Laboratory of Chemical Biology and Signal Transduction, The Rockefeller University, New York, NY, 10065.
Department of Neurobiology, Care Sciences and Society, Division for Neurogeriatrics, Center for Alzheimer Research, Karolinska Institutet, 141 57 Huddinge, Sweden.
Proc Natl Acad Sci U S A. 2017 Nov 7;114(45):12015-12020. doi: 10.1073/pnas.1713074114. Epub 2017 Oct 23.
Receptor activity-modifying proteins (RAMPs) are widely expressed in human tissues and, in some cases, have been shown to affect surface expression or ligand specificity of G-protein-coupled receptors (GPCRs). However, whether RAMP-GPCR interactions are widespread, and the nature of their functional consequences, remains largely unknown. In humans, there are three RAMPs and over 800 expressed GPCRs, making direct experimental approaches challenging. We analyzed relevant genomic data from all currently available sequenced organisms. We discovered that RAMPs and GPCRs tend to have orthologs in the same species and have correlated phylogenetic trees to the same extent, or higher than other interacting protein pairs that play key roles in cellular signaling. In addition, the resulting RAMP-GPCR interaction map suggests that RAMP1 and RAMP3 interact with the same set of GPCRs, which implies functional redundancy. We next analyzed human transcriptomes and found expression correlation for GPCRs and RAMPs. Our results suggest global coevolution of GPCRs and RAMPS and support the hypothesis that GPCRs interact globally with RAMPs in cellular signaling pathways.
受体活性修饰蛋白(RAMPs)广泛表达于人体组织中,在某些情况下,已经证实其会影响 G 蛋白偶联受体(GPCR)的表面表达或配体特异性。然而,RAMP-GPCR 相互作用是否广泛存在,以及其功能后果的性质,在很大程度上仍然未知。在人类中,有三种 RAMPs 和 800 多种表达的 GPCR,使得直接进行实验方法极具挑战性。我们分析了所有现有测序生物的相关基因组数据。我们发现,在同一种物种中,RAMPs 和 GPCR 往往具有同源物,并且它们的系统发育树相关性与其他在细胞信号转导中起关键作用的相互作用蛋白对相同,或者更高。此外,由此产生的 RAMP-GPCR 相互作用图表明,RAMP1 和 RAMP3 与同一组 GPCR 相互作用,这意味着存在功能冗余。我们接下来分析了人类转录组,发现 GPCRs 和 RAMPs 之间存在表达相关性。我们的结果表明 GPCRs 和 RAMPS 存在全局协同进化,并支持 GPCR 在细胞信号通路中与 RAMPs 全局相互作用的假说。