SELECTIVE ACTIVATION OF THE JNK SIGNALING CASCADE AND C-JUN TRANSCRIPTIONAL ACTIVITY BY THE SMALL GTPASES RAC AND CDC42HS

被引:1481
作者
MINDEN, A [1 ]
LIN, AN [1 ]
CLARET, FX [1 ]
ABO, A [1 ]
KARIN, M [1 ]
机构
[1] ONYX PHARMACEUT,RICHMOND,CA 94806
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0092-8674(05)80019-4
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 Rho subfamily of GTPases is involved in control of cell morphology In mammals and yeast. The mammalian Rac and Cdc42 proteins control formation of lamellipodia and filopodia, respectively. These proteins also activate MAP kinase (MAPK) cascades that regulate gene expression. Constitutively activated forms of Rac and Cdc42Hs are efficient activators of a cascade leading to JNK and p38/Mpk2 activation. RhoA did not exhibit this activity, and none of the proteins activated the ERK subgroup of MAPKs. JNK, but not ERK, activation was also observed in response to Dbl, an oncoprotein that acts as a nucleotide exchange factor for Cdc42Hs. Results with dominant interfering alleles place Rac1 as an intermediate between Ha-Ras and MEKK in the signaling cascade leading from growth factor receptors and v-Src to JNK activation. JNK and p38 activation are likely to contribute to the biological effects of Rac, Cdc42Hs, and Dbl on cell growth and proliferation.
引用
收藏
页码:1147 / 1157
页数:11
相关论文
共 66 条
[1]   ACTIVATING TRANSCRIPTION FACTOR-II DNA-BINDING ACTIVITY IS STIMULATED BY PHOSPHORYLATION CATALYZED BY P42 AND P54 MICROTUBULE-ASSOCIATED PROTEIN-KINASES [J].
ABDELHAFIZ, HA ;
HEASLEY, LE ;
KYRIAKIS, JM ;
AVRUCH, J ;
KROLL, DJ ;
JOHNSON, GL ;
HOEFFLER, JP .
MOLECULAR ENDOCRINOLOGY, 1992, 6 (12) :2079-2089
[2]   CDC42 AND CDC43, 2 ADDITIONAL GENES INVOLVED IN BUDDING AND THE ESTABLISHMENT OF CELL POLARITY IN THE YEAST SACCHAROMYCES-CEREVISIAE [J].
ADAMS, AEM ;
JOHNSON, DI ;
LONGNECKER, RM ;
SLOAT, BF ;
PRINGLE, JR .
JOURNAL OF CELL BIOLOGY, 1990, 111 (01) :131-142
[3]  
ADAMS JM, 1992, ONCOGENE, V7, P611
[4]   MEMBRANE TARGETING OF THE NUCLEOTIDE EXCHANGE FACTOR SOS IS SUFFICIENT FOR ACTIVATING THE RAS SIGNALING PATHWAY [J].
ARONHEIM, A ;
ENGELBERG, D ;
LI, NX ;
ALALAWI, N ;
SCHLESSINGER, J ;
KARIN, M .
CELL, 1994, 78 (06) :949-961
[5]   INDUCTION OF MEMBRANE RUFFLING AND FLUID-PHASE PINOCYTOSIS IN QUIESCENT FIBROBLASTS BY RAS PROTEINS [J].
BARSAGI, D ;
FERAMISCO, JR .
SCIENCE, 1986, 233 (4768) :1061-1068
[7]   EMERGING CONCEPTS IN THE RAS SUPERFAMILY OF GTP-BINDING PROTEINS [J].
BOKOCH, GM ;
DER, CJ .
FASEB JOURNAL, 1993, 7 (09) :750-759
[8]   THE GTPASE SUPERFAMILY - A CONSERVED SWITCH FOR DIVERSE CELL FUNCTIONS [J].
BOURNE, HR ;
SANDERS, DA ;
MCCORMICK, F .
NATURE, 1990, 348 (6297) :125-132
[9]   EPIDERMAL GROWTH-FACTOR REGULATES P21(RAS) THROUGH THE FORMATION OF A COMPLEX OF RECEPTOR, GRB2 ADAPTER PROTEIN, AND SOS NUCLEOTIDE EXCHANGE FACTOR [J].
BUDAY, L ;
DOWNWARD, J .
CELL, 1993, 73 (03) :611-620
[10]   COOPERATIVE INTERACTION OF S-POMBE PROTEINS REQUIRED FOR MATING AND MORPHOGENESIS [J].
CHANG, EC ;
BARR, M ;
WANG, Y ;
JUNG, V ;
XU, HP ;
WIGLER, MH .
CELL, 1994, 79 (01) :131-141