Abstract
Background: Alternative RNA splicing allows cells to produce multiple protein isoforms from one gene. These isoforms may have specialized functions, and may be tissue- or stage-specific. Our aim was to use computational analysis of SAGE and genomic data to predict alternatively spliced transcripts expressed in C. elegans. Results: We predicted novel alternatively spliced variants and confirmed five of eighteen candidates selected for experimental validation by RT-PCR tests and DNA sequencing. Conclusion: We show that SAGE data canbe efficiently used to discover alternative mRNA isoforms, including those with skipped exons or retained introns. Our results also imply that C. elegans may produce a larger number of alternatively spliced transcripts than initially estimated. © 2007 Ruzanov et al; licensee BioMed Central Ltd.
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Ruzanov, P., Jones, S. J., & Riddle, D. L. (2007). Discovery of novel alternatively spliced C. elegans transcripts by computational analysis of SAGE data. BMC Genomics, 8. https://doi.org/10.1186/1471-2164-8-447
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