GnRH receptor signalling to ERK: kinetics and compartmentalization

被引:40
作者
Caunt, Christopher James [1 ]
Finch, Ann R. [1 ]
Sedgley, Kathleen R. [1 ]
McArdle, Craig A. [1 ]
机构
[1] Univ Bristol, Henry Wellcome Labs Integrat Neurosci & Endocrino, Bristol BS1 3NY, Avon, England
基金
英国惠康基金;
关键词
D O I
10.1016/j.tem.2006.08.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Many hormones, neurotransmitters and growth factors influence their target cells by activation of mitogen-activated protein kinase cascades. The consequences of such activation reflect not only the magnitude, but also the kinetics and cellular compartmentalization of kinase activity. Gonadotropin-releasing hormone (GnRH) receptors are seven-transmembrane receptors that have undergone a period of rapidly accelerated molecular evolution in which the advent of type I mammalian GnRH receptors has been associated with the loss of the carboxyl-terminal tail, a structure present in all other seven-transmembrane receptors. Here, we review spatiotemporal aspects of extracellular-signal-regulated kinase activation by gonadotropin-releasing hormone receptors, emphasizing how the absence or presence of the carboxyl-terminal tail dictates the receptors' ability to engage and signal via arrestins.
引用
收藏
页码:308 / 313
页数:6
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