Transcriptional oscillation of canonical clock genes in mouse peripheral tissues
© Yamamoto et al; licensee BioMed Central Ltd. 2004
Received: 16 June 2004
Accepted: 09 October 2004
Published: 09 October 2004
The circadian rhythm of about 24 hours is a fundamental physiological function observed in almost all organisms from prokaryotes to humans. Identification of clock genes has allowed us to study the molecular bases for circadian behaviors and temporal physiological processes such as hormonal secretion, and has prompted the idea that molecular clocks reside not only in a central pacemaker, the suprachiasmatic nuclei (SCN) of hypothalamus in mammals, but also in peripheral tissues, even in immortalized cells. Furthermore, previous molecular dissection revealed that the mechanism of circadian oscillation at a molecular level is based on transcriptional regulation of clock and clock-controlled genes.
We systematically analyzed the mRNA expression of clock and clock-controlled genes in mouse peripheral tissues. Eight genes (mBmal1, mNpas2, mRev-erbα, mDbp, mRev-erbβ, mPer3, mPer1 and mPer2; given in the temporal order of the rhythm peak) showed robust circadian expressions of mRNAs in all tissues except testis, suggesting that these genes are core molecules of the molecular biological clock. The bioinformatics analysis revealed that these genes have one or a combination of 3 transcriptional elements (RORE, DBPE, and E-box), which are conserved among human, mouse, and rat genome sequences, and indicated that these 3 elements may be responsible for the biological timing of expression of canonical clock genes.
The observation of oscillatory profiles of canonical clock genes is not only useful for physiological and pathological examination of the circadian clock in various organs but also important for systematic understanding of transcriptional regulation on a genome-wide basis. Our finding of the oscillatory expression of canonical clock genes with a temporal order provides us an interesting hypothesis, that cyclic timing of all clock and clock-controlled genes may be dependent on several transcriptional elements including 3 known elements, E-box, RORE, and DBPE.
The circadian rhythm of about 24 hours is a fundamental physiological function observed in almost all organisms from prokaryotes to humans. Circadian rhythms have been known to be generated in pacemaker cells, the suprachiasmatic nuclei (SCN) of hypothalamus in mammals, and entrained by environmental cues, such as light, temperature, noise, feeding or social cues, whereas a recent analysis using mPer2luciferase knockin mice has demonstrated that peripheral tissues express self-sustained circadian oscillations . The output of circadian oscillation appears as locomotive activity, hormonal secretion, the sleep-wake cycle, and many other physiological functions. Disruption of the circadian rhythms has been associated with various kinds of diseases, such as cardiovascular diseases, psychiatric diseases and cancer in humans [2–6]. Identification of clock genes has allowed study of the molecular bases for circadian behaviors and temporal physiological processes and has prompted the idea that molecular clocks reside not only in a central pacemaker, but also in peripheral tissues, even in immortalized cells [2, 3, 6]. Furthermore, previous molecular dissection revealed that the mechanism of circadian oscillation at a molecular level is based on transcriptional regulation of clock and clock-controlled genes, which consists of interwoven positive and negative feedback loops [2, 7–10].
There is a distinct connection between genes and behaviors in circadian rhythms, which is conserved from fly or other lower organisms to humans [6, 8]. The Drosophila period mutants, originally identified as a circadian mutant brought us the first clock gene, period [8, 11], while a point mutation of hPer2 was recently shown to cause a familial advanced sleep phase syndrome . As described above, circadian rhythms rely on a negative feedback loop in gene expression that involves a limited number of clock genes. Recent molecular dissection has increased our understanding of the molecular nature of the transcriptional regulation of some clock genes. The circadian phenotypes at the cellular level may be represented as temporal mRNA expression. Global gene expression profiling using microarrays has led to the discovery of many circadian-regulated genes, but there is only a minor overlap of cycling transcripts between tissues [10, 13, 14]. Thus, circadian rhythms are an appropriate study target for systems biology.
In this study, we systematically examined the mRNA expression of common circadian-regulated genes in several mouse peripheral tissues and made oscillatory profiles of canonical clock genes. Moreover, by bioinformatics, we identified 3 clock elements for circadian transcription (E-box, RORE, DBPE). These 3 elements and their combination would suffice to explain the biological timing of expression of these clock and clock-controlled genes.
Results and discussion
A molecular mechanism of canonical clock genes is based on transcriptional regulation via interlocked feedback and/or feed-forward loops [2, 4, 7, 8]. One example of the regulation of a known characterized gene in mammals is that of Per1. The transcription of Per1 is activated by binding of the CLOCK/BMAL1 hetero-complex, both members of which are bHLH-PAS (basic helix-loop-helix-Per-Arnt-Sim) proteins, to the E-boxes in the promoter region of Per1 . The translated PER1 is posttranslationally modified by CKI-ε  and, together with other clock proteins such as CRYs , is returned to the nucleus to suppress its own transactivation, resulting in closure of the PER1 loop. E-box elements are also known to be essential for transcriptional regulation of many clock-controlled output genes including the vasopression genes . On the other hand, one of the positive elements, BMAL1, whose mRNA expression is cycled antiphase to Per s, as described above, forms another loop [33, 34]. The orphan nuclear receptors RORα and REV-ERBα regulate circadian transcription positively and negatively, respectively, through ROR/REV-ERB elements (ROREs) in the promoter region of Bmal1 [16, 35]. Moreover, an in silico search identified these 2 ROREs in the promoter region of Npas2 (Table 1, see figure 5), the expression pattern of which was very similar to that of Bmal1. These findings gave us the idea that the circadian pattern of RNA expression might be dependent on transcriptional regulation by specific transcription factors.
Using the NCBI database and Celera Database System, we systematically searched for the above 2 elements and another clock element, a DBP-binding element (DBPE), described below. These elements are conserved among human, mouse, and rat genome sequences in the regions 9-kb upstream and 5-kb downstream of the transcription start site (Table 1, see figure 5). Intriguingly, the transcriptional elements corresponded to the cyclic pattern of the clock genes shown in Figure 4. Bmal1 and Npas2, the circadian peaks of which were both in subjective night at CT20-24, included ROREs in their promoters, as described above. In the promoter of Per1 and Per2, the peaks of which were in subjective day at CT12-16, E-boxes were found. In fact, the conserved E-box in Per2 is not a typical E-box of the molecular clock, CACGTG, but an atypical element, CACGTT. Compared with Per1, which contains 5 conserved E-boxes, Per2 may have other unknown factors and elements responsible for its robust transcriptional oscillation. Per1, whose peak was a bit earlier than that of Per2, has another element, a DBPE, in its promoter region, in addition to the 5 E-boxes well studied in vitro . Per3, the peak of which was even earlier at CT8-12, did not have conserved E-boxes but instead contained DBPEs in its gene. Three genes, Rev-erbα, Dbp, and Rev-erbβ, the peaks of which were between those of Bmal1 and Per, had a mixed combination of the elements. The Rev-erbα genome sequence included 1 RORE, 1 DBPE, and 5 E-boxes, whereas Rev-erbβ included all 3 elements only in the mouse genome sequence. Dbp contained 2 ROREs and 2 E-boxes in each genome. Among the elements described above, some of them in (Bmal1, Dbp, and Per1) were experimentally studied and confirmed [16, 29, 35–38].
Transcripts of 8 genes (mBmal1, mNpas2, mRev-erbα, mDbp, mRev-erbβ, mPer3, mPer1, and mPer2) showed a robust circadian rhythm in different peripheral tissues (see Fig. 1). The amount of mRNA in the trough was nearly zero and the peak-trough amplitude of these genes was clearly higher than that of the others examined. Thus, in terms of mRNA expression among the canonical clock genes examined, these 8 genes likely constitute the core molecules of a molecular circadian clock. The expression timing in a 24-h period appears to be conveyed through 3 kinds of sequence elements bound by specific transcription factors (see Fig. 4). Recent genome-wide analyses using microarrays revealed that many genes (about 10 % of the total number of genes studied) oscillated but only several tens of common genes overlapped between two tissues examined [13, 14]. Among the core candidate genes with similar circadian regulation in those 2 tissues, we examined the circadian transcription of 15 candidate genes besides the known clock genes, but could not find genes with oscillatory behavior in different peripheral tissues comparable to that in the 8 genes described above. The 8 genes studied here may approximate the entirety of the core oscillatory genes in the genome. If so, the 3 elements described here may be sufficient for explaining the biological timing of mRNA expression of clock genes. However, our preliminary results showed that an atypical E-box in Per2 promoter may be insufficient for full transcriptional oscillation (Akashi and Takumi, unpublished data). Further detailed studies of each promoter, combined with systematic analyses using microarrays and real-time RT-PCR, will give us a more detailed comprehension of the intertwined positive and negative regulatory loops of molecular biological clocks.
The current study has clarified the detailed circadian expression of mRNAs for clock and clock-related genes in different peripheral tissues of the mouse. The observation of oscillatory profiles of canonical clock genes is not only useful for physiological and pathological examination of the circadian clock in various organs but also important for systematic understanding of transcriptional regulation on a genome-wide basis. Our finding of the oscillatory expression of canonical clock genes in a temporal order provides us an interesting hypothesis, that cyclic timing of all clock and clock-controlled genes may be dependent on several transcriptional elements including 3 known elements, E-box, RORE, and DBPE.
Male Balb/c mice purchased 5 weeks postpartum from Japan SLC (Hamamatsu, Japan), were exposed to 2 weeks of light-dark (LD) cycles and then kept in complete darkness as a continuation of the dark phase of the last LD cycle. mRNA expression was examined in the third dark-dark (DD) cycle. All protocols of experiments using animals in this study were approved by the OBI (Osaka Bioscience Institute) Animal Research Committee.
Real-time quantitative RT-PCR was performed by using an ABI PRISM 7000 (Applied Biosystems). The PCR primers were designed with Primer Express software (Applied Biosystems), and the sequences of the forward and reverse primers were as follow: mPer1 FW: CAG GCT AAC CAG GAA TAT TAC CAG C, mPer1 RV: CAC AGC CAC AGA GAA GGT GTC CTG G; mPer2 FW: GGC TTC ACC ATG CCT GTT GT, mPer2 RV: GGA GTT ATT TCG GAG GCA AGT GT; mPer3 FW: CTG CTC CAA CTC AGC TTC CTT T, mPer3 RV: TTA GAC AGC AAG GCT CTG GTT CT; mNpas2 FW: GTA TGC ACA GAG CCA AGT GAT GTT, mNpas2 RV: TGC TCA CTG TGC AGA GAT GTT G; mDbp FW: AAT GAC CTT TGA ACC TGA TCC CGC T, mDbp RV: GCT CCA GTA CTT CTC ATC CTT CTG T; mBmal1 FW: GCA GTG CCA CTG ACT ACC AAG A, mBmal1 RV: TCC TGG ACA TTG CAT TGC AT; mRev-erbα FW: CGT TCG CAT CAA TCG CAA CC, mRev-erbα RV: GAT GTG GAG TAG GTG AGG TC; mRev-erbβ FW: ACG GAT TCC CAG GAA CAT GG, mRev-erbβ RV: CCT CCA GTG TTG CAC AGG TA; G3-PDH FW: ACG GGA AGC TCA CTG GCA TGG CCT T, G3-PDH RV: CAT GAG GTC CAC CAC CCT GTT GCT G; mCry1 FW: CCC AGG CTT TTC AAG GAA TGG AAC A, mCry1 RV: TCT CAT CAT GGT CAT CAG ACA GAG G; mCry2 FW: GGG ACT CTG TCT ATT GGC ATC TG, mCry2 RV: GTC ACT CTA GCC CGC TTG GT; mCKIε FW: GGA TGT GAA GCC CGA CAA CTT, mCKIε RV: TCT CGA CGG CTT TGC TCA AT; mCKIδ FW: CCA GCC TGG AAG ACC TGT TC, mCKIδ RV: TGG CCA GCC CAA AGT CAA; mClock FW: CCT ATC CTA CCT TGG CCA CAC A, mClock RV: TCC CGT GGA GCA ACC TAG AT; mTim FW: ACA TGT GGG CAA TGG CTT, mTim RV: CTG CTC CAC AAA GTG AAA GGT. Specificity of gene amplification was confirmed by measuring the size and purity of the PCR product by gel electrophoresis, and by analyzing the dissociation curve with ABI PRISM 7000 SDS software (Applied Biosystems). For a 25-μl PCR reaction, 50 ng cDNA template was mixed with the forward and reverse primers to a final concentration of 300 nM each and 12.5 μl of 2x SYBR Green PCR Master Mix (Applied Biosystems). The reaction was first incubated at 50°C for 2 min, then at 95°C for 10 min, followed by 40 cycles of 95°C for 15 sec and 60°C for 1 min. Each gene-specific PCR was performed in triplicate. G3-PDH primers were used as the control.
Real-time luciferase reporter assay
NIH3T3 cells were cultured, transfected with hBmal1 -Luc or mPer2 -Luc, and incubated for 24 hours. The medium was then exchanged for serum-rich medium (DMEM, supplemented with 50 % serum). Two hours later this medium was replaced with normal culture medium. In the presence of 0.1 mM luciferin, light emission was measured and integrated for 1 min at intervals of 15 min, with a photomultiplier tube (Hamamatsu Photonics).
In silico search
The sequences were downloaded from the Celera Database System and the NCBI Gene database. Each gene sequence spanning from 9 kb upstream to 4 kb downstream of the transcription start site was examined in each database. Multiple sequence alignments of these sequences for each gene were obtained by Clustalw version 1.83 with default parameters. The binding elements were then searched from these alignments using a pattern finding tool, fuzznuc, with the following consensus sequences allowing for a 1-base mismatch:
The accession numbers used and the sequence numbers analyzed are as follow: Bmal1; Human, NT_009237.16, 12054318–12069318, Mouse, NT_081129.1, 107781–122781, Rat, NW_047562.1, 13774073–13789073, Npas2; Human, hCG27614, 95632226–65646226, Mouse, mCG8437, 35980102–35994102, Rat, rCT22431, 39204499–39218499, Rev-erbα; Human, hCG93862, 34926094–34912094, Mouse, mCG15360, 105438925–105424925, Rat, rCG33292, 82492796–82478796, Dbp; Human, NT_011109.15, c21417778–21402778, Mouse, NT_078442.1, 59711–74711, Rat, NW_047558.1, 5120734–5135734, Per3; Human, NT_021937.16, 1962822–1977822, Mouse, NT_039268.2, c4331528–4316528, Rat, NW_047727.1, c8016956–8001956, Per1; Human, NT_010718.14, c6905708–6890708, Moues, NT_039515.2, 65661216–65676216, Rat, rCG34390, 52960430–52974430, Per2; Human, NT_005120.14, c5136562–5121562, Mouse, NT_039173.2, c5833757–5818757, Rat, NW_047817.1, c6827703–6812703.
List of Abbreviations used
reverse transcription-polymerase chain reaction
the National Center for Biotechnology Information.
We thank Setsuko Tsuboi, Chiaki Matsubara, Yoko Sakakida, and Dan Trcka for their technical assistance, Paul Burke for his review of the manuscript, and acknowledge Yasuhiro Sakamoto for his administrative assistance. This work was supported in part by a research grant from MEXT. The support of fellowships from the Japan Society for the Promotion of Science (M.A.) is also acknowledged.
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