Yamamoto-Hino M, Sugiyama T, Hikichi K, Mattei M G, Hasegawa K, Sekine S, Sakurada K, Miyawaki A, Furuichi T, Hasegawa M
Tokyo Research Laboratories, Kyowa Hakko Kogyo Co., Ltd., Japan.
Recept Channels. 1994;2(1):9-22.
We have cloned cDNAs coding for human type 2 and type 3 and part of type 1 inositol 1,4,5-trisphosphate receptors (IP3Rs). The complete nucleotide sequences for type 2 and type 3 receptors were determined and the pharmacological properties of the latter were characterized. Human type 2 and type 3 IP3Rs are 2701 amino acids and 2671 amino acids long, respectively, and have significant sequence homologies as well as structural similarities including the six membrane-spanning regions near the C-termini when compared with the rat or mouse counterpart. COS-7 cells transfected with human type 3 IP3R showed characteristic inositol 1,4,5-trisphosphate (IP3)-binding properties with Kd values of 28.8 nM. The order of potency of competition with IP3 was Ins(1,4,5)P3 (IP3) > Ins(2,4,5)P3 > Ins(1,3,4,5)P4 > Ins(1,2,3,4,5,6)P6. Type 2 and type 3 IP3Rs were mapped to human chromosomes 12p11 and 6p21, respectively, by in situ hybridization. cDNA cloning of the human IP3Rs allowed us to identify the types of the receptor expressed in various human hematopoietic and lymphoma cell lines. The type 3 receptor was present in all of cell lines tested, while the type 1 or 2 receptor was expressed in only particular cell types. The differential expression of the IP3R types could confer the cell-specific regulation on the IP3/Ca2+ signalling.
我们已经克隆了编码人2型、3型以及部分1型肌醇1,4,5-三磷酸受体(IP3Rs)的cDNA。确定了2型和3型受体的完整核苷酸序列,并对后者的药理学特性进行了表征。人2型和3型IP3Rs分别长2701个氨基酸和2671个氨基酸,与大鼠或小鼠相应受体相比,它们具有显著的序列同源性以及结构相似性,包括靠近C末端的六个跨膜区域。用人类3型IP3R转染的COS-7细胞显示出特征性的肌醇1,4,5-三磷酸(IP3)结合特性,Kd值为28.8 nM。与IP3竞争的效力顺序为Ins(1,4,5)P3(IP3)> Ins(2,4,5)P3 > Ins(1,3,4,5)P4 > Ins(1,2,3,4,5,6)P6。通过原位杂交,2型和3型IP3Rs分别定位于人染色体12p11和6p21。人IP3Rs的cDNA克隆使我们能够鉴定在各种人类造血和淋巴瘤细胞系中表达的受体类型。3型受体存在于所有测试的细胞系中,而1型或2型受体仅在特定细胞类型中表达。IP3R类型的差异表达可以赋予IP3/Ca2+信号传导细胞特异性调节作用。