AgBase: a functional genomics resource for agriculture
- Fiona M McCarthy†1, 7Email author,
- Nan Wang†2, 7,
- G Bryce Magee2, 7,
- Bindu Nanduri1, 7,
- Mark L Lawrence1,
- Evelyn B Camon3,
- Daniel G Barrell3,
- David P Hill4,
- Mary E Dolan4,
- W Paul Williams5,
- Dawn S Luthe6, 7,
- Susan M Bridges†2, 7 and
- Shane C Burgess†1, 7
© McCarthy et al; licensee BioMed Central Ltd. 2006
Received: 18 April 2006
Accepted: 08 September 2006
Published: 08 September 2006
Many agricultural species and their pathogens have sequenced genomes and more are in progress. Agricultural species provide food, fiber, xenotransplant tissues, biopharmaceuticals and biomedical models. Moreover, many agricultural microorganisms are human zoonoses. However, systems biology from functional genomics data is hindered in agricultural species because agricultural genome sequences have relatively poor structural and functional annotation and agricultural research communities are smaller with limited funding compared to many model organism communities.
To facilitate systems biology in these traditionally agricultural species we have established "AgBase", a curated, web-accessible, public resource http://www.agbase.msstate.edu for structural and functional annotation of agricultural genomes. The AgBase database includes a suite of computational tools to use GO annotations. We use standardized nomenclature following the Human Genome Organization Gene Nomenclature guidelines and are currently functionally annotating chicken, cow and sheep gene products using the Gene Ontology (GO). The computational tools we have developed accept and batch process data derived from different public databases (with different accession codes), return all existing GO annotations, provide a list of products without GO annotation, identify potential orthologs, model functional genomics data using GO and assist proteomics analysis of ESTs and EST assemblies. Our journal database helps prevent redundant manual GO curation. We encourage and publicly acknowledge GO annotations from researchers and provide a service for researchers interested in GO and analysis of functional genomics data.
The AgBase database is the first database dedicated to functional genomics and systems biology analysis for agriculturally important species and their pathogens. We use experimental data to improve structural annotation of genomes and to functionally characterize gene products. AgBase is also directly relevant for researchers in fields as diverse as agricultural production, cancer biology, biopharmaceuticals, human health and evolutionary biology. Moreover, the experimental methods and bioinformatics tools we provide are widely applicable to many other species including model organisms.
Comparison of human, mouse, rat, chicken and bovine genome statistics.
7 741 746
4 719 380
1 039 059
No. Proteins (NRPD)
No. Proteins (UniProtKB)
% 'Predicted' Proteins
All GO Associations
% IEA Associations
The current state of agricultural genome annotation hinders its utility for systems biology modeling of microarray and other functional genomics datasets. To fully utilize agricultural genome sequence data requires further, computationally accessible, structural and functional annotation. Here we describe "AgBase", a unified resource dedicated to enabling genome-wide structural and functional annotation and modeling of microarray and other functional genomics data in agricultural species. AgBase integrates structural and functional annotations and provides tools in an easy-to-use pipeline, allowing agricultural and biomedical researchers to rapidly and effectively model and derive biological significance from microarray and other functional genomics datasets.
Construction and content
The AgBase server is a dual Xeon 3.0 processor with a 800 Mhz FSB, 4 GB of Ram and five 146 GB hard drives in a RAID-5 configuration. The operating system is Windows 2000 Server. AgBase has a dedicated tape backup system with a total storage capacity of 3.2 TB native and 6.4 TB compressed. The backup software is Veritas Netback. A full backup is done each weekend, an archive backup once a month, and incremental backups nightly.
AgBase is implemented using the mySQL 4.1 database management system, NCBI Blast, and scripts written in Perl CGI. The schema is a protein centric design that is an adaptation of the Chado schema with extensions to accommodate storage of expressed peptide sequence tags (ePSTs). The entity relationship (ER) model for primary objects in the database for each protein is given as supplementary data [see Additional file 1]. A separate schema is implemented for ePST data. Data that is generated in-house includes AgBase GO annotations, the AgBase gene association files and ePSTs. External data that is integrated into the database includes the Gene Ontology, the UniProt database, EBI-GOA and the NCBI Entrez Taxonomy.
The GO annotations are generated by manual curation of the literature and by sequence similarity (GO evidence code ISS) using the GOanna tool followed by manual inspection of the alignments that are produced. AgBase biocurators are trained in a GO curation course that is held periodically. All literature-based AgBase GO annotations are quality checked to GO Consortium standards. The ePSTs are generated using a proteogenomic mapping pipeline implemented in Perl. The pipeline integrates information from experimental proteomics experiments and annotated genomes. Results are visualized using the Apollo genome browser to allow curation by scientists. Each ePST is quality checked by AgBase Biocurators. The generation of ePSTs is discussed in the experimental structural annotation section below.
Users can access protein information by protein name, gene name, GO term, taxon, a variety of accession numbers, or via BLAST searches. The AgBase tools also access the AgBase database. AgBase is updated from external sources every three months and locally generated data is loaded as it is generated. Gene association files of gene products annotated by AgBase are accessible in a tab-delimited format to facilitate data exchange.
We have purposely followed the paradigm of multi-species databases suggested by Stein  and the Reactome database  and are currently focused on plants and animals whose genomes are, or will be, sequenced and microbial pathogens and parasites that have significant economic impact on agricultural production and zoonotic disease. AgBase has four main aims (discussed in detail below): (1) to provide experimentally derived structural annotations of agricultural genomes; (2) to provide highly curated, GO functional annotations; (3) to promote the use of standardized nomenclature in agricultural species; (4) to develop computational pipelines for processing and using structural and functional annotations.
The AgBase database is intended as a resource to assist functional genomics in agricultural species and the tools provided support analysis of large scale datasets. To this end, we provide both experimentally derived structural annotation and functional data in a unified resource. While agriculturally important organisms may have other resources that provide structural annotation or GO annotations, AgBase is unique because (1) the structural data provided is experimentally derived; (2) the structural and functional data is provided from a unified resource; and (3) tools for analysis of this data are freely available via AgBase. The AgBase interface allows users to search for information in several ways. The Text Search performs an exact substring search on the selected database. To facilitate data sharing, searching based on commonly used accession numbers and identifiers is supported in addition to BLAST searches. Multiple query searches are also available.
Experimental structural annotation
The use of experimental data for genome annotation is critical for conclusive identification of the functional sequences within genomes, accurate description of intron/exon structures and determination of the potential products from each gene in different tissues and cellular states . Through AgBase we make available improved structural annotation of agriculturally important genomes from experimental confirmation of electronically predicted proteins/open reading frames, especially via proteogenomic mapping [19–23].
Proteogenomic mapping generates expressed peptide sequence tags (ePSTs) . These ePSTs are derived by identifying novel protein fragments through proteomics, aligning these to the genome sequence and extending to the nearest 3' stop codon. We have used the proteogenomic mapping pipeline to generate ePSTs for a prokaryote (Pasteurella multocida) and a eukaryote (chicken). P. multocida, or chicken "fowl cholera", is a bovine respiratory disease pathogen and human zoonosis. Although the P. multocida genome was sequenced in 2001  and is considered well annotated, our proteogenomic pipeline identified 202 ePSTs that had identifiable methionine start codons [see Additional file 2]. One of these is a 130 amino acid ePST that was identified by six different peptides and is located in a 704 bp intergenic region between accA and guaA in the Pm70 genome [see Additional file 3]. The ePST has 60% identity and 74% similarity at the protein level with the 114 amino acid hypothetical protein HD_1218 (Genbank accession AAP96060) from Haemophilus ducreyi (a major cause of human genital ulcer disease [chancroid] in humans). A database of ePSTs identified from chicken and P. multocida is publicly accessible via the proteogenomics link on the AgBase homepage. The ePST database is fully searchable either by text or Blast searching. Text-searchable fields include taxonID, genome build, chromosome or chromosomal location. Public submissions to the ePST database are cited by submitter name.
Generating ePSTs is time consuming and labor intensive. To facilitate structural annotation we have developed a proteogenomic mapping pipeline for generation of ePSTs (available from AgBase by request). The pipeline for prokaryotes currently includes a visualization component (we currently use Apollo ) that allows the researcher to view the ePSTs in context in the genome. In eukaryote genomes it is possible that the extension is carried beyond a splice signal producing an ePST that includes intronic DNA. We are currently in the process of extending the pipeline to detect splice signals and to show alignments with ESTs in the visualizations to address this shortcoming.
To ensure that structural data is based on high quality proteomics identifications, we have developed a method for assigning probabilities to mass spectral identifications during proteogenomic mapping . Assigning probabilities to mass spectral identifications is important because one issue associated with tandem mass spectral searching against databases is false positive and false negative peptide identifications. Moreover, all of our proteomics data is submitted to the PRIDE database . Mass spectrometry data submitted to PRIDE is further curated for inclusion in UniProtKB, where it is available for uploading into genome browsers, for example Ensembl . To add value to the structural annotations provided by AgBase and enhance biological modeling, we have also developed methods and tools for assigning GO annotations (see below).
Many gene products from agriculturally important organisms have no GO annotation. Practically, this means that experimentalists working with these species must provide their own GO annotations if they wish to use GO to model their microarray and other functional genomics data. While those best qualified to functionally annotate a gene product may be those who work directly with it , few experimentalists can devote the time and resources needed to learn the intricacies of GO biocuration. To facilitate functional modeling in agricultural organisms, we are actively GO annotating chicken, cow, sheep and catfish gene products.
While EBI-GOA uses an electronic mapping strategy to rapidly provide GO annotations for a large number of gene products, these are IEA mappings that rely on curated information from SwissProt, InterPro and the Enzyme Commission (EC) databases . Many agricultural gene products are 'predicted' products based on gene prediction algorithms (Table 1) and do not exist in these curated databases. However, GO annotation can be assigned based on human interpretation of sequence and/or structural similarities (ISS) with well-studied and already GO-annotated gene products. By definition, such gene products can only be annotated to ISS or IEA since they have no experimental functional data as yet.
Our GO annotation strategy first provides breadth by focusing on the large proportion of gene products that currently exist in the UniParc database and have no GO annotation. Since predicted proteins represent approximately half of the gene products from newly sequenced genomes (Table 1.), being able to provide GO annotations for these gene products complements the GO annotations provided by EBI-GOA and dramatically improves our ability to model functional genomics data. We are doing a "first-pass" ISS annotation of chicken, cow and sheep gene products that currently have no GO annotation (using manual inspection of BLAST alignments and, where possible, established orthology). In addition, we have developed DDF-MudPIT , a high-throughput, proteomics-based method that simultaneously confirms expression and experimentally determines the cellular component of gene products . We next provide finer and more precise functional annotations (i.e. improved GO depth) by curating literature. All of our GO annotations are prioritized based on our experimental needs. One example is our recent proteomics model of B-cell development in the chicken bursa of Fabricius . Initially we were hampered because few chicken proteins had any GO functional annotation. We annotated 142 chicken proteins, including curation of 24 PubMed articles. These GO annotations were used to refine cell differentiation, proliferation and cell death modeling in the developing bursa.
AgBase GO annotations by species and evidence code.
No. Proteins Annotated
UniParc Proteins Annotated (ISS)
No. Papers Curated
We actively educate, encourage and seek out researchers in the scientific communities to contribute their own GO annotations. We help these researchers properly format their annotations and they are acknowledged for their annotations on the protein detail page for the gene product in AgBase. As public annotations are submitted to AgBase, research-directed GO annotations from the research community will be acknowledged on the protein detail page. We will also supply maize gene product annotations to Gramene  and MaizeGDB . To avoid duplication of effort in literature curation, we developed a journal database (JDB) based on PubMed identity number (PMID). JDB tracks all PubMed articles used as a source for manual GO annotations. The JDB will aid collaborative GO annotation as it can be used for quality control for GO annotations among interested groups. Non-biocurators may access the JDB as a guest user.
While the GO does not specifically deal with gene nomenclature, unified and unique nomenclature for orthologous genes is essential. Where possible, chicken genes will be assigned nomenclature based on orthologous human nomenclature . We use human orthologs to provide standardized gene symbols to chicken and cow gene products during the process of making GO associations. A chicken gene nomenclature committee is at a formative stage; as yet, no corresponding committee exists for cow.
We have developed freely available computational tools to help researchers use the GO to derive biological significance from their microarray and other functional genomics data. These tools are designed as part of an integrated pipeline to batch process input. In order to improve interoperability with different types of data, the tools accept several input formats. Our GO annotation suite of tools is available online via the Tools link at the AgBase homepage. These tools can also be used for non-agricultural organisms, including newly sequenced species and those without complete genome sequence available. The steps to analyze a microarray or other functional genomics dataset are:
3. After ISS annotation, the user may choose to annotate the data further by curating published literature. We provide advice on GO annotation and are developing a mechanism for researchers to be publicly acknowledged for GO annotations they submit to AgBase.
We are committed to developing tools and pipelines to maximize the payoff gained from expensive high-throughput microarray and other functional genomics experiments. We have designed tools that may be applied across a diverse range of species, including microbes, parasites, viruses, plants and animals. For example, the same tools used to model B-cell development in the chicken allowed us to formulate experimental models for disease resistance in maize. We identified 1,522 unique proteins from the developing maize rachis (cob) using a combination of MudPIT and 2-D electrophoresis. In addition, rachis proteins from Aspergillus flavus resistant and susceptible lines were compared by differential gel electrophoresis: seventy-three proteins that were more abundant in resistant lines (1.5-fold or greater). Using the tools described above we divided these over-expressed proteins into four categories: abiotic stress proteins; antioxidant enzymes; enzymes in the phenylpropanoid pathway leading to flavonoid and lignin biosynthesis; and proteins with various other metabolic functions. Analyses of these data will help us formulate testable hypotheses regarding the role of the maize rachis in resistance to A. flavus infection and aflatoxin accumulation.
Finally, we also develop tools for agriculturally important species that do not yet (or may never have) their genomes sequenced. Researchers working with such species often rely on ESTs and EST assemblies for functional analysis. However, most ESTs (and microarrays derived from these) are not associated with GO annotation. GOanna accepts FASTA files and can be used associate GO function with ESTs. Another tool to enable EST modeling is the ProtIDer tool (freely available by request to AgBase). ProtIDer is a homology-based search program that provides an automated pipeline for the proteomic analysis of ESTs and EST assemblies from TIGR [34–36]. The ProtIDer tool compares EST assemblies or singleton ESTs to the UniProtKB and uses high-matching proteins to correct sequencing errors and to annotate the sequence. We have tested ProtIDer using data obtained from channel catfish, an organism which currently has only 1,108 protein records in the NRPD, but has 45,622 ESTs available from the dbEST (03/20/06). Tandem mass spectra obtained from channel catfish ovary cells was used to search against three databases: all catfish entries in the NRPD (cfNRPD); a database of highly homologous proteins (hpDB) that come from NRPD as a result of TBLASTN-searching the NRPD with all catfish ESTs generated using ProtIDer; and the ESTs themselves translated in all 6 frames (cfESTDB). We identified 1001 proteins and ESTs [see Additional file 4]: 10 from cfNRPD (4 were ribosomal proteins); 48 from the hpDB (only 5 of which were ribosomal) and 962 from cfESTDB. These approaches provide complementary annotation information. Not all of the cfNRPD entries are yet represented in the EST databases; the hpDB allowed us to identify highly conserved proteins and searching the cfESTDB directly indicates ESTs that may be translated. When we used ISS to the hpDB to make GO associations to catfish ESTs we found that the GO terms were distributed over the cellular component, although the biological process had a larger proportion of gene products annotated to response to stimulus and cell communication. From this initial data we will focus on modeling cell communication pathways in developing channel catfish ovary cells.
We are building upon the tools and resources already available at AgBase. The proteogenomics pipeline is being extended to allow more informative visualization of ePSTs in context within the genome and alignment with ESTs and orthologous sequences from other organisms. We will continue to generate ePSTs for newly sequenced agricultural genomes and will also continue to add GO annotations for agriculturally important organisms. We are working to improve the representation of agricultural gene products in the UniProtKB and a tangible example of this is the recent addition of experimentally confirmed chicken 'predicted' gene proteins  added to the UniProtKB database.
We have improved the structural annotation of agriculturally important genomes by experimentally confirming 8,704 predicted proteins in chicken and cow (PRIDE submissions numbers pending) and 723 ePSTs from chicken and P. multocida. In our first nine months (04/22/05–03/20/06) we have provided 5,762 new GO annotations to 759 proteins from five different species. While most of our GO annotations are ISS (97%), we have also manually curated 42 PubMed references. We have developed a suite of tools to associate GO annotation with experimental data and to provide higher-order summaries of the data, and a tool to aid EST analysis. Users external to MSU account for more than one third of the hits recorded at the AgBase website.
Availability and requirements
Access to the AgBase databases is via http://www.agbase.msstate.edu/ and access to data is unrestricted. The tools we have developed are either freely available online at AgBase or by contacting us via the link provided at the AgBase website. The help pages provide information about how to use these tools or technical support can be obtained directly by contacting us. AgBase is an on-going project and interaction with the user community is vital for its success. We encourage the submission of data, correction of errors, and suggestions for making AgBase of greater use, including ideas for new computational tools. Our biocurators make every effort to maintain data integrity by linking data with researchers, references and methods.
We would like to thank MGI and EBI-GOA for their continued help and support with the Gene Ontology aspects of this manuscript. Financial support for our projects has come from the USDA NRI, MSU Office of Research (MAFES contribution number J-10924), MSU Bagley College of Engineering, MSU College of College of Veterinary Medicine and the MSU Life Science and Biotechnology institute. The authors thank T. Pechan, D. Kunec, B. van den Berg, A.M. Cooksey, A. Shack, C. Doffitt, and E. Dimmer for help with preparing the manuscript.
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