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Heterotrimeric G protein signaling outside the realm of seven transmembrane domain receptors.

机译:异源三聚体G蛋白信号传导于七个跨膜结构域受体的领域之外。

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摘要

Heterotrimeric G proteins, consisting of the guanine nucleotide-binding Galpha subunits with GTPase activity and the closely associated Gbeta and Ggamma subunits, are important signaling components for receptors with seven transmembrane domains (7TMRs). These receptors, also termed G protein-coupled receptors (GPCRs), act as guanine nucleotide exchange factors upon agonist stimulation. There is now accumulating evidence for noncanonical functions of heterotrimeric G proteins independent of 7TMR coupling. Galpha proteins belonging to all 4 subfamilies, including G(s), G(i), G(q), and G(12) are found to play important roles in receptor tyrosine kinase signaling, regulation of oxidant production, development, and cell migration, through physical and functional interaction with proteins other than 7TMRs. Association of Galpha with non-7TMR proteins also facilitates presentation of these G proteins to specific cellular microdomains. This Minireview aims to summarize our current understanding of the noncanonical roles of Galpha proteins in cell signaling and to discuss unresolved issues including regulation of Galpha activation by proteins other than the 7TMRs.
机译:异源三聚体G蛋白由具有GTPase活性的鸟嘌呤核苷酸结合Galpha亚基以及紧密相关的Gbeta和Ggamma亚基组成,是具有七个跨膜结构域(7TMR)的受体的重要信号成分。这些受体,也称为G蛋白偶联受体(GPCR),在激动剂刺激时充当鸟嘌呤核苷酸交换因子。现在有越来越多的证据表明异三聚体G蛋白的非规范功能独立于7TMR偶联。发现属于所有4个亚家族的Galpha蛋白,包括G(s),G(i),G(q)和G(12)在受体酪氨酸激酶信号传导,氧化剂产生,发育和细胞调节中起重要作用通过与7TMR以外的蛋白质发生物理和功能相互作用而迁移。 Galpha与非7TMR蛋白的关联也有助于将这些G蛋白呈递到特定的细胞微域。这份Minireview旨在总结我们目前对Galpha蛋白在细胞信号传导中非典型作用的理解,并讨论尚未解决的问题,包括除7TMR以外的其他蛋白对Galpha激活的调控。

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