EuroPineDB: a high-coverage web database for maritime pine transcriptome
- Noé Fernández-Pozo1,
- Javier Canales1,
- Darío Guerrero-Fernández2,
- David P Villalobos1,
- Sara M Díaz-Moreno1,
- Rocío Bautista2,
- Arantxa Flores-Monterroso1,
- M Ángeles Guevara3,
- Pedro Perdiguero4,
- Carmen Collada3, 4,
- M Teresa Cervera3, 4,
- Álvaro Soto3, 4,
- Ricardo Ordás5,
- Francisco R Cantón1,
- Concepción Avila1,
- Francisco M Cánovas1 and
- M Gonzalo Claros1, 2Email author
© Fernández-Pozo et al; licensee BioMed Central Ltd. 2011
Received: 26 May 2011
Accepted: 15 July 2011
Published: 15 July 2011
Pinus pinaster is an economically and ecologically important species that is becoming a woody gymnosperm model. Its enormous genome size makes whole-genome sequencing approaches are hard to apply. Therefore, the expressed portion of the genome has to be characterised and the results and annotations have to be stored in dedicated databases.
EuroPineDB is the largest sequence collection available for a single pine species, Pinus pinaster (maritime pine), since it comprises 951 641 raw sequence reads obtained from non-normalised cDNA libraries and high-throughput sequencing from adult (xylem, phloem, roots, stem, needles, cones, strobili) and embryonic (germinated embryos, buds, callus) maritime pine tissues. Using open-source tools, sequences were optimally pre-processed, assembled, and extensively annotated (GO, EC and KEGG terms, descriptions, SNPs, SSRs, ORFs and InterPro codes). As a result, a 10.5× P. pinaster genome was covered and assembled in 55 322 UniGenes. A total of 32 919 (59.5%) of P. pinaster UniGenes were annotated with at least one description, revealing at least 18 466 different genes. The complete database, which is designed to be scalable, maintainable, and expandable, is freely available at: http://www.scbi.uma.es/pindb/. It can be retrieved by gene libraries, pine species, annotations, UniGenes and microarrays (i.e., the sequences are distributed in two-colour microarrays; this is the only conifer database that provides this information) and will be periodically updated. Small assemblies can be viewed using a dedicated visualisation tool that connects them with SNPs. Any sequence or annotation set shown on-screen can be downloaded. Retrieval mechanisms for sequences and gene annotations are provided.
The EuroPineDB with its integrated information can be used to reveal new knowledge, offers an easy-to-use collection of information to directly support experimental work (including microarray hybridisation), and provides deeper knowledge on the maritime pine transcriptome.
Conifers (Coniferales), the most important group of gymnosperms, represent 650 species, some of which are the largest, tallest, and oldest non-clonal terrestrial organisms on Earth. They are of immense ecological importance, dominating many terrestrial landscapes and representing the largest terrestrial carbon sink. Currently present in a large number of ecosystems, they have evolved very efficient physiological adaptation systems. Given that trees are the great majority of conifers, they provide a different perspective on plant genome biology and evolution taking into account that conifers are separated from angiosperms by more than 300 million years of independent evolution. Studies on the conifer genome are revealing unique information which cannot be inferred from currently sequenced angiosperm genomes (such as poplar, Eucaliptus, Arabidopsis or rice): around 30% of conifer genes have little or no sequence similarity to plant genes of known function [1, 2]. Unfortunately, conifer genomics is hindered by the very large genome (e.g. the pine genome is approximately 160 times larger than Arabidopsis and seven times larger than the human genome; in fact, it is larger than any other genome sequenced to date) that is replete with highly repetitive, non-coding sequences .
Conifers include the economically and ecologically important species of spruces (Picea sp) and pines (Pinus), Pinus being the largest extant genus with approximately 115 species. The importance of pines is due to the fact that: (i) their timber and paper pulp are used for the construction of buildings and furniture; (ii) they are used in reforestation due to their rapid growth and drought tolerance as compared to other tree species; (iii) they help stabilise sandy soils and indirectly act as an atmospheric CO2 sink, helping to reduce global warming; (iv) some pine nuts are widely used in Mediterranean cuisine. Consequently, the genus Pinus is becoming a woody gymnosperm model. The main pine model species in Europe are Pinus pinaster and Pinus sylvestris, whereas Pinus taeda and Pinus contorta are the equivalent in North America. Therefore, it is relevant to investigate and increase our knowledge of the content of the pine genome as this would allow the exploitation of natural genetic resources and the use of new forest reproductive material appropriate to adapt these trees to a changing climate.
The application of genome-based science is playing an important role in understanding the genome content and structure of different organisms. Since whole-genome sequencing approaches are hard to apply to large genomes such as the pine genome, scientists have focused on the expressed portion of the genome using dedicated technologies. For example, the sequencing of clones obtained by suppression subtractive hybridisation (SSH) [4–6] provides gene-enriched sequences that are specific to a particular condition. However, the dominant approach to characterising the transcriptionally active portions of pine genomes has been expressed sequence tags (ESTs) [7, 8] due to the absence of non-coding DNA (mainly introns and intergenic regions). Classic ESTs are subject to artefacts during cDNA library construction and are highly error prone during sequencing procedures. As a result, erroneous clustering and assembling occur during reconstruction of putative transcripts and may ultimately lead to inaccurate gene annotation . However, next-generation sequencing technologies have removed many drawbacks and time-consuming steps involved in classic ESTs and have facilitated transcriptome sequencing of many species at a fraction of the total time and cost previously required . ESTs have also driven the development of pine microarrays [11–14], although there is no easy way to relate the data printed on these microarrays to the corresponding pine sequences.
Sequencing projects should store, organise, and retrieve sequences by means of user-friendly databases. Since many sequences in EST databases are reported to be highly contaminated or incorrectly pre-processed , there is a need for more reliable pre-processing, clustering, assembly and annotation pipelines to yield reliable information. ConiferEST  (now part of ConiferGDB http://www.conifergdb.org/coniferEST.php) was the first attempt to rationalise pine sequences by more precise pre-processing dedicated to Pinus taeda traces only. The DFCI Pine Gene Index http://compbio.dfci.harvard.edu/cgi-bin/tgi/gimain.pl?gudb=pine, a subset of the discontinued TGI Gene Indices , is a non-redundant database of all putative Pinus genes. This is a very large compilation of pine sequences, but only GO and KEGG annotations are available and no separation by species is provided, P. taeda is highly over-represented, and its interface only allows limited interaction. ForestTreeDB was created to centralise large-scale ESTs from diverse tissues of conifer and poplar trees , but it is no longer available. The TreeGenes database http://dendrome.ucdavis.edu/treegenes/ is composed of a wide range of forest tree species . This effort to combine and inter-relate a great variety of different information should be acknowledged, even though EST pre-processing is not optimal. TreeSNPs  and PineSAP  are databases exclusively devoted to single nucleotide polymorphisms (SNPs) in Picea and Pinus species, respectively. Recently, Parchman and co-workers  described the first high-throughput analysis of a pine species, but no database was created for this. It should be noted that none of the above databases are linked to the pine microarrays described in literature.
Our group has been working on pine genomics for many years (e.g., EMBL accession numbers AM982822-AM983454, BX248593-BX255804, BX682240-BX683073, BX784033-BX784385, EC428477-EC428747, FM945441-FM945999 or FN256437-FN257130) and wish to provide high-quality sequences and annotations of pine genomes by means of EuroPineDB. Taking advantage of next-generation sequencing methods, recently released pre-processors , reliable sequence annotators , and the bioinformatics infrastructure of the University of Málaga (Spain), EuroPineDB was designed to gather the most reliable re-pre-processed, assembled, and annotated P. pinaster sequences using different technologies. Retrieval systems based on sequence similarity, description matches or microarray positions are also included, as well as browsing by species, experimental process, and annotation. As a new feature, many of its sequences have been printed on a microarray for expression analysis  and can be freely browsed.
2 Construction and content
2.1 Pine sequences
Although EuroPineDB is mainly devoted to the P. pinaster (maritime pine) genome, several sequences from two other species (P. sylvestris and P. pinea) are also included since their sequences were printed in a pine microarray (see below).
2.1.1 Gene libraries
Gene libraries providing sequences for EuroPineDB
Roots, stem, embryos, callus, cones, male and female strobili, buds, xylem, phloem.
ESTs from several different tissues
ESTs, adult buds
ESTs from normal, compression, opposite, early and late wood
SSH, compression vs. opposite, and juvenile vs. mature
Roots, stem, needles
SSH, drought stress
SSH, ammonium excess vs. ammonium deficiency
SSH, inoculated with Laccaria bicolor vs. not inoculated
SSH, mycorrhizal vs. not mycorrhizal
SSH, adventitious shoot induction
SSH, lack of N vs. normal N
ESTs from photosynthetic tissues
EMBL v. 102
P. pinaster, P. pinea, P. sylvestris
2.1.2 EMBL sequences
Gene library reads were completed with 13 206 sequences from the EMBL v. 102 database including the plant EST (Expressed Sequence Tag) and plant STD (Standard) sets for sequences whose 'source organism' field contained P. pinaster, P. sylvestris or P. pinea, provided that the sequence was not already included as a member of one of the gene libraries, and discarding any organellar sequence or sequences whose length was below 100 bp. The idea was to gather all sequence data on the three species, including their annotations. With P. pinaster as the main contributor (12 673 out of 13 206 EMBL entries), EMBL entries only provided 5667 different UniGenes.
Statistics for the gene libraries shown in Table 1
Discarded nt (%) by
55 431 (59.5%)
EMBL v. 102
55 332 (59.5%)
2.2 Database architecture
The EuroPineDB was built using Ruby On Rails 2.0 http://rubyonrails.org/, a web development framework that uses a model-view-controller pattern to maintain strict separation between the web interface (views) code, database tables (models), and all methods that handle interactions between views and database (controllers). It also maintains different environments for each development phase (development, production and testing). This enabled EuroPineDB to be developed and tested in a redundant Oracle RAC (Real Application Cluster) database. Bulk imports, updates, and database managements were automated by means of Ruby scripts.
An automated pipeline that combines all the tools described here is executed on every EuroPineDB update. An update incorporates new pine sequence retrieval from dbEST and EMBL databases, new user reads, and the re-execution of bioinformatics tools with every new UniGene.
2.3 Pre-processing and assembling entries
Most problems for automated sequence assembly resulted from chimerical clones in the plasmid libraries, bacterial DNA contamination, low-quality sequences, and low-complexity repeats. Since ESTs in databases are commonly inaccurately pre-processed, any data sequence contained in EuroPineDB whose quality values (QV) for each nucleotide are available was pre-processed using SeqTrim http://www.scbi.uma.es/seqtrim with parameter customisation for each type of library . High-quality pre-processed EST and SSH sequences guarantee that only non-chimerical, good-quality sequences (i.e., reads devoid of vectors, adaptors, poly-A/T tails, contaminants, and potential cloning artefacts) are included in the database, while sequences consisting of cloning vectors (AC BX676903) or containing poly-A (AC BX676940) were removed. The better the quality of the trimmed sequences, the more reliable the final assembly. It should be noted that 52.5% of nucleotides from the Pp-454 gene library were discarded due to low quality. The EMBL v. 102 subset included in EuroPineDB was also pre-processed with SeqTrim in order to remove uninformative, contaminant or erroneous sequences, even though these sequences lack a QV.
Curated sequences, i.e. those longer than 100 bp for Sanger's reads and 60 bp for 454 reads that exceed SeqTrim pre-processing, were assembled to produce putative pine transcriptional units (UniGenes) as contigs and singletons. Sanger's reads were de novo assembled with a web version of CAP3 [http://www.scbi.uma.es/cap3, ] since it has been described as a highly reliable sequence assembler for establishing UniGenes  with these types of reads. CAP3 assembly was conducted with default parameters using 85% as the cut-off for overlap percent identity to deal with the sequence variation due to the high heterozygosity of pine genes and genome heterogeneity between samples (Table 1). The 454 reads were de novo assembled with a web version of MIRA3 [http://www.scbi.uma.es/mira, ] using 454 settings for ESTs, which enormously reduces the number of misassembled contigs; moreover, this assembly contains 99.94% of curated reads and provides as few as 471 singletons (0.06%). Each library sequence set (Table 1) was assembled separately to obtain specific UniGene assemblies for every gene library and every pine species (Table 2); P. pinaster comprehensive assembly was also performed with MIRA3 with mixed 454-Sanger settings. A collection of all UniGenes is available for every assembly and the distribution of contig lengths is shown in Figure 1, where the longest reads correspond to Sanger reads and the mean length of GS-FLX Titanium reads are below the expected mean length due to the extremely high number of low quality nucleotides (52.5%, Table 2). SSH libraries account for the small shoulder on 200 bp in Figure 1A for Sanger reads.
The annotation of pine sequences is especially challenging since, phylogenetically, pine is distantly related to angiosperm plant models, for which significantly more data and tools are already available . EuroPineDB contains detailed and reliable annotations on UniGenes. This was achieved by combining the results of several annotation processes (described below). The redundant bioinformatics approach makes the curation and annotation processes highly reliable. During every EuroPineDB update, new sequences and new contigs will be re-annotated to provide the correct link and annotation as knowledge increases. Each sequence and UniGene has a specific page to display its annotation together with the E value associated with it to enable the empirical assessment of annotation quality. The current version of EuroPineDB includes annotations for 59.5% of pine UniGenes.
2.4.1 Putative description
A sequence description is a user-friendly manner to offer information about putative functions. Every Sanger sequence in EuroPineDB is given a definition from up to four different sources, with the advantage that inconsistent descriptions are evidence of misannotation. Descriptions were obtained from: (i) the original description, if the sequence has one in the EMBL; (ii) the user definition, provided by the sequence owner when downloading sequences; (iii) the description retrieved by Blast2GO (see below); and (iv) the PGI definition obtained by the best hit in a low stringency BLAST (E < 10-3). Each UniGene contains only the definition provided by Blast2GO (see below).
2.4.2 GO terms, EC keys, KEGG maps, and interpro codes
Every UniGene sequence was annotated using Blast2GO  using the best 10 sequences providing hits of at least 150 nt with a threshold E-value of 10-10 against the non-redundant GeneBank in order to remove spurious annotations. In addition, GO terms with experimental evidence codes were the most preferred, while computational evidence codes and codes inferred by curator were half-weighted for the final annotation; GO terms without biological evidence data or inferred from electronic annotation were discarded. This provided annotations with a high degree of confidence for UniGenes using an E-value for evidence codes of 10-6. A Ruby script was designed to assign the corresponding metabolic pathway (a KEGG map) to each EC key provided by Blast2GO. InterPro codes obtained from Blast2GO were included to add other high-valued annotations (such as functional sites, protein families or conserved domains) since it is an integrated documentation resource . Entries without annotations are candidates for re-annotation with every database update.
2.4.3 SSRs, SNPs and ORFs
Plant cDNAs contain a high frequency of polymorphisms whose main sources are single nucleotide polymorphisms (SNPs) and single sequence repeats (SSRs). They serve to build molecular markers that form an essential starting point for association studies and other genome scan applications such as comparative genomics. SNPs and SSRs can also be used as templates to design primers that amplify specific genomic DNA in diverse populations . SSRs have been assessed with MREPS (http://bioinfo.lifl.fr/mreps/ ). SNPs have been calculated with an adapted version of AlignMiner . The tentative (complete or incomplete) ORFs were inferred from the results of Full-Lengther .
3 Utility and discussion
Molecular sequence databases are fundamental resources for modern bioscientists. The development of such a genomic resource for Pinus pinaster should facilitate basic and applied research on the genetics and evolution of this species, its role in maintaining forest health and ecosystem function, and the genetic traits that are desirable for the paper pulp and wood industry.
3.1 Web interface
There is an option to download files containing UniGene sequences or sequences displayed on a page in FASTA format (including their QV when available), which facilitates further analyses by laboratories. Cross-links to the EMBL database are always provided by means of the accession numbers.
3.1.1 Navigation tabs
By means of the 'Gene Libraries' tab, the user can see gene libraries, UniGenes and annotations for every gene library included in EuroPineDB. Each one contains a short description and some characteristics, including the statistical distribution of the relevant GO terms. The UniGene dataset consists of a consensus sequence of each contig and the singletons (see above).
Gene library clones are stored in 96-well and/or 384-well plates in the laboratory. Navigation using the '96-Well plates' and '384-Well plates' tabs displays the plate organisation of the libraries. Users can download the sequences of all clones in a plate or browse the plate in which red clones are useless sequences, green clones are those that have successfully passed SeqTrim pre-processing, and black ones are printed controls.
Currently, only one microarray (Pinarray1) has been designed with EuroPineDB sequences . The 'Microarray' tab displays general and statistical information about Pinarray1 (Figure 2), whose printed sequences and annotations can be downloaded. Each microarray block organisation is displayed in the lower part of the page. Coordinates refer to a single sequence. The colours green, red and black have the same meaning as in the plates (see above). The graphic representation offers the possibility of retrieving information from specific clones after analysis of any experimental result using this microarray.
Sequences in EuroPineDB have been assembled by gene library and pine species, and can be accessed using the 'Assemblies' tab. Each assembly can be inspected in detail, showing a paged list of UniGenes and a summary description. The detailed view of every UniGene includes the aligned sequences, their orientation, the contig alignment (as a simple-text), a description for the consensus sequence, and the putative description of each included Sanger sequence.
At the home page, a menu on the left enables filtered browsing by microarray, pine species, or annotation. Filtered browsing only displays entries sharing the same selected annotation. Each item in the list opens a new page with the EuroPineDB entries that share this specific annotation. For example, based on nitrogen metabolism (KEGG 00910), it is possible to know how many sequences are present in the database, since by clicking on 00910 every enzyme from this pathway can be seen, as well as the entries that are annotated as being one of these enzymes. As an additional example, all UniGenes involved in photosynthesis (GO:0015979) that belong to a particular library or pine species can be identified by means of GO term filtering.
3.1.2 Database retrieval
In addition to a guided browsing, EuroPineDB contents can be retrieved by means of text search or sequence similarity. A text search engine has been implemented. It can look for words in annotations (i.e. descriptions for sequences, GOs, ECs and InterPro) or for specific codes (i.e. accession numbers or EuroPineDB identifiers). Search results can be restricted to different database subsets (displayed on the Web page as checkboxes), and they are then grouped by common characteristics and displayed in tabs which show/hide the list of elements that match the request. Results are also linked to their respective description pages.
A low-stringent (E < 10-3) BLAST-based search engine enables users to look for EuroPineDB entries similar to their amino acid or nucleotide sequence. The type of sequence (amino acid or nucleotides) is automatically detected, and either BLASTN or BLASTX will be used from the latest BLAST+ version . BLAST searches may be conducted against different subsets of EuroPineDB: by species (P. pinaster, P. sylvestris and/or P. pinea, which can be chosen and combined as desired); and by single sequence or UniGenes. BLAST executions are queued and the results are accessible for up to 1 month with a custom URL that is sent to the user.
3.2 EuroPineDB is a large maritime pine sequence collection
EuroPineDB is mainly devoted to P. pinaster since its 877 523 curated reads (99.7% of total reads) have produced approximately 5.24 × 108 nt in 55 332 UniGenes (Table 2), 24 937 being > 500 bp. Assuming that a similar number of genes occur in P. pinaster as in Arabidopsis thaliana (25 000, which is close to the number of UniGenes > 500 bp) and a similar average transcript length (2000 nt), average transcriptome coverage was estimated at 10.5×. This amount of data and the high coverage represent a substantial sequence resource for P. pinaster that will contribute significantly to its genomic analysis and make EuroPineDB one of the largest sequence collections available for a pine species. Further evidence of the high coverage is that the number of P. pinaster UniGenes is slightly lower than the number of UniGenes in the Pp-454 library (55 431, Table 2). This indicates that UniGenes from the other gene libraries, which are also longer in size (Figure 1), have served to gather together apparently independent contigs from the 454 sequencing, and that most ESTs revealed by capillary (Sanger) analyses of cDNA libraries (Table 1) were also encountered in the 454-sequenced pooled RNA.
3.3 EuroPineDB sequences include a low occurrence of repetitive and retrotransposon-like sequences
The percentage of retrotransposon-like sequences in EuroPineDB is quite low (127 [0.0001%] reads and 20 [0.0003%] UniGenes), in contrast with the 6.2% found in P. contorta, indicating that mRNA isolation for cDNA synthesis in all gene libraries guarantees the best approach for gene discovery, instead of using total RNA. The reduced amount of repetitive DNA found in the coding sequences and the relatively long reads obtained by the sequencing procedures have enabled an accurate de novo assembly and a reliable UniGene collection of maritime pine. A relative high proportion of reads (876 839 out of 877 523, 99.92%) was assembled into reliable contigs (containing less than 9% mismatches), which is in agreement with other high-coverage assemblies .
3.4 EuroPineDB shed light on pine transcriptome
Since estimating the number of genes and the level of transcript coverage represented in an EST collection is an important issue for transcriptome sequencing projects, functional information of EuroPineDB UniGenes was included by means of the widely-used Blast2GO annotator . A wide range of GO terms was assigned to EuroPineDB UniGenes indicating that a wide diversity of transcripts is represented in the database (results not shown). Therefore, 32 919 (59.5%) out of 55 332 UniGenes of P. pinaster were annotated and corresponded to at least 18 466 different genes (which is the number of unique UniProt hits). Assuming that UniGenes inferred from contigs longer than 500 bp are a reliable view of a transcriptome and observing that the number of P. pinaster UniGenes longer than 500 bp (20 928, including annotated and unannotated UniGenes) is slightly greater than the number of different UniGenes regarding unique UniProt hits (18 466), it can be inferred that much of the P. pinaster genes have been identified with the gene libraries described in Table 1, since both numbers (18 466 and 20 928) are close to the 25 000 genes that are supposed to form the A. thaliana genome.
The 59.5% of annotated maritime pine UniGenes is consistent with the 63.6% (20 928 out of 32 919 UniGenes) obtained when considering only UniGenes longer than 500 bp. Both percentages are only slightly lower than the 65% annotated in Eucawood  and the 67.8% in Melogen , but clearly more than the 32% of annotated sequences of P. contorta. In total, 935 (1.7%) UniGenes were annotated with another pine sequence and 16 113 (29.1%) were annotated with a conifer (mainly Picea), which reflects the paucity of information on conifers in databases. This is further highlighted by the fact that the 12 057 (31%) annotated pine genes are qualified as "unknown" proteins, even though most of these unknown proteins correspond to non-annotated full-length transcripts from Picea glauca. The predicted putative ORF could perhaps provide further support to any future functional annotation. The 40.5% of unannotated UniGenes may then correspond to one or more of the following possibilities: (i) putative new pine genes that do not have an orthologue; (ii) non-coding RNAs (including pseudogenes, antisense transcripts, structured RNAs, microRNAs, etc) that have recently been found in abundance when deep transcriptome analysis is performed [36, 37]; (iii) short sequences from the UTR part that are difficult to match, even though 36.4% (11 991) of annotated UniGenes are shorter than 500 bp; and (iv) artefactual assemblies that do not correspond to valid protein-coding sequences, as occurs in 15% of entries in the human gene catalogue .
Each UniGene also includes information about putative SSRs and SNPs, since the development of SSR and SNP markers in pine species could serve to dissect complex traits given that linkage disequilibrium is low or declines rapidly within the length of an average-sized gene . A total of 4740 SSRs have been found in EuroPineDB for P. pinaster; tri-nucleotide repeats were found to be the most common SSRs in EuroPineDB (55.7%), with tetra-nucleotide (12.6%) and di-nucleotide (10.5%) repeats being present at much smaller frequencies. This contrasts with P. contorta in which di-nucleotide repeats were the most abundant. A total of 44 185 SNPs were also identified. Most SSRs and SNPs (3546 [74.8%] and 41 152 [93.1%], respectively) occur in UniGenes with a putative ORF (2966 and 10 756, respectively), and 1% occurs in start/end codons. These numbers are difficult to compare to other conifers because of the different algorithms used for detection [2, 18, 39]. Due to the enormous size of the pine genome, ORF-based SSRs and SNPs are advantageous since they will reduce the mapping efforts required for the development of high-density maps and association studies. The development of SSR/SNP molecular markers, as well as the ORF predictions contained in EuroPineDB, will facilitate comparative genomics with other well-known conifers like P. taeda, P. contorta, P. glauca and P. sitchensis, and will be very useful to scientists interested in different aspects of pine genomics. In contrast to other plant databases, the SSRs and SNPs included in EuroPineDB are downloadable and can be used within any research project.
3.5 EuroPineDB differential features
EuroPineDB is a dynamic structure since its content is re-assembled and re-annotated when new sequences are added. It is designed to include new tables that display other pine genomic features in the near future. Its purpose is to make UniGenes and their annotations available to the scientific community involved in pine genomics by means of a flexible interface for developing queries. Although overlaps exist with the content of the Pine Gene Index (PGI)  and TreeGenes , each database offers distinct analytical approaches, enabling EuroPineDB to contain sequence relationships that cannot be found elsewhere. Moreover, EuroPineDB only includes sequences that have passed stringent quality filtering and only reliable annotations are assigned. Such a procedure provides a high level of confidence in the putative function and characteristics of P. pinaster UniGenes. Whereas the final aim of TreeGenes is to compare the different Pinaceae species, EuroPineDB, like ConiferEST , is more focused on deep information about a single species. In contrast to PGI and to ConiferEST, EuroPineDB differentiates pine species, contains the highest number of ESTs for a single conifer species, and provides insights on every gene library used to seed the database. ConiferEST attempted to provide reliable P. taeda EST pre-processing, anticipating the finding that at least 4.8% of ESTs in dbEST are contaminated by vectors, linkers, E. coli DNA and mitochondrial sequences . TreeGenes does not fully pre-process chromatograms, since it was started using the high-quality sequence provided by PHRED; this has been described as a suboptimal strategy since it over-trims in relation to terminal structures, representing a loss of directional, positional and structural information on cDNA termini . Since Pine Gene Index 7.0 extracted the sequences directly from databases, it contains untrimmed terminus parts, which has a detrimental impact on many downstream EST applications, thereby compromising the reliability of their resulting tentative contigs.
Early pre-processing of some gene libraries considered in EuroPineDB  have proven to be incorrectly processed and annotated (e.g. accession numbers BX252344, BX255382, BX252627, BX252630 or BX251344), and this is mainly due to using the now-outdated StackPack  workflows based on PHRED and PHRAP algorithms. EuroPineDB was pre-processed with SeqTrim  and assembled using CAP3  and MIRA3 . The use of SeqTrim was advantageous in obtaining reliable trimmed sequences, which is preferable to tailor-made scripts for every kind of sequence. An example of this improvement is indicated by the fact that EMBL v. 102 provided 12 673 out of 13 206 sequence entries (Table 2) devoid of any class of contaminant/artefactual sequences. Although this percentage could be considered too high for the EMBL database, it is clearly under the 4.8% reported for ESTs  because EMBL sequences have a more detailed curation process than ESTs. The use of SeqTrim is also devoid of the original reads of contaminating sequences from several bacteria and fungi genomes. Since contigs established with MIRA3 are highly reliable (the maximal mismatch percent in a contig is below 9%), EuroPineDB assemblies for P. pinaster would provide highly reliable UniGenes that would reflect a realistic set of pine genes.
EuroPineDB can be browsed intuitively (Figures 2 and 3) using several tabs, and data can be retrieved by text terms or sequence similarity using a stand-alone BLAST implementation. As a new feature, location information on sequences in microarrays is provided (Figure 2). UniGenes and its annotations can be browsed and downloaded (Figure 3) by pine species as well as by gene library, thus providing scientists with a comprehensive source of information on genomics and transcriptomics of P. pinaster. All this, together with the detailed sequence information and annotation, user-friendly Web-interface (Figure 2), regular updates, as well as connection to printed microarrays, make EuroPineDB extremely valuable to researchers using pine as a model organism, since its annotations and UniGenes cannot be found elsewhere. Finally, the current EuroPineDB assembly could also be used to design a new generation of pine microarrays comprising more UniGenes that would cover more transcriptome elements. Any scientists wishing to incorporate their sequences in EuroPineDB should contact the administrator to upload the data and obtain a private user account.
Availability and requirements
Project name: EuroPineDB; Web site: http://www.scbi.uma.es/pindb; Operating system(s): platform independent; Programming language: Ruby, HTML; Other requirements: Ruby on Rails; Licence: e.g. GNU Affero Public License; Any restrictions to use by non-academics: licence needed.
Conflict of interests statement
The authors declare that they have no competing interests.
The authors gratefully acknowledge the computer resources and technical support provided by the Plataforma Andaluza de Bioinformática of the University of Málaga, Spain. This study was supported by the Spanish Ministerio de Ciencia e Innovación [AGL2009-12139-C02-02, BIO2009-07490], the European Union [PLE2009-0016] and the Junta de Andalucía [CVI-6075 and BIO-114].
- Pavy N, Johnson JJ, Crow JA, Paule C, Kunau T, MacKay J, Retzel EF: ForestTreeDB: a database dedicated to the mining of tree transcriptomes. Nucleic Acids Res. 2007, D888-894. 35 DatabaseGoogle Scholar
- Parchman TL, Geist KS, Grahnen JA, Benkman CW, Buerkle CA: Transcriptome sequencing in an ecologically important tree species: assembly, annotation, and marker discovery. BMC Genomics. 2010, 11: 180-10.1186/1471-2164-11-180.View ArticlePubMedPubMed CentralGoogle Scholar
- Ahuja MR, Neale DB: Evolution of genome size in conifers. Silvae Genetica. 2005, 54: 126-137.Google Scholar
- Alonso P, Cortizo M, Cantón FR, Fernández B, Rodríguez A, Centeno ML, Cánovas FM, Ordás RJ: Identification of genes differentially expressed during adventitious shoot induction in Pinus pinea cotyledons by subtractive hybridization and quantitative PCR. Tree Physiol. 2007, 27 (12): 1721-1730.View ArticlePubMedGoogle Scholar
- Paiva JAP, Garnier-Géré PH, Rodrigues JC, Alves A, Santos S, Graça J, Le Provost G, Chaumeil G, Da Silva-Perez D, Bosc A, Fevereiro P, Plomion C: Plasticity of maritime pine (Pinus pinaster) wood-forming tissues during a growing season. New Phytol. 2008, 179 (4): 1080-1094.View ArticlePubMedGoogle Scholar
- Wang X, Feuerstein GZ: Suppression subtractive hybridisation: application in the discovery of novel pharmacological targets. Pharmacogenomics. 2000, 1 (1): 101-108. 10.1517/146224184.108.40.206.View ArticlePubMedGoogle Scholar
- Allona I, Quinn M, Shoop E, Swope K, St Cyr S, Carlis J, Riedl J, Retzel E, Campbell MM, Sederoff R, Whetten RW: Analysis of xylem formation in pine by cDNA sequencing. Proc Natl Acad Sci USA. 1998, 95 (16): 9693-9698. 10.1073/pnas.95.16.9693.View ArticlePubMedPubMed CentralGoogle Scholar
- Cantón F, Le Provost G, Garcia V, Barré A, Frigerio J-M, Paiva J, Fevereiro P, Ávila C, Mouret J-F, Brach J, de Daruvar A, Cánovas FM, Plomion C: Transcriptome analysis of wood formation in maritime pine. Sustainable Forestry, Wood Products & Biotechnology. 2003, BIOFOR. Vitoria: DFA-AFA Press, 333-347.Google Scholar
- Lee B, Shin G: CleanEST: a database of cleansed EST libraries. Nucleic Acids Res. 2009, D686-689. 37 DatabaseGoogle Scholar
- Wang Z, Gerstein M, Snyder M: RNA-Seq: a revolutionary tool for transcriptomics. Nat Rev Genet. 2009, 10 (1): 57-63. 10.1038/nrg2484.View ArticlePubMedPubMed CentralGoogle Scholar
- Adomas A, Heller G, Olson A, Osborne J, Karlsson M, Nahalkova J, Van Zyl L, Sederoff R, Stenlid J, Finlay R, Asiegbu FQ: Comparative analysis of transcript abundance in Pinus sylvestris after challenge with a saprotrophic, pathogenic or mutualistic fungus. Tree Physiol. 2008, 28 (6): 885-897.View ArticlePubMedGoogle Scholar
- Brinker M, van Zyl L, Liu W, Craig D, Sederoff RR, Clapham DH, von Arnold S: Microarray analyses of gene expression during adventitious root development in Pinus contorta. Plant Physiol. 2004, 135 (3): 1526-1539. 10.1104/pp.103.032235.View ArticlePubMedPubMed CentralGoogle Scholar
- Heller G, Adomas A, Li G, Osborne J, van Zyl L, Sederoff R, Finlay RD, Stenlid J, Asiegbu FO: Transcriptional analysis of Pinus sylvestris roots challenged with the ectomycorrhizal fungus Laccaria bicolor. BMC Plant Biol. 2008, 8: 19-10.1186/1471-2229-8-19.View ArticlePubMedPubMed CentralGoogle Scholar
- Lorenz WW, Yu Y-S, Simões M, Dean JFD: Processing the loblolly pine PtGen2 cDNA microarray. J Vis Exp. 2009, 25: 1182-Google Scholar
- Liang C, Wang G, Liu L, Ji G, Fang L, Liu Y, Carter K, Webb JS, Dean JFD: ConiferEST: an integrated bioinformatics system for data reprocessing and mining of conifer expressed sequence tags (ESTs). BMC Genomics. 2007, 8: 134-10.1186/1471-2164-8-134.View ArticlePubMedPubMed CentralGoogle Scholar
- Lee Y, Tsai J, Sunkara S, Karamycheva S, Pertea G, Sultana R, Antonescu V, Chan A, Cheung F, Quackenbush J: The TIGR Gene Indices: clustering and assembling EST and known genes and integration with eukaryotic genomes. Nucleic Acids Res. 2005, D71-74. 33 DatabaseGoogle Scholar
- Wegrzyn JL, Lee JM, Tearse BR, Neale DB: TreeGenes: A Forest Tree Genome Database. Int J Plant Genomics. 2008, 2008: 412875-View ArticlePubMedPubMed CentralGoogle Scholar
- Clément S, Fillon J, Bousquet J, Beaulieu J: TreeSNPs: a laboratory information management system (LIMS) dedicated to SNP discovery in trees. Tree Genetics & Genomics. 2010, 6 (3): 435-438. 10.1007/s11295-009-0261-6.View ArticleGoogle Scholar
- Wegrzyn JL, Lee JM, Liechty J, Neale DB: PineSAP--sequence alignment and SNP identification pipeline. Bioinformatics. 2009, 25 (19): 2609-2610. 10.1093/bioinformatics/btp477.View ArticlePubMedPubMed CentralGoogle Scholar
- Falgueras J, Lara AJ, Fernandez-Pozo N, Canton FR, Perez-Trabado G, Claros MG: SeqTrim: a high-throughput pipeline for preprocessing any type of sequence reads. BMC Bioinformatics. 2010, 11 (1): 38-10.1186/1471-2105-11-38.View ArticlePubMedPubMed CentralGoogle Scholar
- Gotz S, Garcia-Gomez JM, Terol J, Williams TD, Nagaraj SH, Nueda MJ, Robles M, Talon M, Dopazo J, Conesa A: High-throughput functional annotation and data mining with the Blast2GO suite. Nucleic Acids Res. 2008, 36 (10): 3420-3435. 10.1093/nar/gkn176.View ArticlePubMedPubMed CentralGoogle Scholar
- Canales J, Flores-Monterrosso A, Rueda-Lopez M, Avila C, Canovas FM: Identification of genes regulated by ammonium availability in the roots of maritime pine trees. Amino Acids. 2010, 39 (4): 991-1001. 10.1007/s00726-010-0483-9.View ArticlePubMedGoogle Scholar
- Huang X, Madan A: CAP3: A DNA Sequence Assembly Program. Genome Research. 1999, 9: 868-877. 10.1101/gr.9.9.868.View ArticlePubMedPubMed CentralGoogle Scholar
- Liang F, Holt I, Pertea G, Karamycheva S, Salzberg SL, Quackenbush J: An optimized protocol for analysis of EST sequences. Nucleic Acids Research. 2000, 28 (18): 3657-3665. 10.1093/nar/28.18.3657.View ArticlePubMedPubMed CentralGoogle Scholar
- Chevreux B, Pfisterer T, Drescher B, Driesel AJ, Muller WE, Wetter T, Suhai S: Using the miraEST assembler for reliable and automated mRNA transcript assembly and SNP detection in sequenced ESTs. Genome Res. 2004, 14 (6): 1147-1159. 10.1101/gr.1917404.View ArticlePubMedPubMed CentralGoogle Scholar
- Kirst M, Johnson AF, Baucom C, Ulrich E, Hubbard K, Staggs R, Paule C, Retzel E, Whetten R, Sederoff R: Apparent homology of expressed genes from wood-forming tissues of loblolly pine (Pinus taeda L.) with Arabidopsis thaliana. Proc Natl Acad Sci USA. 2003, 100 (12): 7383-7388. 10.1073/pnas.1132171100.View ArticlePubMedPubMed CentralGoogle Scholar
- Apweiler R, Attwood TK, Bairoch A, Bateman A, Birney E, Biswas M, Bucher P, Cerutti L, Corpet F, Croning MD, Durbin R, Falquet L, Fleischmann W, Gouzy J, Hermjakob H, Hulo N, Jonassen I, Kahn D, Kanapin A, Karavidopoulou Y, Lopez R, Marx B, Mulder NJ, Oinn TM, Pagni M, Servant F, Sigrist CJ, Zdobnov EM: The InterPro database, an integrated documentation resource for protein families, domains and functional sites. Nucleic Acids Res. 2001, 29 (1): 37-40. 10.1093/nar/29.1.37.View ArticlePubMedPubMed CentralGoogle Scholar
- Guerrero D, Bautista R, Villalobos DP, Canton FR, Claros MG: AlignMiner: a Web-based tool for detection of divergent regions in multiple sequence alignments of conserved sequences. Algorithms Mol Biol. 2010, 5: 24-10.1186/1748-7188-5-24.View ArticlePubMedPubMed CentralGoogle Scholar
- Kolpakov R, Bana G, Kucherov G: mreps: Efficient and flexible detection of tandem repeats in DNA. Nucleic Acids Res. 2003, 31 (13): 3672-3678. 10.1093/nar/gkg617.View ArticlePubMedPubMed CentralGoogle Scholar
- Lara A, Pérez-Trabado G, Villalobos D, Díaz-Moreno S, Cantón F, Claros MG: A Web Tool to Discover Full-Length Sequences: Full-Lengther. Innovations in Hybrid Intelligent Systems. Edited by: Corchado E, Corchado JM, Abraham A. 2007, Berlín Springer, 361-368.View ArticleGoogle Scholar
- Camacho C, Coulouris G, Avagyan V, Ma N, Papadopoulos J, Bealer K, Madden TL: BLAST+: architecture and applications. BMC Bioinformatics. 2009, 10: 421-10.1186/1471-2105-10-421.View ArticlePubMedPubMed CentralGoogle Scholar
- Meyer E, Aglyamova GV, Wang S, Buchanan-Carter J, Abrego D, Colbourne JK, Willis BL, Matz MV: Sequencing and de novo analysis of a coral larval transcriptome using 454 GSFlx. BMC Genomics. 2009, 10: 219-10.1186/1471-2164-10-219.View ArticlePubMedPubMed CentralGoogle Scholar
- Rengel D, San Clemente H, Servant F, Ladouce N, Paux E, Wincker P, Couloux A, Sivadon P, Grima-Pettenati J: A new genomic resource dedicated to wood formation in Eucalyptus. BMC Plant Biol. 2009, 9: 36-10.1186/1471-2229-9-36.View ArticlePubMedPubMed CentralGoogle Scholar
- Gonzalez-Ibeas D, Blanca J, Roig C, González-To M, Picó B, Truniger V, Gómez P, Deleu W, Caño-Delgado A, Arús P, Nuez F, García-Más J, Puigdomènech P, Aranda MA: MELOGEN: an EST database for melon functional genomics. BMC Genomics. 2007, 8: 306-10.1186/1471-2164-8-306.View ArticlePubMedPubMed CentralGoogle Scholar
- Ralph SG, Chun HJ, Kolosova N, Cooper D, Oddy C, Ritland CE, Kirkpatrick R, Moore R, Barber S, Holt RA, Jones SJ, Marra MA, Douglas CJ, Ritland K, Bohlmann J: A conifer genomics resource of 200,000 spruce (Picea spp.) ESTs and 6,464 high-quality, sequence-finished full-length cDNAs for Sitka spruce (Picea sitchensis). BMC Genomics. 2008, 9: 484-10.1186/1471-2164-9-484.View ArticlePubMedPubMed CentralGoogle Scholar
- Mardis ER: Next-generation DNA sequencing methods. Annu Rev Genomics Hum Genet. 2008, 9: 387-402. 10.1146/annurev.genom.9.081307.164359.View ArticlePubMedGoogle Scholar
- Harrow J, Nagy A, Reymond A, Alioto T, Patthy L, Antonarakis SE, Guigo R: Identifying protein-coding genes in genomic sequences. Genome Biol. 2009, 10 (1): 201-10.1186/gb-2009-10-1-201.View ArticlePubMedPubMed CentralGoogle Scholar
- Clamp M, Fry B, Kamal M, Xie X, Cuff J, Lin MF, Kellis M, Lindblad-Toh K, Lander ES: Distinguishing protein-coding and noncoding genes in the human genome. Proc Natl Acad Sci USA. 2007, 104 (49): 19428-19433. 10.1073/pnas.0709013104.View ArticlePubMedPubMed CentralGoogle Scholar
- Pavy N, Parsons LS, Paule C, MacKay J, Bousquet J: Automated SNP detection from a large collection of white spruce expressed sequences: contributing factors and approaches for the categorization of SNPs. BMC Genomics. 2006, 7: 174-10.1186/1471-2164-7-174.View ArticlePubMedPubMed CentralGoogle Scholar
- Gion J-M, Lalanne C, Le Provost G, Ferry-Dumazet H, Paiva J, Chaumeil P, Frigerio J-M, Brach J, Barré A, de Daruvar A, Claverol S, Sommerer N, Negroni L, Plomion C: The proteome of maritime pine wood forming tissue. Proteomics. 2005, 5 (14): 3731-3751. 10.1002/pmic.200401197.View ArticlePubMedGoogle Scholar
- Christoffels A, van Gelder A, Greyling G, Miller R, Hide T, Hide W: STACK: Sequence Tag Alignment and Consensus Knowledgebase. Nucleic Acids Res. 2001, 29 (1): 234-238. 10.1093/nar/29.1.234.View ArticlePubMedPubMed CentralGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.