Research article | Open | Published:
CATMA, a comprehensive genome-scale resource for silencing and transcript profiling of Arabidopsis genes
BMC Bioinformaticsvolume 8, Article number: 400 (2007)
The Complete Arabidopsis Transcript MicroArray (CATMA) initiative combines the efforts of laboratories in eight European countries  to deliver gene-specific sequence tags (GSTs) for the Arabidopsis research community. The CATMA initiative offers the power and flexibility to regularly update the GST collection according to evolving knowledge about the gene repertoire. These GST amplicons can easily be reamplified and shared, subsets can be picked at will to print dedicated arrays, and the GSTs can be cloned and used for other functional studies. This ongoing initiative has already produced approximately 24,000 GSTs that have been made publicly available for spotted microarray printing and RNA interference.
GSTs from the CATMA version 2 repertoire (CATMAv2, created in 2002) were mapped onto the gene models from two independent Arabidopsis nuclear genome annotation efforts, TIGR5 and PSB-EuGène, to consolidate a list of genes that were targeted by previously designed CATMA tags. A total of 9,027 gene models were not tagged by any amplified CATMAv2 GST, and 2,533 amplified GSTs were no longer predicted to tag an updated gene model. To validate the efficacy of GST mapping criteria and design rules, the predicted and experimentally observed hybridization characteristics associated to GST features were correlated in transcript profiling datasets obtained with the CATMAv2 microarray, confirming the reliability of this platform. To complete the CATMA repertoire, all 9,027 gene models for which no GST had yet been designed were processed with an adjusted version of the Specific Primer and Amplicon Design Software (SPADS). A total of 5,756 novel GSTs were designed and amplified by PCR from genomic DNA. Together with the pre-existing GST collection, this new addition constitutes the CATMAv3 repertoire. It comprises 30,343 unique amplified sequences that tag 24,202 and 23,009 protein-encoding nuclear gene models in the TAIR6 and EuGène genome annotations, respectively. To cover the remaining untagged genes, we identified 543 additional GSTs using less stringent design criteria and designed 990 sequence tags matching multiple members of gene families (Gene Family Tags or GFTs) to cover any remaining untagged genes. These latter 1,533 features constitute the CATMAv4 addition.
To update the CATMA GST repertoire, we designed 7,289 additional sequence tags, bringing the total number of tagged TAIR6-annotated Arabidopsis nuclear protein-coding genes to 26,173. This resource is used both for the production of spotted microarrays and the large-scale cloning of hairpin RNA silencing vectors. All information about the resulting updated CATMA repertoire is available through the CATMA database http://www.catma.org.
The Complete Arabidopsis Transcriptome Microarray (CATMA) consortium  was created in 2000 to take advantage of the available Arabidopsis genome sequence to enable novel functional genomics approaches. Eight European plant genomics research groups teamed up to produce a comprehensive set of Gene-specific Sequence Tags (GSTs) originally designed for microarray transcript profiling. These GSTs were 150–500 base pairs in length and were selected to have no significant similarity with any other sequence in the genome . The Specific Primer and Amplicon Design Software (SPADS) was written to automate the design of these tags . The resulting GST amplicons can be used as features on spotted microarrays for transcript profiling experiments. Indeed, such CATMA arrays performed as well as, if not better than, the Affymetrix (ATH1) and Agilent (Arabidopsis oligo 2) platforms in terms of specificity, sensitivity and gene coverage . As an academic initiative, CATMA provide the research community with an independent and flexible alternative to commercial arrays. Furthermore, the GSTs can be utilized for posttranscriptional gene silencing when cloned into hairpin RNA expression vectors . The AGRIKOLA consortium has converted the CATMA GST repertoire into hairpin RNA expression vectors  and over 2,000 such silencing constructs have been transformed into Arabidopsis to produce knock-down lines .
Here, we describe a major effort to create a comprehensive DNA tag repertoire effectively targeting nearly all protein-encoding genes in Arabidopsis. The pre-existing CATMAv2 repertoire was first mapped to recent Arabidopsis genome sequence annotations, TIGR release 5 (TIGR5) (January 2004, [8, 9]) and EuGène 040917 (Additional File 1), with the aim of identifying a GST of the highest possible quality for each documented protein-encoding gene model. EuGène results were taken into account because annotation projects focusing on the genome of various species [10, 11] have confirmed the quality of the EuGène annotation algorithm  and no single algorithm can be perfectly accurate. We implemented the improved and alternative algorithms for the design of GSTs of most of the remaining 'orphan' Arabidopsis protein-encoding genes.
Results and discussion
Mapping of CATMA GSTs and gene classification
To keep up with evolving and increasingly more accurate genome annotations, continued efforts are needed to synchronize probe repertoires with changes in the list of annotated genes. The first CATMA GST design rounds [3, 5] were based on earlier Arabidopsis genome annotation releases, namely EuGène 2003, TIGR3 and TIGR4, that were outdated at the time the present work was initiated. Therefore, we first determined which genes described in the more recent EuGène 040917 and TIGR5 (January 2004) annotation releases were still unambiguously tagged by pre-existing GSTs to identify the list of 'orphan' genes that should be considered for upgrading and expanding the GST repertoire (Figure 1). We finally mapped all newly designed GSTs onto the TAIR6 (October 2005) gene models. This work is part of our ongoing efforts to assure the comprehensive nature of the CATMA resources (see also 'Note added in proof').
The first step of the procedure was to position the coordinates of the amplified CATMAv2 GSTs with respect to both the TIGR5 and EuGène 040917 gene models. Briefly, a gene was considered 'tagged' when it contained one or more exonic regions that sufficiently overlapped with at least one GST. A gene was 'uniquely tagged' when this GST had no significant overlap with any other gene. The following criteria were applied to classify a gene as being 'uniquely tagged' by a GST or, vice versa, to classify a GST as 'uniquely tagging' a gene:
The gene overlaps with the primary BLAST hit of the GSTs so that the percentage sequence identity of the GST with the corresponding gene region must be at least 99%.
At least 100 bp of this matching gene region must be inside an exon.
At most 30 bp of the whole GST sequence might overlap with an exonic region of another gene.
The GST must not have a significant secondary BLAST hit, i.e. the percentage sequence identity of the GST with any exon of any other gene should be lower than 70%.
Five non-overlapping classes of genes (GE1 to GE5) and GSTs (GST1 to GST5) were defined based on these rules (for more details, see Table 1). Class GE5 and GST5 contain the uniquely tagged genes and the uniquely tagging GSTs, respectively. The flowchart for the classification procedure is presented in Additional File 2.
The mapping of the CATMAv2 GSTs onto the 26,207 TIGR5 protein-encoding gene models and the subsequent classification resulted in 19,003 (72.5%) genes classified as GE5. Mapping onto the 27,977 EuGène models resulted in 18,193 (65.0%) GE5 genes. The class distribution statistics, including mapping against the TAIR6 (November 2005, ) genome annotation release, is detailed in Table 2. The GST/gene correspondence (TAIR6 and EuGène 040917) is listed in Additional File 3.
SPADS algorithm adjustments
The GST design procedure presented below was based on the previously described SPADS algorithm . The successive steps encoded in SPADS (represented at the bottom of Figure 1) are described in Methods. The script of SPADS 1.1.4 was debugged and optimized, in particular with regard to (i) the verification of uniqueness of PCR primer binding sites and (ii) the program's performance in identifying novel GSTs. The adjusted SPADS version was numbered 1.1.5.
To obtain a quantitative measure of the performance increase between the SPADS versions, we compared their efficiency on the same set of 'orphan' gene models, consisting of 1,823 TIGR5 protein-encoding genes located on chromosome 1 and untagged by the CATMAv2 repertoire. The efficiency of GST design was improved from 57% to 69%, for SPADS 1.1.4 and 1.1.5, respectively. The increased efficiency was at the cost of a slightly reduced specificity. For details, see 'Characteristics of the CATMAv3 addition'.
Design of the CATMAv3 addition
To design novel GSTs for all the genes not yet uniquely tagged in the CATMAv2 repertoire (classes GE1 to GE4 in Table 2), we first produced an optimized target gene set. This 'orphan' set totaled 9,027 gene models, consisting of 7,204 TIGR5 sequences and 1,823 models predicted additionally by EuGène 040917 that shared no overlap with any genic region in TIGR5 (same or opposite strand). The orphan gene models were slightly modified prior to SPADS processing: (1) as in previous GST design efforts , gene models that ended with the ORF stop codon were extended by 150 bp, as a conservative prediction for the presence of a 3' UTR; this extension is henceforth referred to as the 'artificial 3' UTR' (extensions were added to 3,639 TIGR5 and 1,735 EuGène models); (2) regions shared by two overlapping genes were removed (applied to 1,274 TIGR5 and 95 EuGène models) to avoid GSTs tagging of more than one gene; (3) in the case of splice variants, the gene model presented to SPADS was trimmed to contain the exons present in all variants (only concerning TIGR5 models, of which 431 targets contained splice variants).
With SPADS 1.1.5, a GST was successfully designed for 5,756 out of 9,027 target genes (64%). Table 3 presents a breakdown of results according to the four gene classes (GE1-GE4) requiring the design of novel tags. The new set of GSTs, combined with the CATMAv2 repertoire, constituted CATMAv3. Their correspondence with gene models (TAIR6 and EuGène 040917) is listed in Additional File 3. As a first step toward their use in microarray transcript profiling and gene silencing experiments, the tags of this new set were amplified by PCR as described  from Arabidopsis genomic DNA, with SPADS-selected primer pairs. The size of all PCR products was analyzed by DNA gel electrophoresis. In total, 5,388 GSTs (93.6%) were detected as products with the predicted size. These results are comparable to the two previous synthesis campaigns. The cloning of these amplified GSTs is described elsewhere . All newly designed tags are listed in Additional File 4. This information is also available on line via the CATMA database .
Characteristics of the CATMAv3 addition
Two parameters were analyzed to investigate whether the new GST set (CATMAv3 addition) has properties similar to the previously designed tags (CATMAv2) and to assess the consistency of the subsequent GST batches: (1) the relative position of the tag within the gene (Figure 2, top), with the 3' location being preferable to 5', because transcript labeling techniques often include oligo-dT priming steps; (2) the distribution of GST specificity measured as the percentage sequence identity of a tag with the next best non-trivial genome BLAST hit (Figure 2, bottom), indicating the likelihood that GST microarray features might yield unspecific hybridization. The comparative analysis indicated that both sets are similar with regard to the relative GST position. The CATMAv3 addition did not show an overall decrease in specificity. However, from Figure 2, a larger fraction of the next best non-trivial BLAST hits has a homology closer to 70% (the absolute overall cut-off) in v3 than in v2. Although it is reasonable to assume that the performance of the majority of the added features would be similar to that of the CATMAv2 repertoire in microarray experiments , we examined more closely the cross-hybridization potential for all GSTs. For this purpose, we calculated the melting temperature of the DNA heteroduplex between each GST and their best non-target BLAST hit sequence with the Baldino formula , in commonly adopted CATMA microarray hybridization conditions (4×SSC, 50% formamide, 45°C). Conservatively, a GST was flagged for potential cross-hybridization when this predicted melting temperature was equal to or higher than 45°C. This information is available via the CATMA database . The percentages of flagged GSTs were 3.2%, and 9.7% for CATMAv2 and CATMAv3, respectively.
Experimental validation of GST classification
We reasoned that hybridization signal values would be differently distributed for GST features of different classes (Tables 1 and 2), reflecting their efficacy in detecting expressed sequences. Compared to the best feature class (GST5, tagging a unique gene with sufficient coverage), sequences similar to multiple genes (GST3 and GST4) might hybridize to more than one transcript and, thus display on average a higher signal. Inversely, features with insufficient gene coverage (GST2) or no discernable gene model (GST1) would have a lower signal, with GST1 features theoretically reporting background.
To test this hypothesis, we analyzed the results of 276 CATMA microarray experiments performed in the context of the European FP5 Compendium of Arabidopsis Gene Expression (CAGE) project . The corresponding biological samples consist of various Arabidopsis anatomical parts, harvested at different development stages, after different treatments or stresses, and from mutants (Additional File 5), including links to ArrayExpress experiment accessions [17, 18]. Figure 3 shows the number of experiments in which a GST feature (a microarray probe) was associated with statistically significant foreground signal values (see Methods) in the 276 microarray data sets. The five top graphs represent the experimentally observed hybridization characteristics for each of the five GST classes.
As expected, the median number of significant foreground value experiments per probe for each class could be ranked in the following order: GST1 (54; 19.6% of the total number of experiments) < GST2 (61; 22.1%) < GST5 (141; 51.1%) < GST3 (207; 75.0%). It is important to note that class size varied significantly. The GST4 curve was irregular and difficult to rank because it was constructed with data collected from very few features. Remarkably, GST1 and GST2 medians were far from negligible. This observation could be explained in different ways: (1) the hybridization conditions might yield unspecific signals; (2) GST1 and GST2 tags might still yield residual signal because of partial overlap with actual transcription units; (3) regions currently defined as intergenic, but nevertheless transcribed, might hybridize to GST1 or GST2 tags [19, 20]. We favor the latter two explanations because the Cy3 hybridization signal pattern observed for the Lucidea  background control spikes printed on the CATMA array had a very low median number of experiments with a significant foreground signal (21; 7.6%), distinctly below the median number for probe classes GST1 and GST2. To summarize, our observations confirm that the distribution of hybridization signal values is in agreement with the GST classification established on the basis of DNA sequence analysis and that this analysis correctly predicts the quality of the GST features in microarray experiments.
Design of the CATMAv4 addition including Gene Family Tags
In a final effort to reach comprehensive genome coverage of the CATMA repertoire, we had to resort to alternative strategies to design a tag for the remaining 2,338 untouched Arabidopsis nucleus-encoded TAIR6 cDNA sequences. Many of these genes lacked a matching GST because they belonged to gene families with high sequence similarity (above the 70% threshold previously chosen for GST design). To establish their relationship, the untouched genes were compared with each other and with the CATMAv3-tagged genes with NCBI-BLASTn  and grouped in gene families. The gene families were delimited to minimize the number of CATMAv3-tagged members they contained and the number of genes adhering to multiple families. For each family, a representative sequence was defined as a fragment from one of the members of the family, sharing at least 70% identity with all other untouched members and containing at least 50% of exon sequence. Using the Primer3 software , we designed sequence tags based on the representative family sequences. Tags corresponding to multi-member gene families were referred to as Gene Family Tags (GFTs), whereas tags corresponding to singleton genes were referred to as additional GSTs. An example of sequence alignment leading to the design of a GFT is presented in Additional File 6.
To increase the chance of identifying GFTs or GSTs, the minimum amplicon length was lowered from 150 to 100 bp. Such tags still yield satisfactory hybridization signals (data not shown) , whereas shorter tags are difficult to purify from a PCR mix. As shown in Figure 4, the length of most newly designed tags was between 100 and 150 bp, justifying the choice to lower the length threshold as it greatly improved the ability for the tag design algorithm to identify appropriate sequences. Other criteria whose relaxation markedly affected the design included extension of primer GC content range to 20% to 95% (from 30% to 80%) and restricting the specificity calculation only to cDNA sequences. In all 2,338 genes, only three genes (At2g03937, At3g50250 and At4g19270) did not yield a satisfactory tag because of an unusually high proportion of GC or AT repeats. All additional 990 GFTs and 543 GSTs are listed in Additional File 7 and constitute the CATMAv4 addition. This information is also available online [14, 25]. In addition, we assessed the specificity of the CATMAv4 GSTs, essentially as described above for the CATMAv2 and CATMAv3 probes. For 31% of these GSTs, a flag was added in the CATMA database, warning for potential off-target hybridization. A first amplification round for a subset of the CATMAv4 repertoire addition had an amplification success rate of 95% (data not shown). Note that 65% of the GFTs tagged only two or three genes (Figure 5), so that a positive hybridization result corresponding to a given feature in practice could easily be assigned to the responsible gene(s) in a follow-up study.
We launched a significant effort to extend the existing CATMAv2 repertoire with additional GSTs to reach comprehensive genome coverage. The CATMAv2 GST repertoire was synchronized with two recent Arabidopsis genome annotations to identify 'orphan' genes. In two complementary design rounds, we could increase the number of sequence tags to 31,876. First, SPADS adjustments significantly increased the success of GST design at the cost of only a limited lower specificity. Subsequently, a sequence tag for nearly all remaining genes was selected by applying a markedly different design algorithm in which key design criteria were relaxed and single sequences allowed tagging of multiple genes of the same gene family. Counting all the genes satisfactorily tagged by a CATMAv2 GST (GE5) and the additional genes mapped by a v3 or v4 tag, the CATMA repository addresses 26,173 nuclear protein-coding TAIR6 annotated genes. CATMAv2 GSTs were carefully classified to predict and test their performance in microarray experiments. The analysis of a large set of microarray experiments validated both the correctness of this classification as well as the robustness of the CATMA microarrays. Interestingly, the analysis also revealed a substantial number of GSTs that now map to intergenic regions, but in hybridizations appear to be capable to detect transcripts in microarray experiments. As these GSTs were once designed to target annotated gene models, these gene models might have been incorrectly declared obsolete during subsequent genomic re-annotations.
This work concludes a unique voluntary collaboration of European laboratories funded by national government agencies to generate a valuable community resource that would not have been possible to create on a national basis.
Gene and GST classification
The TIGR5 (January 2004, ) and TAIR6 (November 2005, ) annotations were downloaded from the TAIR website and all gene models (including the splice variants) of the protein-encoding nuclear genes were extracted with a script based on the TIGR XML parser . The EuGène Arabidopsis structural annotation was constructed in a three-step procedure. Firstly, the Arabidopsis nuclear genome sequence (Assembly TIGR5, ) was processed with the EuGène software (version 1.64 with SpliceMachine plugin  and ability to handle full pseudomolecule sequences). External information sources were Swissprot release 44, PIR release 79 and all EST and full-length cDNA sequences publicly available from the EMBL Nucleotide Sequence Database  on 17 September 2004. Secondly, the resulting coding sequences were re-mapped against EST libraries with NCBI-BLASTn , CAP3  and SIM4  to append UTRs to the gene models. Thirdly, Perl scripts removed two types of apparent annotation artifacts: small (<50 bp) outer exons, that were part of extended UTRs and distant by more than 2,000 bp from the main transcription unit, and unspliced UTRs longer than 3,200 bp. These cut-off values were deduced from distribution analysis of UTR, intron and exon size from gene models supported by cDNAs.
All CATMAv2 GST sequences were extracted from the CATMA database . The CATMAv2 repertoire was compared to the nuclear TIGR5 genome sequence using NCBI-BLASTn (q = 1; e = 500; W = 7; filter false). GST BLAST hits and exon information were stored in a MySQL database. For both genome annotations, gene models without a predicted 3' UTR were extended beyond their stop codon with an additional, contiguous 150 bp to create an artificial 3' UTR. The length of 150 bp is a conservative figure below the average annotated 3' UTR length (227.5 bases). For 72% and 88% of the gene models including a 3' UTR, this region is >150 and >100 bases, respectively. Therefore, in the vast majority of cases, the addition of an artificial 3' UTR of 150 bp to predicted gene models lacking transcript support is unlikely to yield misplaced GSTs. Additionally, exons overlapping with exons of other genes were flagged and removed or, where possible, replaced by new 'partial exons' containing only non-overlapping sequences. Perl scripts were used to compare the coordinates of GSTs and gene models, and to sort genes and GSTs. Classification was first performed according to the TIGR5 structural annotation and then complemented with the 'unique' EuGène models. A EuGène model was defined as unique when no exon of a TIGR5 protein-encoding gene could be located between its 5' and 3' ends (both polarities).
GST design for the CATMAv3 addition
As described in more detail elsewhere , SPADS first scans (predicted) transcribed sequences from 3' to 5' to identify with BLASTn  those regions with low similarity compared to the rest of the genome. Within these relatively unique regions, the software finds the best primer pairs for the PCR amplification of a gene-specific tag. The selection criteria are gradually relaxed when no primer pairs could be selected in the most divergent regions. When necessary, the design also allows GSTs to span introns. SPADS also calls on Primer3  to select appropriate primer pairs and BLASTn to guarantee their specificity with regard to the amplification template. SPADS parameters used for GST design were as follows: GSTs should be 150 to 500 bp in length, with a maximum of 70% sequence identity (through its entire length) with any other Arabidopsis nuclear genome sequences, and possibly containing intron regions (at most 50% of intron sequence relative to total GST length in tags containing a minimum of 150-bp exon sequence). SPADS design parameters for PCR amplification primers included: length, 18 to 25 nucleotides; Tm, 50°C to 65°C (ΔTm<5°C); and GC%, 30% to 80%.
Only probes in the GST5 class were taken into account to calculate the quality characteristics of the CATMAv2 repository presented in Figure 3, but not when both probe ends were not positioned within an exon of the cognate gene. The relative position of a GST with regard to its cognate transcript sequence was determined as follows: when a GST started in the first third of the transcript and ended before the last third, it was assigned 5'; when the GST started after the first third and ended in the last third it was declared 3'; in all other cases, the GST was declared to be in central position.
All spotted microarrays were hybridized with two samples simultaneously: the Cy5-labeled Arabidopsis cDNA and the 'universal reference' consisting of the 16 Cy3-labeled oligonucleotides complementary to the universal GST extensions added to the sequences with the PCR amplification primers (denoted as rA-rP in ). In this configuration, the reference label provided stable signal for all properly printed features. A gene was deemed transcribed (present call) when both the biological sample and the universal reference resulted in a significant foreground signal value (Fg) higher than the background signal value (Bg) plus twice the local standard deviation of the background signal (Fg > Bg + 2 σ(Bg)). All TAIR6 and EuGène 040917 gene models were considered to classify the GST features. By definition GST5 features uniquely tagged a gene in at least one of the structural annotations and GST1 features did not correspond to any gene in either annotation. Additional information about the microarray experiments is provided in Additional File 5 and available on line via ArrayExpress .
GST and GFT design for the CATMAv4 repertoire addition
All scripts for designing the CATMAv4 repertoire addition were written in BioPerl. A flowchart of the CATMAv4 repertoire addition is provided in Additional File 8. The design process was started with cDNA sequences from the TAIR6 annotation. To produce a list of 'orphan' gene models, all AGI gene models were removed that were in any way tagged by a CATMAv3 repertoire GST, leaving 3,352 untouched genes classified as GE1 or GE2. We removed another 1,014 genes from this collection because they were smaller than 150 bp or were mitochondrial, chloroplastic or non-coding genes.
The coding sequences of the remaining 2,338 untouched genes were compared with each other with NCBI-BLASTn  to group them into families. A segment was selected in each gene where the number of co-aligned homologous sequences was the lowest. This 'representative family sequence' (RFS) served as reference for the corresponding gene family defined as all genes sharing regions with more than 70% sequence identity with the RFS. An RFS had to be longer than 150 bp and was preferentially positioned toward the 3' end of a gene.
The RFS was compared to the TAIR6 cDNA database with BLAST to assess any sequence similarity with previously tagged genes. RFS ends sharing more than 70% identity with such genes were trimmed down to a minimum length of 150 bp. Any CATMAv3-tagged genes still mapping in these trimmed RFS were included into the cognate gene family for subsequent analyses. Because a gene family was initially constructed for each gene, the resulting groups vastly overlapped. Redundant gene families were removed when all of their members were already represented either in other gene families with fewer members or in other gene families with fewer aggregated CATMAv3-tagged genes. With a Smith and Waterman algorithm  with a gap open penalty of 50 and a gap extension penalty of 10, each RFS was aligned to the genomic sequence of the family members.
Tag design was attempted for each RFS with Primer3 in two successive cycles. First, the primer GC content was constrained between 30% and 70%, the amplicon length between 120 and 500 bp, and the primer Tm had to be between 50°C and 65°C (ΔTm ≤ 5°C). When no satisfactory amplification primers could be identified, the second cycle parameters were GC content between 20% and 95% and minimum amplicon length down to 100 bp. For each successfully designed amplicon, a Smith and Waterman analysis verified whether the identity percentage over the entire amplicon was still exceeding 70% for each family member; if not, a new amplicon design was attempted. If no amplicon tagging the entire gene family could be selected, previously removed redundant gene families were recruited back to tackle 'orphan' family members.
Note added in proof
The latest TAIR7  Arabidopsis genome annotation was released after submission of this manuscript. All CATMAv4 GSTs (excluding GFTs) were classified and mapped onto the updated gene models as listed in Additional File 9 and available on line via the CATMA database . According to the TAIR7 annotation, a few GSTs from the CATMAv2 repertoire (22) now tag a gene model. As expected, on average, the foreground signal for these GSTs was statistically significant in a higher number of microarray experiments in contrast to other GSTs that do not correspond to any TAIR7 gene model (Mann-Whitney U-test: p < 0.01)
Arabidopsis Genome Initiative
Basic Local Alignment Search Tool
Complete Arabidopsis Transcriptome MicroArray
Expressed Sequence Tag
Eukaryotic gene finder
Gene Family Tag
Gene-specific Sequence Tag
National Center for Biotechnology Information
Open Reading Frame
Polymerase Chain Reaction
Practical Extraction and Report Language
Specific Primer and Amplicon Design Software
The Arabidopsis Information Resource
The Institute for Genomic Research
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We are indebted to Stephane Rombauts for providing and curating the EuGène annotation, Pierre Rouzé and Yves Van de Peer for supervising this annotation project, Carine Serizet and Vincent Thareau for their assistance concerning the SPADS program, Eric Bonnet and Martin Trick for their help in transferring the CATMA database from the John Innes Centre to the Department of Plant Systems Biology, and Rudy Vanderhaeghen for helpful discussion, and Martine De Cock for help with the manuscript. We thank the collective CAGE partners for their general support and for sharing their transcript profile data. GS and JA were supported by the European Union 5th Framework Programme via the Compendium of Arabidopsis Gene Expression project (CAGE; QLK3-CT-2002-02035), PR and RL by the Herbette Foundation of the University of Lausanne and by the Swiss State Secretariat for Education and Research SER (Contract Nr SER-02.0346), JB by grants from the Biotechnology and Biological Sciences Research Council, RB by funds from Vetenskapsrådet and WCN, YM by the grants KUL GOA AMBioRICS, KUL CoE EF/05/007 SymBioSys, and BelSPO IUAP P6/25 BioMaGNet. All CATMA microarrays were printed at the VIB Microarray facility in Belgium.
The author(s) declares that there are no competing interests.
GS performed the GST design of the CATMAv3 repertoire addition and all related analyses and drafted the manuscript. RL and PR designed the CATMAv4 repertoire addition, carried out the corresponding analyses, and wrote and integrated the corresponding sections into the manuscript. JA carried out the CATMA microarray data analyses under supervision of YM. JB, RB, WN, JPR, PR, and PH amplified the GSTs of CATMAv3 addition by PCR, resulting in the actual physical upgrade of the CATMAv3 repertoire. BDM was responsible for maintaining, upgrading, and providing direct access to the CATMA database. MK and PH conceived the GST repertoire upgrade, assisted in making the major GST design decisions, and participated actively in the writing of the manuscript. All authors read and approved the final manuscript.
Martin TR Kuiper and Pierre Hilson contributed equally to this work.