Alu-Containing Exons are Alternatively Spliced

  1. Rotem Sorek1,2,4,
  2. Gil Ast3, and
  3. Dan Graur1
  1. 1Department of Zoology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Ramat Aviv 69978, Israel; 2Compugen, Tel Aviv 69512, Israel; 3Department of Human Genetics, Sackler Faculty of Medicine, Tel Aviv University, Ramat Aviv 69978, Israel

Abstract

Alu repetitive elements are found in ∼1.4 million copies in the human genome, comprising more than one-tenth of it. Numerous studies describe exonizations of Alu elements, that is, splicing-mediated insertions of parts of Alu sequences into mature mRNAs. To study the connection between the exonization ofAlu elements and alternative splicing, we used a database of ESTs and cDNAs aligned to the human genome. We compiled two exon sets, one of 1176 alternatively spliced internal exons, and another of 4151 constitutively spliced internal exons. Sixty one alternatively spliced internal exons (5.2%) had a significant BLAST hit to an Alu sequence, but none of the constitutively spliced internal exons had such a hit. The vast majority (84%) of theAlu-containing exons that appeared within the coding region of mRNAs caused a frame-shift or a premature termination codon.Alu-containing exons were included in transcripts at lower frequencies than alternatively spliced exons that do not contain anAlu sequence. These results indicate that internal exons that contain an Alu sequence are predominantly, if not exclusively, alternatively spliced. Presumably, evolutionary events that cause a constitutive insertion of an Alu sequence into an mRNA are deleterious and selected against.

Footnotes

  • 4 Corresponding author.

  • E-MAIL rotem{at}compugen.co.il; FAX +972-3-6409403.

  • Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.229302.

    • Received December 19, 2001.
    • Accepted May 8, 2002.
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