- Open Access
Annotation, submission and screening of repetitive elements in Repbase: RepbaseSubmitter and Censor
© Kohany et al; licensee BioMed Central Ltd. 2006
- Received: 23 May 2006
- Accepted: 25 October 2006
- Published: 25 October 2006
Repbase is a reference database of eukaryotic repetitive DNA, which includes prototypic sequences of repeats and basic information described in annotations. Updating and maintenance of the database requires specialized tools, which we have created and made available for use with Repbase, and which may be useful as a template for other curated databases.
We describe the software tools RepbaseSubmitter and Censor, which are designed to facilitate updating and screening the content of Repbase. RepbaseSubmitter is a java-based interface for formatting and annotating Repbase entries. It eliminates many common formatting errors, and automates actions such as calculation of sequence lengths and composition, thus facilitating curation of Repbase sequences. In addition, it has several features for predicting protein coding regions in sequences; searching and including Pubmed references in Repbase entries; and searching the NCBI taxonomy database for correct inclusion of species information and taxonomic position. Censor is a tool to rapidly identify repetitive elements by comparison to known repeats. It uses WU-BLAST for speed and sensitivity, and can conduct DNA-DNA, DNA-protein, or translated DNA-translated DNA searches of genomic sequence. Defragmented output includes a map of repeats present in the query sequence, with the options to report masked query sequence(s), repeat sequences found in the query, and alignments.
- Transposable Element
- Query Sequence
- Repetitive Element
- Simple Repeat
- Java Virtual Machine
Repbase is the most widely used database of transposable elements, with ~5800 entries as of October 2006, representing over 40 superfamilies of DNA transposons, LTR and non-LTR retrotransposons, and endogenous retroviruses . The current version of Repbase is based on a flexible and extensible relational database schema implemented in mySQL. Ongoing large-scale sequencing of eukaryotic genomes has resulted in a rapid increase in the rate at which new transposable elements are discovered. Rather than relying on error-prone automated processing, the philosophy behind Repbase has been to incorporate a significant amount of manual curation into the database. However, the increasing number of sequences to be annotated and entered led us to develop a standardized submission interface that external users can use to provide information on their sequences, with a minimum of subsequent reformatting being necessary.
Repbase is primarily being used for screening and annotation of genomic DNA. Censor was the first program for Repbase-based repeat detection and masking, originally released in 1994 and later published . Its major drawback was inefficient implementation of the Smith-Waterman algorithm and, therefore, the publicly accessible Censor server ran exclusively on specialized Paracel hardware. In the meantime, other programs, notably RepeatMasker [3, 4], and blaster  became available. RepeatMasker uses a customized version of the Repbase library that can sometimes have significant differences from the original Repbase submission. Furthermore, Censor can be used to search DNA sequences against a library of proteins, or translated nucleotide sequences.
Manual curation of databases has both advantages and drawbacks compared to automated processing. Automatic annotation has the significant advantage of much higher potential throughput, freedom from user error, and elimination of unintended bias in the processing. On the other hand, it is hard to anticipate every contingency in, for example, correct reconstruction of consensus sequences. A particular problem with automated reconstruction of transposable elements is over-fragmentation, where algorithms do not correctly assemble related parts of an element into a complete consensus. The principal source of mistakes in manual curation is user error in entering data. All complex data such as taxonomy, literature references, transposable element classifications are potentially problematic, since simple misspellings can render a database entry unretrievable based on exact string-based searches.
For these reasons, we have chosen to adopt a hybrid approach: keeping the positive aspects of manual curation, while attempting to eliminate the most common sources of user-supplied errors, by automating the import and annotation of complex, but well-defined information including taxonomic information, referencing, etc. The purpose of RepbaseSubmitter is to provide an easy to use interface that permits flexibility in annotation, while at the same time reducing the scope for mistakes in the manual curation process.
RepbaseSubmitter is implemented in Java (requires Java Virtual Machine version 1.5 or above). The interface is structured around six data entry pages, together with an initialization page for creating a new entry, and a final submission page for performing checks and submitting to Repbase. New entries are not directly entered into Repbase, but are submitted to a review database for editorial approval and additional curation.
The new version of Censor described here uses an unaltered version of Repbase (as well as user-supplied libraries if desired), and is composed of Perl and C++ modules for identification of both interspersed and tandem repeats using similarity searches. Censor analyzes DNA/RNA sequences for repeats and provides a description of repetitive elements from their Repbase Update annotation . Censor can optionally use either WU-BLAST or NCBI BLAST as its search engine, and can perform both direct NA-NA searches, as well as any combination of protein-NA or translated NA searches using the appropriate BLAST modules.
The downloadable version of Censor can be installed on virtually any UNIX system (including Mac OSX) with Perl and a C++ compiler, that has WU-BLAST or NCBI BLAST installed. It can also utilize symmetric multiprocessor machines. Censor uses BLAST to detect similarity between repeat libraries and nucleic acid (NA) or protein sequences. For simple NA-NA searches, BLASTN is used (the default). For more sensitive detection of distantly-related protein coding sequences, a six-frame search (using TBLASTX) or protein-NA search (TBLASTN) is available. Censor offers three sensitivity modes: normal, rough and sensitive, each offering a different balance of sensitivity and speed. The difference in performance is determined by the BLAST search parameters (see Additional file 1). Censor automatically determines the type (NA or protein) of input sequences by calculating base composition, and calls the appropriate BLAST program, although this behavior can be overridden as described below. Censor relies on some standard UNIX system commands. For that reason a Unix/Linux operating system is required. Censor requires Perl to work, which is standard on most UNIX systems. WU-BLAST (recommended) or NCBI-BLAST is required to perform searches. If the BLAST installation directory is on the user's path, the configuration script will automatically detect it and assign corresponding variables. Otherwise, users must manually edit the header of Censor's main script to provide this information. GCC or another C++ compiler, and "make' utility, are required to build the Censor distribution.
Data entry pages in RepbaseSubmitter.
Data Entry Form
Specification of entry Accession, Keywords, Definition, Comments
Entry of sequence, calculation of DNA content and lengths
Source organism/taxonomy; classification based on current Repbase structure
Specification of coding regions: prediction of ORFs, annotation on DNA sequence, comments describing protein features/functions
Relevant references to primary literature or databases (Repbase or external such as Genbank, EMBL)
Repbase release, relevant database accessions; consensus references
Display of final version prior to submission, perform final checks, submit to relational database for review
Current Repbase schema for transposable element classification.
Mariner, hAT, MuDR, EnSpm, piggyback, P, Merlin, Harbinger, Transib, Novosib, Mirage, Helitron, Polinton, Rehavkus
Gypsy, Copia, DIRS, BEL
ERV1, ERV2, ERV3
LINE1 (L1), RTE-1, CRE, CR1 (LINE3), I, Jockey, NeSL, R2, R4, Rex1, RandI, Penelope
Satellites (SAT, MSAT)
The Sequence entry page is the simplest, and requires only the sequence data to be input. If a DNA or RNA sequence was loaded from file at the initial entry creation page, it will be displayed here. Otherwise, sequence data can be cut-and-pasted into the window. The base count and composition of the sequence is automatically updated and entered. Sequences can also be complemented, if it is determined that the other strand is more appropriate (for example, if it encodes proteins for autonomous elements).
An important feature of Repbase is the ability to supply references to appropriate scientific literature, or to other Repbase entries and other databases. The submission interface facilitates both types of referencing. References to scientific literature can be added manually i.e. by supplying authors, title, journal etc. in the normal manner; however, in this case entries are not automatically verified in any way. As an alternative, RepbaseSubmitter provides an "Import" option on the References entry page. This allows users to specify partial information such as author names, article title, journal name, and then search the NCBI Pubmed database . A list of matching references is returned, and multiple selections can be made from this list and included in the Repbase entry. In this way, references to literature will correspond exactly to how they appear in Pubmed, which can substantially eliminate errors due to mistyping of reference information. In some cases, a particular reference may only apply to part of a sequence. This is often true if the sequence currently being entered is an extension of a previously-existing partial Repbase entry; or if the element being annotated combines information that has been reported fragmentarily in multiple locations. A reference may also be to another database such as Genbank or EMBL, or to another Repbase entry. In this case, the user needs to supply the author information manually. If the creation of this Repbase entry represents new work, the user will generally want to supply a title, and submit it to Repbase Reports. Entries already described in another publication should be directed to Repbase Update. Repbase Reports provides a medium for publication of novel transposable elements in an online journal form, so that the work may be referred to in other publications. Finally, the Reference page provides an option for "Free Text" references, for those cases which do not correspond to traditional journal references, or links to those databases specifically recognized by Repbase.
The Release and Accessions page summarizes the information supplied on the References page, primarily to allow selection of a primary reference for sequences which are consensi. Additionally, it is possible to specify a "creation date" for this Repbase entry (generally the current date); and a "last update" which will be the same as the creation data for a new sequence, but may be different if this is a refinement of a pre-existing Repbase element. This section is also the appropriate place to specify accession number(s) linking to other databases (Genbank etc.) – one accession number will be the primary accession for the sequence.
The last screen of the submission interface is for actual submission to the Repbase review database. The database entry as it will appear in native Repbase (EMBL) format is displayed, and may be saved to a file. Upon selecting "submit", the entry is checked for correct formatting, and basic consistency such as unique Repbase accession and sequence information; and is then entered into the mySQL database for approval
Pre-processing of data
Before performing each search, input data is checked and formatted. Censor automatically chops long sequences into smaller fragments to reduce BLAST memory requirements and to facilitate splitting of jobs on multiple processor machines. Base composition is calculated for query and database sequences, and based on the total percentage of ATCGN bases, Censor decides whether each sequence is nucleotide or protein. This information is used in automatic selection of the BLAST search program – BLASTN, BLASTP, BLASTX or TBLASTN. In order to run a translated versus translated search of nucleotide against nucleotide sequences, TBLASTX must be specified as the search program (otherwise BLASTN is used). By default, simple tandem repeats are masked using filter modules prior to similarity searching, to prevent false hits. Two approaches are available for dealing with simple repeats. The built-in BLAST filters, SEG and DUST, can be applied in initial sequence processing. However this prevents identification of simple repeats in the Censor output. Another approach is to mask them by first BLASTing the query sequence against a library of simple repeats, which is included with the Censor distribution. In this case simple repeats will be reported in the program's output. Both filtering functions can be disabled if required, but this is not recommended, since it can lead to a significant proportion of false hits between the query sequence and simple repeats that are internal parts of repetitive elements curated in Repbase. However, disabling annotation of simple repeats can lead to a significant decrease in overall processing time.
In the main search phase, Censor uses BLAST to compare the input sequence to annotated repetitive elements in Repbase, or a custom user-supplied library. There are two separately developed and maintained versions of BLAST available: WU-BLAST, copyrighted and maintained by Washington University , and a free version developed by NCBI . Both versions have their advantages and disadvantages. WU-BLAST is faster than NCBI BLAST, and has more options, making it very flexible. However WU-BLAST requires licensing from commercial companies and academic users (this can be done online for the latter), while NCBI BLAST is free for all users. As a result, we created two versions of standalone Censor, with parameters optimized for each version of BLAST. A web-based Censor server is also available, which uses WU-BLAST solely. The default WU-BLAST parameters for Censor's "normal", "sensitive", and "rough" modes are described in the Supplementary Material (see Additional file 1). In addition, all BLAST parameters can be overridden by specification on the command line of standalone Censor. The query sequence is scanned against each library of repeats specified using Censor's "-lib" option, in the order in which they are listed. After processing each library, detected repeats are masked out from the query sequence before comparison to the next library.
Post-processing and output
Maps include simple repeats unless the "-nosimple" option was specified. The web-based version of Censor provides a graphical representation of the map in SVG (Scalable Vector Graphics) format, with colour-coding of different repeat types. By default, Censor also produces a ".masked" file containing the original sequence with all detected repeats masked out; and a ".found" file containing the genomic sequence fragments that were detected as matching a known repeat. General information on the query sequence(s) and their repeat content is stored in ".tab" files.
Finally optional tasks are performed, including classification of repeats into subfamilies based on maximum similarity to consensus sequences. Currently the Censor distribution supports only classification of human ALU subfamilies. However other repeat families can be classified after an easy setup process that requires a list of consensus sequences and a hierarchy of subfamilies. A complete description of Censor parameters can be found in the program documentation. Details of BLAST parameters for the available sensitivity modes are given in the Supplementary Material (see Additional file 1).
The resulting new package, RepbaseSubmitter, facilitates and automates many aspects of Repbase entry creation and maintenance. The program performs numerous checks on formatting of entries, and consistent entry of certain data fields; as well as ensuring that required data are provided.
Project name: Censor
Project home page: http://www.girinst.org/censor/index.php
Operating system(s): Unix/Linux
Programming language: Perl, C++
Any restrictions to use by non-academics: None
Project name: RepbaseSubmitter
Project home page: http://www.girinst.org/repbase/submission.html
Operating system(s): Any, with Java Virtual Machine 1.5 or above
Programming language: Java
Other requirements: Java 1.5 or higher
Any restrictions to use by non-academics: None
Development of Censor was supported by National Institutes of Health grant 5 P41 LM006252-08. We would like to thank Jolanta Walichiewicz for help with preparing the manuscript.
- Jurka J, Kapitonov VV, Pavlicek A, Klonowski P, Kohany O, Walichiewicz J: Repbase Update, a database of eukaryotic repetitive elements. Cytogenet Genome Res 2005, 110: 462–7. 10.1159/000084979View ArticlePubMedGoogle Scholar
- Jurka J, Klonowski P, Dagman V, Pelton P: CENSOR – a program for identification and elimination of repetitive elements from DNA sequences. Comput Chem 1996, 20: 119–21. 10.1016/S0097-8485(96)80013-1View ArticlePubMedGoogle Scholar
- Smit AFA, Hubley R, Green P: 1996–2006 RepeatMasker Open-3.0.1996. [http://www.repeatmasker.org]Google Scholar
- Bedell JA, Korf I, Gish W: MaskerAid: a performance enhancement to RepeatMasker. Bioinformatics 2000, 16: 1040–1041. 10.1093/bioinformatics/16.11.1040View ArticlePubMedGoogle Scholar
- Quesneville H, Nouaud D, Anxolabehere D: Detection of new transposable element families in Drosophila melanogaster and Anopheles gambiae genomes. J Mol Evol 2003, 57(Suppl 1):S50–9. 10.1007/s00239-003-0007-2View ArticlePubMedGoogle Scholar
- NCBI Taxonomy Browser2003. [http://www.ncbi.nlm.nih.gov/Taxonomy/taxonomyhome.html]
- NCBI PubMed2003. [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed]
- Washington University BLAST Archives2003. [http://blast.wustl.edu]
- Reese JT, Pearson WR: Empirical determination of effective gap penalties for sequence comparison. Bioinformatics 2002, 18(11):1500–7. 10.1093/bioinformatics/18.11.1500View ArticlePubMedGoogle Scholar
- Rivas E: Evolutionary models for insertions and deletions in a probabilistic modeling framework. BMC Bioinformatics 2005, 6: 63. 10.1186/1471-2105-6-63PubMed CentralView ArticlePubMedGoogle Scholar
- Vingron M, Waterman MS: Sequence alignment and penalty choice. Review of concepts, case studies and implications. J Mol Biol 1994, 235(1):1–12. 10.1016/S0022-2836(05)80006-3View ArticlePubMedGoogle Scholar
- Altschul SF, Madden TL, Schäffer AA, Zhang J, Zhang Z, Miller W, Lipman DJ: Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 1997, 25: 3389–3402. 10.1093/nar/25.17.3389PubMed CentralView ArticlePubMedGoogle Scholar
- Smith TF, Waterman MS: Identification of common molecular sub sequences. J Mol Biol 1981, 147: 195–198. 10.1016/0022-2836(81)90087-5View ArticlePubMedGoogle 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.