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从COS-7细胞中克隆非洲绿猴(猕猴)促肾上腺皮质激素释放因子受体1型(CRF1)并进行初步表征。

Molecular cloning and initial characterization of African green monkey (Cercopithecus aethiops) corticotropin releasing factor receptor type 1 (CRF1) from COS-7 cells.

作者信息

Slominski Andrzej T, Zmijewski Michal A, Pisarchik Alexander, Wortsman Jacobo

机构信息

Department of Pathology, University of Tennessee Health Science Center, Memphis, TN 38163, USA.

出版信息

Gene. 2007 Mar 15;389(2):154-62. doi: 10.1016/j.gene.2006.11.001. Epub 2006 Nov 10.

Abstract

We report the expression of endogenous CRF1 in COS-7 cells (African green monkey origin). Cloning of the coding region of CRF1 gene identified three alternatively spliced isoforms with nucleotide and predicted amino acid sequences corresponding to the membrane bound alpha and c and soluble e isoforms. DNA sequencing of the main isoform CRF1alpha showed homologies of 99%, 97% and 91% with the rhesus monkey, human and rodent genes, respectively; the deduced protein sequence differed in only one amino acid with rhesus monkey and human. Western blot analysis with antibodies against human CRF1 demonstrated immunoreactive proteins with MW of 37, 52, 70 and 80-85 in crude membrane or cytoplasm preparation; two additional species of 40 and 60 kDa were detected only in the cytoplasmic fraction. On immunocytochemistry CRF1 was localized to both the cell surface and intracellularly. The receptor was functional, e.g., addition of CRF to COS-7 cells inhibited cell proliferation and stimulated release of arachidonic acid; nevertheless, it was poorly coupled to cAMP production (its stimulation was minimal in native cells). In conclusion, COS cells that are routinely used for the study of transfected CRF receptors do express endogenous CRF1 mRNA with splicing behavior similar to that reported in human and rodent cells, and translated into functional CRF1 receptors.

摘要

我们报道了内源性促肾上腺皮质激素释放因子受体1(CRF1)在COS-7细胞(源自非洲绿猴)中的表达。CRF1基因编码区的克隆鉴定出三种选择性剪接的异构体,其核苷酸和预测的氨基酸序列分别对应于膜结合的α和c异构体以及可溶性e异构体。主要异构体CRF1α的DNA测序显示,其与恒河猴、人类和啮齿动物基因的同源性分别为99%、97%和91%;推导的蛋白质序列与恒河猴和人类仅在一个氨基酸上有所不同。用抗人CRF1抗体进行的蛋白质印迹分析表明,在粗制膜或细胞质制剂中存在分子量为37、52、70和80 - 85的免疫反应性蛋白;仅在细胞质组分中检测到另外两种分子量为40和60 kDa的蛋白。免疫细胞化学显示CRF1定位于细胞表面和细胞内。该受体具有功能,例如,向COS-7细胞中添加促肾上腺皮质激素释放因子(CRF)可抑制细胞增殖并刺激花生四烯酸的释放;然而,它与环磷酸腺苷(cAMP)生成的偶联较差(在天然细胞中其刺激作用最小)。总之,常用于研究转染的CRF受体的COS细胞确实表达内源性CRF1 mRNA,其剪接行为与人类和啮齿动物细胞中报道的相似,并可翻译为功能性CRF1受体。

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