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
. 1997 Feb;17(2):537-44.
doi: 10.1128/MCB.17.2.537.

A novel, transformation-relevant activation domain in Fos proteins

Affiliations

A novel, transformation-relevant activation domain in Fos proteins

M Funk et al. Mol Cell Biol. 1997 Feb.

Abstract

We have previously demonstrated that transformation by Fos is critically dependent on an intact DNA-binding domain (bZip) and a functional N-terminal transactivation motif (N-TM). We now show that a novel motif (C-terminal transactivation motif [C-TM]) near the C terminus also plays an important role in both transformation and the activation of AP1-dependent transcription and that the hydrophobic amino acids in the C-TM are functionally essential. The C-TM is the most crucial element in the C-terminal transactivation domain in Fos, as indicated by its relative strength and context-independent function. The C-TM is clearly different from the previously identified HOB2 domain, located N terminally to the C-TM, and the C-terminally positioned TATA-binding protein-binding domain. We also show that the C-terminal transactivation domain strongly synergizes with the HOB1-like N-TM, even when both domains are present on different proteins within a dimeric complex, and that the C-TM plays a crucial role in this cooperation. These observations can be corroborated in a model in which multiple contacts with the basal machinery are established either to stabilize the transcription complex or to facilitate its sequential assembly.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Nature. 1988 Aug 11;334(6182):535-7 - PubMed
    1. Genes Dev. 1992 Sep;6(9):1810-9 - PubMed
    1. Cell. 1989 Feb 10;56(3):507-16 - PubMed
    1. Nature. 1989 Apr 13;338(6216):589-90 - PubMed
    1. Science. 1989 Mar 31;243(4899):1689-94 - PubMed

Publication types

Substances