线虫纲神经肽受体保护的全球分析。

IF 4.4 1区 生物学 Q1 BIOLOGY
Luca Golinelli, Ellen Geens, Allister Irvine, Ciaran J McCoy, Elke Vandewyer, Louise E Atkinson, Angela Mousley, Liesbet Temmerman, Isabel Beets
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引用次数: 0

摘要

背景:线虫门种类繁多,包括许多寄生于人类、家畜和植物的寄生虫。肽激活的 G 蛋白偶联受体(GPCR)是调节生理机能和多种行为的核心,它们是控制寄生虫的诱人药理靶标。目前正在努力研究线虫 GPCR 的功能特征并确定其配体,在秀丽隐杆线虫中已知或预测的多肽 GPCR 已达数百种。然而,对 elegans 和其他线虫物种之间多肽 GPCR 保护情况的比较分析还很有限,许多线虫 GPCR 仍然是 "孤儿"。从整个动物门类的角度来研究多肽 GPCR 将有利于线虫多肽 GPCR 的功能和应用研究:结果:我们利用半自动流水线分析了预测的蛋白质组数据集,在 125 种线虫中构建了线虫多肽 GPCR 同源物的泛门资源。不同系统发育支系的线虫物种之间的多肽 GPCR 特征各不相同,线虫多肽 GPCR 在整个线虫纲中有多个直向同源物。我们发现了两种高度保守的孤儿受体 NPR-9 和 NPR-16 的多肽配体,它们属于双子叶动物的加拉宁/动情素 A(Gal/AstA)和体生长抑素/动情素 C(SST/AstC)受体家族。类似 AstA 的 NLP-1 肽能在培养细胞中激活 NPR-9,在体内也是该受体的同源配体。此外,我们还发现了一种 AstC 型多肽 NLP-99,它能激活 AstC 型受体 NPR-16。在我们的泛门资源中,NPR-9和NPR-16的全门代表性与其同源配体的代表性更相似,而与不激活这些受体的异磷脂素样肽的代表性更相似:结论:在不同的系统发育支系中,秀丽隐杆线虫肽GPCR直向同源物的种类各不相同,而在线虫门中,有几种肽GPCR表现出广泛的保守性。我们的工作从功能上确定了保守受体 NPR-9 和 NPR-16 的特征,它们分别是 AstA 样 NLP-1 肽和 AstC 相关肽 NLP-99 的 GPCR。NLP-1 和 NLP-99 在线虫中广泛保守,它们在大多数物种中的表现与其受体一致。这些发现证明了线虫中功能性 Gal/AstA 和 SST/AstC 信号系统的保守性。我们的线虫多肽 GPCR 同源物数据集还为进一步研究线虫门中多肽 GPCR 的功能奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Global analysis of neuropeptide receptor conservation across phylum Nematoda.

Background: 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.

Results: 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.

Conclusions: 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.

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来源期刊
BMC Biology
BMC Biology 生物-生物学
CiteScore
7.80
自引率
1.90%
发文量
260
审稿时长
3 months
期刊介绍: BMC Biology is a broad scope journal covering all areas of biology. Our content includes research articles, new methods and tools. BMC Biology also publishes reviews, Q&A, and commentaries.
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