Nakagawa T, Okano H, Furuichi T, Aruga J, Mikoshiba K
Division of Regulation of Macromolecular Function, Osaka University, Suita, Japan.
Proc Natl Acad Sci U S A. 1991 Jul 15;88(14):6244-8. doi: 10.1073/pnas.88.14.6244.
Additional subtypes of the inositol 1,4,5-trisphosphate (InsP3) receptor are expressed in a tissue-specific and developmentally specific manner. They differ from the InsP3 receptor structure previously reported in two small variably spliced segments. One segment (SI) is located within the InsP3 binding site, whereas another segment (SII) is located near putative sites for phosphorylation and ATP binding to modulate InsP3 action on Ca2+ flux. Therefore, we speculate that selective use of InsP3 receptor subtypes permits a tissue-specific and developmentally specific expression of functionally distinct channels.
肌醇1,4,5-三磷酸(InsP3)受体的其他亚型以组织特异性和发育特异性的方式表达。它们与先前报道的InsP3受体结构在两个可变剪接的小片段上有所不同。一个片段(SI)位于InsP3结合位点内,而另一个片段(SII)位于磷酸化和ATP结合的假定位点附近,以调节InsP3对Ca2+通量的作用。因此,我们推测InsP3受体亚型的选择性使用允许功能不同的通道在组织和发育上特异性表达。