Different roles of Period2 and Period3 genes in the mouse body clock studied in the lab

Circadian rhythms are self-sustained oscillations in physiology and behavior with endogenous periods of approximately 24 hours that can be entrained to environmental cues such as the light/dark cycle and temperature [1]. In mammals, a light-entrainable circadian pacemaker, located in the suprachiasmatic nuclei (SCN) of the anterior hypothalamus, plays a critical role in the generation of daily rhythms. Surgical destruction of the SCN abolishes most circadian rhythms, including rhythmic locomotor activity [2], [3], [4]. Transplants of fetal SCN tissue to SCN-lesioned animals restore rhythmic behavior that is consistent with the periodicity of the donor's genotype [5], [6], [7], suggesting that the SCN controls the period of the circadian behavioral rhythm.

The SCN is not the only endogenously rhythmic structure. Ex vivo adrenals, liver, and retinas exhibit circadian rhythmicity [8], [9], [10], [11], [12]. In addition, genes important for circadian timekeeping are expressed not only in the SCN, but also in many peripheral tissues [13], [14], [15], [16], [17]. Following the discovery that immortalized rat embryonic fibroblasts have circadian rhythms of gene expression [18], real-time monitoring of circadian promoter-driven reporters revealed that peripheral tissues and extra-SCN brain regions exhibit circadian oscillations in vitro[19], [20], [21]. Consequently, there is now direct evidence that the mammalian circadian system is composed of multiple circadian oscillators: a light-entrainable central pacemaker in the SCN and many oscillators in other regions of the brain and peripheral tissues.

The molecular mechanism of endogenous rhythm generation in the SCN is modeled as interlocking positive and negative transcriptional and translational feedback loops of circadian gene expression [22], [23], [24]. According to this model, BMAL1/CLOCK or BMAL1/NPAS2 heterodimers activate the transcription of the Period (Per) and Cryptochrome (Cry) genes. As PER and CRY proteins accumulate, they form complexes and directly bind to BMAL1-CLOCK/NPAS2 heterodimers, thereby inhibiting their own transcription. In addition, post-translational modifications regulate the stability and cellular localization of circadian proteins. The mRNAs of three Period homologs (Per1, 2, and 3) are rhythmically expressed in the SCN, yet only Per1 and Per2 have been implicated as important negative elements in the feedback loops that generate the endogenous SCN rhythm [14], [15], [17], [25], [26], [27]. Per1^−/− or Per2^−/− mice, for example, have more severe behavioral phenotypes than Per3^−/− mice. The periods of wheel-running activity of Per1^−/− and Per2^−/− mice can be 1.5 hrs shorter than wildtype mice (depending on the line and genetic background) and they sometimes become arrhythmic in constant darkness (DD), while only a 0.5 h period difference between Per3^−/− and wildtype mice has been observed and Per3^−/− mice never become arrhythmic in DD [28], [29], [30], [31], [32]. In addition, Per1/Per2 double mutants, but not Per1/Per3 or Per2/Per3 double mutants, have arrhythmic locomotor activity in DD [28]. While most of these experiments have been performed in mice with mixed genetic backgrounds or congenic with the 129/sv strain, one study found that Per2^−/− mice congenic with the C57BL/6J strain have periods of wheel-running activity that are indistinguishable from wildtype mice and they do not become arrhythmic in DD [33].

The C57BL/6J strain is ideal for analysis of circadian behavior because the mice have high amplitude (robust), consolidated (not dissociated or fragmented) locomotor activity with a stable free-running period in DD [34], [35]. Since the phenotypes of Per mutant mice may vary depending on the genetic background, we sought to investigate the circadian phenotypes of wheel-running behavior and of SCN and peripheral tissue explants in Per2^−/− and Per3^−/− mice congenic with the C57BL/6J strain. In our previous study of C57BL/6J Per1^−/− mice, we found that the real-time circadian gene promoter activity rhythm was weak or absent in SCN slices in vitro even though the free-running wheel-running activity rhythm was indistinguishable from wildtype mice [36]. Pituitary and lung explants were also arrhythmic in C57BL/6J Per1^−/− mice. In the current study, we assessed wheel-running activity and rhythmicity in the SCN and peripheral tissues in Per2^−/− and Per3^−/− mice congenic with the C57BL/6J strain. Our approach allowed us to compare the behavioral rhythms to the rhythms of explanted tissues of Per2^−/− and Per3^−/− mice with genetic background held constant.

Previous studies have demonstrated that the SCN controls the period of the circadian locomotor activity rhythm in mammals [7], [37], [38]. Therefore, it is reasonable to predict that if a molecular alteration of the timekeeping mechanism changes the period of the circadian rhythm in the SCN, then the period of locomotor activity should also change (in a similar direction and magnitude). This hypothesis is supported by previous studies in tau mutant hamsters and Clock (Δ19) mutant mice [39], [40], [41]. In contrast, we found that clock gene promoter-driven luciferase activity was arrhythmic or had low amplitude, irregular rhythms in SCN explants from C57BL/6J Per1^−/− mice even though their locomotor behavior was indistinguishable from wildtype mice [36]. In the current study we assessed locomotor activity and rhythmicity in the SCN of Per2^−/− and Per3^−/− mice to determine if the in vitro phenotypes of the mutant SCN were congruent with behavior.

We found that the period of wheel-running activity was 11 minutes shorter and the phase angle of entrainment was advanced by 25 minutes in C57BL/6J Per2^−/− mice compared to Per2^+/+ mice. Since we observed only small differences in behavior between Per2^−/− and Per2^+/+ mice, we expected to observe a mild phenotype of Per1-luc expression in the Per2^−/− SCN. Surprisingly, though, we found that the period of Per1-luc expression in the Per2^−/− SCN was 1.5 hours shorter than in the Per2^+/+ SCN. The period was shorter in both the SCN and behavior, but the Per2 mutant phenotype was enhanced in SCN explants. Since the phenotype was more pronounced in vitro compared to in vivo, we hypothesize that in vivo factors such as temperature fluctuations, activity feedback, or coupling to extra-SCN oscillators may compensate for the mutant phenotype.

To our knowledge, our study is the first to analyze real-time circadian rhythms of gene expression in SCN explants from Per2^−/− mice. A previous study found that bioluminescence was arrhythmic or had low amplitude, irregular rhythms in immortalized fibroblasts derived from Per2^−/− mice and infected with a lentiviral construct in which the Per2 promoter drives the expression of luciferase (mPer2-dluc) [42]. SCN explants (or dissociated SCN neurons) were not investigated using this lentivirally-mediated method [42]. In contrast to the dissociated Per2^−/− fibroblasts analyzed by Liu et al. [42], we found that SCN, pituitary, and lung explants from C57BL/6J Per2^−/− mice had robust, rhythmic expression of Per1-luc. While the period of Per1-luc expression in Per2^−/− SCN explants was significantly shorter than in Per2^+/+ SCN, circadian rhythms in ex vivo pituitary and lung from Per2^−/− mice were largely unaffected compared to Per2^+/+ mice.

In contrast to Per2^−/− mice, wheel-running behavior and rhythmicity in the SCN of C57BL/6J Per3^−/− mice were indistinguishable from Per3^+/+ mice. Interestingly, though, we found that the period and phase of Per1-luc expression in the pituitary and lung were altered when PER3 was not functional. Our findings in Per3^−/− SCN and lung explants are in agreement with a previous study that assessed the expression of the PERIOD2::LUCIFERASE fusion protein in ex vivo Per3^−/− tissues [42]. Since we also found that circadian rhythms were altered in pituitary explants from Per3^−/− mice compared to Per3^+/+ mice, it is possible that Per3 is important for timekeeping in peripheral tissues. Future studies could assess the physiological outputs of peripheral tissues to determine if the in vitro phenotypes of Per3^−/− tissues are present in vivo.

Taken together, our data suggest that the function of each Per gene may differ between tissues. Per2 appears to be important for period determination in the SCN, while Per3 participates in timekeeping in the pituitary and lung.