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
. 1991 Mar;11(3):1270-80.
doi: 10.1128/mcb.11.3.1270-1280.1991.

Multiple basal promoter elements determine the level of human c-fos transcription

Affiliations

Multiple basal promoter elements determine the level of human c-fos transcription

L Runkel et al. Mol Cell Biol. 1991 Mar.

Abstract

Three cis-acting domains that contribute to the basal promoter activity of the human c-fos gene were identified. One encompasses the serum response element and has been previously described. Another spans an NF1-like site situated at -170. Mutations and in vitro protein binding assays pinpoint this site as the sole basal element of the medial domain. The third, or promoter-proximal, domain can be divided into several distinct sites, one containing a directly repeated GC-rich element and the other consisting of partially overlapping recognition sites for transcription factors ATF/CREB and MLTF/USF. Each of these sites contributes to basal activity as assayed by transient transfections and by in vitro transcription. Consistent with this, several complexes could be visualized between this region and nuclear proteins in vitro and genomic footprinting demonstrated that both elements are constitutively bound in vivo. On the basis of these results, we conclude that all three domains are necessary for full c-fos promoter function.

PubMed Disclaimer

References

    1. Genes Dev. 1987 Mar;1(1):65-74 - PubMed
    1. Nature. 1989 Jul 6;340(6228):64-6 - PubMed
    1. Genes Dev. 1990 Oct;4(10):1730-40 - PubMed
    1. Cell. 1988 Sep 23;54(7):1043-51 - PubMed
    1. Cell. 1988 Sep 23;54(7):1033-42 - PubMed

Publication types