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PMID: 11125105 Published · ppublish English Journal Article

SpliceDB: database of canonical and non-canonical mammalian splice sites.

Nucleic acids research ·Vol. 29 ·No. 1 ·2001-01-01 ·Pages 255-9

Burset M, Seledtsov IA, Solovyev VV

Abstract

A database (SpliceDB) of known mammalian splice site sequences has been developed. We extracted 43 337 splice pairs from mammalian divisions of the gene-centered Infogene database, including sites from incomplete or alternatively spliced genes. Known EST sequences supported 22 815 of them. After discarding sequences with putative errors and ambiguous location of splice junctions the verified dataset includes 22 489 entries. Of these, 98.71% contain canonical GT-AG junctions (22 199 entries) and 0.56% have non-canonical GC-AG splice site pairs. The remainder (0.73%) occurs in a lot of small groups (with a maximum size of 0.05%). We especially studied non-canonical splice sites, which comprise 3.73% of GenBank annotated splice pairs. EST alignments allowed us to verify only the exonic part of splice sites. To check the conservative dinucleotides we compared sequences of human non-canonical splice sites with sequences from the high throughput genome sequencing project (HTG). Out of 171 human non-canonical and EST-supported splice pairs, 156 (91.23%) had a clear match in the human HTG. They can be classified after sequence analysis as: 79 GC-AG pairs (of which one was an error that corrected to GC-AG), 61 errors corrected to GT-AG canonical pairs, six AT-AC pairs (of which two were errors corrected to AT-AC), one case was produced from a non-existent intron, seven cases were found in HTG that were deposited to GenBank and finally there were only two other cases left of supported non-canonical splice pairs. The information about verified splice site sequences for canonical and non-canonical sites is presented in SpliceDB with the supporting evidence. We also built weight matrices for the major splice groups, which can be incorporated into gene prediction programs. SpliceDB is available at the computational genomic Web server of the Sanger Centre: http://genomic.sanger.ac. uk/spldb/SpliceDB.html and at http://www.softberry. com/spldb/SpliceDB.html.

MeSH Terms
Animals Base Sequence Databases, Factual Exons Expressed Sequence Tags Genes/genetics Humans Internet Introns RNA Splicing/genetics
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Burset M
The Sanger Centre, Hinxton, Cambridge CB10 1SA, UK and Softberry Inc., 108 Corporate Park Drive, Suite 120, White Plains, NY 10604, USA.
Seledtsov I A
Solovyev V V
References (7)
7 references, click to expand
  1. Ab initio gene finding in Drosophila genomic DNA.
    Genome Res. 2000 Apr;10(4):516-22 PMID: 10779491
  2. Analysis of canonical and non-canonical splice sites in mammalian genomes.
    Nucleic Acids Res. 2000 Nov 1;28(21):4364-75 PMID: 11058137
  3. A reappraisal of non-consensus mRNA splice sites.
    Nucleic Acids Res. 1991 Jul 25;19(14):3795-8 PMID: 1713664
  4. A clean data set of EST-confirmed splice sites from Homo sapiens and standards for clean-up procedures.
    Nucleic Acids Res. 1999 Jul 1;27(13):2627-37 PMID: 10373578
  5. GenBank.
    Nucleic Acids Res. 1999 Jan 1;27(1):12-7 PMID: 9847132
  6. INFOGENE: a database of known gene structures and predicted genes and proteins in sequences of genome sequencing projects.
    Nucleic Acids Res. 1999 Jan 1;27(1):248-50 PMID: 9847192
  7. Human pre-mRNA splicing signals.
    J Theor Biol. 1991 Jun 7;150(3):385-420 PMID: 1798333
Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
1362-4962
Published
2001-01-01
Pages
255-9
Language
English
Region
England
NLM ID
0411011
PMCID
PMC29840
Subset
IM
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