Spliceosome-mediated RNA trans-splicing as a tool for gene therapy

被引:154
作者
Puttaraju, M
Jamison, SF
Mansfield, SG
Garcia-Blanco, MA [1 ]
Mitchell, LG
机构
[1] Intronn LLC, Durham, NC 27701 USA
[2] Duke Univ, Med Ctr, Durham, NC 27710 USA
关键词
spliceosome; trans-splicing; gene therapy; RNA repair;
D O I
10.1038/6986
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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 p-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 transsplicing. RNA repair In a splicing model of a nonfunctional lacZ transcript was effected in cells by a PTM, which restored significant beta-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.
引用
收藏
页码:246 / 252
页数:7
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