Abstract
We mapped the collection of The Institute of Physical and Chemical Research (Japan) (RIKEN) 21,076 full-length mouse cDNA clone sequences and the mouse RefSeq sequences to the recently completed draft of the mouse genome. Using this mapping, we identified 3674 mouse genes with multiple transcripts, of which 1098 have splice variants. All but 532 of 21,076 clones (97.5%) mapped to the genome assembly. Alignments of cDNA clone sequences with proteins show that much of the detected splice variation alters coding regions and affects the translated protein. We developed novel analytical techniques to classify observed splice variation and to assess the relation between splice variation and alternative transcription. This analysis indicates that an alternative choice of transcription start or polyadenylation signal frequently induces splice variation.
MeSH Terms
Alternative Splicing/genetics,physiology
Animals
Chromosome Mapping/methods
Codon, Terminator/genetics
DNA, Complementary/genetics
Exons/genetics,physiology
Genes/genetics,physiology
Genetic Variation/genetics,physiology
Genome
Introns/genetics
Mice
Transcription Initiation Site
Chemicals
Codon, Terminator
DNA, Complementary
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Zavolan Mihaela
Laboratory for Computational Genomics, The Rockefeller University, New York, New York 10021, USA. mihaela@genomes.rockefeller.edu
van Nimwegen Erik
Gaasterland Terry
References (18)
18 references, click to expand
-
Functional annotation of a full-length mouse cDNA collection.
Nature. 2001 Feb 8;409(6821):685-90
PMID: 11217851
-
SPLASH (PLA2IID), a novel member of phospholipase A2 family, is associated with lymphotoxin deficiency.
Genes Immun. 2000 Feb;1(3):191-9
PMID: 11196711
-
Gene structure prediction and alternative splicing analysis using genomically aligned ESTs.
Genome Res. 2001 May;11(5):889-900
PMID: 11337482
-
Assembly, annotation, and integration of UNIGENE clusters into the human genome draft.
Genome Res. 2001 May;11(5):904-18
PMID: 11337484
-
Coordination between transcription and pre-mRNA processing.
FEBS Lett. 2001 Jun 8;498(2-3):179-82
PMID: 11412852
-
Genome-wide detection of alternative splicing in expressed sequences of human genes.
Nucleic Acids Res. 2001 Jul 1;29(13):2850-9
PMID: 11433032
-
Computational analysis of full-length mouse cDNAs compared with human genome sequences.
Mamm Genome. 2001 Sep;12(9):673-7
PMID: 11641714
-
Basic local alignment search tool.
J Mol Biol. 1990 Oct 5;215(3):403-10
PMID: 2231712
-
dbEST--database for "expressed sequence tags".
Nat Genet. 1993 Aug;4(4):332-3
PMID: 8401577
-
Fully automated genome analysis that reflects user needs and preferences. A detailed introduction to the MAGPIE system architecture.
Biochimie. 1996;78(5):302-10
PMID: 8905148
-
A computer program for aligning a cDNA sequence with a genomic DNA sequence.
Genome Res. 1998 Sep;8(9):967-74
PMID: 9750195
-
GenBank.
Nucleic Acids Res. 2000 Jan 1;28(1):15-8
PMID: 10592170
-
Frequent alternative splicing of human genes.
Genome Res. 1999 Dec;9(12):1288-93
PMID: 10613851
-
ISIS, the intron information system, reveals the high frequency of alternative splicing in the human genome.
Nat Genet. 2000 Apr;24(4):340-1
PMID: 10742092
-
Using GeneWise in the Drosophila annotation experiment.
Genome Res. 2000 Apr;10(4):547-8
PMID: 10779496
-
RefSeq and LocusLink: NCBI gene-centered resources.
Nucleic Acids Res. 2001 Jan 1;29(1):137-40
PMID: 11125071
-
SpliceDB: database of canonical and non-canonical mammalian splice sites.
Nucleic Acids Res. 2001 Jan 1;29(1):255-9
PMID: 11125105
-
An alternative-exon database and its statistical analysis.
DNA Cell Biol. 2000 Dec;19(12):739-56
PMID: 11177572