Numerical analysis of a comprehensive model of M-phase control in Xenopus oocyte extracts and intact embryos

J Cell Sci. 1993 Dec;106 ( Pt 4):1153-68. doi: 10.1242/jcs.106.4.1153.


To contribute to a deeper understanding of M-phase control in eukaryotic cells, we have constructed a model based on the biochemistry of M-phase promoting factor (MPF) in Xenopus oocyte extracts, where there is evidence for two positive feedback loops (MPF stimulates its own production by activating Cdc25 and inhibiting Wee1) and a negative feedback loop (MPF stimulates its own destruction by indirectly activating the ubiquitin pathway that degrades its cyclin subunit). To uncover the full dynamical possibilities of the control system, we translate the regulatory network into a set of differential equations and study these equations by graphical techniques and computer simulation. The positive feedback loops in the model account for thresholds and time lags in cyclin-induced and MPF-induced activation of MPF, and the model can be fitted quantitatively to these experimental observations. The negative feedback loop is consistent with observed time lags in MPF-induced cyclin degradation. Furthermore, our model indicates that there are two possible mechanisms for autonomous oscillations. One is driven by the positive feedback loops, resulting in phosphorylation and abrupt dephosphorylation of the Cdc2 subunit at an inhibitory tyrosine residue. These oscillations are typical of oocyte extracts. The other type is driven by the negative feedback loop, involving rapid cyclin turnover and negligible phosphorylation of the tyrosine residue of Cdc2. The early mitotic cycles of intact embryos exhibit such characteristics. In addition, by assuming that unreplicated DNA interferes with M-phase initiation by activating the phosphatases that oppose MPF in the positive feedback loops, we can simulate the effect of addition of sperm nuclei to oocyte extracts, and the lengthening of cycle times at the mid-blastula transition of intact embryos.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • CDC2 Protein Kinase / metabolism
  • Cell Cycle Proteins*
  • Cell Nucleus
  • Cell-Free System
  • Cyclins
  • Male
  • Maturation-Promoting Factor / metabolism
  • Mitosis / physiology*
  • Models, Biological*
  • Nuclear Proteins*
  • Oocytes / physiology*
  • Periodicity
  • Protein Kinases / metabolism
  • Protein-Tyrosine Kinases*
  • Proteins / metabolism
  • S Phase / physiology
  • Spermatozoa
  • Time Factors
  • Xenopus / embryology
  • Xenopus / physiology*
  • Xenopus Proteins
  • cdc25 Phosphatases


  • Cell Cycle Proteins
  • Cyclins
  • Nuclear Proteins
  • Proteins
  • Xenopus Proteins
  • Protein Kinases
  • WEE1 protein, Xenopus
  • Protein-Tyrosine Kinases
  • CDC2 Protein Kinase
  • Maturation-Promoting Factor
  • cdc25 Phosphatases