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在黑腹果蝇中进行的系统性G蛋白偶联受体分析鉴定出一种具有新功能的促白细胞激素受体。

Systematic G-protein-coupled receptor analysis in Drosophila melanogaster identifies a leucokinin receptor with novel roles.

作者信息

Radford Jonathan C, Davies Shireen A, Dow Julian A T

机构信息

Division of Molecular Genetics, Institute of Biomedical & Life Sciences, University of Glasgow, Glasgow G11 6NU, United Kingdom.

出版信息

J Biol Chem. 2002 Oct 11;277(41):38810-7. doi: 10.1074/jbc.M203694200. Epub 2002 Aug 5.

Abstract

Leucokinins are insect neuropeptides that stimulate hindgut motility and renal fluid secretion. Drosophila has a single leucokinin gene, pp, encoding the longest known leucokinin, Drosokinin. To identify its receptor, a genome-wide scan for G-protein-coupled receptors was performed in silico and candidate receptors identified by similarity to known tachykinin receptors. The deduced peptides were expressed, with a transgene for the calcium reporter aequorin, in S2 cells and only one gene (CG10626) encoded a protein that responded to Drosokinin. The properties of the heterologously expressed receptor (action through intracellular calcium with an EC(50) of 4 x 10(-11) m and a t(1/2) <1 s) match closely those reported for the action of Drosokinin on Malpighian (renal) tubules. Antibodies raised against the receptor identified known sites of leucokinin action: stellate cells of the Malpighian tubule, two triplets of cells in the pars intercerebralis of the adult central nervous system, and additional cells in larval central nervous system. Western blots and reverse transcription-PCR confirmed these locations, but also identified expression in male and female gonads. These tissues also displayed elevated calcium in response to Drosokinin, demonstrating novel roles for leucokinin. A functional genomic approach has thus yielded the first complete characterization of a leucokinin receptor in an insect.

摘要

亮激肽是一类昆虫神经肽,可刺激后肠蠕动和肾液分泌。果蝇有一个单一的亮激肽基因pp,编码已知最长的亮激肽——果蝇激肽。为了鉴定其受体,通过计算机模拟在全基因组范围内扫描G蛋白偶联受体,并通过与已知速激肽受体的相似性鉴定候选受体。将推导的肽与钙报告蛋白水母发光蛋白的转基因一起在S2细胞中表达,只有一个基因(CG10626)编码对果蝇激肽有反应的蛋白质。异源表达受体的特性(通过细胞内钙起作用,EC(50)为4×10(-11) m,t(1/2) <1 s)与报道的果蝇激肽对马尔皮基(肾)小管作用的特性密切匹配。针对该受体产生的抗体确定了亮激肽作用的已知位点:马尔皮基小管的星状细胞、成年中枢神经系统脑间部的两组三联体细胞以及幼虫中枢神经系统中的其他细胞。蛋白质免疫印迹和逆转录PCR证实了这些位置,但也确定了在雄性和雌性性腺中的表达。这些组织对果蝇激肽也有钙升高反应,证明了亮激肽的新作用。因此,一种功能基因组学方法首次完整地鉴定了昆虫中的亮激肽受体。

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