| Literature DB >> 23395799 |
Hitoshi Suzuki1, Toshiki Kameyama, Kenji Ohe, Toshifumi Tsukahara, Akila Mayeda.
Abstract
The mechanisms by which huge human introns are spliced out precisely are poorly understood. We analyzed large intron 7 (110199 nucleotides) generated from the human dystrophin (DMD) pre-mRNA by RT-PCR. We identified branching between the authentic 5' splice site and the branch point; however, the sequences far from the branch site were not detectable. This RT-PCR product was resistant to exoribonuclease (RNase R) digestion, suggesting that the detected lariat intron has a closed loop structure but contains gaps in its sequence. Transient and concomitant generation of at least two branched fragments from nested introns within large intron 7 suggests internal nested splicing events before the ultimate splicing at the authentic 5' and 3' splice sites. Nested splicing events, which bring the authentic 5' and 3' splice sites into close proximity, could be one of the splicing mechanisms for the extremely large introns.Entities:
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Year: 2013 PMID: 23395799 DOI: 10.1016/j.febslet.2013.01.057
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124