The evidence for G-protein-coupled receptors and heterotrimeric G proteins in protozoa and ancestral metazoa.

D C New, J T Wong
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引用次数: 36

Abstract

In higher eukaryotes G-protein-coupled signal transduction pathways are a common mechanism used to detect an extracellular message and transmit a signal, via a membrane-bound receptor and a heterotrimeric G protein, to second messenger producing enzymes and effector proteins. The techniques used to identify components of these pathways are increasingly being applied to protozoa and ancestral metazoa. Many of the organisms studied do seem to express functional homologues of those found in higher eukaryotes and increasingly genes encoding these proteins are being cloned. Sequence analysis of the isolated alpha-subunits of heterotrimeric G proteins shows that these proteins have extensive homology to their mammalian counterparts, and often show absolute sequence identity in functionally significant regions. The receptor clones isolated clearly establish that protozoa and early metazoa express proteins with seven transmembrane spanning domains. Comparisons with mammalian receptors indicate that these proteins are likely to be regulated by phosphorylation and dephosphorylation events, although the pathways which control these are yet to be identified. The postulated regulatory mechanisms and the number of homologous clones isolated from some protozoa suggest that a highly regulated system of transmembrane signalling appeared at a relatively early stage in evolution.

原生动物和原始后生动物中G蛋白偶联受体和异三聚体G蛋白存在的证据。
在高等真核生物中,G蛋白偶联信号转导途径是一种常见的机制,用于检测细胞外信息并通过膜结合受体和异源三聚体G蛋白将信号传递给第二信使产生酶和效应蛋白。用于鉴定这些通路成分的技术越来越多地应用于原生动物和祖先后生动物。许多被研究的生物似乎确实表达了在高等真核生物中发现的功能同源物,并且越来越多的编码这些蛋白质的基因正在被克隆。对异三聚体G蛋白α -亚基的序列分析表明,这些蛋白与哺乳动物的α -亚基具有广泛的同源性,并且在功能显著的区域表现出绝对的序列一致性。受体克隆的分离清楚地表明,原生动物和早期后生动物表达具有7个跨膜结构域的蛋白。与哺乳动物受体的比较表明,这些蛋白质可能受到磷酸化和去磷酸化事件的调节,尽管控制这些事件的途径尚未确定。从一些原生动物中分离出的调控机制和同源克隆的数量表明,一个高度调控的跨膜信号系统出现在进化的相对早期阶段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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