The kinetic origins of the restriction point in the mammalian cell cycle

被引:75
作者
Aguda, BD [1 ]
Tang, Y [1 ]
机构
[1] Laurentian Univ, Dept Biochem & Chem, Sudbury, ON P3E 2C6, Canada
关键词
D O I
10.1046/j.1365-2184.1999.3250321.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A detailed model mechanism for the G1/S transition in the mammalian cell cycle is presented and analysed by computer simulation to investigate whether the kinetic origins of the restriction point (R-point) can be identified. The R-point occurs in mid-to-late G1 phase and marks the transition between mitogen-dependent to mitogen-independent progression of the cell cycle. For purposes of computer simulations, the R-point is defined as the first point in time after mitosis where cutting off mitogen stimulation does not prevent the cell reaching the threshold activity of cyclin-E/cdk2 required for entry into S phase. The key components of the network that generate a dynamic switching behaviour associated with the R-point include a positive feedback loop between cyclin-E/cdk2. and Cdc25A, along with the mutually negative interaction between the cdk inhibitor p27(Kip1) and cyclin-E/cdk2. Simulations of the passage through the R-point were carried out and the factors affecting the position of the R-point in G1 are determined. The detailed model also shows various points in the network where the activation of cyclin-E/cdk2 can be initiated with or without the involvement of the retinoblastoma protein.
引用
收藏
页码:321 / 335
页数:15
相关论文
共 46 条
[21]   Collaborative role of E2F transcriptional activity and G1 cyclin-dependent kinase activity in the induction of S phase [J].
Leone, G ;
DeGregori, J ;
Jakoi, L ;
Cook, JG ;
Nevins, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (12) :6626-6631
[22]   Myc and Ras collaborate in inducing accumulation of active cyclin E/Cdk2 and E2F [J].
Leone, G ;
DeGregori, J ;
Sears, R ;
Jakoi, L ;
Nevins, JR .
NATURE, 1997, 387 (6631) :422-426
[23]  
LI Y, 1994, CANCER RES, V54, P6078
[24]   Cyclin E-induced S phase without activation of the pRb/E2F pathway [J].
Lukas, J ;
Herzinger, T ;
Hansen, K ;
Moroni, MC ;
Resnitzky, D ;
Helin, K ;
Reed, SI ;
Bartek, J .
GENES & DEVELOPMENT, 1997, 11 (11) :1479-1492
[25]   Functional inactivation of the retinoblastoma protein requires sequential modification by at least two distinct cyclin-cdk complexes [J].
Lundberg, AS ;
Weinberg, RA .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (02) :753-761
[26]   Control of pRB phosphorylation [J].
Mittnacht, S .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1998, 8 (01) :21-27
[27]  
Moroy T, 1998, TUMORDIAGN THER, V19, P93
[28]   TRANSCRIPTION OF THE E2F-1 GENE IS RENDERED CELL-CYCLE DEPENDENT BY E2F DNA-BINDING SITES WITHIN ITS PROMOTER [J].
NEUMAN, E ;
FLEMINGTON, EK ;
SELLERS, WR ;
KAELIN, WG .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (10) :6607-6615
[29]   A mathematical model of the regulation of the G(1) phase of Rb+/+ and Rb-/- mouse embryonic fibroblasts and an osteosarcoma cell line [J].
Obeyesekere, MN ;
Knudsen, ES ;
Wang, JYJ ;
Zimmerman, SO .
CELL PROLIFERATION, 1997, 30 (3-4) :171-194
[30]   Regulation of the cyclin E gene by transcription factor E2F1 [J].
Ohtani, K ;
DeGregori, J ;
Nevins, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (26) :12146-12150