09) are indicated. GenBank accession numbers of MYBs in the phylogenetic tree are as follows: AmMIXTA (CAA55725), AmROSEA1 (ABB83826), AmROSEA2 (ABB83827), AmVENOSA (ABB83828), Am308 (JQ0960), AtTT2 (Q9FJA2), AtPAP1 (ABB03879), AtPAP2 (NP_176813), AtMYB4 (BAA21619), AtMYB12 (ABB03913), AtWER (AAF18939), AtGL1 (AAC97387), DkMYB2 (AB503699), DkMYB4 (AB503671), FaMYB1 (AAK84064), GMYB10 (CAD87010), LeANT1 (AAQ55181), MdMYB1 (DQ886414), PmMBF1 (AAA82943), PhAN2 (AAF66727), PhPH4 (AAY51377.1), PhODO1 (AAV98200), PtMYB134 (ACR83705), ZmC1 (AAA33482), ZmPl (AAA19821), ZmP (AAC49394), VvMybPA1 (CAJ90831), VvMybPA2 (EU919682), VvMYBPA1 (BAD18977), VvMYBPA2 (BAD18978), VvMYB4 (ABL61515), and VvMYB5a (AAS68190).

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To further investigate the homology of SsMYB3 to 33 function-known plant-R2R3 MYB-type proteins, a phylogenetic tree was constructed using the full-length amino acid sequences. These MYBs were clustered into distinct groups according to their functions and structural characterizations (Fig 2B). All MYBs characterized as PA regulators could be placed in two separate subclades: PA-clade 1 contained SsMYB3, VvMYBPA1, and DkMyb4; PA-clade 2 contained AtTT2, PtMYB134, VvMYBPA2, and DkMyb2. The result of this phylogenetic analysis was consistent with previous reports on PA regulators PtMYB134 [22] and DkMyb2 [21]. In addition, by comparative analysis of the genomic structure of several PA-regulatory genes, we found that the two PA clades had different gene structures: genes in PA-clade 1 had one intron, while those in PA-clade 2 had two (Fig 2B). Previous studies have shown that the two types of PA regulators have different expression patterns. For examples, in V. vinifera, VvMYBPA1 [17] and VvMYBPA2 [18], which are from PA-clade 1 and 2, respectively, have different expression profiles in seeds, skin and leaves. In persimmon (Diospyroskaki), DkMyb4 [20] and DkMyb2 [21] belong to PA-clade 1 and 2, and are orthologs of VvMYBPA1 and VvMYBPA2, respectively. The expression level of DkMyb4 is considerably higher than that of DkMyb2 in each plant organ. Furthermore, the PA-clade 1 regulators, such as VvMYBPA1 and DkMyb4, mainly recognized the MYBCORE cis-motif, but PA-clade 2 regulators, such as DkMyb2 and PtMYB134, mainly recognized the AC element of MYB-binding cis-motif, in the promoter regions of PA pathway genes.

These differences in gene structure, protein C-terminal conserved motifs, expression patterns and identification of conserved motifs implied that the two PA regulatory clades controlled the transcription of PA-specific genes in different ways, which might form diverse regulatory strategies in plant PA biosynthesis. These results strongly suggested that SsMYB3 is a PA-clade 1 regulatory gene.

Expression of SsMYB3 is correlated with PA accumulation and is induced by light and wounding in coleus

To confirm the relationship between expression of SsMYB3 and PA accumulation, qPCR expression analysis of the gene and determination of PA content were performed in different tissues of coleus. SsMYB3 was expressed in all tested tissues, with highest level in young leaves (YL) and lowest level in roots (R) (Fig 3A). The SsMYB3expression declined gradually in leaves as developed and matured. The concentration of PAs changed in accordance with the changing level of gene expression in different coleus tissues. These results indicated that the expression pattern of SsMYB3 was consistent with the accumulation of PAs in coleus tissues. Similar results were described for PA regulators in grapevine (VvMYBPA1) [17] and persimmon (DkMyb4) [20].

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Fig 3. Accumulation of PAs and the gene expression profiles of SsMYB3.

(A) The expression pattern of SsMYB3 and accumulation of PAs in various tissues of coleus: R (root), S (stem), YL (young leaf), ML (mature leaf), OL (old leaf), and F (flower). Transcription pattern of SsMYB3 in leaves under different treatments: (B) light, (C) dark, and (D) wounding. All expression data were normalized to the coleus SsActin gene, and values represent averages of three technical replicates.

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Current studies have shown that visible light primarily induces biosynthesis of PAs in grapevine by upregulating expression of the key genes involved in this pathway [39]. To investigate whether light induces SsMYB3 expression, dark- and light-induction treatments were performed. When coleus leaves were exposed to high intensity of light, transcript numbers of SsMYB3 increased rapidly to approximately 5-fold higher at 0.5 h than at 0 h (CK) and continued to increase at 8 h treatment (Fig 3B). In the dark treatment, the expression level of SsMYB3 decreased gradually during the first hour and reached a minimum at 48 h dark (Fig 3C). These results demonstrated that SsMYB3 expression is light-inducible, and suggested that light may be an important factor for PA biosynthesis in coleus. Because several PA regulators (e.g., PtMYB134, DkMyb2, and DkMyb4) are reported to be induced by wounding [18, 21], the possibility of wound induction of SsMYB3 was explored; the transcript level of SsMYB3 clearly increased in the wound-stress treatment (Fig 3D). From this result, we speculated that other MYB-type PA regulators may be induced by wound stress, although the stress-induction mechanism is unclear and requires further investigation.

Complementation of the Arabidopsis tt2 mutant

In the Arabidopsis tt2 mutant, the MBW ternary transcription complex (AtTT2-AtTT8-AtTTG1) could not be formed and PA-specific AtANR gene could not be activated because of the loss of function of AtTT2 [16, 24]. The lack of PAs in the tt2 mutant seed coat creates the yellow-colored seed phenotype.

To test whether the cloned SsMYB3 was a functional PA regulator, the SsMYB3 gene, under the control of the CaMV35S promoter in pCAMBIA2301G, was introduced into the tt2 mutant by A. tumefaciens-mediated transformation. The transgenic T₁ seeds showed the wild-type brown-colored seed coat, which could be stained black using DMACA reagent to indicate the accumulation of CTs (Fig 4A), consistent with the complementary phenotype of the tt2 seed coat using AtTT2 [16] and VvMYBPA1 [17]. DMACA is a useful and specific reagent for detecting PAs by its reaction with both PA monomers and polymers [40]. This result demonstrated that the SsMYB3 overexpression can complement the tt2 mutant seed coat phenotype. Although SsMYB3 and VvMYBPA1 are from PA-clade 1, they can complement the PA-clade 2 Arabidopsis tt2 mutant, which indicated that the two types of PA-clade factors have the functional conservation to regulate PA biosynthesis.

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Fig 4. Complementation of Arabidopsis PA-deficient tt2 mutant seed phenotype by overexpression of SsMYB3.

(A) Seed coat pigmentation and DMACA staining of wild-type (WT), tt2 mutant, and tt2 35S::SsMYB3 seeds. Seeds of WT and tt2 35S::SsMYB3 show brown pigmentation due to the accumulation of PAs, and their seed coats display dark coloration from staining by DMACA. The PA-deficient tt2 mutant seed coat is yellow and cannot be stained by DMACA. (B) RT-PCR analysis of key structural genes related to PA biosynthesis in immature siliques of WT, tt2 mutant, and tt2 35S::SsMYB3 lines. (C) Protein–protein interactions between SsMYB3 and Arabidopsis PA-related regulator AtTT8 or AtTTG1. In a Y2H assay, SsMYB3 fused to the GAL4-activation domain (pAD-SsMYB3) and GAL4-DNA-binding domain (pBD-SsMYB3); pAD-SsMYB3 was co-transformed with fusion constructs of the GAL4 DNA-binding domain with the WD40 protein AtTTG1 (pBD-AtTTG1) and the MYB-interaction regions from AtTT8 (pBD-AtTT8^aa1-204).

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Further RT-PCR analyses showed that the PA-specific gene ANR and two closely related anthocyanin structural genes DFR and ANS were induced in immature siliques of tt2 35S::SsMYB3T₁ lines (Fig 4B), while these early structural genes (AtCHS, AtCHI and AtF3H) of flavonoid pathway have not been affected (S3 Fig). This was similar to Arabidopsis TT2 [16] and grapevine VvMYBPA1 [17], which control PA-specific genes and related DFR and ANS genes. In addition, Y2H assays revealed that SsMYB3 could interact with AtTT8 and AtTTG1 to reform the MBW complex and form a homodimer with itself (Fig 4C), similar to the role played by AtTT2 [24]. Taken together, our Arabidopsis complementation experiments provided direct evidence that SsMYB3 is a functional MYB-type PA regulator.

Functional characterization of the SsMYB3 gene in tobacco

Recent studies have shown that TFs, with their potential ability to activate multiple structural genes, are more effective tools than single structural genes (encoding enzymes) for plant metabolic engineering [41]. For example, ectopic expression of DkMyb4, which increased or activated the expression of multiple structural genes involved in the PA or anthocyanin pathway, resulted in massive accumulation of PAs in the callus of kiwifruit (Actinidia deliciosa) [20]. However, similar approaches for regulating PA biosynthesis in the model plant tobacco have not yet been reported. And it is unknown that whether ectopic expression of MYB PA-regulators would affect the flower color.

To test the regulatory function of SsMYB3 in tobacco, a 35S::SsMYB3 construct was transferred into tobacco by Agrobacterium-mediated transformation of leaf discs, and several transgenic lines were generated in which the flowers showed a visible decrease in color (Fig 5A). Compared with wild-type control plants that produced pink flowers, the flower colors of all T₁ transgenic lines showed clear phenotypic changes in petal pigmentation patterns, from pink to almost white. For example, some lines (e.g., OX-2) displayed very pale pink flowers with pale red veins, and other lines (e.g., OX-15) produced almost-white flowers with a small, pale-pink region on the edge of petal. Further, anthocyanin and CT contents of transgenic and wild-type flowers were measured, respectively; anthocyanin levels of all transgenic lines were significantly lower than those of the wild-type (Fig 5B), while their CT contents were significantly higher (Fig 5C). In each transgenic line, an inverse relationship between anthocyanin and CT level was detected. For example, transgenic line OX-15 accumulated the highest levels of CTs and the lowest levels of anthocyanin. RT-PCR analyses revealed that line OX-15 exhibited the highest transcription levels of SsMYB3, while the lowest expression level of this gene was detected in line OX-2, which had the highest anthocyanin and lowest CT content (Fig 5D).

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Fig 5. Functional characterization of SsMYB3 by its ectopic expression in tobacco.

(A) Overexpression of SsMYB3 resulted in visibly decreased color in the corolla of transgenic tobacco flowers. (B) Relative anthocyanin contents quantified as (A530–0.25 × A650)/fresh weight (g). (C) The measured relative condensed tannin contents at 500-nm absorbance. (D) RT-PCR expression analysis of SsMYB3 and flavonoid-related regulators in transgenic tobacco flowers. Asterisks indicate a statistically significant difference between wild-type and transgenic plants (P≤ 0.05 by Student’s t-test).

https://doi.org/10.1371/journal.pone.0139392.g005

Our results are similar with those of previous studies that overexpression of PA structural gene ANRs resulted in a visible decrease of flower color in tobacco. And the degree of reduction of anthocyanin content and increase of CT content was negatively or positively correlated, respectively, with the expression level of ANRs gene [3, 7, 9–12]. These combined findings suggest that SsMYB3 is a functional gene in tobacco and its ectopic expression can promote biosynthesis of CTs, but reduce accumulation of anthocyanins to change flower color form pink to almost white, in transgenic flowers.

Ectopic expression of SsMYB3 affects expression of key genes for anthocyanin and PA biosynthesis in transgenic tobacco

To analyze the effects of ectopic expression of SsMYB3 on TFs involved in biosynthesis of tobacco flavonoids, RT-PCR analysis were performed. The results showed that the overexpression of SsMYB3 affected expression of the PA-related genes (Fig 5D). The expression levels of two bHLH-type genes, NtAn1a [42]and NtJAF13-1, showed slight changes, but the R2R3 MYB-type NtAn2 gene was downregulated and the WD40-type NtAn11-1 gene was upregulated in all transgenic lines. The overexpression of SsMYB3 may have competitively inhibited expression of the endogenous same-type gene NtAn2, thereby affecting transcription of other genes of the complex.

Further qPCR analysis showed that overexpressing SsMYB3 strongly influenced expression of the key structural genes of the anthocyanin and PA pathways in transgenic tobacco flowers (Fig 6). For example, expression patterns of early anthocyanin structural genes encoding NtCHS, NtCHI, and NtF3H were complicated and showed no obvious rules in transgenic flowers. These early genes were upregulated in some lines and downregulated in others. Late anthocyanin structural genes (NtDFR and NtANS) and key PA-biosynthetic genes (NtLAR and NtANR) were upregulated and showed higher levels of expression in all transgenic lines. However, accumulation of transcripts of NtUFGT was significantly lower in all transgenic plants than in the wild type. NtUFGT is responsible for the last step inanthocyanin biosynthesis, which transfers the glucosyl moiety from UDP-glucose to the 3-hydroxyl group of anthocyanidins forming stable and water soluble anthocyanins. The loss of function or low expression of NtUFGT leads to loss or reduced accumulation of anthocyanin [43–46]. The lowest expression level of NtUFGT was found in line OX-15, which produced almost-white flowers with the lowest anthocyanin content. These data indicated that SsMYB3 can upregulate or activate PA biosynthetic key genes NtLAR and NtANR, but downregulate or not activate transcript accumulation of the key anthocyanin gene NtUFGT in transgenic tobacco flower.

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Fig 6. Transcript expression profiles of anthocyanin-related structural genes in flowers of WT and SsMYB3-overexpressing transgenic tobacco lines.

All transcripts expressed in transgenic flowers were quantified relative to those expressed in WT tobacco flowers (2^-ΔΔCt).

https://doi.org/10.1371/journal.pone.0139392.g006

SsMYB3 may form a temporary transcription complex to regulate PA biosynthesis in transgenic tobacco

The tobacco flavonoid regulatory genes NtAn1, NtJAF13, NtAn2 [36], and NtAn11 are homologues of model plant petunia PhAn1, PhJAF13, PhAn2, and PhAn11, respectively. Bai et al. [42] and our studies (unpublished) indicated that these regulators can form a protein complex NtAn2-NtAn1/NtJAF13-NtAn11 (NtAn2-complex) to control biosynthesis of tobacco flavonoids, like the role of their homologues in petunia [47]. Because the overexpression of SsMYB3 can rescue the brown phenotype in the PA-deficient Arabidopsis tt2 mutant seed coat, and SsMYB3 protein can interact with AtTT8 and AtTTG1 in yeast, we speculate that there is a similar interaction between SsMYB3 and tobacco flavonoid regulators. We performed Y2H assays to examine whether SsMYB3 could interact with regulators of flavonoid biosynthesis in tobacco. In yeast, SsMYB3 interacted with two bHLH proteins (NtAn1a and NtJAF13-1) and a WD40 protein NtAn11-1(Fig 7), which implied that SsMYB3 may form a temporary transcription complex SsMYB3-bHLH-WD40 (SsMYB3-complex) to control PA biosynthesis in transgenic tobacco flowers.

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Fig 7. Protein–protein interactions between SsMYB3 and tobacco flavonoid-related regulators.

In a yeast two-hybrid assay, the SsMYB3/GAL4-activation domain fusion (pAD-SsMYB3) was co-transformed with fusion constructs of the GAL4-DNA-binding domain with the WD40 protein NtAn11-1 (pBD-NtAn11), the MYB-interaction regions from NtAn1a (pBD-NtAn1a^aa1–195), or NtJAF13-1 (pBD-NtJAF13-1^aa1-203).

https://doi.org/10.1371/journal.pone.0139392.g007

On the basis of these analyses, we propose a model for how CTs content, anthocyanins accumulation and flower color are affected by a PA regulator SsMYB3 in transgenic tobacco (Fig 8). The exogenous SsMYB3 may compete with endogenous anthocyanin regulator NtAn2 for binding to the bHLH regulators (NtAn1/NtJAF13), and the formative SsMYB3-complex may inhibit or destabilize the formation of NtAn2-complex in SsMYB3-overexpressing transgenic tobacco flowers. As a result of this competition, the SsMYB3-complex may specially activate or upregulate expression levels of key PA-biosynthetic genes NtLAR and NtANR to increase the content of CTs, but the anthocyanin final key gene NtUFGT could not be activated. Meanwhile, the lack of NtAn2-complex may result in lower expression levels of the NtUFGT. The low levels of NtUFGT directly lead to an almost white-flowered phenotype with limited accumulation of anthocyanins. Furthermore, the reduced biosynthesis of anthocyanin probably provided more substrates for biosynthesis of CTs.

Download:

Fig 8. A model for regulation of PAs and anthocyanins biosynthesis by SsMYB3 in transgenic tobacco.

In wild tobacco (A), the NtAn2-complex controls anthocyanins biosynthesis by activating expression of late anthocyanin structural genes, such as F3H, DFR, ANS, and UFGT. In SsMYB3-overexpressing tobacco (B), high levels of SsMYB3 compete with NtAn2 to form SsMYB3-complex promoting PAs biosynthesis by specially activating expression of LAR and ANR, and repressing anthocyanins accumulation by inactivating expression of UFGT, through inhibition or destabilization of the formation of NtAn2-complex.

https://doi.org/10.1371/journal.pone.0139392.g008

This was similar to findings for PA regulators AtTT2, VvMYBPA1 and nectarine/peach PpMYBPA1. In Arabidopsis, the MYB-type regulator AtPAP1/2 and AtTT2 can interact with AtTT8 and AtTTG1 to form different transcription complexes that regulate anthocyanin and PA biosynthesis, respectively [13]. The key late anthocyanin structural gene AtUFGT can be specially activated by the AtPAP1/2-complex rather than the AtTT2-complex [48]. In grapevine, VvMYBPA1 controls key PA-biosynthetic genes VvLAR and VvANR, but cannot regulate the key late anthocyanin structural gene VvUFGT [17]. In nectarine (Prunus persica), PpMYBPA1 trans-activates the promoters of PA pathway genes DFR and LAR, but not UFGT [49].

Over all, overexpression of SsMYB3 in tobacco results in a significant white flower phenotype with high CT content and low accumulation of anthocyanins. On the basis of functional characterization of SsMYB3 in the Arabidopsis tt2 mutant and transgenic tobacco, we concluded that SsMYB3 gene is an R2R3 MYB-type PA regulator involved in the regulation of PA biosynthesis in coleus. This study contributes to our understanding of regulation of secondary metabolites in coleus, and provides a potential molecular tool for enhancing PA biosynthesis in other fruits and crops using metabolic engineering.

Supporting Information

S1 Fig. Isolation of the SsMYB3 gene by RACE amplification (A) and full-length PCR amplification (B).

https://doi.org/10.1371/journal.pone.0139392.s001

(TIF)

S2 Fig. Nucleotide and deduced amino acid sequences of SsMYB3.

The start codon ATG and stop codon TAG are in bold and underlined; the predicted Kozak sequence including ATG is boxed and introns are underlined with dashes. The predicted conserved R2R3 domain is denoted with gray background; the conserved bHLH motif is underlined in gray. The presumed polyadenylation signal AATTAA is wave-underlined.

https://doi.org/10.1371/journal.pone.0139392.s002

(TIF)

S3 Fig. RT-PCR analyses of early structural genes related to flavonoid biosynthesis in Arabidopsis WT, tt2 mutant, and transgenic lines.

https://doi.org/10.1371/journal.pone.0139392.s003

(TIF)

S1 Table. List of primers used for SsMYB3 isolation and characterization.

https://doi.org/10.1371/journal.pone.0139392.s004

(PDF)

S2 Table. List of primers used for the RT-PCR assay.

https://doi.org/10.1371/journal.pone.0139392.s005

(PDF)

S3 Table. List of primers used for the qPCR assay.

https://doi.org/10.1371/journal.pone.0139392.s006

(PDF)

Acknowledgments

We are grateful to Prof. Letian Chen (State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, College of Life Sciences, South China Agricultural University) for editing and revising this manuscript.

Author Contributions

Conceived and designed the experiments: QZ ML. Performed the experiments: QZ SS XL ZY. Analyzed the data: QZ ML. Contributed reagents/materials/analysis tools: GL Y-GL KL. Wrote the paper: QZ.

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Figures

Abstract

Introduction

Materials and Methods

Plant materials, stress treatments, and isolation of total RNA

Cloning of the full-length SsMYB3 gene

Sequence analysis and construction of expression vector

Arabidopsis complementation analysis

Transformation of tobacco plants

Yeast two-hybrid analysis

Expression analysis of RT-PCR and quantitative real-time PCR (qPCR)

Measurement of anthocyanin and condensed tannins

Results and Discussion

Isolation and characterization of SsMYB3 gene

Expression of SsMYB3 is correlated with PA accumulation and is induced by light and wounding in coleus

Complementation of the Arabidopsis tt2 mutant

Functional characterization of the SsMYB3 gene in tobacco

Ectopic expression of SsMYB3 affects expression of key genes for anthocyanin and PA biosynthesis in transgenic tobacco

SsMYB3 may form a temporary transcription complex to regulate PA biosynthesis in transgenic tobacco

Supporting Information

S1 Fig. Isolation of the SsMYB3 gene by RACE amplification (A) and full-length PCR amplification (B).

S2 Fig. Nucleotide and deduced amino acid sequences of SsMYB3.

S3 Fig. RT-PCR analyses of early structural genes related to flavonoid biosynthesis in Arabidopsis WT, tt2 mutant, and transgenic lines.

S1 Table. List of primers used for SsMYB3 isolation and characterization.

S2 Table. List of primers used for the RT-PCR assay.

S3 Table. List of primers used for the qPCR assay.

Acknowledgments

Author Contributions

References