Identification of a novel protein kinase mediating Akt survival signaling to the ATM protein


Autoria(s): Suzuki, A; Kusakai, G; Kishimoto, A; Lu, J; Ogura, T; Lavin, MF; Esumi, H
Contribuinte(s)

H. Tabor

Data(s)

01/01/2003

Resumo

We identified a novel human AMP-activated protein kinase (AMPK) family member, designated ARK5, encoding 661 amino acids with an estimated molecular mass of 74 kDa. The putative amino acid sequence reveals 47, 45.8, 42.4, and 55% homology to AMPK-alpha1, AMPK-alpha2, MELK and SNARE respectively, suggesting that it is a new member of the AMPK family. It has a putative Akt phosphorylation motif at amino acids 595600, and Ser(600) was found to be phosphorylated by active Akt resulting in the activation of kinase activity toward the SAMS peptide, a consensus AMPK substrate. During nutrient starvation, ARK5 supported the survival of cells in an Akt-dependent manner. In addition, we also demonstrated that ARK5, when activated by Akt, phosphorylated the ATM protein that is mutated in the human genetic disorder ataxia-telangiectasia and also induced the phosphorylation of p53. On the basis of our current findings, we propose that a novel AMPK family member, ARK5, is the tumor cell survival factor activated by Akt and acts as an ATM kinase under the conditions of nutrient starvation.

Identificador

http://espace.library.uq.edu.au/view/UQ:65358

Idioma(s)

eng

Publicador

American Society for Biochemistry & Molecular Biology

Palavras-Chave #Biochemistry & Molecular Biology #Cell-cycle Checkpoint #Ataxia-telangiectasia #Phosphorylation #Activation #Subfamily #Cloning #Gene #P53 #Pathways #Damage #C1 #320305 Medical Biochemistry - Proteins and Peptides #730107 Inherited diseases (incl. gene therapy)
Tipo

Journal Article