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Tubulin Polymerization Promoting Protein 1 (Tppp1) Phosphorylation by Rho-associated Coiled-coil Kinase (Rock) and Cyclin-dependent Kinase 1 (Cdk1) Inhibits Microtubule Dynamics to Increase Cell Proliferation
被引:39
作者:
Schofield, Alice V.
[1
,3
]
Gamell, Cristina
[1
]
Suryadinata, Randy
[2
]
Sarcevic, Boris
[2
,3
]
Bernard, Ora
[1
,3
]
机构:
[1] Univ Melbourne, St Vincents Hosp, Cytoskeleton & Canc Unit, Fitzroy, Vic 3065, Australia
[2] Univ Melbourne, St Vincents Hosp, St Vincents Inst Med Res, Cell Cycle & Canc Unit, Fitzroy, Vic 3065, Australia
[3] Univ Melbourne, St Vincents Hosp, Dept Med, Fitzroy, Vic 3065, Australia
基金:
澳大利亚国家健康与医学研究理事会;
澳大利亚研究理事会;
英国医学研究理事会;
关键词:
S-PHASE;
IDENTIFICATION;
TPPP/P25;
PROGRESSION;
SUBSTRATE;
ASSEMBLIES;
ACTIVATION;
TRANSITION;
EXPRESSION;
MITOSIS;
D O I:
10.1074/jbc.M112.441048
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:
Tubulin polymerization promoting protein 1 (Tppp1) regulates microtubule (MT) dynamics via promoting MT polymerization and inhibiting histone deacetylase 6 (Hdac6) activity to increase MT acetylation. Our results reveal that as a consequence, Tppp1 inhibits cell proliferation by delaying the G(1)/S-phase and the mitosis to G(1)-phase transitions. We show that phosphorylation of Tppp1 by Rho-associated coiled-coil kinase (Rock) prevents its Hdac6 inhibitory activity to enable cells to enter S-phase. Whereas, our analysis of the role of Tppp1 during mitosis revealed that inhibition of its MT polymerizing and Hdac6 regulatory activities were necessary for cells to re-enter the G(1)-phase. During this investigation, we also discovered that Tppp1 is a novel Cyclin B/Cdk1 (cyclin-dependent kinase) substrate and that Cdk phosphorylation of Tppp1 inhibits its MT polymerizing activity. Overall, our results show that dual Rock and Cdk phosphorylation of Tppp1 inhibits its regulation of the cell cycle to increase cell proliferation.
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页码:7907 / 7917
页数:11
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