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Resources » Reference Databases » Citations Database
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Gene Synthesis> | A synthetic 778 base-pair DNA fragment corresponding to the wild-type human PER2promoter (from 238288785 to 238289562 of Homo sapiens chromosome 2, GRCh38.p12 primary assembly, sequence ID: NC_000002.12) and a corresponding fragment containing the E’-box sequence CACGTT mutated in CCCCCC were synthetized by and cloned in pBluescript II KS (−) vector by GenScript (USA). Wild-type and mutated PER2 promoter sequences were then sub-cloned in pGreenFire1-mCMV (EF1α-neo) (System Biosciences, catalog# TR010PA-N) upstream the minimal CMV promoter driving the expression of the copGFP protein. The resulting E’-box-GFP and E’mut-box-GFP vectors were sequenced with a specific primers in reverse orientation respect with the copGFP gene (copGFP RV primer, 5’-GATGATCTTGTCGGTGAAGATCACG-3’) to confirm the correct cloning. | Get A Quote |
The circadian transcriptional network is based on a competition between transcriptional activator and repressor complexes regulating the rhythmic expression of clock-controlled genes. We show here that the MYC-Associated factor X, MAX, plays a repressive role in this network and operates through its MYC-independent binding to E-box-containing regulatory regions within the promoters of circadian BMAL1 targets. This clock function of MAX is essential for maintaining a proper circadian rhythm but separated by the role of MAX as a partner of MYC in controlling cell proliferation. We also identified MAX Network Transcriptional repressor, MNT, as a fundamental partner of MAX-mediated circadian regulation. Collectivel... More