Abstract
A recombinant plasmid containing the gene for bacterial beta-galactosidase, situated close to the simian virus 40 early promoter, has been constructed. Transfection of CHO, L, and COS-1 cells with this plasmid led to the expression and appearance of the enzyme. Using this system, we have developed a series of promoter cloning vehicles capable of accepting promoter signals for animal genes.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Bacterial Proteins / biosynthesis*
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Bacterial Proteins / genetics
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Cell Line
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Escherichia coli / genetics
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Gene Expression Regulation
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Genes, Bacterial
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Plasmids / genetics
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Plasmids / metabolism
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Promoter Regions, Genetic
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Recombinant Proteins / biosynthesis
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beta-Galactosidase / biosynthesis*
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beta-Galactosidase / genetics
Substances
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Bacterial Proteins
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Recombinant Proteins
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beta-Galactosidase