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A novel computational model of the circadian clock in Arabidopsis that incorporates PRR7 and PRR9
被引:175
作者:
Zeilinger, Melanie N.
Farre, Eva M.
Taylor, Stephanie R.
Kay, Steve A.
Doyle, Francis J., III
[1
]
机构:
[1] Univ Calif Santa Barbara, Dept Chem Engn, Biomol Sci & Engn Program, Santa Barbara, CA 93106 USA
[2] Scripps Res Inst, Dept Biochem, La Jolla, CA USA
[3] Univ Calif Santa Barbara, Dept Comp Sci, Santa Barbara, CA 93106 USA
关键词:
Arabidopsis;
circadian rhythms;
mathematical modeling;
parameter optimization;
sensitivity analysis;
D O I:
10.1038/msb4100101
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
In plants, as in animals, the core mechanism to retain rhythmic gene expression relies on the interaction of multiple feedback loops. In recent years, molecular genetic techniques have revealed a complex network of clock components in Arabidopsis. To gain insight into the dynamics of these interactions, new components need to be integrated into the mathematical model of the plant clock. Our approach accelerates the iterative process of model identification, to incorporate new components, and to systematically test different proposed structural hypotheses. Recent studies indicate that the pseudo-response regulators PRR7 and PRR9 play a key role in the core clock of Arabidopsis. We incorporate PRR7 and PRR9 into an existing model involving the transcription factors TIMING OF CAB (TOC1), LATE ELONGATED HYPOCOTYL (LHY) and CIRCADIAN CLOCK ASSOCIATED (CCA1). We propose candidate models based on experimental hypotheses and identify the computational models with the application of an optimization routine. Validation is accomplished through systematic analysis of various mutant phenotypes. We introduce and apply sensitivity analysis as a novel tool for analyzing and distinguishing the characteristics of proposed architectures, which also allows for further validation of the hypothesized structures.
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页数:13
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