Biology – Quantitative Biology – Molecular Networks
Scientific paper
2004-01-23
Biology
Quantitative Biology
Molecular Networks
Accepted to Biophysical Journal, 1/16/04. Single PDF file, 7 figures at end
Scientific paper
10.1016/S0006-3495(04)74332-5
A model of Drosophila circadian rhythm generation was developed to represent feedback loops based on transcriptional regulation of per, Clk (dclock), Pdp-1, and vri (vrille). The model postulates that histone acetylation kinetics make transcriptional activation a nonlinear function of [CLK]. Such a nonlinearity is essential to simulate robust circadian oscillations of transcription in our model and in previous models. Simulations suggest two positive feedback loops involving Clk are not essential for oscillations, because oscillations of [PER] were preserved when Clk, vri, or Pdp-1 expression was fixed. Eliminating the negative feedback loop in which PER represses per expression abolished oscillations. Simulations of per or Clk null mutations and of vri, Clk, or Pdp-1 heterozygous null mutations altered model behavior in ways similar to experimental data. The model simulated a photic phase-response curve resembling experimental curves, and oscillations entrained to simulated light-dark cycles. The model makes experimental predictions, some of which could be tested in transgenic Drosophila.
Baxter Douglas A.
Byrne John H.
Hardin Paul E.
Lo Brian S.
Smolen Paul
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