- Research article
- Open Access
Analysis of the P1promoter in response to UV-B radiation in allelic variants of high-altitude maize
© Rius et al.; licensee BioMed Central Ltd. 2012
- Received: 1 March 2012
- Accepted: 28 May 2012
- Published: 15 June 2012
Plants living at high altitudes are typically exposed to elevated UV-B radiation, and harbor mechanisms to prevent the induced damage, such as the accumulation of UV-absorbing compounds. The maize R2R3-MYB transcription factor P1 controls the accumulation of several UV-B absorbing phenolics by activating a subset of flavonoid biosynthetic genes in leaves of maize landraces adapted to high altitudes.
Here, we studied the UV-B regulation of P1 in maize leaves of high altitude landraces, and we investigated how UV-B regulates P1binding to the CHS promoter in both low and high altitude lines. In addition, we analyzed whether the expansion in the P1 expression domain between these maize landraces and inbred lines is associated to changes in the molecular structure of the proximal promoter, distal enhancer and first intron of P1. Finally, using transient expression experiments in protoplasts from various maize genotypes, we investigated whether the different expression patterns of P1 in the high altitude landraces could be attributed to trans- or cis-acting elements.
Together, our results demonstrate that, although differences in cis-acting elements exist between the different lines under study, the different patterns of P1 expression are largely a consequence of effects in trans.
- UV-B radiation
- Maize landraces
- P1 transcription factor
Plants, because of their sessile lifestyle, have evolved adaptations to live under diverse environmental variables, including solar radiation. Sunlight contains qualities of light that are essential for photosynthesis, and also provides informational signals that control plant growth and development. At least three different types of photoreceptor systems exist in plant cells, perceiving red/far-red (phytochromes), blue/UV-A (cryptochromes and phototropins), and there is at least one putative UV-B receptor (UVR8), which was recently identified .
UV-B (280 to 315 nm) is part of the solar radiation, and therefore plants are inevitably exposed to UV-B. UV photons cause cellular damage by generating DNA photoproducts and through direct damage to proteins, lipids, and RNA [2–4]. Plant responses to UV-B damage include repair [5, 6] and avoidance [7, 8]. Solar UV-B radiation flux varies over time and location on earth. It is higher at increased elevation, because there is less air mass and greater atmospheric transparency to shorter wavelength radiation, although local climatic conditions, such as cloud cover, can modulate the dosage . UV-B increases are most critical in specific ecosystems, for example, ozone depletion was extensive at a 3420-m site in the Andes Mountains compared with values from equal latitude to the west and east . Consequently, determining the molecular bases for acclimation to higher UV-B fluence is an important factor in sustaining crop yield as the world’s population continues to increase.
Because plants living at high altitudes are typically exposed to elevated UV-B, they are predicted to have mechanisms to prevent damage from this radiation, such as the accumulation of UV-absorbing compounds [7, 11] and the use of UV-A photons by photolyase enzymes to repair most UV-B induced DNA damage . The plant epidermis, by virtue of the accumulation of numerous phenolic compounds and cuticular waxes, absorbs 90–99% of solar UV-B radiation. In many flowering plants, flavonoids accumulate in the vacuoles of epidermal cells where they attenuate the UV component of sunlight with minimal absorption of photosynthetically active radiation [11, 12].
The P1 gene encodes an R2R3-MYB transcription factor that regulates the accumulation of a specific group of flavonoids in maize floral tissues, the flavones and the phlobaphenes . P1 controls the accumulation of these pigments by activating a subset of maize flavonoid biosynthetic genes [13–15] and is primarily expressed in floral tissues, including the pericarp, cob glumes, silks and husk tissues. The phlobaphene pigments have been historically used as markers to uncover some of the fundaments of modern genetics. Among the compounds controlled by P1 are the flavones, important phytochemicals that provide protection against a number of maize pathogens, furnish a powerful UV shield and are significant nutraceutical components of the human diet . Previously, we established that some maize landraces, specifically those adapted to high altitudes, accumulate flavones and express P1 in leaves and other green tissues in the presence of UV-B, in sharp departure to the floral-organ specific expression domain of P1 found in most other maize inbred lines . These results suggest the potential for a large P1 allelic diversity as a consequence of growing in diverse environments.
An important challenge is to define the molecular bases that permit acclimation responses of maize to UV-B. Maize races have a complex history, having been derived from multiple open pollinated varieties and transported by people to diverse locations . Maize genotypes exhibit immense allelic diversity, and this represents a fundamental resource for both genetics and breeding. This crop requires a high light environment for good yield , and it is safe therefore to assume that indigenous farmers would grow high-altitude maize in sunny locations. Therefore, these indigenous landraces are predicted to have improved UV-B tolerance, reflecting recurrent selection against visible symptoms of UV-B stress.
In this study, we analyzed whether the expansion in the expression domain of P1 in specific maize landraces that have adapted to high altitude (and hence to higher UV-B levels) can be associated to changes in the molecular structure of the corresponding P1 alleles, in particular, changes in cis-regulatory elements sequences in promoter regions that allow as-yet to be identified regulators to activate P1 expression in vegetative tissues. To gain insight of the participation of this transcription factor in UV-B regulated synthesis of flavones in maize leaves, we first studied the regulation of P1 by UV-B in maize leaves of five maize landraces from high altitudes: three from Mexico (Cacahuacintle, Conico Norteño and Arrocillo Amarillo, collected from altitudes between 2200- and 2800-m) and two from the Andes mountains (Mishca from altitudes between 2200-and 2800-m and Confite Puneño from altitudes between 3600- and 3900 m). We then analyzed the molecular structure of the P1 promoter alleles in these landraces, and investigated which regulatory motifs may be responsible of the regulation of P1 by UV-B. Finally, to study if the different expression patterns of P1 in the high altitude landraces can be attributed to the presence of trans- or cis-acting elements in the landraces, transient expression analysis using leaf protoplasts from W23 and Mishca, and proximal promoter constructs fused to the luciferase gene reporter were analyzed.
P1is expressed in maize leaves and is induced by UV-B in maize high altitude landraces
Furthermore, P1 protein levels were analyzed by western blots, using polyclonal antibodies against P1 , in nuclear extracts from leaves of a low altitude inbred line (W23) and the five landraces, under control and UV-B conditions. The densitometric quantification of the western blots showed increases of P1 protein levels in the high altitude landraces (with the exception of Arrocillo) after the UV-B treatment (Figure 1B). Consistent with the RT-PCR results (Figure 1A), W23 did not show changes in P1 levels after irradiation with supplemental UV-B (Figure 1B). Thus, mRNA changes by UV-B parallels the protein changes measured. It is interesting that, despite the low levels of P1 transcript measured in leaves, in some cases almost undetectable as determined by nested RT-PCR, it was possible to distinguish the presence of the protein in nuclear extracts in all samples at different levels.
UV-B increases the binding of P1 to the CHSpromoter in high altitude landraces
An 8 h-long UV-B-treatment can induce the expression of enzymes of the flavonoid pathway in maize, including chalcone synthase (CHS) . Maize has two CHS genes, C2 and WHP . Thus, we analyzed the association of P1 to the promoter region of C2 in one high-altitude landrace, Confite Puneño (CFT), and in the W23 low altitude line under control conditions (without UV-B) and after an 8 h UV-B treatment.
Variable P1 copy number in maize landraces
Figure 3B shows that Arrocillo has only 1 copy of the P1 gene, Cacahuacintle has 2 copies, Confite has 4, Conico has 3 and Mishca has 8 copies of the P1 gene. On the other hand, our assays show that B73 has 15 P1 copies (Figure 3), which is close to the eleven copies of P1 reported by sequencing different BAC clones from this inbred line by Goettel and Messing . Our results show that the landraces under study have a variable number of P1 copies, suggesting that the UV-B regulation of this gene in the landraces in vegetative tissues is unlikely to be linked to the structure of the P1 cluster.
Analysis of P1promoters from maize lines and landraces
We first cloned and analyzed promoter regions which cover ~1.1kbp upstream the P1 transcription start site, and which include the basal promoter and part of the proximal enhancer described  from four of the high altitude landraces (Arrocillo, Confite, Cacahuacintle and Mishca). For comparison, we included in our analysis promoter regions from B73 and W23 lines. We obtained two clones with distinct promoter sequences from Confite and Mishca, and one from Arrocillo and Cacahuacintle, a good correlation, but not the complete set, of the copy number present in the genome (Figure 3). It is however possible that the different copies might be identical in the regions analyzed, or that the primers used to amplify the promoter regions may not hybridize with all the different copies in each landrace.
When the proximal promoter sequences of all lines was compared, a total of 19 indels were identified in this ~1.1kbp region, with single-nucleotide indels accounting for more than half (59.1%), followed by two nucleotide indels (9.1%, Additional file 1: Figure S1A). Thus, more than 68% of all the indels identified were less than 2 bps in length. Moreover, in the middle region of 783 bps sequence analyzed (from −1020 to −237, Figure 4A); there are no indels longer than 2 bps.
It is interesting to note that there is also a relatively high frequency of indels ≥ 15 bases, that include four indels of 18, 19, 24 and 36 bps in length located in the region extending from −253 to +1 (referred to the B73 promoter); and a 15 bps indel is located at −1084. With exception of the 19 bps indel, these long indels are multiples of 3 bps. The 36 bps insertion is exclusively present in the B73 line; the 24 bps insertion is absent in Mishca; the 19 bps insertion is absent in B73 and Cacahuacintle, and the 18 bps insertion is absent only in Cacahuacintle. The 15 bps indel, positioned at −1084 bps (referred to B73), is absent in W23, Arrocillo, and Confite. The sequences included in these long indels do not have any characterized box linked to UV-B or light response elements described in other promoters [27, 28]. However, the absence or presence of these indels could affect the relative distance of cis-regulatory element to others boxes, which may be involved not only in response to light but also in the modulation of P1 expression levels.
The high indel frequency observed in maize, and specifically in the cloned promoter regions of the landraces analyzed, may lead to PCR failure when primers are designed from a sequence derived from a genotype different to B73 from the one used in the DNA amplification experiment . This could at least partially explain why we were not able to amplify by PCR the proximal promoter region from Conico.
We also analyzed the sequences described as a distal P1 enhancer that covers ~630 bp, and it is located 4.6kbp upstream the transcription start site (region from −5282 to −4653, Figure 4A). This sequence includes a sub-fragment of 458 bp of the P1.2 enhancer described by Sidorenko and Peterson . The primers used to clone these sequences are listed in Additional file 2: Table S1. We were able to get only one sequence from this region for each of the five landraces, and of the inbred lines B73 and W23. In this region, we identify three elements that have been described to correspond to binding sites for transcription factors in response to UV-B : a MRE CHS core (ACCTA sequence), which is present only in the landraces with the exception of Cacahuacintle (CACGT sequence), and two UVBox ANAC13 boxes (CCAAG sequence) and one core corresponding to this box (CAAG) (Additional file 1: Figure S1B). Both 5 bps long UVBox ANAC13 boxes are present in all analyzed promoter distal sequences, and are separated by only 5 bps with the sequence AGC/ACC. The UVBox core sequence, present in all the sequences analyzed, is located nine nucleotides upstream an UVBox ANAC13 box (Additional file 1: Figure S1B). These UVBoxes ANAC13 were found significantly enriched in late induced UV-B genes .
We also cloned and analyzed the first P1 intron from B73, W23 and 4 landraces. This intron is usually very small (less than 200 bps) in MYB transcription factors . Within the 120 bps of this intron, we only identified five and one nucleotide changes with respect to B73 and W23 in Confite and Mishca, respectively (Additional file 1: Figure S1C). The remaining sequence resulted identical between them and respect to B73 and W23.
The six 1st intron sequences harbor an ACECHS core, located 33 bps from the start of the intron (CACGT sequence). In the case of Mishca, two of the three changes are located at each side of the ACE CHS core (Additional file 1: Figure S1C).
Recently, sequencing data has demonstrated that the maize genome exhibits variable levels of genetic diversity depending on the lines under comparison. On average, the frequency of single nucleotide polymorphisms between two maize inbred lines is approximately 1 substitution per 100 bases . In our case, the comparison of both the proximal and the distal promoter regions, and the 1st intron of P1 between inbred lines and high altitude landraces showed some minor, but possibly still important, sequence variation that may be responsible for the differences observed in P1 expression patterns.
Together, our analysis of the P1promoter and 1st intron nucleotide sequences in the high altitude landraces and inbred lines suggests that there may be a selective pressure over some regulatory regions that may explain the different UV-B regulation of P1.
Nucleotide diversity in P1non-coding regions
Finally, nucleotide diversity among the analyzed non-coding regions of the P1 alleles was calculated. A total of 19 indels and 30 polymorphic sites were found in the proximal promoter; while in the distal enhancer, a total of 1 indel and 17 polymorphic sites were identified. For the 1stP1 intron, no indels were found, and a total of 6 polymorphic sites were detected (Additional file 1: Figure S1C), for this region the analysis of diversity denotes a high level of conservation (π-value 0.01667). We calculated two estimates of diversity from our data. Nucleotide polymorphism (θ) is calculated from the total number of segregating sites with correction to the sample size , and nucleotide diversity (π) is the probability that two randomly selected sequences will possess different nucleotides at a site . The nucleotide polymorphism (θ) and diversity (π) estimated indicated that the distal enhancer region is more diverse than the proximal promoter region (Additional file 2: Table S2). This suggests that the distal enhancer may contain critical regulatory regions for P1 expression. The analysis of variability can be correlated with the analysis performed for both phylograms on the non-coding regions of P1.
The radial trees show the diversity present between the landraces and the inbred lines for the proximal and distal promoter regions (Figure 4A). Evidently this region, near to the SST, may have found a greater selective pressure than the rest of the promoter during selection for better environmental traits under higher radiation levels found at high altitudes or even during domestication to obtain greater yield.
Small RNAs expressed are complementary to a discrete region of the P1proximal enhancer
Using probes complementary to fifteen smRNA sequences, a microfluidic microarray-based assay was performed as described in Methods. After hybridizing with small RNAs extracted from B73 maize leaves, ten mature siRNAs showed significant expression levels (intensity >3fold background levels). However, siRNAs were detected at different intensity levels, ranging from 158.9 ± 33.2 to 11.2 ± 0.5 (Figure 5B). In addition, we were able to detect two smRNA which bind to 2nd intron. This 2nd intron region has also been demonstrated to be subject to epigenetic regulation . The levels of expression observed for the smRNAs are in the same order of magnitude as those complementary to the Mutator transposon and gypsy-type retrotransposon (Figure 5B) [37, 38]. It is interesting to note that the region of higher density of siRNAs is highly correlated with a zone of palindromes and repeated/inverted sequence within the P1 gene (Additional file 3: Figure S2). Increased DNA and histone methylation are proposed to be triggered by double-stranded RNA, which is processed into 21–25 nucleotide RNA molecules . Taking this into account, this short region of the proximal promoter could also be a fine regulation point of the expression of P1 through a siRNA/methylation manner dependent.
Mishca protoplasts activate P1expression in response to UV-B
The different P1 expression pattern in the high altitude landraces can be attributed to the presence of cis- and/or trans- acting elements in the landraces, which may be absent or inactive in the inbred lines like B73 or W23. To address this point, P1 promoter constructions using the P1 basal promoter region (~1.1-kbp upstream from +1, Figure 4A) from Mishca and W23 were fused to the luciferase reporter gene, and these constructs were then used to transform Mishca, W23 and B73 protoplasts. These protoplasts were irradiated during 8 h with UV-B after transformation with pP1MIS::LUC or pP1W23::LUC, or kept under control conditions in the absence of UV-B, and luciferase activity was analyzed. As a control, protoplasts were co-transformed using a plasmid expressing Renilla under the constitutive promoter CaMV35S promoter (p35S::Renilla).
P1 is one of the transcription factors that control the flavonoid biosynthesis pathway in maize. While the mechanisms by which P1 controls gene expression have been well established ([13, 40]), little is known on how the expression of P1 is controlled. DNA methylation is clearly at play, evidenced by the distinct phenotypes of P1-wr and P1-rr ears [35, 36]. In addition, the Unstable Factor Orange1 (UFO1) allele plays a role controlling whether P1 is expressed in vegetative tissues or not [35, 41–43]. The number of P1 copies varies depending on the maize genotype. The P1-rr allele has been well characterized at the molecular level [44, 45] and contains a single coding sequence, which when expressed, confers pigmentation to both the kernel pericarp and the cob . Other allelic variants contain different P1 copy numbers within their genomes. For example, the P1-wr allele is composed of six gene copies arranged in a tandem head-to-tail array (), and the B73 inbred line present a multiple copy P1 cluster .
In addition, the multicopy P1 allele is epigenetically regulated, resulting in the phenotype P1-wr (white pericarp/red cob) due to hypermethylation [34, 35]. However, the degree of methylation is modulated by the presence of Unstable factor for orange1 (Ufo1), which leads to ectopic pigmentation of pericarp and other organs when induces progressive hypomethylation over generations . Paramutation was first described for the maize Red1 (R1) gene . Subsequently, three more regulatory genes of the flavonoid biosynthetic pathway, B1 (Booster1), PL1 (Plant color1), and P1[26, 49, 50] were shown to undergo paramutation in maize . For example, the P1-wr gene copies are hypermethylated in their coding and non-coding regions relative to the P1-rr allele; the P1-wr multi-copy structure possibly results in intra-allelic interactions that give rise to silencing of P1-wr expression in the kernel pericarp . Functional analysis of P1-wr promoter and coding sequences in transgenic maize plants, as well as studies of natural P1 variants, have provided further support for the hypothesis that the organ-specific expression pattern of P1-wr is epigenetically regulated .
Here, we focused on the analysis of P1 expression in leaves and its regulation by UV-B radiation in high altitude maize landraces, and its comparison with low altitude inbred lines, like B73 and W23. Using young leaves of five different maize high-altitude landraces, we found that P1 is induced by UV-B, both at the transcript and at the protein levels, in contrast to B73 or W23, which showed almost undetectable expression levels, and very low induction by UV-B. In addition, P1 is able to increase the transcription of the CHS gene after a UV-B treatment in Confite, while up-regulation of this gene by UV-B is not observed in W23 (Figure 2). Previously, we found that an 8 h-long UV-B-treatment can induce the expression of enzymes of the flavonoid pathway in maize . Chalcone synthase (CHS) is a key enzyme in flavonoid biosynthesis. Maize has two CHS genes, C2 and WHP . It had been shown that the expression of the C2 gene is induced by low levels of UV-B/UV-A/blue light, and its function is largely regulated at the level of transcription [51–53]. In addition, ectopic expression of P1 in maize protoplasts is also sufficient to induce C2 in vivo. Thus, it is clear that P1 participates in the UV-B induction of the flavonoid pathway in leaves of high altitude landraces, but not in leaves of low altitude lines.
Taking into account the high allelic variability already described for P1[25, 44, 45, 47], ranging from the simple-copy P1-rr allele, to the multiple-copy tandem organization present in the B73 genome, we estimated the copy number of P1 in each genome of the high altitude landraces. Besides the high divergence that we found exists in the number of alleles present between the landraces (Figure 3), there is a correlation between the P1 copy number and the place of origin of the different races. For instance, Arrocillo, Cacahuacintle and Conico, with the lowest copy number (1 to 3), were collected in Mexico, from altitudes ranging between 2200 and 2800 m.; while both the Andean South American races Mishca, which grows at 2200–2800 m, and Confite Puneño, which has adapted to live at 3600–3900 m, have 4 and 8 copies of P1, respectively. Evidently, this variability could be related to the selective pressure during the domestication to select adaptive traits, in this case to be able to grow under conditions of high incidence of UV-B.
We also cloned and sequenced two fragments of the P1 promoter region (a distal and a proximal segment) and the first intron from the landraces under study, and from B73 and W23. The analysis allowed us to determinate the presence of different allelic variants, the presence of variable numbers of indels and the location of them within these promoter sequences. We also analyzed the presence of different DNA motifs that may participate in the regulation by UV-B in the promoter regions. For example, both the Mishca and the W23 P1 promoter regions contain seven UVBoxes (CAAG) distributed within the ~1.1-kbp proximal promoter analyzed and one ACE CHS core (CACGT)  (Additional file 1: Figure S1). Assuming that this element is of importance in the induction by UV-B, we found only one difference between both promoter regions that could give different UV-B regulation, which is the unequal number of core ACE ANAC13 (ACGTG) located near the TSS, Mishca having three and only two present in W23. Another difference is the presence of a 24 bps sequence in the W23 promoter, which includes a sequence highly similar to a SIR (sub terminal inverted repeat, GCTCGGCGCCATAG) described by Goettel and Messing  of 14 bp that is also present the terminal inverted repeats of Mutator-like transposons. This indel produces a displacement of the ACE CHS and all the UVBoxes from the ACE ANAC13 core in W23. However, when transient expression analysis using leaf protoplasts from W23 and Mishca, and proximal promoter constructs fused to the luciferase gene reporter from both lines were done (Figure 6), we found that differences in gene regulation by UV-B are largely a consequence of effects in trans-, suggesting that these regulatory sequence differences are not the causal reasons for the difference in expression. Rather, our results suggest the presence of a regulatory protein in Mishca protoplasts that responds to UV-B, which may be able to bind to regulatory sequences in the promoter of P1.
To further analyze other possible mechanisms that may participate in the regulation of the expression of P1 in maize leaves, an analysis of the presence of small RNAs in leaves of the B73 line was conducted. Our results indicate that there is a high number of smRNAs complementary to a specific region in the basal P1 promoter of about 100 bps, which includes a repeated-inverted sequence. This region is a target of more than 40 smRNAs (from 21 to 24 bps in length). Until now, little evidence existed respect to the mechanism and participation of these small RNAs in P1 silencing. Analysis of these smRNAs levels in leaves of high altitude landraces, and their levels after UV-B exposure are currently under study to understand their possible involvement in the induction of P1.
We have demonstrated that P1 expression is increased in response to UV-B in high altitude maize landraces, and P1 binding to the C2 promoter is increased by UV-B in at least one if these landraces. Although polymorphisms exist between the P1 basal promoter sequences of the landraces and low altitude lines, we found that differences in gene regulation by UV-B are largely a consequence of effects in trans-, suggesting that these regulatory sequence differences are not the causal reasons for the difference in expression. The analysis of the presence of small RNAs in leaves of the B73 line show that there is a high number of smRNAs complementary to a specific region in the basal P1 promoter, the role of these smRNAs in the regulation of P1 leaf expression and UV-B regulation is under study.
Plant material and radiation treatments
Two Zea mays inbred lines, B73 and W23 b,pl , and five high-altitude landraces (Arrocillo Amarillo (ARR), Cacahuacintle (CCH), Conico Norteño (CNC), from altitudes between 2200 and 2800 m., Mexico), and Mishca (MIS, from altitudes between 2200 and 2800 m.) and Confite Puneño (CFT, from altitudes between 3600 and 3900 m.a.s.l.), native from the South American Andes were used. The highland lines where obtained from the Maize Genetics Cooperation Stock Center, http://maizecoop.cropsci.uiuc.edu/USDA/ARS, University of Illinois, Urbana/Champaign National Plant Germplasm System (NPGS) and from International Maize and Wheat Improvement Center (CIMMYT), D.F. Mexico, Mexico. B73 seeds were obtained from the Instituto Nacional de Tecnología Agropecuaria (INTA, http://www.inta.gov.ar/) and the W23 b,pl maize line is a lab stock as previously described . The landraces P1 phenotype alleles are summarized in Table S2.
Kernels from the different ears were selected and grown in the greenhouse with supplemental visible light to 10% of summer noon radiation with approximately 15 h light/9 h dark without UV-B for 28 d. UV-B was provided once for 8 h, starting 3 h after the beginning of the light period, using fixtures mounted 30 cm above the plants (Phillips, F40UVB 40 W and TL 20 W/12) at a UV-B intensity of 2 W m-2, UV-A: 0.65 W m-2. The bulbs were covered with cellulose acetate to exclude wavelengths <280 nm. As a control, plants were exposed for 8 h under the same lamps covered with polyester film (no UV-B treatment, UV-B: 0.04 W m-2, UV-A: 0.4 W m-2). Lamp output was recorded using a UV-B/UV-A radiometer (UV203 A + B radiometer, Macam Photometrics, Ltd, Livingston, UK) to ensure that both the bulbs and filters provided the designated UV dosage in all treatments. The UV-B treatment experiments were repeated at least three times, and biological replicate leaf samples were collected immediately after each experiment.
RNA isolation and reverse transcription reaction
RNA samples were isolated using Trizol (Invitrogen, Carlsbad, CA) as described by Casati and Walbot . RNA was isolated from a pool of young leaves from 6 plants; pooling minimizes organismal variation. Five μg of total RNA from each genotype/treatment combination was used for cDNA synthesis using Superscript II reverse transcriptase (Invitrogen). Three biological replicates were used for each sample plus a negative control (reaction without reverse transcriptase).
For P1 expression analyses of inbred and landraces lines under control and UV- B conditions, nested RT-PCR was performed as previously described . For the first round PCR reaction, EP5-8 and P1-23568 primers were used . A 5-μl portion of cDNA was added, and amplification conditions were as follows: 2 min denaturation at 94°C; 40 cycles at 94°C for 15 s, 60°C for 1 min and 72°C for 1 min, followed by 5 min at 72°C. For the second round PCR reaction, EP5-8-1 and ZFRT-8 primers were used . After first-round PCR, the reaction product was diluted 1:10 with dH2O. The diluted samples were used for the second-round (nested) PCR. A 0.1 μl of the PCR product from the first PCR reaction was added, and amplification conditions were as follows: 2 min denaturation at 94°C; 40 cycles at 94°C for 15 sec, 50°C for 1 min and 72°C for 1 min, followed by 5 min at 72°C. Primers for a non-UV-B regulated gene, encoding a putative thioredoxin-like protein were used as a control .
Quantitative real-time PCR (qRT-PCR) was carried out in a MiniOPTICON2 (Bio-Rad, Richmond CA) as described in Casati and Walbot . For qRT-PCR, three biological replicates were performed for each sample plus template-free samples and other negative controls (reaction without reverse transcriptase). Amplification of a thioredoxin-like transcript was used for data normalization. To confirm the size of the PCR products and to check for correspondence to a unique and expected PCR product, the final PCR products were analyzed on a 2% agarose gel.
Antibodies and western blot
The P1 polyclonal antibodies (#344) generated against the C-terminal region of P1, which has no homology with other maize proteins (excluding the MYB domain), were used. The P1 polyclonal antibodies (#344) were generated against 125aa corresponding to the C-terminal region of P1 (excluding the MYB domain), were expressed as aHis6-tagged fusion protein in E. coli followed by affinity purification. For immunodetection, maize leaf nuclear proteins were obtained from nuclei enrichment extracts according to the procedure described by Casati et al. . Nuclear proteins extracts from control and UV-B treated leaf samples were resolved on a 15% SDS-PAGE, transferred to a nitrocellulose membrane and probed with antibodies against P1 . Thirty micrograms of nuclear proteins were loaded in each lane. Densitometric analysis of the gels and blots was performed using the Gel Pro Analyzer program (Media Cybernetics, Silver Spring, MD, USA).
Total genomic DNA was extracted from leaf tissue as previously described . To amplify the fragments corresponding to the basal promoter (~1.1 kb), distal promoter (~0.6 kb), and 1st intron of P1, primers were designed based on the EF165349 sequence (http://www.maizesequence.com). The fragments were amplified using the FailSafe™ PCR System Kit (Epicentre®) and cloned in the pGEMT-easy® (Promega) vector and sequenced. The basal promoter fragments were re-amplified by PCR using primers with the restriction sites NotI and KpnI included in the forward and reverse primers, respectively (see Table S1). The PCR products were purified from gels, cut with the corresponding restriction enzymes and purified. The pA1::Luc construct (pMSZ011)  was restricted with NotI and KpnI and the A1 promoter was replaced by the ZmP1 basal promoter (~1.1 kb), resulting in the pP1::Luc construct.
Chromatin immunoprecipitation (ChIP) experiments
Mature leaves from CFT and W23 lines that were treated with UV-B and were kept under control conditions in the absence of UV-B were used for ChIP experiments. The antibody (#344) which specifically recognized the C-terminus of P1 was used for immunoprecipitation. Both PCR (25 cycles) and qPCR were carried out for the quantification of enrichment of P1 binding to sequences from −380 to −280 in the chalcone synthase promoter, primers used for the PCR analyses are shown in Table S1. Three biological replicates were performed from each genotype/treatment sample type, and three PCR experiments were done with each sample.
The miRNA microarray was custom synthesized by LC Sciences (Houston, Texas, USA) using their protocols . Briefly, poly-A tails were added to the 3’ ends of small RNAs using a poly(A) polymerase, and Cy3 and Cy5 was then ligated to the poly-A tails of samples from control and UV-B treated maize plants. The tagged RNAs were hybridized to the microfluidic hybridization chip. Hybridization images were scanned with a Gene- Pix 4000B microarray scanner (Molecular Devices, Sunnyvale, USA). Data extraction and image processing were performed using ArrayPro™ image analysis software (Media Cybernetics, Silver Spring, USA). A smRNA was scored as detectable if the signal intensity was higher than 3 times the standard deviation of the background signal, and the spot CV <0.5. CV is calculated as standard deviation/signal intensity; above background significant intensities had p-values < 0.05 using the SIGMA STAT package (SciencesSoftware.com, http://www.sciencessoftware.com). Normalization was performed with a LOWESS method to remove system-related variations.
Maize protoplast transient assay for P1promoter activity
Protoplasts were isolated from etiolated maize seedlings (W23, B73 and Mishca) as described by Sheen . Approximately 320.000 protoplasts were used in each of 200 μL reactions. For transient experiments, 20 μg of plasmid test DNA (pP1MIS::LUC or pP1W23::LUC) along with 5 μg renilla luciferase reporter plasmid were transformed into protoplasts. The reporter gene was driven by enhanced 35 S promoter and terminated by the 3’UTR of the nopaline synthase gene. Protoplasts without plasmid were used as controls. The protoplasts were transformed using a 40% PEG solution for 5 min at room temperature. Protoplasts were incubated for 8 h at 26°C under control and UV-B conditions in 16-well plates and then harvested by centrifugation (100 × g for 3 min). For the luciferase assays, 100 μL of the protoplast solution was removed to a 96-well assay plated and added 3 mL of 5X passive lysis buffer (Promega, Madison, WI, USA). The Dual-Luciferase Reporter assay kit from Promega was used to measure the renilla luciferase and firefly luciferase activities. The renilla luciferase and firefly luciferase activities were read on a LD-400 Luminescence detector (Beckman-Coulter) and the units were counts per second. To analyze the effect of the UV-B treatment on protoplast stability, protoplasts were transformed with a plasmid with the 35 S::GFP construct, and the integrity of the protoplasts was analyzed using an inverted confocal microscope Nikon C1/Eclipse TE-2000-E2 (see Additional file 4: Figure S3). Transient expression experiments in maize W23, MIS and B73 protoplast cells were performed with the p-P1 (~1.1kpb)::LUC + p35S::Renilla, and p35S::Renilla plasmids. Transformation conditions of maize protoplast cells and transient expression assays for luciferase Firefly and Renilla were performed essentially as previously described [40, 62].
Accession numbers for the nucleotide sequences of the different landraces promoters and distal enhancer of P1 are deposited in GenBank®: proximal promoters: ARR (JX033024), CCH (JX033025), CFT-1 (JX033026), CFT-2(JX033027), MIS-1 (JX033028) and MIS-2 (JX033029). Distal enhancers: ARR (JX033030), CCH (JX033031), CFT (JX033032), CNC (JX033033) and MIS (JX033034).
Data presented were analyzed using either the t-student test, or one-way analysis of variance (ANOVA). Minimum significant differences were calculated by the Bonferroni, Holm–Sidak, Dunett, and Duncan tests (p < 0.05) using the SIGMA STAT package (SciencesSoftware.com, http://www.sciencessoftware.com).
This work was supported in part by NSF-DBI-0701405 grant to E.G. FONCyT grant PICT-2006-00957 and PICT-2010-00105 to PC and EG. PC and SR are members of the Research Career of the Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) of Argentina.
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