Alu -Containing Exons are Alternatively Spliced
Citations Over Time
Abstract
Alu repetitive elements are found in approximately 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 of Alu 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 the Alu-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 an Alu 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.
Related Papers
- → Complete exon-intron organization of the human leukocyte common antigen (CD45) gene.(1988)106 cited
- → Human cystathionine β-synthase: gene organization and expression of different 5′ alternative splicing(1997)17 cited
- → Identification of an Alu-mediated tandem duplication of exons 8 and 9 in a patient with mitochondrial acetoacetyl-CoA thiolase (T2) deficiency(2007)17 cited
- → Novel cryptic exons identified in introns 2 and 3 of the human dystrophin gene with duplication of exons 8-11.(2006)6 cited
- → Organization, structure and alternate splicing of the murine RFC-1 gene encoding a folate transporter(1997)31 cited