Important note: Information in this article was accurate in 1993. The state of the art may have changed since the publication date.
Ribozyme-mediated cleavage of an HIV-1 gag RNA: the effects of nontargeted sequences and secondary structure on ribozyme cleavage activity.
Antisense Res Dev. 1991 Summer;1(2):173-86. Unique Identifier : AIDSLINE MED/93044231 Taylor NR; Rossi JJ; Department of Molecular Genetics, Beckman Research Institute of; the City of Hope, Duarte, CA 91010.
Abstract:
Catalytic antisense RNAs, or ribozymes, have great potential as inhibitors of gene expression and as antiviral therapeutic agents. The major advantage of ribozymes versus standard antisense RNAs is their catalytic capability, enabling these RNAs to cleave multiple substrates. We have been investigating the antiviral activity of ribozymes targeted to the HIV-1 genome. The successful use of these antisense agents in an intracellular milieu requires stabilization of the ribozymes by flanking, non-base-pairing sequences, or some modification of the sugar-phosphate backbone. We describe a systematic investigation of the effects of flanking, non-base-pairing sequences on the catalytic activity of an anti-HIV-1 gag ribozyme embedded in radically different transcripts. Amazingly, these complex ribozyme-containing transcripts maintain substantial catalytic activity. Finally, we describe a bacterial gene fusion system that has potential for the large scale production of catalytically active ribozymes.
Keywords: Base Sequence Cloning, Molecular Comparative Study Escherichia coli/GENETICS *Genes, gag Genes, Bacterial Genome, Viral HIV-1/*GENETICS/METABOLISM Kinetics Molecular Sequence Data Nucleic Acid Conformation Plasmids Restriction Mapping RNA, Bacterial/GENETICS/METABOLISM RNA, Catalytic/GENETICS/*METABOLISM RNA, Viral/*METABOLISM Support, Non-U.S. Gov't Support, U.S. Gov't, P.H.S. Thermodynamics JOURNAL ARTICLE 930228
M9320847
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