The kinetic origins of the restriction point in the mammalian cell cycle
- PMID: 10619492
- PMCID: PMC6726334
- DOI: 10.1046/j.1365-2184.1999.3250321.x
The kinetic origins of the restriction point in the mammalian cell cycle
Abstract
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 p27Kip1 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.
References
-
- Aguda BD. (1999) Instabilities in phosphorylation‐dephosphorylation cascades and cell cycle checkpoints. Oncogene 18, 2846. - PubMed
-
- Bartek J, Bartkova J, Lukas J. (1996) The retinoblastoma protein pathway and the restriction point. Curr. Opin. Cell Biol. 8, 805. - PubMed
-
- Bartek J, Bartkova J, Lukas J. (1997) The retinoblastoma protein pathway in cell cycle control and cancer. Exptl. Cell Res. 237, 1. - PubMed
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