Abstract
During the last decade, several elegant and disparate RNA-repair strategies have been developed for use as therapeutic interventions. One such approach, spliceosome-mediated RNA trans-splicing (SMaRT™), uses specialized constructs called pre-trans-splicing molecules (PTMs) that can bind to specific endogenous mutant nuclear RNAs and effect a trans-splicing event to create a composite repaired product. This and other RNA modifying technologies are a distinct departure from the traditional gene-therapy approach of ubiquitously expressing a full-length cDNA. RNA repair offers the potential advantages of maintaining endogenous regulation and the elimination of ectopic expression of the transgene. Here, we review the different RNA-repair strategies and discuss the advances that have been made for SMaRT™ technology to date and the potential advantages and limitations of SMaRT™ compared with traditional gene therapy.
| Original language | English |
|---|---|
| Pages (from-to) | 263-268 |
| Number of pages | 6 |
| Journal | Trends in Molecular Medicine |
| Volume | 10 |
| Issue number | 6 |
| DOIs | |
| State | Published - 1 Jun 2004 |
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