Dual-specificity MAP kinase phosphatases (MKPs): Shaping the outcome of MAP kinase signalling

被引:403
作者
Caunt, Christopher J. [1 ]
Keyse, Stephen M. [2 ]
机构
[1] Univ Bath, Dept Biol & Biochem, Bath BA2 7AY, Avon, England
[2] Univ Dundee, Ninewells Hosp & Med Sch, CR UK Stress Response Lab, Med Res Inst,Div Canc Res,Jacqui Wood Canc Ctr, Dundee DD1 9SY, Scotland
关键词
dual specificity protein phosphatase; DUSP; ERK; JNK mitogen activated protein kinase; MAPK; MAPK localisation; MAPK phosphatase; MKP; p38; ACTIVATED PROTEIN-KINASE; NUCLEAR EXPORT SIGNAL; REGULATED KINASE; CATALYTIC ACTIVATION; CRYSTAL-STRUCTURE; GROWTH-FACTOR; DIFFERENTIAL REGULATION; TYROSINE-PHOSPHATASE; FEEDBACK-REGULATION; CANCER CELLS;
D O I
10.1111/j.1742-4658.2012.08716.x
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
Dual-specificity MAP kinase phosphatases (MKPs) provide a complex negative regulatory network that acts to shape the duration, magnitude and spatiotemporal profile of MAP kinase activities in response to both physiological and pathological stimuli. Individual MKPs may exhibit either exquisite specificity towards a single mitogen-activated protein kinase (MAPK) isoform or be able to regulate multiple MAPK pathways in a single cell or tissue. They can act as negative feedback regulators of MAPK activity, but can also provide mechanisms of crosstalk between distinct MAPK pathways and between MAPK signalling and other intracellular signalling modules. In this review, we explore the current state of knowledge with respect to the regulation of MKP expression levels and activities, the mechanisms by which individual MKPs recognize and interact with different MAPK isoforms and their role in the spatiotemporal regulation of MAPK signalling.
引用
收藏
页码:489 / 504
页数:16
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