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Publication Detail

Title: RNAi or overexpression: alternative therapies for Spinocerebellar Ataxia Type 1.

Authors: Keiser, Megan S; Geoghegan, James C; Boudreau, Ryan L; Lennox, Kim A; Davidson, Beverly L

Published In Neurobiol Dis, (2013 Aug)

Abstract: Spinocerebellar Ataxia Type 1 (SCA1) is an autosomal dominant late onset neurodegenerative disease caused by an expanded polyglutamine tract in ataxin-1. Here, we compared the protective effects of overexpressing ataxin-1-like using recombinant AAVs, or reducing expression of mutant ataxin-1 using virally delivered RNA interference (RNAi), in a transgenic mouse model of SCA1. For the latter, we used an artificial microRNA (miR) design that optimizes potency, efficacy and safety to suppress ataxin-1 expression (miS1). Delivery of either ataxin-1-like or miS1 viral vectors to SCA1 mice cerebella resulted in widespread cerebellar Purkinje cell transduction and improved behavioral and histological phenotypes. Our data indicate the utility of either approach as a possible therapy for SCA1 patients.

PubMed ID: 23583610 Exiting the NIEHS site

MeSH Terms: No MeSH terms associated with this publication

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