Li Y, Jaiswal A K
Department of Pharmacology, Fox Chase Cancer Center, Philadelphia, PA 19111.
Biochem Biophys Res Commun. 1992 Nov 16;188(3):992-6. doi: 10.1016/0006-291x(92)91329-o.
Deletion mutagenesis in human NAD(P)H:Quinone Oxidoreductase (NQO1) gene and transfection studies into mammalian cells identified a segment of DNA designated as human Antioxidant Response Element (hARE) responsible for high basal expression in tumor cells and its induction by beta-naphthoflavone (beta-NF). The twenty four base pairs of the hARE contains an essential cis-element AP1 binding site and has been shown to bind to jun-D and c-fos proteins from mouse hepatoma (Hepa-1) nuclear extract. In the present report, we have identified jun-B as the third major protein in the hARE-Hepa-1 proteins complex observed in the band shift assays.