Mechanisms of regulating the Raf kinase family

被引:325
作者
Chong, H
Vikis, HG
Guan, KL
机构
[1] Univ Michigan, Dept Biol Chem, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Inst Gerontol, Ann Arbor, MI 48109 USA
关键词
MAPK signalling; Ras; phosphorylation; scaffolding proteins; ACTIVATED PROTEIN-KINASE; KSR-1 GENE ENCODES; B-RAF; A-RAF; C-ELEGANS; TYROSINE PHOSPHORYLATION; SERINE/THREONINE KINASE; SIGNAL-TRANSDUCTION; NEGATIVE REGULATION; BIOLOGICAL-ACTIVITY;
D O I
10.1016/S0898-6568(02)00139-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The MAP Kinase pathway is a key signalling mechanism that regulates many cellular functions such as cell growth, transformation and apoptosis. One of the essential components of this pathway is the serine/threonine kinase, Raf. Raf (MAPKK kinase, MAPKKK) relays the extracellular signal from the receptor/Ras complex to a cascade of cytosolic kinases by phosphorylating and activating MAPK/ERK kinase (MEK; MAPK kinase, MAPKK) that phosphorylates and activates extracellular signal regulated kinase (ERK; mitogen-activated protein kinase, MAPK), which phosphorylates various cytoplasmic and nuclear proteins. Regulation of both Ras and Raf is crucial in the proper maintenance of cell growth as oncogenic mutations in these genes lead to high transforming activity. Ras is mutated in 30% of all human cancers and B-Raf is mutated in 60% of malignant melanomas. The mechanisms that regulate the small GTPase Ras as well as the downstream kinases MEK and extracellular signal regulated kinase (ERK) are well understood. However, the regulation of Raf is complex and involves the integration of other signalling pathways as well as intramolecular interactions, phosphorylation, dephosphorylation and protein-protein interactions. From studies using mammalian isoforms of Raf, as well as C elegans lin45-Raf, common patterns and unique differences of regulation have emerged. This review will summarize recent findings on the regulation of Raf kinase. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:463 / 469
页数:7
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