Control of the eukaryotic cell cycle by MAP kinase signaling pathways

被引:237
|
作者
Wilkinson, MG
Millar, JBA
机构
[1] SmithKline Beecham Pharmaceut PLC, Dept Mol Neurobiol, Harlow CM19 5AW, Essex, England
[2] Natl Inst Med Res, Div Yeast Genet, London NW7 1AA, England
来源
FASEB JOURNAL | 2000年 / 14卷 / 14期
基金
英国医学研究理事会;
关键词
CDK; proliferation; MAPK; signal transduction;
D O I
10.1096/fj.00-0102rev
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
In an often rapidly changing environment, cells must adapt by monitoring and reacting quickly to extracellular stimuli detected by membrane-bound receptors and proteins, Reversible phosphorylation of intracellular regulatory proteins has emerged as a crucial mechanism effecting the transmission and modulation of such signals and is determined by the relative activities of protein kinases and phosphatases within the cell, These are often arranged into complex signaling networks that may function independently or be subject to cross-regulation. Recently, genetic and biochemical analyses have identified the universally conserved mitogen-activated protein (MAP) kinase cascade as one of the most ubiquitous signal transduction systems. This pathway is activated after a variety of cellular stimuli and regulates numerous physiological processes, particularly the cell division cycle, Progression through the cell cycle is critically dependent on the presence of environmental growth factors and stress stimuli, and failure to correctly integrate such signals into the cell cycle machinery can lead to the accumulation of genetic damage and genomic instability characteristic of cancer cells. Here we focus on the MAP kinase cascade and discuss the molecular mechanisms by which these extensively studied signaling pathways influence cell growth and proliferation.
引用
收藏
页码:2147 / 2157
页数:11
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