Diversity and specificity of the mitogen-activated protein kinase phosphatase-1 functions

被引:65
作者
Lawan, Ahmed [1 ]
Shi, Hao [1 ]
Gatzke, Florian [1 ]
Bennett, Anton M. [1 ,2 ]
机构
[1] Yale Univ, Sch Med, Dept Pharmacol, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Program Integrat Cell Signaling & Neurobiol Metab, New Haven, CT 06520 USA
基金
美国国家卫生研究院;
关键词
MAP kinase; MAP kinase phosphatase; Cell signaling; Knock-out mouse; Phosphatases; Dephosphorylation; IMMEDIATE-EARLY GENE; LEPTIN-DEFICIENT MICE; MAP KINASE; REGULATED KINASE; P38; MAPK; TYROSINE-PHOSPHATASE; CATALYTIC ACTIVATION; HEPATIC STEATOSIS; CRYSTAL-STRUCTURE; PPAR-GAMMA;
D O I
10.1007/s00018-012-1041-2
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
The balance of protein phosphorylation is achieved through the actions of a family of protein serine/threonine kinases called the mitogen-activated protein kinases (MAPKs). The propagation of MAPK signals is attenuated through the actions of the MAPK phosphatases (MKPs). The MKPs specifically inactivate the MAPKs by direct dephosphorylation. The archetypal MKP family member, MKP-1 has garnered much of the attention amongst its ten other MKP family members. Initially viewed to play a redundant role in the control of MAPK signaling, it is now clear that MKP-1 exerts profound regulatory functions on the immune, metabolic, musculoskeletal and nervous systems. This review focuses on the physiological functions of MKP-1 that have been revealed using mouse genetic approaches. The implications from studies using MKP-1-deficient mice to uncover the role of MKP-1 in disease will be discussed.
引用
收藏
页码:223 / 237
页数:15
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