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 Aug 25;16(16):8057-76.
doi: 10.1093/nar/16.16.8057.

Multiple elements are required for expression of an intermediate filament gene

Affiliations
Free PMC article

Multiple elements are required for expression of an intermediate filament gene

C M Sax et al. Nucleic Acids Res. .
Free PMC article

Abstract

The expression of vimentin is unique within the intermediate filament multigene family. It is the only member which deviates from its usual tissue-specific expression pattern and whose 5'-flanking region contains multiple GC boxes, the binding site for Sp1. The activity of vimentin 5'-end:CAT fusions has been compared in cells where vimentin is highly expressed (mouse L cells) or not expressed at all (MH1C1). In addition, CAT activity has been examined by microinjection into Xenopus oocytes. Both in vivo expression and in vitro binding studies implicate Sp1 as a general regulatory factor in vimentin gene expression. Increased expression of 5'-end:CAT fusions in mouse L cells suggests that a fibroblast-specific enhancer element resides in the region -321 to -160. Low transcriptional activity in MH1C1 cells may be due to either the lack of this positive transcription factor(s) or the presence of a repressor element. Here, we demonstrate that the unique and complex pattern of vimentin gene expression is controlled by multiple cis-acting elements.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Virology. 1973 Apr;52(2):456-67 - PubMed
    1. J Cell Biol. 1979 Aug;82(2):577-84 - PubMed
    1. Exp Cell Res. 1979 Oct 1;123(1):25-46 - PubMed
    1. Cell. 1979 Dec;18(4):1285-97 - PubMed
    1. Nature. 1980 Jan 17;283(5744):249-256 - PubMed

Publication types