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      A novel computational model of the circadian clock in Arabidopsis that incorporates PRR7 and PRR9

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          Abstract

          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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          Most cited references52

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          Reciprocal regulation between TOC1 and LHY/CCA1 within the Arabidopsis circadian clock.

          The interactive regulation between clock genes is central for oscillator function. Here, we show interactions between the Arabidopsis clock genes LATE ELONGATED HYPOCOTYL (LHY), CIRCADIAN CLOCK ASSOCIATED 1 (CCA1), and TIMING OF CAB EXPRESSION 1 (TOC1). The MYB transcription factors LHY and CCA1 negatively regulate TOC1 expression. We show that both proteins bind to a region in the TOC1 promoter that is critical for its clock regulation. Conversely, TOC1 appears to participate in the positive regulation of LHY and CCA1 expression. Our results indicate that these interactions form a loop critical for clock function in Arabidopsis.
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            Cloning of the Arabidopsis clock gene TOC1, an autoregulatory response regulator homolog.

            The toc1 mutation causes shortened circadian rhythms in light-grown Arabidopsis plants. Here, we report the same toc1 effect in the absence of light input to the clock. We also show that TOC1 controls photoperiodic flowering response through clock function. The TOC1 gene was isolated and found to encode a nuclear protein containing an atypical response regulator receiver domain and two motifs that suggest a role in transcriptional regulation: a basic motif conserved within the CONSTANS family of transcription factors and an acidic domain. TOC1 is itself circadianly regulated and participates in a feedback loop to control its own expression.
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              LHY and CCA1 are partially redundant genes required to maintain circadian rhythms in Arabidopsis.

              Several genes are known to regulate circadian rhythms in Arabidopsis, but the identity of the central oscillator has not been established. LHY and CCA1 are related MYB-like transcription factors proposed to be closely involved. Here we demonstrate that, as shown previously for CCA1, inactivation of LHY shortens the period of circadian rhythms in gene expression and leaf movements. By constructing lhy cca1-1 double mutants, we show that LHY and CCA1 are partially redundant and essential for the maintenance of circadian rhythms in constant light. Under light/dark cycles the lhy cca1-1 plants show dramatically earlier phases of expression of GI and TOC1, genes associated with the generation of circadian rhythms and the promotion of LHY and CCA1 expression. We conclude that LHY and CCA1 appear to be negative regulatory elements required for central oscillator function.
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                Author and article information

                Journal
                Mol Syst Biol
                Molecular Systems Biology
                1744-4292
                2006
                14 November 2006
                : 2
                : 58
                Affiliations
                [1 ]Department of Chemical Engineering, University of California, Santa Barbara, CA, USA
                [2 ]Department of Biochemistry, The Scripps Research Institute, La Jolla, CA, USA
                [3 ]Department of Computer Science, University of California, Santa Barbara, CA, USA
                Author notes
                [a ]Department of Chemical Engineering, Biomolecular Science and Engineering Program, University of California Santa Barbara, Santa Barbara, CA 93106-5080, USA. Tel.: +1 805 893 8133; Fax: +1 805 893 4731; doyle@ 123456engineering.ucsb.edu
                [*]

                Present address: Institute for Systems Theory and Automatic Control, University of Stuttgart, Stuttgart, Germany

                [†]

                These authors contributed equally to this work

                Article
                msb4100101
                10.1038/msb4100101
                1682023
                17102803
                6f2de662-a5c4-4f53-aa9b-1c5333053190
                Copyright © 2006, EMBO and Nature Publishing Group
                History
                : 22 May 2006
                : 17 August 2006
                Page count
                Pages: 1
                Categories
                Article

                Quantitative & Systems biology
                parameter optimization,arabidopsis,mathematical modeling,sensitivity analysis,circadian rhythms

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