Circadian clocks are biological timekeepers that allow living cells to time their activity in anticipation of predictable daily changes in light and other environmental factors. The complexity of the circadian clock in higher plants makes it difficult to understand the role of individual genes or molecular interactions, and mathematical modelling has been useful in guiding clock research in model organisms such as Arabidopsis thaliana.
We present a model of the circadian clock in Arabidopsis, based on a large corpus of published time course data. It appears from experimental evidence in the literature that most interactions in the clock are repressive. Hence, we remove all transcriptional activation found in previous models of this system, and instead extend the system by including two new components, the morning-expressed activator RVE8 and the nightly repressor/activator NOX.
Our modelling results demonstrate that the clock does not need a large number of activators in order to reproduce the observed gene expression patterns. For example, the sequential expression of the PRR genes does not require the genes to be connected as a series of activators. In the presented model, transcriptional activation is exclusively the task of RVE8. Predictions of how strongly RVE8 affects its targets are found to agree with earlier interpretations of the experimental data, but generally we find that the many negative feedbacks in the system should discourage intuitive interpretations of mutant phenotypes. The dynamics of the clock are difficult to predict without mathematical modelling, and the clock is better viewed as a tangled web than as a series of loops.
Like most living organisms, plants are dependent on sunlight, and evolution has endowed them with an internal clock by which they can predict sunrise and sunset. The clock consists of many genes that control each other in a complex network, leading to daily oscillations in protein levels. The interactions between genes can be positive or negative, causing target genes to be turned on or off. By constructing mathematical models that incorporate our knowledge of this network, we can interpret experimental data by comparing with results from the models. Any discrepancy between experimental data and model predictions will highlight where we are lacking in understanding. We compiled more than 800 sets of measured data from published articles about the clock in the model organism thale cress (Arabidopsis thaliana). Using these data, we constructed a mathematical model which compares favourably with previous models for simulating the clock. We used our model to investigate the role of positive interactions between genes, whether they are necessary for the function of the clock and if they can be identified in the model.
Citation: Fogelmark K, Troein C (2014) Rethinking Transcriptional Activation in the Arabidopsis Circadian Clock. PLoS Comput Biol 10(7): e1003705. doi:10.1371/journal.pcbi.1003705
Editor: Jason M. Haugh, North Carolina State University, United States of America
Received: February 3, 2014; Accepted: May 19, 2014; Published: July 17, 2014
Copyright: © 2014 Fogelmark, Troein. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: CT was supported by grant 2010-5219 from the Swedish Research Council, http://vr.se/. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
The task of the circadian clock is to synchronize a multitude of biological processes to the daily rhythms of the environment. In plants, the primary rhythmic input is sunlight, which acts through photoreceptive proteins to reset the phase of the clock to local time. The expression levels of the genes at the core of the circadian clock oscillate due to mutual transcriptional and post-translational feedbacks, and the complexity of the feedbacks makes it difficult to predict and understand the response of the system to mutations and other perturbations without the use of mathematical modelling .
Early modelling of the system by Locke et al. demonstrated the feasibility of gaining new biological insights into the clock through the use of model predictions . The earliest model described the system as a negative feedback loop between the two homologous MYB-like transcription factors CIRCADIAN CLOCK ASSOCIATED 1 (CCA1) and LATE ELONGATED HYPOCOTYL (LHY) ,  on one hand and TIMING OF CAB EXPRESSION 1 (TOC1/PRR1)  on the other. Over the past decade, models have progressed to describing the system in terms of multiple interacting loops, still centred around LHY/CCA1 (treated as one component) and TOC1. The latest published model by Pokhilko et al. (2013) describes transcriptional and post-translational interactions between more than dozen components. We refer to that model as P2012 , in keeping with the tradition of naming the Arabidopsis clock models after author and submission year (cf. L2005 , L2006 , P2010  and P2011 ).
The clock depends on several genes in the PSEUDO RESPONSE REGULATOR (PRR) family: PRR9, PRR7, PRR5, PRR3 and TOC1/PRR1 are expressed in a clear temporal pattern, with PRR9 mRNA peaking in the morning, PRR7 and PRR5 before and after noon, respectively, and PRR3 and TOC1 near dusk . PRR9, PRR7 and PRR5 act to repress expression of CCA1 and LHY during the day , but, until recently, TOC1 was thought to be a nightly activator of CCA1 and LHY, acting through some unknown intermediate. However, TOC1 has firmly been shown to be a repressor of both CCA1 and LHY, and it now takes its place in the models as the final repressor of the “PRR wave” , –. PRR3 has yet to be included in the clock models and the roles of the other PRRs are being reevaluated following the realization that TOC1 acts as a repressor .
The GIGANTEA (GI) protein has long been thought to form part of the clock , whereas EARLY FLOWERING 3 (ELF3) was known to affect clock function  but was only more recently found to be inside the clock, rather than upstream of it , . GI and ELF3 interact with each other and with other clock-related proteins such as the E3 ubiquitin-ligase COP1 . GI plays an important role in regulating the level and activity of ZEITLUPE (ZTL) , which in turn affects the degradation of TOC1  and PRR5  but not of the other PRRs . The clock models by Pokhilko et al. include GI and ZTL; GI regulates the level of ZTL by sequestering it in a GI-ZTL complex during the day and releasing it at night .
Together with EARLY FLOWERING 4 (ELF4) and LUX ARRHYTHMO (LUX), ELF3 is necessary for maintaining rhythmicity in the clock –. The three proteins are localized to the nucleus, and ELF3 is both necessary and sufficient for binding ELF4 and LUX into a complex termed the evening complex (EC) . In recent models, EC is a major repressor; it was introduced in P2011 to repress the transcription of PRR9, LUX, TOC1, ELF4 and GI .
We here present a model (F2014) of the circadian clock in Arabidopsis, extending and revising the earlier models by Pokhilko et al. (P2010–P2012). To incorporate as much as possible of the available knowledge about the circadian clock into the framework of a mathematical model, we have compiled a large amount of published data to use for model fitting. These curated data are made available for download as described in Methods.
The aim of this work is to clarify the role of transcriptional activation in the Arabidopsis circadian clock. Specifically, we use modelling to test whether the available data are compatible with models with and without activation. There is no direct experimental evidence for any of the activators postulated in earlier models, and as a crucial step in remodelling the system we have removed all transcriptional activation from the equations. Instead, we have added a major clock component missing from earlier models: the transcription factor REVEILLE 8 (RVE8), which positively regulates the expression of a large fraction of the clock genes , . A further addition is the nightly transcription factor NOX/BROTHER OF LUX ARRHYTHMO (NOX/BOA), which is similar to LUX but may also act as an activator of CCA1 . By examining transcriptional activation within the framework of our model, we have clarified the relative contributions of the activators to their different targets.
Based on available experimental data and interpretations in the published literature, we have developed a revised model of the Arabidopsis circadian clock. The new model is presented in Figure 1, and a comparison with the most recently published model, P2012 , is shown in Figure S1. Five major alterations are discussed below: remodelling of EC, addition of the LUX homologue NOX, removal of sequential activation in the PRR wave, repression of the PRRs by CCA1, and addition of RVE8 as the main transcriptional activator. For brevity, we refer to Text S1 for further details and results concerning nuclear localization of TOC1 by PRR5, splitting of LHY/CCA1 and removal of unmotivated components and light inputs.
Components of the clock are laid out according to approximate time of peak mRNA expression, clockwise with zeitgeber time 0 (lights on) at the bottom. Yellow and grey boxes indicate proteins that are active primarily during the day and night, respectively. Solid lines indicate transcriptional regulation and dashed lines indicate protein–protein interactions, with arrows for activation and bars for repression or degradation. Additions to the model relative to P2012 are shown in blue. The green line indicates a hypothetical interaction, and the light grey line indicates an interaction that the model predicts to be extremely weak. The light blue boxes show three main modules of the clock, and interactions between them are shown with thick black lines. EC is the evening complex between ELF3, ELF4 and LUX or NOX, and the dark grey line indicates the ELF3-ELF4 complex. Lightning and yellow circles symbolize light input at the transcriptional and post-transcriptional level, respectively. For an alternative version comparing F2014 with P2012  (published 2013), see Figure S1.
To increase the robustness of the conclusions drawn from the modelling, all our model simulations are presented as eight curves, derived from an ensemble of eight independent parameter sets as described in Methods.
A remodelled evening complex
Overexpression of ELF3 rescues clock function in the otherwise arrythmic elf4-1 mutant . This suggests that the function of ELF4 is to amplify the effects of ELF3 through the ELF3-ELF4 complex, which led us to consider an evening complex (EC) where free ELF3 protein can play the role of ELF3-ELF4, albeit with highly reduced efficacy. This, together with our aim to add the NOX protein in parallel with LUX, as described in the next section, prompted us to rethink how to model this part of the clock.
EC is not given its own variable in the differential equations, unlike in the earlier models. Instead, EC activity is seen as rate-limited by LUX and NOX on one hand and by ELF3-ELF4 and free ELF3 on the other. In either pair, the first component is given higher importance, in accordance with previous knowledge. For details, see the equations in Text S1. This simplified description requires few parameters, which was desirable because the model had to be constrained using time course data for the individual components of EC, mainly at the mRNA level.
The effects of our changes to EC are illustrated in Figure 2, which shows EC and related model components in the transition from cycles of 12 h light, 12 h dark (LD 12:12) to constant light (LL). ELF3, which is central to EC in our model, behaved quite differently at the mRNA level compared with the P2011 and P2012 models, and more closely resembled the available experimental data, with a broad nightly peak and a trough in the morning at zeitgeber time (ZT) 0–4 (Figure 2A).
Concentration levels of a selection of model components relevant to EC, in the transition from LD 12:12 (light/dark cycles) to LL (constant light), comparing our ensemble of models (eight parameter sets, black lines), to the previous models P2011 (dashed red line) and P2012 (dotted blue line). (A) ELF3 mRNA in wild type (wt), compared with a typical experiment (green triangles, data from ). (B) ELF3 protein in the nucleus, not counting complexes. (C) The ELF3-ELF4 protein complex. (D) The resulting evening complex. Each curve was normalized to a peak level of 1. Grey background signifies the night of the last day of LD before the transition to LL at ZT 24.
The differences in the dynamics of the EC components between our eight parameter sets demonstrate an interesting and more general point: The components that are most reliably constrained are not always those that were fitted to measured data. In our case, the model was fitted to data for the amount of ELF3 mRNA (Figure 2A) and total ELF3 protein (not shown), but the distribution between free ELF3 and ELF3 bound in the ELF3-ELF4 complex was not directly constrained by any data. As expected, the variation between parameter sets was indeed greater for the levels of free ELF3 protein and the ELF3-ELF4 complex, as shown in Figure 2B–C. However, the predicted level of EC (Figure 2D) showed less variation than even the experimentally constrained ELF3 mRNA. This indicates that the shape and timing of EC were of such importance that the EC profile was, in effect, tightly constrained by data for the seven EC repression targets (PRR9, PRR7, PRR5, TOC1, GI, LUX and ELF4).
NOX as a brother of LUX
NOX is a close homologue of LUX, with a highly similar DNA-binding domain and a similar expression pattern which peaks in the evening. Like LUX, NOX can form a complex with ELF3 and ELF4, but it is only partially redundant with LUX, which has a stronger clock phenotype . The recruitment of ELF3 to the PRR9 promoter is reduced in the lux-4 mutant and abolished in the LUX/NOX double amiRNA line . To explain these findings, we introduced NOX into the model as a component acting in parallel with LUX; we assumed that NOX and LUX play similar roles as transcriptional repressors in the evening complex.
There is evidence that NOX binds to the promoter of CCA1 (and possibly LHY) in vivo and activates its transcription. Accordingly, the peak level of CCA1 expression is higher when NOX is overexpressed, and the period of the clock is longer . This possible role of NOX as an activator fits badly with its reported redundancy with LUX as a repressor. In an attempt to resolve this issue, we first modelled the system with NOX only acting as a repressor in EC, and then investigated the effects of adding the activation of CCA1 expression.
Figure 3 illustrates the role of NOX in the model in comparison with LUX. The differences in their expression profiles (Figure 3A–B) reflect the differences in their transcriptional regulation (cf. Figure 1). CCA1 expression is decreased only marginally in the nox mutant (Figure 3C–D) but more so in lux (Figure 3E). Because of the redundancy between NOX and LUX, the model predicted that the double mutant lux;nox has a stronger impact on circadian rhythms, with CCA1 transcription cut at least in half compared with lux (Figure S2A). According to the model, the loss of LUX and NOX renders the evening complex completely ineffective, which in turn allows the PRR genes (including TOC1) to be expressed at high levels and thereby repress LHY and CCA1.
Comparison between the F2014 model (eight parameter sets, black lines) and experimental data (green triangles , blue circles , red squares  and purple diamonds ), and the earlier models P2011 (dashed red lines) and P2012 (dotted blue lines), where applicable, in the transition from LD to LL. (A) NOX mRNA in wt. (B) LUX mRNA in wt. (C–F) CCA1 mRNA in (C) wt, (D) nox mutant (boa-1), (E) lux mutant (pcl1-1), and (F) NOX-ox. The peak mRNA levels for the models were normalized to 1 in wt, and the same normalization was kept for the mutants. Experimental data were scaled to match the model in panel C, and the same normalization was used in panels D–F. Note the different y scales.
A comparison with the P2011 and P2012 models, which include LUX but not NOX, is shown in Figure 3B, C and E. Here, the most noticeable improvement in our model was the more accurate peak timing after entry into LL, where in the earlier models the clock phase was delayed during the first subjective night .
Period lengthening and increased CCA1 expression was observed in NOX-ox only for some of the parameter sets (Figure 3F). The four parameter sets with increased CCA1 all had a very weakly repressing NOX whose main effect was to counter LUX by taking its place in EC. Removing NOX from EC in the equations and reoptimizing a relevant subset of the parameters worsened the fit to the data (Figure S3). These results support the idea of NOX acting through EC in manner that makes it only partially redundant with LUX.
The possibility that NOX is a transcriptional activator of CCA1 and LHY was probed by adding an activating term to the equations (see Text S1) and reoptimizing the parameters that control transcription of CCA1 and LHY. The resulting activation was very weak in all parameter sets, and had negligible effect on the expression of CCA1 in NOX-ox (Figure S2B–C). Accordingly, the addition of the activation term did not improve the fit to data as measured by the cost function described in Methods (Figure S3).
Sequential PRR expression without activation
In earlier models that included the PRR genes, the PRRs were described as a series of activators; during the day, PRR9 activated the transcription of PRR7, which similarly activated PRR5. These interactions improved the clock's entrainability to different LD cycles . However, this sequential activation disagrees with experimental data for prr knockout mutants, which indicate that loss of function of one PRR leaves the following PRR virtually unaffected. For instance, experiments have shown that the expression levels of PRR5 and TOC1 (as well as LHY and CCA1) are unaffected in both prr9-1 and prr7-3 knockout mutants , .
Instead, direct interactions between the PRRs have been found to be negative and directed from the later PRRs in the sequence to the earlier ones , . A strong case has been made for TOC1 as a repressor of the PRR genes , . As in P2012, we modelled transcription of PRR9, PRR7 and PRR5 as repressed by TOC1, but we also included negative auto-regulation of TOC1, as suggested by the ChIP-seq data that identified the TOC1 target genes . Likewise, PRR5 directly represses expression of PRR9 and PRR7 , and we have added these interactions to the model.
As illustrated in Figure 4A–C, this reformulation of the PRR wave is compatible with correct timing of the expression of the PRRs in the wild type, and the timing and shape of the expression curves were improved compared with the P2012 model. An earlier version of our model gave similar profiles despite missing the repression by PRR5, which suggests that such repression is not of great importance to the clock.
(A–C) The mRNA levels of PRR9 (solid red), PRR7 (long dashed green), PRR5 (short dashed blue) and TOC1 (dotted black) in the transition from LD to LL. (A) The F2014 model with eight different parameter sets. (B) Experimental data: PRR9 , , , PRR7 , , , PRR5 , ,  and TOC1 , , . (C) The P2012 and P2011 models (thick and thin lines, respectively). (D) Total PRR5 protein level in prr9;prr7 in LD in F2014 (solid black), P2011 (dashed red), P2012 (dotted blue) and experimental data (green triangles ). (E) The predicted repression of PRR transcription by CCA1 and LHY, as a multiplicative factor, with colours as in (A–C). (F) PRR9 mRNA in cca1-11;lhy-21 in LD, normalized to the corresponding wt curves in (A–C); colours as in (D) but data from . The peak levels in (A), (C) and (D) were normalized to 1, whereas the levels in (B) were adjusted manually.
A nightly repressor appears to be acting on the PRR7 promoter, as seen in the rhythmic expression of PRR7 in LD in the cca1-11;lhy-21;toc1-21 mutant . An observed increase in PRR7 expression at ZT 0 in the lux-1 mutant relative to wild type  points to EC as a possible candidate. Although Helfer et al. report that LUX does not bind to the LUX binding site motif found in the PRR7 promoter , we included EC among the repressors of PRR7. This interaction was confirmed by Mizuno et al. while this manuscript was in review , demonstrating the power of modelling and of timely publication of models.
We further let EC repress PRR5. We are not aware of any evidence for such a connection, but the parameter fitting consistently assigned a high value to the connection strength, as was also the case with PRR7. This result hints that nightly repression of PRR5 is of importance, whether it is caused by EC or some related clock component.
The real test of the model came with knocking out members of the PRR wave. Here, the model generally outperformed the P2012 model, as judged by eye, but we are missing data for some important experiments such as PRR7 in prr9. As an example, Figure 4D shows the level of PRR5 protein in the prr9;prr7 double mutant, where half of our parameter sets predict the correct profile and peak phase. In the earlier models, the only remaining inputs to PRR5 were (a hypothetical delayed LHY/CCA1), TOC1 (in P2012 only) and light (which stabilized the protein), and these were unable to shape the PRR5 profile correctly. The crucial difference in our model was the repression of PRR5 by CCA1 and LHY, as described in the next section.
Regulation of the PRRs by CCA1 and LHY
CCA1 and LHY appear to work as transcriptional repressors in most contexts in the clock (see e.g. ), but knockdown and overexpression experiments seem to suggest that they act as activators of PRR9 and PRR7 . Accordingly, previous models have used activation by LHY/CCA1, combined with an acute light response, to accomplish the rapid increase observed in PRR9 mRNA in the morning. However, with the misinterpretation of TOC1 regulation of CCA1  in mind, we were reluctant to assume that the activation is a direct effect.
To investigate this issue, we modelled the clock with CCA1 and LHY acting as repressors of all four PRRs. If repression was incompatible with the data for any of the PRRs, parameter fitting should reduce the strength of that repression term to near zero. As is shown in Figure 4E, the model consistently made CCA1 and LHY strongly repress PRR5 and TOC1. PRR7 was also repressed, but in a narrower time window that acted to modulate the phase of its expression peak. In contrast, PRR9 was virtually unaffected; CCA1 and LHY do not directly repress PRR9 in the model.
Even though CCA1 and LHY were not modelled as activators, the model reproduced the reduction in PRR9 expression observed in the cca1-11;lhy-21 double mutant (Figure 4F and Figure S4). PRR7 behaved similarly to PRR9 in both experiments and model. Conversely, in the P2011 and P2012 models, where LHY/CCA1 was supposed to activate PRR9, there was no reduction in the peak level of PRR9 mRNA in cca1;lhy compared to wild type (Figure S5A).
To explore whether CCA1 and LHY may be activating PRR9 transcription, we temporarily added an activation term to the equations (see Text S1) and reoptimized the relevant model parameters. The activation term came to increase PRR9 expression around ZT 2 at least twofold in two of the eight parameter sets, and by a smaller amount in several (Figure S5B). This would seem to suggest that activation improved the fit between data and model. Surprisingly, there was no improvement as measured by the cost function (Figure S3). With the added activation, PRR9 was reduced only marginally more in cca1;lhy than in the original model (Figure S5C). A likely explanation is that feedbacks through EC and TOC1, which repress PRR9, almost completely negate the removed activation of PRR9 in the cca1;lhy mutant. Thus the model neither requires nor rules out activation of PRR9 by CCA1 and LHY.
Transcriptional activation by RVE8
Like CCA1 and LHY, RVE8 is a morning expressed MYB-domain transcription factor. However, unlike CCA1 and LHY, RVE8 functions as an activator of genes with the evening element motif, and its peak activity in the afternoon is strongly delayed in relation to its expression . Based on experimentally identified targets, we introduced RVE8 into our model as an activator of the five evening expressed clock components PRR5, TOC1, GI, LUX and ELF4, as well as the morning expressed PRR9 .
PRR5 binds directly to the promoter of RVE8 to repress its transcription , and it is likely that PRR7 and PRR9 share this function , . Using only these three PRRs as repressors of RVE8 was sufficient to capture the expression profile and timing of RVE8, both in LL and LD (Figure 5A).
(A–C) Expression levels in the transition from LD to LL, comparing the model (eight parameter sets, solid black lines) with experimental data (green triangles , red squares , blue circles  and purple diamonds ). (A) RVE8 mRNA in wt, (B) LHY in wt, and (C) LHY in rve4;rve6;rve8. (D–F) The effect of RVE8 on each of its target genes, as a time-dependent multiplicative factor, in the eight parameter sets. (D) PRR9 (solid red) and PRR5 (dotted blue), (E) GI (solid green) and TOC1 (dotted black), and (F) LUX (solid purple) and ELF4 (dotted light blue).
RVE8 is partially redundant with RVE4 and RVE6 , which led us to model the rve8 mutant as a 60% reduction in the production of RVE8. To clearly see the effects of RVE8 in the model, we instead compared with the rve4;rve6;rve8 triple mutant, which we modelled as a total knockout of RVE8 function. The phase of the clock was delayed in LD, and the period lengthened by approximately two hours in LL in the simulated triple mutant, in agreement with with data for LHY (Figure 5B–C), though we note that CAB::LUC showed a greater period lengthening in experiments .
To investigate the significance of RVE8 as an activator in the model, we made a version of the model without RVE8. The model parameters were reoptimized against the time course data (excluding data for RVE8 and from rve mutants). As with NOX, we found that removing the activation had no clear effect on the costs of the parameter sets after refitting (Figure S3). It appears that activators such as RVE8 are not necessary for clock function. Still, the effects of the rve mutants can only be explained when RVE8 is present in the model, motivating its inclusion.
The model used RVE8 as an activator for four of its targets in a majority of the parameter sets (Figure 5D–F). The exceptions were TOC1 and ELF4. Although TOC1 is a binding target of RVE8 in vivo, TOC1 expression is not strongly affected by RVE8-ox or rve8-1 , . This was confirmed by our model, where the parameter fitting disfavoured the activation of TOC1 in most of the parameter sets (Figure 5E). The eight parameter sets may not represent an exhaustive exploration of the parameter space, but the results nevertheless support the notion that the effect of RVE8 on TOC1 is of marginal importance.
As with previous models of the Arabidopsis clock, our model consists of a set of ordinary differential equations (ODEs) with parameters that need to be fitted against experimental observations. The final F2014 model consists of equations for 35 variables, with a total of 119 parameters. The number of variables has increased compared with previous models (see Table 1), but the number of parameters has been reduced relative to P2012, due to the simplifications described in Results and Text S1.
Constraining the many parameters in our model requires a cost function based on a large number of experiments. To this end, we compiled time course data from the published literature, mainly by digitizing data points from figures using the free software package g3data . We extracted more than 11000 data points from 800 time courses in 150 different mutants or light conditions, from 59 different papers published between 1998 and 2013. The median time resolution was 3 hours. The list of time courses and publications can be found in Text S2, and the raw time course data and parameter values are available for download from http://cbbp.thep.lu.se/activities/clocksim.
Most of the compiled data refer to the mRNA level, from measurements using Northern blots or qPCR, but there are also data at the protein level (67 time courses) and measurements of gene expression using luciferase assays (12 time courses). About one third of the time courses can be considered as replicates, mainly from wild type plants in the most common light conditions. Many of these data are controls for different mutants. Where wild type and mutant data were plotted with the same normalization, we made note of this, as their relative levels provide crucial information that is lost if the curves are individually normalized.
Model fitting and constraining
To find suitable values for the model parameters, we constructed a minimalistic cost function based on the mean squared error between simulations and time course data. This approach was chosen to allow the model to capture as many features of the gene expression profiles as possible, with a minimum of human input.
The cost function consists of two parts, corresponding to the profiles and levels of the time course data, respectively. For each time course with experimental data points the corresponding simulated data were obtained from the model. The simulations were performed with the mutant background represented in the model equations, with entrainment for up to 50 days in light/dark cycles followed by measurements, all in the experimental light conditions. The cost for the concentration profile was computed as(1)
Since the profile levels are thus normalized, eq. (1) is independent of the units of measurements. The parameters (see Text S2 for values) allowed us to weight time courses to reflect their relative importance, e.g. where less data was available to constrain some part of the model.
Where several experimental time courses had the same normalization, e.g. in comparisons between wild type and mutants, the model should reproduce the relative changes in expression levels between the time courses. For each group of time courses, we could minimize the sum(2)
Unlike eq. (1), the nominators in this sum are guaranteed to be non-zero, which allows us to operate in log-space where fold changes up or down from the mean will be equally penalized. Replacing with and likewise for we write the final scaling cost for group as(3)
This cost term thus penalizes non-uniform scaling between experiment and data within the group.
where sets the balance between fitting the simulation to the profile or the level of the data. We used
A downside to our approach is that period and phase differences between different data sets result in fitting to a mean behaviour that is more damped than any individual data set. To reduce this problem, we removed the most obvious outliers from the fitting procedure. We also considered distorting the time axis (e.g. dynamic time warping) to normalize the period of oscillations in constant conditions, in order to better capture the effects of mutants relative to the wild type. This process would be cumbersome and arbitrary, which is why it was deemed outside the scope of our efforts.
Compared to previous models by Pokhilko et al., fewer parameters were manually constrained in our model. In the P2010–P2012 models, roughly 40% of the parameters were constrained based on the experimental data , , , and the remaining free parameters were fitted to mRNA profiles in LD and the free running period in LL and DD (constant dark) in wild type and mutants . For the F2014 model, we completely constrained 16 parameters in order to obtain correct dynamics for parts of the system where we lacked sufficient time course data. Specifically, the parameters governing COP1 were taken from P2011 where they were introduced, whereas the parameters for the ZTL and GI proteins (except the GI production and transport rates) were fitted by hand to the figures in . All other parameters were fitted to the collected time course data through the cost function.
The eight parameter sets presented here were selected from a group of 30, where each was independently seeded from the best of 1000 random points in parameter space, then optimized using parallel tempering for iterations at four different temperatures which were gradually lowered. The resulting parameter values, which are listed in Text S1, typically span at least an order of magnitude between the different parameter sets (Figure S6). The sensitivity of the cost function to parameter perturbations is presented in Figure S7 and further discussed in Text S1. Plots of the single best parameter set against all experimental data is shown in Figure S8.
To simulate the system and evaluate the cost function rapidly enough for parameter optimization to be feasible, we developed a C++ program that implements ODE integration and parameter optimization using the GNU Scientific Library . Evaluating the cost function for a single point in parameter space, against the full set of experiments and data, took about 10 seconds on a 3 GHz Intel Core i7 processor. Our software is released under the GNU General Public License (GPL)  and is available from http://cbbp.thep.lu.se/activities/clocksim/.
Modelling and data
Accurately modelling the circadian clock as a network of a dozen or more genes is challenging. Previous modelling work (e.g. P2010–P2012) , ,  has drawn on existing data and knowledge to constrain the models, but as the amount of data increases it becomes ever more difficult to keep track of the effects of mutations and other perturbations. For a system as large as the plant circadian clock, it is desirable to automate the parameter search as much as possible, but encoding the uncertainties surrounding experimental data in a computer-evaluated cost function is not trivial.
Our modelling demonstrates the feasibility of fitting a model of an oscillating system against a large set of data without the construction of a complicated cost function based on qualitative aspects of the model output, such as entrainability, free-running period or amplitude. Instead, we relied on the large amount of compiled time course data to constrain the model, using a direct comparison between simulations and data. This minimalistic cost function had the additional advantage of allowing the use of time courses that span a transition in environmental conditions, e.g. from rhythmic to constant light, where the transient behaviour of the system may contain valuable information. Consequently, our model correctly reproduces the phase of the clock after such transitions (see e.g. Figure 3C).
Our approach makes it easy to add new data, at the price of ignoring previous knowledge (e.g., clock period) from reporters that are not represented in the model. Accordingly, our primary modelling goal was not to reproduce the correct periods of different clock mutants, but rather to capture the profiles of mRNA and protein curves, and the changes in amplitude and profile between mutants and different light conditions. Compiling a large amount of data from different sources has allowed us to see patterns in expression profiles that were not apparent without independent replication. For example, the TOC1 mRNA profile shows a secondary peak during the night in many data sets (see examples in Figure 4B).
All collected time course data were used in fitting the parameters. To validate the model, we instead used independently obtained period data from clock period mutants. The results are shown in Text S1. In brief, most predictions in LL are in good agreement with experiments, with the exception of elf4 where the period changes in the wrong direction.
To experimentally measure a specific parameter value, such as the nuclear translocation rate of a protein, is exceptionally challenging. Hence, constraining a model with measured parameters can introduce large uncertainties in the model predictions, especially when the understanding of the full system is incomplete. Fitting the model with free parameters can instead give a large spread in individual parameter values, but result in a set of models that make well constrained predictions. For this reason, we have based our results on an ensemble of independently optimized parameter sets, as recommended by Gutenkunst et al. . At the cost of computational time, this approach gives a more accurate picture of the uncertainties in the model and its predictions, rather than focusing on individual parameter values.
Based on our experience of curation of time course data, we offer some suggestions for how data can be compiled and treated to be more useful to modellers. These points arose in the context of the circadian clock, but they apply to experiments that are to be used for modelling in a broader context.
- If the raw data contain information about the relative levels between experiments, for example between mutant and wild type, do not discard this information by normalizing the peak levels of the curves individually.
- If possible, provide data from both before and after treatment, preferably as one uninterrupted time course, so that changes in expression levels become clear. In clock experiments, this would entail including data from the last day of entrainment before a shift into constant light.
- Increase the time resolution of measurements where expression levels are expected to change rapidly, as this adds valuable information about timing. This is especially important around light/dark transitions to distinguish between acute light responses and circadian rhythms.
- Be clear about the conditions during entrainment, especially if they were varied between experiments.
- If possible, apply background correction so that the data reflect the true ratio between peak and trough levels. Alternatively, be clear about whether background correction has been applied.
- Use supplementary figures or files to present data that were not included in the figures and that would otherwise be lost to the research community.
Two of these suggestions concern the preservation of information about the relative expression levels between experiments. One example of the value of such information comes from the dramatic reduction in PRR9 expression in cca1;lhy (Figure 4F). As implied in the section on PRR9 activation in Results, clock models ought to be able to explain both shape and level of expression curves in such mutant experiments, but this is only possible if that information is present in the data.
RVE8 as an activator
Based on the current knowledge of the clock, most clock components are exclusively or primarily repressive, and RVE8 sets itself apart by functioning mainly (or solely) as an activator. According to our model, RVE8 has only a marginal effect on the expression of TOC1, but activates PRR5 and other genes more strongly, in agreement with earlier interpretations of the experimental data .
We note that all six targets of RVE8 in the model (PRR9, PRR5, TOC1, GI, LUX and ELF4) are also binding targets of TOC1 . This may be a coincidence, because TOC1 is a repressor of a majority of the genes in the model. It is conceivable, however, that activation by RVE8 around noon is gated by TOC1 to confer sensitivity to the timing of RVE8 relative to TOC1 in a controlled fashion.
We were surprised by the ease with which we could remove RVE8 from the model. After reoptimization of the parameters, the cost was decreased in three of the eight parameter sets compared with the original model (Figure S3). Thus, the clock is not dependent on activation for its function (although it should be noted that the model without RVE8 lost the ability to explain any RVE8-related experiments). This result indicates that the model possesses a high degree of flexibility, whereby the remaining components and parameters are able to adjust and restore the behaviour of the system. Such flexibility challenges our ability to test hypotheses about individual interactions in the model, but we argue that predictions can also be made based on entropy.
Even if an alteration to the model, such as the addition of RVE8, does not result in a significant change in the cost function, it may open up new parts of the high-dimensional parameter space. If, following local optimization, most parameter sets indicate that a certain interaction is activating, we may conclude that the activation is likely to be true. The parameter space is sampled in accordance with the prior belief that the model should roughly minimize the cost function, and the same reasoning motivates the use an ensemble of parameter sets to explore the model. The conclusion about activation is indeed strengthened by the use of multiple parameter sets, because we learn whether it is valid in different areas of the parameter space.
Problems and predictions
Our model agrees with a majority of the compiled data sets, but like earlier models it also fails to fit to data for some mutants. This indicates that important clock components or interactions may yet be unknown or misinterpreted. We here give a few examples.
NOX expression is rhythmic in the short period double mutant cca1;lhy , but our model predicts a constant high NOX level in constant light (Figure S4F). If NOX is repressed by PRR7 as assumed in the model (see Text S1), the rhythmicity can only be explained if PRR7 is also rhythmic and drives the NOX oscillations. Unfortunately, the model predicts that PRR7 oscillates only for a single cycle in cca1;lhy, before going to a constant low level (Figure S4B). This is a prediction shared with the P2012 model; we are not aware of any data that invalidate the prediction, but given that PRR7 is only slightly reduced in cca1;lhy in light/dark cycles , we believe that PRR7 may be rhythmic in constant light in this mutant.
The addition of NOX as a component partly redundant with LUX leads to an untested prediction regarding CCA1 and LHY. Their peak expression levels are reduced only marginally in nox but roughly by half in lux compated with wt. In the lux;nox double mutant, the model predicts that their expression is cut by at least half again, to nearly zero even in light/dark cycles (see Figure 3 and Figure S2).
The modelling suggests that nightly repression of PRR5 and PRR7 is of importance. The evening complex (EC) is thought to repress PRR9 and TOC1, and our prediction that EC also represses PRR7 was experimentally confirmed while this manuscript was in review .
Several known clock components were not included in the model, partly due to a lack of suitable data. Examples of genes that could be included in future models are CHE  and EBI . More experiments and data are also needed to clarify the differences between CCA1 and LHY, the role of NOX as a part of the evening complex, and how PRR5 affects the localization of TOC1.
Additional non-transcriptional interactions should also be considered in future work. This includes protein interactions such as the regulation of LHY degradation by DET1 , . Most importantly, the recently discovered and highly conserved redox-related circadian oscillator is linked to the transcriptional clock , . Understanding that link may help explain why some clock components more easily remain rhythmic in experiments than in simulations.
The complexity of the clock
The insensitivity of PRR9 to LHY/CCA1 in the P2011–P2012 models, as illustrated by its unchanged level in the cca1;lhy mutant (Figure S5A), shows one of the problems of constructing and fitting large models: The transcriptional activation of PRR9 by LHY/CCA1 looks like an important term in the model equations, but the effects of this term are small. To reduce the prevalence of such “dead” terms and parameters in the equations, we recommend examining their effects in isolation, as was done with the corresponding repression terms in Figure 4E.
The ability of our model to reduce PRR9 expression in cca1;lhy (Figure 4F) can only be explained by indirect effects. CCA1 and LHY repress TOC1, which in turn represses PRR7 and PRR9, and the resulting indirect activation may be sufficient to counteract the direct repression by CCA1 and LHY. In general, in a highly interconnected system such as the circadian clock, it is perilous to draw conclusions about whether interactions are activating or repressing based only on altered expression levels in mutants.
Previous models (L2006–P2012) described the Arabidopsis circadian clock as primarily divided into two interacting feedback loops, the “morning loop” and the “evening loop”. In contrast, we describe the clock in terms of three main modules linked by transcriptional repression and many additional connections (Figure 1). Our results and experiences support an important point formulated by Hsu et al. : The plant clock is best viewed as a highly interconnected, complex regulatory network, in which discrete feedback loops are virtually impossible to identify.
NOX interaction with CCA1. (A) The predicted CCA1 expression level in the lux;nox double mutant, in the transition from LD to LL in F2014. The peak levels were normalized to 1 in wt, as in Figure 3. (B) The activation of CCA1 expression by NOX in a variant of the model, expressed as a multiplicative factor. (C) CCA1 mRNA in NOX-ox in same model variant as (B), shown as in Figure 3F.
Cost function values. The value of the cost function for the eight best parameter sets in the six different model variants discussed in the text. Note that all parameters were reoptimized in the model without RVE8, whereas only a subset of the parameters were reoptimized in the variants with CCA1 activating PRR9 or with different NOX function. Furthermore, the original model improved somewhat as it was optimized in parallel with the other variants.
PRR7, PPR9 and NOX mRNA in wt and cca1;lhy. Comparison between our model (solid black lines), P2011 (dashed red lines), P2012 (dotted blue lines) and data (green triangles) between wt (left panels) and cca1;lhy (right panels), in the transition from LD to LL. (A–B) PPR7, (C–D) PPR9, and (E–F) NOX. Data from  (A–D) and  (E–F). Peak levels were normalized to 1 in wt.
Effects of activation of PRR9 by CCA1. (A) PRR9 mRNA in P2011 (dashed red) and P2012 (dotted blue) in wt (thin lines, higher) and cca1;lhy (thick lines, lower), in the transition from LD to LL. Activation by LHY/CCA1 affects the expression of PRR9 in the afternoon, but the peak level is unaffected in the double mutant. (B) The activation of PRR9 by CCA1, after refitting our model with such an activation term. The activation is shown as a multiplicative factor, whose peak is >1.2 for half of the eight parameter sets. (C) Expression of PRR9 in cca1;lhy in the day (LD or first day of LL), in the model where CCA1 activates PRR9 transcription, with peak levels normalized to 1 in wt. The difference between the model (black lines) and data (green triangles ) is comparable to the difference without the activation term (Figure 4F).
Parameter variability between parameter sets. A visual representation of the values of the model parameters in the eight best parameter sets (eight different symbols). These values are also presented as a table in Text S1.
Parameter sensitivity analysis. The relative change in cost function in each of the eight best parameter sets (eight different symbols) when each parameter is altered. Symbols above (below) the zero cost line refer to multiplication (division) of the parameter by 1.1.
Model simulations compared with all data. Simulations with the single best parameter set, plotted against all 800 time courses used for fitting the model. As described in Methods, simulations and data are normalized to the same mean. Time courses with identical normalization are shown on the same page (“Scale group ), with the total scaling cost in the title. The profile and scaling costs ( and ) for each individual time course are shown in the legend. The time courses are named after the data files used; these are available for download as described in Methods. The naming convention is as follows: initial letters denote light condition, dd (constant dark), ll (constant light), rr (constant red light), bb (constant blue light), ld (light dark LD 12:12), lgd (long day LD 16:8), and shd (short day LD 8:16); followed by gene name, C (CCA1), L (LHY), T or P1 (TOC1), G (GI), P5,7,9 (PRR5,7,9), LUX (LUX), NOX (NOX), R8 (RVE8), E3 (ELF3), E4 (ELF4), Z (ZTL); suffixed by “_m” for mRNA data and an arbitrary number for uniqueness, or just the number for protein data. The last part of the filename is “-ox” for overexpression, and/or lower case gene names for mutants. A combination of LL and another light condition indicates entrainment in something other than LD 12:12, followed by LL. Where all data come from the same light conditions, the background is shaded for night; exceptions include scaling groups with data from different photoperiods.
Additional results and equations. Further information about the modelling, covering details about the evening complex, the regulation of NOX, the splitting of CCA1 and LHY into two variables, the localization of TOC1 and PRR5, and the removal of the ABA circuit, and some light inputs. This text also includes the differential equations of the model, a table of periods comparing model to experiments, and the parameter values of the eight best fitted parameter sets. The equations are presented in their wild type forms, which do not include modifications used when simulating the many different mutants.
Overview of the compiled time course data. A list of the roughly 800 experimental data sets that were compiled and used for fitting the model.
We are grateful to James Locke for suggesting the inclusion of RVE8, to Andrew Millar for encouragement, to Carsten Peterson for proofreading and comments, to Patrik Edén for improvements to the cost function and to Maria Eriksson for bioinformatics analyses and fruitful discussions.
Analyzed the data: CT KF. Wrote the paper: KF CT. Compiled the published time course data used for fitting: KF. Designed the software: CT.
- 1. McClung CR, Gutierrez RA (2010) Network news: prime time for systems biology of the plant circadian clock. Curr Opin Genet Dev 20: 588–598.
- 2. Locke JC, Southern MM, Kozma-Bognár L, Hibberd V, Brown PE, et al. (2005) Extension of a genetic network model by iterative experimentation and mathematical analysis. Mol Syst Biol 1: 2005.0013.
- 3. Wang ZY, Tobin EM (1998) Constitutive expression of the CIRCADIAN CLOCK ASSOCIATED 1 (CCA1) gene disrupts circadian rhythms and suppresses its own expression. Cell 93: 1207–1218.
- 4. Schaffer R, Ramsay N, Samach A, Corden S, Putterill J, et al. (1998) The late elongated hypocotyl mutation of Arabidopsis disrupts circadian rhythms and the photoperiodic control of flowering. Cell 93: 1219–1229.
- 5. Somers DE, Webb A, Pearson M, Kay SA (1998) The short-period mutant, toc1-1, alters circadian clock regulation of multiple outputs throughout development in Arabidopsis thaliana. Development 125: 485–494.
- 6. Pokhilko A, Más P, Millar AJ (2013) Modelling the widespread effects of TOC1 signalling on the plant circadian clock and its outputs. BMC Syst Biol 7: 1–12.
- 7. Locke JC, Kozma-Bognár L, Gould PD, Fehér B, Kevei E, et al. (2006) Experimental validation of a predicted feedback loop in the multi-oscillator clock of Arabidopsis thaliana. Mol Syst Biol 2: 59.
- 8. Pokhilko A, Hodge SK, Stratford K, Knox K, Edwards KD, et al. (2010) Data assimilation constrains new connections and components in a complex, eukaryotic circadian clock model. Mol Syst Biol 6: 416.
- 9. Pokhilko A, Fernández AP, Edwards KD, Southern MM, Halliday KJ, et al. (2012) The clock gene circuit in Arabidopsis includes a repressilator with additional feedback loops. Mol Syst Biol 8: 574.
- 10. Matsushika A, Makino S, Kojima M, Mizuno T (2000) Circadian waves of expression of the APRR1/TOC1 family of pseudo-response regulators in Arabidopsis thaliana: insight into the plant circadian clock. Plant Cell Physiol 41: 1002–1012.
- 11. Nakamichi N, Kiba T, Henriques R, Mizuno T, Chua NH, et al. (2010) PSEUDO-RESPONSE REGULATORS 9, 7, and 5 are transcriptional repressors in the Arabidopsis circadian clock. Plant Cell 22: 594–605.
- 12. Somers DE (2012) The Arabidopsis clock: time for an about-face? Genome Biol 13: 153.
- 13. Gendron JM, Pruneda-Paz JL, Doherty CJ, Gross AM, Kang SE, et al. (2012) Arabidopsis circadian clock protein, TOC1, is a DNA-binding transcription factor. Proc Natl Acad Sci USA 109: 3167–3172.
- 14. Huang W, Pérez-García P, Pokhilko A, Millar A, Antoshechkin I, et al. (2012) Mapping the core of the Arabidopsis circadian clock defines the network structure of the oscillator. Science 336: 75–79.
- 15. Carré I, Veflingstad SR (2013) Emerging design principles in the Arabidopsis circadian clock. Semin Cell Dev Biol 24: 393–398.
- 16. Park DH, Somers DE, Kim YS, Choy YH, Lim HK, et al. (1999) Control of circadian rhythms and photoperiodic flowering by the Arabidopsis GIGANTEA gene. Science 285: 1579–1582.
- 17. Hicks KA, Millar AJ, Carré IA, Somers DE, Straume M, et al. (1996) Conditional circadian dysfunction of the Arabidopsis early-flowering 3 mutant. Science 274: 790–792.
- 18. Thines B, Harmon FG (2010) Ambient temperature response establishes ELF3 as a required component of the core Arabidopsis circadian clock. Proc Natl Acad Sci USA 107: 3257–3262.
- 19. Nusinow DA, Helfer A, Hamilton EE, King JJ, Imaizumi T, et al. (2011) The ELF4-ELF3-LUX complex links the circadian clock to diurnal control of hypocotyl growth. Nature 475: 398–402.
- 20. Yu JW, Rubio V, Lee NY, Bai S, Lee SY, et al. (2008) COP1 and ELF3 control circadian function and photoperiodic flowering by regulating GI stability. Mol Cell 32: 617–630.
- 21. Kim WY, Fujiwara S, Suh SS, Kim J, Kim Y, et al. (2007) ZEITLUPE is a circadian photoreceptor stabilized by GIGANTEA in blue light. Nature 449: 356–360.
- 22. Más P, Kim WY, Somers DE, Kay SA (2003) Targeted degradation of TOC1 by ZTL modulates circadian function in Arabidopsis thaliana. Nature 426: 567–570.
- 23. Kiba T, Henriques R, Sakakibara H, Chua NH (2007) Targeted degradation of PSEUDO-RESPONSE REGULATOR 5 by an SCFZTL complex regulates clock function and photomor-phogenesis in Arabidopsis thaliana. Plant Cell 19: 2516–2530.
- 24. Fujiwara S, Wang L, Han L, Suh SS, Salomé PA, et al. (2008) Post-translational regulation of the Arabidopsis circadian clock through selective proteolysis and phosphorylation of pseudo-response regulator proteins. J Biol Chem 283: 23073–23083.
- 25. Hazen SP, Schultz TF, Pruneda-Paz JL, Borevitz JO, Ecker JR, et al. (2005) LUX ARRHYTHMO encodes a MYB domain protein essential for circadian rhythms. Proc Natl Acad Sci USA 102: 10387–10392.
- 26. Kolmos E, Davis SJ (2007) ELF4 as a central gene in the circadian clock. Plant Signal Behav 2: 370–372.
- 27. Herrero E, Kolmos E, Bujdoso N, Yuan Y, Wang M, et al. (2012) EARLY FLOWERING 4 recruitment of EARLY FLOWERING 3 in the nucleus sustains the Arabidopsis circadian clock. Plant Cell 24: 428–443.
- 28. Rawat R, Takahashi N, Hsu PY, Jones MA, Schwartz J, et al. (2011) REVEILLE 8 and PSEUDO-REPONSE REGULATOR 5 form a negative feedback loop within the Arabidopsis circadian clock. PLoS Genet 7: e1001350.
- 29. Hsu PY, Devisetty UK, Harmer SL (2013) Accurate timekeeping is controlled by a cycling activator in Arabidopsis. eLife 2: e00473.
- 30. Dai S, Wei X, Pei L, Thompson RL, Liu Y, et al. (2011) BROTHER OF LUX ARRHYTHMO is a component of the Arabidopsis circadian clock. Plant Cell 23: 961–972.
- 31. Helfer A, Nusinow DA, Chow BY, Gehrke AR, Bulyk ML, et al. (2011) LUX ARRHYTHMO encodes a nighttime repressor of circadian gene expression in the Arabidopsis core clock. Curr Biol 21: 126–133.
- 32. Chow BY, Helfer A, Nusinow DA, Kay SA (2012) ELF3 recruitment to the PRR9 promoter requires other evening complex members in the Arabidopsis circadian clock. Plant Signal Behav 7: 170–173.
- 33. Dodd AN, Dalchau N, Gardner MJ, Baek SJ, Webb AA (2014) The circadian clock has transient plasticity of period and is required for timing of nocturnal processes in Arabidopsis. New Phytol 201: 168–179.
- 34. Farré EM, Harmer SL, Harmon FG, Yanovsky MJ, Kay SA (2005) Overlapping and distinct roles of PRR7 and PRR9 in the Arabidopsis circadian clock. Curr Biol 15: 47–54.
- 35. Nakamichi N, Kiba T, Kamioka M, Suzuki T, Yamashino T, et al. (2012) Transcriptional repressor PRR5 directly regulates clock-output pathways. Proc Natl Acad Sci USA 109: 17123–17128.
- 36. Ding Z, Doyle MR, Amasino RM, Davis SJ (2007) A complex genetic interaction between Arabidopsis thaliana TOC1 and CCA1/LHY in driving the circadian clock and in output regulation. Genetics 176: 1501–1510.
- 37. Mizuno T, Nomoto Y, Oka H, Kitayama M, Takeuchi A, et al. (2014) Ambient temperature signal feeds into the circadian clock transcriptional circuitry through the EC nighttime repressor in Arabidopsis thaliana. Plant Cell Physiol 55: 958–976.
- 38. Mizoguchi T, Wheatley K, Hanzawa Y, Wright L, Mizoguchi M, et al. (2002) LHY and CCA1 are partially redundant genes required to maintain circadian rhythms in Arabidopsis. Dev Cell 2: 629–641.
- 39. Farinas B, Mas P (2011) Functional implication of the MYB transcription factor RVE8/LCL5 in the circadian control of histone acetylation. Plant J 66: 318–329.
- 40. Frantz J (2009). g3data. URL http://www.frantz.fi/software/g3data.php/. Version 1.5.2.
- 41. Kim JY, Song HR, Taylor BL, Carré IA (2003) Light-regulated translationmediates gated induction of the Arabidopsis clock protein LHY. EMBO J 22: 935–944.
- 42. Galassi M, Davies J, Theiler J, Gough B, Jungman G, et al.. (2009) GNU Scientific Library Reference Manual. Network Theory Ltd., third edition.
- 43. GNU General Public License. URL http://www.gnu.org/licenses/gpl.html.
- 44. Gutenkunst RN, Waterfall JJ, Casey FP, Brown KS, Myers CR, et al. (2007) Universally sloppy parameter sensitivities in systems biology models. PLoS Comput Biol 3: e189.
- 45. Pruneda-Paz JL, Breton G, Para A, Kay SA (2009) A functional genomics approach reveals CHE as a component of the Arabidopsis circadian clock. Science 323: 1481–1485.
- 46. Johansson M, McWatters HG, Bakó L, Takata N, Gyula P, et al. (2011) Partners in time: EARLY BIRD associates with ZEITLUPE and regulates the speed of the Arabidopsis clock. Plant Physiol 155: 2108–2122.
- 47. Song HR, Carré IA (2005) DET1 regulates the proteasomal degradation of LHY, a component of the Arabidopsis circadian clock. Plant Mol Biol 57: 761–771.
- 48. Lau OS, Huang X, Charron JB, Lee JH, Li G, et al. (2011) Interaction of Arabidopsis DET1 with CCA1 and LHY in mediating transcriptional repression in the plant circadian clock. Mol Cell 43: 703–712.
- 49. O′Neill JS, Van Ooijen G, Dixon LE, Troein C, Corellou F, et al. (2011) Circadian rhythms persist without transcription in a eukaryote. Nature 469: 554–558.
- 50. Edgar RS, Green EW, Zhao Y, van Ooijen G, Olmedo M, et al. (2012) Peroxiredoxins are conserved markers of circadian rhythms. Nature 485: 459–464.
- 51. Lu SX, Webb CJ, Knowles SM, Kim SH, Wang Z, et al. (2012) CCA1 and ELF3 interact in the control of hypocotyl length and flowering time in Arabidopsis. Plant Physiol 158: 1079–1088.
- 52. Onai K, Ishiura M (2005) PHYTOCLOCK 1 encoding a novel GARP protein essential for the Arabidopsis circadian clock. Genes Cells 10: 963–972.
- 53. Edwards KD, Akman OE, Knox K, Lumsden PJ, Thomson AW, et al. (2010) Quantitative analysis of regulatory flexibility under changing environmental conditions. Mol Syst Biol 6: 424.
- 54. Dixon LE, Knox K, Kozma-Bognar L, Southern MM, Pokhilko A, et al. (2011) Temporal repression of core circadian genes is mediated through EARLY FLOWERING 3 in Arabidopsis. Curr Biol 21: 120–125.
- 55. Baudry A, Ito S, Song YH, Strait AA, Kiba T, et al. (2010) F-box proteins FKF1 and LKP2 act in concert with ZEITLUPE to control Arabidopsis clock progression. Plant Cell 22: 606–622.
- 56. Matsushika A, Imamura A, Yamashino T, Mizuno T (2002) Aberrant expression of the light-inducible and circadian-regulated APRR9 gene belonging to the circadian-associated APRR1/TOC1 quintet results in the phenotype of early flowering in Arabidopsis thaliana. Plant Cell Physiol 43: 833–843.
- 57. Farré EM, Kay SA (2007) PRR7 protein levels are regulated by light and the circadian clock in Arabidopsis. Plant J 52: 548–560.
- 58. Sato E, Nakamichi N, Yamashino T, Mizuno T (2002) Aberrant expression of the Arabidopsis circadian-regulated APRR5 gene belonging to the APRR1/TOC1 quintet results in early flowering and hypersensitiveness to light in early photomorphogenesis. Plant Cell Physiol 43: 1374–1385.
- 59. GongW, He K, Covington M, Dinesh-Kumar S, Snyder M, et al. (2008) The development of protein microarrays and their applications in DNA–protein and protein–protein interaction analyses of Arabidopsis transcription factors. Mol Plant 1: 27–41.
- 60. Hsu PY, Harmer SL (2012) Circadian phase has profound effects on differential expression analysis. PLoS One 7: e49853.