The bottleneck of JNK signaling: Molecular and functional characteristics of MKK4 and MKK7

被引:106
作者
Haeusgen, Wiebke [1 ]
Herdegen, Thomas [1 ]
Waetzig, Vicki [1 ]
机构
[1] Univ Hosp Schleswig Holstein, Inst Expt & Clin Pharmacol, D-24105 Kiel, Germany
关键词
MKK4; MKK7; SEK1; JNKK1; JNKK2; JNK; c-Jun N-terminal kinase; Scaffolds; Signalosome; ACTIVATED PROTEIN-KINASE; N-TERMINAL KINASE; METASTASIS SUPPRESSOR GENE; JUN NH2-TERMINAL KINASE; EMBRYONIC STEM-CELLS; DEATH IN-VIVO; C-JUN; MAP KINASE; SCAFFOLD PROTEIN; DOCKING SITES;
D O I
10.1016/j.ejcb.2010.11.008
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The functions of mitogen-activated protein kinases (MKKs) 4 and 7 are typically associated with the c-Jun N-terminal kinase (INK) signaling pathway. Both MKKs synergistically phosphorylate different JNK isoforms and are therefore involved in numerous physiological (e.g. differentiation and proliferation) and pathological (e.g. apoptosis and tumorigenesis) processes. MKK4 and MKK7 share similar molecular characteristics as well as several upstream activators and scaffold proteins. However, their functions are non-redundant and determined by different stimuli, biochemical interactions and differential tissue distribution. The central question is how two MKKs regulate or affect the multiple actions of their JNK substrates. Similar to JNKs. MKK4 and MKK7 can simultaneously exert divergent functions in different cellular compartments and signalosomes. It is also important to realize that the MKK effects are splice variant-specific. The present review not only summarizes the various modes of MKK4 and MKK7 activation and activity, but also their functions. We also extensively describe their impact on JNK signaling, their molecular interactions resulting in the formation of context-specific signalosomes and the functional consequences of JNK deficiency. (C) 2011 Elsevier GmbH. All rights reserved.
引用
收藏
页码:536 / 544
页数:9
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