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Biophys J, November 2002, p. 2349-2359, Vol. 83, No. 5
Department of Neurobiology and Anatomy, W. M. Keck Center for the Neurobiology of Learning and Memory, The University of Texas-Houston Medical School, Houston, Texas 77225 USA
Although several detailed models of molecular processes
essential for circadian oscillations have been developed, their
complexity makes intuitive understanding of the oscillation mechanism
difficult. The goal of the present study was to reduce a previously
developed, detailed model to a minimal representation of the
transcriptional regulation essential for circadian rhythmicity in
Drosophila. The reduced model contains only two
differential equations, each with time delays. A negative feedback loop
is included, in which PER protein represses per
transcription by binding the dCLOCK transcription factor. A positive
feedback loop is also included, in which dCLOCK indirectly enhances its
own formation. The model simulated circadian oscillations, light
entrainment, and a phase-response curve with qualitative similarities
to experiment. Time delays were found to be essential for simulation of
circadian oscillations with this model. To examine the robustness of
the simplified model to fluctuations in molecule numbers, a stochastic
variant was constructed. Robust circadian oscillations and entrainment
to light pulses were simulated with fewer than 80 molecules of each gene product present on average. Circadian oscillations persisted when
the positive feedback loop was removed. Moreover, elimination of
positive feedback did not decrease the robustness of oscillations to
stochastic fluctuations or to variations in parameter values. Such
reduced models can aid understanding of the oscillation mechanisms in
Drosophila and in other organisms in which feedback
regulation of transcription may play an important role.
Biophys J, November 2002, p. 2349-2359, Vol. 83, No. 5
© 2002 by the Biophysical Society 0006-3495/02/11/2349/11 $2.00
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