ATF1 phosphorylation by the ERK MAPK pathway is required for epidermal growth factor-induced c-jun expression

被引:71
作者
Gupta, P [1 ]
Prywes, R [1 ]
机构
[1] Columbia Univ, Dept Sci Biol, New York, NY 10027 USA
关键词
D O I
10.1074/jbc.M209799200
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
Epidermal growth factor induction of c-jun expression requires ATF1 and MEF2 sites in the c-jun promoter. We find that activation of the c-jun promoter through the ATF1 site requires phosphorylation of ATF1 at serine 63. A serine 63 to alanine mutation of ATF1 acts to block epidermal growth factor (EGF) induction of a transfected c-jun gene. ATF1 can be phosphorylated by mitogen- and stress-activated protein kinase 1 (MSK1), which is activated by EGF and ERK1/2. Kinase-dead MSK1 mutants blocked EGF induction of a transfected c-jun gene suggesting that MSK1 or a similar family member is required for induced c-jun expression. Use of the MEK1 inhibitor U0126 and dominant negative MEK1 further showed that MSK1 activation and c-jun induction require the ERK pathway. In contrast, a JNK inhibitor blocked EGF induction of c-jun expression but not ATF1 phosphorylation. These results show that the two MAPK pathways, ERK and JNK, are required for EGF-induced c-jun expression and that the ERK pathway acts through downstream phosphorylation of ATF1.
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收藏
页码:50550 / 50556
页数:7
相关论文
共 63 条
[1]   THE ROLE OF JUN, FOS AND THE AP-1 COMPLEX IN CELL-PROLIFERATION AND TRANSFORMATION [J].
ANGEL, P ;
KARIN, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1072 (2-3) :129-157
[2]   SP600125, an anthrapyrazolone inhibitor of Jun N-terminal kinase [J].
Bennett, BL ;
Sasaki, DT ;
Murray, BW ;
O'Leary, EC ;
Sakata, ST ;
Xu, WM ;
Leisten, JC ;
Motiwala, A ;
Pierce, S ;
Satoh, Y ;
Bhagwat, SS ;
Manning, AM ;
Anderson, DW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (24) :13681-13686
[3]   SERUM-INDUCED, TPA-INDUCED, AND RAS-INDUCED EXPRESSION FROM AP-1/ETS-DRIVEN PROMOTERS REQUIRES RAF-1 KINASE [J].
BRUDER, JT ;
HEIDECKER, G ;
RAPP, UR .
GENES & DEVELOPMENT, 1992, 6 (04) :545-556
[4]   Ribosomal subunit kinase-2 is required for growth factor-stimulated transcription of the c-Fos gene [J].
Brüning, JC ;
Gillette, JA ;
Zhao, Y ;
Bjorbaeck, C ;
Kotzka, J ;
Knebel, B ;
Avci, H ;
Hanstein, B ;
Lingohr, P ;
Moller, DE ;
Krone, W ;
Kahn, CR ;
Müller-Wieland, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (06) :2462-2467
[5]   Mammalian MAP kinase signalling cascades [J].
Chang, LF ;
Karin, M .
NATURE, 2001, 410 (6824) :37-40
[6]   MEKK3 directly regulates MEK5 activity as part of the big mitogen-activated protein kinase 1 (BMK1) signaling pathway [J].
Chao, TH ;
Hayashi, M ;
Tapping, RI ;
Kato, Y ;
Lee, JD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (51) :36035-36038
[7]  
Chen X, 1999, MOL CELL BIOL, V19, P4695
[8]   Epidermal growth factor induction of the c-jun promoter by a Rac pathway [J].
Clarke, N ;
Arenzana, N ;
Hai, TW ;
Minden, A ;
Prywes, R .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (02) :1065-1073
[9]   Specificity and mechanism of action of some commonly used protein kinase inhibitors [J].
Davies, SP ;
Reddy, H ;
Caivano, M ;
Cohen, P .
BIOCHEMICAL JOURNAL, 2000, 351 (351) :95-105
[10]   Signal transduction by the JNK group of MAP kinases [J].
Davis, RJ .
CELL, 2000, 103 (02) :239-252