INDUCTION OF C-FOS EXPRESSION THROUGH JNK-MEDIATED TCF/ELK-1 PHOSPHORYLATION

被引:484
作者
CAVIGELLI, M
DOLFI, F
CLARET, FX
KARIN, M
机构
[1] Department of Pharmacology, Program in Biomedical Sciences, Univ. California School of Medicine, La Jolla
关键词
C-FOS; GROWTH FACTOR; TRANSCRIPTION REGULATION;
D O I
10.1002/j.1460-2075.1995.tb00284.x
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
Growth factors induce c-fos transcription by stimulating phosphorylation of transcription factor TCF/Elk-1, which binds to the serum response element (SRE). Under such conditions Elk-1 could be phosphorylated by the mitogen-activated protein kinases (MAPKs) ERK1 and ERK2, However, c-fos transcription and SRE activity are also induced by stimuli, such as UV irradiation and activation of the protein kinase MEKK1, that cause only an insignificant increase in ERK1/2 activity. However, both of these stimuli strongly activate two other MAPKs, JNK1 and JNK2, and stimulate Elk-1 transcriptional activity and phosphorylation. We find that the JNKs are the predominant Elk-1 activation domain kinases in extracts of UV-irradiated cells and that immunopurified JNK1/2 phosphorylate Elk-1 on the same major sites recognized by ERK1/2, that potentiate its transcriptional activity. Finally, we show that UV irradiation, but not serum or phorbol esters, stimulate translocation of JNK1 to the nucleus. As Elk-l is most likely phosphorylated while bound to the c-fos promoter, these results suggest that UV irradiation and MEKK1 activation stimulate TCF/Elk-1 activity through JNK activation, while growth factors induce c-fos through ERK activation.
引用
收藏
页码:5957 / 5964
页数:8
相关论文
共 43 条
[1]  
BOYLE WJ, 1991, METHOD ENZYMOL, V201, P110
[2]  
BUSCHER M, 1988, ONCOGENE, V3, P301
[3]   JAK-STAT PATHWAYS AND TRANSCRIPTIONAL ACTIVATION IN RESPONSE TO IFNS AND OTHER EXTRACELLULAR SIGNALING PROTEINS [J].
DARNELL, JE ;
KERR, IM ;
STARK, GR .
SCIENCE, 1994, 264 (5164) :1415-1421
[4]   JNK1 - A PROTEIN-KINASE STIMULATED BY UV-LIGHT AND HA-RAS THAT BINDS AND PHOSPHORYLATES THE C-JUN ACTIVATION DOMAIN [J].
DERIJARD, B ;
HIBI, M ;
WU, IH ;
BARRETT, T ;
SU, B ;
DENG, TL ;
KARIN, M ;
DAVIS, RJ .
CELL, 1994, 76 (06) :1025-1037
[5]   INDEPENDENT HUMAN MAP KINASE SIGNAL-TRANSDUCTION PATHWAYS DEFINED BY MEK AND MKK ISOFORMS [J].
DERIJARD, B ;
RAINGEAUD, J ;
BARRETT, T ;
WU, IH ;
HAN, JH ;
ULEVITCH, RJ ;
DAVIS, RJ .
SCIENCE, 1995, 267 (5198) :682-685
[6]   RAPID AND PREFERENTIAL ACTIVATION OF THE C-JUN GENE DURING THE MAMMALIAN UV RESPONSE [J].
DEVARY, Y ;
GOTTLIEB, RA ;
LAU, LF ;
KARIN, M .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (05) :2804-2811
[7]  
DIDONATO JA, 1995, MOL CELL BIOL, V15, P1302
[8]   PHOSPHORYLATION OF TRANSCRIPTION FACTOR P62TCF BY MAP KINASE STIMULATES TERNARY COMPLEX-FORMATION AT C-FOS PROMOTER [J].
GILLE, H ;
SHARROCKS, AD ;
SHAW, PE .
NATURE, 1992, 358 (6385) :414-417
[9]   ERK PHOSPHORYLATION POTENTIATES ELK-1-MEDIATED TERNARY COMPLEX-FORMATION AND TRANSACTIVATION [J].
GILLE, H ;
KORTENJANN, M ;
THOMAE, O ;
MOOMAW, C ;
SLAUGHTER, C ;
COBB, MH ;
SHAW, PE .
EMBO JOURNAL, 1995, 14 (05) :951-962
[10]   SERUM-INDUCED TRANSLOCATION OF MITOGEN-ACTIVATED PROTEIN-KINASE TO THE CELL-SURFACE RUFFLING MEMBRANE AND THE NUCLEUS [J].
GONZALEZ, FA ;
SETH, A ;
RADEN, DL ;
BOWMAN, DS ;
FAY, FS ;
DAVIS, RJ .
JOURNAL OF CELL BIOLOGY, 1993, 122 (05) :1089-1101