The PRK2 kinase is a potential effector target of both Rho and Rac GTPases and regulates actin cytoskeletal organization

被引:178
作者
Vincent, S
Settleman, J
机构
[1] MASSACHUSETTS GEN HOSP,CTR CANC,CHARLESTOWN,MA 02129
[2] HARVARD UNIV,SCH MED,CHARLESTOWN,MA 02129
关键词
D O I
10.1128/MCB.17.4.2247
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 Pas-related Rho family GTPases mediate signal transduction pathways that regulate a variety of cellular processes, Like Ras, the Rho proteins (which include Rho, Pac, and CDC42) interact directly with protein kinases, which are likely to serve as downstream effector targets of the activated GTPase, Activated RhoA has recently been reported to interact directly with several protein kinases, p120 PKN, p150 ROK alpha and -beta, p160 ROCK, and p164 Rho kinase, Here, we describe the purification of a novel Rho-associated kinase, p140, which appears to be the major Rho-associated kinase activity in most tissues, Peptide microsequencing revealed that p140 is probably identical to the previously reported PRK2 kinase, a close relative of PKN, However, unlike the previously described Rho-binding kinases, which are Rho specific, p140 associates with Rac as well as Rho, Moreover, the interaction of p140 with Rho in vitro is nucleotide independent, whereas the interaction,vith Pac is completely GTP dependent, The association of p140 with either GTPase promotes kinase activity substantially, and expression of a kinase-deficient form of p140 in microinjected fibroblasts disrupts actin stress fibers, These results indicate that p140 may be a shared kinase target of both Rho and Rac GTPases that mediates their effects on rearrangements of the actin cytoskeleton.
引用
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页码:2247 / 2256
页数:10
相关论文
共 49 条
[1]   Identification of a putative target for Rho as the serine-threonine kinase protein kinase N [J].
Amano, M ;
Mukai, H ;
Ono, Y ;
Chihara, K ;
Matsui, T ;
Hamajima, Y ;
Okawa, K ;
Iwamatsu, A ;
Kaibuchi, K .
SCIENCE, 1996, 271 (5249) :648-650
[2]  
BAGRODIA S, 1995, J BIOL CHEM, V270, P27995
[3]   HA-RAS AUGMENTS C-JUN ACTIVITY AND STIMULATES PHOSPHORYLATION OF ITS ACTIVATION DOMAIN [J].
BINETRUY, B ;
SMEAL, T ;
KARIN, M .
NATURE, 1991, 351 (6322) :122-127
[4]   THE GTPASE SUPERFAMILY - A CONSERVED SWITCH FOR DIVERSE CELL FUNCTIONS [J].
BOURNE, HR ;
SANDERS, DA ;
MCCORMICK, F .
NATURE, 1990, 348 (6297) :125-132
[5]  
Brill S, 1996, MOL CELL BIOL, V16, P4869
[6]   A CONSERVED BINDING MOTIF DEFINES NUMEROUS CANDIDATE TARGET PROTEINS FOR BOTH CDC42 AND RAC GTPASES [J].
BURBELO, PD ;
DRECHSEL, D ;
HALL, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (49) :29071-29074
[7]   THE MAMMALIAN G-PROTEIN RHOC IS ADP-RIBOSYLATED BY CLOSTRIDIUM-BOTULINUM EXOENZYME C-3 AND AFFECTS ACTIN MICROFILAMENTS IN VERO CELLS [J].
CHARDIN, P ;
BOQUET, P ;
MADAULE, P ;
POPOFF, MR ;
RUBIN, EJ ;
GILL, DM .
EMBO JOURNAL, 1989, 8 (04) :1087-1092
[8]   THE SMALL GTP-BINDING PROTEINS RAC1 AND CDC42 REGULATE THE ACTIVITY OF THE JNK/SAPK SIGNALING PATHWAY [J].
COSO, OA ;
CHIARIELLO, M ;
YU, JC ;
TERAMOTO, H ;
CRESPO, P ;
XU, NG ;
MIKI, T ;
GUTKIND, JS .
CELL, 1995, 81 (07) :1137-1146
[9]   The multidomain protein Trio binds the LAR transmembrane tyrosine phosphatase, contains a protein kinase domain, and has separate rac-specific and rho-specific guanine nucleotide exchange factor domains [J].
Debant, A ;
SerraPages, C ;
Seipel, K ;
OBrien, S ;
Tang, M ;
Park, SH ;
Streuli, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (11) :5466-5471
[10]   SMALL GTP-BINDING PROTEINS AND THE REGULATION OF THE ACTIN CYTOSKELETON [J].
HALL, A .
ANNUAL REVIEW OF CELL BIOLOGY, 1994, 10 :31-54