Publication Cover
Chronobiology International
The Journal of Biological and Medical Rhythm Research
Volume 30, 2013 - Issue 5
603
Views
67
CrossRef citations to date
0
Altmetric
Research Article

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

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

References

  • Altschul SF, Gish W, Miller W, et al. (1990). Basic local alignment search tool. J Mol Biol, 215, 403–10
  • Amaral IPG, Jhonston IA. (2012). Circadian expression of clock and putative clock-controlled genes in skeletal muscle of the zebrafish. Am J Physiol Regul Integr Comp Physiol, 302, R193–R206
  • Azzaydi M, Rubio VC, Martínez-López FJ, et al. (2007). Effects of restricted feeding schedule on seasonal shifting of daily demand-feeding pattern and food anticipatory activity in European sea bass (Dicentrarchus labrax L.). Chronobiol Int, 24, 859–74
  • Bertolucci C, Sovrano VA, Magnone MC, Foà A. (2000). The role of the suprachiasmatic nuclei in circadian and light–entrained behavioral rhythms of lizard. Am J Physiol Regul Integr Comp Physiol, 279, R2121–R2131
  • Blum ID, Lamont EW, Abizaid A. (2012a). Competing clocks: metabolic status moderates signals from the master circadian pacemaker. Neurosci Biobehav Rev, 36, 254–70
  • Blum ID, Waddington Lamont E, Rodrigues T, Abizaid A. (2012b). Isolating neural correlates of the pacemaker for food anticipation. PLoS ONE, 7, e36117 . doi: 10.1371/journal.pone.0036117
  • Cahill GM. (2002). Clock mechanisms in zebrafish. Cell Tissue Res, 309, 27–34
  • Cavallari N, Frigato E, Vallone D, et al. (2011). A blind circadian clock in cavefish reveals that opsins mediate peripheral clock photoreception. PLoS Biol, 9, e1001142. doi: 10.1371/journal.pbio.1001142
  • Cermakian N, Whitmore D, Foulkes NS, Sassone-Corsi P. (2000). Asynchronus oscillations of two zebrafish CLOCK partners reveal differential clock control and function. Proc Nat Acad Sci U S A, 97, 4339–44
  • Challet E, Mendoza J, Dardente H, Pevet P. (2009). Neurogenetics of food anticipation. Eur J Neurosci, 30, 1676–87
  • Comperatore CA, Stephan FK. (1987). Entrainment of duodenal activity to periodic feeding. J Biol Rhythms, 2, 227–42
  • Damiola F, Le Minh N, Preitner N, et al. (2000). Restricted feeding uncouples circadian oscillators in peripheral tissues from the central pacemaker in the suprachiasmatic nucleus. Genes Dev, 14, 2950–61
  • Dardente H, Cermakian N. (2007). Review: molecular circadian rhythms in central and peripheral clocks in mammals. Chronobiol Int, 24, 195–213
  • Davidson AJ. (2009). Lesion studies targeting food-anticipatory activity. Eur J Neurosci, 30, 1658–64
  • Davie A, Minghetti M, Migaud H. (2009). Seasonal variations in clock-gene expression in Atlantic salmon (Salmo salar). Chronobiol Int, 26, 379–95
  • Del Pozo A, Sánchez-Férez JA, Sánchez-Vázquez FJ. (2011). Circadian rhythms of self-feeding and locomotor activity in zebrafish (Danio rerio). Chronobiol Int, 28, 39–47
  • Feliciano A, Vivas Y, De Pedro N, et al. (2011). Feeding time synchronizes clock gene rhythmic expression in brain and liver of goldfish (Carassius auratus). J Biol Rhythms, 26, 24–33
  • Gu YZ, Hogenesch JB, Bradfield CA. (2000). The PAS superfamily sensors of environmental and developmental signals. Annu Rev Pharmacol Toxicol, 40, 519–61
  • Idda ML, Bertolucci C, Vallone D, et al. (2012). Circadian clocks: lessons from fish. Prog Brain Res, 199, 49–57
  • Iijima M, Yamaguchi S, van der Horst GTJ, et al. (2005). Altered food-anticipatory activity rhythm in Cryptochrome-deficient mice. Neurosci Res, 52, 166–73
  • Ko CH, Takahashi JS. (2006). Molecular components of the mammalian circadian clock. Hum Mol Genet, 15, 271–7
  • Lamia KA, Sachdeva UM, DiTacchio L, et al. (2009). AMPK regulates the circadian clock by cryptochrome phosphorylation and degradation. Science, 326, 437–40
  • Livak KJ, Schmittgen TD. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2(−Delta Delta C(T)) Method. Methods, 25, 402–8
  • López-Olmeda JF, Sánchez-Vázquez FJ. (2010). Feeding rhythms in fish: from behavioral to molecular approach. In: Kulczykowska E, ed. Biological Clock in Fish. Enfield, NH: Science Publishers, 155–84
  • López-Olmeda JF, Tartaglione EV, de la Iglesia HO, Sánchez-Vázquez FJ. (2010). Feeding entrainment of food-anticipatory activity and per1 expression in the brain and liver of zebrafish under different lighting and feeding conditions. Chronobiol Int, 27, 1380–400
  • López-Patiño MA, Rodríguez-Illamola A, Conde-Sieira M, et al. (2011). Daily rhythmic expression patterns of Clock1a, Bmal1, and Per1 genes in retina and hypothalamus of the rainbow trout, Oncorhynchus mykiss. Chronobiol Int, 28, 381–9
  • Malloy JN, Jaclyn N, Paulose JK, et al. (2012). Circadian rhythms of gastrointestinal function are regulated by both central and peripheral oscillators. Am J Physiol Gastrointest Liver Physiol, 303, 461–73
  • Martín-Robles AJ, Isorna E, Whitmore D, et al. (2011). The clock gene Period3 in the nocturnal flatfish Solea senegalensis: molecular cloning, tissue expression and daily rhythms in central areas. Comp Biochem Physiol A Mol Integr Physiol, 159, 7–15
  • McIntosh BE, Hogenesch JB, Bradfield CA. (2010). Mammalian Per-Arnt-Sim proteins in environmental adaptation. Annu Rev Physiol, 72, 625–45
  • Mistlberger RE. (1994). Circadian food-anticipatory activity: formal models and physiological mechanisms. Neurosci Biobehav Rev, 18, 171–95
  • Mistlberger RE. (2011). Neurobiology of food anticipatory circadian rhythms. Physiol Behav, 104, 535–45
  • Mistlberger RE, Antle MC. (2011). Entainment of circadian clocks in mammals by arousal and food. Essays Biochem, 49, 119–36
  • Montoya A, López-Olmeda JF, Garayzar ABS, Sánchez-Vázquez FJ. (2010a). Synchronization of daily rhythms of locomotor activity and plasma glucose, cortisol and thyroid hormones to feeding in Gilthead sea bream (Sparus aurata) under a light-dark cycle. Physiol Behav, 101, 101–7
  • Montoya A, López-Olmeda JF, Yúfera M, et al. (2010b). Feeding time synchronises daily rhythms of behaviour and digestive physiology in gilthead sea bream (Sparus aurata). Aquaculture, 306, 315–21
  • Mistlberger RE. (1994). Circadian food-anticipatory activity: formal models and physiological mechanisms. Neurosci Biobehav Rev, 18, 171–95
  • Mistlberger RE, Antle MC. (2011). Entainment of circadian clocks in mammals by arousal and food. Essays Biochem, 49, 119–36
  • Nisembaum LG, Velarde E, Tinoco AB, et al. (2012). Light-dark cycle and feeding time differentially entrains the gut molecular clock of the goldfish (Carassius auratus). Chronobiol Int, 29, 665–73
  • Pando MP, Pinchak AB, Cermakian N, Sassone-Corsi P. (2001). A cell-based system that recapitulates the dynamic light-dependent regulation of the vertebrate clock. Proc Natl Acad Sci U S A, 98, 10178–83
  • Park JG, Park YJ, Sugama N, et al. (2007). Molecular cloning and daily variations of the Period gene in a reef fish Siganus guttaus. J Comp Physiol A, 193, 403–11
  • Pegoraro M, Tauber E. (2011). Animal clocks: a multitude of molecular mechanisms for circadian timekeeping. Wiley Interdiscip Rev RNA, 2, 312–20
  • Portaluppi F, Smolensky M, Touitou Y. (2010). Ethics and methods for biological rhythm research in animals and human beings. Chronobiol Int, 27, 1911–29
  • Rensing L, Ruoff P. (2002). Temperature effect on entrainment, phase shifting, and amplitude of circadian clocks and its molecular bases. Chronobiol Int, 19, 807–864
  • Reppert SM, Weaver DR. (2001). Molecular analysis of mammalian circadian rhythms. Annu Rev Physiol, 63, 647–76
  • Rozen S, Skaletsky HJ. (2000). Primer3 on the WWW for general users and for biologist programmers. Methods Mol Biol, 132, 365–386
  • Sancar A. (2000). The second photoactive pigment in the eye and its role in circadian photoreception. Annu Rev Biochem, 69, 31–67
  • Sánchez JA, Sánchez-Vázquez FJ. (2009). Feeding entrainment of daily rhythms of locomotor activity and clock gene expression in zebrafish brain. Chronobiol Int, 26, 1120–1135
  • Sánchez JA, López-Olmeda JF, Blanco-Vives B, Sánchez-Vázquez FJ. (2009). Effects of feeding schedule on locomotor activity rhythms and stress response in sea bream. Physiol Behav, 98, 125–9
  • Sánchez JA, Madrid J, Sánchez-Vázquez FJ. (2010). Molecular cloning, tissue distribution and daily rhythms of expression of per1 gene in European sea bass (Dicentrarchus labrax). Chronobiol Int, 27, 19–33
  • Sánchez-Vázquez FJ, Aranda A, Madrid JA. (2001). Differential effects of meal size and food energy density on feeding entrainment in goldfish. J Biol Rhythms, 16, 58–65
  • Shibata S, Tominaga K. (1991). Brain neuronal mechanisms of circadian rhythms in mammalians. Yakugaku Zasshi, 111, 270–83
  • Schmutz I, Albrecht U, Ripperger, JA. (2012). The role of clock genes and rhythmicity in the liver. Mol Cell Endocrinol, 349, 38–44
  • Stephan FK. (2002). The “other” circadian system: food as a zeitgeber. J Biol Rhythms, 17, 284–92
  • Strubbe JH, Van Dijk G. (2002). The temporal organization of ingestive behaviour and its interactions with regulation of energy balance. Neurosci Biobehav Rev, 26, 485–98
  • Vatine G, Vallone D, Appelbaum L, et al. (2009). Light Directs Zebrafish period2 Expression via Conserved D and E Boxes. PLoS Biol, 7, e1000223 . doi: 10.1371/journal.pbio.1000223
  • Velarde E, Haque R, Iuvone PM, et al. (2009). Circadian clock genes of goldfish, Carassius auratus: cDNA cloning and rhythmic expression of period and cryptochrome transcrips in retina, liver and gut. J Biol Rhythms, 24, 104–13
  • Vera LM, De Pedro N, Gómez-Milán E, et al. (2007). Feeding entrainment of locomotor activity rhythms, digestive enzymes and neuroendocrine factors in goldfish. Physiol Behav, 90, 518–24
  • Wang H. (2008). Comparative analysis of period genes in teleost fish genomes. J Mol Evol, 67, 29–40
  • Welsh DK, Takahashi JS, Kay SA. (2010). Suprachiasmatic nucleus: cell autonomy and network properties. Annu Rev Physiol, 72, 551–77
  • Whitmore D, Foulkes NS, Strahle U, Sassone-Corsi P. (1998). Zebrafish clock rhythmic expression reveals independent peripheral circadian oscillators. Nat Neurosci, 1, 701–7
  • Zilberman-Peled B, Appelbaum L, Vallone D, et al. (2006). Transcriptional regulation of arylalkylamine-N-acetyltransferase-2 gene in the pineal gland of the gilthead sea bream. J Neuroendocrinol, 19, 46–53
  • Ziv L, Levkovitz S, Toyama R, et al. (2005). Functional development of the zebrafish pineal gland: light-induced expression of period2 is required for onset of the circadian clock. J Neuroendocrinol, 17, 314–20

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.