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Volume 582, Issue 5, Pages 661-665 (5 March 2008)


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14-3-3 Proteins directly regulate Ca2+/calmodulin-dependent protein kinase kinase α through phosphorylation-dependent multisite binding

Edited by Jesus Avila

Tohru IchimuraaCorresponding Author Informationemail address, Masato Taokaa, Yasukazu Hozumib, Kaoru Gotob, Hiroshi Tokumitsuc

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.

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 InformationCorresponding 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


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