Abstract
We have developed RNA molecules capable of effecting spliceosome- mediated RNA trans-splicing reactions with a target messenger RNA precursor (pre-mRNA). Targeted trans-splicing was demonstrated in a HeLa nuclear extract, cultured human cells, and H1299 human lung cancer tumors in athymic mice. Trans-splicing between a cancer-associated pre-mRNA encoding the β- subunit of human chorionic gonadotropin gene 6 and pre-trans-splicing molecule (PTM) RNA was accurate both in vitro and in vivo. Comparison of targeted versus nontargeted trans-splicing revealed a moderate level of specificity, which was improved by the addition of an internal inverted repeat encompassing the PTM splice site. Competition between cis- and trans- splicing demonstrated that cis-splicing can be inhibited by trans-splicing. RNA repair in a splicing model of a nonfunctional lacZ transcript was effected in cells by a PTM, which restored significant β-galactosidase activity. These observations suggest that spliceosome-mediated RNA trans- splicing may represent a general approach for reprogramming the sequence of targeted transcripts, providing a novel approach to gene therapy.
Original language | English (US) |
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Pages (from-to) | 246-252 |
Number of pages | 7 |
Journal | Nature Biotechnology |
Volume | 17 |
Issue number | 3 |
DOIs | |
State | Published - 1999 |
Externally published | Yes |
Keywords
- Gene therapy
- RNA repair
- Spliceosome
- Trans-splicing
ASJC Scopus subject areas
- Microbiology