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Proc Natl Acad Sci U S A. 2009 Jul 7;106(27):11107-12. doi: 10.1073/pnas.0904837106. Epub 2009 Jun 19.

A model of the cell-autonomous mammalian circadian clock.

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  • 1Program in Biomolecular Science and Engineering, University of California, Santa Barbara, CA 93106-9611, USA.

Abstract

Circadian timekeeping by intracellular molecular clocks is evident widely in prokaryotes and eukaryotes. The clockworks are driven by autoregulatory feedback loops that lead to oscillating levels of components whose maxima are in fixed phase relationships with one another. These phase relationships are the key metric characterizing the operation of the clocks. In this study, we built a mathematical model from the regulatory structure of the intracellular circadian clock in mice and identified its parameters using an iterative evolutionary strategy, with minimum cost achieved through conformance to phase separations seen in cell-autonomous oscillators. The model was evaluated against the experimentally observed cell-autonomous circadian phenotypes of gene knockouts, particularly retention of rhythmicity and changes in expression level of molecular clock components. These tests reveal excellent de novo predictive ability of the model. Furthermore, sensitivity analysis shows that these knockout phenotypes are robust to parameter perturbation.

PMID:
19549830
PMCID:
PMC2699375
DOI:
10.1073/pnas.0904837106
[PubMed - indexed for MEDLINE]
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