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Chronobiology International
The Journal of Biological and Medical Rhythm Research
Volume 30, 2013 - Issue 5
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Research Article

Light and feeding entrainment of the molecular circadian clock in a marine teleost (Sparus aurata)

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Pages 649-661 | Received 19 Jun 2012, Accepted 07 Feb 2013, Published online: 20 May 2013
 

Abstract

Daily light and feeding cycles act as powerful synchronizers of circadian rhythmicity. Ultimately, these external cues entrain the expression of clock genes, which generate daily rhythmic behavioral and physiological responses in vertebrates. In the present study, we investigated clock genes in a marine teleost (gilthead sea bream). Partial cDNA sequences of key elements from both positive (Bmal1, Clock) and negative (Per2, Cry1) regulatory loops were cloned before studying how feeding time affects the daily rhythms of locomotor activity and clock gene expression in the central (brain) and peripheral (liver) oscillators. To this end, all fish were kept under a light-dark (LD) cycle and were divided into three experimental groups, depending on the time of their daily meal: mid-light (ML), mid-darkness (MD), or at random (RD) times. Finally, the existence of circadian control on gene expression was investigated in the absence of external cues (DD + RD). The behavioral results showed that seabream fed at ML or RD displayed a diurnal activity pattern (>91% of activity during the day), whereas fish fed at MD were nocturnal (89% of activity during the night). Moreover, seabream subjected to regular feeding cycles (ML and MD groups) showed food-anticipatory activity (FAA). Regardless of the mealtime, the daily rhythm of clock gene expression in the brain peaked close to the light-dark transition in the case of Bmal1 and Clock, and at the beginning of the light phase in the case of Per2 and Cry1, showing the existence of phase delay between the positive and negative elements of the molecular clock. In the liver, however, the acrophases of the daily rhythms differed depending on the feeding regime: the maximum expression of Bmal1 and Clock in the ML and RD groups was in antiphase to the expression pattern observed in the fish fed at MD. Under constant conditions (DD + RD), Per2 and Cry1 showed circadian rhythmicity in the brain, whereas Bmal1, Clock, and Per2 did in the liver. Our results indicate that the seabream clock gene expression is endogenously controlled and in liver it is strongly entrained by food signals, rather than by the LD cycle, and that scheduled feeding can shift the phase of the daily rhythm of clock gene expression in a peripheral organ (liver) without changing the phase of these rhythms in a central oscillator (brain), suggesting uncoupling of the light-entrainable oscillator (LEO) from the food-entrainable oscillator (FEO). These findings provide the basis and new tools for improving our knowledge of the circadian system and entraining pathways of this fish species, which is of great interest for the Mediterranean aquaculture. (Author correspondence: [email protected]).

Acknowledgments

The authors would like to thank José Antonio Oliver, Ana del Pozo, Ander Montoya, and Juan Fernando Paredes for their help in daily fish management and sampling. Financial support was provided by the project AQUAGENOMICS (Consolider-Ingenio 2010 Programme), by the Integrated Action Spain-Italy (IT2009-0057) from the Spanish Ministry of Economy and Competitiveness (MINECO) and the Italian Ministry of Education, University and Research (MIUR), and by University of Ferrara research grants. L. M. Vera has a postdoctoral contract (Juan de la Cierva) awarded by the Spanish MINECO. Thanks are also due to the Spanish Ministry of Defense for allowing use of the ENA aquaculture facilities.

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