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
. 1988 Mar;85(5):1447-51.
doi: 10.1073/pnas.85.5.1447.

Overlapping positive and negative regulatory domains of the human beta-interferon gene

Affiliations

Overlapping positive and negative regulatory domains of the human beta-interferon gene

S Goodbourn et al. Proc Natl Acad Sci U S A. 1988 Mar.

Abstract

Virus or poly(I).poly(C) induction of human beta-interferon gene expression requires a 40-base-pair DNA sequence designated the interferon gene regulatory element (IRE). Previous studies have shown that the IRE contains both positive and negative regulatory DNA sequences. To localize these sequences and study their interactions, we have examined the effects of a large number of single-base mutations within the IRE on beta-interferon gene regulation. We find that the IRE consists of two genetically separable positive regulatory domains and an overlapping negative control sequence. We propose that the beta-interferon gene is switched off in uninduced cells by a repressor that blocks the interaction between one of the two positive regulatory sequences and a specific transcription factor. Induction would then lead to inactivation or displacement of the repressor and binding of transcription factors to both positive regulatory domains.

PubMed Disclaimer

References

    1. Proc Natl Acad Sci U S A. 1983 Jul;80(13):3923-7 - PubMed
    1. Cell. 1983 Oct;34(3):865-79 - PubMed
    1. Nucleic Acids Res. 1984 Sep 25;12(18):6979-93 - PubMed
    1. Cell. 1985 Jun;41(2):489-96 - PubMed
    1. Cell. 1985 Jun;41(2):509-20 - PubMed

Publication types

MeSH terms

LinkOut - more resources