Activation of the c-fos enhancer by the Erk MAP kinase pathway through two sequence elements:: the c-fos AP-1 and p62TCF sites

被引:106
作者
Wang, Y [1 ]
Prywes, R [1 ]
机构
[1] Columbia Univ, Dept Biol Sci, New York, NY 10027 USA
关键词
c-fos; FAP1; Erk; MAPK;
D O I
10.1038/sj.onc.1203443
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The c-fos enhancer can be activated by many signaling pathways through distinct elements of the enhancer. The enhancer contains at its core the serum response element (SRE) that binds serum response factor (SRF), On the 5' side of the SRE is a site for p62(TCF) which binds only when SRF is bound as well. p62(TCF) is encoded by three ets-related genes, Elk-l, SAP1 and SAP2, Each of these factors contain a transcriptional activation domain that is activated by phosphorylation by MAP kinases, On the 3' side of the SRE is the 'c-fos API site) (FAP1) whose role has been less clear, We find here that the FAP1 site contributes strongly to phorbol ester (TPA) and Erk MAP kinase activation of the c-fos enhancer and that both the p62(TCF) and FAP1 sites are required for effective activation of the enhancer. We further find that the FAP1 site binds ATF1 and CREB from HeLa nuclear extracts and that the phosphorylation of these factors is induced by TPA. ATF1 and CREB can be phosphorylated by Rsk2 which is a protein kinase directly activated by Erk MAP kinases, These results suggest a signaling pathway in which Erk MAP kinase activates the c-fos enhancer by direct phosphorylation of p62(TCF) and by activation of Rsk related kinases that phosphorylate ATF1 and CREB.
引用
收藏
页码:1379 / 1385
页数:7
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