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寄生线虫FLP能神经肽补体的新见解:为去孤儿化方法提供信息

New insights into the FLPergic complements of parasitic nematodes: Informing deorphanisation approaches.

作者信息

McCoy Ciaran J, Atkinson Louise E, Zamanian Mostafa, McVeigh Paul, Day Tim A, Kimber Michael J, Marks Nikki J, Maule Aaron G, Mousley Angela

机构信息

Molecular Biosciences-Parasitology, Institute for Global Food Security, School of Biological Sciences, Queen's University Belfast, Belfast, UK.

Department of Biomedical Sciences, Iowa State University, Ames, IA, USA.

出版信息

EuPA Open Proteom. 2014 Apr 19;3:262-272. doi: 10.1016/j.euprot.2014.04.002. eCollection 2014 Jun.

Abstract

FMRFamide-like peptide (FLP) receptors are appealing as putative anthelmintic targets. To date, 31 -encoding genes have been identified in and thirteen FLP-activated G-protein coupled receptors (FLP-GPCRs) have been reported. The lack of knowledge on FLPs and FLP-GPCRs in parasites impedes their functional characterisation and chemotherapeutic exploitation. Using homology-based BLAST searches and phylogenetic analyses this study describes the identification of putative and -GPCR gene homologues in 17 nematode parasites providing the first pan-phylum genome-based overview of the FLPergic complement. These data will facilitate FLP-receptor deorphanisation efforts in the quest for novel control targets for nematode parasites.

摘要

FMRF酰胺样肽(FLP)受体作为潜在的驱虫靶点很有吸引力。迄今为止,已在[具体物种]中鉴定出31个编码基因,并报道了13种FLP激活的G蛋白偶联受体(FLP-GPCRs)。对寄生虫中FLP和FLP-GPCRs缺乏了解阻碍了它们的功能表征和化疗应用。本研究通过基于同源性的BLAST搜索和系统发育分析,描述了在17种线虫寄生虫中推定的[具体基因]和-GPCR基因同源物的鉴定,提供了首个基于全门类基因组的FLP能系统概述。这些数据将有助于在寻找线虫寄生虫新控制靶点的过程中推动FLP受体的去孤儿化工作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7100/4405611/ed84bdce092e/fx1.jpg

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