Circadian (∼24 hr) rhythms of behavior and physiology are driven by molecular clocks that are endogenous to most organisms. The mechanisms underlying these clocks are remarkably conserved across evolution and typically consist of auto-regulatory loops in which specific proteins (clock proteins) rhythmically repress expression of their own genes. Such regulation maintains 24-hr cycles of RNA and protein expression. Despite the conservation of these mechanisms, however, questions are now being raised about the relevance of different molecular oscillations. Indeed, several studies have demonstrated that oscillations of some critical clock genes can be eliminated without loss of basic clock function. Here, we describe the multiple levels at which clock gene/protein expression and function can be rhythmically regulated—transcription, protein expression, post-translational modification, and localization—and speculate as to which aspect of this regulation is most critical. While the review is focused on Drosophila, we include some discussion of mammalian clocks to indicate the extent to which the questions concerning clock mechanisms are similar, regardless of the organism under study.
THE light:dark cycle generated by the earth's rotation is the driving force of daily behavioral and physiological rhythms exhibited by most organisms. However, these daily (∼24 hr) rhythms are not just a passive response to the light:dark cycle; instead, an intrinsic timekeeping mechanism synchronizes physiological processes to the cyclic environment. The endogenous timekeeper is a self-sustained oscillator, termed the circadian clock, which can be entrained to environmental cues such as light and temperature (such environmental time signals are called zeitgebers), but more importantly, it free runs in constant conditions that lack environmental cues. In the past ∼20 years, genetic analysis of circadian rhythms in model organisms such as Drosophila, Neurospora, Arabidopsis, cyanobacteria, and mice has yielded considerable insight into the molecular mechanisms of circadian oscillators. Despite these advances, the question of how exactly a rhythm is generated is getting some attention again because a number of recent studies have challenged the simple models proposed initially. This review traces these developments in the field and then proposes a revised model that incorporates the old and new findings. While the focus is on the molecular mechanisms of the Drosophila melanogaster circadian clock, advances in other circadian systems will also be discussed to illustrate conserved mechanisms. Readers interested in circadian clock mechanisms of other organisms are encouraged to read recent reviews (Hastings and Herzog 2004; Gardner et al. 2006; Ko and Takahashi 2006; Williams 2006; Woelfle and Johnson 2006; Heintzen and Liu 2007; Levi and Schibler 2007).
THE BASIC CIRCADIAN FRAMEWORK: THE per–tim FEEDBACK LOOP
Genetic analysis has identified four proteins in Drosophila that are essential for, and largely dedicated to, circadian clock function: CLOCK (CLK), CYCLE (CYC), PERIOD (PER), and TIMELESS (TIM) (Konopka and Benzer 1971; Bargiello et al. 1984; Reddy et al. 1984; Zehring et al. 1984; Sehgal et al. 1994; Myers et al. 1995; Allada et al. 1998; Rutila et al. 1998). The manner in which a molecular clock is generated through the actions of these proteins has been investigated in some detail. During the day and early evening, CLK and CYC form a heterodimer, which activates per and tim expression through binding to specific enhancer elements (E-box) in their promoters (Darlington et al. 1998), resulting in a peak of per and tim transcripts during the early night. The PER and TIM proteins accumulate and associate with each other (Gekakis et al. 1995; Meyer et al. 2006) in the late night and translocate into the nucleus to repress the transcriptional activity of the CLK–CYC heterodimer (Hardin 2005) (Figure 1). Recent studies suggest that each of the two proteins can enter the nucleus alone (Shafer et al. 2002); however, nuclear TIM alone does not function as an efficient repressor of CLK–CYC activity (Ashmore et al. 2003; Chang and Reppert 2003). In contrast, PER alone can repress CLK–CYC activity (Rothenfluh et al. 2000; Chang and Reppert 2003; Nawathean and Rosbash 2004; Cyran et al. 2005), although the repression efficiency is greatly increased when TIM is present. After lights on, PER–TIM proteins are degraded, allowing a new cycle of transcription to start (Figure 1). The turnover of PER and TIM proteins during the daytime, the delay of their accumulation during early night, and their nuclear translocation during the late night appears to be crucial to maintaining the 24-hr cycle. These dynamic cyclic processes persist in constant dark conditions. Mammals have a similar framework, where the circadian clock consists of CLOCK, BMAL1 (mammalian ortholog of CYC), and PER and its partner, which is a molecule called cryptochrome (mCRY), rather than TIM (Ko and Takahashi 2006).
The mechanisms described above are usually synchronized to light:dark cycles through the process described below. However, they are sustained in constant darkness; indeed, they can even be initiated in the absence of light. When flies are raised under constant dark conditions, they are able to manifest rhythmic behavior (Sehgal et al. 1992; Tomioka et al. 1997), although individual flies are not in phase with each other.
The simplest model, then, is that rhythmic transcription produces rhythmic RNA expression, which leads to rhythmic protein expression. The protein, in turn, regulates transcription of its own gene, maintaining a 24-hr loop, which drives overt rhythms. However, a number of observations have challenged this model. Even when per and tim mRNA are held constant, the two proteins continue to cycle, and behavioral rhythms persist in a significant proportion of flies (Yang and Sehgal 2001). This contradicts the original model because the prediction was that abolishing rhythmic transcription would abolish the feedback loop, and thereby behavioral rhythms. Thus, mechanisms other than rhythmic transcription are able to maintain cyclic expression of the core clock proteins, and it would appear that cyclic expression of the two proteins is essential for clock function. Consistent with this idea, overexpression of either protein renders flies arrhythmic (Yang and Sehgal 2001). However, it may also be that overexpression of the proteins prevents necessary post-translational modifications (discussed further below).
In the mammalian circadian clock, even the significance of clock protein cycling has been questioned. Although overexpression of mCry1 was reported to impair molecular oscillations in cultured fibroblasts (Ueda et al. 2005), infusion of constant levels of mCRY into cultured cells did not disrupt the molecular clock (Fan et al. 2007). One could argue that the overall levels of mCRY, or its post-translational modifications, were different in the two studies, but the latter study does suggest that robust cycling of mCRY is not necessary for a functional molecular oscillation, at least in the cell system used. Thus, it appears that rhythms can be generated in the absence of rhythmic mRNA expression, and perhaps even rhythmic protein expression, of one or more essential clock genes. In fact, as alluded to above, post-translational control of clock proteins is critical, if not sufficient for generating a rhythm.
LIGHT RESPONSE OF THE CIRCADIAN CLOCK
Light is the major entraining signal for the circadian clock. Since the clock's response to light is based largely upon the function of proteins introduced above, we will discuss it here before describing other aspects of the clock mechanism. The clock can be entrained to light by the visual system and by nonvisual, dedicated circadian mechanisms (Ashmore and Sehgal 2003). The dedicated circadian photoreceptor in Drosophila is cryptochrome (CRY) (Emery et al. 1998; Stanewsky et al. 1998), ortholog of the protein that in mammals is a component of the molecular clock. Upon light treatment, CRY is activated and transmits a signal that targets TIM for degradation by the proteasome (Hunter-Ensor et al. 1996; Myers et al. 1996; Zeng et al. 1996; Naidoo et al. 1999). Light-dependent degradation of TIM is mediated by a specific E3 ligase protein termed JETLAG (JET) (Koh et al. 2006). The name was derived from the phenotype of mutant flies that fail to efficiently adjust their circadian behavior to a shift in the light:dark schedule, thus displaying extended “jetlag.” jetlag (jet) mutants also have aberrent behavior in the presence of constant light. Unlike wild-type flies that are arrhythmic in the presence of constant light due to the constant degradation of TIM, jet flies are rhythmic under such conditions.
Although tyrosine kinase activity appears to be required for TIM degradation by light (Naidoo et al. 1999), the specific enzyme involved has not yet been identified. However, the serine/threonine kinase, glycogen synthese kinase [SHAGGY (SGG) in Drosophila], is involved in this process. Serotonin signaling increases SGG phosphorylation, thereby lowering its activity (SGG activity is lowered by phosphorylation at the Ser9 residue), and reduces TIM degradation by light (Yuan et al. 2005). On the other hand, a recent study showed that increased SGG stabilizes TIM and also reduces its response to light (Stoleru et al. 2007). This apparent contradiction cannot be simply explained by SGG activity toward TIM and may involve effects of SGG on CRY (Stoleru et al. 2007).
With respect to how the effect of light on TIM resets the clock, the association of TIM with CRY abrogates negative feedback by PER–TIM, and the subsequent degradation of TIM disrupts the PER–TIM complex (Lee et al. 1996; Ceriani et al. 1999). Thus, light alters the levels of a clock component, which resets the timing of all other events in the cycle. Interestingly, pulses of light delivered at night will reset the phase of the clock, but the effect is different depending upon the time of delivery: in the early night, a light pulse delays the clock (resetting to dusk) while in the late night it advances the clock (resetting to dawn). In molecular terms, a possible explanation may be provided by the levels of tim mRNA and the subcellular localization of PER and TIM. In the early night, the two proteins are cytoplasmic and mRNA levels are high and able to resynthesize the protein lost by degradation. Thus, the clock is delayed by the number of hours it takes to produce that amount of protein. In the late night, the PER–TIM complex is in the nucleus, repressing transcription. Thus, the protein cannot be replenished and the clock moves forward to the next cycle.
POST-TRANSLATIONAL REGULATION OF PER AND TIM
As may be evident from the description of the light response above, post-translational mechanisms are critical for the entrainment of the clock to light. Likewise, free-running clock function relies upon regulated post-translational events, even when per and tim mRNA are expressed with a robust rhythm. PER stability is regulated by phosphorylation carried out largely by a casein kinase I gene called doubletime (dbt). Mutations in dbt result in long or short period or arrhythmia, depending on the specific molecular lesion (Price et al. 1998). It is clear that in strong hypomorphic alleles of dbt PER levels are constantly high, consistent with the idea that DBT phosphorylates PER and destabilizes it. In the dbtS mutant, PER accumulates more slowly in the nucleus in the early evening phase and is degraded faster in the late night and early morning (Bao et al. 2001). A mutation in a serine residue of PER (perS) produced a similar late-night effect as dbtS (Marrus et al. 1996). PER is also phosphorylated by casein kinase 2, and mutations in CK2 affect circadian periodicity most likely by affecting the timing of the nuclear entry of PER (Lin et al. 2002, 2005; Akten et al. 2003).
DBT phosphorylated PER is recognized by protein phosphatase 2A (PP2A). Elevated PP2A activity stabilizes PER and retains it in the nucleus throughout the day, resulting in arrhythmic behavior (Sathyanarayanan et al. 2004). Normally, PER phosphorylation displays a robust circadian oscillation (Edery et al. 1994). There is no obvious cycling of dbt RNA (Kloss et al. 1998) and protein (Preuss et al. 2004), but the PP2A regulatory subunit, tws, is expressed rhythmically, suggesting that cyclic PER phosphorylation and subsequent nuclear localization and degradation may be driven by cyclic phosphatase activity. Alternatively, cyclic expression of TIM may modulate the accessibility of PER to DBT, thereby affecting cyclic PER phosphorylation (Kloss et al. 2001). Indeed, PER is unstable, and its rhythmic phosphorylation is abolished in tim null mutants (Price et al. 1995). However, since there is no functional clock in tim null mutants, presumably cyclic tws expression is also abolished, as it is in cyc mutants (Sathyanarayanan et al. 2004); thus these two possibilities to explain rhythmic PER phosphorylation cannot be distinguished.
It is clear that TIM stabilizes PER although the mechanisms are not known. It is possible that TIM binding prevents DBT from phosphorylating PER (Kloss et al. 2001); without TIM, PER is hyperphosphorylated by DBT and subsequently degraded (Cyran et al. 2005). Alternatively, protein phosphatases may have better access to the TIM-bound PER (Sathyanarayanan et al. 2004; Fang et al. 2007). In fact, PER is dephosphorylated and stabilized by protein phosphatase 1 (PP1) in a TIM-regulated fashion (Fang et al. 2007). Thus, TIM does not affect PP2A action on PER, but it influences the stabilizing effect of PP1.
TIM stability and nuclear entry are likewise regulated by phosphorylation and dephosphorylation. In addition to its role in modulating light-dependent degradation of TIM, SGG also regulates TIM phosphorylation under constant dark conditions. Flies overexpressing SGG have short periods, while sgg mutants have long periods. SGG phosphorylation promotes TIM nuclear entry, which may account for the faster clock (Martinek et al. 2001). Presumably, reduced expression of SGG decreases phosphorylation of TIM and delays its nuclear entry, thereby slowing down the clock. Although TIM levels are increased in sgg mutants, it seems that TIM degradation is not a direct consequence of SGG phosphorylation because TIM levels are not reduced in SGG overexpressing cells (Martinek et al. 2001; Stoleru et al. 2007). Since protein phosphatase 1 (PP1) dephosphorylates TIM (Fang et al. 2007), one might expect that inhibition of PP1 would produce similar effects on circadian period as SGG overexpression. However, inhibition of PP1 actually lengthens circadian period. Moreover, inhibition of PP1 does not affect the initiation of nuclear translocation although it delays the accumulation of TIM in the nucleus due to an effect on TIM stability. It is possible that SGG and PP1 target different sites and thus regulate different aspects of TIM nuclear entry and stability (Fang et al. 2007).
Hyperphosphorylated PER is a substrate for the ubiquitin–proteasome degradation machinery. Slimb, an F-box/WD40-repeat E3 ligase protein, is essential for the degradation of phosphorylated PER and perhaps TIM (Grima et al. 2002; Ko et al. 2002). In Slimb mutants, high levels of hyperphosphorylated PER and TIM are observed under constant dark conditions; in contrast, both PER and TIM continue to oscillate under light:dark conditions. Since PER stability depends upon TIM, the normal cycling of PER levels in Slimb mutants under light:dark conditions might be a secondary effect of light-dependent TIM degradation. Thus, light-dependent degradation of TIM does not rely on Slimb. As noted above, another ubiquitin E3 ligase, JET, targets TIM for degradation in response to light (Koh et al. 2006).
In the mammalian system also, post-translational regulation of clock proteins plays an important role. PER, CRY, and BMAL1 are phosphorylated by casein kinase 1 and PP1 dephosphorylates PER (Lowrey et al. 2000; Lee et al. 2001; Akashi et al. 2002; Eide et al. 2002; Gallego et al. 2006). A mutation in CK1ε as well as a mutation in a putative CK1ε phosphorylation site on PER2 have even been implicated in a human circadian disorder, familial advanced sleep phase syndrome (FASPS) (Toh et al. 2001; Xu et al. 2005). In addition, similar to Drosophila TIM and PER, CRY is targeted for proteasomal degradation by an E3 ligase F-box protein FBXL3. Loss-of-function alleles of this gene have long circadian periods, consistent with the role of mCRY as a repressor of CLOCK activity (Godinho et al. 2007; Siepka et al. 2007).
THE Clk FEEDBACK LOOP
Interaction of the PER–TIM complex with CLK not only represses CLK–CYC activity, but also brings DBT in close proximity to CLK. Thus CLK is phosphorylated by DBT and apparently dephosphorylated by PP2A (Kim and Edery 2006). Under normal light:dark conditions, Clk mRNA levels cycle with a robust circadian rhythm (Bae et al. 1998; Darlington et al. 1998). However, this robust mRNA cycling does not result in a corresponding cycle of CLK protein abundance: Clk mRNA levels change three to fivefold over the course of the day, while CLK protein levels remain constant (Houl et al. 2006; Yu et al. 2006). It is possible that the turnover of CLK has a rhythm that counters the effect of Clk mRNA cycling, although the purpose of such regulation would be difficult to explain. In fact, CLK is regulated in a circadian fashion at the level of phosphorylation, with the peak of phosphorylation occurring in the late night and early morning (Kim and Edery 2006; Yu et al. 2006), which is the same phase as the cycling of Clk mRNA. Since phosphorylated CLK is turned over by the proteasome degradation pathway, high levels of Clk mRNA at these times may allow sufficient CLK protein to be produced, thus keeping total CLK protein levels constant. However, the significance of this constant CLK protein level is unknown. One possibility is that constant CLK protein levels serve to jump-start transcription when repressors are removed, such as when flies are light pulsed in the late night. In response to such a pulse, TIM is degraded, releasing the repression of the PER–TIM complex on the CLK–CYC heterodimer and promoting a new cycle of transcription.
The CLK–CYC heterodimer regulates the expession of another two transcription factors, PAR domain protein 1 (Pdp1) and basic leucine zipper (bZIP) transcription factor vrille (vri), both Pdp1 and vri are activated by CLK–CYC, so both have a robust circadian expression pattern. And both proteins feed back to regulate Clk expression although in opposing ways (Blau and Young 1999; Cyran et al. 2003). PDP1 binds to the Clk promoter via an E4BP4-binding site to activate Clk transcription while VRI competes with PDP1 for binding to the same site to repress Clk transcription. The PDP1 peak lags behind that of VRI, thus enabling sequential repression and activation of Clk and giving rise to rhythmic Clk mRNA expression (Blau and Young 1999; Cyran et al. 2003; Glossop et al. 2003) (Figure 1). Other factors may also be involved in regulating Clk mRNA cycling because expression of a Pdp1 RNA interference construct or wild-type Pdp1 in tim-expressing cells does not disrupt cycling of Clk mRNA or of VRI (Benito et al. 2007). However, the overall significance of Clk mRNA cycling and of the feedback loop generated through the mutual regulation of Clk and vri/Pdp1 remains unclear. As noted above, the CLK protein does not cycle. In addition, its overexpression does not affect free-running rhythms, supporting the idea that levels of CLK do not constitute timekeeping cues (Kim et al. 2002). Expression of Clk under the control of the per promoter, which reverses the phase of mRNA expression, also has no significant effect on free-running behavioral rhythms although it affects the morning peak of locomotor activity in the presence of light:dark cycles (Kim et al. 2002). We speculate that the Clk feedback loop exists primarily to allow interfaces between the clock and other pathways. For instance, vri and Pdp1 may be regulated by inputs to the clock, and they may also cyclically activate/repress downstream genes. In this scenario, the cycling of Clk mRNA would be an epiphenomenon generated through the cyclic activity of VRI and PDP1.
In mammals, Bmal1 is regulated through a feedback loop similar to the Clk loop in Drosophila. The nuclear receptors Rev-erb α and Rora are expressed cyclically under the control of CLOCK–BMAL1 activity, and they repress and activate Bmal1 expression respectively. This feedback mechanism maintains robust oscillations of Bmal1 mRNA (see reviews by Ko and Takahashi 2006; Levi and Schibler 2007).
RELEVANCE OF THE DIFFERENT MOLECULAR OSCILLATIONS IN THE CLOCK
We have just questioned the importance of the Clk feedback loop for the essential timekeeping mechanism. Similar concerns may apply to the Bmal1 loop in mammals, given that a knockout of Rev-erbα, which loses Bmal1 oscillations, is able to maintain basic clock function (Preitner et al. 2002). In addition, we pointed out studies that show that all components of the per–tim feedback loop, or of the per–Cry loop in mammals, need not necessarily cycle. The question, then, is what must cycle to generate a functional clock? While there is, as yet, no definitive answer to this question, it is worth examining the clock mechanism in the simplest organism known to have a clock—cyanobacteria.
Although a feedback loop similar to the one described above exists in cyanobacteria, a rhythm of autophosphorylation of the clock protein KaiC persists without cyclic RNA and protein expression (Tomita et al. 2005). Remarkably, cyclic phosphorylation of KaiC can be reconstituted in a test tube by incubating it with ATP and two other clock proteins, KaiA and KaiB (Nakajima et al. 2005). Thus the transcription–translation feedback loop is not necessary for this circadian clock. However, this clock drives rhythmic transcription of much of the cyanobacteria genome, perhaps in response to a cellular metabolism zeitgeber (Lakin-Thomas 2006; Woelfle and Johnson 2006). Interestingly, metabolic cues can also affect circadian clocks in other organisms. The redox state modulates mammalian CLOCK activity by regulating its DNA-binding efficiency (Rutter et al. 2001). Recently, we showed that oxidative stress affects the molecular circadian clock in Drosophila. Mutations in a FOXO transcription factor increase the sensitivity of the Drosophila clock to oxidative stress and result in degeneration of circadian rhythms (Zheng et al. 2007).
RHYTHMIC CLK–CYC ACTIVITY MAY BE ESSENTIAL FOR A FUNCTIONAL CLOCK
While it is tempting to speculate that circadian clocks in eukaryotic organisms are generated through mechanisms similar to those in cyanobacteria, this is not likely to be the case. It may be possible to dispense with rhythmic transcription for some genes, but we predict that some clock mRNAs continue to cycle. In the experiments described earlier where per and tim mRNA were kept constant (Yang and Sehgal 2001), mRNA levels of the PP2A regulatory subunit, tws, were probably still cycling and may have been sufficient to drive the rhythmic phosphorylation and thereby the cycling of PER. Cycling PER, in turn, would have rhythmically regulated activity of CLK–CYC. In the mammalian cell culture experiment where rhythms persisted despite constant levels of mCRY (Fan et al. 2007), some genes relevant to post-translational control of mCRY may have been expressed rhythmically. For example, mPER serves as a scaffold to mediate CKI ε phosphorylation of mCRY (Eide et al. 2002). This may have been sufficient for mCRY to rhythmically repress CLOCK–BMAL1. Experiments in the mammalian system have, in fact, demonstrated that repression of CLOCK–BMAL1 activity is essential for clock function (Sato et al. 2006).
As noted above, although levels of Drosophila CLK are constant throughout the day, there are robust daily oscillations of its phosphorylation (Houl et al. 2006; Yu et al. 2006). In addition, phosphorylation of CLK appears to directly affect its transcriptional activity (Kim and Edery 2006; Yu et al. 2006) [Likewise, transcriptional activity of mammalian BMAL1 and the cyanobacterial clock protein KaiC is regulated by phosphorylation (Eide et al. 2002; Nishiwaki et al. 2004; Xu et al. 2004).] Since the phosphorylation of CLK is PER dependent (Kim and Edery 2006; Yu et al. 2006), oscillations of PER could confer rhythmic regulation of CLK activity. Thus it seems that an oscillation of PER is a prerequisite for a functional clock. This oscillation has several components: cyclic PER protein expression and phosphorylation (Edery et al. 1994), rhythmic nuclear localization (Vosshall et al. 1994; Price et al. 1998), and subsequent binding to CLK–CYC (Lee et al. 1999) (Figure 2).
Overexpression of per or tim in the central clock cells abolishes protein cycling and results in arrhythmic behavior in many flies (Kaneko et al. 2000; Blanchardon et al. 2001; Yang and Sehgal 2001). The arrhythmicity may be due to increased levels of PER or TIM per se or due to the loss of rhythmic protein phosphorylation or due to a disruption in cyclic nuclear entry (these mechanisms are not mutually exclusive). Regardless of the precise mechanism, rhythmic repression of CLK–CYC by the PER–TIM complex, which involves PER-dependent phosphorylation of CLK by DBT, would be disrupted. This would lead to noncyclic expression of clock-controlled downstream target genes. On the basis of the mammalian study that indicates that the cycling of CRY is not essential, we predict that it is not the loss of PER or TIM cycling per se that causes the arrhythmia, but rather the loss of cyclic nuclear entry, which may, in turn, be regulated by phosphorylation. We propose that the critical function of PER–TIM in the clock is to rhythmically enter the nucleus and repress CLK–CYC, perhaps by providing DBT kinase activity.
Having argued that rhythmic activity of clock proteins, rather than rhythmic levels, is key to the timekeeping process, some aspects of clock function may require alterations in protein levels. For instance, in all organisms examined, light alters the levels of a clock component. Thus, it seems that the initial event in resetting a clock, or perhaps even in initiating a clock, is a change in the levels of a clock protein. In this context, it is interesting that ectopic expression of Clk is sufficient to generate molecular cycling of tim and cry under light:dark conditions (Zhao et al. 2003). It appears that CLK is able to activate and orchestrate the oscillation of necessary components when ectopically expressed. How this cycling is initiated is not clear. Since it is possible that light-driven TIM degradation jump-starts the feedback loop in nonclock cells, it would be interesting to see if ectopic CLK expression can start an oscillator in constant darkness.
Despite this emphasis on CLK, it is important to note that the transcriptional heterodimer at the center of the timekeeping mechanism does not have to include CLK in particular. Indeed, mice with a deficiency of Clock have functional clocks (Debruyne et al. 2006). Most mammalian circadian phenotypes are based on a dominant negative allele of Clk, which produces phenotypes more severe than those produced by a Clk deficiency, perhaps because dominant negative CLK interferes with BMAL1 binding to another partner. Indeed, BMAL1 can partner with the mCLK paralog NPAS2 that functions in the basal forebrain and other tissues (Reick et al. 2001). Recent findings demonstrate that CLK and NPAS2 act redundantly in the master pacemaker, the suprachiasmatic nucleus (SCN) (Debruyne et al. 2007a,b). In contrast, mCLK is necessary for circadian clock function in some peripheral tissues (Kennaway et al. 2006; Debruyne et al. 2007b).
Finally, it is important to note that while rhythmic transcription of some clock genes can be experimentally dispensed with, this is not to say that it is without function. Rhythms are less robust and penetrant, and periods are less precise when these genes are expressed noncyclically. Moreover, flies that express per and tim constitutively show defects in their response to pulses of light (Yang and Sehgal 2001). Overexpression of mPer1 also impairs normal entrainment and molecular oscillations in mammals (Numano et al. 2006), supporting the idea that these responses depend upon cycling RNA. In further support of a role for transcription, new transcription factors continue to be identified as part of the clock mechanism. A bHLH ORANGE family protein CLOCKWORK ORANGE (CWO) is one such recently identified factor. Cwo is activated by CLK–CYC through the E-box in its promoter, and it also feeds back to synergize with PER to repress CLK–CYC activity. These feedback loops thus are able to amplify the oscillation and maintain a robust 24-hr cycle (Kadener et al. 2007; Lim et al. 2007; Matsumoto et al. 2007).
In summary, we are learning that the mechanism of the clock is much more intricate than previously thought. There are likely multiple feedback loops that lie at the heart of the clock, and some aspects of clock function may be maintained through redundant mechanisms. While post-translational regulation is clearly critical to maintaining a clock, we believe it is unlikely that eukaryotic clocks will turn out to be entirely free of transcriptional control as is the cyanobacteria clock. Thus, while a subset of clock mRNAs, and even clock proteins, may be held at constant levels without complete loss of clock function, others are likely cycling under these conditions. In addition, even the dispensable oscillations probably serve functions that may sometimes be too subtle to detect.
Due to space limitations, many important original findings could not be cited. This work was supported by a National Institutes of Health grant R01 NS048471.
Communicating editor: A. Spradling
- Copyright © 2008 by the Genetics Society of America