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小鼠血管紧张素II 2型受体cDNA的克隆及基因分析

Cloning of cDNA and analysis of the gene for mouse angiotensin II type 2 receptor.

作者信息

Nakajima M, Mukoyama M, Pratt R E, Horiuchi M, Dzau V J

机构信息

Falk Cardiovascular Research Center, Stanford University School of Medicine, California 94305-5246.

出版信息

Biochem Biophys Res Commun. 1993 Dec 15;197(2):393-9. doi: 10.1006/bbrc.1993.2492.

Abstract

A cDNA clone encoding the mouse angiotensin receptor subtype 2 (AT2 receptor) was isolated from a mouse fetal cDNA library. Mouse AT2 receptor full-length cDNA contains a 1089-base-pair open reading frame which encodes a protein of 363 amino acid residues. Hydropathy analysis reveals seven putative transmembrane domains. Specific binding of [125I]CGP42112A was demonstrated in membranes of COS-7 cells transfected with the cDNA. Scatchard analysis and ligand displacement profile were typical of the AT2 receptor. Northern blot and reverse transcription-polymerase chain reaction analyses demonstrated that AT2 receptor mRNA was expressed abundantly in fetus and in a lesser amount in adult brain. Analysis of the mouse AT2 receptor gene reveals that the mouse AT2 receptor locus exists as a single copy in the genome, and that the gene does not contain introns in the coding region.

摘要

从小鼠胎儿cDNA文库中分离出一个编码小鼠血管紧张素受体2型(AT2受体)的cDNA克隆。小鼠AT2受体全长cDNA包含一个1089个碱基对的开放阅读框,编码一个由363个氨基酸残基组成的蛋白质。亲水性分析揭示了七个推定的跨膜结构域。在用该cDNA转染的COS-7细胞膜中证实了[125I]CGP42112A的特异性结合。Scatchard分析和配体置换图谱是AT2受体的典型特征。Northern印迹和逆转录-聚合酶链反应分析表明,AT2受体mRNA在胎儿中大量表达,在成体脑中表达量较少。对小鼠AT2受体基因的分析表明,小鼠AT2受体基因座在基因组中以单拷贝形式存在,并且该基因在编码区不包含内含子。

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