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 Apr;8(4):1551-7.
doi: 10.1128/mcb.8.4.1551-1557.1988.

Role of the promoter in the regulation of the thymidine kinase gene

Affiliations

Role of the promoter in the regulation of the thymidine kinase gene

S Travali et al. Mol Cell Biol. 1988 Apr.

Abstract

To identify the regulatory elements of the human thymidine kinase (TK) gene, we have established stable cell lines carrying different chimeric constructs of the TK gene. Our results can be summarized as follows. (i) When the TK coding sequence is under the control of the calcyclin promoter (a promoter that is activated when G0 cells are stimulated by growth factors), TK mRNA levels are higher in G1-arrested cells than in proliferating cells; (ii) when the TK coding sequence is under the control of the promoter of heat shock protein HSP70, steady-state levels of TK mRNA are highest after heat shock, regardless of the position of the cells in the cell cycle; (iii) the bacterial CAT gene under the control of the human TK promoter is maximally expressed in the S phase; (iv) the TK cDNA driven by the simian virus 40 promoter is also maximally expressed in the S phase; and (v) TK enzyme activity is always at a maximum in the S phase, even when the levels of TK mRNA are highest in nonproliferating cells. We conclude that although the TK coding sequence may also play some role, the TK promoter has an important role in the cell cycle regulation of TK mRNA levels.

PubMed Disclaimer

References

    1. Biochem Biophys Res Commun. 1965 Aug 16;20(4):535-8 - PubMed
    1. Mol Cell Biol. 1987 Aug;7(8):2803-13 - PubMed
    1. Biochim Biophys Acta. 1966 Feb 21;114(2):398-403 - PubMed
    1. J Cell Physiol. 1977 Sep;92(3):425-36 - PubMed
    1. Cell. 1979 Mar;16(3):575-88 - PubMed

Publication types

Substances