de Mendoza Alex, Sebé-Pedrós Arnau, Ruiz-Trillo Iñaki
Institut de Biologia Evolutiva (CSIC-Universitat Pompeu Fabra) Passeig Marítim de la Barceloneta, Barcelona, Spain.
Genome Biol Evol. 2014 Mar;6(3):606-19. doi: 10.1093/gbe/evu038.
The G-protein-coupled receptor (GPCR) signaling system is one of the main signaling pathways in eukaryotes. Here, we analyze the evolutionary history of all its components, from receptors to regulators, to gain a broad picture of its system-level evolution. Using eukaryotic genomes covering most lineages sampled to date, we find that the various components of the GPCR signaling pathway evolved independently, highlighting the modular nature of this system. Our data show that some GPCR families, G proteins, and regulators of G proteins diversified through lineage-specific diversifications and recurrent domain shuffling. Moreover, most of the gene families involved in the GPCR signaling system were already present in the last common ancestor of eukaryotes. Furthermore, we show that the unicellular ancestor of Metazoa already had most of the cytoplasmic components of the GPCR signaling system, including, remarkably, all the G protein alpha subunits, which are typical of metazoans. Thus, we show how the transition to multicellularity involved conservation of the signaling transduction machinery, as well as a burst of receptor diversification to cope with the new multicellular necessities.
G蛋白偶联受体(GPCR)信号系统是真核生物中的主要信号通路之一。在此,我们分析了其所有组成部分从受体到调节因子的进化历史,以全面了解其系统层面的进化。利用涵盖迄今采样的大多数谱系的真核生物基因组,我们发现GPCR信号通路的各个组成部分是独立进化的,突出了该系统的模块化性质。我们的数据表明,一些GPCR家族、G蛋白和G蛋白调节因子通过谱系特异性多样化和反复的结构域改组而多样化。此外,参与GPCR信号系统的大多数基因家族在真核生物的最后一个共同祖先中就已存在。此外,我们表明后生动物的单细胞祖先已经拥有GPCR信号系统的大部分细胞质成分,值得注意的是,包括所有典型的后生动物G蛋白α亚基。因此,我们展示了向多细胞性的转变如何涉及信号转导机制的保守性,以及为应对新的多细胞需求而出现的受体多样化爆发。