Scrambled exons

Janice M. Nigro, Kathleen R. Cho, Eric R. Fearon, Scott E. Kern, J. Michael Ruppert, Jonathan D. Oliner, Kenneth W. Kinzler, Bert Vogelstein

Research output: Contribution to journalArticle

Abstract

Using a sensitive assay for RNA expression, we identified several abnormally spliced transcripts in which exons from a candidate tumor suppressor gene (DCC) were scrambled during the splicing process in vivo. Cloning and sequencing of PCR-amplified segments of the abnormally spliced transcripts showed that exons were joined accurately at consensus splice sites, but in an order different from that present in the primary transcript. Four scrambled transcripts were identified, each involving a different pair of exons. The scrambled transcripts were found at relatively low levels in a variety of normal and neoplastic cells of rodent and human origin, primarily in the nonpolyadenylated component of cytoplasmic RNA. These results demonstrate that the splicing process does not always pair sequential exons in the order predicted from their positions in genomic DNA, thus creating a novel type of RNA product.

Original languageEnglish (US)
Pages (from-to)607-613
Number of pages7
JournalCell
Volume64
Issue number3
DOIs
StatePublished - Feb 8 1991

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ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)

Cite this

Nigro, J. M., Cho, K. R., Fearon, E. R., Kern, S. E., Ruppert, J. M., Oliner, J. D., Kinzler, K. W., & Vogelstein, B. (1991). Scrambled exons. Cell, 64(3), 607-613. https://doi.org/10.1016/0092-8674(91)90244-S