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Exon-trapping mediated by the human retrotransposon SVA
- Source :
- Genome Research. 19:1983-1991
- Publication Year :
- 2009
- Publisher :
- Cold Spring Harbor Laboratory, 2009.
-
Abstract
- Although most human retrotransposons are inactive, both inactive and active retrotransposons drive genome evolution and may influence transcription through various mechanisms. In humans, three retrotransposon families are still active, but one of these, SVA, remains mysterious. Here we report the identification of a new subfamily of SVA, which apparently formed after an alternative splicing event where the first exon of the MAST2 gene spliced into an intronic SVA and subsequently retrotransposed. Additional examples of SVA retrotransposing upstream exons due to splicing into SVA were also identified in other primate genomes. After molecular and computational experiments, we found a number of functional 3′ splice sites within many different transcribed SVAs across the human and chimpanzee genomes. Using a minigene splicing construct containing an SVA, we observed splicing in cell culture, along with SVA exonization events that introduced premature termination codons (PTCs). These data imply that an SVA residing within an intron in the same orientation as the gene may alter normal gene transcription either by gene-trapping or by introducing PTCs through exonization, possibly creating differences within and across species.
- Subjects :
- Male
Primates
Genome evolution
Letter
Retroelements
Transcription, Genetic
Green Fluorescent Proteins
Molecular Sequence Data
Retrotransposon
Protein Serine-Threonine Kinases
Biology
Transfection
Cell Line
Exon
Exon trapping
Genetics
Animals
Humans
Protein Kinase C
Genetics (clinical)
Expressed Sequence Tags
Reverse Transcriptase Polymerase Chain Reaction
Alternative splicing
Intron
Exons
Sequence Analysis, DNA
Alternative Splicing
Mutagenesis, Insertional
RNA splicing
RNA Splice Sites
Transcription Initiation Site
Microtubule-Associated Proteins
HeLa Cells
Minigene
Subjects
Details
- ISSN :
- 10889051
- Volume :
- 19
- Database :
- OpenAIRE
- Journal :
- Genome Research
- Accession number :
- edsair.doi.dedup.....20da25edbbb7534def65a6c8ba593263
- Full Text :
- https://doi.org/10.1101/gr.093153.109