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Genome Biol DOI:10.1186/gb-2008-9-3-r50

Cross-kingdom patterns of alternative splicing and splice recognition.

Publication TypeJournal Article
Year of Publication2008
AuthorsMcGuire, AM, Pearson, MD, Neafsey, DE, Galagan, JE
JournalGenome Biol
Volume9
Issue3
PagesR50
Date Published2008
ISSN1474-760X
KeywordsAlternative Splicing, Animals, Base Sequence, Evolution, Molecular, Exons, Expressed Sequence Tags, Genome, Introns, Phylogeny, RNA Splice Sites, Transcription, Genetic
Abstract

BACKGROUND: Variations in transcript splicing can reveal how eukaryotes recognize intronic splice sites. Retained introns (RIs) commonly appear when the intron definition (ID) mechanism of splice site recognition inconsistently identifies intron-exon boundaries, and cassette exons (CEs) are often caused by variable recognition of splice junctions by the exon definition (ED) mechanism. We have performed a comprehensive survey of alternative splicing across 42 eukaryotes to gain insight into how spliceosomal introns are recognized.

RESULTS: All eukaryotes we studied exhibit RIs, which appear more frequently than previously thought. CEs are also present in all kingdoms and most of the organisms in our analysis. We observe that the ratio of CEs to RIs varies substantially among kingdoms, while the ratio of competing 3' acceptor and competing 5' donor sites remains nearly constant. In addition, we find the ratio of CEs to RIs in each organism correlates with the length of its introns. In all 14 fungi we examined, as well as in most of the 9 protists, RIs far outnumber CEs. This differs from the trend seen in 13 multicellular animals, where CEs occur much more frequently than RIs. The six plants we analyzed exhibit intermediate proportions of CEs and RIs.

CONCLUSION: Our results suggest that most extant eukaryotes are capable of recognizing splice sites via both ID and ED, although ED is most common in multicellular animals and ID predominates in fungi and most protists.

URLhttp://genomebiology.com/content/9/3/R50
DOI10.1186/gb-2008-9-3-r50
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/18321378?dopt=Abstract

Alternate JournalGenome Biol.
PubMed ID18321378
PubMed Central IDPMC2397502
Grant ListHHSN26620040001C / / PHS HHS / United States