Growth factors signal to steroid receptors through mitogen-activated protein kinase regulation of p160 coactivator activity

被引:116
作者
Lopez, GN
Turck, CW
Schaufele, F
Stallcup, MR
Kushner, PJ [1 ]
机构
[1] Univ Calif San Francisco, Metab Res Unit, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94143 USA
[4] Univ So Calif, Dept Pathol, Los Angeles, CA 90033 USA
关键词
D O I
10.1074/jbc.M010718200
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
Promoter-bound steroid receptors activate gene expression by recruiting members of the p160 family of coactivators. Many steroid receptors, most notably the progesterone and estrogen receptors, are regulated both by cognate hormone and independently by growth factors, Here we show that epidermal growth factor regulates the activities of the p160 GRIP1 through the extracellular signal-regulated kinase (ERK) family of mitogen-activated protein kinases. ERKs phosphorylate GRIP1 at a specific site, Ser-736, the integrity of which is required for full growth factor induction of GRIP1 transcriptional activation and coactivator function. We propose that growth factors signal to nuclear receptors in part by targeting the p160 coactivators.
引用
收藏
页码:22177 / 22182
页数:6
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