An apple MYB transcription factor, MdMYB3, is involved in regulation of anthocyanin biosynthesis and flower development
© Vimolmangkang et al.; licensee BioMed Central Ltd. 2013
Received: 13 September 2013
Accepted: 4 November 2013
Published: 7 November 2013
Red coloration of fruit is an important trait in apple, and it is mainly attributed to the accumulation of anthocyanins, a class of plant flavonoid metabolites. Anthocyanin biosynthesis is genetically determined by structural and regulatory genes. Plant tissue pigmentation patterns are mainly controlled by expression profiles of regulatory genes. Among these regulatory genes are MYB transcription factors (TFs), wherein the class of two-repeats (R2R3) is deemed the largest, and these are associated with the anthocyanin biosynthesis pathway. Although three MdMYB genes, almost identical in nucleotide sequences, have been identified in apple, it is likely that there are other R2R3 MYB TFs that are present in the apple genome that are also involved in the regulation of coloration of red color pigmentation of the skin of apple fruits.
In this study, a novel R2R3 MYB gene has been isolated and characterized in apple. This MYB gene is closely related to the Arabidopsis thaliana AtMYB3, and has been designated as MdMYB3. This TF belongs to the subgroup 4 R2R3 family of plant MYB transcription factors. This apple MdMYB3 gene is mapped onto linkage group 15 of the integrated apple genetic map. Transcripts of MdMYB3 are detected in all analyzed tissues including leaves, flowers, and fruits. However, transcripts of MdMYB3 are higher in excocarp of red-skinned apple cultivars than that in yellowish-green skinned apple cultivars. When this gene is ectopically expressed in Nicotiana tabacum cv. Petite Havana SR1, flowers of transgenic tobacco lines carrying MdMYB3 have exhibited increased pigmentation and accumulate higher levels of anthocyanins and flavonols than wild-type flowers. Overexpression of MdMYB3 has resulted in transcriptional activation of several flavonoid pathway genes, including CHS, CHI, UFGT, and FLS. Moreover, peduncles of flowers and styles of pistils of transgenic plants overexpressing MdMYB3 are longer than those of wild-type plants, thus suggesting that this TF is involved in regulation of flower development.
This study has identified a novel MYB transcription factor in the apple genome. This TF, designated as MdMYB3, is involved in transcriptional activation of several flavonoid pathway genes. Moreover, this TF not only regulates the accumulation of anthocyanin in the skin of apple fruits, but it is also involved in the regulation of flower development, particularly that of pistil development.
KeywordsAnthocyanin Apple MYB transcription factors Malus × domestica Flavonoids Reproductive tissues
Skin color is an important determinant of apple fruit quality. Generally, consumers prefer red-skinned apples as they are perceived to be associated with better taste and flavor . Coloration of apple fruit is attributed to accumulation of anthocyanins, a class of plant flavonoid metabolites. Flavonoids are ubiquitous in plants, and play important roles throughout plant growth, including UV protection, disease resistance, herbivore defense, and providing flowers and seeds with pigmentation to attract pollinators and seed dispersers [2, 3]. More importantly, there is increasing evidence that flavonoids benefit human health such as lowering the incidence of cardiovascular disease, obesity, diabetes, pulmonary disease, and cancer [4–8].
The biosynthetic pathway of anthocyanins has been well established, and anthocyanin pathway genes have been isolated and characterized in a variety of model plants such as petunia, snapdragon, and Arabidopsis [9, 10]. Anthocyanin biosynthesis is genetically determined by structural and regulatory genes. The structural genes are regulated at the transcriptional level by regulatory genes, and thus plant pigmentation patterns are mainly controlled by the expression profiles of regulatory genes [11, 12].
Three transcription factors (TFs), including the basic helix-loop-helix (bHLH), R2R3 MYB, and WD40 proteins, predominantly regulate genes in the anthocyanin biosynthesis pathway across all plant species reported to date, including apple [13, 14]. MYB TFs have been reported to play diverse functions in controlling pathways such as secondary metabolism, development, signal transduction, and disease resistance in plants . They are classified by the numbers of highly conserved imperfect repeats in the DNA-binding domain, and consisting of either single or multiple repeats. Among these MYB TFs, the class of two-repeats (R2R3) is deemed the largest, with 339 TFs reported in Arabidopsis , and it is associated with the anthocyanin biosynthesis pathway.
Regulation of R2R3 MYB TFs can occur at different steps of the anthocyanin biosynthesis pathway. For example, R2R3 MYB TFs in perilla (Perilla frutescens) control transcription of all structural genes involved in anthocyanin biosynthesis . MYBA in grape (Vitis vinifera) specifically regulates genes down-stream of anthocyanin production, but not those of earlier steps . As with other transcription factors, regulation of R2R3 MYB TFs could serve to either activate or repress expression of these genes. For example, MYB TFs such as Arabidopsis PAP1, AtPAP2, AtMYB113, and AtMYB114 [19, 20], grape VvMYB1a , and Gerbera hybrid GhMYB10  positively regulate anthocyanin biosynthesis. Suppression of flavonoid accumulation has been observed in transgenic plants overexpressing strawberry FaMYB1 , Antirrhinum AmMYB308 , Arabidopsis AtMYB4 , and Arabidopsis AtMYBL2 which encode a single-repeat R3-MYB protein [26, 27].
In recent years, several studies have been reported on the characterization of structural and regulatory genes involved in fruit coloration in apple (Malus × domestica Borkh.). For example, induction of most structural genes in the anthocyanin biosynthesis pathway can significantly increase accumulation of anthocyanin in apple skin . Three transcription factors, MdMYB10, MdMYB1, and MdMYBA, have been isolated and characterized in apple [29–31]. Of the three TFs, MdMYB10 is responsible for red flesh coloration, while MdMYB1 and MdMYBA control red skin coloration of apple fruit. The three MdMYB genes are almost identical in nucleotide sequences, and have been subsequently reported to be of different alleles on linkage group 9 [32, 33]. Recently, Chagné et al.  have reported that the red-flesh cortex phenotype of apple fruit is associated with enhanced expression of MYB110a, a paralog of MYB10, and functional analysis of MYB110a in tobacco has revealed that it is involved in up-regulation of anthocyanin biosynthesis. Apple fruits vary considerably in color, ranging from yellow, green, or red, along with varied differences in red color pigmentation patterns. It seems unlikely that apple fruit skin red coloration is simply controlled by a single locus.
Isolation and characterization of MYB TFs associated with anthocyanin biosynthesis is an important key step towards understanding and manipulating fruit coloration. In this study, a MYB TF, designated MdMYB3, has been identified using an apple expressed sequence tag (EST) database  and a BAC-based physical map of the apple genome . The MdMYB3 gene shows higher levels of expression in exocarp of red-skinned apple cultivars than that of yellowish-green skinned apple cultivars. Transgenic flowers overexpressing MdMYB3 accumulate higher levels of anthocyanin and have longer peduncles and styles when compared with those of wild-type flowers. These results strongly suggest that MdMYB3 not only regulates anthocyanin biosynthesis, but is also involved in flower and pistil development.
Sequence characterization of MdMYB3in apple
Mapping of the MdMYB3gene onto the apple genetic map
Two pairs of primers flanking the SSR1 and SSR2 repeats within the MdMYB3 gene were designed and used to screen the two parents of the F1 population of the ′Co-op 16′ x 'Co-op 17′ cross. The two parents were found to be heterozygous and homozygous at SSR1 and SSR2 loci, respectively (Figure 1B). The primers flanking the SSR1 locus was then selected to screen F1 progenies of 'Co-op 16′ x 'Co-op 17′ cross. As a result, three genotypes, designated 'hh’ (upper band), 'hk’ (upper and lower bands), and 'kk’ (lower band), respectively, were identified for the SSR1 locus among this progeny (Figure 1C). Based on our recently constructed apple genetic linkage map , the apple MdMYB3 gene was anchored onto linkage group 15 (Figure 1D).
Expression profiles of MdMYB3in apple
Subsequently, a total of 10 apple cultivars were selected and used to investigate the association of MdMYB3 gene expression with anthocyanin accumulation in excocarp of fruits at maturity. Overall, MdMYB3 transcripts were highly expressed in excocarp of red-skinned fruits, but were either low or undetectable in yellowish-green skinned fruits (Figure 4B). These expression profiles were accompanied with similar anthocyanin content profiles in cortex tissues of these apple cultivars (Figure 4B). This finding further confirmed that MdMYB3 was involved in anthocyanin accumulation in apple.
Functional analysis of MdMYB3in tobacco
Analysis of flavonoid contents in tobacco flowers of wild-type and transgenic lines using LC/MS/MS method*
Expression profiles of structural genes of phenylpropanoid and flavonoid pathways in tobacco transgenic flowers overexpressing MdMYB3
Multiple R2R3 TFs have been reported to be involved in anthocyanin biosynthesis in many plant species . However, it is not clear whether or not there are additional loci, other than the MdMYB10 locus. Using second-generation resequencing, Chagné et al.  have identified 33 SNPs within a 60-kb region surrounding the two alleles MYB110a and MYB110b that are involved in the regulation of red flesh (or cortex) color pigmentation of apple fruit. Chromosomal location of MYB110a has been attributed to whole-genome duplication event that occurred during the evolution of apple within the Maloideae family . This is to be expected as integration of an apple physical and genetic maps have demonstrated presence of both genome-wide and segmental duplications in the apple genome and providing further insights into the complex polyploid ancestral origin of the apple . In this study, a novel R2R3 MYB transcription factor MdMYB3 in apple has been isolated, and its ectopic expression in tobacco flowers indicates that it is involved in flower coloration, peduncle length, and style/stigma development.
The apple MdMYB3is involved in regulation of the anthocyanin biosynthesis pathway
When the coding DNA sequence of MdMYB3 was BLASTed against the Arabidopsis genome sequence database (http://www.arabidopsis.org/Blast/index.jsp), hits to subgroup 4 of MYB TFs were detected, including those of AtMYB3, AtMYB7, and AtMYB4 with E-values of 3e-25, 2e-23, and 1e-21, respectively. Although AtMYB3 and AtMYB7 have not been functionally characterized, AtMYB4 has been reported to function as a repressor of the lignin biosynthesis pathway . It is noteworthy to point out that the MdMYB3 gene identified in this study is different from MYB repressors reported by Lin-Wang et al. . Although, it is originally anticipated that MdMYB3 would have a similar function to that of AtMYB4, flowers of transgenic tobacco lines overexpressing MdMYB3 have accumulated higher levels of anthocyanin than those of wild-type plants, resulting in increased color pigmentation. Analysis of gene expression profiles in flowers of T2 transgenic lines has further revealed that MdMYB3 contributes to activation of NtCHI, NtCHS, NtANS, NtUFGT, and NtAn2 genes, and some degree of repression of the NtDFR gene. These results clearly indicate that MdMYB3 is involved in regulation of the anthocyanin biosynthesis pathway. The functionality of subgroup 4 MYB genes involved in activation of anthocyanin synthesis has also been reported in maize . The maize ZmMYB31 gene is closely related to MdMYB3, and its overexpression in Arabidopsis has been reported to enhance transcription of anthocyanin pathway genes including those of CHI, F3H, F3′H, and DFR.
More recently, an R2R3 MYB regulator from tobacco, NtAn2, has been isolated and reported to be a key gene controlling anthocyanin production in reproductive tissues of tobacco . Interestingly in this study, expression levels of NtAn2 in flowers of transgenic tobacco lines overexpressing MdMYB3 are significantly higher than those of wild-type plants (Figure 7). Zhao et al.  have reported that Arabidopsis MYB4 contains a MYB binding site motif A(A/C)C(A/T)A(A/C)C. The MYB4 protein can interact with its own MYB binding motif, thus regulating its own expression through an autoregulatory mechanism. We have analyzed the promoter sequence of the tobacco NtAn2 (Genbank accession no. FJ472650), and found a MYB binding site motif, AACTAAC, located at -817 to -811 bp upstream of the start codon. To clarify the role of MdMYB3 in regulation of anthocyanin biosynthesis, it is worthy to investigate as whether or not the MdMYB3 protein can bind to the promoter region of the NtAn2 that may subsequently lead to transcriptional activation of NtAn2. However, it cannot be ruled out that MdMYB3 may positively regulate expression of flavonoid structural genes such as CHS and UFGT. Previously it has been reported that expression levels of UFGT in the red-skinned cv. Red Delicious are significantly higher than those in the yellow-skinned cv. Golden Delicious . Herein, we further demonstrate that MdMYB3 strongly activates transcription of the UFGT gene in flowers of transgenic tobacco lines. Further studies are needed to determine whether or not the MdMYB3 protein can bind to the promoter region of MdUFGT and contributing to increased accumulation of anthocyanin.
In this study, ectopic expression of MdMYB3 in tobacco has contributed to anthocyanin accumulation, predominantly detected in reproductive tissues. Similar findings have been reported for transgenic tobacco lines carrying an apple MdMYBA gene  as well as transgenic Arabidopsis lines carrying an apple MdMYB1. In contrast, several other anthocyanin-related TFs such as the grape VlMybA1-1, Gerbera GMYB10, tomato LeANT1, and Arabidopsis AtPAP1 are capable of inducing anthocyanin accumulation in whole plants [18, 19, 22, 44]. Previously, it has been reported that these MYB genes are capable of activating bHLH transcription, and thus forming a complex with bHLH to promote accumulation of anthocyanin [45, 46]. In this study, MdMYB3 may not function as a bHLH activator. Instead, it may combine with a tissue-specific bHLH to activate transcription of either NtAn2 or other anthocyanin pathway genes, resulting in anthocyanin accumulation in flowers.
In apple, MdMYB10 and MdMYB1 strongly up-regulate most flavonoid structural genes, including MdCHI, MdCHS, MdF3H, MdLDOX, MdDFR, and MdUFGT [29, 31]. In contrast in this study, MdMYB3 activates transcription of NtCHI, NtCHS, and NtUFGT genes in tobacco flowers, but it inhibits transcription of the NtDFR gene. Moreover, expression levels of structural genes such as NtF3H, NtF3′H, NtFLS, and NtLDOX in flowers of transgenic tobacco in this study are on average similar to those detected in flowers of wild-type plants. These findings suggest that the role of MdMYB3 in regulation of the anthocyanin biosynthesis pathway may be different from those of MdMYB10 and MdMYB1. This is consistent with the phylogenetic analysis that revealed that MdMYB3 is separated from MdMYB10/MdMYB1. Moreover, MdMYB3 is located on chromosome 15, and is expressed at higher levels in the cortex of red-skinned apple cultivars than in yellowish-green skinned apple cultivars. Therefore, it seems that MYB TFs other than MdMYB10/MdMYB1, located on chromosome 9, may also be involved in the regulation of apple red skin coloration.
The phylogenetic analysis indicates that MdMYB3 has a close relationship with Arabidopsis AtMYB12 and AtMYB111. These two Arabidopsis MYB TFs positively regulate expression of CHS, FLS, and F3H genes, and are thus responsible for accumulation of flavonol . Similarly in this study, MdMYB3 is activating transcription of NtCHS and NtFLS in flowers of transgenic tobacco. Overall, levels of kaempferol and quercetin in flowers of transgenic tobacco plants are higher than those in wild-type plants (Table 1). Therefore, it seems that the apple MdMYB3 gene is also involved in positive regulation of flavonol accumulation. Interestingly, the Arabidopsis AtMYB12 does not contain an R/B-like bHLH binding motif, thus it functions independently of a bHLH cofactor . However, MdMYB3 has an R/B-like bHLH binding motif, suggesting it can form a complex with bHLH to regulate anthocyanin biosynthesis. Thus, it is likely that the apple MdMYB3 gene has functionally diverged from the Arabidopsis AtMYB12.
Functional divergence of the apple MdMYB3from its closely related genes
The MdMYB3 gene is clustered together with the strawberry FaMYB1 (Figure 2). Ectopic expression of FaMYB1 in tobacco inhibits accumulation of both anthocyanins and flavonols, resulting in strong reduction in flower pigmentation . Overexpression of FaMYB1 in tobacco flowers down-regulates transcription of late flavonoid biosynthesis genes. In contrast, the MdMYB3 gene in this study strongly up-regulates expression of genes involved in anthocyanin and flavonol synthesis, including CHS, CHI, UFGT, ANS, and FLS genes. FaMYB1 contains a conserved C2-motif pdLNLD/ELxiG/S at the C-terminal, which is responsible for repression of transcription . The C2-motif is also present in the C-terminus of MdMYB3, but its first amino acid sequence has been changed from Phe to Ser (Figure 3). It remains unclear if a single amino acid substitution is responsible for observed functional differences between MdMYB3 and FaMYB1.
The apple MdMYB3 gene is also closely related to the maize ZmMYB31 gene and the Arabidopsis AtMYB32 and AtMYB4 genes. These three latter genes have been previously reported to function as repressors in the lignin biosynthesis pathway. For example, AtMYB4 and AtMYB32 down-regulate expression of C4H and COMT genes, respectively, and are thus deemed as repressors of lignin biosynthesis [25, 49]. It is likely that ZmMYB31 inhibits transcription of COMT, F5H, C3H, and 4CL genes, resulting in reduced levels of lignin biosynthesis . Thus, it has been presumed that MdMYB3 will have a similar function to those of its closely related genes. As expected, overexpression of MdMYB3 in tobacco flowers significantly represses transcription of genes involved in the lignin biosynthesis pathway such as C4H and 4CL2; moreover, it also severely inhibits expression of the CAD gene involved in monolignol biosynthesis (Figure 7). However, expression of NtCOMT in flowers of transgenic lines overexpressing MdMYB3 is significantly higher than that in wild-type plants (Figure 7). These results suggest that MdMYB3 may have functionally diverged from subgroup 4 MYB genes such as those of AtMYB4 and AtMYB32.
The apple MdMYB3is involved in regulation of style development in pistils of flowers
It has been reported that changes in expression levels of AtMYB32 and AtMYB4 can influence pollen development by changing the flux of the phenylpropanoid pathway, and influencing composition of pollen wall . For example, an AtMYB32 insertion mutant of Arabidopsis shows abnormal pollen grains that are either partially or completely devoid of cellular contents . In this study, the subgroup 4 R2R3 family is also involved in the development of reproductive tissues. Transgenic tobacco lines expressing MdMYB3 have developed flowers with longer peduncles and longer styles than those of wild-type flowers. Of particular interest are those elongated styles as they result in stigmas that are positioned anthers of a flower. This suggests that MdMYB3 is also involved in the regulation of pistil development. Similar observations have been previously reported for an Antirrhinum AmMYB308, a homolog of MdMYB3 . When AmMYB308 is overexpressed in transgenic tobacco, elongated styles have been observed, resulting in protruded stigmas and contributing to infrequent self-pollination . However, unlike morphological observations noted in this study, flowers of transgenic tobacco overexpressing AmMYB308 are smaller in size and accumulate lower levels of anthocyanin than those of wild-type tobacco.
Taken together, this study demonstrates that MdMYB3 plays important and multiple roles in plant growth and development. Based on functional analysis of transgenic tobacco lines, overexpression of MdMYB3 in tobacco flowers enhances accumulation of anthocyanins and increases length of peduncles and more importantly lengths of styles.
In this study, a new R2R3 MYB transcription factor (TF), MdMYB3, involved in the anthocyanin biosynthesis pathway was identified in the apple genome. This TF has been characterized and mapped onto Linkage group (LG) 15 of the apple genetic map. Transcripts of this TF are detected in leaves, flowers, and fruits; however, transcripts of MdMYB3 are higher in excocarp of red-skinned apple cultivars than that in yellowish-green skinned apple cultivars thus regulating accumulation of anthocyanin accumulation in the skin of apple fruit. Ectopic expression of this TF in tobacco revealed that it has a regulatory role by activating the transcription of NtAn2 and thus inducing several flavonoid biosynthesis pathway genes. More interestingly, this TF is also involved in floral development by modifying pistil length in flowers.
Leaves, flowers, and fruits at different stages of development were collected from trees of apple cvs. Red Delicious and Golden Delicious. In addition, fruits of cvs. Baihaitang, Gala, Huangtaiping, Jinhong, Dolgo, Jiguan, Golden Delicious, Sompain, Baishaguo, and Mutsu were also collected at maturity.
Isolation of genomic DNA encoding MdMYB3 in apple
Arabidopsis AtMYB3 (AT1G22640) was BLASTed against our apple EST database (http://titan.biotec.uiuc.edu/cgi-bin/ESTWebsite/estima_start?seqSet=apple), and a homologous EST contig (accession no. Apple_0223.1923.C1.Contig3505) was identified. The EST contig sequence was then BLASTed against apple EST database in NCBI, and an EST sequence (GenBank accession no. CO868594) containing both R2 and R3 domains was recovered. Based on the EST sequence, a pair of primers (5′-GGGAGAGCACCTTGTTGTGAG-3′/5′-GATCTCGTTGTCGGTTCTTCC-3′) was then designed and subjected to screen BAC library of cv. GoldRush using a PCR-based screening method as previously described by Xu et al. . The reaction consisted of 94°C for 3 min, followed by 33 cycles of 94°C for 35 s, 55°C for 30 s, 72°C for 60 s, and followed by a final 8 min extension at 72°C. A positive BAC clones was randomly selected and subjected to sequencing to recover genomic sequence encoding MdMYB3 in apple.
Recovery of cDNA sequence encoding MdMYB3 in apple
The genomic sequences encoding MdMYB3 were analyzed using FGENESH-M program (http://www.softberry.com), and an open reading frame (ORF) was predicted. A pair of primers (5′-GGAGAGCACCTTGTTGTGAG-3′/5′-ACTGACAATTGCTGCATGCC-3′) was designed based on the predicted ORF, and used to amplify cDNA from leaves of cv. GoldRush. The PCR product was sequenced, and a cDNA fragment 872 bp in size was recovered. The cDNA fragment sequence was BLASTed against NCBI EST database (http://blast.ncbi.nlm.nih.gov/Blast.cgi), and a cDNA containing the full coding region was identified. Subsequently, a pair of primers (5′-CTGATCCAGAAGAAGAAACAGATG-3′/5′-TGGATTCAAAGCAGGTCTGTG-3′) was designed to amplify the full coding region of MdMYB3 from cv. GoldRush to further verify the predicted ORF.
Expression vector construction and tobacco transformation
A pair of primers (5′-TGACTCTAGACTGATCCAGAAGAAGAAAC-3′/5′-ATACGAGCTCTGGATTCAA AGCAG-3′) was designed to amplify the coding region of MdMYB3 using the proofreading DNA polymerase Platinum® Pfx (Invitrogen) following the manufacturer′s instructions. Forward and reverse primers contained XbaI and SacI restriction sites at the 5′ end, respectively. The blunt-end PCR product was ligated into the pCR®-Blunt vector using Zero Blunt® PCR cloning kit (Invitrogen) according to the manufacturer′s protocol. The expression vector was confirmed by direct sequencing. The coding sequence of MdMYB3 was introduced into the pBI121 cloning vector, and the construct was used for Agrobacterium-mediated transformation of tobacco (Nicotiana tabacum cv. Petite Havana SR1) as described by Han et al. . T1 seed from three confirmed independent transgenic T0 lines overexpressing MdMYB3 and carrying a single copy of the transgene, including OE-1, OE-5, and OE-8 were selfed to generate T2 plants.
Wild-type and T2 transgenic tobacco plants were grown in the greenhouse, and flowers at full-bloom (completely open flowers) were collected for analysis of gene expression as well as for analysis of contents of flavonoid compounds. Upon collection, all samples were frozen in liquid nitrogen and stored at -80°C until needed.
Mapping of the MdMYB3gene onto the apple linkage map
An SSR marker within a 5′ un-translated region of MdMYB3 was used to screen an F1 mapping opulation derived from a cross between 'Co-op 16′ and 'Co-op 17′. The primer sequences of the SSR marker were as follows: forward 5′-TCACCTCTTCAAACAACACACC-3′ and reverse 5′-TGCTCTCCCCATCTGTTTCT-3′. The PCR product was run on 2% (w/v) metaphor gel. The linkage map was constructed using JoinMap version 4.0, according to Han et al. .
Real-time PCR analysis
Total RNA from leaf and flower tissues were extracted using an RNAqueous Kit (Ambion) according to the manufacturer’s instructions. RNA from fruit tissues was isolated according to the protocol described by Gasic et al. . Total RNA (2 μg) from each tissue was treated with DNaseI (Invitrogen), and used for cDNA synthesis. The first-strand cDNA synthesis was performed with Oligo (dT) primer using the SuperScript III RT kit (Invitrogen), according to the manufacturer’s instructions. Specific primers for MdMYB3 and each flavonoid-related gene were designed using Biology Workbench version 3.2 (http://workbench.sdsc.edu). Specific primer sequences and accession numbers of genes used to design primers have been listed in Additional file 1: Table S1.
The SYBR Green real-time PCR assay was carried out in a total volume of 25 μl, consisting of 12.5 μL of 2× SYBR Green I Master Mix (Applied Biosystems), 0.2 μM (each) specific primers, and 100 ng of template cDNA. The amplification program consisted of 1 cycle of 95°C for 10 min, followed by 40 cycles of 95°C for 15 s, and 60°C for 1 min. The fluorescent product was detected at the last step of each cycle. Following amplification, melting temperatures of PCR products were analyzed to determine specificity of the PCR product. Melting curves were obtained by slow-heating at 0.5°C/sec, from 60°C to 90°C, while continuously monitoring the fluorescence signal. A negative control without a cDNA template was run with each analysis to evaluate the overall specificity. Amplifications were carried out in a 96-well plate in a 7300 Real Time PCR System (Applied Biosystems). All experimental samples were run in triplicates. An apple Actin gene was used as a constitutive control. Differences between the cycle threshold (Ct) of the target gene and the Actin gene were used to obtain relative transcript levels of the target gene, and calculated as 2 exp-(Cttarget - Ctactin).
Anthocyanins and flavonols were extracted from 50 mg of finely ground tissue in 1 ml 1% HCl/methanol (v/v), at room temperature in the dark, with continuous shaking for 1 h, and centrifuged at 13,000 rpm for 15 min. An aliquot of 100 μL of the supernatant was transferred to a fresh tube, and acid-hydrolyzed by adding 30 μL of 3 N HCl, and incubated at 70°C for 1 h in a thermal cycler (Thermo Hybaid MBS 0.25 s, Thermo Scientific). Proanthocyanins (PAs) were extracted using 1 ml 70% (v/v) acetone containing 0.1% (w/v) ascorbate, and incubated at room temperature for 24 h in darkness as described by Takos et al. . The extract was centrifuged at 13,000 rpm for 15 min at room temperature, and the clear supernatant was transferred to a new tube. An aliquot of 200 μL extract was dried at 35°C, and resuspended in 100 μL of 1% (v/v) HCl-methanol and 100 μL of 200 mM sodium acetate (pH 7.5).
Flavonoid contents were determined using LC/MS/MS along with use of commercial standards for kaempferol, quercetin, cyanidin, catechin, and epicatechin (Sigma). The LC/MS/MS analysis was performed on a 5500 QTRAP mass spectrometer (AB Sciex) equipped with a 1200 Agilent HPLC Analyst (version 1.5.1, Applied Biosytems) for data acquisition and processing. A Phenomenex column (3 μ C6-Phenly 11A, 4.6 × 50 mm) was used for separation. The HPLC flow rate was set at 0.3 mL/min, and HPLC mobile phases consisted of A (0.1% formic acid in H2O) and B (0.1% formic acid in acetonitrile). The autosampler was maintained at 5°C. The gradient for catechin and epicatechin was as follows: 0 min, 90% A; 10 min, 50% A; 13-18 min, 0% A; and 18.1-25 min, 90% A. The injection volume was 20 μl. The gradient for cyanidin, kaempferol, and quercetin was as follows: 0 min, 70% A; 7-12.5 min, 0% A; and 13-20 min, 70% A. The injection volume was 10 μL. The mass spectrometer was operated with positive electrospray ionization. Multiple reaction monitoring (MRM) was used to quantify catechin and epicatechin (m/z 291.0-- > 139.2), cyanidin (m/z 287.2-- > 213.2), kaempferol (m/z 287.1-- > 153.2), and quercetin (m/z 303.1-- > 153.1). The electrospray voltage was set to 5500 V; the heater was set at 600°C; the curtain gas was at 35 psi; and GS1 and GS2 were both at 60 psi. Analysis of each sample was repeated three times using three biological replicates.
Chalcone flavanone isomerase
Days after pollination
Production of anthocyanin pigment1
Simple sequence repeat
Udp glucose-flavonoid 3-o-glucosyl transferase.
The authors would like to thank Prof. Zhenhai Han and Prof. Xinzhong Zhang for providing apple fruits. This project was supported by funds from USDA-NIFA-SCRI grant AG 2009-51181-06023. Also, funding was provided by the Office of Research Project no. 65-325, the National 863 program of China grant No. 2011AA0020401, and the Chinese Academy of Sciences Visiting Professorship for Senior International Scientists Grant No. 2011T2S25.
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