p115 Rho GTPase activating protein interacts with MEKK1

被引:24
作者
Christerson, LB [1 ]
Gallagher, E [1 ]
Vanderbilt, CA [1 ]
Whitehurst, AW [1 ]
Wells, C [1 ]
Kazempour, R [1 ]
Sternweis, PC [1 ]
Cobb, MH [1 ]
机构
[1] Univ Texas, SW Med Ctr, Dept Pharmacol, Dallas, TX 75390 USA
关键词
D O I
10.1002/jcp.10125
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mammalian MAP/ERK kinase kinase 1 (MEKK1) was identified as a mammalian homolog of Ste11p of the yeast pheromone-induced mating pathway. Like Ste11p, MEKK1 is a MAP3 kinase linked to at least two MAP kinase cascades and regulatory events that require cytoskeletal reorganization. MEKK1 is activated by molecules that impact cytoskeletal function. MEKK1 -/- cells are defective in cell migration, demonstrating that it is required for cell motility. MEKK1 has a 1,200 residue N-terminal regulatory domain that interacts with a dozen identified proteins. Using part of the MEKK1 N-terminus in a yeast two-hybrid screen, we discovered a novel interaction with p115 Rho GTPase-activating protein (GAP). The p115 Rho GAP binds to MEKK1 in vitro and in intact cells. The p115 Rho GAP has selectivity for RhoA over other Rho family members. Expression of p115 Rho GAP reduces MEKK1-induced signaling to AP-1. The reduced activation of AP-1 is dependent on the association of MEKK1 with p115 Rho GAP, because deletion of the Rho GAP SH3 domain, which abrogates their interaction, restores the stimulatory effect of MEKK1 on AP-1 activity. Here we have identified an MEKK1 binding partner that offers a connection between this protein kinase and the machinery regulating cytoskeletal reorganization. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:200 / 208
页数:9
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共 34 条
[31]   Tumor necrosis factor signaling to stress-activated protein kinase (SAPK)/Jun NH2-terminal kinase (JNK) and p38 -: Germinal center kinase couples TRAF2 to mitogen-activated protein kinase/ERK kinase kinase 1 and SAPK while receptor interacting protein associates with a mitogen-activated protein kinase kinase kinase upstream of MKK6 and p38 [J].
Yuasa, T ;
Ohno, S ;
Kehrl, JH ;
Kyriakis, JM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (35) :22681-22692
[32]   MEK kinase 1 gene disruption alters cell migration and c-Jun NH2-terminal kinase regulation but does not cause a measurable defect in NF-κB activation [J].
Yujiri, T ;
Ware, M ;
Widmann, C ;
Oyer, R ;
Russell, D ;
Chan, E ;
Zaitsu, Y ;
Clarke, P ;
Tyler, K ;
Oka, Y ;
Fanger, GR ;
Henson, P ;
Johnson, GL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (13) :7272-7277
[33]   MEK kinase 1 (MEKK1) transduces c-Jun NH2-terminal kinase activation in response to changes in the microtubule cytoskeleton [J].
Yujiri, T ;
Fanger, GR ;
Garrington, TP ;
Schlesinger, TK ;
Gibson, S ;
Johnson, GL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (18) :12605-12610
[34]   Role of MEKK1 in cell survival and activation of JNK and ERK pathways defined by targeted gene disruption [J].
Yujiri, T ;
Sather, S ;
Fanger, CR ;
Johnson, GL .
SCIENCE, 1998, 282 (5395) :1911-1914