Miyake A
Molecular Medicine Research Laboratories, Yamanouchi Pharmaceutical Co. Ltd, Tukuba-city, Japan.
Biochem Biophys Res Commun. 1995 Mar 8;208(1):230-7. doi: 10.1006/bbrc.1995.1328.
An isoform cDNA of CCK-B/gastrin receptor was isolated from human stomach. This cDNA differed from initially cloned cDNA only in the 5'-end region and encoded a truncated isoform (delta CCK-B) in which the putative N-terminal extracellular domain of the CCK-B/gastrin receptor was completely lost. Isolation of genomic CCK-B/gastrin receptor DNA revealed that this transcript is generated by alternative usage of a novel exon, termed exon 1b. Human stomach expressed both transcripts of delta CCK-B and entire CCK-B/gastrin receptor (CCK-BR), whereas human stomach cancer cell line AGS exclusively expressed delta CCK-B transcripts. Transfection of COS-7 with delta CCK-B cDNA led to the appearance of binding sites for 125I-CCK-8. Its ligand selectivity was different from that of CCK-BR. These results suggest the molecular diversity in CCK-B/gastrin receptor subtypes.
从人胃中分离出CCK - B/胃泌素受体的一种亚型cDNA。该cDNA与最初克隆的cDNA仅在5'端区域有所不同,编码一种截短的亚型(δCCK - B),其中CCK - B/胃泌素受体假定的N端胞外结构域完全缺失。基因组CCK - B/胃泌素受体DNA的分离表明,该转录本是由一个称为外显子1b的新外显子的选择性使用产生的。人胃表达δCCK - B和完整的CCK - B/胃泌素受体(CCK - BR)的两种转录本,而人胃癌细胞系AGS仅表达δCCK - B转录本。用δCCK - B cDNA转染COS - 7细胞导致出现125I - CCK - 8的结合位点。其配体选择性与CCK - BR不同。这些结果表明CCK - B/胃泌素受体亚型存在分子多样性。