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Bioinformatics Advance Access published online on November 24, 2005

Bioinformatics, doi:10.1093/bioinformatics/bti795
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© The Author (2005). Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org
Received July 20, 2005
Revised November 3, 2005
Accepted November 18, 2005

Article

Bioinformatic analysis of exon repetition, exon scrambling and trans-splicing in humans

Xiang Shao 1, Valery Shepelev 2, and Alexei Fedorov 3 *

1 Department of Medicine and Program in Bioinformatics and Proteomics/Genomics, Medical University of Ohio, Toledo, OH 43614, USA; Present address: Zebrafish Information Network, University of Oregon, Eugene, OR 97403-5291
2 Department of Bioinformatics, Institute of Molecular Genetics, RAS, Moscow 123182, Russia
3 Department of Medicine and Program in Bioinformatics and Proteomics/Genomics, Medical University of Ohio, Toledo, OH 43614, USA

* To whom correspondence should be addressed.
Alexei Fedorov, E-mail: afedorov{at}meduohio.edu


   Abstract

Motivation: Using bioinformatic approaches we aimed to characterize poorly-understood abnormalities in splicing known as exon scrambling, exon repetition, and trans-splicing.

Results: We developed a software package that allows large-scale comparison of all human EST sequences to the entire set of human gene sequences. Among 5,992,495 Expressed Sequence Tag (EST) sequences, 401 cases of exon repetition and 416 cases of exon scrambling were found. The vast majority of identified ESTs contains fragments rather than full-length repeated or scrambled exons. Their structures suggest that the scrambled or repeated exon fragments may have arisen in the process of cDNA cloning and not from splicing abnormalities. Nevertheless, we found 11 cases of full-length exon repetition showing that this phenomenon is real yet very rare. In searching for examples of trans-splicing, we looked only at reproducible events where at least two independent ESTs represent the same putative trans-splicing event. We found 15 ESTs representing five types of putative trans-splicing. However, all 15 cases were derived from human malignant tissues and could have resulted from genomic rearrangements. Our results provide support for a very rare but physiological occurrence of exon repetition, but suggest that apparent exon scrambling and trans-splicing result respectively from in vitro artifact and gene-level abnormalities.

Availability: Exon-Intron Database (EID) at http://www.meduohio.edu/bioinfo/eid.

Programs and supplementary file at http://www.meduohio.edu/bioinfo/software.html.

Lab website at http://www.meduohio.edu/medicine/fedorov.


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