Abstract
Ribozymes are potentially very powerful agents for perturbing intracellular gene expression. However, pilot experiments in eukaryotes have met with mixed success. We now report that a ribozyme designed to cleave the integrase gene of the human immunodeficiency virus (HIV), when transcribed from a plasmid in Escherichia coli, led to destruction of integrase RNA and complete blockage of integrase protein synthesis. These results indicate that ribozymes can be used to study intracellular gene expression in bacteria and that the HIV-1 integrase gene may be a useful target for therapeutic ribozymes.
MeSH Terms
Base Sequence
Cloning, Molecular
DNA Nucleotidyltransferases/antagonists & inhibitors,biosynthesis,genetics
Escherichia coli/enzymology,genetics
HIV-1/enzymology,genetics
Integrases
Kinetics
Models, Structural
Molecular Sequence Data
Nucleic Acid Conformation
Plasmids
RNA, Catalytic/metabolism
Recombinant Proteins/antagonists & inhibitors,biosynthesis
Chemicals
RNA, Catalytic
Recombinant Proteins
DNA Nucleotidyltransferases
Integrases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Sioud M
Public Health Research Institute, New York, NY 10016.
Drlica K
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