CIN85 regulates the ability of MEKK4 to activate the p38 MAP kinase pathway

被引:21
作者
Aissouni, Y
Zapart, G
Iovanna, JL
Dikic, I [1 ]
Soubeyran, P
机构
[1] INSERM, U624, F-13288 Marseille, France
[2] Goethe Univ, Sch Med, Inst Biochem 2, D-60590 Frankfurt, Germany
关键词
multi-adaptor; signaling; regulation; stress; MAP kinase; interaction;
D O I
10.1016/j.bbrc.2005.10.032
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
CIN85 is a multi-adaptor protein involved in different cellular functions including the down-regulation of activated receptor tyrosine kinases and survival of neuronal cells. CIN85 contains three SH3 domains that specifically bind a unique proline-arginine motif (PxxxPR) found in several CIN85 effectors. In this report, we show that the MAP kinase kinase kinase MEKK4 is a new CIN85-interacting partner. This interaction is mediated by the engagement of the SH3 domains of CIN85 to three PxxxPR motifs located within MEKK4 sequence. By disrupting this interaction we demonstrated that CIN85 binding to MEKK4 enhances the activation of MKK6 and of the downstream p38 MAP kinase following oxidative stress and growth factor stimulation. CIN85 was also shown to regulate the activation of MEKK4 by GADD45 proteins and promote multi-ubiquitination of MEKK4. Taken together, these results indicate a novel role for CIN85 in the regulation of cellular stress response via the MAPK pathways. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:808 / 814
页数:7
相关论文
共 26 条
[1]   Adaptor proteins Grb2 and Crk couple Pyk2 with activation of specific mitogen-activated protein kinase cascades [J].
Blaukat, A ;
Ivankovic-Dikic, I ;
Grönroos, E ;
Dolfi, F ;
Tokiwa, G ;
Vuori, K ;
Dikic, I .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (21) :14893-14901
[2]   Oncogenic kinase signalling [J].
Blume-Jensen, P ;
Hunter, T .
NATURE, 2001, 411 (6835) :355-365
[3]   Cbl signaling networks in the regulation of cell function [J].
Dikic, I ;
Szymkiewicz, I ;
Soubeyran, P .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2003, 60 (09) :1805-1827
[4]   Negative receptor signalling [J].
Dikic, I ;
Giordano, S .
CURRENT OPINION IN CELL BIOLOGY, 2003, 15 (02) :128-135
[5]   Transforming growth factor-β1 (TGF-β)-induced apoptosis of prostate cancer cells involves Smad7-dependent activation of p38 by TGF-β-activated kinase 1 and mitogen-activated protein kinase kinase 3 [J].
Edlund, S ;
Bu, SH ;
Schuster, N ;
Aspenström, P ;
Heuchel, R ;
Heldin, NE ;
ten Dijke, P ;
Heldin, CH ;
Landström, M .
MOLECULAR BIOLOGY OF THE CELL, 2003, 14 (02) :529-544
[6]   Cloning of a novel mitogen-activated protein kinase kinase kinase, MEKK4, that selectively regulates the c-Jun amino terminal kinase pathway [J].
Gerwins, P ;
Blank, JL ;
Johnson, GL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (13) :8288-8295
[7]   Multiple monoubiquitination of RTKs is sufficient for their endocytosis and degradation [J].
Haglund, K ;
Sigismund, S ;
Polo, S ;
Szymkiewicz, I ;
Di Fiore, PP ;
Dikic, I .
NATURE CELL BIOLOGY, 2003, 5 (05) :461-466
[8]   Mitogen-activated protein kinase pathways mediated by ERK, JNK, and p38 protein kinases [J].
Johnson, GL ;
Lapadat, R .
SCIENCE, 2002, 298 (5600) :1911-1912
[9]   Oligomerization of human Gadd45a protein [J].
Kovalsky, O ;
Lung, FDT ;
Roller, PP ;
Fornace, AJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (42) :39330-39339
[10]   CIN85 associates with multiple effectors controlling intracellular trafficking of epidermal growth factor receptors [J].
Kowanetz, K ;
Husnjak, K ;
Höller, D ;
Kowanetz, M ;
Soubeyran, P ;
Hirsch, D ;
Schmidt, MHH ;
Pavelic, K ;
De Camilli, P ;
Randazzo, PA ;
Dikic, I .
MOLECULAR BIOLOGY OF THE CELL, 2004, 15 (07) :3155-3166