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pubmed-article:20833635pubmed:abstractTextDNAzymes are easier to prepare and less sensitive to chemical and enzymatic degradation than ribozymes; however, a DNA enzyme expression system has not yet been developed. In this study, we exploited the mechanism of HIV-1 reverse transcription (RT) in a DNA enzyme expression system. We constructed HIV-1 RT-dependent lentiviral DNAzyme expression vectors including the HIV-1 primer binding site, the DNA enzyme, and either a native tRNA (Lys-3), tR(M)DtR(L), or one of two truncated tRNAs (Lys-3), tR(M)D?ARMtR(L) or tR(M)D3'-endtR(L). Lentiviral vector-mediated DNAzyme expression showed high levels of inhibition of HIV-1 replication in SupT1 cells. We also demonstrated the usefulness of this approach in a long-term assay, in which we found that the DNAzymes prevented escape from inhibition of HIV. These results suggest that HIV-1 RT-dependent lentiviral vector-derived DNAzymes prevent the emergence of escape mutations.lld:pubmed
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pubmed-article:20833635pubmed:authorpubmed-author:YamamotoNorio...lld:pubmed
pubmed-article:20833635pubmed:authorpubmed-author:TakakuHiroshi...lld:pubmed
pubmed-article:20833635pubmed:authorpubmed-author:HayafuneMasaa...lld:pubmed
pubmed-article:20833635pubmed:authorpubmed-author:HabuYuichiroYlld:pubmed
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pubmed-article:20833635pubmed:articleTitleHIV-1 RT-dependent DNAzyme expression inhibits HIV-1 replication without the emergence of escape viruses.lld:pubmed
pubmed-article:20833635pubmed:affiliationDepartment of Life and Environmental Science, Chiba Institute of Technology, Narashino-shi, Chiba, Japan.lld:pubmed
pubmed-article:20833635pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:20833635pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed