GPCRs globally coevolved with receptor activity-modifying proteins, RAMPs

被引:29
作者
Barbash, Shahar [1 ]
Lorenzen, Emily [1 ]
Persson, Torbjorn [1 ,2 ]
Huber, Thomas [1 ]
Sakmar, Thomas P. [1 ,2 ]
机构
[1] Rockefeller Univ, Lab Chem Biol & Signal Transduct, New York, NY 10065 USA
[2] Karolinska Inst, Dept Neurobiol Care Sci & Soc, Div Neurogeriatr, Ctr Alzheimer Res, S-14157 Huddinge, Sweden
关键词
coevolution; G-protein-coupled receptor; phylogenetic analysis; receptor activity-modifying protein; signal transduction; COEVOLUTION; MODULATION; PROFILES;
D O I
10.1073/pnas.1713074114
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:12015 / 12020
页数:6
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