Regulation of CDK4

被引:61
作者
Bockstaele, Laurence [1 ]
Coulonval, Katia [1 ]
Kooken, Hugues [1 ]
Paternot, Sabine [1 ]
Roger, Pierre P. [1 ]
机构
[1] Univ Libre Bruxelles, Fac Med, Inst Interdisciplinary Res IRIBHM, B-1070 Brussels, Belgium
关键词
Nuclear Import; T98G Cell; CDK4 Activity; Master Integrator; Mitogenic Stimulation;
D O I
10.1186/1747-1028-1-25
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cyclin-dependent kinase (CDK)4 is a master integrator that couples mitogenic and antimitogenic extracellular signals with the cell cycle. It is also crucial for many oncogenic transformation processes. In this overview, we address various molecular features of CDK4 activation that are critical but remain poorly known or debated, including the regulation of its association with D-type cyclins, its subcellular location, its activating Thr172-phosphorylation and the roles of Cip/Kip CDK "inhibitors" in these processes. We have recently identified the T-loop phosphorylation of CDK4, but not of CDK6, as a determining target for cell cycle control by extracellular factors, indicating that CDK4-activating kinase(s) might have to be reconsidered.
引用
收藏
页数:16
相关论文
共 199 条
[1]   Cdc2-cyclin E complexes regulate the G1/S phase transition [J].
Aleem, E ;
Kiyokawa, H ;
Kaldis, P .
NATURE CELL BIOLOGY, 2005, 7 (08) :831-U93
[2]   p21Cip1 promotes cyclin D1 nuclear accumulation via direct inhibition of nuclear export [J].
Alt, JR ;
Gladden, AB ;
Diehl, JA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (10) :8517-8523
[3]   Phosphorylation-dependent regulation of cyclin D1 nuclear export and cyclin D1-dependent cellular transformation [J].
Alt, JR ;
Cleveland, JL ;
Hannink, M ;
Diehl, JA .
GENES & DEVELOPMENT, 2000, 14 (24) :3102-3114
[4]   BOTH P16 AND P21 FAMILIES OF CYCLIN-DEPENDENT KINASE (CDK) INHIBITORS BLOCK THE PHOSPHORYLATION OF CYCLIN-DEPENDENT KINASES BY THE CDK-ACTIVATING KINASE [J].
APRELIKOVA, O ;
XIONG, Y ;
LIU, ET .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (31) :18195-18197
[5]   p27Kip1 and p21Cip1 are not required for the formation of active D cyclin-cdk4 complexes [J].
Bagui, TK ;
Mohapatra, S ;
Haura, E ;
Pledger, WJ .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (20) :7285-7290
[6]   Analysis of cyclin D3-cdk4 complexes in fibroblasts expressing and lacking p27kip1 and p21cip1 [J].
Bagui, TK ;
Jackson, RJ ;
Agrawal, D ;
Pledger, WJ .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (23) :8748-8757
[7]   The retinoblastoma protein pathway and the restriction point [J].
Bartek, J ;
Bartkova, J ;
Lukas, J .
CURRENT OPINION IN CELL BIOLOGY, 1996, 8 (06) :805-814
[8]   Cyclin D3: requirement for G1/S transition and high abundance in quiescent tissues suggest a dual role in proliferation and differentiation [J].
Bartkova, J ;
Lukas, J ;
Strauss, M ;
Bartek, J .
ONCOGENE, 1998, 17 (08) :1027-1037
[9]  
Bartkova J, 1999, J PATHOL, V187, P573, DOI 10.1002/(SICI)1096-9896(199904)187:5<573::AID-PATH289>3.0.CO
[10]  
2-H