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

被引:124
作者
Suzuki, A
Kusakai, G
Kishimoto, A
Lu, J
Ogura, T
Lavin, MF
Esumi, H
机构
[1] Natl Canc Ctr, Res Inst E, Invest Treatment Div, Kashiwa, Chiba 2778577, Japan
[2] Univ Queensland, Queensland Inst Med Res, Brisbane, Qld 4029, Australia
[3] Univ Queensland, Dept Surg, Brisbane, Qld 4029, Australia
关键词
D O I
10.1074/jbc.M206025200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:48 / 53
页数:6
相关论文
共 38 条
[1]   CHARACTERIZATION AND CHROMOSOMAL LOCALIZATION OF THE HUMAN HOMOLOG OF A RAT AMP-ACTIVATED PROTEIN KINASE-ENCODING GENE - A MAJOR REGULATOR OF LIPID-METABOLISM IN MAMMALS [J].
AGUAN, K ;
SCOTT, J ;
SEE, CG ;
SARKAR, NH .
GENE, 1994, 149 (02) :345-350
[2]   Enhanced phosphorylation of p53 by ATN in response to DNA damage [J].
Banin, S ;
Moyal, L ;
Shieh, SY ;
Taya, Y ;
Anderson, CW ;
Chessa, L ;
Smorodinsky, NI ;
Prives, C ;
Reiss, Y ;
Shiloh, Y ;
Ziv, Y .
SCIENCE, 1998, 281 (5383) :1674-1677
[3]   Atm selectively regulates distinct p53-dependent cell-cycle checkpoint and apoptotic pathways [J].
Barlow, C ;
Brown, KD ;
Deng, CX ;
Tagle, DA ;
WynshawBoris, A .
NATURE GENETICS, 1997, 17 (04) :453-456
[4]   Molecular cloning and characterization of a novel mammalian protein kinase harboring a homology domain that defines a subfamily of serine threonine kinases [J].
Becker, W ;
Heukelbach, J ;
Kentrup, H ;
Joost, HG .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 235 (03) :736-743
[5]   Activation of the ATM kinase by ionizing radiation and phosphorylation of p53 [J].
Canman, CE ;
Lim, DS ;
Cimprich, KA ;
Taya, Y ;
Tamai, K ;
Sakaguchi, K ;
Appella, E ;
Kastan, MB ;
Siliciano, JD .
SCIENCE, 1998, 281 (5383) :1677-1679
[6]   PURIFICATION AND CHARACTERIZATION OF THE AMP-ACTIVATED PROTEIN-KINASE - COPURIFICATION OF ACETYL-COA CARBOXYLASE KINASE AND 3-HYDROXY-3-METHYLGLUTARYL-COA REDUCTASE KINASE-ACTIVITIES [J].
CARLING, D ;
CLARKE, PR ;
ZAMMIT, VA ;
HARDIE, DG .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1989, 186 (1-2) :129-136
[7]   Glucose repression in yeast [J].
Carlson, M .
CURRENT OPINION IN MICROBIOLOGY, 1999, 2 (02) :202-207
[8]   TISSUE DISTRIBUTION OF THE AMP-ACTIVATED PROTEIN-KINASE, AND LACK OF ACTIVATION BY CYCLIC-AMP-DEPENDENT PROTEIN-KINASE, STUDIED USING A SPECIFIC AND SENSITIVE PEPTIDE ASSAY [J].
DAVIES, SP ;
CARLING, D ;
HARDIE, DG .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1989, 186 (1-2) :123-128
[9]   Hypoxia and nitric oxide treatment confer tolerance to glucose starvation in a 5′-AMP-activated protein kinase-dependent manner [J].
Esumi, H ;
Izuishi, K ;
Kato, K ;
Hashimoto, K ;
Kurashima, Y ;
Kishimoto, A ;
Ogura, T ;
Ozawa, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (36) :32791-32798
[10]   Cloning and characterization of Hunk, a novel mammalian SNF1-related protein kinase [J].
Gardner, HP ;
Wertheim, GBW ;
Ha, SI ;
Copeland, NG ;
Gilbert, DJ ;
Jenkins, NA ;
Marquis, ST ;
Chodosh, LA .
GENOMICS, 2000, 63 (01) :46-59