The Clock–Cycle (CLK–CYC) heterodimer constitutes a key circadian transcription complex in Drosophila. CYC has a DNA-binding domain but lacks an activation domain. Previous experiments also indicate that most of the transcriptional activity of CLK–CYC derives from the glutamine-rich region of its partner CLK. To address the role of transcription in core circadian timekeeping, we have analyzed the effects of a CYC–viral protein 16 (VP16) fusion protein in the Drosophila system. The addition of this potent and well-studied viral transcriptional activator (VP16) to CYC imparts to the CLK–CYC-VP16 complex strongly enhanced transcriptional activity relative to that of CLK–CYC. This increase is manifested in flies expressing CYC-VP16 as well as in S2 cells. These flies also have increased levels of CLK–CYC direct target gene mRNAs as well as a short period, implicating circadian transcription in period determination. A more detailed examination of reporter gene expression in CYC-VP16–expressing flies suggests that the short period is due at least in part to a more rapid transcriptional phase. Importantly, the behavioral effects require a period (per) promoter and are therefore unlikely to be merely a consequence of generally higher PER levels. This indicates that the CLK–CYC-VP16 behavioral effects are a consequence of increased per transcription. All of this also suggests that the timing of transcriptional activation and not the activation itself is the key event responsible for the behavioral effects observed in CYC-VP16-expressing flies. The results taken together indicate that circadian transcription contributes to core circadian function in Drosophila.
The existence of circadian clocks, which allow organisms to predict daily changes in their environments, have been recognized for centuries, yet only recently has the molecular machinery responsible for their generation been uncovered. The current model in animals posits that interlocked feedback loops of transcription-translation produce these 24-hour rhythms. In fruit flies, the transcription loop contains a key activator complex, composed of the transcription factors Clock and Cycle. This CLK-CYC complex stimulates the synthesis of repressor proteins like Period and Timeless, which repress the activator complex. The synthesis–repression cycle takes precisely 24 hours under environmental conditions that influence the circadian period. An almost identical process relies on the ortholog proteins CLK-BMAL in mammals. Recent findings have challenged the transcription-translation feedback model and suggest that circadian transcription is an output process and that the post-translational modification of clock proteins is the real central pacemaker mechanism. In the present study, we have manipulated the levels and strength of the CLK-CYC complex. The results demonstrate that its activity is vital for proper period determination and thus indicate that the transcriptional feedback loop is part of the core circadian mechanism.
Citation: Kadener S, Menet JS, Schoer R, Rosbash M (2008) Circadian Transcription Contributes to Core Period Determination in Drosophila. PLoS Biol 6(5): e119. doi:10.1371/journal.pbio.0060119
Academic Editor: John B. Hogenesch, University of Pennsylvania, United States of America
Received: October 4, 2007; Accepted: April 2, 2008; Published: May 20, 2008
Copyright: © 2008 Kadener et al. 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: SK is a recipient of a Human Frontier Science Program postdoctoral fellowship and JSM is a recipient of an European Molecular Biology Organization long term postdoctoral fellowship. The work was supported in part by National Institutes of Health grants NS44232, NS45713, and GM66778 to MR.
Competing interests: The authors have declared that no competing interests exist.
Abbreviations: clk , clock ; cyc , cycle ; cwo , clockwork orange ; dbt , doubletime ; DD, constant darkness; dsRNA, double-stranded RNA; LD, light–dark; luc , luciferase ; pdp1 , par domain protein 1 ; per , period ; rp49 , ribosomal protein 49 ; tim , timeless ; VP16, viral protein 16; vri , vrille ; ZT, Zeitgeber time
Circadian rhythms are widespread in nature and help to maintain internal temporal order as well as anticipate daily environmental changes . They use self-sustained biochemical oscillators that generate oscillations at the molecular, physiological, and behavioral levels [2,3].
Results over the past 15 years have highlighted the importance of transcription to circadian biology . In eukaryotic systems, a large fraction of mRNAs, perhaps 10% or more, undergoes circadian transcription (e.g., [5,6]). Circadian transcriptional oscillations contribute to myriad physiological and behavioral outputs in diverse tissues of eukaryotic organisms (e.g., [5,7–10]). Recent data from humans, mice, and flies indicate that numerous syndromes and even pathologies result from a disruption of these daily oscillations [11–16].
A conserved heterodimeric transcription factor, constituted by the proteins Clock and BMAL1 (CLK–BMAL) in mammals and Clock and Cycle (CLK–CYC) in flies, sits at the top of the system that generates circadian transcriptional oscillations [17–22]. These complexes direct the transcription of direct target genes, some of which encode repressors of the activity that leads to their transcription. These repressor proteins, chiefly Timeless and Period in flies or Cryptochrome and Period in mammals, accumulate over the course of many hours and ultimately result in the repression of CLK–CYC or CLK–BMAL activity, respectively [23–28]. A complete cycle takes approximately 24 h and is entrained or reset to exactly 24 h by the daily light–dark (LD) cycle.
These transcriptional cycles constitute the core circadian transcriptional feedback loop of flies and mammals. There are also subsidiary loops involving additional repressors and activators, but genetic evidence indicates that they are less important to circadian timekeeping [29–31]. The circadian transcriptional feedback loop was originally proposed in flies and based on the circadian oscillation of per transcription as well as the role of PER in the parallel timing of behavioral and transcriptional oscillations [23,25]. Subsequent evidence made a direct role of PER in transcriptional repression more likely [18,24,32–34].
There is also an important contribution of post-transcriptional and post-translational regulation to circadian timekeeping in both the fly and the mammalian systems. In Drosophila, genetic evidence indicates that major alterations in circadian period result from mutations of key kinase genes, and there is similar evidence in mammals. For example, the key Drosophila clock gene doubletime (dbt) encodes CKIε, and its mammalian relative is also a clock gene [35–37]. This importance of phosphorylation to circadian timekeeping even derives from studies of humans with advanced sleep phase syndrome [11–13,38]. Manipulation of phosphatase activities within Drosophila clock cells also affects circadian period [39,40].
Major targets of these post-translational modifications appear to be the transcriptional repressors PER and TIM. Their modification status as well as the rates with which these modifications take place have a major influence on their degradation rate [35,38,41–50]. Modification of PER may additionally influence its transcriptional repressor activity or the timing of this activity [34,38,51–53]. It is also likely that the repression of CLK–CYC activity occurs at least in part via CLK phosphorylation, which may be mediated by a PER–DBT complex and/or a PER–TIM–DBT complex [42–44,54].
The importance of post-translational modification to period determination has been strengthened by recent results from cyanobacteria . The three key clock proteins—KaiA, KaiB, and KaiC—are transcription factors. However, recombinant versions of these proteins undergo circadian oscillations of association and modification state in vitro (KaiC has autokinase and autophosphatase activity) in the absence of transcription and without nucleic acids [56,57]. These results make it very likely that the core circadian system in cyanobacteria is predominantly if not exclusively post-translational and suggest that circadian transcriptional regulation is a downstream output feature, unnecessary for core circadian timekeeping. This raises the possibility that a similar situation occurs in flies and mammals: the core circadian system may be primarily post-translational (e.g., based on the temporal modification of PER and TIM). Consistent with this notion, Yang and Sehgal have shown that circadian locomotor activity rhythms can occur with per- and tim-expressing transgenes missing their natural promoters . This work extended previous indications that behavioral rhythms require PER activity but do not require circadian transcription of the per gene .
To pursue the contribution of transcription to core circadian timekeeping in Drosophila, we have analyzed the in vivo effects of a CYC–viral protein 16 (VP16) fusion gene. VP16 is a potent transcriptional activator derived from Herpes virus  and imparts to the CLK–CYC-VP16 complex enhanced transcriptional activity relative to the normal CLK–CYC heterodimeric complex. This is based on activity in S2 cells as well as flies expressing CYC-VP16. These flies also have increased levels of CLK–CYC direct target gene mRNAs, including those from per and tim. Moreover, the CYC-VP16-expressing flies have short periods, implicating circadian transcription in period determination. Taken together with more detailed molecular analyses of these flies as well as behavioral assays of strains missing the normal per promoter, we suggest that CLK–CYC-mediated transcription of the per gene is important for period determination.
To manipulate the transcriptional activation potential of the CLK–CYC heterodimer, we generated a fusion protein between the CYC protein and the strong and well-characterized viral transcriptional activator VP16 (Figure 1A) . Current indications are that all activator activity of the CLK–CYC heterodimer normally comes from the polyglutamine region of CLK (Figure 1A) , so we considered that VP16 might increase the activity of a CLK–CYC-VP16 heterodimer. As an initial assay, DNA encoding the fusion protein was transfected into S2 cells along with a standard timeless promoter-luciferase (tim-luc) reporter gene [18,61], which responds well to CLK–CYC activity.
(A) Schematic diagram of the CLK protein (top) and of the CYC-VP16 hybrid protein (bottom) showing the protein domains of those molecules.
(B) Effect of cyc-vp16 expression (100 ng of cyc-vp16-expressing plasmid, pAc-cyc-vp16) and/or Clk expression (10 ng of pAc-Clk) on the transcription of tim-luc (first five bars) or tim(mut)-luc (last two bars) in S2 cells. Some cells were treated with dsRNA against the 5′ and 3′ UTR regions of the cyc gene as described in the Materials and Methods section (fourth and fifth bars). In all cases, cotransfection with pCopia-Renilla luciferase was performed to normalize for cell number, transfection efficiency, and general effects on transcription. For each condition a normalized firefly/Renilla luciferase value was obtained by setting the ratio without any addition of cyc-vp16 or clk to 1. A representative experiment is shown. For each condition two experiments with duplicates were performed. Error bars represent standard error of the mean.
(C) Similar experiment to the one performed in (B) but assessing the levels of tim and cyc mRNAs by real-time PCR. Control or cyc(i) refers to dsRNAs against green fluorescent protein or untranslated regions of cyc. Expression values are reported as a ratio of tim or cyc over control (rp49). The experiment was performed twice, and the results were averaged. The error bars indicate standard error of the mean.
(D) PER repression of CLK-mediated transcription in presence (100 ng of pAc-cyc-vp16) or absence of cyc-vp16; 0, 50. or 150 ng of pAc-per were used. For each condition a normalized firefly/Renilla luciferase value was obtained by setting the ratio with the addition of pActin-Clk to 1. A representative experiment is shown. Two experiments with duplicates for each condition were performed.
Transfection of the fusion protein gene has little or no activity (Figure 1B). This is expected and reflects the absence of its partner CLK from S2 cells . In contrast, transfection of a CLK gene alone partners with endogenous CYC and potently increases reporter gene activity (Figure 1B), identically to what has been reported previously . Cotransfection of CLK with CYC-VP16 increases activity a further 5-fold (Figure 1B), which presumably reflects the transcriptional activation potential of VP16. Importantly, cotransfection of CLK with CYC or with another VP16 fusion protein (GAL4-VP16) has no effect over transfection with CLK alone (Figure S1A and unpublished data). An assay of endogenous tim mRNA expression by real-time PCR and TIM protein by western blotting gives rise to similar results: CYC-VP16 alone has no activity, whereas CLK plus CYC-VP16 cotransfection has considerably more activity than CLK alone (Figure 1C and Figure S1B). Moreover, coexpression of CYC-VP16 rescues activity of the truncated CLKJrk protein in this tissue culture assay system (Figure S1C); CLKJrk is missing most of its activation domain .
CLK-driven transcription is inhibited by double-stranded RNAs (dsRNAs) against the 5′ and 3′ untranslated regions (UTRs) of the endogenous cyc mRNA present in S2 cells (Figure 1B and 1C). In contrast, activity due to cotransfection of CLK and CYC-VP16 is insensitive to incubation with the same dsRNAs (Figure 1B and 1C). This is because the CYC-VP16 expression plasmid does not carry the cyc UTRs. The result indicates that most CLK activity is derived from the CLK–CYC-VP16 heterodimer. Neither CLK–CYC nor CLK–CYC-VP16 has activity on a tim-luc reporter with mutant E-boxes , indicating that the CLK–CYC-VP16 fusion has DNA-binding properties similar to wild-type CLK–CYC (Figure 1B). Because there is no detectable endogenous per expression in S2 cells, even after clk expression , the higher target gene mRNA levels are likely the consequence of a stronger transcriptional activation independent of any possible weaker PER-mediated repression on CYC-VP16.
Cotransfection with per cDNA inhibits CLK–CYC-VP16 activity, similar to what is observed for CLK–CYC activity (Figure 1D) [18,34] Given the entirely different nature of the VP16 activator compared to the polyglutamine region of CLK and the 5-fold increase in activity, this suggests that per repression involves a similar inhibition of CLK–CYC and CLK–CYC-VP16, probably an inhibition of DNA binding . The similar properties of the two heterodimers are despite the much more potent activity of the former.
To generate flies with cyc-vp16 expression in circadian cells, we created uas-cyc-vp16 transgenic flies and crossed them to tim-gal4 driver lines. We then assayed circadian locomotor behavior in these tim-cyc-vp16 flies (Figure 2A and 2B, top). They were robustly rhythmic with ~22-h periods, approximately 2 h shorter than those of wild-type flies. Figure 2C summarizes comparable period shortening by uas-cyc-vp16 combined with a highly spatially restricted circadian driver (pdf-gal4) and with two broader expression drivers (actin-gal4 and the pan-neuronal elav-gal4). This indicates that the ~22-h period is not an idiosyncrasy of the tim-gal4 driver. Moreover, the short period was not simply caused by cyc overexpression. This is because elav-cyc flies (uas-cyc rather than uas-cyc-vp16 in combination with the same elav-gal4 driver) have a wild-type–like period (Figure 2C, bottom). We thus attribute the period-shortening effect to increased transcriptional activity from the CLK–CYC-VP16 heterodimer within circadian cells.
(A) Comparison of circadian locomotor behavior of control flies (uas-cyc-vp16/+, top tracing) and flies expressing cyc-vp16 under the control of the tim driver (tim-gal4/uas-cyc-vp16, middle tracing). In each case, the behavior is shown in average actograms. The arrow indicates the phase of evening anticipation for each fly strain. The light timing is indicated by alternating white and gray background areas, with white representing the illuminated interval of the LD condition (ZT0–12) and gray representing the dark period (ZT12–24 and DD period). To facilitate the identification of peaks in the control and tim-cyc-vp16 datasets the data were smoothed with a low-pass filter set with a cutoff of 12 h (bottom tracing).
(B) Period length of fly strains overexpressing uas-cyc-vp16 using the tim-gal4 driver and control flies.
(C) Behavioral analysis of fly strains expressing the uas-cyc-vp16 or uas-cyc transgenes in combination with different gal4 drivers.
Consistent with this interpretation is the period of tim-cyc-vp16 in combination with the classic pers allele; these flies have ~17-h periods, 2 h shorter than the canonical pers 19–20 h phenotype (Figure 2B, bottom). The additive nature of tim-cyc-vp16 and pers suggests that they shorten period in independent ways, the former by increasing transcription of CLK–CYC direct target genes and the latter by causing more rapid PER turnover .
To further study the period-shortening effect of tim-cyc-vp16, we characterized the molecular clock of these flies. To this end, we added a tim-luc or a per-luc reporter gene to the tim-cyc-vp16 strain (generating tim-luc-cyc-vp16 flies or per-luc-cyc-vp16 flies).
The expression of luciferase is robustly rhythmic in tim-luc-cyc-vp16 flies and isolated wings. The patterns are similar to those of wild-type tim-luc flies, but luciferase levels were about 2–3 times higher (Figure 3A for isolated wings and Figure S2A for intact flies). This is a comparable activity difference to what was observed above between CLK–CYC and CLK–CYC-VP16 in S2 cells (Figure 1B and 1C). Robust cycling and an even greater activity difference are observed with the per-luc reporter gene (Figure 3B).
(A) Luciferase recordings from control (uas-cyc-vp16/+) and tim-cyc-vp16 flies using the tim-luc reporter. Light timing is indicated by alternating white and gray background areas, with white representing the illuminated interval of LD (ZT0–12) and gray representing the dark period (ZT12–24). After 3 d in LD conditions the assay was conducted in DD conitions. The results are the average of ten (tim-cyc-vp16) and 13 (control) pairs of fly wings.
(B) Luciferase recordings from control (uas-cyc-vp16/+) and tim-cyc-vp16 flies utilizing the per-luc reporter. The results are the average of 24 pairs of fly wings of each genotype.
(C) Both curves in (B) were normalized to their maximum and then plotted together.
Normalization to the first peak of the oscillations in Figure 3B and 3A allowed a useful comparison between the controls and the per-luc-cyc-vp16 and the tim-luc-cyc-vp16 profiles (Figure 3C and Figure S2B). The normalized pairs are very similar, but the CYC-VP16 curves are phase-advanced as they decrease more rapidly and then increase more rapidly during the next cycle (Figure 3C and Figure S2B). The peaks remain coincident, almost certainly reflecting entrainment to the superimposed 24-h LD cycle. Careful observation of the tim-luc reporter in constant darkness (DD) conditions reveals shorter circadian period in CYC-VP16 flies, in parallel with the behavior (Figure S2B). The damping oscillations of the wing transcriptional reporters in DD (always true in our hands) precluded a precise period determination.
To compare these reporter effects with those on bona-fide circadian mRNAs, microarray assays were performed on tim-cyc-vp16 head RNA from Zeitgeber time 15 (ZT15) and ZT3 (the timepoints when the CLK target genes have the peak and trough mRNA amounts in wild-type flies) and compared to the same timepoints from wild-type flies (Figure 4A and 4B). CLK–CYC direct target gene (tim, per, vrille (vri), and par domaine protein 1 (pdp1)) mRNA peak levels increase 2–3-fold, and an increase is also observed in trough levels (Figure 4A). The increase in trough levels suggests that they normally result from residual CLK–CYC activity that resists repression and/or that there is a minority of CLK–CYC-expressing cells that lack a robust circadian repression system. The microarray results are qualitatively similar although quantitatively less striking than the reporter gene assays shown above (Figure 3A and 3B). This may reflect the longer half-lives of the CLK–CYC direct target gene mRNAs relative to the luciferase reporter mRNAs or another level of post-transcriptional regulation. It is also possible that the reporter genes have a larger transcriptional response to CYC-VP16 than the CLK–CYC direct target genes.
(A) mRNA expression value for control (uas-cyc-vp16/+, white) and tim-cyc-vp16 flies (black) for two timepoints (ZT3 and ZT15) of four direct Clk targets: tim, vri, per, and pdp1. The data were obtained by microarray (n = 2 for each genotype and timepoint). The data were normalized to the maximum value obtained in the control flies. Error bars indicate standard error of the mean.
(B) mRNA expression value for control (uas-cyc-vp16/+, red) and tim-cyc-vp16 flies (blue) for two timepoints (ZT3 and ZT15) of four genes (Clk, cry, Ugt35B, and CG9649) that are not direct CLK targets and that oscillate in control flies with opposite phase than the genes shown in (A). The data were obtained by microarray (n = 2 for each genotype and timepoint). The data were normalized to the maximum value obtained in the control flies. Error bars indicate standard error of the mean.
(C) Effect of cyc-vp16 in per01 mutants flies measured by quantitative PCR. Un-entrained per01 or per01; tim-gal4; uas-cyc-vp16 flies were harvested. RNA was extracted from fly heads, and quantitative PCR was performed. Expression values for each transcript and timepoint were generated by dividing the vri or tim mRNA signal by the expression value for a control non-circadian mRNA (rp49). Expression values are reported as a ratio of tim or vri over rp49 expression. We assigned a value of 1 to the ratio obtained for control flies and proceed as in (A). The data are the average of the normalized vri or tim expression values for three independent RNA samples. The error bars indicate standard error of the mean.
In contrast to these direct target genes, maximal values for cycling mRNAs that peak at the opposite time of day are not increased in tim-cyc-vp16 flies (Figure 4B). Trough levels are decreased, however, suggesting that this might reflect an increase in the level of a transcriptional repressor protein, itself the product of a CLK–CYC direct target gene (e.g., VRI [29,30]).
We also tested whether the increase in CLK-mediated transcription was predominantly due to impaired per repression. To this end, we measured the effect of the CYC-VP16 protein in a per null mutant (per01) background . The tim and vri mRNA levels are increased in per01 flies, comparable to the increase in the S2 cell (also without PER) experiments (Figure 1B). This indicates that transcription is increased independent of any more subtle effects on per repression.
Although we attribute the shorter period of the cyc-vp16 flies to a direct enhancement of transcription, it is still possible that the VP16 activation domain has a subtle effect on some other aspect of repression, which then only indirectly enhances transcription. Therefore we decided to assay the periods of transgenic flies carrying increasing numbers of copies of the Clk genomic region. Introduction of additional copies of the Clk transgene shortens circadian period and increases CLK–CYC-mediated transcription similar to the effects of the cyc-vp16 transgene (Figure 4A and 4B).
Homozygous ClkAR flies have significantly diminished levels of functional CLK and very low amplitude transcriptional oscillations of core clock genes . As a consequence, these mutant flies do not have circadian activity patterns in DD or even in standard LD conditions. In addition they do not show the typical burst of activity at the beginning of the light cycle present in wild-type flies (lights-on startle response). Because CYC-VP16 increases CLK-driven transcription, we tested it for rescue of circadian activity in the ClkAR mutant background. Although introduction of CYC-VP16 into the ClkAR background failed to rescue circadian locomotor activity rhythms in DD conditions, most of the abnormal features of LD behavior conditions were restored: this included the presence of behavioral cycles (higher diurnal than night activity) as well as the lights-on startle response (Figure 6).
(A) Locomotor behavior of ClkAR mutant flies in LD conditions. Four standard days are shown, with timing indicated by alternating white and gray background areas with white representing the illuminated interval of LD (ZT0-12) and gray representing the dark period (ZT12-24). The behavior is shown in actograms (left) and averaged actograms (right).
(B) Same as in (A), but using tim-gal4/uas-cyc-vp16; ClkAR/ClkAR flies.
The effect of CYC-VP16 on the transcriptional profiles of the reporters and CLK–CYC direct target mRNAs suggested that the period-shortening effect might be simply due to a CYC-VP16-mediated change in the timing or level of per transcription. To test this possibility, we assayed the period of tim-cyc-vp16 flies in the context of uas-per (i.e., a period gene that can be driven constitutively by GAL4 but not by CLK–CYC or by CLK–CYC-VP16). Importantly, Sehgal and co-workers  have shown previously that uas-per can rescue the arrhythmic per01 genotype (per01; elav-gal4; uas-per), and we verified this finding (Figure 7A). Importantly, the elav-gal4 driver in combination with uas-cyc-vp16 (and a wild-type per gene) also manifests the ~2-h period shortening as shown above (Figure 2C). However, these two transgenes in combination with the uas-per and per01 only shorten circadian period by 20 min (Figure 7A–7C, and Figure S3B). This indicates that an increase in the levels and/or timing of per transcription is a major contributor to CLK–CYC-VP16 period shortening. We also note the broad distribution of individual fly periods from genotypes containing the uas-per; per01 combination compared to the much tighter distribution in genotypes containing a proper per promoter (Figure 7C and Figure S3C); this is an additional indication that per transcription contributes to period determination (see Discussion section).
(A) Period length analysis of fly strains overexpressing uas-cyc-vp16 using the elav-gal4 driver and control flies in different genetic backgrounds.
(B) Locomotor behavior of per01; elav-gal4; uas-per flies with or without a uas-cyc-vp16 transgene in DD conditions. The behavior is shown in actograms (left) and averaged actograms (right).
(C) Box plot showing the period distribution of the specified flies. The p-values correspond to a t-test performed among the indicated samples.
This role of per transcription is consistent with previous reports showing a relationship between per gene dose and behavioral period: more per genes cause shorter periods [65–67]. To determine if other ways of increasing per transcription also give rise to period shortening, we compared behavioral period between genotypes with one or two doses of uas-per (Figure 7A and Figure S3C). Rather than shortening period, however, the extra copy of uas-per slightly lengthens it. This is consistent with previous reports showing that overexpression of a uas-per transgene does not shorten period [44,58,68]. Taken together with other data shown above, we conclude that the short period of tim-cyc-vp16 requires not just increased levels of per mRNA but proper timing of the per transcriptional increase.
To address the role of transcription in core circadian timekeeping in the Drosophila system, we have analyzed the effects of a cyc-vp16 fusion gene in S2 cells as well as in flies. VP16 is a potent and well-studied transcriptional activator, which imparts to the CLK–CYC-VP16 heterodimer enhanced activity relative to that of the normal CLK–CYC complex. This increased activity is manifested with reporter genes, and transgenic flies also have increased levels of CLK–CYC direct target gene mRNAs, including those from per and tim. Importantly, the cyc-vp16-expressing flies have a short period, implicating circadian transcription in period determination. As this short period and proper period control more generally require a per promoter, we suggest that CLK–CYC-VP16 drives increased per transcription, which leads to more rapid accumulation of PER and a consequent advanced phase of per repression. This is also consistent with reporter gene profiles in cyc-vp16-expressing flies. The results indicate that circadian transcription contributes to core period determination in Drosophila.
This conclusion fits with several other pieces of data from the Drosophila system. First, recent studies have identified the transcriptional repressor–encoding gene clockwork orange (cwo) as a clock gene [62,69,70]. The protein product synergizes with PER and aids the repression of CLK–CYC direct target genes. Importantly, mutations in cwo or changes in cwo expression cause substantial period changes. Second, an increase in per gene dose leads to flies with short periods. There is a decrease of approximately 0.5 h for each additional gene copy up to about four copies, which have a ~22-h period (e.g., ). Third, a hemizygous deletion that includes clock lengthens circadian period by about 0.5 h . Although this deletion removes more DNA than just clk (including the adjacent clock gene pdp1), our results indicate that additional copies of the clk locus indeed shorten the circadian period of otherwise wild-type flies (Figure 5). All of these observations are qualitatively similar to the increase in transcription and period shortening caused by expression of cyc-vp16 in flies.
(A) Behavioral analysis of fly strains with one, two, or three doses of a Clk transgene. Transgenes in the second and third chromosome were used. All of the flies assayed are wild type for the endogenous Clk locus.
(B) Luciferase recordings from control (yw) and flies carrying two doses of a Clk transgene utilizing the tim-luc reporter. Light timing is indicated by alternating white and gray background areas, with white representing the illuminated interval of the LD condition (ZT0–12) and gray representing the dark period (ZT12–24). The results are the average of 13 (two copies of the Clk transgene) and 18 (control) pairs of fly wings.
Because of the molecular analyses (Figure 3 and Figure S2), we suspect that it is the timing of per transcription rather than a simple increase in per mRNA levels that causes the period shortening by expression of cyc-vp16. As the reporter genes contain proper per and tim promoters, their profiles indicate that per and tim transcription decreases more steeply and then increases more steeply in the cyc-vp16 flies (Figure 3C and Figure S2B). The steeper decrease presumably reflects a faster accumulation of active PER repressor, and the steeper increase reflects the enhanced potency of CLK–CYC-VP16. In addition, we note that an increase in per dose with a uas-per transgene slightly increases rather than decreases period (Figure 7A and Figure S3C) [44,58]. This genetic requirement for the per promoter also emphasizes the contribution of proper transcriptional regulation to period determination.
The increased transcriptional potency of CLK–CYC-VP16 is unlikely to be a consequence of impaired PER-mediated repression, due in turn to some structurally anomalous feature of the artificial fusion protein. This is because the stronger activation of CLK direct targets by the CLK–CYC-VP16 dimer is apparent even in the absence of PER (Figures 1C and 4C). Shorter periods due to more potent transcription is also the conclusion of Figure 5, which shows that increasing clk gene dose (an independent and “more natural” way to increase CLK-mediated transcription) leads to molecular and behavioral changes that resemble those observed in tim-cyc-vp16 flies. Finally, cyc-vp16 expression rescues several aspects of the ClkAR phenotype (Figure 6). This suggests that these features are due to low direct target mRNA levels, which are increased by the more potent CLK–CYC-VP16 complex. The failure to rescue the behavioral arrhythmicity of homozygous ClkAR flies may reflect a requirement for minimal CLK levels, which would not be expected to increase by the addition of CYC-VP16.
The robust behavioral and molecular rhythms of cyc-vp16 flies (Figure 2 and 3) more generally indicate that CLK–CYC-VP16 circadian function, including the mechanism(s) that temporally activate or repress transcription of this hyperactive complex, must be similar to those that regulate the activity of the wild-type CLK–CYC complex. This is also because the increased transcription as well as RNA levels in tim-cyc-vp16 flies suggests that most CLK–CYC direct target gene transcription is carried out by CYC-VP16 rather than endogenous CYC. Because the VP16 activation domain almost certainly functions differently from the CLK polyglutamine region, this indicates that the recruitment of specific activator and/or repressor proteins is unlikely to play a prominent, mechanistic role in the circadian regulation of transcription. A more likely mechanism involves the cyclical inhibition of CLK–CYC DNA binding. Importantly, this notion is consistent with recent chromatin immunoprecipitation results from the mammalian as well as the fly system [54,71]. Nonetheless, we suggest that per transcription as well as DNA binding of the CLK–CYC dimer to per E-boxes is the actual timekeeper of the circadian cycle during the mid-late day, when they are both increasing. This predicts that the additional activation power of VP16 indirectly shortens the DNA binding time of the CLK–CYC-VP16 dimer by accelerating the rate of PER accumulation and function. This hypothesis also fits well with the behavioral and molecular defects observed in cwo mutant flies [62,69,70].
The emphasis on the per promoter is seemingly contradicted by the rhythmicity of flies missing not only this promoter but also the tim promoter . In our hands as well, per01; elav-gal4; uas-per flies are largely rhythmic despite weak rhythms, and their average period is near-normal. However, the period distribution of individual flies is unusually broad (Figure 7C and Figure S3C), indicating a contribution of the per promoter to the proper control of period within individual flies—even without CYC-VP16. Moreover, luciferase recordings from these transgenic flies show poor or no transcriptional oscillations (unpublished data). These observations suggest that individual neurons from this per01; elav-gal4; uas-per strain might be impaired even more than indicated by the behavioral rhythms of this strain (i.e., circadian brain circuitry might help to compensate for poor core circadian function within individual cells). This is analogous to the superior circadian performance of behavioral rhythmicity and the suprachiasmatic nucleus (SCN) from mutant mouse strains compared to that of individual tissue culture cells (mouse embryonic fibroblasts) derived from the same strains .
The role of circadian transcription described in this study complements the well-documented role of PER, TIM, and CLK post-translational regulation in period determination [34,35,43,44,48,49,54,73–75]. Given the parallel role of mammalian CLK and BMAL1 to CLK and CYC, it would be surprising were there not a similar contribution of circadian transcription to mammals. This suggests that there is a division of labor in animals between transcriptional and post-translational regulation of circadian timekeeping, which may even be temporally segregated. In contrast and as mentioned above, recent indications are that post-translational regulation is the pre-eminent mechanism in cyanobacteria. It is also the case that individual bacterial cells keep excellent circadian time, essentially indistinguishable from the culture . This contrasts with individual eukaryotic cells, for example, separated SCN cells, which show substantially more variation in period than the intact SCN or organism [72,77]. All of these considerations suggest that the intracellular timekeeping mechanism of animals is different from that of cyanobacteria. We suggest that this important difference between systems reflects their separate origins, a view that is supported by the lack of sequence conservation between cyanobacterial and animal clock proteins.
Materials and Methods
pAc-clk, pAc-per, Copia Renilla luciferase, and tim-luc have been described previously . pAc-cyc-vp16 was constructed by amplifying the cyc coding region and the vp16 activation domain by PCR and ligating in-frame into pAcA V5/His6 (Invitrogen). pAc-cyc was constructed by amplifying the cyc coding region and ligating in-frame into pAcA V5/His6.
S2 cell transfection.
S2 cells were maintained in 10% fetal bovine serum (Invitrogen) insect tissue culture medium (HyClone). Cells were seeded in a six-well plate. Transfection was performed at 70–90% confluence according to company recommendations (12 μl of Cellfectin (Invitrogen) and 2 μg of total DNA). In all experiments 50 ng of pCopia Renilla luciferase plus 50 ng of the luciferase firefly reporter were used. pBS-KS+ (Stratagene) was used to bring the total amount of DNA to 2 μg.
dsRNA synthesis and RNAi treatment.
For both procedures we follow the RNAi protocol in S2 cells previously described . Two dsRNAs were synthesized against cyc: one containing its 5′ UTR and another containing the 3′ UTR.
Analysis of gene expression by real-time PCR.
Total RNA was prepared from S2 cells or adult fly heads using Trizol reagent (Invitrogen) according to the manufacturer's protocol. cDNA derived from this RNA (using Invitrogen Superscript II) was utilized as a template for quantitative real-time PCR performed with the Corbett Research Rotor-Gene 3000 real-time cycler. The PCR mixture contained Platinum Taq polymerase (Invitrogen), optimized concentrations of Sybr-green, and the corresponding primers. tim: 5′-CCTTTTCGTACACAGATGCC-3′, 5′ –GGTCCGTCTGGTGATCCCAG-3′; vri: 5′-GCGCTCGCGATAAGTCTCTA-3′, 5′-CTTTGTTGTGGCTGTTGGTG-3′; rp49: 5′-ATCCGCCCAGCATACAG-3′, 5′-TCCGACCAGGTTACAAGAA-3′; and cyc: 5′-GGACGAGCGAGATTGACTATA-3′, 5′-TTTGGAGTGTATACAAATGTCG-3′.
Cycling parameters were 95 °C for 3 min, followed by 40 cycles of 95 °C for 30 s, 55 °C for 45 s, and 72 °C for 45 s. Fluorescence intensities were plotted versus the number of cycles by using an algorithm provided by the manufacturer. mRNA levels were quantified using a calibration curve based upon dilution of concentrated cDNA. mRNA values from heads were normalized to that from ribosomal protein 49 (rp49).
Luciferase activity assay.
Forty-eight hours after transfection cells were assayed using the Dual Luciferase Assay Kit (Promega) following the manufacturer's instructions.
Lysate for the luciferase activity assay was electrophoresed in 6% SDS-PAGE. The protein was transferred to a membrane. The membrane was blocked and probed with primary and secondary antibodies according to standard techniques. Rat anti-TIM antibody  and horseradish-peroxidase-conjugated anti-rat antibody (Sigma) were used.
The following drivers were utilized: tim-gal4 , pdf-gal4 , and elav-gal4 . per-luc, tim-luc, pers, uas-cycHA, and per-rescued flies (per01 elav-gal4; uas-per) were previously described [58,63,64,81,82].
Construction of uas-cyc-vp16 transgenic lines.
The uas-cyc-vp16 plasmids were generated by cloning a PCR fragment from pAc-cyc-vp16 into pUAST . This construct was used to generate germ-line transformants by injecting yw; Ki pp P[ry+Δ2–3]/+.
Construction of dClk-V5 14.8 kb transgenic lines.
D. melanogaster RP98-5K6 bacterial artificial chromosome, which contains the complete dClk gene, was used as a template (BACPAC Resources Center at Children's Hospital Oakland Research Institute). Four different fragments covering the entire gene were first PCR amplified and cloned into pBS vector (first fragment from 7751817 to 7747254 with KpnI and SacI; second fragment from 7747617 to 7745531 with KpnI and SacII; third fragment from 7745570 to 7741748 with KpnI and SacI; fourth fragment from 7741779 to 7736982 with XhoI and NotI; the position of nucleotides refer to D. melanogaster 3L chromosome sequence). A V5 tag was inserted in the fourth fragment by quick change PCR (Stratagene) in the C terminus just before the stop codon at 7738162. The four fragments were then cut and ligated together in the pBS vector using three endogenous restriction sites, BglII at 7747320, NheI at 7745537, and NcoI at 7741772, resulting in a final dClk transgene of 14878 bp (14836 bp of dClk and 42 bp of V5 tag) with KpnI on the 5′ and NotI on the 3′ ends. The dClk-V5 transgene was then cut and ligated in the pCaSpeR 4.0 vector, sequenced, and injected into yw embryo (CBRC Transgenic Drosophila Fly Core).
Male flies were monitored for 4 d in LD conditions, followed by 4–5 d in DD conditions using Trikinetics Drosophila Activity Monitors. Analyses were performed with a signal-processing toolbox . We utilized autocorrelation and spectral analysis to estimate behavioral cycle durations (periods) and the Rhythm Index to assess rhythm strength .
Real-time monitoring of luciferase activity from whole flies and dissected wings.
Adult male flies and dissected wings were cultured in 12:12 LD conditions, and luciferase was measured as described previously . In the case of the experiments described in Figure 3A and Figure S2B, the assay was performed for three days in LD (12:12 LD) and then in DD conditions.
Probe preparation. Total RNA was extracted from fly heads, using Trizol reagent (Invitrogen) according to the manufacturer's protocol. cDNA synthesis was carried out as described in the Expression Analysis Technical Manual (Affymetrix). The cRNA reactions were carried out using the IVT Transcript Labeling Kit (Affymetrix). Affymetrix high-density arrays for D. melanogaster Genome 2.0 were probed, hybridized, stained, and washed according to the manufacturer's protocol.
Data analysis. GeneChip.CEL files were analyzed using R (http://www.r-project.org/) and the bioconductor package (gcrma algorithm; http://www.bioconductor.org/). An anti-logarithm (base 2) was applied to the data to obtain the expression values.
Figure S1. Specific Effects of CYCVP16 in S2 Cells
(A) Expression of cyc does not affect CLK-mediated transcription in S2 cells. S2 cells were transfected with 5 ng of pAc-clk, a tim-luc reporter and different amounts of pAc-cyc plasmid. The data analysis was performed as in Figure 1B.
(B) Protein was isolated from nontransfected S2 cells or cells transfected with pAc-clk (10 ng) and/or pAc-cyc-vp16 (100 ng). Western blotting with anti-TIM was performed to determine TIM levels.
(C) S2 cells were transfected with 100 ng of pAc-ClkJrk or 100 ng of pAc-ClkJrk plus 100 ng of pAc-cyc-vp16 plasmid.
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Figure S2. Luciferase Real-Time Recordings from Control and tim-cyc-vp16 Flies
(A) Luciferase recordings from whole flies for the different fly strains were performed as described in the Materials and Methods section.
(B) Each of the curves in (A) (fly wing Luciferase recordings) was normalized to its maximum value and then plotted together. In the lower right box, an amplification of the marked region is shown.
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Figure S3. Representation of the Period Spread among Individuals of Different Fly Strains
The y-axis corresponds to the relative frequency. The dataset is identical to that displayed in Figure 7A.
(166 KB PPT)
Accession numbers for genetic sequences mentioned in this paper from the National Center for Biotechnology Information (http://www.ncbi.nlm.nih.gov) are the D. melanogaster RP98-5K6 bacterial artificial chromosome, which contains the complete dClk gene, (AC010042) and the D. melanogaster 3L chromosome sequence (NT_037436.2).
We thank our colleagues in the Rosbash lab for helpful discussions, especially D. Stoleru, P. Nawathean, and J. Agosto. We also thank R. Allada, P. Emery, M. Merr, W. Luo, and E. Nagoshi for comments on the manuscript; K. Palm for help with the fly genetics; and Heather Felton for administrative assistance.
SK and MR conceived and designed the experiments. SK, JSM, and RAS performed the experiments. SK analyzed the data. SK and MR wrote the paper.
- 1. Panda S, Hogenesch J, Kay S (2002) Circadian rhythms from flies to human. Nature 417: 329–335.
- 2. Dunlap JC (1999) Molecular bases for circadian clocks. Cell 96: 271–290.
- 3. Roenneberg T, Merrow M (2003) The network of time: understanding the molecular circadian system. Curr Biol 13: R198–R207.
- 4. Hall J (2003) Genetics and molecular biology of rhythms in Drosophila and other insects. Adv Genet 48: 1–280.
- 5. Panda S, Antoch MP, Miller BH, Su AI, Schook AB, et al. (2002) Coordinated transcription of key pathways in the mouse by the circadian clock. Cell 109: 307–320.
- 6. Ptitsyn AA, Zvonic S, Gimble JM (2007) Digital signal processing reveals circadian baseline oscillation in majority of mammalian genes. PLoS Comput Biol 3(6): e120. doi:10.1371/journal.pcbi.0030120.
- 7. McDonald MJ, Rosbash M (2001) Microarray analysis and organization of circadian gene expression in Drosophila. Cell 107: 567–578.
- 8. Schaffer R, Landgraf J, Accerbi M, Simon VV, Larson M, et al. (2001) Microarray analysis of diurnal and circadian-regulated genes in Arabidopsis. Plant Cell 13: 113–123.
- 9. Storch KF, Paz C, Signorovitch J, Raviola E, Pawlyk B, et al. (2007) Intrinsic circadian clock of the mammalian retina: importance for retinal processing of visual information. Cell 130: 730–741.
- 10. Claridge-Chang A, Wijnen H, Naef F, Boothroyd C, Rajewsky N, et al. (2001) Circadian regulation of gene expression systems in the Drosophila head. Neuron 32: 657–671.
- 11. Jones CR, Campbell SS, Zone SE, Cooper F, DeSano A, et al. (1999) Familial advanced sleep-phase syndrome: a short-period circadian rhythm variant in humans. Nat Med 5: 1062–1065.
- 12. Toh KL, Jones CR, He Y, Eide EJ, Hinz WA, et al. (2001) An hPer2 phosphorylation site mutation in familial advanced sleep-phase syndrome. Science 291: 1040–1043.
- 13. Xu Y, Padiath QS, Shapiro RE, Jones CR, Wu SC, et al. (2005) Functional consequences of a CKIδ delta mutation causing familial advanced sleep phase syndrome. Nature 434: 640–644.
- 14. Lamont EW, James FO, Boivin DB, Cermakian N (2007) From circadian clock gene expression to pathologies. Sleep Med 8: 547–556.
- 15. Davis S, Mirick DK (2006) Circadian disruption, shift work and the risk of cancer: a summary of the evidence and studies in Seattle. Cancer Causes Control 17: 539–545.
- 16. Shaw PJ, Tononi G, Greenspan RJ, Robinson DF (2002) Stress response genes protect against lethal effects of sleep deprivation in Drosophila. Nature 417: 287–291.
- 17. Allada R, White N, So W, Hall J, Rosbash M (1998) A mutant Drosophila homolog of mammalian Clock disrupts circadian rhythms and transcription of period and timeless. Cell 93: 791–804.
- 18. Darlington TK, Wager-Smith K, Ceriani MF, Staknis D, Gekakis N, et al. (1998) Closing the circadian loop: CLOCK-induced transcription of its own inhibitors per and tim. Science 280: 1599–1603.
- 19. Gekakis N, Staknis D, Nguyen HB, Davis CF, Wilsbacher LD, et al. (1998) Role of the CLOCK protein in the mammalian circadian mechanism. Science 280: 1564–1569.
- 20. Antoch MP, Song E-J, Chang A-M, Vitaterna MH, Zhao Y, et al. (1997) Functional identification of the mouse circadian clock gene by transgenic BAC rescue. Cell 89: 655–667.
- 21. King DP, Zhao Y, Sangoram AM, Wilsbacher LD, Tanaka M, et al. (1997) Positional cloning of the mouse circadian clock gene. Cell 89: 641–653.
- 22. Rutila JE, Suri V, Le M, So WV, Rosbash M, et al. (1998) CYCLE is a second bHLH-PAS clock protein essential for circadian rhythmicity and transcription of Drosophila period and timeless. Cell 93: 805–814.
- 23. Hardin PE, Hall JC, Rosbash M (1990) Feedback of the Drosophila period gene product on circadian cycling of its messenger RNA levels. Nature 343: 536–540.
- 24. Sehgal A, Price JL, Man B, Young MW (1994) Loss of circadian behavioral rhythms and per RNA oscillations in the Drosophila mutant timeless. Science 263: 1603–1606.
- 25. Hardin PE, Hall JC, Rosbash M (1992) Circadian oscillations in period gene mRNA levels are transcriptionally regulated. Proc Natl Acad Sci U S A 89: 11711–11715.
- 26. Sun ZS, Albrecht U, Zhuchenko O, Bailey J, Eichele G, et al. (1997) RIGUI, a putative mammalian ortholog of the Drosophila period gene. Cell 90: 1003–1011.
- 27. Tei H, Okamura H, Shigeyoshi Y, Fukuhara C, Ozawa R, et al. (1997) Circadian oscillation of a mammalian homologue of the Drosophila period gene. Nature 389: 512–516.
- 28. Kume K, Zylka MJ, Sriram S, Shearman LP, Weaver DR, et al. (1999) mCRY1 and mCRY2 are essential components of the negative limb of the circadian clock feedback loop. Cell 98: 193–205.
- 29. Cyran S, Buchsbaum A, Reddy K, Lin M, Glossop N, et al. (2003) vrille, Pdp1, and dClock form a second feedback loop in the Drosophila circadian clock. Cell 112: 329–341.
- 30. Glossop NR, Houl JH, Zheng H, Ng FS, Dudek SM, et al. (2003) VRILLE feeds back to control circadian transcription of clock in the Drosophila circadian oscillator. Neuron 37: 249–261.
- 31. Ko CH, Takahashi JS (2006) Molecular components of the mammalian circadian clock. Hum Mol Genet 15(Spec No 2): R271–R277.
- 32. Zeng H, Hardin PE, Rosbash M (1994) Constitutive overexpression of the Drosophila Period protein inhibits period mRNA cycling. EMBO J 13: 3590–3598.
- 33. Rothenfluh A, Young MW, Saez L (2000) A TIMELESS-independent function for PERIOD proteins in the Drosophila clock. Neuron 26: 505–515.
- 34. Nawathean P, Rosbash M (2004) The doubletime and CKII kinases collaborate to potentiate Drosophila PER transcriptional repressor activity. Mol Cell 13: 213–223.
- 35. Price JL, Blau J, Rothenfluh-Hilfiker A, Abodeely M, Kloss B, et al. (1998) double-time is a novel Drosophila clock gene that regulates PERIOD protein accumulation. Cell 94: 83–95.
- 36. Lowrey PL, Shimomura K, Antoch MP, Yamazaki S, Zemenides PD, et al. (2000) Positional syntenic cloning and functional characterization of the mammalian circadian mutation tau. Science 288: 483–492.
- 37. Kloss B, Price JL, Saez L, Blau J, Rothenfluh-Hilfiker A, et al. (1998) The Drosophila clock gene double-time encodes a protein closely related to human casein kinase Iε. Cell 94: 97–107.
- 38. Vanselow K, Vanselow JT, Westermark PO, Reischl S, Maier B, et al. (2006) Differential effects of PER2 phosphorylation: molecular basis for the human familial advanced sleep phase syndrome (FASPS). Genes Dev 20: 2660–2672.
- 39. Sathyanarayanan S, Zheng X, Xiao R, Sehgal A (2004) Posttranslational regulation of Drosophila PERIOD protein by protein phosphatase 2A. Cell 116: 603–615.
- 40. Fang Y, Sathyanarayanan S, Sehgal A (2007) Post-translational regulation of the Drosophila circadian clock requires protein phosphatase 1 (PP1). Genes Dev 21: 1506–1518.
- 41. Rothenfluh A, Abodeely M, Price JL, Young MW (2000) Isolation and analysis of six timeless alleles that cause short or long-period circadian rhythms in Drosophila. Genetics 156: 665–675.
- 42. Kim EY, Edery I (2006) Balance between DBT/CKIε kinase and protein phosphatase activities regulate phosphorylation and stability of Drosophila CLOCK protein. Proc Natl Acad Sci U S A 103: 6178–6183.
- 43. Kim EY, Ko HW, Yu W, Hardin PE, Edery I (2007) A DOUBLETIME kinase binding domain on the Drosophila PERIOD protein is essential for its hyperphosphorylation, transcriptional repression, and circadian clock function. Mol Cell Biol 27: 5014–5028.
- 44. Nawathean P, Stoleru D, Rosbash M (2007) A small conserved domain of Drosophila PERIOD is important for circadian phosphorylation, nuclear localization, and transcriptional repressor activity. Mol Cell Biol 27: 5002–5013.
- 45. Ko HW, Jiang J, Edery I (2002) Role for Slimb in the degradation of Drosophila Period protein phosphorylated by Doubletime. Nature 420: 673–678.
- 46. Curtin K, Huang ZJ, Rosbash M (1995) Temporally regulated nuclear entry of the Drosophila period protein contributes to the circadian clock. Neuron 14: 365–372.
- 47. Dembinska ME, Stanewsky R, Hall JC, Rosbash M (1997) Circadian cycling of a period-lacZ fusion protein in Drosophila: evidence for an instability cycling element in PER. J Biol Rhythms 12: 157–172.
- 48. Akten B, Jauch E, Genova GK, Kim EY, Edery I, et al. (2003) A role for CK2 in the Drosophila circadian oscillator. Nat Neurosci 6: 251–257.
- 49. Lin JM, Kilman VL, Keegan K, Paddock B, Emery-Le M, et al. (2002) A role for casein kinase 2α in the Drosophila circadian clock. Nature 420: 816–820.
- 50. Marrus SB, Zeng H, Rosbash M (1996) Effect of constant light and circadian entrainment of pers flies: evidence for light-mediated delay of the negative feedback loop in Drosophila. EMBO J 15: 6877–6886.
- 51. Curtin KD, Huang ZJ, Rosbash M (1995) Temporally regulated nuclear entry of the Drosophila period protein contributes to the circadian clock. Neuron 14: 365–372.
- 52. Bao S, Rihel J, Bjes E, Fan JY, Price JL (2001) The Drosophila double-timeS mutation delays the nuclear accumulation of period protein and affects the feedback regulation of period mRNA. J Neurosci 21: 7117–7126.
- 53. Vielhaber E, Eide E, Rivers A, Gao ZH, Virshup DM (2000) Nuclear entry of the circadian regulator mPER1 is controlled by mammalian casein kinase Iε. Mol Cell Biol 20: 4888–4899.
- 54. Yu W, Zheng H, Houl JH, Dauwalder B, Hardin PE (2006) PER-dependent rhythms in CLK phosphorylation and E-box binding regulate circadian transcription. Genes Dev 20: 723–733.
- 55. Woelfle MA, Johnson CH (2006) No promoter left behind: global circadian gene expression in cyanobacteria. J Biol Rhythms 21: 419–431.
- 56. Tomita J, Nakajima M, Kondo T, Iwasaki H (2005) No transcription-translation feedback in circadian rhythm of KaiC phosphorylation. Science 307: 251–254.
- 57. Nakajima M, Imai K, Ito H, Nishiwaki T, Murayama Y, et al. (2005) Reconstitution of circadian oscillation of cyanobacterial KaiC phosphorylation in vitro. Science 308: 414–415.
- 58. Yang Z, Sehgal A (2001) Role of molecular oscillations in generating behavioral rhythms in Drosophila. Neuron 29: 453–467.
- 59. Frisch B, Hardin PE, Hamblen-Coyle MJ, Rosbash M, Hall JC (1994) A promoterless DNA fragment from the period locus rescues behavioral rhythmicity and mediates cyclical gene expression in a restricted subset of the Drosophila nervous system. Neuron 12: 555–570.
- 60. Wysocka J, Herr W (2003) The herpes simplex virus VP16-induced complex: the makings of a regulatory switch. Trends Biochem Sci 28: 294–304.
- 61. McDonald MJ, Rosbash M, Emery P (2001) Wild-type circadian rhythmicity is dependent on closely spaced E boxes in the Drosophila timeless promoter. Mol Cell Biol 21: 1207–1217.
- 62. Kadener S, Stoleru D, McDonald M, Nawathean P, Rosbash M (2007) Clockwork Orange is a transcriptional repressor and a new Drosophila circadian pacemaker component. Genes Dev 21: 1675–1686.
- 63. Konopka RJ, Benzer S (1971) Clock mutants of Drosophila melanogaster. Proc Natl Acad Sci U S A 68: 2112–2116.
- 64. Allada R, Kadener S, Nandakumar N, Rosbash M (2003) A recessive mutant of Drosophila Clock reveals a role in circadian rhythm amplitude. EMBO J 22: 3367–3375.
- 65. Rutila JE, Edery I, Hall JC, Rosbash M (1992) The analysis of new short-period circadian rhythm mutants suggests features of D. melanogaster period gene function. J Neurogenet 8: 101–113.
- 66. Baylies MK, Bargiello TA, Jackson FR, Young MW (1987) Changes in abundance and structure of the per gene product can alter periodicity of the Drosophila clock. Nature 326: 390–392.
- 67. Smith RF, Konopka RJ (1981) Circadian clock phenotypes of chromosome aberrations with a breakpoint at the per locus. Mol Gen Genet 183: 243–251.
- 68. Kaneko M, Park J, Cheng Y, Hardin P, Hall J (2000) Disruption of synaptic transmission or clock-gene-product oscillations in circadian pacemaker cells of Drosophila cause abnormal behavioral rhythms. J Neurobiol 43: 207–233.
- 69. Matsumoto A, Ukai-Tadenuma M, Yamada RG, Houl J, Uno KD, et al. (2007) A functional genomics strategy reveals clockwork orange as a transcriptional regulator in the Drosophila circadian clock. Genes Dev 21: 1687–1700.
- 70. Lim C, Chung BY, Pitman JL, McGill JJ, Pradhan S, et al. (2007) Clockwork orange encodes a transcriptional repressor important for circadian-clock amplitude in Drosophila. Curr Biol 17: 1082–1089.
- 71. Ripperger JA, Schibler U (2006) Rhythmic CLOCK-BMAL1 binding to multiple E-box motifs drives circadian Dbp transcription and chromatin transitions. Nat Genet 38: 369–374.
- 72. Liu AC, Welsh DK, Ko CH, Tran HG, Zhang EE, et al. (2007) Intercellular coupling confers robustness against mutations in the SCN circadian clock network. Cell 129: 605–616.
- 73. Martinek S, Inonog S, Manoukian AS, Young MW (2001) A role for the segment polarity gene shaggy/GSK-3 in the Drosophila circadian clock. Cell 105: 769–779.
- 74. Kim EY, Bae K, Ng FS, Glossop NR, Hardin PE, et al. (2002) Drosophila CLOCK protein is under posttranscriptional control and influences light-induced activity. Neuron 34: 69–81.
- 75. Edery I, Zwiebel LJ, Dembinska ME, Rosbash M (1994) Temporal phosphorylation of the Drosophila period protein. Proc Natl Acad Sci U S A 91: 2260–2264.
- 76. Mihalcescu I, Hsing W, Leibler S (2004) Resilient circadian oscillator revealed in individual cyanobacteria. Nature 430: 81–85.
- 77. Welsh DK, Logothetis DE, Meister M, Reppert SM (1995) Individual neurons dissociated from rat suprachiasmatic nucleus express independently phased circadian firing rhythms. Neuron 14: 697–706.
- 78. Zeng H, Qian Z, Myers MP, Rosbash M (1996) A light-entrainment mechanism for the Drosophila circadian clock. Nature 380: 129–135.
- 79. Kaneko M, Hall JC (2000) Neuroanatomy of cells expressing clock genes in Drosophila: transgenic manipulation of the period and timeless genes to mark the perikarya of circadian pacemaker neurons and their projections. J Comp Neurol 422: 66–94.
- 80. Renn SC, Park JH, Rosbash M, Hall JC, Taghert PH (1999) A pdf neuropeptide gene mutation and ablation of PDF neurons each cause severe abnormalities of behavioral circadian rhythms in Drosophila. Cell 99: 791–802.
- 81. Peng Y, Stoleru D, Levine JD, Hall JC, Rosbash M (2003) Drosophila free-running rhythms require intercellular communication. PLoS Biol 1: e13.
- 82. Stanewsky R, Jamison CF, Plautz JD, Kay SA, Hall JC (1997) Multiple circadian-regulated elements contribute to cycling period gene expression in Drosophila. EMBO J 16: 5006–5018.
- 83. Brand AH, Perrimon N (1993) Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. Development 118: 401–415.
- 84. Levine JD, Funes P, Dowse HB, Hall JC (2002) Signal analysis of behavioral and molecular cycles. BMC Neurosci 3: 1.
- 85. Krishnan B, Levine JD, Lynch MK, Dowse HB, Funes P, et al. (2001) A new role for cryptochrome in a Drosophila circadian oscillator. Nature 411: 313–317.