Figures
Abstract
Despite the prominent roles played by R2R3-MYB transcription factors in the regulation of plant gene expression, little is known about the details of how these proteins interact with their DNA targets. For example, while Arabidopsis thaliana R2R3-MYB protein AtMYB61 is known to alter transcript abundance of a specific set of target genes, little is known about the specific DNA sequences to which AtMYB61 binds. To address this gap in knowledge, DNA sequences bound by AtMYB61 were identified using cyclic amplification and selection of targets (CASTing). The DNA targets identified using this approach corresponded to AC elements, sequences enriched in adenosine and cytosine nucleotides. The preferred target sequence that bound with the greatest affinity to AtMYB61 recombinant protein was ACCTAC, the AC-I element. Mutational analyses based on the AC-I element showed that ACC nucleotides in the AC-I element served as the core recognition motif, critical for AtMYB61 binding. Molecular modelling predicted interactions between AtMYB61 amino acid residues and corresponding nucleotides in the DNA targets. The affinity between AtMYB61 and specific target DNA sequences did not correlate with AtMYB61-driven transcriptional activation with each of the target sequences. CASTing-selected motifs were found in the regulatory regions of genes previously shown to be regulated by AtMYB61. Taken together, these findings are consistent with the hypothesis that AtMYB61 regulates transcription from specific cis-acting AC elements in vivo. The results shed light on the specifics of DNA binding by an important family of plant-specific transcriptional regulators.
Citation: Prouse MB, Campbell MM (2013) Interactions between the R2R3-MYB Transcription Factor, AtMYB61, and Target DNA Binding Sites. PLoS ONE 8(5): e65132. https://doi.org/10.1371/journal.pone.0065132
Editor: Turgay Unver, Cankiri Karatekin University, Turkey
Received: February 4, 2013; Accepted: April 22, 2013; Published: May 31, 2013
Copyright: © 2013 Prouse, Campbell. 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.
Funding: This work was generously supported by a Natural Science and Engineering Research Council of Canada (NSERC) Canadian Graduate Scholarship (CGSD) awarded to MBP, and funding from NSERC to MMC. 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
Much of plant growth and development is shaped by sequence-specific transcription factors, proteins that act in response to external and internal cues to modulate gene expression. The MYB family is the largest family of plant sequence-specific transcription factors, with greater than 100 family members in individual plant species [1], [2], [3], [4], [5], [6]. MYB transcription factors are recognised by the presence of the MYB domain, which comprises characteristic helix-helix-loop-helix repeats of approximately 50 amino acids. The MYB domain binds DNA in a sequence-specific manner and is highly conserved in yeast, vertebrates, and plants [7]. The MYB domain is normally found near the amino terminus of the protein, and generally contains either 1, 2, or 3 of the 50 amino-acid MYB repeat. R2R3-MYB proteins have two such repeats, and comprise the largest sub-family of the MYB family. Moreover, R2R3-MYB proteins are plant specific, regulating facets of plant growth, development and metabolism [3], [5], [8], [9], [10], [11], [12], [13], [14], [15].
While members of the R2R3-MYB family are being characterised in increasing numbers, these investigations largely focus on the involvement of a particular MYB in the manifestation of a specific plant phenotype. That is, most of these analyses do not extend to a more detailed examination of MYB function at the molecular level. Nevertheless, some general themes with respect to R2R3-MYB function at the molecular level are emerging [16]. For example, many R2R3-MYB transcription factors bind to DNA motifs that are enriched in adenosine (A) and cytosine (C) residues [8], [17], where guanine (G) residues are either absent or depleted [16], [18]. These motifs have been variously referred to as AC elements, H boxes, or PAL boxes [18], [19], [20], [21], [22], [23], [24], [25], [26], [27]. Some R2R3-MYB proteins function as transcriptional activators at these sites [15], [17], while others function as transcriptional repressors [28]. AC elements are relatively short, comprising 5 or 6 nucleotides, where 3 residues form a relatively invariant core [29], [30], [31]. R2R3-MYB proteins bind to AC elements in a manner that relies on specific amino acid residues in the R2R3-MYB domain [29], [30], [31], [32], [33]. To date, the details of such interactions have been relatively scant, aside from their putative involvement in the regulation of plant-specific gene expression.
AtMYB61, a member of the Arabidopsis thaliana R2R3-MYB family of transcription factors, illustrates the involvement of R2R3-MYB family members in the regulation of plant-specific processes. AtMYB61 is a pleiotropic regulator of three major facets of the plant transpiration system: xylem cell differentiation; lateral root outgrowth; and, stomatal aperture [13], [34]. AtMYB61 modifies gene expression in response to diurnal cues so as to appropriately modify the aperture of stomata [13], the pore-like structures on leaf surfaces that enable gas exchange. Thus, AtMYB61 plays a role in modifying the capacity to take up carbon dioxide for photosynthesis, while limiting the loss of water from the plant body. AtMYB61 also alters gene expression in response to sugars, resulting in modification of plant architecture and cell wall structure [14], [35], [36]. As is the case for most R2R3-MYB transcription factors, the precise mechanisms that enable AtMYB61 to bring about important changes in plant function are unknown. Furthermore, although AtMYB61 has been shown to bind to certain consensus motifs [34], the preferential binding of AtMYB61 has not yet been determined quantitatively.
Given that R2R3-MYB proteins are involved in a rich variety of plant-specific processes [2], it would be desirable to have a more detailed understanding of R2R3-MYB and DNA motif interactions. The work described herein focuses on the interplay between AtMYB61 and its DNA target sequences. Cyclic amplification and selection of targets (CASTing), which enables identification of a transcription factor’s DNA-binding sites from a pool of random oligonucleotides, was used to identify target DNA-binding sites for AtMYB61 [37]. The sequences identified served as a useful foundation to examine mechanisms responsible for AtMYB61 sequence-specific binding, and to hypotheses about the roles these may play in shaping AtMYB61 function in vivo.
Materials and Methods
Ethics Statement
Antibody generation was carried out in strict accordance with the Province of Ontario’s Animals for Research Act, and the requirements of the federal Canadian Council on Animal Care. The protocol was approved at the University of Toronto, which involved full committee review by the Local Animal Care Committee (LACC), followed by approval by the University of Toronto Office of Research Ethics, the University Veterinarian, and finally the University of Toronto Animal Care Committee (UACC) (Permit Number: 20007080, approved 14/01/08). All efforts were made to minimise suffering.
Expression of Recombinant Protein in Bacteria
Recombinant AtMYB61 protein was produced in E. coli using the coding sequence cloned in frame into the NdeI and BamHI sites of the pET15b vector (Novagen). Recombinant AtMYB61 protein was produced, extracted and affinity purified as described previously for pine MYB proteins [17].
Antibody Production and Western Blot Analysis
Anti-AtMYB61 polyclonal antibodies were produced against the recombinant fusion protein in rabbits as described previously [38]. Affinity-purified recombinant antigen was gel-purified on a 10% SDS-PAGE gel and shipped in phosphate buffered saline to University of Toronto BioScience Support Laboratories for antibody production. In brief, 2 rabbits were each injected a total of 4 times with 300 µg of antigen per injection over a 6 week period. Production bleeds were performed after nitrocellulose dot blot assays indicated acceptable titre.
For western blot analysis, total soluble protein extracts were separated by SDS-PAGE and transferred to Bio-Rad Laboratories Nitrocellulose Trans-Blot Transfer Medium (0.45 µm) by electrophoretic transfer (BioRad, Mississauga, ON, Canada). Chemiluminescent western blot analysis was performed on the filters with Invitrogen’s Western Breeze Chemiluminescent kit as described by the manufacturer (Invitrogen, Burlington, ON, Canada). Primary antibody dilutions were done at a final dilution of 1/20000.
Cyclic Amplification and Selection of Targets (CASTing)
The CASTing assay was completed according to Wright et al [37]. CASTing was completed by incubating 15 µg of double stranded random olionucleotides (27 mers) flanked in between two constant priming sequences with the AtMYB61 full length recombinant protein. This complex was added to a Protein G Dynabead (Invitrogen, Burlington, ON, Canada) plus post-injection AtMYB61 antibody complex, causing the complex to immunoprecipitate. The immunoprecipitated complex was then washed 3 times, resuspended in 100 µL PCR buffer, boiled and then PCR amplified for 30 cycles with 15 pmol of forward and reverse primers. 10 µl of the amplified selected targets were kept for analysis and 90 µL were used to continue with the next cycle. This cycle was repeated four more times to select for AtMYB61 consensus DNA target sequences. The selected targets were then cloned into Invitrogen’s pCR4 TOPO vector and sequenced (Invitrogen, Burlington, ON, Canada).
MEME (Multiple Em for Motif Elicitation)
MEME was conducted as described previously [39]. The MEME filter criteria was set for a min/max motif width of 6, any number of repetitions of a single motif distributed among the sequences, and no restrictions on the number of motifs identified. This allowed for the identification of all over-represented hexamer sequences in the recovered CASTing-enriched oligonucleotides. Moreover, it allowed for the identification of repeats of over-represented hexamer sequences in a given CASTing-enriched oligonucleotide.
Nitrocellulose Filter-binding Assay
The nitrocellulose filter-binding assay was conducted as described by Hall and Kranz [40]. The CASTing targets that were over-represented were ordered from Invitrogen and PCR amplified (Invitrogen, Burlington, ON, Canada). These PCR products were Qiagen nucleotide purified according to the Qiagen manufacturer (Qiagen, Toronto, ON, Canada). The cleaned up PCR products were then radioactively labelled with P-32 via primer extension and further Qiagen nucleotide purified according to the Qiagen manufacturer (Qiagen, Toronto, ON, Canada). The CPM levels were measured via a liquid scintillation counter to measure the incorporation of P-32 into the probe. The radioactively labelled probes were combined in a binding reaction with recombinant AtMYB61 protein and passed through BioRad nitrocellulose filters (0.2 µm) (BioRad, Mississauga, ON, Canada). The relative binding of recombinant AtMYB61 protein to the CASTing motifs and mutated AC-I sequences were recorded. The dissociation constants (Kd) of the CASTing targets to AtMYB61 were determined by GRAFIT program which linearised the nonlinear regression via scatchard plots to calculate the point at which half of the ligand was bound to AtMYB61.
Electrophoretic Mobility-Shift Assay (EMSA)
Recombinant AtMYB61 protein was produced, extracted and affinity purified as described previously for pine MYB proteins [17]. EMSA conditions were exactly as described previously [8], [17] but using recombinant AtMYB61 protein in place of pine MYB protein.
Molecular Modelling
The tertiary structure of AtMYB61 was predicted using the tool PHYRE [41]; www.sbg.bio.ic.ac.uk/phyre/html/index.html). PHYRE proposed that the resolved structure that shared the most homology to AtMYB61 was the animal c-MYB DNA-binding domain, which was resolved previously with its DNA consensus motif (AACNG) by heteronuclear multidimensional NMR [31]. This solution structure was used to predict a 3D protein model of AtMYB61 with an E-value of 3.8e-13 and an estimated precision of 100%. The two protein sequences were 44% alike using amino acid sequence alignment. The PBD (protein data bank) file recovered from the PHYRE analysis (PBD ID = c1msfC) was used to superimpose the predicted AtMYB61 crystal structure with the c-MYB crystal structure using DaliLite [42]. The c-MYB protein was resolved along with its DNA binding sequence allowing one to predict the binding domain of AtMYB61 using homology. The PBD files for the AC-I and NBS nucleotide motifs were created from the http://structure.usc.edu/make-na/server.html server. Using Pymol [43] the two structures were modelled and superimposed [44]. Polar interactions were determined using Pymol.
Transcriptional Activation Assay
Transcriptional activation assays using yeast were as described previously [17], but substituting the AtMYB61 coding sequence in place of pine MYB sequences. Transcriptional activation assays were conducted with three biologically independent replicates per condition.
Results and Discussion
AtMYB61 Bound a Discrete Subset of DNA Target Sequences
To generate an antibody of adequate specificity for the cyclic amplification and selection of targets (CASTing) assay, antibodies were raised against a non-conserved region in the AtMYB61 C-terminus (Figure S1). CASTing was initiated with a pool of 63-base-pair double-stranded oligonucleotides, where each oligonucleotide consisted of a segment of 27 random nucleotides flanked by designed sequences for PCR priming. A 15 µg (2.21×1014 DNA molecules) pool of “randomers” was incubated with AtMYB61 full-length recombinant protein (Figure 1A). Assuming the average protein-binding site is a hexamer, the 27-bp degenerate core of each double-stranded oligomer contained 21 possible positions. Therefore, in the initial round of CASTing, 21×1014 unique sites were available for binding, when using 15 µg of randomers.
(A) 27 bp random sequences flanked by two primer sites (63 bp in total) were used in the CASTing assay. (B) Sequence logo of CASTing targets discovered by MEME. The ACC motif was conserved among all target sequences. Two nucleotides upstream and downstream of the over-represented hexamer target sequences were included to analyse if the over-represented motifs could be extended beyond a hexameric sequence.
Five CASTing cycles were undertaken to enrich the pool of oligonucleotides in DNA binding-sites bound by AtMYB61. The enriched oligonucleotides were cloned into pCR4 TOPO (Invitrogen, Burlington, ON, Canada) and sequenced. Following enrichment, 89 CASTing-derived oligonucleotides were sequenced. Sequences were subjected to analysis to discover over-represented motifs using MEME (Multiple Em for Motif Elicitation) [39] (Table 1, Table 2, Figure 1B). MEME filtering criteria identified sequences with a min/max motif width of 6, any number of repetitions of a single motif distributed among the sequences, and no restrictions on the number of motifs identified. Following MEME analysis, all CASTing-enriched sequences contained over-represented motifs characterised by an abundance of adenosine and cytosine residues. These over-represented motifs had a conserved set of ACC nucleotides present at the beginning of the motifs, suggesting that these nucleotides may be essential for recognition and binding (Table 1, Table 2, Figure 1B). These motifs correspond to canonical AC elements, also known as H-boxes or PAL-boxes (Table 1, Table 2, Figure 1B). Notably, a subset of CASTing-enriched oligonucleotides had multiple AC elements present in individual target sequences (Table 1). That said, a CASTing assay is a method to identify novel DNA-binding targets of a transcription factor of interest, and further characterisations are required to determine preferred targets.
AC elements, also known as PAL boxes or H-boxes, play key roles in regulating transcription for a variety of genes, particularly those encoding enzymes implicated in phenylpropanoid metabolism [18], [19], [20], [21], [22], [23], [24], [25], [26], [27]. R2R3-MYB proteins are known to bind AC elements and activate transcription from these motifs in yeast and in planta [16]. For example, pine (Pinus taeda) MYB1 [15] and MYB4 [17] and eucalyptus (Eucalyptus grandis) MYB2 [45], were all able to bind to AC elements present in the promoters of lignin biosynthetic genes. Similarly, pine (Pinus taeda) MYB1 and MYB4 bound AC elements present in the gene regulatory sequences of a pine gene encoding glutamate synthetase (GS1b) [8]. R2R3-MYB binding to AC elements is predicted to play a role in dictating xylem-localised expression of the aforementioned genes [8], [15], [17], [45]. Given the xylem-localised expression of AtMYB61 [34], it is likely that it functions in an equivalent manner to drive AC-element-mediated expression in Arabidopsis thaliana.
AtMYB61 Bound to DNA Target Sequences with Varying Degrees of Affinity
The relative binding affinities of recombinant AtMYB61 protein to the CASTing-derived sequences were determined (Table S1). Dissociation constants for each CASTing target were calculated by GRAFIT software program by using Scatchard plots (Table 3). The CASTing target that bound with the highest affinity (9.12E−09 M) was ACCTAC (AC-I) (Table 3). Since the AC-I motif was the preferred target of AtMYB61, a mutational assay was conducted on this motif to examine which nucleotides were essential for binding (Table 4). A guanine nucleotide was substituted one nucleotide at a time and shifted along the motif. A nitrocellulose filter-binding assay was used to calculate the Kds of the mutated AC-I motifs (Table 4). Binding diminished when a mutation was present in the first three nucleotides of the AC-I motif (Kd>5.00E−06 M); however, when a mutation is present in the last three nucleotides of the AC-I motif, the binding is reduced but not completely abolished (Table 4). The relative binding affinities of recombinant AtMYB61 protein to CASTing targets and mutated motifs were validated by EMSAs (Figure 2AB). EMSAs were conducted at a protein concentration of 5×10−08 M because this was the protein concentration at which not all the targets reached their binding max as determined by nitrocellulose filter-binding assay (Figure 2AB, Table S1). This enabled detection of differential binding via EMSAs.
(A) EMSA of recombinant AtMYB61 protein binding to 6 labelled CASTing target sequences. The protein concentration used was 5×10–08M. Protein concentrations were conducted at 5×10–08M because this was the protein concentration at which targets had not all reached their binding max as determined by nitrocellulose filter-binding assay, allowing one to observe differential binding. (B) EMSA validating relative binding affinities of AtMYB61 to mutated ACCTAC motif. The protein concentration used was 5×10–08M. Mutations were conducted by substituting a single guanine nucleotide along the AC1 element. Black arrow indicates gel shift by the probe. Non-binding site (NBS) is a sequence that does not bind AtMYB61, acting as a negative control. Probes were engineered for the EMSA reaction by inserting the hexamer CASTing sequence or mutated AC1 element sequence into the underlined area.
AtMYB61 bound its preferred target AC-I (ACCTAC) with a binding constant of 9.12E−09 M (Table 3), which is similar to the tight binding of the vertebrate c-MYB R2R3 domain to the MYB binding site ((T/C)AAC(G/T)G(A/C/T)(A/C/T)) (binding constant = 1.5E−09 M±28% ) [46], [47]. Tanikawa et al. found that AACG nucleotides in the MYBSI binding site were critical for binding [47]. The second adenine, fourth cytosine, and sixth guanine were particularly important in determining binding specificity. If any of these core nucleotides were mutated, binding affinity decreased by greater than 500 fold. The third adenine was not as crucial - if it was mutated, the binding affinity would be decreased up to 15 fold. Consistent with this, AtMYB61 had a set of core recognition nucleotides – ACC – that could not be mutated without abolishing binding (Figure 2b, Table 4). Moreover, mutation of the latter half of the binding site, occurring at residues TAC, reduced binding but did not abolish it completely.
The Affinity of AtMYB61 to Specific Target DNA Sequences was Predicted by Molecular Interactions Determined in Silico
Computational analysis of the 3-dimensional structure of the N-terminal DNA-binding region of AtMYB61 was conducted in order to validate the role of this domain in sequence-specific binding. Previously, the structure of the N-terminal DNA-binding domain of animal c-MYB bound to its DNA consensus motif (AACNG) was solved by heteronuclear multidimensional NMR [31]. Animal c-MYB DNA-binding region contains a conserved R2R3-MYB domain that exhibits high similarity to plant R2R3-MYB DNA binding domains. This NMR structure was used as a template to model the structure of AtMYB61. The AC-I (ACCTAC) and NBS (GAGACC) nucleotide models were then docked into the predicted binding sites of the AtMYB61 model (Figure 3).
(A) Pymol models of ACCTAC motif docked into the binding site of AtMYB61. Molecular modelling was completed by using the online program PHYRE (Protein Homology/analogY Recognition Engine) to predict a crystal structure of AtMYB61 using homology to the c-MYB DNA binding domain. The PBD (protein data bank) file recovered from the PHYRE analysis was used to superimpose the predicted AtMYB61 crystal structure with the c-MYB crystal structure using DaliLite. Using Pymol the 3D sequence model – ACCTAC – was docked into the predicted binding sites of AtMYB61. The AC1 element model is displayed in yellow, the loop secondary structure of AtMYB61 inferred model is displayed in green, and the helix secondary structure of AtMYB61 inferred model is displayed in red. (B) Model of AtMYB61 binding site with the first three ACC nucleotides in the ACCTAC sequence determines that these nucleotides are essential for binding. The AC1 (ACCTAC) nucleotide model was docked into the predicted binding site of AtMYB61. The specific hydrogen bonding between the amino acids of AtMYB61 binding site to the ACC nucleotides of AC1 were predicted by Pymol and listed as follows: asparagine-59 (R3 helix) hydrogen to adenine-1 nitrogen; asparagine-106 (R3 helix) oxygen to adenine-1 hydrogen; asparagine-59 (R3 helix) oxygen to cytosine-2 hydrogen; asparagine-102 (R3 helix) oxygen to cytosine-3 hydrogen; and arginine-56 (R2 helix) oxygen to cytosine-3 hydrogen. This confirms binding data determined by the nitrocellulose filter-binding assay and EMSAs, iterating that the ACC motif is the core recognition motif of AtMYB61. (C) Model of AtMYB61 binding site with the TAC nucleotides in the ACCTAC sequence determine that these nucleotides are less essential for binding. The AC1 (ACCTAC) nucleotide models were docked into the predicted binding sites of AtMYB61. The molecular interactions between the amino acids of AtMYB61 binding site and the TAC nucleotides of AC1 were analyzed by Pymol and are listed as follows: leucine-55 (R2 helix) methyl group was predicted to form a non-polar bond with thymidine-4 methyl group; Arginine-54 (R2 helix) hydrogen was predicted to form a hydrogen bound with thymidine-4 oxygen; lysine-51 (R2 helix) hydrogen was predicted to form a hydrogen bound with adenine-5 nitrogen; and cytosine-6 remained unbound in the model. (D) Model of AtMYB61 binding site with non-binding site (GAGACC) predicts that this motif is not recognised by AtMYB61. The non binding site model was docked into AtMYB61 binding site via Pymol and hydrogen bonding was analyzed. Only one hydrogen bond was predicted between AtMYB61 asparagine-59 (R3 helix) oxygen and the non-binding site adenine-2 hydrogen. Yellow dashed lines indicate hydrogen bonding established by Pymol program, and blue dashed lines indicate non-polar interactions.
Based on the model of AtMYB61, the molecular interactions shared between the binding sites of AtMYB61 to its targets supported in vitro binding data (Figure 3BCD). For example, there were more hydrogen bonds shared between AtMYB61 DNA-binding domain and AC-I compared to NBS (Figure 3BCD). Based on the model of AtMYB61 bound to AC-I, several specific intermolecular interactions are predicted to create binding specificity. These include hydrogen bonds between the following residues: asparagine-59 (R3 helix) of AtMYB61 with adenine-1 nitrogen of AC-I; asparagine-106 (R3 helix) oxygen of AtMYB61 with adenine-1 hydrogen of AC-I; asparagine-59 (R3 helix) oxygen of AtMYB61 with cytosine-2 hydrogen of AC-I; asparagine-102 (R3 helix) oxygen of AtMYB61 with cytosine-3 hydrogen of AC-I; arginine-56 (R2 helix) oxygen of AtMYB61 with cytosine-3 hydrogen of AC-I; arginine-54 (R2 helix) hydrogen of AtMYB61 with thymidine-4 oxygen of AC-I; and, lysine-51 (R2 helix) of AtMYB61 with adenine-5 nitrogen of AC-I. The leucine-55 (R2 helix) methyl group of AtMYB61 is predicted to form a non-polar bond with thymidine-4 methyl group of AC-I. Cytosine-6 remained unbound in the model. In comparison, the NBS model had only one hydrogen bond present, involving asparagine-59 (R3 helix) oxygen of AtMYB61 with adenine-2 hydrogen of AC-I.
The Affinity of AtMYB61 to Specific Target DNA Sequences did not Correlate with AtMYB61-driven Transcriptional Activation with each of the Target Sequences
Previous studies have shown that AtMYB61 protein is sufficient to drive transcription in yeast from promoter sequences that contain AC elements [34]. Consequently, yeast transcriptional activation assays were used to determine the relationship between AtMYB61 affinity to specific DNA sequences and its capacity to drive transcription (Figure 4). Reporter constructs comprised the coding sequence for β-galactosidase under the control of the yeast minimal CYC1 promoter fused to triple repeats of a given CASTing target or a mutated AC-I motif (Figure 4). The minimal CYC1 promoter is unable to support transcription, so reporter expression would be contingent on the capacity of AtMYB61 to bind to the fused motifs, which would function as gene regulatory sequences. The expression of AtMYB61 was under the control of the galactose-inducible GAL1 promoter. As determined by the quantification of β-galactosidase activity, when AtMYB61 protein was induced by galactose, the protein was able to activate transcription from the CASTing target sequences but not from the mutated AC-I elements (Figure 4). The extent of transcriptional activation varied for each CASTing target (Figure 4C). Notably, CASTing target sequences ACCATA, ACCAAT, and ACCAAA supported greater amounts of β-galactosidase induction relative to the AC-I element, which bound with the greatest affinity to AtMYB61 (Figure 4C).
(A) The sequence of the oligonucleotides cloned into the reporter vector using EcoRI and SalI sites. Each AC element or mutated ACI element is triplicated within the segment. (B) Schematic representations of the Effector (pYES2TRP::AtMYB61) and Reporter (pLacZi::AC) constructs used in this assay (CYC1: minimal yeast promoter). (C) Quantitative analysis of β-galactosidase activity in yeast after induction. The measurements in liquid assay were made from three biological independent replicates. Activation of artificial genes comprising a minimal CYC1 promoter fused to a tandem AC element or mutated ACI element upstream of the lacZ gene by AtMYB61 protein, upon growth of the yeast in galactose (light grey bars), gave rise to β-galactosidase activity that was significantly greater than the controls, as determined by analysis of variance (P<0.005); including each vector alone, or both together after growth on non-inducing glucose (dark grey bars). Error bars represent standard deviations. *indicates statistically significant, P<0.005, determined by t-test. Underlined bases corresponds to a substituted guanine.
Previously, R2R3-MYB proteins have been shown to bind to AC elements and activate transcription in yeast and in planta; however, these studies did not correlate binding affinity with ability to activate transcription [8], [15], [17], [28]. Yeast activation assays determined that the affinity of AtMYB61 to specific target DNA sequences did not correlate with AtMYB61-driven transcriptional activation with each of the target sequences. This is not surprising given the multitude of studies that have observed that in vitro binding and endogenous transcriptional regulation frequently disagree [48], [49], [50], [51], [52]. Consistent with this are results obtained using the glucocorticoid receptor (GR), where no correlation between in vitro binding affinities and in vivo transcriptional activities was observed [53]. GR target sequences, differing by as little as a single nucleotide, differentially affected GR DNA binding and transcriptional activity, with no correlation between these parameters. Similarly, binding affinity of AtMYB61 to specific target DNA sequences did not correlate with AtMYB61-driven transcriptional activation with each of the target sequences. It may be that conformation of AtMYB61 changes when binding to a specific DNA sequence, altering its ability to activate transcription.
CASTing Target Sequences were Found in the Promoter Regions of Three Putative Direct Downstream Targets of AtMYB61
Previous experiments predicted three putative direct downstream target genes of AtMYB61 [34]. The predicted targets of AtMYB61 were determined by a two-stage comparative transcriptome analysis. This transcriptome analysis entailed identification and comparison of genes whose transcript abundance was modulated by differences in AtMYB61 activity, relative to those genes whose transcript abundance profiles paralleled AtMYB61 across development and in different organs. In the first stage of the analysis, publicly available, complete Arabidopsis transcriptome microarray data were used to identify those genes sharing the same transcript abundance profile as AtMYB61 across multiple stages of development. The second stage of transcriptome analysis identified genes whose transcript abundance was influenced by the presence or absence of AtMYB61. A complete transcriptome microarray dataset was generated using WT, myb61 loss-of-function mutants and 35S::MYB61 gain-of-function transgenic plants, enabling comparison of the impact of AtMYB61 on transcriptome activity. Genes were identified in this dataset whose transcript abundance was contingent on the relative abundance of AtMYB61. Both gene lists were then compared to identify genes that were most likely direct targets of AtMYB61. Three genes were identified in the intersection set. They encode the following gene products: a KNOTTED1-like transcription factor (KNAT7, At1g62990); a Caffeoyl-CoA 3-O-methyltransferase (CCoAOMT7, At4g26220); and a pectin-methylesterase (PME, At2g45220). In keeping with their role as putative AtMYB61 targets, loss-of-function mutants corresponding to each of the genes phenocopy aspects of the myb61 loss-of-function mutant phenotype.
The CASTing targets were identified in the 1000 bp 5′ non-coding regions of the three putative direct target genes and were determined by algorithm-based screening to be statistically over-represented (Figure 5). AtMYB61 bound to the 5′ gene regulatory sequences of all three putative direct target genes in an AC dependent manner [34]. These data support the hypothesis that AtMYB61 binds to AC elements in a distinct set of target genes to modify gene expression.
(A) Sequence logo of the over-represented motifs in the promoter sequences of the three target genes of AtMYB61, as determined by the Promomer algorithm [54] (average = 2.9; Z-score = 13; significance = 0.001). Right: Schematic representation of the promoter regions of the three putative AtMYB61 downstream target genes. (B) The three putative AtMYB61 direct downstream target genes,, KNOTTED1-like transcription factor (KNAT7, At1g62990); Caffeoyl-CoA 3-O-methyltransferase (CCoAOMT7, At4g26220), and pectin-methylesterase (PME, At2g45220), were identified by Romano et al (33). 1000 bp upstream regulatory regions were examined of the three genes. +/− indicate the orientation of CASTing target sequences relative to the sense coding strand; whereas, numbers indicate the position of these motifs relative to the putative transcriptional start (indicated by an arrow). Triangle represents ACCAAA, square represents ACCAAT, and circle represents ACCATA.
Conclusion
Despite the size and importance of the plant R2R3-MYB family of transcriptional regulators, little is known about the molecular functioning of given family members. The work described herein casts greater light on the interaction between an R2R3-MYB family member and its cognate DNA targets. The findings support the hypothesis that AtMYB61 is recruited to target genes via its interactions with a set of unique sequences, and thereby modifies gene expression. Surprisingly, the affinity of AtMYB61 to specific target DNA sequences did not correlate with AtMYB61-driven transcriptional activation with each of the target sequences, suggesting that the conformation of AtMYB61 may be altered allosterically when bound to specific target sequences. These findings point to additional complexities in the regulation of plant gene expression, and argue for the need for greater exploration of the molecular intricacies involved in the interactions between plant transcription factors and their DNA targets.
Supporting Information
Figure S1.
AtMYB61 antibody generation and validation. (A) Amino acid sequence similarity of AtMYB61 along with its closest family member AtMYB50. The two proteins have conserved N-terminal amino acid sequences but unique C-terminal domains, which was the domain selected to generate AtMYB61 antibodies against (highlighted region). (B) A chemiluminescent western blot validate anti-AtMYB61 antibody specificity. Lanes correspond to full-length recombinant AtMYB61 protein (Lane 1), of antibody alone (Lane 2), and AtMYB61 recombinant protein immunoprecipitated with pre-immune serum (Lane 3) and with AtMYB61-specific antiserum (Lane 4). Western blot was done with 1∶20000 dilution of immune serum. Western blot shows greater quantities of AtMYB61 protein eluted from the Magnetic Dynabeads Protein G antibody complex compared to the Magnetic Dynabeads Protein G pre-immune serum complex, showing that the immunoprecipitation was successful.
https://doi.org/10.1371/journal.pone.0065132.s001
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Table S1.
Relative binding of CASTing targets and mutated AC-I sequences to AtMYB61.
https://doi.org/10.1371/journal.pone.0065132.s002
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Acknowledgments
We are very grateful to Ms. Joan Ouellette for technical assistance, Mr. Ke Wu for assistance on the CASTing assay and to Ms. Stephanie Tung, Ms. Kate Lee and Ms. Trisha Min for assistance with the yeast experiments.
Author Contributions
Conceived and designed the experiments: MBP MMC. Performed the experiments: MBP. Analyzed the data: MBP MMC. Contributed reagents/materials/analysis tools: MBP MMC. Wrote the paper: MBP MMC.
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