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pubmed-article:10023439pubmed:abstractTextRecombinant adeno-associated virus (rAAV) vectors hold promise for treating a number of neurological disorders due to the ability to deliver long-term gene expression without toxicity or immune response. Critical to these endeavors will be controlled expression of the therapeutic gene in target cells. We have constructed and tested a dual cassette rAAV vector carrying a reporter gene under the control of the tetracycline-responsive system and the tetracycline transactivator. Transduction in vitro resulted in stable expression from the vector that can be suppressed 20-fold by tetracycline treatment. In vivo experiments, carried out to 6 weeks, demonstrated that vector-transduced expression is sustained until doxycycline administration upon which reporter gene expression is reduced. Moreover, the suppression of vector-driven expression can be reversed by removal of the drug. These studies demonstrate long-term regulated gene expression from rAAV vectors. This system will provide a valuable approach for controlling vector gene expression both in vitro and in vivo.lld:pubmed
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pubmed-article:10023439pubmed:authorpubmed-author:SamulskiR JRJlld:pubmed
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pubmed-article:10023439pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:10023439pubmed:articleTitleInducible long-term gene expression in brain with adeno-associated virus gene transfer.lld:pubmed
pubmed-article:10023439pubmed:affiliationUNC Gene Therapy Center, University of North Carolina, Chapel Hill 27599, USA.lld:pubmed
pubmed-article:10023439pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:10023439pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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