Hershey A D, Dykema P E, Krause J E
Department of Anatomy and Neurobiology, Washington University School of Medicine, St. Louis, Missouri 63110.
J Biol Chem. 1991 Mar 5;266(7):4366-74.
The gene for the rat substance P receptor has been cloned, its genomic structure determined, and the patterns of mRNA expression extensively analyzed. Unlike many genes encoding G protein-coupled receptors, the protein-coding region of this gene is divided into five exons consisting of 965, 195, 151, 197, and 2,010 base pairs. The substance P receptor gene extends more than 45 kilobases in length, and the splice sites for the exons occur at the borders of the sequences encoding putative membrane-spanning domains. The transcription initiation site has been defined by solution hybridization-nuclease protection and nucleotide sequence analyses, and lies downstream of a conventional TATA sequence. Substance P receptor mRNA levels in various tissues have been quantitated using solution hybridization-nuclease protection assays and were found to comprise from 0.00008 to 0.0016% of total RNA levels. Relatively high levels of substance P receptor mRNA are seen in the urinary bladder and the sublingual salivary gland, whereas moderate levels are observed for the submandibular salivary gland, striatum, hippocampus, midbrain, and olfactory bulb with lower levels in the remainder of the central nervous system and alimentary canal. These results are discussed in relation to the evolutionary role of multiple exons for a G protein-coupled receptor and with regard to the locations and mechanisms of substance P receptor gene expression.
大鼠P物质受体的基因已被克隆,其基因组结构已确定,并且对其mRNA表达模式进行了广泛分析。与许多编码G蛋白偶联受体的基因不同,该基因的蛋白质编码区被分为五个外显子,分别由965、195、151、197和2010个碱基对组成。P物质受体基因长度超过45千碱基,外显子的剪接位点出现在编码假定跨膜结构域的序列边界处。转录起始位点已通过溶液杂交-核酸酶保护和核苷酸序列分析确定,位于传统TATA序列的下游。使用溶液杂交-核酸酶保护试验对各种组织中的P物质受体mRNA水平进行了定量,发现其占总RNA水平的0.00008%至0.0016%。在膀胱和舌下唾液腺中可见相对较高水平的P物质受体mRNA,而在下颌下唾液腺、纹状体、海马体、中脑和嗅球中观察到中等水平,在中枢神经系统和消化道的其余部分中水平较低。本文结合G蛋白偶联受体多个外显子的进化作用以及P物质受体基因表达的位置和机制对这些结果进行了讨论。