Serine/arginine-rich protein-dependent suppression of exon skipping by exonic splicing enhancers.
basic_science · Level V
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- Record sourced from PubMed, PMID 15753297.
- Also identified by PMC identifier 555999.
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Abstract
The 5' and 3' splice sites within an intron can, in principle, be joined to those within any other intron during pre-mRNA splicing. However, exons are joined in a strict 5' to 3' linear order in constitutively spliced pre-mRNAs. Thus, specific mechanisms must exist to prevent the random joining of exons. Here we report that insertion of exon sequences into an intron can inhibit splicing to the downstream 3' splice site and that this inhibition is independent of intron size. The exon sequences required for splicing inhibition were found to be exonic enhancer elements, and their inhibitory activity requires the binding of serine/arginine-rich splicing factors. We conclude that exonic enhancers can act as barriers to prevent exon skipping and thereby may play a key role in ensuring the correct 5' to 3' linear order of exons in spliced mRNA.
Medical subject headings
- Exons
- Nuclear Proteins
- Phosphoproteins
- RNA Splicing