| | 14-3-3 Proteins directly regulate Ca2+/calmodulin-dependent protein kinase kinase α through phosphorylation-dependent multisite bindingEdited by Jesus Avila Received 7 December 2007; accepted 23 January 2008. published online 31 January 2008. Abstract Ca2+/calmodulin-dependent protein kinase kinase α (CaMKKα) plays critical roles in the modulation of neuronal cell survival as well as many other cellular activities. Here we show that 14-3-3 proteins directly regulate CaMKKα when the enzyme is phosphorylated by protein kinase A on either Ser74 or Ser475. Mutational analysis revealed that these two serines are both functional: the CaMKKα mutant with a mutation at either of these residues, but not the double mutant, was inhibited significantly by 14-3-3. The mode of regulation described herein differs the recently described mode of 14-3-3 regulation of CaMKKα. Abbreviations: CaMKKα, Ca2+/calmodulin-dependent protein kinase kinase α, CaMKI, Ca2+/calmodulin-dependent protein kinase I, CaMKIV, Ca2+/calmodulin-dependent protein kinase IV, PKA, cAMP-dependent protein kinase A, MAPK, mitogen-activated protein kinase, PKB, protein kinase B, CaM, calmodulin, GST, glutathione S-transferase, WT, wild-type a Department of Chemistry, Graduate School of Science, Tokyo Metropolitan University, Tokyo 192-0397, Japan b Department of Anatomy and Cell Biology, Yamagata University School of Medicine, Yamagata 990-9585, Japan c Department of Signal Transduction Sciences, Faculty of Medicine, Kagawa University, Kagawa 761-0793, Japan Corresponding author. Present Address: Department of Applied Chemistry, National Defense Academy, Yokosuka, Kanagawa 239-8686, Japan. Fax: +81 468 44 5901.
PII: S0014-5793(08)00062-8 doi:10.1016/j.febslet.2008.01.037 © 2008 Federation of European Biochemical Societies | |
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