Abstract
The human immunodeficiency virus-1 transactivator protein (tat) was codelivered efficiently with a reporter gene under the control of a tat-responsive DNA element using different formulations of cationic liposomes. Expression of a tat-responsive reporter gene was induced by incubating cells with a mixture of purified recombinant tat protein, reporter DNA, and liposomes. Different cell lines were tested successfully as targets for the codelivery. Tat was shown to trans-activate the codelivered virus promoter specifically in the cells tested. Codelivery of tat with DNA is a useful model for studying the function of trans-acting factors and their cis-acting DNA elements. The currently available methods such as foot-printing only reveal the binding, but not the functional consequence of the binding, of the factor with the element. In addition, this system may prove useful as a model for high level and regulated transgene expression in target cells.
Publication types
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Comparative Study
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Base Sequence
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CHO Cells
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Carcinoma, Squamous Cell
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Cell Line
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Chloramphenicol O-Acetyltransferase / analysis
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Chloramphenicol O-Acetyltransferase / biosynthesis
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Cricetinae
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DNA Primers
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Drug Carriers
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Gene Products, tat / administration & dosage*
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Gene Products, tat / biosynthesis
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HIV Long Terminal Repeat
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HIV-1 / metabolism*
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HeLa Cells
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Humans
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Kidney
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Liposomes
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Molecular Sequence Data
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Mutagenesis
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Phosphatidylethanolamines
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Plasmids
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Polymerase Chain Reaction / methods
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Recombinant Proteins / administration & dosage
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Recombinant Proteins / analysis
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Recombinant Proteins / biosynthesis
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Sequence Deletion
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Transcriptional Activation*
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Transfection / methods*
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Tumor Cells, Cultured
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tat Gene Products, Human Immunodeficiency Virus
Substances
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DNA Primers
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Drug Carriers
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Gene Products, tat
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Liposomes
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Phosphatidylethanolamines
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Recombinant Proteins
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tat Gene Products, Human Immunodeficiency Virus
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1,2-dielaidoylphosphatidylethanolamine
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Chloramphenicol O-Acetyltransferase