E-box function in a period gene repressed by light
- *Max-Planck-Institut für Entwicklungsbiologie, Spemannstrasse 35-39, Tübingen, D-72076 Germany; and †Centre for Cell and Molecular Dynamics, Department of Anatomy and Developmental Biology, University College London, 21 University Street, London WC1E 6JJ, England
-
Edited by Jeffrey C. Hall, Brandeis University, Waltham, MA, and approved January 14, 2004 (received for review September 11, 2003)
Abstract
In most organisms, light plays a key role in the synchronization of the circadian timing system with the environmental day–night cycle. Light pulses that phase-shift the circadian clock also induce the expression of period (per) genes in vertebrates. Here, we report the cloning of a zebrafish per gene, zfper4, which is remarkable in being repressed by light. We have developed an in vivo luciferase reporter assay for this gene in cells that contain a light-entrainable clock. High-definition bioluminescence traces have enabled us to accurately measure phase-shifting of the clock by light. We have also exploited this model to study how four E-box elements in the zfper4 promoter regulate expression. Mutagenesis reveals that the integrity of these four E-boxes is crucial for maintaining low basal expression together with robust rhythmicity and repression by light. Importantly, in the context of a minimal heterologous promoter, the E-box elements also direct a robust circadian rhythm of expression that is significantly phase-advanced compared with the original zfper4 promoter and lacks the light-repression property. Thus, these results reveal flexibility in the phase and light responsiveness of E-box-directed rhythmic expression, depending on the promoter context.
Footnotes
-
↵ ‡ To whom correspondence should be addressed. E-mail: nix{at}tuebingen.mpg.de.
-
This paper was submitted directly (Track II) to the PNAS office.
-
Abbreviations: LD, light–dark; DD, constant darkness; LL, constant light; BMAL brain and muscle arnt-like protein.
-
Data deposition: The sequence reported in this paper has been deposited in the GenBank database (accession no. AY359820).
- Copyright © 2004, The National Academy of Sciences





