Antagonistic role of E4BP4 and PAR proteins in the circadian oscillatory mechanism

• Published in: Genes & development Vol. 15; no. 8; pp. 995 - 1006
• Main Authors: Mitsui, S, Yamaguchi, S, Matsuo, T, Ishida, Y, Okamura, H
• Format: Journal Article
• Language: English
• Published: United States Cold Spring Harbor Laboratory Press 15.04.2001
• Subjects: Animals; Basic-Leucine Zipper Transcription Factors; Blotting, Northern; Blotting, Western; Cell Nucleus - metabolism; Circadian Rhythm - physiology; Dimerization; DNA-Binding Proteins - biosynthesis; DNA-Binding Proteins - physiology; G-Box Binding Factors; Genetic Vectors; Immunohistochemistry; In Situ Hybridization; Kinetics; Leucine Zippers; Liver - metabolism; Male; Membrane Proteins; Mice; Mice, Inbred BALB C; Models, Biological; Molecular Sequence Data; Neoplasm Proteins; Plasmids - metabolism; Protein Binding; Protein Biosynthesis; Protein Structure, Tertiary; Proteins - physiology; Research Paper; RNA, Messenger - metabolism; Time Factors; Tissue Distribution; Transcription Factors - biosynthesis; Transcription Factors - physiology; Transcription, Genetic
• ISSN: 0890-9369; 1549-5477
• DOI: 10.1101/gad.873501

E4BP4, a basic leucine zipper transcription factor, contains a DNA-binding domain closely related to DBP, HLF, and TEF, which are PAR proteins. Here, we show that the phase of e4bp4 mRNA rhythm is opposite to that of the dbp, hlf, and tef rhythms in the suprachiasmatic nucleus (SCN), the mammalian circadian center, and the liver. The protein levels of E4BP4 and DBP also fluctuate in almost the opposite phase. Moreover, all PAR proteins activate, whereas E4BP4 suppresses, the transcriptional activity of the reporter gene containing a common binding sequence in transcriptional assays in vitro. An electrophoretic mobility shift assay demonstrated that E4BP4 is not able to dimerize with the PAR proteins, but is able to compete for the same binding sites with them. Furthermore, we showed sustained low e4bp4 and high dbp mRNA levels in mCry-deficient mice. These results indicate that the E4BP4 and PAR proteins are paired components of a reciprocating mechanism wherein E4BP4 suppresses the transcription of target genes during the time of day when E4BP4 is abundant, and the PAR proteins activate them at another time of day. E4BP4 and the PAR proteins may switch back and forth between the on-off conditions of the target genes.