Abstract
The development of systemic approaches in biology has put emphasis on
identifying genetic modules whose behavior can be modeled accurately so as to
gain insight into their structure and function. However most gene circuits in a
cell are under control of external signals and thus quantitative agreement
between experimental data and a mathematical model is difficult. Circadian
biology has been one notable exception: quantitative models of the internal
clock that orchestrates biological processes over the 24-hour diurnal cycle
have been constructed for a few organisms, from cyanobacteria to plants and
mammals. In most cases, a complex architecture with interlocked feedback loops
has been evidenced. Here we present first modeling results for the circadian
clock of the green unicellular alga Ostreococcus tauri. Two plant-like
clock genes have been shown to play a central role in Ostreococcus
clock. We find that their expression time profiles can be accurately reproduced
by a minimal model of a two-gene transcriptional feedback loop. Remarkably,
best adjustment of data recorded under light/dark alternation is obtained for
vanishing coupling between the oscillator and the forcing cycle. This suggests
that coupling to light is confined to specific time intervals and has no effect
when the oscillator is entrained by the diurnal cycle. This intringuing
property may reflect a strategy to minimize the impact of fluctuations in
daylight intensity on the core circadian oscillator, a type of perturbation
that has been rarely considered when assessing the robustness of circadian
clocks.
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