Bruno J F, Xu Y, Song J, Berelowitz M
Department of Medicine, State University of New York, Stony Brook 11794-8154.
Proc Natl Acad Sci U S A. 1992 Dec 1;89(23):11151-5. doi: 10.1073/pnas.89.23.11151.
The PCR and conventional library screening were used to clone the brain-specific somatostatin receptor rSSTR-4 from a rat genomic library. The deduced amino acid sequence encodes a protein of 384 amino acids and displays structural and sequence homologies with members of the G protein-receptor superfamily. The amino acid sequence of rSSTR-4 is 60% and 48% identical to that of somatostatin receptors SSTR-1 and SSTR-2, respectively, two recently cloned subtypes. Competition curve analysis of the binding properties of the receptor transiently expressed in COS-1 cells revealed a higher apparent affinity for somatostatin 14 than for somatostatin 28. In contrast, the somatostatin analogs SMS 201-995, IM 4-28, and MK-678 failed to displace specific binding in transfected cells. These characteristics resemble the pharmacological binding properties of the previously described brain-specific somatostatin-receptor subtype. Examination of the tissue distribution of mRNA for rSSTR-4 revealed expression limited to various brain regions with highest levels in the cortex and hippocampus. Thus, based on the pharmacology and tissue localization of this receptor, we conclude that rSSTR-4 represents a brain-specific somatostatin receptor.
采用聚合酶链反应(PCR)和传统文库筛选方法,从大鼠基因组文库中克隆出脑特异性生长抑素受体rSSTR - 4。推导的氨基酸序列编码一个由384个氨基酸组成的蛋白质,与G蛋白受体超家族成员具有结构和序列同源性。rSSTR - 4的氨基酸序列分别与最近克隆的两种亚型生长抑素受体SSTR - 1和SSTR - 2的氨基酸序列有60%和48%的同一性。对在COS - 1细胞中瞬时表达的受体结合特性进行竞争曲线分析,结果显示其对生长抑素14的表观亲和力高于对生长抑素28的亲和力。相反,生长抑素类似物SMS 201 - 995、IM 4 - 28和MK - 678未能取代转染细胞中的特异性结合。这些特性类似于先前描述的脑特异性生长抑素受体亚型的药理学结合特性。对rSSTR - 4的mRNA组织分布进行检测,结果显示其表达仅限于大脑的各个区域,在皮质和海马中水平最高。因此,基于该受体的药理学特性和组织定位,我们得出结论,rSSTR - 4代表一种脑特异性生长抑素受体。