Sugita R, Mochizuki H, Ito T, Yokokura H, Kobayashi R, Hidaka H
Department of Pharmacology, Nagoya University School of Medicine, Japan.
Biochem Biophys Res Commun. 1994 Aug 30;203(1):694-701. doi: 10.1006/bbrc.1994.2238.
Recently we obtained evidence for the existence of Ca2+/calmodulin-dependent protein kinase kinase (CaMKK), which was partially purified in the process of the purification step of Ca2+/calmodulin-dependent protein kinase V (CaM kinase V). This enzyme promoted phosphorylation of the autophosphorylation site on CaM kinase V and activated the activity (Mochizuki, H. et al. (1993) Biochem. Biophys. Res. Commun. 197, 1595-1600). Present study revealed that CaMKK also phosphorylated CaM kinase IV associated with the activation of its activity. Phosphorylation of CaM kinase IV by CaMKK occurred on multiple sites. Furthermore, CaM kinase IV and CaM kinase V phosphorylated each other which resulted in their activation. The phosphorylation site of CaM kinase V by CaM kinase IV was the same as the autophosphorylation site. Our study suggests the existence of a heretofore CaM kinases cascade consisting of a sequential activation of each CaM kinase.
最近,我们获得了钙调蛋白依赖性蛋白激酶激酶(CaMKK)存在的证据,它是在钙调蛋白依赖性蛋白激酶V(CaM激酶V)的纯化步骤中部分纯化得到的。这种酶促进了CaM激酶V上自身磷酸化位点的磷酸化,并激活了其活性(望月,H.等人(1993年)《生物化学与生物物理学研究通讯》197,1595 - 1600)。目前的研究表明,CaMKK还能磷酸化与CaM激酶IV活性激活相关的CaM激酶IV。CaMKK对CaM激酶IV的磷酸化发生在多个位点。此外,CaM激酶IV和CaM激酶V相互磷酸化,从而导致它们的激活。CaM激酶IV对CaM激酶V的磷酸化位点与自身磷酸化位点相同。我们的研究表明存在一种迄今为止由每种CaM激酶依次激活组成的CaM激酶级联反应。