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Mol Ther. 2005 Sep;12(3):555-61.

Toward a gene therapy for dominant disease: validation of an RNA interference-based mutation-independent approach.

Author information

1
Ocular Genetics Unit, Department of Genetics, Trinity College Dublin, Dublin 2, Ireland. skiang@tcd.ie

Abstract

The intragenic heterogeneity encountered in many dominant disease-causing genes represents a significant challenge with respect to development of economically viable therapeutics. For example, 25% of autosomal dominant retinitis pigmentosa is caused by over 100 different mutations within the gene encoding rhodopsin, each of which could require a unique gene therapy. We describe here an RNA interference (RNAi)-based mutation-independent approach, targeting as an example murine rhodopsin. Native transcripts are suppressed by a single RNAi molecular species, whereas transcripts from replacement genes engineered at degenerate third-codon wobble positions are resistant to suppression. We demonstrate suppression of murine rhodopsin transcript by up to 90% with full concomitant expression of replacement transcript and establish the validity of this approach in cell culture, retinal explants, and mouse liver in vivo.

PMID:
15967729
DOI:
10.1016/j.ymthe.2005.03.028
[Indexed for MEDLINE]
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