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鸡和鸭中四个孤儿受体(GPR3、GPR6、GPR12 和 GPR12L)的特征鉴定以及孕酮对卵巢颗粒细胞表达的调控。

Characterization of Four Orphan Receptors (GPR3, GPR6, GPR12 and GPR12L) in Chickens and Ducks and Regulation of Expression in Ovarian Granulosa Cells by Progesterone.

机构信息

Key Laboratory of Bio-Resources and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu 610065, China.

China Conservation and Research Centre for the Giant Panda, Wolong Nature Reserve, Wolong 623006, China.

出版信息

Genes (Basel). 2021 Mar 27;12(4):489. doi: 10.3390/genes12040489.

DOI:10.3390/genes12040489
PMID:33801713
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8065388/
Abstract

The three structurally related orphan G protein-coupled receptors, GRP3, GPR6, and GPR12, are reported to be constitutively active and likely involved in the regulation of many physiological/pathological processes, such as neuronal outgrowth and oocyte meiotic arrest in mammals. However, the information regarding these orphan receptors in nonmammalian vertebrates is extremely limited. Here, we reported the structure, constitutive activity, and tissue expression of these receptors in two representative avian models: chickens and ducks. The cloned duck and duck/chicken and are intron-less and encode receptors that show high amino acid (a.a.) sequence identities (66-88%) with their respective mammalian orthologs. Interestingly, a novel GPR12-like receptor (named GPR12L) sharing 66% a.a. identity to that in vertebrates was reported in the present study. Using dual-luciferase reporter assay and Western blot, we demonstrated that GPR3, GPR6, GPR12, and GPR12L are constitutively active and capable of stimulating the cAMP/PKA signaling pathway without ligand stimulation in birds (and zebrafish), indicating their conserved signaling property across vertebrates. RNA-seq data/qRT-PCR assays revealed that and expression is mainly restricted to the chicken brain, while is highly expressed in chicken ovarian granulosa cells (GCs) and oocytes of 6 mm growing follicles and its expression in cultured GCs is upregulated by progesterone. Taken together, our data reveal the structure, function, and expression of GPR3, GPR6, GPR12, and GPR12L in birds, thus providing the first piece of evidence that expression is upregulated by gonadal steroid (i.e., progesterone) in vertebrates.

摘要

三种结构相关的孤儿 G 蛋白偶联受体,GRP3、GPR6 和 GPR12,被报道为组成型激活,可能参与许多生理/病理过程的调节,如哺乳动物中的神经元生长和卵母细胞减数分裂阻滞。然而,关于这些非哺乳动物脊椎动物孤儿受体的信息极其有限。在这里,我们报告了两个代表性鸟类模型:鸡和鸭中这些受体的结构、组成型活性和组织表达。克隆的鸭[Duck]和鸭/鸡[Duck/Chicken]和[Duck/Chicken]没有内含子,编码的受体与各自的哺乳动物同源物具有高氨基酸(a.a.)序列同一性(66-88%)。有趣的是,本研究报道了一种新型 GPR12 样受体(命名为 GPR12L),与脊椎动物中的 GPR12 具有 66%的 a.a.同一性。使用双荧光素酶报告基因检测和 Western blot 实验,我们证明了 GPR3、GPR6、GPR12 和 GPR12L 在鸟类(和斑马鱼)中是组成型激活的,能够在没有配体刺激的情况下刺激 cAMP/PKA 信号通路,表明它们在脊椎动物中的信号转导特性是保守的。RNA-seq 数据/qRT-PCR 检测表明[Duck/Chicken]和[Duck/Chicken]的表达主要局限于鸡脑,而[Duck/Chicken]在鸡卵巢颗粒细胞(GCs)和 6mm 生长卵泡的卵母细胞中高度表达,其在培养的 GCs 中的表达受孕激素上调。综上所述,我们的数据揭示了 GPR3、GPR6、GPR12 和 GPR12L 在鸟类中的结构、功能和表达,从而首次提供了证据表明,在脊椎动物中,性腺类固醇(即孕激素)上调了[Duck/Chicken]的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f0f/8065388/9e7d93f81252/genes-12-00489-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f0f/8065388/8f4107033500/genes-12-00489-g001a.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f0f/8065388/ce39c7ea1bab/genes-12-00489-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f0f/8065388/a24b041b880a/genes-12-00489-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f0f/8065388/ff24ab6f277f/genes-12-00489-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f0f/8065388/e39188044df9/genes-12-00489-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f0f/8065388/4b9e4447cea2/genes-12-00489-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f0f/8065388/9e7d93f81252/genes-12-00489-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f0f/8065388/8f4107033500/genes-12-00489-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f0f/8065388/2a076a905a6c/genes-12-00489-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f0f/8065388/ce39c7ea1bab/genes-12-00489-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f0f/8065388/a24b041b880a/genes-12-00489-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f0f/8065388/ff24ab6f277f/genes-12-00489-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f0f/8065388/e39188044df9/genes-12-00489-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f0f/8065388/4b9e4447cea2/genes-12-00489-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f0f/8065388/9e7d93f81252/genes-12-00489-g008.jpg

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