The role of Clock in the plasticity of circadian entrainment

Biochemical and Biophysical Research Communications

Volumn 318, Issue 4, 2004, Pages 893-898

  Udo, Ryuta ^a   Hamada, Toshiyuki ^b   Horikawa, Kazumasa ^a   Iwahana, Eiko ^a   Miyakawa, Kazuko ^a   Otsuka, Kuniaki ^c   Shibata, Shigenobu ^a  

^a WASEDA UNIVERSITY   (Japan)

^b NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY AIST   (Japan)

^c TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

Author keywords

Body temperature; Circadian rhythm; Clock; Period 1; Period 2; Suprachiasmatic nucleus

Indexed keywords

TRANSCRIPTION FACTOR CLOCK;

ANIMAL EXPERIMENT; ARTICLE; CIRCADIAN RHYTHM; CONTROLLED STUDY; ENVIRONMENTAL FACTOR; LIGHT DARK CYCLE; MALE; MOUSE; NONHUMAN; OSCILLATION; PLASTICITY; PRIORITY JOURNAL; PROTEIN EXPRESSION; SUPRACHIASMATIC NUCLEUS; WILD TYPE;

ANIMALS; BODY TEMPERATURE; CELL CYCLE PROTEINS; CIRCADIAN RHYTHM; DARKNESS; GENE EXPRESSION; GENOTYPE; LIGHT; MALE; MICE; MICE, MUTANT STRAINS; MOTOR ACTIVITY; MUTATION; NUCLEAR PROTEINS; RNA, MESSENGER; SUPRACHIASMATIC NUCLEUS; TRANS-ACTIVATORS; TRANSCRIPTION FACTORS;

MAMMALIA;

EID: 2442607830     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbrc.2004.04.113     Document Type: Article

References (22)

1. Ashoff J. Handbook of behavioral neurobiology. Biological Rhythms. vol. 4:1981;Plenum Press, New York
2. Kriegsfeld L.J., LeSauter J., Hamada T., Pitts S.M., Silver R. Circadian rhythms in the endocrine system. Pfaff D., Etgen A. Hormones, Brain and Behavior. 2002;33-91 Academic Press, NY
3. Ashoff J. Circadian system properties. Obal F., Benedek G. Advances in Physiological Sciences-Environmental Physiology. vol. 18:1981;1-17 Akademiai Kiado, Budapest
4. Vitaterna M.H., King D.P., Chang A.M., Kornhauser J.M., Lowrey P.L., McDonald J.D., Dove W.F., Pinto L.H., Turek F.W., Takahashi J.S. Mutagenesis and mapping of a mouse gene, Clock, essential for circadian behavior. Science. 264:1994;719-725
5. Nakamura W., Honma S., Shirakawa T., Honma K. Clock mutation lengthens the circadian period without damping rhythms in individual SCN neurons. Nat. Neurosci. 5:2002;399-400
6. Herzog E.D., Takahashi J.S., Block G.D. Clock controls circadian period in isolated suprachiasmatic nucleus neurons. Nat. Neurosci. 1:1998;708-713
7. Low-Zeddies S.S., Takahashi J.S. Chimera analysis of the Clock mutation in mice shows that complex cellular integration determines circadian behavior. Cell. 105:2001;25-42
8. Sokolove P.G., Bushell W.N. The chi square periodogram: its utility for analysis of circadian rhythms. J. Theor. Biol. 72:1978;131-160
9. Ohtomo N., Terachi S., Tanaka Y., Tokiwano K., Kaneko N. New method of time series analysis and its application to Wolf's sunspot number data. Jpn. J. Appl. Phys. 33:1994;2821-2831
10. Horikawa K., Yokota S., Fuji K., Akiyama M., Moriya T., Okamura H., Shibata S. Nonphotic entrainment by 5-HT1A/7 receptor agonists accompanied by reduced Per1 and Per2 mRNA levels in the suprachiasmatic nuclei. J. Neurosci. 20:2000;5867-5873
11. Akiyama M., Kouzu Y., Takahashi S., Wakamatsu H., Moriya T., Maetani M., Watanabe S., Tei H., Sakaki Y., Shibata S. Inhibition of light- or glutamate-induced mPer1 expression represses the phase shifts into the mouse circadian locomotor and suprachiasmatic firing rhythms. J. Neurosci. 19:1999;1115-1121
12. Shigeyoshi Y., Taguchi K., Yamamoto S., Takekida S., Yan L., Tei H., Moriya T., Shibata S., Loros J.J., Dunlap J.C., Okamura H. Light-induced resetting of a mammalian circadian clock is associated with rapid induction of the mPer1 transcript. Cell. 91:1997;1043-1053
13. Shearman L.P., Weaver D.R. Photic induction of period gene expression is reduced in clock mutant mice. Neuroreport. 10:1999;613-618
14. Zheng B., Larkin D.W., Albrecht U., Sun Z.S., Sage M., Eichele G., Lee C.C., Bradley A. The mPer2 gene encodes a functional component of the mammalian circadian clock. Nature. 400:1999;169-173
15. Moore R.Y., Silver R. Suprachiasmatic nucleus organization. Chronobiol. Int. 15:1998;475-487
16. Hamada T., LeSauter J., Venuti J.M., Silver R. Expression of Period genes: rhythmic and nonrhythmic compartments of the suprachiasmatic nucleus pacemaker. J. Neurosci. 21:2001;7742-7750
17. LeSauter J., Yan L., Vishnubhotla B., Quintero J.E., Kuhlman S.J., McMahon D.G., Silver R. A short half-life GFP mouse model for analysis of suprachiasmatic nucleus organization. Brain Res. 964:2003;279-287
18. Hamada T., LeSauter J., Lokshin M., Romero M.T., Yan L., Venuti J.M., Silver R. Calbindin influences response to photic input in suprachiasmatic nucleus. J. Neurosci. 23:2003;8820-8826
19. Karatsoreos I.N., Yan L., LeSauter J., Silver R. Phenotype matters: identification of light-responsive cells in the mouse suprachiasmatic nucleus. J. Neurosci. 24:2004;68-75
20. Nakamura W., Honma S., Shirakawa T., Honma K. Regional pacemakers composed of multiple oscillator neurons in the rat suprachiasmatic nucleus. Eur. J. Neurosci. 14:2001;666-674
21. Jobst E.E, Allen C.N. Calbindin neurons in the hamster suprachiasmatic nucleus do not exhibit a circadian variation in spontaneous firing rate. Eur. J. Neurosci. 16:2002;2469-2474
22. Oishi K., Miyazaki K., Ishida N. Functional CLOCK is not involved in the entrainment of peripheral clocks to the restricted feeding: entrainable expression of mPer2 and BMAL1 mRNAs in the heart of Clock mutant mice on Jcl:ICR background. Biochem. Biophys. Res. Commun. 298:2002;198-202