首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Cloning molecular characterization and chromosomal assignment of a gene encoding a second D1 dopamine receptor subtype: differential expression pattern in rat brain compared with the D1A receptor.
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Cloning molecular characterization and chromosomal assignment of a gene encoding a second D1 dopamine receptor subtype: differential expression pattern in rat brain compared with the D1A receptor.

机译:编码第二种D1多巴胺受体亚型的基因的克隆分子表征和染色体分配:与D1A受体相比大鼠脑中的差异表达模式。

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摘要

Multiple D1 dopaminergic receptor subtypes have been postulated on the basis of pharmacological, biochemical, and genetic studies. We describe the isolation and characterization of a rat gene encoding a dopamine receptor that is structurally and functionally similar to the D1 dopamine receptor. The coding region, which is intronless, encodes a protein of 475 amino acids (Mr 52,834) with structural features that are consistent with receptors coupled to guanine nucleotide-binding regulatory proteins. The expressed protein binds dopaminergic ligands and mediates stimulation of adenylyl cyclase with pharmacological properties similar to those of the D1 dopamine receptor. The gene encoding the human homologue of this receptor subtype is located to the short arm of chromosome 4 (4p16.3), the same region as the Huntington disease gene. In striking contrast to the previously cloned D1 receptor, little or no mRNA for the receptor described here was observed in striatum, nucleus accumbens, olfactory tubercle, and frontal cortex. High levels of mRNA for this receptor were found in distinct layers of the hippocampus, the mammillary nuclei, and the anterior pretectal nuclei, brain regions that have been shown to exhibit little or no D1 dopamine receptor binding. On the basis of its properties we propose that this dopamine receptor subtype be called D1B.
机译:在药理学,生化和遗传学研究的基础上,假定了多种D1多巴胺能受体亚型。我们描述了编码多巴胺受体的大鼠基因的分离和表征,该基因在结构和功能上与D1多巴胺受体相似。该编码区是无内含子,编码一个475个氨基酸的蛋白质(Mr 52,834),其结构特征与与鸟嘌呤核苷酸结合的调节蛋白偶联的受体一致。表达的蛋白结合多巴胺能配体并介导腺苷酸环化酶的刺激,其药理特性类似于D1多巴胺受体的药理特性。编码该受体亚型的人类同源物的基因位于4号染色体的短臂(4p16.3),与亨廷顿病基因相同。与先前克隆的D1受体形成鲜明对比的是,在纹状体,伏隔核,嗅结节和额叶皮层中观察到很少或没有本文所述受体的mRNA。在海马,乳突和前额前核的不同层中发现了该受体的高水平mRNA,这些脑区域已显示出很少或没有D1多巴胺受体结合。根据其性质,我们建议将该多巴胺受体亚型称为D1B。

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