Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1992 Jun 15;89(12):5547-51.
doi: 10.1073/pnas.89.12.5547.

Tight control of gene expression in mammalian cells by tetracycline-responsive promoters

Affiliations

Tight control of gene expression in mammalian cells by tetracycline-responsive promoters

M Gossen et al. Proc Natl Acad Sci U S A. .

Abstract

Control elements of the tetracycline-resistance operon encoded in Tn10 of Escherichia coli have been utilized to establish a highly efficient regulatory system in mammalian cells. By fusing the tet repressor with the activating domain of virion protein 16 of herpes simplex virus, a tetracycline-controlled transactivator (tTA) was generated that is constitutively expressed in HeLa cells. This transactivator stimulates transcription from a minimal promoter sequence derived from the human cytomegalovirus promoter IE combined with tet operator sequences. Upon integration of a luciferase gene controlled by a tTA-dependent promoter into a tTA-producing HeLa cell line, high levels of luciferase expression were monitored. These activities are sensitive to tetracycline. Depending on the concentration of the antibiotic in the culture medium (0-1 microgram/ml), the luciferase activity can be regulated over up to five orders of magnitude. Thus, the system not only allows differential control of the activity of an individual gene in mammalian cells but also is suitable for creation of "on/off" situations for such genes in a reversible way.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Biotechniques. 1988 May;6(5):454-8 - PubMed
    1. Cell. 1982 May;29(1):99-108 - PubMed
    1. Mol Cell Biol. 1985 Jun;5(6):1480-9 - PubMed
    1. Cell. 1987 Jun 5;49(5):603-12 - PubMed
    1. EMBO J. 1988 Dec 1;7(12):4011-7 - PubMed

Publication types

MeSH terms

LinkOut - more resources

-