Van Lookeren Campagne M M, Erneux C, Van Eijk R, Van Haastert P J
Zoological Laboratory, University of Leiden, The Netherlands.
Biochem J. 1988 Sep 1;254(2):343-50. doi: 10.1042/bj2540343.
Dictyostelium discoideum homogenates contain phosphatase activity which rapidly dephosphorylates Ins(1,4,5)P3 (D-myo-inositol 1,4,5-trisphosphate) to Ins (myo-inositol). When assayed in Mg2+, Ins(1,4,5)P3 is dephosphorylated by the soluble Dictyostelium cell fraction to 20% Ins(1,4)P2 (D-myo-inositol 1,4-bisphosphate) and 80% Ins(4,5)P2 (D-myo-inositol 4,5-bisphosphate). In the particulate fraction Ins(1,4,5)P3 5-phosphatase is relatively more active than the Ins(1,4,5)P3 1-phosphatase. CaCl2 can replace MgCl2 only for the Ins(1,4,5)P3 5-phosphatase activity. Ins(1,4)P2 and Ins(4,5)P2 are both further dephosphorylated to Ins4P (D-myo-inositol 4-monophosphate), and ultimately to Ins. Li+ ions inhibit Ins(1,4,5)P3 1-phosphatase, Ins(1,4)P2 1-phosphatase, Ins4P phosphatase and L-Ins1P (L-myo-inositol 1-monophosphate) phosphatase activities; Ins(1,4,5)P3 1-phosphatase is 10-fold more sensitive to Li+ (half-maximal inhibition at about 0.25 mM) than are the other phosphatases (half-maximal inhibition at about 2.5 mM). Ins(1,4,5)P3 5-phosphatase activity is potently inhibited by 2,3-bisphosphoglycerate (half-maximal inhibition at 3 microM). Furthermore, 2,3-bisphosphoglycerate also inhibits dephosphorylation of Ins(4,5)P2. These characteristics point to a number of similarities between Dictyostelium phospho-inositol phosphatases and those from higher organisms. The presence of an hitherto undescribed Ins(1,4,5)P3 1-phosphatase, however, causes the formation of a different inositol bisphosphatase isomer [Ins(4,5)P2] from that found in higher organisms [Ins(1,4)P2]. The high sensitivity of some of these phosphatases for Li+ suggests that they may be the targets for Li+ during the alteration of cell pattern by Li+ in Dictyostelium.
盘基网柄菌匀浆含有磷酸酶活性,该活性可迅速将肌醇-1,4,5-三磷酸(Ins(1,4,5)P3)去磷酸化为肌醇(Ins)。在Mg2+存在下进行测定时,可溶性盘基网柄菌细胞组分可将Ins(1,4,5)P3去磷酸化为20%的肌醇-1,4-二磷酸(Ins(1,4)P2)和80%的肌醇-4,5-二磷酸(Ins(4,5)P2)。在颗粒组分中,Ins(1,4,5)P3 5-磷酸酶比Ins(1,4,5)P3 1-磷酸酶相对更具活性。CaCl2仅能替代MgCl2用于Ins(1,4,5)P3 5-磷酸酶活性的测定。Ins(1,4)P2和Ins(4,5)P2都会进一步去磷酸化为肌醇-4-磷酸(Ins4P),最终转化为Ins。Li+离子抑制Ins(1,4,5)P3 1-磷酸酶、Ins(1,4)P2 1-磷酸酶、Ins4P磷酸酶和L-肌醇-1-磷酸(L-Ins1P)磷酸酶的活性;Ins(1,4,5)P3 1-磷酸酶对Li+的敏感性是其他磷酸酶的10倍(约0.25 mM时达到半数最大抑制)(约2.5 mM时达到半数最大抑制)。Ins(1,4,5)P3 5-磷酸酶活性受到2,3-二磷酸甘油酸的强烈抑制(3 microM时达到半数最大抑制)。此外,2,3-二磷酸甘油酸也抑制Ins(4,5)P2的去磷酸化。这些特性表明盘基网柄菌磷酸肌醇磷酸酶与高等生物的磷酸肌醇磷酸酶之间存在许多相似之处。然而,一种迄今未描述的Ins(1,4,5)P3 1-磷酸酶的存在导致形成了与高等生物中不同的肌醇二磷酸酶异构体[Ins(4,5)P2] [Ins(1,4)P2]。其中一些磷酸酶对Li+的高敏感性表明,它们可能是盘基网柄菌中Li+改变细胞模式过程中Li+的作用靶点。