Abstract

Genetic oscillatory networks can be mathematically modeled with delay differential equations (DDEs). Interpreting genetic networks with DDEs gives a more intuitive understanding from a biological standpoint. However, it presents a problem mathematically, for DDEs are by construction infinitely-dimensional and thus cannot be analyzed using methods common for systems of ordinary differential equations (ODEs). In our study, we address this problem by developing a method for reducing infinitely-dimensional DDEs to two- and three-dimensional systems of ODEs. We find that the three-dimensional reductions provide qualitative improvements over the two-dimensional reductions. We find that the reducibility of a DDE corresponds to its robustness. For non-robust DDEs that exhibit high-dimensional dynamics, we calculate analytic dimension lines to predict the dependence of the DDEs’ correlation dimension on parameters. From these lines, we deduce that the correlation dimension of non-robust DDEs grows linearly with the delay. On the other hand, for robust DDEs, we find that the period of oscillation grows linearly with delay. We find that DDEs with exclusively negative feedback are robust, whereas DDEs with feedback that changes its sign are not robust. We find that non-saturable degradation damps oscillations and narrows the range of parameter values for which oscillations exist. Finally, we deduce that natural genetic oscillators with highly-regular periods likely have solely negative feedback.

Highlights

  • Genetic oscillatory networks are networks of interacting proteins that regulate gene expression

  • We extend the definition of an equilibrium state for an ordinary differential equations (ODEs), which states that xà is an equilibrium state of the system x_ ~ f (x) if and only if f ~ 0, to delay differential equations (DDEs)

  • Our project has answered a number of questions concerning DDEs, but they have highlighted a number of new research directions which could lead to further understanding of genetic oscillatory networks

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Summary

Introduction

Genetic oscillatory networks are networks of interacting proteins that regulate gene expression They are found in many biological pathways, including the circadian rhythm [1], cell cycle regulation [2], apoptosis [3], metabolism [4], and morphogenesis [5,6]. Such networks involve hundreds of reactions and are extremely difficult to characterize biologically and mathematically. DDEs are easier to interpret biologically than systems of ordinary differential equations (ODEs), which must account for each individual reaction with an additional differential equation

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