Mechanism Of The Generation Of Autonomous Activity Of Ca2+/Calmodulin-Dependent Protein Kinase Iv

Ca2+/calmodulin-dependent protein kinase IV (CaM-KIV) is phosphorylated at Thr(196) by Ca2+/calmodulin-dependent protein kinase kinase (CaM-KK), resulting in induction of both autonomous activity and a high level of Ca2+/CaM-dependent activity. We have shown that the kinetics of Thr(196) phosphorylation of CaM-KIV by CaM-KK is well correlated with the generation of its autonomous activity, although Thr(177) phosphorylation of CaM-KI does not induce its autonomous activity. The activities of CaM-KI chimera mutants fused with C-terminal regions ( residues 296 - 469 and 296 - 350) of CaM-KIV are completely dependent on Ca2+/CaM, which is also the case for CaM-KI. Unlike wild-type CaM-KI, however, phosphorylation of Thr177 in the chimera mutants by CaM-KK resulted in generation of significant autonomous activities, indicating that the phosphorylation of Thr in the activation loop is sufficient to partially release the autoinhibitory region of CaM-KIV from the catalytic core. Indeed, the CaM-KIV peptide ( residues 304 - 325) containing minimum autoinhibitory sequences ( residues 314 - 321) suppressed the activity of non-phosphorylated CaM-KIV with an IC50 of similar to50 muM, and this suppression was competitive with respect to the peptide substrate; however, the CaM-KIV peptide was not capable of inhibiting Thr(196)-phosphorylated CaM-KIV. Taken together, these results indicated that the Thr(196) phosphorylation of CaM-KIV by CaM-KK reduced the interaction of the catalytic core with the autoinhibitory region, resulting in generation of the autonomous activity.