Gankyrin is an ankyrin-repeat oncoprotein that interacts with CDK4 kinase and the S6 ATPase of the 26 S proteasome

被引:109
作者
Dawson, S [1 ]
Apcher, S
Mee, M
Higashitsuji, H
Baker, R
Uhle, S
Dubiel, W
Fujita, J
Mayer, RJ
机构
[1] Univ Nottingham, Sch Med, Queens Med Ctr, Sch Biomed Sci,Lab Intracellular Proteolysis, Nottingham NG7 2UH, England
[2] Australian Natl Univ, John Curtin Sch Med Res, Div Mol Med, Ubiquitin Lab, Canberra, ACT 2601, Australia
[3] Kyoto Univ, Fac Med, Dept Clin Mol Biol, Sakyo Ku, Kyoto 606, Japan
[4] Humboldt Univ, Div Mol Biol, Dept Surg, Fac Med Charite, D-10117 Berlin, Germany
关键词
D O I
10.1074/jbc.M107313200
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
A yeast two-hybrid screen with the human S6 (TBP7, RPT3) ATPase of the 26 S proteasome has identified gankyrin, a liver oncoprotein, as an interacting protein. Gankyrin interacts with both free and regulatory complex-associated S6 ATPase and is not stably associated with the 26 S particle. Deletional mutagenesis shows that the C-terminal 78 amino acids of the S6 ATPase are necessary and sufficient to mediate the interaction with gankyrin. Deletion of an orthologous gene in Saccharomyces cerevisiae suggests that it is dispensable for cell growth and viability. Overexpression and precipitation of tagged gankyrin from cultured cells detects a complex containing co-transfected tagged S6 ATPase (or endogenous S6) and endogenous cyclin D-dependent kinase CDK4. The proteasomal ATPases are part of the AAA (ATPases associated with diverse cellular activities) family, members of which are molecular chaperones; gankyrin complexes may therefore influence CDK4 function during oncogenesis.
引用
收藏
页码:10893 / 10902
页数:10
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