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与生长激素促分泌素及神经降压素受体相关的两个人类G蛋白偶联受体基因(GPR38和GPR39)的克隆与特性分析

Cloning and characterization of two human G protein-coupled receptor genes (GPR38 and GPR39) related to the growth hormone secretagogue and neurotensin receptors.

作者信息

McKee K K, Tan C P, Palyha O C, Liu J, Feighner S D, Hreniuk D L, Smith R G, Howard A D, Van der Ploeg L H

机构信息

Department of Biochemistry and Physiology, Merck Research Laboratories, Rahway, New Jersey 07065, USA.

出版信息

Genomics. 1997 Dec 15;46(3):426-34. doi: 10.1006/geno.1997.5069.

Abstract

The recent cloning of a growth hormone secretagogue receptor (GHS-R) from human pituitary gland and brain identified a third G protein-coupled receptor (GPC-R) involved in the control of growth hormone release. The nucleotide sequence of the GHS-R is most closely related to the neurotensin receptor-1 (NT-R1) (35% overall protein identity). Two human GPC-Rs related to both the type 1a GHS-R and NT-Rs were cloned and characterized. Hybridization at low posthybridizational stringency with restriction enzyme-digested human genomic DNA resulted in the identification of a genomic clone encoding a first GHS-R/NT-R family member (GPR38). A cDNA clone was identified encoding a second GHS-R-related gene (GPR39). GPR38 and GPR39 share significant amino acid sequence identity with the GHS-R and NT-Rs 1 and 2. An acidic residue (E124) in TM-3, essential for the binding and activation of the GHS-R by structurally dissimilar GHSs, was conserved in GPR38 and GPR39. GPR38 is encoded by a single gene expressed in thyroid gland, stomach, and bone marrow. GPR39 is encoded by a highly conserved single-copy gene, expressed in brain and other peripheral tissues. Fluorescence in situ hybridization localized the genes for GPR38 and GPR39 to separate chromosomes, distinct from the gene encoding the GHS-R and NT-R type 1. The ligand-binding and functional properties of GPR38 and GPR39 remain to be determined.

摘要

最近从人垂体和大脑中克隆出一种生长激素促分泌素受体(GHS-R),这确定了参与生长激素释放控制的第三种G蛋白偶联受体(GPC-R)。GHS-R的核苷酸序列与神经降压素受体-1(NT-R1)关系最为密切(总体蛋白质同一性为35%)。克隆并鉴定了两种与1a型GHS-R和NT-Rs相关的人GPC-R。用限制性内切酶消化的人基因组DNA在低杂交后严格度下进行杂交,从而鉴定出一个编码首个GHS-R/NT-R家族成员(GPR38)的基因组克隆。鉴定出一个编码第二个GHS-R相关基因(GPR39)的cDNA克隆。GPR38和GPR39与GHS-R以及NT-Rs 1和2具有显著的氨基酸序列同一性。跨膜区3(TM-3)中的一个酸性残基(E124)对于结构不同的生长激素促分泌素与GHS-R的结合和激活至关重要,该残基在GPR38和GPR39中保守。GPR38由在甲状腺、胃和骨髓中表达的单个基因编码。GPR39由一个高度保守的单拷贝基因编码,在大脑和其他外周组织中表达。荧光原位杂交将GPR38和GPR39的基因定位到不同的染色体上,这与编码GHS-R和1型NT-R的基因不同。GPR38和GPR39的配体结合和功能特性仍有待确定。

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