Abstract
In zebrafish, the expression of long-wavelength cone (LC) opsin mRNA fluctuated rhythmically between the day and night. In a 24-h period, expression was high in the afternoon and low in the early morning. This pattern of fluctuation persisted in zebrafish that were kept in constant darkness, suggesting an involvement of circadian clocks. Functional expression of Clock, a circadian clock gene that contributes to the central circadian pacemaker, was found to play an important role in maintaining the circadian rhythms of LC opsin mRNA expression. In zebrafish embryos, in which the translation of Clock was inhibited by anti-Clock morpholinos, the circadian rhythms of LC opsin mRNA expression diminished. CLOCK may regulate the circadian rhythms of LC opsin mRNA expression via cyclic adenosine monophosphate (cAMP)-dependent signaling pathways. In control retinas, the concentration of cAMP was high in the early morning and low in the remainder of the day and night. Inhibition of Clock translation abolished the fluctuation in the concentration of cAMP, thereby diminishing the circadian rhythms of opsin mRNA expression. Transient increase of cAMP concentrations in the early morning (i.e. by treating the embryos with 8-bromo-cAMP) restored the circadian rhythms of LC opsin mRNA expression in morpholino-treated embryos. Together, the data suggest that Clock plays important roles in regulating the circadian rhythms in photoreceptor cells.
Highlights
The neural retina is considered an important part of the circadian system
We demonstrate that functional expression of Clock is required for maintaining the circadian rhythms of the expression of long-wavelength cone (LC) opsin mRNA in photoreceptor cells
Circadian Rhythms of LC mRNA Expression—LC opsin mRNA is expressed in red cone photoreceptor cells
Summary
Animals and Maintenance—Zebrafish (Danio rerio) were maintained as described [14]. The embryos were maintained under cyclic light and darkness (LD; fluorescent light, 07:00 to 21:00). For DD experiments, the embryos were removed from LD at 21:00 the day before the experiment and thereafter kept in DD. All of the experimental procedures adhered to the National Institutes of Health Guidelines for Animals in Research.
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