Fisch T M, Prywes R, Roeder R G
Laboratory of Biochemistry and Molecular Biology, Rockefeller University, New York, New York 10021.
Mol Cell Biol. 1989 Mar;9(3):1327-31. doi: 10.1128/mcb.9.3.1327-1331.1989.
We have demonstrated that two sequence elements in the c-fos promoter can mediate the response of the gene to epidermal growth factor and the tumor promoter 12-O-tetradecanoyl phorbol-13-acetate (TPA). The first is the previously described serum response element. The second is a sequence element highly homologous to the consensus binding site for the HeLa cell transcription factor AP1. Although recent reports have shown that fos protein binds to AP1-binding sites through an interaction with AP1 protein and have raised the speculation that fos protein may negatively regulate expression of the c-fos gene via this interaction, we found no role for the AP1 consensus homology in the downregulation of c-fos expression following induction by epidermal growth factor and TPA.
我们已经证明,c-fos启动子中的两个序列元件可介导该基因对表皮生长因子和肿瘤启动子十四烷酰佛波醇乙酯(TPA)的反应。第一个是先前描述的血清反应元件。第二个是与HeLa细胞转录因子AP1的共有结合位点高度同源的序列元件。尽管最近的报道表明fos蛋白通过与AP1蛋白的相互作用与AP1结合位点结合,并引发了fos蛋白可能通过这种相互作用负调控c-fos基因表达的推测,但我们发现在表皮生长因子和TPA诱导后,AP1共有同源性在c-fos表达的下调中不起作用。