PUBLICATION
Zebrafish CRY represses transcription mediated by CLOCK-BMAL heterodimer without inhibiting its binding to DNA
- Authors
- Ishikawa, T., Hirayama, J., Kobayashi, Y., and Todo, T.
- ID
- ZDB-PUB-021015-19
- Date
- 2002
- Source
- Genes to cells : devoted to molecular & cellular mechanisms 7(10): 1073-1086 (Journal)
- Registered Authors
- Hirayama, Jun
- Keywords
- none
- MeSH Terms
-
- Flavoproteins/physiology*
- Zebrafish
- Base Sequence
- Transcription, Genetic/physiology*
- Animals
- ARNTL Transcription Factors
- Transcription Factors/genetics
- Transcription Factors/metabolism
- Transcription Factors/physiology*
- Trans-Activators/genetics
- Trans-Activators/metabolism
- Trans-Activators/physiology*
- Dimerization
- DNA Primers
- Cloning, Molecular
- Protein Binding
- Basic Helix-Loop-Helix Transcription Factors
- Cryptochromes
- DNA/metabolism*
- Zebrafish Proteins/physiology*
- CLOCK Proteins
- Plasmids
- PubMed
- 12354100 Full text @ Genes Cells
Citation
Ishikawa, T., Hirayama, J., Kobayashi, Y., and Todo, T. (2002) Zebrafish CRY represses transcription mediated by CLOCK-BMAL heterodimer without inhibiting its binding to DNA. Genes to cells : devoted to molecular & cellular mechanisms. 7(10):1073-1086.
Abstract
BACKGROUND: CLOCK and BMAL1 proteins, members of the basic helix-loop- helix PAS (PER-ARNT-SIM) superfamily of transcription factors which bind to the E-box DNA motif, are required for the high-level expression of the circadian clock genes period (per) and cryptochrome (cry). CRY inhibits transcriptional activity of the CLOCK-BMAL1 heterodimer, generating a negative-feedback loop that is the core element of the circadian oscillator. RESULTS: We show that zebrafish CRY (zCRY1a) neither disrupts the association between zfCLOCK and zfBMAL nor inhibits binding of the zfCLOCK-zfBMAL heterodimer to an E-box-bearing DNA fragment. Instead it binds to the heterodimer to form a stable zCRY1a- zfCLOCK-zfBMAL-E-box complex. Another zebrafish CRY protein, zCRY4, does not have transcriptional inhibitor activity, whereas zCRY1a has strong activity. zCRY4 does not associate with zfCLOCK and zfBMAL. We also show that the presence of a chemical reductant in the reaction mixture is crucial for efficient binding of the CLOCK-BMAL heterodimer to E-box bearing DNA, which is indicative of the reduction/oxidation (redox)- sensitive character of the heterodimer. CONCLUSIONS: Our findings suggest that CRY represses CLOCK-BMAL-mediated transcription by interacting directly with the zfCLOCK-zfBMAL-E-box complex.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping