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Conceived and designed the experiments: JV. Performed the experiments: CC CIC. Analyzed the data: JV CIC. Contributed reagents/materials/analysis tools: JV. Wrote the paper: JV.
In part due to the ease of visual detection of phenotypic changes, anthocyanin pigment production has long been the target of genetic and molecular research in plants. Specific members of the large family of plant myb transcription factors have been found to play critical roles in regulating expression of anthocyanin biosynthetic genes and these genes continue to serve as important tools in dissecting the molecular mechanisms of plant gene regulation.
A spontaneous mutation within the coding region of an Arabidopsis 35S::AtMYB90 transgene converted the activator of plant-wide anthocyanin production to a dominant-negative allele (PG-1) that inhibits normal pigment production within tobacco petals. Sequence analysis identified a single base change that created a premature nonsense codon, truncating the encoded myb protein. The resulting mutant protein lacks 78 amino acids from the wild type C-terminus and was confirmed as the source of the white-flower phenotype. A putative tobacco homolog of AtMYB90 (NtAN2) was isolated and found to be expressed in flower petals but not leaves of all tobacco plants tested. Using transgenic tobacco constitutively expressing the NtAN2 gene confirmed the NtAN2 protein as the likely target of PG-1-based inhibition of tobacco pigment production.
Messenger RNA and anthocyanin analysis of PG-1Sh transgenic lines (and PG-1Sh x purple 35S::NtAN2 seedlings) support a model in which the mutant myb transgene product acts as a competitive inhibitor of the native tobacco NtAN2 protein. This finding is important to researchers in the field of plant transcription factor analysis, representing a potential outcome for experiments analyzing in vivo protein function in test transgenic systems that over-express or mutate plant transcription factors.
Anthocyanins represent a broad family of plant pigments that contribute to flower and fruit pigmentation , plant stress response ,  and have been implicated as helpful nutrients that contribute to improved human health . The production of anthocyanins and related pigments in plants has been the target of extensive genetic and molecular research and represents one of the better understood plant gene regulatory systems. Specific members of the Myb family of plant transcription factors have been found to play critical roles in controlling the expression of genes associated with anthocyanin production, often in conjunction with members of the basic helix-loop-helix (bHLH) and WD40 families of trans factors (e.g. , , , , , , , , ). A classic example of this form of gene regulation was originally identified through genetic mapping of maize mutations affecting seed-coat color. Many of these maize mutant alleles mapped to the C1 (MYB) , , R (bHLH) , , or PAC1 (WD40)  loci . More recently, other examples of plant MYB genes in the R2R3 family ,  have been found to play significant roles in controlling pigment production in flowers, fruit and vegetative tissues of several plant species , . Transgenic ectopic over-expression of several of these MYB genes has been shown to dramatically impact anthocyanin accumulation, in many cases affecting pigmentation within plant species other than those from which the MYB transgenes originated , , , , , , , , , , , , . Ectopic expression of either of two closely related Arabidopsis MYB genes, AtMYB75 (PAP1) and AtMYB90 (PAP2) in Nicotiana tabacum produced striking levels of anthocyanin pigmentation in most parts of transgenic plants, providing a clear visual indicator of transgene activity . A similar dark purple 35S::AtMYB90 transgenic tobacco line was created in this laboratory (Myb-27, Fig. 1 & 2) and used as test material in a visual screen for molecular mechanisms that can alter transgene expression levels and/or patterns during in vitro de-differentiated growth, and subsequent de novo shoot production, processes that are normally part of plant genetic transformation protocols. A single plant line (PG-1) regenerated from purple Myb-27 callus, was initially identified by a complete loss of the darkly pigmented phenotype of the parental line. Upon reaching maturity, the PG-1 line was found to display a white flower phenotype that differed from the dark purple flowers of MYB-27 and the lightly pigmented red flowers of wild-type tobacco [N. tabacum, cv SR1 ]. Genetic and molecular analysis of the PG-1 line indicate that both the loss of hyper-pigmentation and the white flower phenotype are the result of a spontaneous dominant-negative nonsense mutation within the coding region of the AtMYB90 transgene. The observed dominant-negative white flower phenotype seen with the PG-1 allele is similar to that reported in transgenic tobacco lines expressing the maize C1-I mutant allele ; and a wild type strawberry myb (FaMYB1 ). The structure and properties of the PG-1 dominant-negative mutation demonstrate a mechanism for manipulating Myb gene structure that can provide useful insight into the mechanisms by which MYB transcription factors function to regulate gene expression in plants.
The AtMYB90 coding region, under control of a CaMV 35S promoter  and the T-DNA gene-7 transcription termination/polyadenylation signal sequence (, Fig. 1A), was introduced into tobacco (N. tabacum cv SR1) and resulting transgenic shoots screened visually for ectopic anthocyanin production. The Myb-27 line was selected as a purple shoot from callus associated with the initial Agrobacterium-treated tobacco leaf explants. Subsequent phosphinothricin treatment of R1 Myb-27 seedlings indicated that the line was not herbicide resistant, consistent with PCR scans spanning the introduced T-DNA (Fig. 1B). Other transgenic lines also chosen for their purple phenotypes (e.g. Myb-237 and Myb-155) were found to harbor functional glufosinate resistance genes (Fig. 1B). The transgenic line, Myb-27, was selected for additional analysis based upon its dominant, heavily pigmented phenotype (Fig. 2A). Although the purple Myb-27 plants grow more slowly than their wild-type tobacco parent under low light conditions (~60 uMol quanta m−2 s−1), they otherwise display no obvious developmental or morphological changes. Actively growing cultured callus derived from surface sterilized hemizygous Myb-27 leaf material was found to display extensive anthocyanin pigmentation and was capable of producing new shoots, most of which displayed anthocyanin pigment patterns and levels similar to the parent Myb-27 plant (Fig. 2A).
Of ~100 plantlets regenerated and rooted from hemizygous purple Myb-27 callus, 4 completely lacked ectopic purple pigmentation (Fig. 2A). These 4 green regenerants were subsequently screened by PCR for the presence of the 35S::AtMYB90 transgene (primer set 7a, Fig. 1A). Only one plant, designated line PG-1, gave a positive PCR signal, with the other three green plants apparently having lost the transgene during callus growth and/or plant regeneration. After reaching maturity the PG-1 line was found to display a white flower phenotype, producing flower petals that not only lacked the dark pigmentation of Myb-27 flowers, but also failed to produce the normal lightly pigmented red petals seen in wild-type tobacco (Fig. 2B).
Plants grown from seed of the selfed R0 PG-1 plant displayed an approximately 31 ratio of white to pink flowered plants (29 white, 11 pink), results consistent with the original PG-1 transgenic plant being hemizygous for a single, dominant-negative, white-flower locus. The dominant-negative character of the PG-1 allele was confirmed by crossing the PG-1 R0 plant to wild-type tobacco, producing an approximate 11 ratio of white (18) to red (21) flower phenotypes in the resulting seedlings.
PCR analysis using primers targeting additional sites within the T-DNA used to create the Myb-27, and subsequent PG-1, transgenic lines failed to indicate any gross rearrangements of the PG-1 T-DNA relative to that present in Myb-27 plants (Fig. 1B). DNA isolated from Myb-27, PG-1 and Myb-237 lines was used to produce PCR products covering the area flanked by primer set 7 (extending from the 35S promoter to the g7 termination signal, Fig. 1A). Sequence derived from these PCR products indicated that, relative to the wild-type Myb-27 AtMYB90 allele, the PG-1 allele contains a single base change within the myb coding region. This mutation, an A to T transversion, converts an AAG (lysine) codon to a TAG (ocher) nonsense triplet at the 172nd codon (Fig. 3), and is predicted to produce a truncated AtMYB90 protein that lacks the C-terminal 78 amino acids of the 249 amino acid AtMYB90 protein (Fig. 4). The A to T mutation also creates a new XbaI cleavage site (Fig. 4), allowing direct detection of the PG-1 allele by XbaI digestion of PCR products from flanking primers, followed by electrophoretic separation of the resulting two DNA fragments. The new XbaI site was used to confirm the presence of the PG-1 allele in all experiments involving PG-1 plant lines.
To test the hypothesis that the predicted shortened PG-1 protein is responsible for the observed white-flower phenotype, a new 35S::AtMYB90 variant (PG-1 Short, or PG-1Sh) was generated and introduced into tobacco plants. The PG-1Sh construct lacks DNA encoding the 78 C-terminal amino acids downstream from the site of the PG-1 mutant stop codon (Fig. 1A), and should produce the same shortened AtMYB90 protein as is predicted for the PG-1 mutant allele. Transgenic tobacco lines expressing the PG-1Sh transgene displayed a range of flower color phenotypes, including plants with completely white flowers similar to those seen with the PG-1 line (Fig. 2B). Quantitative reverse-transcriptase PCR (qRTPCR) using mRNA from flowers of PG-1Sh lines chosen for their broad range in flower pigmentation indicated that expression of the PG-1Sh transgene was inversely proportional (R2=0.93) to flower anthocyanin pigment levels (Fig. 3A&B). These results support a model in which the PG-1 or PG-1Sh gene product interferes competitively with the normal functioning of an endogenous tobacco myb factor controlling anthocyanin production.
Alignment of the AtMYB90 sequence against those contained in the tobacco transcription factor sequence database, TOBFAC, (<http://compsysbio.achs.virginia.edu/tobfac/>, ) identified a tobacco myb gene (gnl|tobfac|R2R3-MYB_141) with sequence similarity to the AtMYB90 coding region. A PCR primer targeting the N-terminus of the predicted R2R3-MYB_141 coding region was designed and used to amplify and clone a cDNA for this putative tobacco AtMYB90 homolog (PCR from start codon to a poly-A adaptor sequence, primers in Table 1)). The cloned tobacco Myb cDNA was sequenced and found to match that of a tobacco homolog (NtAN2) of the Petunia AN2 myb gene recently added to the NCBI Genbank (FJ472647). In the spirit of standardized nomenclature we will refer to our tobacco myb homolog as NtAN2.
A protein BLAST search using the NtAN2 sequence identified AtMyb113, 75, 90 and 114 genes (BLAST scores: 205, 194, 183, and 180) as the Arabidopsis proteins most closely related to NtAN2. All of these Arabidopsis Myb genes have been implicated in regulation of Anthrocyanin production and the next closest Arabidopsis gene in the search, transparent testa 2 (TT2, AtMYB123) is associated with proanthocyanin production in the seed coat. Consistent with a role as an activator of anthocyanin production in tobacco, qRTPCR analysis of NtAN2 mRNA (primers listed in Table 1) detected NtAN2 expression in flowers but none in leaf tissue (leaf Ct>35, at least 1000 fold less than flower mRNA levels [Ct~23]). Further support for NtAN2′s role as a myb activator of anthocyanin production was provided by generation of transgenic N. tabacum (SR1) plants expressing a 35S::NtAN2 transgene (the 35S::NtAN2 construct substitutes the NtAN2 coding region for that of AtMYB90 in Fig. 1A). Several NtAN2-expressing R0 lines (12 of 71) displayed extensive ectopic purple pigmentation similar to patterns observed in tobacco lines expressing the 35S::AtMYB90 transgene (e.g. Fig. 2A and 2B). Finally, transgenic tobacco plants expressing a double-stranded hairpin construct targeting the entire NtAN2 coding region for RNAi (ihpNtAN2, a 35S::antisense-intron-sense hairpin within the pKO vector, ) was able to produce white flowers similar to those of PG-1 plants (2 of 12 lines showed a white flower phenotype, with the remaining lines displaying varying levels of pigment reduction, Fig. 2B and and3A).3A). These findings are consistent with those reported by Pattanaik et al, at the ASPB Plant Biology Symposium, 2009 <http://abstracts.aspb.org/pb2009/public/P30/P30031.html>, and strongly suggest that NtAN2 is a likely target for the interference with anthocyanin production seen in plants expressing the PG-1 allele or PG-1Sh transgenes.
qRTPCR analysis of NtAN2 gene expression in flowers from the set of representative PG-1Sh plants analyzed for PG-1Sh mRNA (Fig. 3A) did not indicate any correlation between flower NtAN2 mRNA levels and anthocyanin pigmentation (R2=0.01). These results strongly suggest that PG-1Sh-associated interference in pigment production does not result from transgene-induced alterations in NtAN2 transcription or from post transcriptional gene silencing of the NtAN2 gene, leaving competitive protein-protein interaction as the most likely mechanism for the observed white flower phenotype.
Alignment of the NtAN2 cDNA with that of AtMYB90 showed very little sequence similarity outside of that occurring within the 5′ repeats that are definitive of the R2R3 family of plant myb genes (Fig. 4). The only clear exception was a small region of sequence similarity just downstream from the R2R3 repeats (at ~625 bp) which, interestingly, overlaps the area of the AtMYB90 transcript targeted by an Arabidopsis trans-acting small interfering RNA [tasiRNA, specifically TAS4-siR81(−)] . The tobacco sequence is not a perfect complement to the TAS4-siR81 (2 mismatches and a G::T pairing) and there is as yet no direct evidence suggesting that the observed sequence similarity reflects evolutionary conservation of a functional mRNA::siRNA interaction. In fact, alignment of the predicted amino acid sequences (Probcons, ) from the NtAN2 and AtMYB90 genes at the TAS4-siRN81 target site indicated only highly conservative amino acid substitutions (Arginine for Lysine and Threonine for Serine, Fig. 5) within a conserved nine amino acid segment. It is thus conceivable that the observed sequence similarity at the TAS4-siRN81 site is the result of an evolutionarily conserved protein function.
To confirm functional in vivo interaction between the PG1 and NtAN2 gene products, PG-1Sh #32 transgenic plants were crossed with a 35S::NtAN2 transgenic line (NtAN2-1-59) that displays enhanced anthocyanin production (Fig. 2A and 2B). The phenotypes (anthocyanin pigmentation) and genotypes (determined by gene-specific PCR, Table 1) of resulting F1 seedlings were compared (Fig. 6). As expected, plants containing only the 35S::NtAN2 transgene displayed enhanced anthocyanin production within their leaves (Fig. 6). Seedlings containing both the 35S::NtAN2 and PG-1Sh transgenes showed dramatically reduced anthocyanin production in leaves, in most cases appearing phenotypically identical to leaves from wildtype SR1 seedlings or plants containing only the PG-1Sh construct (Fig. 6). These data confirm the ability of the PG1 gene product to interfere with NtAN2 function in tissues other than flower petals, and indicate that the observed interference is independent of the promoter associated with NtAN2 expression (the native NtAN2 promoter drives expression in tobacco flower petals, while the virally derived CaMV-35S promoter controls NtAN2 expression in NtAN2-1-59 transgenic leaves).
A single-base nonsense mutation within the coding region of an active Arabidopsis AtMYB90 transgene (the PG-1 allele) was found to convert the R2R3-myb gene from a transcriptional activator of plant-wide anthocyanin biosynthesis to a dominant-negative allele that was able to interfere with normal tobacco pigment production within flower petals. Confirmation that the PG-1 gene product is responsible for the observed white-flower phenotype was provided by expression in transgenic tobacco of a truncated AtMYB90 gene (PG-1Sh) engineered to produce the same shortened myb protein as that predicted for the mutant PG-1 allele. The PG-1Sh transgenic lines displayed a range of flower pigmentation phenotypes, including white flowers similar to those seen with PG-1 plants. Furthermore, anthocyanin content in representative PG-1Sh flowers was found to be inversely proportional to PG-1Sh transgene expression levels (Fig. 3A & 3B), supporting a negative function for the PG-1Sh gene product.
Based upon the highly pigmented phenotype of the Myb-27 tobacco line, the AtMYB90 protein is able to interact with those native tobacco transcription factors and promoters required to activate transcription of anthocyanin biosynthetic genes. This ability of an anthocyanin-associated myb factor to function in a non-native plant system is not unique, as similar pigmented phenotypes have been seen with ectopic over-expressed Myb transgenes in several heterologous plant species (e.g.: Maize C1 expressed in tobacco; , Apple MdMYB1 expressed in Arabidopsis ; Daisy GMYB10 expressed in tobacco ; Arabidopsis AtMYB75 expressed in petunia , tobacco  or tomato ; Sweet potato IbMYB1 expressed in Arabidopsis ; Grape VvMYB5a expressed in tobacco ; and Medicago truncatula LAP1 in legumes and tobacco ). The predicted PG-1 and PG-1Sh protein is a shortened version of the AtMYB90 gene product, retaining the highly conserved R2R3 domains but lacking 78 amino acids at the C-terminus (Fig. 5).
Based on our results, the truncated PG-1 protein has lost the ability to induce pigment production but retained sufficient function to allow it to interfere with the tobacco anthocyanin regulatory system active in flower petals. The observed interference in flower anthocyanin biosynthesis does not appear to be the result of altered transcription or message stability (e.g. RNAi) of the presumed functional tobacco myb homolog (NtAN2) since steady-state NtAN2 mRNA levels show no correlative relationship with PG-1Sh mRNA content or anthocyanin levels in transgenic flowers displaying a wide range of pigmentation (Fig. 3A).
A literature search identified two other examples of myb-based genes that effectively eliminate flower pigment production when over-expressed in tobacco, the C1-I allele from maize  and a wild-type strawberry myb gene (FaMYB1 ). It was proposed that FaMYB1 may act directly as a transcriptional repressor , while the mutant transcriptional activator, C1-I, was assumed to act as a competitor to a native tobacco Myb protein, replacing the native protein within specific transcription initiation complexes , , . The high ratios of PG-1Sh to NtAN2 expression seen in the least pigmented PG-1Sh transgenic flowers (~40-fold PG-1Sh mRNA excess in the mostly white flower line #42 or ~120-fold excess in the white-flower line #32], Fig. 3A), support a model that proposes competition between the ‘inactive’ PG-1 and ‘active’ NtAN2 proteins for a common site within anthocyanin-associated transcription complexes. A similar competitive inhibition of transcription complexes may explain the loss of pigmentation associated with over-expression of AtMYB60 in lettuce . The ability of an active PG-1Sh gene (PG-1Sh #32) to dramatically reduce anthocyanin production when crossed into the purple 35S::NtAN2 transgenic line, NtAN2-1-59 (Fig. 6), further supports a model of protein competition since the observed interference occurs in non-flower tissues and affects NtAN2 activity controlled by a promoter unrelated to that which regulates expression of the native NtAN2 gene in flower petals.
Alignment of predicted C1, C1-I, FaMYB1, AtMYB90/PG-1 and NtAN2 protein sequences indicates that sequence similarity is primarily limited to the highly conserved R2R3 DNA-binding domains common to this family of plant myb genes (Fig. 5). All of the aligned anthocyanin-associated myb proteins do, however, share sequence motifs (Fig. 5) linked to myb-bHLH binding (L--R--RL , DL--R---L------L---R ). The presence of the conserved bHLH binding motif is consistent with possible competition between the dominant-negative PG1 gene product and NtAN2 protein for association with one or more tobacco bHLH proteins. Just downstream from the R2R3 domains there is a noticeable short segment of protein similarity between the AtMYB90 and NtAN2 sequences, KI--F[K/R]PRP[R/T]FS. This sequence overlaps with an active tasiRNA target site identified in the AtMYB90 mRNA (TAS4-siR81−, ) and it is not clear whether the common amino acids represent a conserved protein domain or reflect a possible homologous tobacco tasiRNA target within the NtAN2 message. Our current results do not directly support any interaction between the PG-1 and NtAN2 genes at the level of mRNA regulation.
The simplest model for a competitive interaction between the PG-1 and NtAN2 myb proteins assumes that the 78 C-terminal amino acids missing in the PG-1 product contain, or overlap with, a transcriptional regulatory domain required for gene activation. Although sequences downstream from the conserved R2R3 domains are generally assumed to contain protein sequences responsible for transcription activation and/or repression, very few specific motifs or functional domains have been confirmed in plant myb proteins (e.g. , , , ). Support for this model of plant myb protein function comes from work in which fusion of a 12 amino acid EAR repressor motif to the 3′ end of the AtMYB75 protein transformed the transcriptional activator into a gene specific repressor . A search for conserved protein motifs in the AtMYB90, C1, NtAN2 and FaMYB1 protein sequences (online MEME analysis, ) failed to identify any motifs outside those already identified by protein alignment, specifically the R2, R3 domains, and for AtMYB90 and NtAN2, the TAS4 target region. Specifically, the short conserved ‘C2’ motif (LNL[D/E]L-[G/S] , ), which contains the core EAR motif (LXLXL, ), present in the proposed myb repressor, FaMYB1 was not identified in any of the other myb protein sequences examined.
The PG-1 allele is the result of a spontaneous single-base mutation within a AtMYB90 transgene that acts as a dominant-negative ‘repressor’ of pigment production in tobacco flowers. The AtMYB114 gene present in the Arabidopsis Columbia ecotype (AtMYB114 is one of three Arabidopsis genes with very high sequence similarity to the AtMYB90 gene) contains a premature stop codon located 31 amino acids upstream from the PG1 mutation, and over-production of the AtMYB114 (Col) truncated myb protein was recently shown to negatively impact anthocyanin production in Arabidopsis . Similar dominant-negative mutations that produce truncated Myb proteins have been identified as naturally occurring alleles of the maize C1 gene , . Both gene systems demonstrate a potential evolutionary mechanism that can convert myb transcriptional activators into repressors. In the case of PG-1, repression of tobacco anthocyanin production appears to be the result of competitive inhibition of one or more tobacco myb proteins. This mechanism is different from that proposed for plant myb proteins that contain a functional repressor domain such as the conserved C2 domain  implicated in the regulatory function of AtMYB4  and FaMYB1 , and should be considered as a possibility when plant myb genes are over-expressed to test their function in vivo . The authors are unaware of any documented examples of native plant gene regulatory systems that use competitive inhibition by an ‘inactive’ R2R3 myb protein to down-regulate gene expression. It is, however, important that the potential for such regulatory mechanism be kept in mind when dissecting plant gene control pathways that make use of myb genes.
Plasmids were prepared using standard cloning techniques  and appropriate DNA segments sequenced to confirm final constructs. When possible, different promoter, terminator, reporter and selectable marker cassettes were used within constructs to reduce the potential for recombination within plasmids. The 35S::AtMYB90 constructs (T-DNA depicted in Fig. 1A) used the pPZP200 vector  modified to contain a glufosinate-resistance plant selectable marker near the T-DNA right border. The plant resistance construct consists of the bar gene coding region (552 bp) encoding phosphinothricin acetyl transferase (Accession number: AX235900), regulated by the peanut chlorotic streak virus promoter (240 to +1 bp)  and CaMV 35S transcript termination signal.
Transformation of tobacco (N. tabacum cv SR1) was accomplished using the Agrobacterium tumefaciens line EHA105 . Plasmid constructs were electroporated into EHA105 as previously described  and transformation of tobacco carried out by the conventional leaf disc method , . Regenerated transgenic shoots were rooted on MS-agar medium  containing B5 vitamins  and 500 µg/ml Claforan (sodium cefotaxime, Hoechst).
Callus was produced de novo from Myb-27 leaf tissue by placing surface sterilized material on MS-agar media supplemented with plant hormones (MS Salt; B5 Vitamins; Sucrose 2% [w/v]; indol-3-acetic acid (0.5 mg/mL); benzlaminopurine (0.5 mg/mL). After 2–3 weeks shoot production was induced by transfer of actively growing purple callus to the same media lacking indol-3-acetic acid. Shoots that displayed altered anthocyanin pigmentation levels or patterns were excised above the callus and moved to the same media lacking hormones for root induction and eventually transferred to soil.
Routine PCR used MJ Research PTC-100 thermocyclers (95°C-8 Min, 30 cycles-[94C-45 Sec, 56°C-30 Sec, 72°C-60 Sec], 74°C-5 Min) and reagents from Applied Biosystems®. Primer sets and product sizes are listed in Table 1.
Quantitative reverse transcriptase PCR (qRT-PCR, primers listed in Table 1) was performed using a LightCycler® 480 System and SYBR green kits (LightCycler® DNA Master SYBR Green I) from Roche Applied Science according to protocols provided by the manufacturer (2-step; 60°–72°, read once per second, ramp at 4.4°C/s up & 2.2°C/s down). Total RNA was prepared using either Ambion mirVana™ RNA isolation kits and suggested protocols or using Tri-Reagent® reagent from Ambion®. To control for potential variability in the biochemical processes that precede qRTPCR reactions, total RNA samples (5 µg each) were spiked with a synthetic control internal control (IC) mRNA (250 pg/reaction) produced in vitro using T7 RNA polymerase (using Ambion® MEGAscript® and MEGAclear™ kits) acting on a PCR product template (IC2r, Genebank Accession # GQ215228). Spiked samples were treated with RNAse-free DNAase (TURBO® DNase, from Ambion®) and cleaned post reaction as per manufacturer's instructions. Reverse transcription was performed using RETROscript® from Ambion® (following the manufacturer's protocols). Relative RNA values were calculated using formulas for ΔΔCt, the Pfaffl method , and according to Norgard, et al , applied to qRT-PCR data from total RNA samples (triplicate technical assays and the indicated number of biological replicates).
Anthocyanin levels were determined by extraction of soluble anthocyanins as described by Martin et al , and spectrophotometic measurement at 530 nm and 657 nm. The formula used for relative anthocyanin content is: A530-(0.25xA657)/g tissue extracted.
Our appreciation goes out to: Drs. John Burke, Junping Chen and Zhanguo Xin for critical reading of the manuscript; Ryan Mize, Natalie Bizzell and Gracie Mahan for technical assistance and for keeping our precious plants alive; Kay McCrary and DeeDee Laumbach for tobacco transformation; and Nancy Layland for excellent technical support. The source plasmid for the AtMYB90 cDNA was graciously provided by Mendel Biotechnology. Mention of a commercial or proprietary product does not constitute an endorsement by the USDA. USDA offers its programs to all eligible persons regardless of race, color, age, sex, or national origin.
Competing Interests: The authors have declared that no competing interests exist.
Funding: This research was funded by the United States Department of Agriculture, Agricultural Research Service (CRIS project number 6208-21000-016-00D) <http://www.ars.usda.gov/main/main.htm>. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.