wDBTF: an integrated database resource for studying wheat transcription factor families
BMC Genomics volume 11, Article number: 185 (2010)
Transcription factors (TFs) regulate gene expression by interacting with promoters of their target genes and are classified into families based on their DNA-binding domains. Genes coding for TFs have been identified in the sequences of model plant genomes. The rice (Oryza sativa spp. japonica) genome contains 2,384 TF gene models, which represent the mRNA transcript of a locus, classed into 63 families.
We have created an extensive list of wheat (Triticum aestivum L) TF sequences based on sequence homology with rice TFs identified and classified in the Database of Rice Transcription Factors (DRTF). We have identified 7,112 wheat sequences (contigs and singletons) from a dataset of 1,033,960 expressed sequence tag and mRNA (ET) sequences available. This number is about three times the number of TFs in rice so proportionally is very similar if allowance is made for the hexaploidy of wheat. Of these sequences 3,820 encode gene products with a DNA-binding domain and thus were confirmed as potential regulators. These 3,820 sequences were classified into 40 families and 84 subfamilies and some members defined orphan families. The results were compiled in the Database of Wheat Transcription Factor (wDBTF), an inventory available on the web http://wwwappli.nantes.inra.fr:8180/wDBFT/. For each accession, a link to its library source and its Affymetrix identification number is provided. The positions of Pfam (protein family database) motifs were given when known.
wDBTF collates 3,820 wheat TF sequences validated by the presence of a DNA-binding domain out of 7,112 potential TF sequences identified from publicly available gene expression data. We also incorporated in silico expression data on these TFs into the database. Thus this database provides a major resource for systematic studies of TF families and their expression in wheat as illustrated here in a study of DOF family members expressed during seed development.
Gene expression at the level of mRNA transcription from DNA is regulated through different mechanisms, the most widely studied being regulation by transcription factors (TFs). These DNA-binding proteins control gene expression by interacting with cis-regulatory elements (CREs) in the promoters of their target genes. DNA-binding domains are in general highly conserved among species so their characteristics are used to classify TFs into families. Transcriptional control of gene expression influences many biological processes such as responses to the environment or stress and regulation of metabolic pathways.
The sequencing of model plant genomes has allowed many genes coding for TFs to be identified. A total of 1,533 TFs were identified in the Arabidopsis thaliana genome  and classified into 34 families. Comparing these with TF genes in other eukaryotic genomes, i.e., of Drosophila, Caenorhabditis elegans, and Saccharomyces cerevisiae, the size of TF families differs considerably across the eukaryote kingdoms and about 45% of Arabidopsis TFs are from families specific to plants . In Oryza sativa spp. japonica, Xiong et al.  identified 1,611 TF genes belonging to 37 gene families. Most TF families are of similar size in rice and in Arabidopsis .
Information on the TFs of model species has been organized into databases. Arabidopsis TF sequences were compiled and classified into families by several groups: the Riechmann group, the Sheen group http://genetics.mgh.harvard.edu/sheenweb/AraTRs.html, OHIO-ATTFDB , RARTF http://rarge.gsc.riken.jp/rartf/, TRANSFAC  and TrSDB . Another Arabidopsis TF database (DATF, http://datf.cbi.pku.edu.cn/) was created that integrates information from multiple sources (expressed sequence tags (ESTs), transcription factor binding sites) and contains 1,922 known or predicted TF sequences, classified in 64 families . The same approach was taken for both O. sativa spp. japonica and spp. indica to create DRTF http://drtf.cbi.pku.edu.cn/, which contains 2,384 rice TF sequences classified in 63 families . The discrepancies in the total number of TFs included in databases and the classification into families for the same species depends on the methods used for predicting TFs. For example, the differences between the dataset in DRTF and the results of Xiong et al.  are mostly because of new annotation in the latest version (Release 4) of the TIGR database that uses a broader definition of TFs. The sensu stricto definition of TFs is based on the DNA binding domain, but in the broader sense proteins having co-activator activity can also be considered as TFs. This broader definition explains why more TF families (63 versus 37) were found more recently.
Wheat is the most important crop in world food production. Triticum aestivum and other cereal genomes are substantially larger than those of A. thaliana and O. sativa. The genome of hexaploid wheat is about 16,000 Mb which is 38 times larger than that of the monocotyledon model O. sativa. It is an allohexaploid composed of three homoeologous subgenomes, AA, BB, and DD, thus generally each gene is represented by three homoeologous copies. The large hexaploid nature of the genome is a drawback in determining the complete sequence which is not yet available. Nevertheless, many wheat cDNA libraries have been constructed generating a rich source of ESTs; more than one million wheat ESTs are currently available in dbEST . These ESTs have been assembled into contigs such as Tentative consensus (TC) contigs (; http://compbio.dfci.harvard.edu/cgi-bin/tgi/gimain.pl?gudb=Wheat) along with data collated from the NCBI GenBank nucleotide database (full length and partial cDNAs). ESTs directly represent the transcribed portions of the genome so while waiting for the full genome to be sequenced, the analysis of expressed sequences is a good starting point for gene discovery.
Recently some T. aestivum TF families have been described such as MIKC-type MADS-box , NF-Y and Dr1 , Myb  and the plant-specific DOF (DNA-binding with One Finger) gene families [14, 15]. The DNA-binding domain of DOF proteins contains 52 amino acids structured as a Cys2/Cys2 zinc finger . This domain recognizes and binds a core motif 5'-AAAG-3' on gene promoters . In the Arabidopsis and rice genomes 36 and 30 Dof genes have been identified, respectively, and phylogenetic relationships between the genes have been established such that four major orthologous clusters have been defined [1, 15]. Recently, 26 different Dof genes were identified in barley by sequence analysis of clones isolated by screening genomic libraries and ESTs . By analysing soybean ESTs, 39 putative unigenes that encode DOF proteins were identified , 27 of which were confirmed as having the highly conserved domain .
DOF TFs participate in the regulation of many processes exclusive to plants. For example in barley, DOF TFs are involved at several developmental stages in seeds, in the accumulation of storage proteins and in germination [21–23]. In wheat, two Dof genes have been reported: wheat prolamin-box binding factor (WPBF), shown to be an activator of T. aestivum L. storage protein genes , and TaDof1. The three homoeologous genes encoding WPBF were sequenced and shown to be specifically expressed in seeds between 3 and 39 days after anthesis .
The aim of this study was to identify all unique T. aestivum TFs (i.e. each homoeolog is considered independently) by using generally available wheat transcript sequences and the model plant rice genome. We constructed a database compiling the wheat TF sequences identified, the corresponding in silico expression data and the predicted DNA-binding domains. The study of DOF family members illustrates the utility of wDBTF and the overall analytical approach.
Construction and content
Source data and database construction
The 2,384 putative TF protein sequences of O. sativa japonica were downloaded from the DRTF database http://drtf.cbi.pku.edu.cn/. T. aestivum sequences were downloaded from the Gene Indices database (wheat latest release 11.0, http://compbio.dfci.harvard.edu/tgi/plant.html) which represents 1,036,933 sequences either as TC contigs or singletons. The wheat sequences were translated to peptide sequences and compared using the BlastX program  with O. sativa japonica TF proteins. We used an e-value cut-off of 1e-05 with other parameters at the default setting, keeping only the best Blast hit. As TFs are composed of several conserved domains, some BlastX results gave a high Blast score against a rice TF protein because of particular conserved domains but were not really related to the query TF. To avoid such false associations, all Blast results were checked by eye and the database was edited to remove 2,296 sequences. The wheat TF sequences identified were compiled in the wDBTF database (Figure 1).
The amino acid sequences from T. aestivum were deduced from BlastX alignment against O. sativa proteins using the method described by Sado et al. . Only the protein sequence regions that matched a TF sequence were taken into account. The presence of DNA-binding domain for each wheat TF sequence identified was searched against the Pfam database. The e-value cut-off 1e-01 was used in the initial Hidden Markov Model (HMMer) searches. For families which have no DNA-binding domain profiles available in the Pfam database, each sequence was analyzed individually to decide the cut-off value and sequences with more than 60% identity with their respective sequences from rice were considered to be bona fide members.
The Affymetrix wheat genome array contains 61,127 probe sets which represent 55,052 transcripts. Blast searches were performed against the probe set data to assign an Affymetrix ID to individual sequences.
Details of the all the original EST libraries were collated from the NCBI Unigene site http://www.ncbi.nlm.nih.gov/unigene. The list of 226 libraries used for this database is provided in Additional file 1. The origins of expressed sequences were classified in six categories: root, crown, shoot, leaf, whole plant if the origin is unknown, and spike for whole organs and tissues within the spike at different developmental stages from flowering to maturation (Figure 2).
All data were imported and formatted using custom PERL scripts and stored in a PostgreSQL database, named wDBTF, publicly available at http://wwwappli.nantes.inra.fr:8180/wDBFT/. The web site was developed with Java applet and servlet technologies. The wDBTF web pages are conceptual views of the PostgreSQL relational database.
Identification of TFs in T. aestivum
Comparative analysis of wheat and rice TFs based on sequence identity was performed to identify all unique TFs in public transcript sequences of wheat.
Each of the 216,452 unique wheat sequences (contigs and singletons) from the TIGR assembly of ESTs and transcripts was systematically compared with rice TF proteins using Blastx. The sequences matching rice TFs (e-value < 1e-05) were defined as TF-encoding sequences. Any sequences which did not correspond to potential TFs were discarded. In this way we found 7,112 accessions from TIGR correspond to T. aestivum TFs. These sequences were represented by 3,790 TCs and 3,322 singletons (Table 1). Evidence of a conserved DNA-binding domain was detected for 51.8% of the wheat sequences identified, i.e. 3,681 sequences (Table 1). For 8 (GRF, LUG, NZZ, Trihelix, ULT, Whirly, HRT-like and VOZ) out of 84 subfamilies, no DNA-binding domain motifs are available in the Pfam database, so we established whether a wheat sequence belongs to a specific TF subfamily according to its degree of similarity to the respective subfamily member from rice. After this step 3,820 sequences were found to correspond to bona fide wheat TFs as they have the DNA-binding domain required to validate their status as transcriptional regulators.
We chose to keep all sequences identified by their overall similarity with rice TF proteins in wDBTF and gave information on the positions of Pfam motifs on the table of subfamilies web page.
Classification of wheat TF families
The wheat sequences were assigned to TF families by taking into account the best BLAST hit against rice TF proteins classified in the DRTF database http://drtf.cbi.pku.edu.cn/. In the wheat data set we found members corresponding to every rice TF family suggesting that TF families are conserved between rice and wheat. In wDBTF, wheat TF members were distributed across 40 families and 84 subfamilies. The NAC subfamily is the largest with at least 269 members. Among the other large TF subfamilies in wheat are the EREBP, AUX/IAA, bHLH, R2R3-MYB, bZIP, WRKY and C3H zinc finger families each with more than 150 members. At the other extreme, three subfamilies (LFY, SRS and LS) are each represented by a single gene. Wheat appears to have more AUX/IAA, CCATT-Dr1, HMG, MBF, S1Fa-like, Whirly and VOZ genes than would be predicted by comparing the number of genes proportionally to the number in rice, i.e. more than three times more. For each TF subfamily, a web page is available listing all accession numbers either for contigs or singletons.
Wheat TF expression in silico
Almost 50% of sequences identified as wheat TFs are singletons and the majority (70%) of wheat TF contigs are made up of 2-5 ESTs. For all the families, the average number of ESTs per contig is 6.8. This suggests that wheat TFs, like other plant TFs, are not highly expressed.
By referring to the source of the material used to make each EST library, in silico expression data for each accession was compiled and is provided in the database.
We found 4,305 wDBTF wheat sequences are represented on the Affymetrix wheat genome array using Blast searches against the probe data sets. However, several sequences correspond to the same Affymetrix ID so only 2,036 are unique. This information was added to wDBTF as it could facilitate the study of families or organ-specific TF expression as the expression information relating to each probe can be analyzed across all publicly available Affymetrix results.
Plant material for C2C2-Dof expression analysis
The wheat Dof TF sequences identified in silico were validated biologically by testing for their gene expression in seeds of T. aestivum line RE99006. Seeds were sown in 294-cm3 pots filled with a peat moss mix and kept in a greenhouse for 2 weeks. After 8 weeks of vernalization, the plants were transplanted to soil beds in a greenhouse with daily maximum/minimum air temperatures averaging 21°C/15°C and day/night relative humidity averaging 50%/60%. At anthesis, spikes were tagged when the anthers of the central florets appeared and the temperature was monitored every 30 min by four HOBO® H8 Indoor 8K Data Loggers (Onset Computer Corp., Bourne, MA). Two ears per plant were harvested every 50°C days from ovary stage until 600°C days after anthesis. All samples were taken at 11.00am to avoid possible diurnal effects on gene expression. Three independent biological replicates were used. The grains of central florets were collected, the embryo and the external pericarp were rapidly removed, and the endosperm was frozen in liquid nitrogen and stored at -80°C prior to RNA extraction.
C2C2-Dof expression during seed development
Total RNA was extracted from ovaries and developing grains (without the embryo and external pericarp) as described in Khaled et al. . Dof transcripts were amplified by PCR with an ABI Prism 7900HT sequence detection system (Applied Biosystems) using Power SYBR® Green PCR Master Mix (Applied Biosystems) according to the manufacturer's instructions. Gene-specific primer pairs used for Dof amplification were designed with Oligo6® and are listed in Additional file 2. Amplification of transcripts coding for actin, glyceraldehyde 3-phosphate dehydrogenase (GAPDH), elongation factor 1 alpha (eF1α), β-tubulin, and 18S was used for internal controls. The geometric mean was calculated and the normalized quantity of each gene transcript and standard deviation of the three replicates was then calculated . All primer pairs gave an amplification efficiency of 100% ± 10% and were comparable. The specificity of amplification products was assessed by analyzing their melting curves and by gel electrophoresis (giving a single band). Amplification plots and predicted threshold cycle values were obtained from three independent biological replicates with the SDS software version 2.1 (Applied Biosystems).
wDBTF is an integrated database which compiles all wheat sequences identified as TFs from publicly available expression data. Brought together in this form the data constitute a major resource for the study of gene expression in wheat and of plant TF families in general.
The wDBTF home page is the main web interface for all information contained in the database (Figure 3). The TF family names link to individual TF family or subfamily pages. Each TF family has its own dedicated page that contains 2 tables, either contigs or singletons, with all TF sequence accessions from the group.
The results page returns essential and comprehensive information, such as accession ID, best rice protein Blast hit, positions of Pfam domains and corresponding Affymetrix ID. In silico expression data is available for each accession referring to EST library sources. TF protein and DNA sequences and expression data can be downloaded from the wDBTF web site. Therefore, each family's results page integrates a large amount of data from multiple sources and is a good tool for research on the whole set of 7,112 TFs. Furthermore, classification associated with information on gene expression can be used to link candidate TFs to a given biological process.
Analysis of C2C2-Dof family
To illustrate our approach to in silico data analysis, we focused on the plant-specific Dof family. We identified 59 unique Dof sequences which are made of 186 expressed sequences in the above T. aestivum sequence output. In the wheat data set, 28 sequences cover Dof domains but only 22 cover it entirely. Dof domains of previously identified Dof genes from O. sativa japonica and Hordeum vulgare, described by Moreno-Risueno et al. , were downloaded from Genbank and were compared to the deduced amino acid sequences of the 22 wheat genes to establish relationships between the genes from different species. The conserved 50-amino acid Dof domains of the DOF proteins were aligned using CLUSTALW  and the resultant multiple alignment (Additional file 3) was represented as an unrooted neighbor-joining tree edited with the Treeview© (v1.6.6) program  (Figure 4). Wheat Dof were present in the seven groups observed for the Dof family thus Dof members from the three cereals appeared in all the subfamilies independently of the species. Members were found for all major orthologous clusters (MCOG-A, -B, -C and -D) defined by Lijavetzky et al. . Group I was shown to correspond to MCOG-B, group II to MCOG-A, groups III and VII to MCOG-C, and groups IV, V and VI to MCOG-D.
Expression of T. aestivum Dof genes
We found 59 wheat Dof represented by 25 contigs and 34 singletons. Of the Dof contigs 60% are made up of 1-5 sequences, while only 5 have more than 10 ESTs indicative of high in silico expression.
Of all the wheat Dof expressed sequences 48% come from spike libraries (Figure 5). In silico expression data show that 25 expressed Dof sequences from six contigs (Figure 6) and 19 singletons (Additional file 4) were detected only in spikes. Our primary focus is on identifying wheat Dof involved in endosperm development. cDNA made from RNA extracted from seed (300 degree-days after anthesis) of an INRA breeding line RE99006 was tested for the presence of 20 Dof transcripts using gene-specific PCR primers (Additional file 2); all these Dof transcripts were confirmed to be expressed in seeds (data not shown). To establish whether they are involved in wheat grain development, we tested the expression of 12 transcripts in endosperm at different seed developmental stages (Figure 7) by real time PCR. The same primers as above were used that gave efficient amplification and only one PCR-product in dissociation curves. Wheat Dof can be classified into 3 classes according to their expression profiles. Three Dof (TC298479, BE497753 and BE516595) are preferentially expressed during the first step of development when the grain is growing and their expression decreases down to a basal level in the grain-filling and drying-down stages. According to the second expression profile TC332787, TC285930 and CK208471 can be grouped together. These transcripts are detected through all developmental stages with three expression peaks: at the ovary stage, at early (150 degree-days) and mid grain-filling. Conversely to the first class, the third class groups Dof that are expressed at a basal level at the beginning of grain development increasing to a maximum midway through grain-filling when starch and storage proteins accumulate.
TFs are important for the regulation of eukaryotic gene expression. In constructing wDBTF the goal was to be comprehensive in collating both the wheat TF sequences and the information about each TF. Instead of relying entirely on computational prediction, we combined automated searches and manual curation to improve the quality of the database. In wDBTF, we define TFs as proteins that show sequence-specific DNA binding and are able to activate and/or repress transcription.
The large genome size of wheat (approximately 16,000 Mb) and its polyploid nature make the goal of sequencing the wheat genome a difficult one. ESTs are created by partially sequencing randomly isolated gene transcripts and they play an important role in gene discovery. The availability of more than 1 million T. aestivum ESTs derived from more than 250 libraries has proved an adequate resource for identifying wheat TFs with the added advantage that it can be used to identify tissue-specific expression patterns. In wDBTF, we considered 226 libraries that represent 98% of the publicly available wheat sequences of this kind.
The genomes of grasses are very different in terms of size, ploidy level and chromosome number. Despite these significant differences, the linear order of genes and protein coding sequences are very well conserved between genomes. Thus, the rice genome can serve as a good model for identifying genes in larger non sequenced genomes like the wheat genome. In addition, O. sativa TFs have been well defined [3, 8] and information on these TFs has been organized into databases. Thus this species is ideally suited for comparative genomics like identifying wheat TFs. In the first step of our study, we used all TF protein sequences from rice DRTF as seed in Blast searches to better identify wheat TFs compared to using HMMER or core-consensus sequences. Significant similarity between known rice TF proteins and wheat accessions showed that 7,112 wheat accessions potentially belong to TF gene families. A minimum of 3,820 genes really corresponded to wheat TFs as they have a DNA-binding domain characteristic of a regulatory protein. Within the wheat data, we found members corresponding to every rice TF family suggesting that TF families are conserved between rice and wheat. Previous global approaches to studying plant TFs have already led to some TFs being identified from bread wheat ESTs . PlantTFDB http://planttfdb.cbi.pku.edu.cn is a plant TF database for five model organisms, including Arabidopsis (DATF) and rice (DRTF), and 17 other plant species including wheat . In October 2006 1,127 TFs were identified from wheat transcripts available in PlantGDB (v155a; http://www.plantgdb.org/) based on HMMER searches of the Pfam database (v20.0). These 1,127 TFs were classified into 57 families. For six families - GARP-ARR-B, HRT-like, LFY, NZZ, SRS, and ZF-HD - no TF was identified based on these criteria and no detail was given on whether allowance was made for the polyploidy of wheat. Two reasons could explain the differences between the results of this previous study and the work we report here. First, the results depend on the methods and cut-offs used, more or less stringent, to predict TFs. Depending on how the data is to be used, either high sensitivity or high specificity may be more desirable. Generally, stringent filtering is used to avoid false positives. To increase the chances of isolating TF genes from expressed sequences, especially for short or incomplete sequences and divergent members of gene families, we used less stringent criteria. Second, progress in generating DNA sequences in recent years has vastly increased the number of expressed sequences available in databanks to be searched. As the full genome sequence of wheat is not yet available, using all these sequences to update the catalogue of TF genes is useful.
To evaluate the accuracy and reliability of TFs identified in this way, we compared our results to other recent studies of wheat TF families. Using rice TF proteins from PlnTFDB v2.0 as seed in Tblastn searches, Shaw et al.  identified wheat Dof. Sequences containing the Dof domain were re-assembled with the criterion of 98% nucleotide identity thus defining 31 Dof genes. Similarly, we identified 28 Dof-domain genes using a different strategy based on another source of rice protein sequences. The differences observed may come from the way ESTs are assembled and from the discovery of a previously unpublished Dof member. Another TF family has been studied in detail by Stephenson et al.  who identified 37 CCAAT binding factors based in a Tblastn search of several EST sources (available in October 2006) with an e-value cutoff of 1e-08 using the core-conserved sequences of O. sativa and A. thaliana. With recent data and less stringent criteria we detected 81 CCAAT binding factors including those TFs previously detected. The results obtained with Dof and CCAAT TFs suggest that our approach performs well and with acceptable accuracy.
In plants, 5% to 7% of all the protein-encoding genes are for TFs [1, 35]. Because many of the grass genomes are not yet completely sequenced or annotated, the total number of TFs expected is hard to predict. Based on the information available for four sequenced genomes, i.e. from Arabidopsis, rice, poplar (Populus trichocarpa), and Chlamydomonas (Chlamydomonas reinhardtii), linear regression was used to predict the number of TFs in non sequenced genomes from the total number of genes . Studies based on the annotation of BAC sequences suggest that the hexaploid wheat genome could contain 108,000 genes  or between 164,000 and 334,000 protein-encoding genes including pseudogenes . Thus, applying the linear regression to wheat would give 9,676 TFs. We have found a minimum of 3,820 sequences coding for TFs in data currently available, i.e. almost 40% of the expected number. However, 7,112 (about 73% of the expected number) wheat accessions have similarity with known rice TF proteins and could be potential TFs. Although further experimental evidence is needed to validate whether they really belong to TF families, we decided to keep all sequences in wDBTF so users can themselves judge the sequences with no DNA-binding domain.
The 3,820 wheat sequences identified as TFs represent 1.8% of all available unique wheat sequences. TF expression is mostly specific to a particular tissue or developmental stage and most TFs are also known to be expressed at a low level. We have shown that almost 50% of sequences identified as wheat TFs are singletons and 70% of contigs comprised just a few ESTs. This confirms that wheat TFs are expressed at a low level and suggests that perhaps not all TF sequences are represented in the EST libraries available. Therefore in our analysis of wheat expressed sequences, the number of TF genes could be underestimated. Until the whole genome sequence is available, it is unlikely that all the TFs can be identified based only on transcript sequences.
TFs have evolved by accumulating mutations, so the complexity in gene regulation patterns has increased. Much of the innovation in biological function has been attributed to events of gene duplication. Wheat appears to have more AUX/IAA, CCATT-Dr1, HMG, MBF, S1Fa-like, Whirly and VOZ compared with the predicted number, i.e. three times more than in rice. However, the largest families (EREBP, NAC, bHLH, R2R3-MYB, bZIP, WRKY and C3H zinc finger) do not exceed the proportional number predicted from rice. These preliminary results tend to confirm the coding theory that predicts that there are limits to the TF repertoire of cells. From each superfamily, the maximal number of TFs seems to correlate with the number of DNA bases effectively recognized by the binding mechanism of that superfamily. This limit of expansion is thought to minimize cross-binding errors between TFs .
Comprehensive Affymetrix GeneChip platforms have now been developed for wheat based on extensive EST collections http://www.plexdb.org/index.php. The Affymetrix wheat genome array can provide useful data on organ and developmental stage expression. We found 4,305 out of the 7,112 wDBTF wheat sequences represented on the Affymetrix wheat genome array. However, several sequences correspond to the same Affymetrix ID and only 2,036 are unique. Thus, this result is in agreement with those of Wan et al.  who found about 2,000 probe sets for potential TFs. Analysis of expression using this microarray platform can be difficult because of the often confounding presence of multiple splice forms, paralogs and orthologs, and, in the case of polyploids, homoeologs with near-identical sequences . In general the wheat GeneChip is not able to distinguish contributions from individual homoeologs. As the probe sequences were specifically taken from conserved regions of consensus sequences, the expression profiles measured represent a sum of the individual profiles of the relevant homoeologs for ~90% of genes . Furthermore, the expression measured could also be the sum of the expression of several splicing variants. TFs derived from the same precursor mRNA by alternative splicing may have distinct regulatory functions. In wheat, this kind of mRNA processing has been shown for some TF genes like the A and D copies of Viviparous 1 (TaVp1)  and for wDreb2 . Parameters used in TIGR assembly often place homoeologous genes and alternative splicing variants in separate contigs and thus the difference observed between the number of sequences matching Affymetrix ID probes and the number of probes might be expected. On the other hand, singleton ESTs, relatively abundant in our study, tend to be shorter increasing the chances of confusion when trying to match them to a particular sequence present on GeneChip.
We used the Dof TF family to validate our strategy for identifying wheat TFs. Based on sequence identity with rice gene models, 59 potential Dof genes were identified. Multiple alignment of the entire Dof domain showed that wheat sequences were distributed in seven groups among all four major orthologous clusters suggesting this TF family is organized similarly in the species studied.
We used the database to select Dof involved in wheat grain development based on in silico expression criteria. First we verified these genes were indeed expressed in seed and then established the pattern of expression of 12 transcripts during seed development. For seven Dof (TC289916, TC277573, TC339845, CA484955, TC316155 and TC315813), expression reached a maximum in the middle of the grain-filling phase when starch and storage proteins accumulate. Accession TC315813 is wheat prolamin-box binding factor (WPBF), which was shown to be an activator of storage protein genes . Its expression parallels the increase in abundance of transcripts encoding low molecular weight glutenin subunits and alpha gliadin genes consistent with a role in prolamin gene expression . Thus, Dof TF expression profiles like that of Wpbf could be potential regulators of grain filling. In expressed sequences, there are few nucleotide variations between homoeologs. Thus the probability of designing primers specific to one or two copies is low. All the primers used amplified products from T. urartu, Aegilops speltoides and A. taushii which confirms that potentially all copies which are expressed in hexaploid wheat are amplified. Thus, the expression profiles measured for any particular gene may represent the expression of all its homoeologs. Plant responses to allopolyploidy include unequal expression of duplicated genes and gene silencing. Studies in wheat [45, 46] have shown that novel patterns of gene expression occur in polyploids that are not observed in diploid progenitor species. Furthermore, in silico analysis of gene expression has shown that there may be preferential expression of homoeologous genes between genomes and a uniform level of expression of all three homoeologs is only observed for about 20% of the genes . A recent study on the wheat TF Spa has demonstrated that the three copies were expressed during all stages of grain development in similar patterns. However, there was more Spa transcript from B genome than A and D transcripts . To study patterns of gene expression in bread wheat, it will be essential to develop an assay that allows genome/homoeolog-specific gene expression to be quantified. Our preliminary results provide an overview of Dof expression and further research will confirm which homoeologous genes are implicated in the grain-filling mechanism.
The genome sequence of wheat is not yet available so analyzing the systematically produced sequences of cDNA libraries is a powerful way to identify many transcripts that can then be studied in terms of their gene expression and functional genomics. In our study, wheat TF sequences were identified based on their similarity to those in the model plant rice. Organized in a dedicated database available on our web site, and classified in families are 7,112 potential unique wheat TFs, 3,820 of which have a DNA-binding domain. For each sequence, in silico expression data is given. The database will therefore be a major resource for the plant research community for future studies of wheat TFs.
Availability and requirements
The wheat transcription factor inventory database wDBTF is now available at http://wwwappli.nantes.inra.fr:8180/wDBFT/
Any restrictions to use by non-academics: none.
Riechmann JL, Heard J, Martin G, Reuber L, Jiang C, Keddie J, Adam L, Pineda O, Ratcliffe OJ, Samaha RR, Creelman R, Pilgrim M, Broun P, Zhang JZ, Ghandehari D, Sherman BK, Yu G: Arabidopsis transcription factors: genome-wide comparative analysis among eukaryotes. Science. 2000, 290: 2105-2110. 10.1126/science.290.5499.2105.
Riechmann JL: Transcriptional regulation: a genomic overview. Edited by: Meyerowitz CsaE. 2002, Amerian Society of Plant Biologists, Rockville
Xiong Y, Liu T, Tian C, Sun S, Li J, Chen M: Transcription factors in rice: a genome-wide comparative analysis between monocots and eudicots. Plant Mol Biol. 2005, 59: 191-203. 10.1007/s11103-005-6503-6.
Davuluri RV, Sun H, Palaniswamy SK, Matthews N, Molina C, Kurtz M, Grotewold E: AGRIS: Arabidopsis gene regulatory information server, an information resource of Arabidopsis cis-regulatory elements and transcription factors. BMC Bioinformatics. 2003, 4: 25-10.1186/1471-2105-4-25.
Matys V, Fricke E, Geffers R, Gössling E, Haubrock M, Hehl R, Hornischer K, Karas D, Kel AE, Kel-Margoulis OV, Kloos DU, Land S, Lewicki-Potapov B, Michael H, Münch R, Reuter I, Rotert S, Saxel H, Scheer M, Thiele S, Wingender E: TRANSFAC: transcriptional regulation, from patterns to profiles. Nucleic Acids Res. 2000, 31: 374-378. 10.1093/nar/gkg108.
Hermoso A, Aguilar D, Aviles FX, Querol E: TrSDB: a proteome database of transcription factors. Nucleic acids Res. 2004, D171-173. 10.1093/nar/gkh101. 32 Database
Guo A, He K, Liu D, Bai S, Gu X, Wei L, Luo J: DATF: a database of Arabidopsis transcription factors. Bioinformatics. 2005, 21: 2568-2569. 10.1093/bioinformatics/bti334.
Gao G, Zhong Y, Guo A, Zhu Q, Tang W, Zheng W, Gu X, Wei L, Luo J: DRTF: a database of rice transcription factors. Bioinformatics. 2006, 22: 1286-1287. 10.1093/bioinformatics/btl107.
Boguski MS, Lowe TMJ, Tolstoshev CM: DbEST - Database for expressed sequence tags. Nature Genet. 1993, 4: 332-333. 10.1038/ng0893-332.
Quackenbush J, Liang F, Holt I, Pertea G, Upton J: The TIGR Gene Indices: reconstruction and representation of expressed gene sequences. Nucleic Acids Research. 2000, 28: 141-145. 10.1093/nar/28.1.141.
Paolacci AR, Tanzarella OA, Porceddu E, Varotto S, Ciaffi M: Molecular and phylogenetic analysis of MADS-box genes of MIKC type and chromosome location of SEP-like genes in wheat (Triticum aestivum L.). Mol Genet Genomics. 2007, 278: 689-708. 10.1007/s00438-007-0285-2.
Stephenson TJ, McIntyre CL, Collet C, Xue GP: Genome-wide identification and expression analysis of the NF-Y family of transcription factors in Triticum aestivum. Plant Mol Biol. 2007, 65: 77-92. 10.1007/s11103-007-9200-9.
Chen R, Ni Z, Nie X, Qin Y, Dong G, Sun Q: Isolation and characterization of genes encoding Myb transcription factor in wheat (Triticum aestivum L.). Plant Science. 2005, 169: 1146-1154. 10.1016/j.plantsci.2005.07.018.
Yanagisawa S: The Dof family of plant transcription factors. Trends Plant Sci. 2002, 7: 555-560. 10.1016/S1360-1385(02)02362-2.
Lijavetzky D, Carbonero P, Vicente-Carbajosa J: Genome-wide comparative phylogenetic analysis of the rice and Arabidopsis Dof gene families. BMC Evol Biol. 2003, 3: 17-28. 10.1186/1471-2148-3-17.
Umemura Y, Ishiduka T, Yamamoto R, Esaka M: The Dof domain, a zinc finger DNA-binding domain conserved only in higher plants, truly functions as a Cys2/Cys2 Zn finger domain. Plant J. 2004, 37: 741-749. 10.1111/j.1365-313X.2003.01997.x.
Yanagisawa S, Schmidt RJ: Diversity and similarity among recognition sequences of Dof transcription factors. Plant J. 1999, 17: 209-214. 10.1046/j.1365-313X.1999.00363.x.
Moreno-Risueno MA, Martínez M, Vicente-Carbajosa J, Carbonero P: The family of DOF transcription factors: from green unicellular algae to vascular plants. Mol Genet Genomics. 2007, 277: 379-390. 10.1007/s00438-006-0186-9.
Tian AG, Wang J, Cui P, Han YJ, Xu H, Cong LJ, Huang XG, Wang XL, Jiao YZ, Wang BJ, Wang YJ, Zhang JS, Chen SY: Characterization of soybean genomic features by analysis of its expressed sequence tags. Theor Appl Genet. 2004, 108: 903-13. 10.1007/s00122-003-1499-2.
Wang HW, Zhang B, Hao YJ, Huang J, Tian AG, Liao Y, Zhang JS, Chen SY: The soybean Dof-type transcription factor genes, GmDof4 and GmDof11, enhance lipid content in the seeds of transgenic Arabidopsis plants. Plant J. 2007, 52: 716-29. 10.1111/j.1365-313X.2007.03268.x.
Mena M, Vicente-Carbajosa J, Schmidt RJ, Carbonero P: An endosperm-specific DOF protein from barley, highly conserved in wheat, binds to and activates transcription from prolamin-box of a native B-hordein promoter in barley endosperm. Plant J. 1998, 16: 53-62. 10.1046/j.1365-313x.1998.00275.x.
Isabel-LaMoneda I, Diaz I, Martinez M, Mena M, Carbonero P: SAD: a new DOF protein from barley that activates transcription of a cathepsin B-like thiol protease gene in the aleurone of germinating seeds. Plant J. 2003, 33: 329-340. 10.1046/j.1365-313X.2003.01628.x.
Moreno-Risueno MA, Diaz I, Carrillo L, Fuentes R, Carbonero P: The HvDOF19 transcription factor mediates the abscisic acid-dependent repression of hydrolase genes in germinating barley aleurone. Plant J. 2007, 51: 352-365. 10.1111/j.1365-313X.2007.03146.x.
Conlan RS, Hammond-Kosack M, Bevan M: Transcription activation mediated by the bZIP factor SPA on the endosperm box is modulated by ESBF-1 in vitro. Plant J. 1999, 19: 173-181. 10.1046/j.1365-313X.1999.00522.x.
Chen R, Ni Z, Qin Y, Nie X, Lin Z, Dong G, Sun Q: Isolation and characterization of TaDof1 transcription factor in wheat (Triticum aestivum L). DNA Seq. 2005, 16: 358-63.
Ravel C, Nagy IJ, Martre P, Sourdille P, Dardevet M, Balfourier F, Pont C, Giancola S, Praud S, Charmet G: Single nucleotide polymorphism, genetic mapping, and expression of genes coding for the DOF wheat prolamin-box binding factor. Funct Integr Genomics. 2006, 6: 310-321. 10.1007/s10142-006-0022-7.
Altschul SF, Madden TL, Schaffer AA, Zhang J, Zhang Z, Miller W, Lipman DJ: Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 1997, 25: 3389-3402. 10.1093/nar/25.17.3389.
Sado PE, Tessier D, Vasseur M, Elmorjani K, Guillon F, Saulnier L: Integrating genes and phenotype: a wheat-Arabidopsis-rice glycosyltransferase database for candidate gene analyses. Funct Integr Genomics. 2009, 9: 43-58. 10.1007/s10142-008-0100-0.
Khaled AS, Vernoud V, Ingram GC, Perez P, Sarda X, Rogowsky PM: Engrailed ZmOCL1 fusions cause a transient reduction of kernel size in maize. Plant Mol Biol. 2005, 58: 123-139. 10.1007/s11103-005-5219-y.
Pfaffl MW, Tichopad A, Prgomet C, Neuvians TP: Determination of stable housekeeping genes, differentially regulated target genes and sample integrity: BestKeeper -Excel-based tool using pair-wise correlations. Biotechnol Lett. 2004, 26: 509-515. 10.1023/B:BILE.0000019559.84305.47.
Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG: The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res. 1997, 25: 4876-82. 10.1093/nar/25.24.4876.
Page RD: Treeview: an application to display phylogenetic trees on personal computers. Comput Appl Biosci. 1996, 12: 537-538.
Guo AY, Chen X, Gao G, Zhang H, Zhu QH, Liu XC, Zhong YF, Gu X, He K, Luo J: PlantTFDB: a comprehensive plant transcription factor database. Nucleic Acids Res. 2008, D966-9. 36 Database
Shaw LM, McIntyre CL, Gresshoff PM, Xue GP: Members of the Dof transcription factor family in Triticum aestivum are associated with light-mediated gene regulation. Funct Integr Genomics. 2009, 9: 485-98. 10.1007/s10142-009-0130-2.
Riechmann JL, Ratcliffe OJ: A genomic perspective on plant transcription factors. Curr Opin Plant Biol. 2000, 3: 423-434. 10.1016/S1369-5266(00)00107-2.
Yilmaz A, Nishiyama MY, Fuentes BG, Souza GM, Janies D, Gray J, Grotewold E: GRASSIUS: a platform for comparative regulatory genomics across the grasses. Plant Physiol. 2009, 149: 171-80. 10.1104/pp.108.128579.
Paux E, Roger D, Badaeva E, Gay G, Bernard M, Sourdille P, Feuillet C: Characterizing the composition and evolution of homoeologous genomes in hexaploid wheat through BAC-end sequencing on chromosome 3B. Plant J. 2006, 48: 463-74. 10.1111/j.1365-313X.2006.02891.x.
Devos KM, Costa de Oliveira A, Xu X, Estill JC, Estep M, Jogi A, Morales M, Pinheiro J, San Miguel P, Bennetzen FL: Structure and organization of the wheat genome- the number of genes in the hexaploid wheat genome. [http://hdl.handle.net/2123/3389]
Itzkovitz S, Tlusty T, Alon U: Coding limits on the number of transcription factors. BMC Genomics. 2006, 7: 239-10.1186/1471-2164-7-239.
Wan Y, Poole RL, Huttly AK, Toscano-Underwood C, Feeney K, Welham S, Gooding MJ, Mills C, Edwards KJ, Shewry PR, Mitchell RA: Transcriptome analysis of grain development in hexaploid wheat. BMC Genomics. 2008, 9: 121-10.1186/1471-2164-9-121.
Poole R, Barker G, Wilson ID, Coghill JA, Edwards KJ: Measuring global gene expression in polyploidy; a cautionary note from allohexaploid wheat. Funct Integr Genomics. 2007, 7: 207-219. 10.1007/s10142-007-0046-7. doi: 10.1007/s10142-007-0046-7
Schreiber AW, Sutton T, Caldo RA, Kalashyan E, Lovell B, Mayo G, Muehlbauer GJ, Druka A, Waugh R, Wise RP, Langridge P, Baumann U: Comparative transcriptomics in the Triticeae. BMC Genomics. 2009, 10: 285-10.1186/1471-2164-10-285.
Utsugi S, Nakamura S, Noda K, Maekawa M: Structural and functional properties of Viviparous1 genes in dormant wheat. Genes Genet Syst. 2008, 83: 153-66. 10.1266/ggs.83.153.
Egawa C, Kobayashi F, Ishibashi M, Nakamura T, Nakamura C, Takumi S: Differential regulation of transcript accumulation and alternative splicing of a DREB2 homolog under abiotic stress conditions in common wheat. Genes Genet Syst. 2006, 81: 77-91. 10.1266/ggs.81.77.
Mochida K, Yamazaki Y, Ogihara Y: Discrimination of homoeologous gene expression in hexaploid wheat by SNP analysis of contigs grouped from a large number of expressed sequence tags. Mol Genet Genomics. 2003, 270: 371-7. 10.1007/s00438-003-0939-7.
Chantret N, Salse J, Sabot F, Rahman S, Bellec A, Laubin B, Dubois I, Dossat C, Sourdille P, Joudrier P, Gautier MF, Cattolico L, Beckert M, Aubourg S, Weissenbach J, Caboche M, Bernard M, Leroy P, Chalhoub B: Molecular basis of evolutionary events that shaped the hardness locus in diploid and polyploid wheat species (Triticum and Aegilops). Plant Cell. 2005, 17: 1033-45. 10.1105/tpc.104.029181.
Ravel C, Martre P, Romeuf I, Dardevet M, El-Malki R, Bordes J, Duchateau N, Brunel D, Balfourier F, Charmet G: Nucleotide Polymorphism in the Wheat Transcriptional Activator Spa Influences Its Pattern of Expression and Has Pleiotropic Effects on Grain Protein Composition, Dough Viscoelasticity and Grain Hardness. Plant Physiol. 2009
We thank Christophe Troquier and his team for growing the plants and Stéphanie Verrier for RNA extraction. We also thank Rachel Carol from Emendo Bioscience http://www.emendo.co.uk for editing the manuscript.
IR analyzed data, designed and assessed specific primers for Dof transcript amplification and wrote the manuscript. DT has developed bioinformatics tools. MD carried out the RNA extraction and PCR amplification. CR performed the Blast searches against Affymetrix probes, participated in coordination and in the design of the study and helped to draft the manuscript. GB and GC participated in coordination and helped to draft the manuscript. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 1: The 226 wheat ESTs libraries used for TF analysis. A table showing banks used for this database construction and corresponding tissue and EST number. (PDF 12 KB)
Additional file 2: Sequences of primers used for detection of Dof transcripts. A table of sequence accession names and DNA probe sequences of forward and reverse primers used for Dof transcripts PCR amplification. (PDF 11 KB)
Additional file 3: Multiple sequence alignment of the Dof DNA-binding domain from wheat, rice and barley. A protein sequence alignment of the Dof domain resulting from CLUSTALW. The levels of amino acid conservation at each position among the Dof members are indicated in the first histogram with the highest bars representing 100% amino acid identity. The black histogram represents the consensus amino acid sequence. (PDF 26 KB)
Additional file 4: Tissue-specific in silico expression of wheat Dof singletons. A table showing EST accession names of wheat Dof singletons and their corresponding tissue of origin. (PDF 4 KB)
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Romeuf, I., Tessier, D., Dardevet, M. et al. wDBTF: an integrated database resource for studying wheat transcription factor families. BMC Genomics 11, 185 (2010). https://doi.org/10.1186/1471-2164-11-185