Interaction of circadian clock proteins PER2 and CRY with BMAL1 and CLOCK
© Langmesser et al; licensee BioMed Central Ltd. 2008
Received: 17 December 2007
Accepted: 22 April 2008
Published: 22 April 2008
Circadian oscillation of clock-controlled gene expression is mainly regulated at the transcriptional level. Heterodimers of CLOCK and BMAL1 act as activators of target gene transcription; however, interactions of PER and CRY proteins with the heterodimer abolish its transcriptional activation capacity. PER and CRY are therefore referred to as negative regulators of the circadian clock. To further elucidate the mechanism how positive and negative components of the clock interplay, we characterized the interactions of PER2, CRY1 and CRY2 with BMAL1 and CLOCK using a mammalian two-hybrid system and co-immunoprecipitation assays.
Both PER2 and the CRY proteins were found to interact with BMAL1 whereas only PER2 interacts with CLOCK. CRY proteins seem to have a higher affinity to BMAL1 than PER2. Moreover, we provide evidence that PER2, CRY1 and CRY2 bind to different domains in the BMAL1 protein.
The regulators of clock-controlled transcription PER2, CRY1 and CRY2 differ in their capacity to interact with each single component of the BMAL1-CLOCK heterodimer and, in the case of BMAL1, also in their interaction sites. Our data supports the hypothesis that CRY proteins, especially CRY1, are stronger repressors than PER proteins.
Circadian rhythms are recurring fluctuations with a period of about 24 hours that can be observed in the physiology and behavior of most living organisms from cyanobacteria to humans . They are controlled by an autonomous circadian clock, which can be synchronized to the environmental day-night cycle. In mammals, the suprachiasmatic nucleus (SCN), a structure in the ventral part of the hypothalamus, appears to be the main coordinator of the circadian timing system [2, 3] synchronizing peripheral clocks present in all tissues throughout the body .
The oscillatory mechanism underlying the circadian clock has been unraveled by means of genetic analysis in Drosophila and mammals . In the latter, a heterodimeric complex of two transcriptional activators, CLOCK and BMAL1, binds to E-box enhancer elements present in the promoters of target genes and thereby activates the expression of three Period (Per1, Per2 and Per3) and two Cryptochrome genes (Cry1 and Cry2). PER and CRY proteins translocate to the nucleus where CRY proteins act as potent (and PER proteins as mild) inhibitors of CLOCK-BMAL1-induced transcription [6, 7]. The positive (CLOCK-BMAL1) and negative (CRY, PER) arms of the feedback loop are coupled via the nuclear orphan receptor REV-ERBα  generating a stabilized feedback loop that drives recurrent rhythms in mRNA and protein levels of clock components.
Transcriptional reporter assays, yeast two-hybrid screens and co-immunoprecipitation experiments have been successfully used to identify molecular interactions of clock components at the protein level [6, 7, 9–12]. Interactions of BMAL1 with CLOCK, NPAS2, DEC1 and DEC2 have been identified. Furthermore it has been suggested that the transactivation activity of BMAL1 is mediated by interaction with CREB binding protein (CBP) or p300 .
Many different approaches have been employed to characterize the interactions between the repressors PER2, CRY1 and CRY2 and the BMAL1-CLOCK heterodimer, but still the picture is far from being clear. It is thought that CRY1 plays a key role in repressing the transcriptional activation potential of the heterodimer, and recently, various attempts have been made to elucidate the mechanism by which interaction of CRY1 with BMAL1 and/or CLOCK inhibits transcription [14–17]. However, many of these studies use multimeric protein complexes, which do not always satisfactorily identify the exact interactions between two individual components of the complex.
We decided to choose a complementary approach and to investigate the interactions of PER2, CRY1 and CRY2 with BMAL1 and CLOCK using a mammalian two-hybrid system where we only overexpressed two of the components – one part of the activating heterodimer and one repressor – at a time. All interactions identified in the two-hybrid system were confirmed by co-immunoprecipitation. Our results indicate that in our conditions, CRY1, CRY2 and PER2 proteins interact with BMAL1 by binding to different sites of BMAL1, but that only PER2 interacts with CLOCK alone. Moreover, in keeping with the idea that the CRY proteins are more potent inhibitors than PER2, we found that CRY1 and CRY2 both modify the interaction between PER2 and BMAL1, but not vice versa.
Results and Discussion
Interaction of PER2, CRY1 and CRY2 with BMAL1
Both PER2 (Fig. 1B) and the CRY proteins (Fig. 1D, E) could be co-immunoprecipitated from extracts of HER911 cells co-transfected with Bmal1-GFP and the respective interaction partner using an anti-GFP antibody. We therefore conclude that all three proteins are able to bind to BMAL1, which is in line with previous reports [6, 15, 18, 19]. The fact that each of the three repressors can interact with BMAL1 and thus has the potential to influence BMAL1-CLOCK mediated transcription would also explain why Per2, Cry1 and Cry2 mutant mice all display an altered expression of genes regulated by BMAL1 and CLOCK [18, 20–22].
Interactions with CLOCK
CRY, especially CRY1, binding to BMAL1 has been described many times in various systems. For CRY binding to CLOCK, however, contradictory findings have been published. Griffin et al. do not observe clear interactions between CRY1/2 and CLOCK in a yeast two-hybrid system , whereas Shearman et al. do . Kiyohara et al.  report that they were not able to co-immunoprecipitate CLOCK with CRY1 in the absence of BMAL1, and also in other cases BMAL1/CLOCK(/PER2)/CRY1 complexes, rather than individual components, have been used to characterize interactions [17, 24]. In the SCN and the piriform cortex, though, CRY1 co-immunoprecipitated with CLOCK , and the same group was able to demonstrate CRY1 binding to CLOCK in co-transfected HeLa cells. Therefore, it appears likely that in this case the respective results depend strongly on the system and cell type used and that cell-specific factors might be involved in mediating the interaction. In the mammalian two-hybrid system we employed in HER911 cells, CRY1 and 2 do not interact with CLOCK.
CRY1 and CRY2 influence the interaction between PER2 and BMAL1
Our results indicate that CRY1 and CRY2 have different effects on PER2-BMAL1 interaction. We wished to find out whether this would still be true in the presence of CLOCK and repeated the co-transfections as described above, but additionally co-transfected Clock. We observed an overall higher reporter activity but were able to reproduce the differences between Cry1 (Fig. 3A, solid squares) and Cry2 (Fig. 3A, solid triangles). A two-way ANOVA analysis of the data showed highly significant differences between Cry1 and Cry2 (p < 0.001), a highly significant dose-dependence (p < 0.001) and an equally highly significant interaction between the two parameters (p < 0.001).
To exclude that the modulations of reporter activity were only due to an increase or decrease in GAL4-BMAL1 or PER2-VP16 expression, we analyzed the total expression levels of the two proteins by Western blot. Co-transfection of 1 ng-1 μg Cry1 expression plasmid led to a dose-dependent increase in PER2-VP16 expression whereas it did not influence GAL4-BMAL1 levels, co-transfection of Cry2 caused a slight increase in both PER2-VP16 and GAL4-BMAL1 expression only with the highest amount tested (Fig. 3B). Additional co-transfection of Clock had no effect on GAL4-BMAL1 levels. PER2-VP16 expression levels were slightly elevated when Clock, but not Cry, was co-transfected whereas no further increase was seen with Clock in the presence of Cry (Fig. 3C).
A crucial role of CRY proteins in the nuclear entry of PER1/2 has been reported . It has also been described that CRY expression has an effect on BMAL1 localization . Since in the mammalian two-hybrid system used in this study only fusion proteins that are present in the nucleus can activate the transcription of the reporter, we determined the subcellular localization of GAL4-BMAL1 and PER2-VP16. To this end, we performed Western blots on nuclear and cytoplasmic fractions of HER911 cells transfected as described above (Fig. 3D). The effects of Cry1/2 and Clock basically followed the pattern observed in total extracts for both fractions, we did not detect any gross redistributions of the fusion proteins. If anything, the influence was stronger in the cytoplasm, which would not influence mammalian two-hybrid results.
In summary, fusion protein expression levels do not correlate with the degree of reporter activation, since e.g. the highest amount of Cry1 leads to a marked increase in PER2-VP16 expression and nonetheless significantly decreases luciferase activity. We therefore conclude that the modulations of luciferase activity we observe in the mammalian two-hybrid system reflect true modulations of PER2-BMAL1 interaction by the respective co-expressed proteins. In this scenario, CLOCK would strengthen the interaction because the increase in luciferase activity caused by co-transfection of Clock (Fig. 3A) is markedly higher than the slight increase in PER2-VP16 expression. A similar effect has in fact been observed by Kiyohara et al. for the interaction of CRY1 with the heterodimer . Given that in our system, PER2 interacts with both BMAL1 and CLOCK (and those two in turn with each other), a stabilization of PER2-BMAL1 interactions by CLOCK might be envisaged through the formation of a heterotrimer where each component interacts with the other two. The increase in PER2-VP16 expression after co-transfection of Cry1 is very likely due to a stabilization of PER2-VP16 by CRY1, an effect that has been reported before [18, 25, 26].
CRY1 appears to be more effective than CRY2 in disrupting PER2-BMAL1 interactions. The observed decrease in luciferase activity is not due to less PER2-VP16 or GAL4-BMAL1 available, on the contrary, there is clearly elevated PER2-VP16 expression. For Cry2, a less pronounced increase in expression is observed, especially with low amounts of co-transfected Cry2, which, however, already cause a marked increase in reporter activation. Of course, these effects might be cell-specific; however, they fit in with previous observations. Recently, CRY1 has been proposed as the main repressor of BMAL1-CLOCK-mediated transcription [15, 24], and previous studies in mice also show that the Cry1 gene has a dominant role over Cry2, because one normal Cry1 allele sustains normal circadian rhythms in behavior, while one Cry2 allele leads to arrhythmicity . Since the PER proteins have been reported to be weaker repressors than CRY1/2 [7, 27], the ability of CRY1 (and, to a lesser extent, CRY2) to disrupt PER2-BMAL1 interactions might be important to allow stronger repression of the transcription activation potential of the heterodimer.
PER2 does not significantly affect the interaction between CRY and BMAL1
Although in our system, we could not detect any interaction between CRY1 and CLOCK, it has been described in other systems, indicating that CLOCK might have an impact on CRY1-BMAL1 interaction. Indeed, when we co-transfected increasing amounts of Clock expression plasmid together with Gal4-Bmal1 and Cry1-VP16, we observed a dose-dependent increase in luciferase activity (Fig. 4E) whereas GAL4-BMAL1 and CRY1-VP16 expression levels remained almost constant (Fig. 4F). CLOCK thus appears to stabilize the interaction, possibly by inducing conformational changes in BMAL1 that facilitate CRY1 binding. As for PER2, a heterotrimer might be formed that is more stable than the CRY1-BMAL1 complex alone, even in the absence of direct CRY1-CLOCK interactions. The results of Kiyohara et al.  support a heterotrimer formation as well, since they co-immunoprecipitate CRY1 with CLOCK only in the presence of BMAL1.
Lee et al. report impaired nuclear translocation of CRY proteins in the livers of Per1/Per2 double mutant mice , and it has been demonstrated that PER2 lacking the nuclear localization signal can retain CRY proteins in the cytoplasm . However, overexpressed CRY1 and 2 have been shown to be nuclear proteins in cells . Co-transfection of (full-length) Per2 should therefore in principle not influence the sub-cellular localization of at least the CRY proteins. To our knowledge, no dependence of sub-cellular localization of BMAL1 on PER2 has been reported, either, and since BMAL1 is a predominantly nuclear protein , its nuclear availability should not drastically vary. Thus, we did not perform any cell fractionations for CRY1/2-VP16 and GAL4-BMAL1.
PER2, CRY1 and CRY2 bind different domains of BMAL1
To map the regions of the BMAL1 protein that are critical for interactions with CRY1/2 and PER2 we constructed three deletion mutants of Bmal1 fused to the Gal4 DBD (Gal4-Bmal1ΔHLH/PAS A; Gal4-Bmal1ΔPAS B/C-term and Gal4-Bmal1ΔC-term). We confirmed that their expression levels were comparable to those of full-length GAL4-BMAL1 (data not shown) and tested their capacity to activate the luciferase reporter in the mammalian two-hybrid system when co-expressed together with PER2-VP16, CRY1-VP16 or CRY2-VP16, respectively.
When we tested Gal4-Bmal1ΔPAS B/C-term, a deletion mutant lacking not only the C-terminus but also the PAS B domain, only co-transfection with Per2-VP16 led to a slight (5-fold) elevation in luciferase activity. Neither Cry1-VP16 nor Cry2-VP16 had any statistically significant effect (Fig. 5C). PER2 consequently still appears to be able to bind to this BMAL1-mutant, although to a much lesser extent than to GAL4-BMAL1ΔC-term, which indicates that the PAS domain of BMAL1 might be involved in PER2 binding. It also seems to play a role in CRY1 binding since the residual reporter transactivation observed with GAL4-BMAL1ΔC-term and CRY1-VP16 disappears when the deletion in Bmal1 is extended to the PAS B domain.
GAL4-BMAL1ΔHLH/PAS A was able to activate the luciferase reporter to a considerable extent already in the absence of any VP16 fusion protein. Co-transfection with all three VP16 fusion constructs thus caused only slight, but nonetheless significant, increases in luciferase activity (1.5-fold for Per2-VP16, 2.5-fold for Cry1-VP16 and 3-fold for Cry2-VP16 as compared to Gal4-Bmal1ΔHLH/PAS A alone; Fig. 5D). Although it is difficult to draw any conclusions due to the high background activity of this Bmal 1 mutant, these results confirm the observations made using the other two truncated forms, namely that the N-terminal portion of BMAL1 appears to be most important for PER2 binding, less crucial for the binding of CRY1 and not essential for interactions with CRY2.
In summary, our interaction data leads to a model where PER2 binds to the N-terminus of BMAL1, where the PAS A domain is located. Since PER2 itself also contains a PAS domain, a direct interaction between these two domains could be envisaged. CRY1 would bind more towards the PAS B domain and CRY2 even further C-terminally. This hypothesis is in line with observations of Kiyohara et al.  who report normal binding of PER2, but not of CRY1, to a C-terminally truncated version of BMAL1. Others have also identified mutations in the C-terminus of BMAL1 that weaken BMAL1-CRY1 interactions . To our knowledge, the binding site for CRY2 has not been mapped in BMAL1 so far. However, given that CRY2 was less effective than CRY1 in disrupting PER2-BMAL1 interactions in our system, it can be expected to be further away than the binding site for CRY1, which, in our model, would actually be the case.
CBP and p300, transcriptional co-activators found to interact with BMAL1, have also been hypothesized to bind to the extreme C-terminus that harbors a putative transcription activation domain . Thus, the fact that CRY1 and CRY2 bind more C-terminally to BMAL1 than PER2 might also explain why they have a stronger capacity to inhibit BMAL1-CLOCK-mediated transcriptional activation.
Confirmation of the interactions in cos-7 cells
We were not able to confirm the interactions identified in the mammalian two-hybrid system by co-immunoprecipitation of in vitro transcribed/translated proteins (data not shown). This might be due either to the presence of bridging proteins in HER911 cells or to post-translational modifications of the interaction partners, which are vital for circadian clock function in vivo . We tried to precipitate one in vitro expressed interaction partner together with one expressed in HER911 cells in order to reconstitute potential post-translational modifications on at least one of the proteins. However, in our hands, this was not possible either (data not shown), indicating that modifications of both partners might be necessary for interactions.
GAL4-CLOCK activated the reporter to such a high extent already in the absence of interaction partners that no further significant increase in luciferase activity could be detected upon co-expression of PER2-VP16, CRY1-VP16 or CRY2-VP16 (Fig. 7B).
To be able to analyze interactions with CLOCK, we constructed plasmids that encoded fusions of the GAL4 DBD to PER2, CRY1 and CRY2 and a fusion of VP16 to CLOCK and repeated the two-hybrid assay. Neither one of the GAL4 DBD fusion proteins caused a more than 10-fold increase in luciferase activity as compared to the reporter alone. When Clock-VP16 was co-transfected, significantly enhanced (55-fold) activity values were only observed for Gal4-Per2, indicating that indeed only PER2 interacts directly with CLOCK. Co-transfection of Gal4-Cry1 with Clock-VP16 also led to higher luciferase values; however, there were considerable inter-experimental variations, and moreover, luciferase activity was already elevated when VP16 alone was co-transfected. This hints at an interaction between CRY1 and VP16 rather than between CRY1 and CLOCK. The difference in luciferase activity between co-transfection of Clock-VP16 and VP16 was not statistically significant (Fig. 7C).
We wished to confirm the results obtained using the new plasmids in HER911 cells and performed the same two-hybrid assay as in cos-7 cells. In this cell line, however, all three GAL4 DBD fusion proteins in combination with CLOCK-VP16 significantly augmented reporter activity levels (110-fold for GAL4-PER2, 190-fold for GAL4-CRY1 and 30-fold for GAL4-CRY2 as compared to the reporter alone; Fig. 7D).
Since the interaction between CRY2 and CLOCK can only be observed in HER911 cells, and only when using GAL4-CRY2 and CLOCK-VP16 but not with GAL4-CLOCK and CRY2-VP16 (Fig. 2D), we think that it might actually be an artefact arising from an interaction of CRY2 with endogenous PER2 and/or BMAL1 that, in turn, interacts with CLOCK-VP16. Since for CRY1 and CLOCK, the results were not quite clear in cos-7 cells, either, we co-transfected HER911 cells with Cry1 and HA-Clock and tried to co-immunoprecipitate CRY1 with an anti-HA antibody, which did not work, however (data not shown). We therefore believe that also this alleged direct interaction is rather indirect and mediated by endogenous PER2 and/or BMAL1.
Co-transfection of the newly generated Gal4 fusion constructs with Bmal1-VP16 confirmed the results obtained previously both in HER911 and in cos-7 cells. All three proteins, GAL4-PER2, GAL4-CRY1 and GAL4-CRY2, caused a significant increased in luciferase activity when co-expressed together with BMAL1-VP16 (cos-7: 2900-fold for GAL4-PER2, 450-fold for GAL4-CRY1 and 125-fold for GAL4-CRY2, Fig. 7E; HER91: 110-fold for GAL4-PER2, 70-fold for GAL4-CRY1 and 10-fold for GAL4-CRY2, Fig. 7F).
In summary, our two-hybrid assays in cos-7 cells confirm the interactions identified using the same system in HER911 cells, namely PER2-BMAL1, PER2-CLOCK, CRY1-BMAL1 and CRY2-BMAL1. We still cannot exclude the involvement of endogenous bridging proteins that are present in both cell lines. However, the fact that the interactions still take place in a cell line devoid of endogenous clock genes strongly argues against the notion that endogenous clock components are necessary to stabilize the observed interactions.
Full-length mouse cDNAs encoding BMAL1 [EMBL:BC011080], CLOCK [EMBL:AF000998], and PER2 [EMBL:AF036893] were cloned into pSCT1, a pUC18-based expression vector carrying the CMV promoter and intron 2, exon 3, and the 3' UTR of the β-globin gene to enhance expression . The fusion constructs for BMAL1-GFP, GAL4-BMAL1, GAL4-CLOCK, GAL4-PER2, GAL4-CRY1, GAL4-CRY2, CLOCK-VP16, PER2-VP16, CRY1-VP16, CRY2-VP16, PAX5-VP15 and the VP16 tag alone were expressed from the same vector. pSCT1 was also used to express full-length bacterial β-galactosidase and chloramphenicol acetyl transferase ; these constructs will be referred to as pCMV-lacZ and pCMV-CAT, respectively.
To construct the Bmal1 deletions fused to Gal4, a 1051 bp Hin dIII-Bam HI fragment was excised from pSCT1-Gal4-Bmal1 to yield pSCT1-Gal4-Bmal1ΔPAS BΔC-term (aa 1–278 of the full-length protein). Excision of a 1912 bp Bsr FI-Hin dIII fragment from the same vector gave rise to pSCT1-Gal4-Bma1lΔHLHΔPAS A (aa 276–625), and a 488 bp Sph I-Bam HI fragment was excised to construct pSCT1-Gal4-Bmal1ΔC-term (aa 1–467).
For the expression of CRY1 [EMBL:AF156986] and CRY2 [EMBL:AF156987], the respective full-length mouse cDNAs were cloned into pSTC-TK, an expression vector similar to pSCT1, which additionally contains a thymidine kinase leader sequence after the CMV promoter. This vector was also used to express HA-CLOCK.
GFP was expressed from pEGFP-N3 (Clontech, Saint-Germain-en-Laye, France). The Gal4 DNA binding domain was expressed from a modified version of pFA-CMV (Stratagene, Amsterdam, The Netherlands), which will be referred to as pFC-Gal4. pFR-luc (Stratagene, Amsterdam, The Netherlands) is a GAL4-based luciferase reporter vector containing the luciferase gene under the control of a promoter with 5 GAL4 binding sites.
Cell culture and maintenance
HER911 human retinoblastoma cells  and cos-7 African green monkey kidney cells  were routinely cultured in DMEM High Glucose supplemented with 10% FCS, 2 mM L-glutamine, and 100 U/ml penicillin/streptomycin (all from Bioconcept, Allschwil, Switzerland) at 37°C in a humidified atmosphere containing 5% CO2 and split when confluent.
Reporter gene assays
Cells were seeded in 5 cm dishes, grown to 70% confluency and transfected with the calcium phosphate co-precipitation method. All transfection mixtures excluding those for mock transfections contained 3 μg pFR-luc, 0.1 μg pCMV-lacZ to allow normalization of the luciferase activity values. Unless indicated otherwise, 0.1 μg were transfected for pSCT1-Gal4-Bmal1 and its deletion mutants, pSCT1-Cry1/2-VP16, pSCT1-Gal4-Per2, pSCT1-Clock-VP16, pSCT1-Bmal1-VP16, 0.3 μg for pSCT1-Gal4-Clock and 0.5 μg for pSCT1-Per2-VP16. For pFC-Gal4, pSCT1-VP16 and pSCT1-Pax5-VP16, an amount corresponding to that of the respective Gal4 or VP16 fusion construct tested was used.pCMV-CAT was used to obtain the same amount of CMV promoter/enhancer in all samples. The total DNA amount was brought to 10 μg with calf thymus DNA. The volume was brought to 125 μl, 125 μl 0.5 M CaCl2 in 0.1 M Hepes, pH 7.0 were added, and samples were mixed well. After addition of 250 μl 0.75 mM Na2HPO4/0.75 mM NaH2PO4/.28 M NaCl in 0.05 M Hepes, pH 7.0, samples were mixed again and incubated for 1 minute at room temperature before adding the transfection mixture to the cells. Cells were incubated overnight, washed twice with TBS, supplied with fresh medium, incubated for another 24 h and subsequently lysed in 10% glycerol/10 mM MgAc/0.2% Triton X-100 in 50 mM Tris-HCl, pH 8.0.
Luciferase activity was measured according to . 10 μl lysate were added to 100 μl 1 mM ATP (Sigma, Buchs, Switzerland)/10 mM MgAc/0.1 mg/ml BSA in 250 mM Tris-HCl, pH 7.5. Samples were injected with 100 μl 200 μg coenzyme A/30 μg luciferine (both Sigma, Buchs, Switzerland)/ml in 12.5 mM PIPES, pH 6.5 and light emission was measured after a delay of 0.3 seconds during a 10 second interval in a MicroLumatPlus luminometer (Berthold Technologies, Bad Wildbach, Germany).
β-galactosidase activity was measured as described in . 10 μl lysate diluted 1:10 in lysis buffer were incubated with 250 μl 1 mg/ml MUG (Sigma, Buchs, Switzerland)/DMF in 90 mM Na3PO4/18 mM MgCl2, pH 8.0 for 20 minutes at 37°C protected from light. The reaction was stopped by addition of 100 μl 120 mM glycine/6 mM EDTA, pH 11.5, and the fluorescence of the samples was measured at 360 nm excitation and 460 nm emission wave length in a Lambda Fluoro 320 fluorimeter (MWG Biotech, Ebersberg, Germany).
For statistical analysis, values obtained for mock-transfected cells were subtracted from all other values. Subsequently, luciferase activity was normalized to β-galactosidase activity to correct for transfection efficiency. All experiments were performed at least three times, samples were measured in duplicates.
Preparation of total, nuclear and cytoplasmic extracts
Cells were seeded in 5 cm dishes for total extracts or in 10 cm dishes for IPs and fractionations, grown to 70% confluency and transfected with linear polyethylenimine of 25 kDa (LINPEI25, Polysciences Europe, Eppelheim, Germany). Again, pCMV-CAT was used to obtain equal amounts of CMV promoter in each sample. For IPs, 10 μg pSCT1-Bmal1-GFP and pSCT1-HA-Clock and 5 μg pSCT1-Per2, pSTC-TK-Cry1 and pSTC-TK-Cry2 were transfected. For fractionations and total extracts that were not used for IPs, 1 μg pSCT1-Per2-VP16, 3 μg pSCT1-Cry1/2-VP16 and 0.5 μg pSCT1-Gal4-Bmal1 were used for 5 cm dishes; for 10 cm dishes, amounts were increased 3-fold. 0.2 μg pEGFP-N3 were included in each transfection to control transfection efficiency and to allow normalization of expression levels. Plasmid DNA was brought to 200 μl with 150 mM NaCl in 20 mM HEPES pH 7.4 and mixed with 13 equivalents of LINPEI25. Samples were incubated for 10 minutes at room temperature before adding the DNA-LINPEI25 complexes directly to the culture medium. After 6 hours cells were washed once with TBS, supplied with fresh medium and incubated for another 24 hours before lysis.
For total extracts, cells were lysed in 1 mM EDTA/150 mM NaCl/1% Triton X-100/10% glycerol/0.05% β-mercaptoethanol/protease inhibitor cocktail (complete EDTA-free; Roche, Rotkreuz, Switzerland) in 20 mM Tris-HCl, pH 7.5.
Nuclear and cytoplasmic fractions were obtained according to . Cells were incubated in 10 mM KCl/1.5 mM MgCl2/0.5 mM DTT/protease inhibitor cocktail in 10 mM HEPES-KOH, pH 7.9 for 15 minutes on ice. After centrifugation for 5 minutes at 1200 g and 4°C, the supernatant was stored as the cytosolic fraction. The pellet was washed twice with the same buffer and resuspended in 25% glycerol/0.42 M NaCl/1.5 mM MgCl2/0.2 mM EDTA/0.5 mM DTT/protease inhibitor cocktail in 20 mM Hepes-KOH, pH 7.9. Samples were incubated in rotation for 20 minutes at 4°C and centrifuged for 15 minutes at 13000 g and 4°C. The supernatant was stored as the nuclear fraction.
Protein concentration of total extracts or fractions was determined using the BioRad Protein Assay (BioRad, Reinach, Switzerland) according to manufacturer's instructions. 4× loading dye (4% SDS/4% β-mercaptoethanol/40% glycerol in 200 mM Tris-HCl, pH 6.8) was added to all samples and they were boiled before subjection to SDS-PAGE.
Cells were transfected with linear polyethylenimine of 25 kDa as described above. For co-immunoprecipitations with BMAL1-GFP, 600 μg total protein were brought to a final volume of 800 μl with lysis buffer and incubated with 2 μg Anti-GFP antibody (Roche, Rotkreuz, Switzerland) and 50 μl protein G agarose beads (Roche, Rotkreuz, Switzerland) in rotation over night at 4°C. Beads were washed twice with lysis buffer and once with 250 mM NaCl/10% glycerol/0.1% NP-40 in 50 mM Tris-HCl, pH 7.5.
For co-immunoprecipitations with HA-CLOCK, 600 μg total protein were incubated with 0.5 μg anti-HA high affinity antibody (Roche, Rotkreuz, Switzerland) in rotation over night at 4°C. 50 μl protein G agarose beads were added and samples were incubated for another 3 hours at 4°C. Beads were washed three times using 0.1 mM EDTA/10% glycerol/1% Triton-X 100/0.3% β-mercaptoethanol in 30 mM Tris-HCl, pH 7.5 supplemented with 1 M, 0.1 M and no NaCl, respectively. In both cases, beads were resuspended in 2% SDS/2% β-mercaptoethanol/20% glycerol in 100 mM Tris-HCl, pH 6.8. Samples were boiled and subsequently subjected to SDS-PAGE.
Total lysates, cellular fractions or immunoprecipitates were separated by SDS-PAGE and transferred onto nitrocellulose membranes. Membranes were blocked for 1 h at room temperature in 5% milk/0.1% Tween-20 in TBS for PER2, CRY1, CRY2, GFP and BMAL1 and in 1% milk/0.1% Tween-20 in TBS for HA and incubated with primary antibodies diluted in blocking buffer at 4°C over night. Antibodies and dilution were anti-PER2 1:1000 (BD Biosciences, Allschwil, Switzerland for total lysates and immunoprecipitations; gift from J. Ripperger and S. Brown for fractions ), anti-BMAL1 1:1000 (gift from J. Ripperger and S. Brown ), anti-CRY1 1:500, anti-CRY2 1:750 (both Alpha Diagnostics, San Antonio, USA), anti-GFP 1:3000, anti-HA 1:1000 (both Roche, Rotkreuz, Switzerland). Membranes were washed and incubated with appropriate HRP-conjugated secondary antibodies (anti-rabbit, anti-mouse and anti-rat; all Sigma, Buchs, Switzerland) for 1 h at room temperature. Detection was performed using the Western blotting detection reagents kit (Amersham Biosciences, Freiburg, Germany) according to manufacturer's instructions. Membranes were exposed on Hyperfilm (Amersham Biosciences, Freiburg, Germany).
HER911 cells were seeded in 10 cm dishes and grown to 80% confluency. Cells were washed once with TBS and lysed in 1 ml RNA bee (AMS Biotechnology, Abingdon, UK) directly in the dish. Total RNA was isolated according to manufacturer's instructions and RNA integrity was checked on an agarose gel. cDNA was synthesized from 2 μg total RNA using SuperScript II (Invitrogen, Basel, Switzerland) according to manufacturer's instructions. Human genomic DNA (for primer optimization and as positive control) was from Promega (Wallisellen, Switzerland).
Primers for the amplification of human clock genes were 5'-CCCACCCCACCAGCCACTAC-3' and 5'-CCTGTGCCGGAGCGCGAGTC-3' for hPer1 (GenBank GeneID:5187), 5'-TGGATGTGGCTGTCTTGTAG-3' and 5'-GCCGGTGGATCTGCTCTGTG-3' for hPer2 (GenBank GeneID:8864), 5'-TGGATGTGGCTGTCTTGTAG-3' and 5'-TTTGGCTACCTTTTGGATAC-3' for hCry1 (GenBank GeneID:1407), 5'-AAGCGTTCCCCTCTCGATAC-3' and 5'-AGGGACAGATGCCAGTAGAC-3' for hCry2 (GenBank GeneID:1408), 5'-CATTCCTTCCAGTGGCCTAC-3' and 5'-GTCAACAGGGCCACCCAGTC-3' for hBmal1 (hARNTL; GenBank GeneID:406) and 5'-TCATCGGCAACAAGAAGAAC-3' and 5'-GCTTCCGGCTGCAGGCTGAG-3' for hClock (GenBank GeneID:9575). All primers were designed based on the genomic sequence so that amplicons would contain an intron to distinguish between products obtained from genomic and cDNA (1003/562 bp for hPer1, 590/237 bp for hPer2, 412/188 bp for hCry1, 511/202 bp for hCry2, 1017/213 bp for hBmal1, 2187/399 bp for hClock). 40 PCR cycles (30 seconds denaturation at 95°C, 30 seconds annealing, 2 minutes elongation at 72°C) were run, annealing temperatures were 62°C for hPer1, 60°C for hPer2, hBmal1 and hClock, 56°C for hCry2 and 50°C for hCry1.
This work was supported by the Swiss National Science Foundation, the State of Fribourg and the EC grant 'Euclock'. The authors thank Dr. Jürgen Ripperger and Dr. Stephen Brown for the BMAL1 and PER2 antibodies.
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