Nagai Y, Ueno S, Saeki Y, Soga F, Yanagihara T
Department of Neurology, Osaka University Medical School, Japan.
Biochem Biophys Res Commun. 1993 Jul 15;194(1):368-74. doi: 10.1006/bbrc.1993.1829.
The sequential reverse transcription and polymerase chain reaction amplified the mRNA coding for the D3 dopamine receptor (D3R) in human peripheral blood lymphocytes. Pharmacological analysis confirmed the binding of the D3R specific ligand to the lymphocytes. In addition, there was a novel shorter variant transcript of the D3R gene generated by alternative splicing in lymphocytes and brain. This variant, termed D3(TM4-del), has a 143 bp deletion and encodes a 138 amino acid protein containing the first three transmembrane domains of the native D3R.
连续逆转录和聚合酶链反应扩增了人外周血淋巴细胞中编码D3多巴胺受体(D3R)的mRNA。药理学分析证实了D3R特异性配体与淋巴细胞的结合。此外,淋巴细胞和大脑中通过可变剪接产生了一种新的、较短的D3R基因变体转录本。这种变体称为D3(TM4-del),有143 bp的缺失,编码一种含天然D3R前三个跨膜结构域的138个氨基酸的蛋白质。