Animal Physiology and Neurobiology, Department of Biology, University of Leuven (KU Leuven), Naamsestraat 59, 3000, Leuven, Belgium.
Microbes & Pathogen Biology, School of Biological Sciences, The Institute for Global Food Security, Queen's University Belfast, 19 Chlorine Gardens, Belfast, BT9 5DL, UK.
BMC Biol. 2024 Oct 8;22(1):223. doi: 10.1186/s12915-024-02017-6.
The phylum Nematoda is incredibly diverse and includes many parasites of humans, livestock, and plants. Peptide-activated G protein-coupled receptors (GPCRs) are central to the regulation of physiology and numerous behaviors, and they represent appealing pharmacological targets for parasite control. Efforts are ongoing to characterize the functions and define the ligands of nematode GPCRs, with already most peptide GPCRs known or predicted in Caenorhabditis elegans. However, comparative analyses of peptide GPCR conservation between C. elegans and other nematode species are limited, and many nematode GPCRs remain orphan. A phylum-wide perspective on peptide GPCR profiles will benefit functional and applied studies of nematode peptide GPCRs.
We constructed a pan-phylum resource of C. elegans peptide GPCR orthologs in 125 nematode species using a semi-automated pipeline for analysis of predicted proteome datasets. The peptide GPCR profile varies between nematode species of different phylogenetic clades and multiple C. elegans peptide GPCRs have orthologs across the phylum Nematoda. We identified peptide ligands for two highly conserved orphan receptors, NPR-9 and NPR-16, that belong to the bilaterian galanin/allatostatin A (Gal/AstA) and somatostatin/allatostatin C (SST/AstC) receptor families. The AstA-like NLP-1 peptides activate NPR-9 in cultured cells and are cognate ligands of this receptor in vivo. In addition, we discovered an AstC-type peptide, NLP-99, that activates the AstC-type receptor NPR-16. In our pan-phylum resource, the phylum-wide representation of NPR-9 and NPR-16 resembles that of their cognate ligands more than those of allatostatin-like peptides that do not activate these receptors.
The repertoire of C. elegans peptide GPCR orthologs varies across phylogenetic clades and several peptide GPCRs show broad conservation in the phylum Nematoda. Our work functionally characterizes the conserved receptors NPR-9 and NPR-16 as the respective GPCRs for the AstA-like NLP-1 peptides and the AstC-related peptide NLP-99. NLP-1 and NLP-99 are widely conserved in nematodes and their representation matches that of their receptor in most species. These findings demonstrate the conservation of a functional Gal/AstA and SST/AstC signaling system in nematodes. Our dataset of C. elegans peptide GPCR orthologs also lays a foundation for further functional studies of peptide GPCRs in the widely diverse nematode phylum.
线虫门是一个非常多样化的门,包括许多人类、家畜和植物寄生虫。肽激活的 G 蛋白偶联受体(GPCR)是调节生理和许多行为的核心,它们是寄生虫控制的有吸引力的药理学靶点。人们正在努力描述线虫 GPCR 的功能和定义其配体,在秀丽隐杆线虫中已经确定或预测了大多数肽 GPCR。然而,对线虫门中肽 GPCR 保守性的比较分析受到限制,许多线虫 GPCR 仍然是孤儿。对线虫门肽 GPCR 谱的全门研究将有助于线虫肽 GPCR 的功能和应用研究。
我们使用半自动化的分析预测蛋白质组数据集的管道,在 125 种线虫物种中构建了一个半自动化的线虫门肽 GPCR 直系同源物的泛门资源。线虫物种的肽 GPCR 谱在不同的系统发育枝系之间有所不同,并且在线虫门中,许多秀丽隐杆线虫肽 GPCR 都有直系同源物。我们确定了两个高度保守的孤儿受体 NPR-9 和 NPR-16 的肽配体,它们属于两侧动物的甘丙肽/脑肠肽 A(Gal/AstA)和生长抑素/脑肠肽 C(SST/AstC)受体家族。AstA 样 NLP-1 肽在培养细胞中激活 NPR-9,并在体内是该受体的同源配体。此外,我们发现了一种 AstC 型肽 NLP-99,它激活 AstC 型受体 NPR-16。在我们的泛门资源中,NPR-9 和 NPR-16 的全门代表性与它们的同源配体相似,而与不激活这些受体的脑肠肽样肽的代表性不同。
秀丽隐杆线虫肽 GPCR 直系同源物的 repertoire 在系统发育枝系之间有所不同,并且几个肽 GPCR 在线虫门中表现出广泛的保守性。我们的工作将保守受体 NPR-9 和 NPR-16 功能表征为 AstA 样 NLP-1 肽和相关肽 NLP-99 的相应 GPCR。NLP-1 和 NLP-99 在线虫中广泛保守,其在大多数物种中的代表性与受体相符。这些发现表明线虫门中 Gal/AstA 和 SST/AstC 信号系统的功能保守。我们的秀丽隐杆线虫肽 GPCR 直系同源物数据集也为进一步研究广泛多样的线虫门中的肽 GPCR 功能奠定了基础。