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大鼠组胺H1受体的基因组克隆

Genomic cloning of the rat histamine H1 receptor.

作者信息

Fujimoto K, Horio Y, Sugama K, Ito S, Liu Y Q, Fukui H

机构信息

Department of Pharmacology II, Faculty of Medicine, Osaka University, Suita, Japan.

出版信息

Biochem Biophys Res Commun. 1993 Jan 15;190(1):294-301. doi: 10.1006/bbrc.1993.1045.

Abstract

A rat histamine H1 receptor gene which lacked introns was isolated from a rat genomic library using recently cloned bovine histamine H1 receptor cDNA [Yamashita et al., Proc. Natl. Acad. Sci. USA, 88, 11515-11519 (1991)]. The receptor protein deduced from this isolated gene was composed of 486 amino acids and showed characteristic properties of G protein-coupled receptors. At the 5'-flanking region of the receptor gene, we have located potential TATA box sequences and consensus sequences for the glucocorticoid response element and AP-2 element. After being subcloned into a mammalian expression vector, the isolated gene was transfected to C6 glioma cells. These cells showed significant binding toward [3H]mepyramine. The binding was inhibited by H1 antagonists or histamine. The mode of this binding was comparable to the binding of membranes derived from rat tissues toward [3H]mepyramine. Northern blot analysis detected a 3.0 kb nucleotide band for histamine H1 receptor mRNAs from rat brain and small intestine when these mRNAs were hybridized with the isolated rat H1 gene. The present results demonstrate the isolation of the rat histamine H1 receptor gene.

摘要

利用最近克隆的牛组胺H1受体cDNA[山下等人,《美国国家科学院院刊》,88,11515 - 11519(1991)],从大鼠基因组文库中分离出一个不含内含子的大鼠组胺H1受体基因。从这个分离出的基因推导的受体蛋白由486个氨基酸组成,并显示出G蛋白偶联受体的特征性质。在受体基因的5'-侧翼区,我们定位了潜在的TATA盒序列以及糖皮质激素反应元件和AP-2元件的共有序列。在被亚克隆到哺乳动物表达载体后,将分离出的基因转染到C6胶质瘤细胞中。这些细胞对[3H]美吡拉敏显示出显著的结合。该结合被H1拮抗剂或组胺抑制。这种结合模式与源自大鼠组织的膜对[3H]美吡拉敏的结合相当。当大鼠脑和小肠的组胺H1受体mRNA与分离出的大鼠H1基因杂交时,Northern印迹分析检测到一条3.0 kb的核苷酸带。目前的结果证明了大鼠组胺H1受体基因的分离。

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