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Nucleic Acids Research Advance Access originally published online on October 25, 2008
Nucleic Acids Research 2009 37(Database issue):D946-D950; doi:10.1093/nar/gkn819
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Nucleic Acids Research, 2009, Vol. 37, Database issue D946-D950
© 2008 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

This article appears in the following Nucleic Acids Research issue: Database issue [View the issue table of contents]

Articles

GOBASE: an organelle genome database

Emmet A. O’Brien*, Yue Zhang, Eric Wang, Veronique Marie, Wole Badejoko, B. Franz Lang and Gertraud Burger

Robert-Cedergren Center for Bioinformatics and Genomics, Département de Biochimie, Pavillon Roger-Gaudry, Université de Montréal, 2900 Edouard-Montpetit, Montreal QC, Canada H3T 1J4

*To whom correspondence should be addressed. Tel: +1 514 343 6111; Fax: +1 514 343 2210; Email: eobrien{at}bch.umontreal.ca

Received September 11, 2008. Revised October 10, 2008. Accepted October 13, 2008.


   ABSTRACT
TOP
 ABSTRACT
INTRODUCTION
 DATA CONTENT
 ENHANCEMENTS TO FUNCTIONALITY
 IMPLEMENTATION
 FUTURE PLANS
 FUNDING
 REFERENCES
 
The organelle genome database GOBASE, now in its 21st release (June 2008), contains all published mitochondrion-encoded sequences (~913 000) and chloroplast-encoded sequences (~250 000) from a wide range of eukaryotic taxa. For all sequences, information on related genes, exons, introns, gene products and taxonomy is available, as well as selected genome maps and RNA secondary structures. Recent major enhancements to database functionality include: (i) addition of an interface for RNA editing data, with substitutions, insertions and deletions displayed using multiple alignments; (ii) addition of medically relevant information, such as haplotypes, SNPs and associated disease states, to human mitochondrial sequence data; (iii) addition of fully reannotated genome sequences for Escherichia coli and Nostoc sp., for reference and comparison; and (iv) a number of interface enhancements, such as the availability of both genomic and gene-coding sequence downloads, and a more sophisticated literature reference search functionality with links to PubMed where available. Future projects include the transfer of GOBASE features to NCBI/GenBank, allowing long-term preservation of accumulated expert information. The GOBASE database can be found at http://gobase.bcm.umontreal.ca/. Queries about custom and large-scale data retrievals should be addressed to gobase{at}bch.umontreal.ca.


   INTRODUCTION
TOP
 ABSTRACT
 INTRODUCTION
DATA CONTENT
 ENHANCEMENTS TO FUNCTIONALITY
 IMPLEMENTATION
 FUTURE PLANS
 FUNDING
 REFERENCES
 
The amount of information available in generalist molecular sequence databases such as GenBank (1) continues to grow, and this information becomes more diverse and complex as we discover new biological phenomena. Therefore, there is an increasing need for expert databases specializing in particular areas of molecular biology. Specialist databases provide expert curation of data, and access to that data in a flexible and well-integrated fashion serves a purpose complementary to generalist databases such as GenBank.

GOBASE is one such specialist database, which has been collecting, curating and publishing data concerning mitochondrial and chloroplast genomes since 1995 (2–5). Organelle genomes are of biological interest for a wide range of studies, such as molecular taxonomy, molecular mechanisms of trans-splicing and RNA editing, and non-Mendelian inherited metabolism-related disease in humans. GOBASE contains a number of different categories of data, such as nucleic acid and protein sequences, genetic maps, taxonomic data and RNA secondary structures. All gene and product names have been assigned from a locally maintained standard list, and this combines with a powerful and flexible interface to allow a wide range of complex searches. While initially GOBASE was designed primarily to address issues of comparative biology, such as the diversity of organelle genome structure in eukaryotes (e.g. 6,7), we have more recently added functionality specific to the human mitochondrial genome in GOBASE, such as searches by haplotype and disease state, which are of medical interest.


   DATA CONTENT
TOP
 ABSTRACT
 INTRODUCTION
 DATA CONTENT
ENHANCEMENTS TO FUNCTIONALITY
 IMPLEMENTATION
 FUTURE PLANS
 FUNDING
 REFERENCES
 
GOBASE release 21 (June 2008) contains 913 000 mitochondrial sequences including 737 000 genes, and 250 000 chloroplast-encoded sequences including 174 000 genes, derived mostly from GenBank releases up to 164. The large number of complete organelle genomes available makes GOBASE a valuable resource for phylogenomics, with 6300 complete mitochondrial genomes and 213 chloroplast genomes. This number has increased almost 4-fold since the previous report.

More recently (5), we have added bacterial genome sequences for reference purposes. As of release 21 GOBASE includes three complete bacterial genomes: Escherichia coli K12; the alpha-proteobacterium Rickettsia prowazekii strain Madrid E, closely related to the bacterial ancestor of mitochondria; and the cyanobacterium Nostoc sp., closely related to the bacterial ancestor of chloroplasts. In order to provide a consistent comparative view of these genomes, they have each been reannotated using the AutoFACT functional annotation tool (8), including assignation of Gene Ontology terms. GOBASE now contains 10 700 bacterial genes in total.


   ENHANCEMENTS TO FUNCTIONALITY
TOP
 ABSTRACT
 INTRODUCTION
 DATA CONTENT
 ENHANCEMENTS TO FUNCTIONALITY
IMPLEMENTATION
 FUTURE PLANS
 FUNDING
 REFERENCES
 
RNA editing
RNA editing refers to a molecular process by which the sequence of a transcribed RNA is modified. This has been seen to occur in the mitochondria of several eukaryotic taxa, such as plants (9) and trypanosomes (10), and in chloroplasts (11). At the level of basic changes, examples exist in the database of sequences being modified by the substitution of one residue for another, by deletion of residues, and by the addition of residues, usually uracil.

The RNA editing interface in GOBASE is based primarily on the previously existing RNA query page, with the addition of editing-specific selection parameters such as the type of modification (insertion, deletion or substitution). A query result is shown in Figure 1. In addition to the sequence itself, edited positions are displayed, both as a list specifying the exact change made at each position, and marked in red on an alignment of the relevant sections of sequence for a straightforward and intuitive visual representation. The interface displays only the regions of the sequence where editing occurs. Coding and intronic regions of the sequence are distinguished by background color. Complete unedited and edited sequences can be downloaded from the interface page. Future development will include the possibility of downloading the sequence alignment as displayed, and the addition of multiple rows to the alignment in cases where edits to a sequence are known to occur sequentially, so that observed intermediate stages in the editing process can be represented.


Figure 1
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  		Figure 1. RNA editing result page, showing sequence-specific data, location of edited positions and alignment of gene sequence with edited sequence. Hyperlinks lead to database pages for details of appropriate Gene Product, Taxonomy, Sequence and Gene, and to the Entrez page for the appropriate gi. Start and end positions of the gene, and locations of edited positions, are numbered relative to the start of the sequence entry containing the gene.

 
Human-specific data
Information specific to the ~3000 complete human mitochondrial genome sequences in GOBASE has been added from a number of sources, including HmtDB (http://www.hmtdb/uniba.it/) (12), OMIM (http://www.ncbi.nlm.nih.gov/omim/) (13) and MitoMap (http://www.mitomap.org/) (14). Two different interface pages provide access to these new data.

The Human Sequence query page allows the user to select a set of human mitochondrial sequences based on haplogroup and disease state. More than 450 different haplogroup assignments are available in GOBASE, so a full list might become unwieldy for some queries. As haplogroup designators always start with a letter, the user is offered the option of first selecting an initial letter or letters, and then picking a range of individual haplogroups from the corresponding subset of haplogroup assignments shown in a menu. The results page (Figure 2) provides relevant information from the standard GOBASE Sequence page, and also shows all the positions at which this sequence differs from the reference human mitochondrial genome as defined in GenBank (accession no NC_001807 [GenBank] ) using an alignment. On this alignment, mutations that have been associated with disease are marked in yellow, and other polymorphic mutations are indicated in red.


Figure 2
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  		Figure 2. Human sequence result page, showing the difference between the queried sequence and the reference human mitochondrial genome sequence, both as a list of divergent positions and as an alignment of relevant sections of the sequences.

 
The Human Mutation query page (Figure 3a) allows the user to search the dataset for mutations of interest within a specified range of positions on the human mitochondrial genome sequence, either by specifying start and end positions directly or by selecting one or more genes from a list on the interface. This search returns a list of positions at which mutations are documented. For each mutation (Figure 3b), the result page provides data on its disease associations, a section of the reference sequence showing the location and neighborhood of the mutation, and a list of the sequences in GOBASE containing this mutation.


Figure 3
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  		Figure 3. (a) Human mutation query page, allowing the user to select the gene(s) of interest and specify the range of positions on the sequence to search for mutations. (b) Result page showing details for an individual mutation.

 
Other functional enhancements
The DNA sequence download functionality has been modified to allow the user to download either genomic sequence or gene-coding regions, selectable via buttons from the Gene query page. There are a small number of unusual cases, such as trans-spliced genes, where there is no straightforward correspondence between a single gene and a contiguous linear region of the source sequence record. The GOBASE database structure has now been modified to address these cases transparently. Sequences of complex gene-coding regions are assembled in advance, stored and made available in query results through the same interface as conventional linear genes.

All sequences retrieved from GOBASE now come with detailed literature references derived from the source GenBank records. Journal, author and title are provided, and a direct link to the appropriate PubMed entry if one exists.

Because of practical constraints, any given query in GOBASE returns at most 5000 results. Users wishing to execute custom queries retrieving larger amounts of data are invited to contact the GOBASE team at gobase{at}bch.umontreal.ca so that the query can be run directly on the database via SQL.


   IMPLEMENTATION
TOP
 ABSTRACT
 INTRODUCTION
 DATA CONTENT
 ENHANCEMENTS TO FUNCTIONALITY
 IMPLEMENTATION
FUTURE PLANS
 FUNDING
 REFERENCES
 
The GOBASE database is implemented in version 7.4.1 of the PostgreSQL relational database management system with a web interface written in v4.3.8 of the PHP scripting language. The graphics on the gene pages are generated using the GD module for Perl/PHP, version 2.0.25. Perl (5.8.0) scripts are used to download data from GenBank and process it into GOBASE. All procedures are executed on PCs with two 2.4 GHz or 2.8 GHz Intel Xeon CPUs.


   FUTURE PLANS
TOP
 ABSTRACT
 INTRODUCTION
 DATA CONTENT
 ENHANCEMENTS TO FUNCTIONALITY
 IMPLEMENTATION
 FUTURE PLANS
FUNDING
 REFERENCES
 
Specialized databases with all their valuable information are prone to disappearance (15), mostly because of funding constraints, unless transferred to sustainable public databases. We are therefore collaborating with scientists at NCBI to establish a database based on the content of GOBASE as an auxiliary to GenBank. This database will focus on the additional data that expert curation at GOBASE has generated, notably the curated gene and product names and synonyms and RNA secondary structure data, thus providing a permanent repository for two decades of curation of organelle genome data.


   FUNDING
TOP
 ABSTRACT
 INTRODUCTION
 DATA CONTENT
 ENHANCEMENTS TO FUNCTIONALITY
 IMPLEMENTATION
 FUTURE PLANS
 FUNDING
REFERENCES
 
This project was funded by grants MOP-15331 and MOP-84453 from the Canadian Institute for Health Research (CIHR, Genetics Institute). Funding for open access charge: CIHR.

Conflict of interest statement. None declared.


   ACKNOWLEDGEMENTS
 
The authors would like to thank Ilene Mizrachi, Susan Schaefer, Tatiana Tatusova and Jim Ostell at NCBI; Chris Cesaire, Ousman Diallo, and Olivier Tremblay-Savard for contributions to the development of the RNA editing functionality in GOBASE, and Allan Sun for systems administration.


   REFERENCES
TOP
 ABSTRACT
 INTRODUCTION
 DATA CONTENT
 ENHANCEMENTS TO FUNCTIONALITY
 IMPLEMENTATION
 FUTURE PLANS
 FUNDING
 REFERENCES
 

  1. Benson DA, Karsch-Mizrachi I, Lipman DJ, Ostell J, Wheeler DL. GenBank. Nucleic Acids Res. (2008) 36:D25–D30.[Abstract/Free Full Text]

  2. Korab-Laskowska M, Rioux P, Brossard N, Littlejohn TG, Gray MW, Lang BF, Burger G. The Organelle Genome Database Project (GOBASE). Nucleic Acids Res. (1998) 26:138–144.[Abstract/Free Full Text]

  3. Shimko N, Liu L, Lang BF, Burger G. GOBASE: the organelle genome database. Nucleic Acids Res. (2001) 29:128–132.[Abstract/Free Full Text]

  4. O’Brien EA, Badidi E, Barbasiewicz A, deSousa C, Lang BF, Burger G. GOBASE – a database of mitochondrial and chloroplast information. Nucleic Acids Res. (2003) 31:176–178.[Abstract/Free Full Text]

  5. O’Brien EA, Zhang Y, Yang L, Wang E, Marie V, Lang BF, Burger G. GOBASE – a database of organelle and bacterial genome information. Nucleic Acids Res. (2006) 34:D697–D699.[Abstract/Free Full Text]

  6. Lang BF, Gray MW, Burger G. Mitochondrial genome evolution and the orgin of eukaryotes. Annu. Rev. Genetics. (1999) 33:351–397.[CrossRef][Web of Science][Medline]

  7. Burger G, Gray MW, Lang BF. Mitochondrial genomes: anything goes. Trends Genet. (2003) 19:709–716.[CrossRef][Web of Science][Medline]

  8. Koski LB, Gray MW, Lang BF, Burger G. AutoFACT: an automatic functional annotation and classification tool. BMC Bioinform. (2005) 6:151.[CrossRef][Medline]

  9. Covello PS, Gray MW. RNA editing in plant mitochondria. Nature (1989) 341:662–666.[CrossRef][Web of Science][Medline]

  10. Benne R, Van den Burg J, Brakenhoff JP, Sloof P, Van Boom JH, Tromp MC. Major transcript of the frameshifted coxII gene from trypanosome mitochondria contains four nucleotides that are not encoded in the DNA. Cell (1986) 46:819–826.[CrossRef][Web of Science][Medline]

  11. Hoch B, Maier RM, Appel K, Igloi GL, Kössel H. Editing of a chloroplast mRNA by creation of an initiation codon. Nature (1991) 353:178–180.[CrossRef][Web of Science][Medline]

  12. Attimonelli M, Acceturro M, Santamaria M, Lascaro D, Scioscia G, Pappad G, Russo L, Zanchetta L, Tommaseo-Ponzetta M. HmtDB, a human mitochondrial genomic resource based on variability studies supporting population genetics and biomedical research. BMC Bioinform. (2005) 1:S4.

  13. Wheeler DL, Barrett T, Benson DA, Bryant SH, Canese K, Chetvernin V, Church DM, Dicuccio M, Edgar R, Federhen S, et al. Database resources of the National Center for Biotechnology Information. Nucleic Acids Res. (2008) 36:D13–D21.[Abstract/Free Full Text]

  14. Ruiz-Pesini E, Lott MT, Procaccio V, Poole JC, Brandon MC, Mishmar D, Yi C, Kreuziger J, Baldi P, Wallace DC. An enhanced MITOMAP with a global mtDNA mutational phylogeny. Nucleic Acids Res. (2007) 35:D823–D828.[Abstract/Free Full Text]

  15. Merali Z, Giles G. Databases in peril. Nature (2005) 23:1010–1011.


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