Setting the biological time in central and peripheral clocks during ontogenesis

FEBS Letters

Volumn 580, Issue 12, 2006, Pages 2836-2842

  Sumová, Alena ^a   Bendová, Zdenka ^a   Sládek, Martin ^a   El Hennamy, Rehab ^a   Laurinová, Kristýna ^a   Jindráková, Zuzana ^a   Illnerová, Helena ^a  

^a INSTITUTE OF PHYSIOLOGY   (Czech Republic)

Author keywords

Circadian system; Ontogenesis; Peripheral circadian clocks; Suprachiasmatic nucleus

Indexed keywords

CORTICOTROPIN RELEASING FACTOR; DEXAMETHASONE; GLUCOCORTICOID; GLUCOCORTICOID RECEPTOR; PER1 PROTEIN; RYANODINE RECEPTOR; SEROTONIN AGONIST;

CIRCADIAN RHYTHM; FEEDING BEHAVIOR; MATERNAL CARE; MOLECULAR CLOCK; MOTHER; MOTHER FETUS RELATIONSHIP; NONHUMAN; ONTOGENY; PERINATAL PERIOD; PHOTOSTIMULATION; PRENATAL PERIOD; PRIORITY JOURNAL; SHORT SURVEY; SIGNAL TRANSDUCTION; SUPRACHIASMATIC NUCLEUS; TIME; ANIMAL; BIOLOGICAL RHYTHM; DARKNESS; LIGHT; PHYSIOLOGY; REVIEW;

ANIMALIA; MAMMALIA;

ANIMALS; BIOLOGICAL CLOCKS; DARKNESS; LIGHT; SUPRACHIASMATIC NUCLEUS;

EID: 33746399067     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.febslet.2006.03.023     Document Type: Short Survey

References (51)

1. Klein D.C., Moore R.J., and Reppert S.M. In: Klein D.C., Moore R.J., and Reppert S.M. (Eds). Suprachiasmatic Nucleus: The Mind's Clock (1991), Oxford University Press, New York 197-216
2. Welsh D.K., Logothetis D.E., Meister M., and Reppert S.M. Individual neurons dissociated from rat suprachiasmatic nucleus express independently phased circadian firing rhythms. Neuron 14 (1995) 697-706
3. Kornhauser J.M., Nelson D.E., Mayo K.E., and Takahashi J.S. Regulation of jun-B messenger RNA and AP-1 activity by light and a circadian clock. Science 255 (1992) 1581-1584
4. Jáč M., Kiss A., Sumová A., Illnerová H., and Ježová D. Daily profiles of arginine vasopressin mRNA in the suprachiasmatic, supraoptic and paraventricular nuclei of the rat hypothalamus under various photoperiods. Brain Res. 887 (2000) 472-476
5. Sumová A., Trávni{dotless}́čková Z., Mikkelsen J.D., and Illnerová H. Spontaneous rhythm in c-Fos immunoreactivity in the dorsomedial part of the rat suprachiasmatic nucleus. Brain Res. 801 (1998) 254-258
6. Schibler U., Ripperger J., and Brown S.A. Peripheral circadian oscillators in mammals: time and food. J. Biol. Rhythms 18 (2003) 250-260
7. Yoo S.H., Yamazaki S., Lowrey P.L., Shimomura K., Ko C.H., Buhr E.D., Siepka S.M., Hong H.K., Oh W.J., Yoo O.J., Menaker M., and Takahashi J.S. PERIOD2::LUCIFERASE real-time reporting of circadian dynamics reveals persistent circadian oscillations in mouse peripheral tissues. Proc. Natl. Acad. Sci. USA 101 (2004) 5339-5346
8. Emery P., and Reppert S.M. A rhythmic Ror. Neuron 43 (2004) 443-446
9. Oishi K., Fukui H., and Ishida N. Rhythmic expression of BMAL1 mRNA is altered in Clock mutant mice: differential regulation in the suprachiasmatic nucleus and peripheral tissues. Biochem. Biophys. Res. Commun. 268 (2000) 164-171
10. Jin X., Shearman L.P., Weaver D.R., Zylka M.J., de Vries G.J., and Reppert S.M. A molecular mechanism regulating rhythmic output from the suprachiasmatic circadian clock. Cell 96 (1999) 57-68
11. Panda S., Antoch M.P., Miller B.H., Su A.I., Schook A.B., Straume M., Schultz P.G., Kay S.A., Takahashi J.S., and Hogenesch J.B. Coordinated transcription of key pathways in the mouse by the circadian clock. Cell 109 (2002) 307-320
12. Akhtar R.A., Reddy A.B., Maywood E.S., Clayton J.D., King V.M., Smith A.G., Gant T.W., Hastings M.H., and Kyriacou C.P. Circadian cycling of the mouse liver transcriptome, as revealed by cDNA microarray, is driven by the suprachiasmatic nucleus. Curr. Biol. 12 (2002) 540-550
13. Reppert S.M., and Weaver D.R. Molecular analysis of mammalian circadian rhythms. Annu. Rev. Physiol. 63 (2001) 647-676
14. Aschoff J., Hoffmann K., Pohl H., and Wever R. Re-entrainment of circadian rhythms after phase-shifts of the Zeitgeber. Chronobiologia 2 (1975) 23-78
15. Beaule C., Robinson B., Lamont E.W., and Amir S. Melanopsin in the circadian timing system. J. Mol. Neurosci. 21 (2003) 73-89
16. Gamble K.L., Novak C.M., and Albers H.E. Neuropeptide Y and N-methyl-d-aspartic acid interact within the suprachiasmatic nuclei to alter circadian phase. Neuroscience 126 (2004) 559-565
17. Meijer J.H., and Schwartz W.J. In search of the pathways for light-induced pacemaker resetting in the suprachiasmatic nucleus. J. Biol. Rhythms 18 (2003) 235-249
18. Ding J.M., Buchanan G.F., Tischkau S.A., Chen D., Kuriashkina L., Faiman L.E., Alster J.M., McPherson P.S., Campbell K.P., and Gillette M.U. A neuronal ryanodine receptor mediates light-induced phase delays of the circadian clock. Nature 394 (1998) 381-384
19. Ginty D.D., Kornhauser J.M., Thompson M.A., Bading H., Mayo K.E., Takahashi J.S., and Greenberg M.E. Regulation of CREB phosphorylation in the suprachiasmatic nucleus by light and a circadian clock. Science 260 (1993) 238-241
20. Shearman L.P., Zylka M.J., Weaver D.R., Kolakowski Jr. L.F., and Reppert S.M. Two period homologs: circadian expression and photic regulation in the suprachiasmatic nuclei. Neuron 19 (1997) 1261-1269
21. Trávni{dotless}́čková-BCermakian Z., Cermakian N., Reppert S.M., and Sassone-Corsi P. Bimodal regulation of mPeriod promoters by CREB-dependent signaling and CLOCK/BMAL1 activity. Proc. Natl. Acad. Sci. USA 99 (2002) 7728-7733
22. Sumová A., Bendová Z., Sládek M., Kováčiková Z., and Illnerová H. Seasonal molecular timekeeping within the rat circadian clock. Physiol. Res. 53 Suppl. 1 (2004) S167-S176
23. Challet E., and Pevet P. Interactions between photic and nonphotic stimuli to synchronize the master circadian clock in mammals. Front. Biosci. 8 (2003) 246-257
24. Damiola F., Le Minh N., Preitner N., Kornmann B., Fleury-Olela F., and Schibler U. Restricted feeding uncouples circadian oscillators in peripheral tissues from the central pacemaker in the suprachiasmatic nucleus. Genes Dev. 14 (2000) 2950-2961
25. Balsalobre A., Brown S.A., Marcacci L., Tronche F., Kellendonk C., Reichardt H.M., Schutz G., and Schibler U. Resetting of circadian time in peripheral tissues by glucocorticoid signaling. Science 289 (2000) 2344-2347
26. Terazono H., Mutoh T., Yamaguchi S., Kobayashi M., Akiyama M., Udo R., Ohdo S., Okamura H., and Shibata S. Adrenergic regulation of clock gene expression in mouse liver. Proc. Natl. Acad. Sci. USA 100 (2003) 6795-6800
27. Moore R.Y. Development of the suprachiasmatic nucleus. In: Klein D.C., Moore R.J., and Reppert S.M. (Eds). Suprachiasmatic Nucleus: The Mind's Clock (1991), Oxford University Press, New York 197-216
28. Sládek M., Sumová A., Kováčiková Z., Bendová Z., Laurinová K., and Illnerová H. Insight into molecular core clock mechanism of embryonic and early postnatal rat suprachiasmatic nucleus. Proc. Natl. Acad. Sci. USA 101 (2004) 6231-6236
29. Kováčiková Z., Sládek M., Bendová Z., Illnerová H., and Sumová A. Expression of clock and clock-driven genes in the rat suprachiasmatic nucleus during late fetal and early postnatal development. J. Biol. Rhythms (2006)
30. Ohta H., Honma S., Abe H., and Honma K. Effects of nursing mothers on rPer1 and rPer2 circadian expressions in the neonatal rat suprachiasmatic nuclei vary with developmental stage. Eur. J. Neurosci. 15 (2002) 1953-1960
31. Ohta H., Honma S., Abe H., and Honma K. Periodic absence of nursing mothers phase-shifts circadian rhythms of clock genes in the suprachiasmatic nucleus of rat pups. Eur. J. Neurosci. 17 (2003) 1628-1634
32. Li X., and Davis F.C. Developmental expression of clock genes in the Syrian hamster. Dev. Brain Res. 158 (2005) 31-40
33. Reppert S.M., and Uhl G.R. Vasopressin messenger ribonucleic acid in supraoptic and suprachiasmatic nuclei: appearance and circadian regulation during development. Endocrinology 120 (1987) 2483-2487
34. Shibata S., and Moore R.Y. Development of neuronal activity in the rat suprachiasmatic nucleus. Brain Res. 431 (1987) 311-315
35. Reppert S.M., and Schwartz W.J. The suprachiasmatic nuclei of the fetal rat: characterization of a functional circadian clock using 14C-labeled deoxyglucose. J. Neurosci. 4 (1984) 1677-1682
36. Sakamoto K., Oishi K., Nagase T., Miyazaki K., and Ishida N. Circadian expression of clock genes during ontogeny in the rat heart. Neuroreport 13 (2002) 1239-1242
37. Shimomura H., Moriya T., Sudo M., Wakamatsu H., Akiyama M., Miyake Y., and Shibata S. Differential daily expression of Per1 and Per2 mRNA in the suprachiasmatic nucleus of fetal and early postnatal mice. Eur. J. Neurosci. 13 (2001) 687-693
38. Weaver D.R., and Reppert S.M. Direct in utero perception of light by the mammalian fetus. Dev. Brain Res. 47 (1989) 151-155
39. Reppert S.M., and Schwartz W.J. Maternal suprachiasmatic nuclei are necessary for maternal coordination of the developing circadian system. J. Neurosci. 6 (1986) 2724-2729
40. Weinert D. Ontogenetic development of the mammalian circadian system. Chronobiol. Int. 22 (2005) 179-205
41. Davis F.C., and Gorski R.A. Development of hamster circadian rhythms: role of the maternal suprachiasmatic nucleus. J. Comp. Physiol. [A] 162 (1988) 601-610
42. Honma S., Honma K.I., Shirakawa T., and Hiroshige T. Effects of elimination of maternal circadian rhythms during pregnancy on the postnatal development of circadian corticosterone rhythm in blinded infantile rats. Endocrinology 114 (1984) 44-50
43. Kováčiková Z., Sládek M., Laurinová K., Bendová Z., Illnerová H., and Sumová A. Ontogenesis of photoperiodic entrainment of the molecular core clockwork in the rat suprachiasmatic nucleus. Brain Res. 1064 (2005) 83-89
44. Bendová Z., Sumová A., and Illnerová H. Development of circadian rhythmicity and photoperiodic response in subdivisions of the rat suprachiasmatic nucleus. Dev. Brain Res. 148 (2004) 105-112
45. Balsalobre A., Damiola F., and Schibler U. A serum shock induces circadian gene expression in mammalian tissue culture cells. Cell 93 (1998) 929-937
46. Viswanathan N., Weaver D.R., Reppert S.M., and Davis F.C. Entrainment of the fetal hamster circadian pacemaker by prenatal injections of the dopamine agonist SKF 38393. J. Neurosci. 14 (1994) 5393-5398
47. Weaver D.R., Rivkees S.A., and Reppert S.M. D1-dopamine receptors activate c-fos expression in the fetal suprachiasmatic nuclei. Proc. Natl. Acad. Sci. USA 89 (1992) 9201-9204
48. Weaver D.R., and Reppert S.M. Definition of the developmental transition from dopaminergic to photic regulation of c-fos gene expression in the rat suprachiasmatic nucleus. Mol. Brain Res. 33 (1995) 136-148
49. Takahashi S., Yokota S., Hara R., Kobayashi T., Akiyama M., Moriya T., and Shibata S. Physical and inflammatory stressors elevate circadian clock gene mPer1 mRNA levels in the paraventricular nucleus of the mouse. Endocrinology 142 (2001) 4910-4917
50. Leard L.E., Macdonald E.S., Heller H.C., and Kilduff T.S. Ontogeny of photic-induced c-fos mRNA expression in rat suprachiasmatic nuclei. Neuroreport 5 (1994) 2683-2687
51. Sumová A., Jáč M., Sládek M., Šauman I., and Illnerová H. Clock gene daily profiles and their phase relationship in the rat suprachiasmatic nucleus are affected by photoperiod. J. Biol. Rhythms 18 (2003) 134-144