Ross C A, Danoff S K, Schell M J, Snyder S H, Ullrich A
Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205-2195.
Proc Natl Acad Sci U S A. 1992 May 15;89(10):4265-9. doi: 10.1073/pnas.89.10.4265.
Three inositol 1,4,5-trisphosphate receptor (IP3R) cDNAs, designated IP3R-II, -III, and -IV, were cloned from a mouse placenta cDNA library. All three display strong homology in membrane-spanning domains M7 and M8 to the originally cloned cerebellar IP3R-I, with divergences predominantly in cytoplasmic domains. Levels of mRNA for the three additional IP3Rs in general are substantially lower than for IP3R-I, though in the gastrointestinal tract the levels of IP3R-III may be comparable to IP3R-I. Cerebellar Purkinje cells express at least two and possibly three distinct IP3Rs, suggesting heterogeneity of IP3 action within a single cell.
从一个小鼠胎盘cDNA文库中克隆出了三个肌醇1,4,5-三磷酸受体(IP3R)cDNA,分别命名为IP3R-II、-III和-IV。这三个受体在跨膜结构域M7和M8中与最初克隆的小脑IP3R-I具有很强的同源性,差异主要存在于细胞质结构域。一般来说,另外三个IP3R的mRNA水平明显低于IP3R-I,不过在胃肠道中,IP3R-III的水平可能与IP3R-I相当。小脑浦肯野细胞表达至少两种,也可能是三种不同的IP3R,这表明在单个细胞内IP3的作用具有异质性。