Differential expressions of mPer1 and mPer2 mRNAs under a skeleton photoperiod and a complete light-dark cycle

Molecular Brain Research

Volumn 109, Issue 1-2, 2002, Pages 11-17

  Oishi, Katsutaka ^a   Fukui, Hiromi ^a   Sakamoto, Katsuhiko ^a   Miyazaki, Koyomi ^a   Kobayashi, Hisato ^a,b   Ishida, Norio ^a,c,d  

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

^b IBARAKI UNIVERSITY   (Japan)

^c TOKYO INSTITUTE OF TECHNOLOGY   (Japan)

^d TOHOKU UNIVERSITY   (Japan)

Author keywords

Circadian rhythm; Mouse; Period homologues; Skeleton photoperiod; Suprachiasmatic nucleus

Indexed keywords

MESSENGER RNA; PER1 PROTEIN; PER2 PROTEIN; PROTEIN DERIVATIVE; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CIRCADIAN RHYTHM; CONTROLLED STUDY; ILLUMINATION; LIGHT DARK CYCLE; MALE; MOLECULAR MECHANICS; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PHOTOSTIMULATION; PRIORITY JOURNAL; PROTEIN DETERMINATION; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; REGULATORY MECHANISM; SKIN; SUPRACHIASMATIC NUCLEUS; TISSUE DISTRIBUTION;

ANIMALS; BEHAVIOR, ANIMAL; CELL CYCLE PROTEINS; CIRCADIAN RHYTHM; DARKNESS; GENE EXPRESSION REGULATION; LIGHT; MALE; MICE; NUCLEAR PROTEINS; PHOTOPERIOD; SKIN; SUPRACHIASMATIC NUCLEUS; TRANSCRIPTION FACTORS;

EID: 0037203292     PISSN: 0169328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0169-328X(02)00457-6     Document Type: Article

References (35)

1. Balsalobre A., Marcacci L., Schibler U. Multiple signaling pathways elicit circadian gene expression in cultured Rat-1 fibroblasts. Curr. Biol. 10:2000;1291-1294.
2. Bae K., Jin X., Maywood E.S., Hastings M.H., Reppert S.M., Weaver D.R. Differential functions of mPer1, mPer2, and mPer3 in the SCN circadian clock. Neuron. 30:2001;525-536.
3. Brinkhof M.W.G., Daan S., Strubbe J.H. Forced dissociation of food- and light-entrainable circadian rhythms of rats in a skeleton photoperiod. Physiol. Behav. 65:1998;225-231.
4. Cermakian N., Monaco L., Pando M.P., Dierich A., Sassone-Corsi P. Altered behavioral rhythms and clock gene expression in mice with a targeted mutation in the Period1 gene. EMBO J. 20:2001;3967-3974.
5. DeCoursey P.J. LD ratios and the entrainment of circadian activity in a nocturnal and diurnal rodent. J. Comp. Physiol. 78:1972;221-235.
6. Drucker-Colín R., Aguilar-Roblero R., García-Hernández F., Fernández-Cancino F., Rattoni F.B. Fetal suprachiasmatic nucleus transplants: diurnal rhythm recovery of lesioned rats. Brain Res. 311:1984;353-357.
7. Dunlap J.C. Molecular bases for circadian clocks. Cell. 96:1999;271-290.
8. Earnest D.J., Liang F.-Q., Ratcliff M., Cassone V.M. Immortal time: circadian clock properties of rat suprachiasmatic cell lines. Science. 283:1999;693-695.
9. Edelstein K., Amir S. The role of the intergeniculate leaflet in entrainment of circadian rhythms to a skeleton photoperiod. J. Neurosci. 19:1999;372-380.
10. Gekakis N., Staknis D., Nguyen H.B., Davis F.C., Wilsbacher L.D., King D.P., Takahashi J.S., Weitz C.J. Role of the CLOCK protein in the mammalian circadian mechanism. Science. 280:1998;1564-1569.
11. Gillette M.U., Tischkau S.A. Suprachiasmatic nucleus: the brain's circadian clock. Recent Prog. Horm. Res. 54:1999;33-58.
12. Ishida N. A DIG in situ hybridization method for newcomers. Part 1. Preparation of DIG-labeled probes. Neurosci. Prot. 1:1996;1-9.
13. Ishida N., Kaneko M., Allada R. Biological clocks. Proc. Natl. Acad. Sci. USA. 96:1999;8819-8820.
14. Jin X., Shearman L.P., Weaver D.R., Zylka M.J., De Vries G.J., Reppert S.M. A molecular mechanism regulating rhythmic output from the suprachiasmatic circadian clock. Cell. 96:1999;57-68.
15. Lopez-Molina L., Conquet F., Dubois-Dauphin M., Schibler U. The DBP gene is expressed according to a circadian rhythm in the suprachiasmatic nucleus and influences circadian behavior. EMBO J. 16:1997;6762-6771.
16. Matsui M., Mitsui Y., Ishida N. A DIG in situ hybridization method for newcomers. Part 2. Application of the method to paraffin brain sections. Neurosci. Prot. 2:1996;1-13.
17. Messager S., Ross A.W., Barrett P., Morgan P.J. Decoding photoperiodic time through Per1 and ICER gene amplitude. Proc. Natl. Acad. Sci. USA. 96:1999;9938-9943.
18. Oishi K., Fukui H., 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.
19. Oishi K., Sakamoto K., Okada T., Nagase T., Ishida N. Humoral signals mediate the circadian expression of rat period homologue (rPer2) mRNA in peripheral tissues. Neurosci. Lett. 256:1998;117-119.
20. Pittendrigh C.S., Dann S. A functional analysis of circadian pacemakers in nocturnal rodents. IV. Entrainment: pacemaker as clock. J. Comp. Physiol. 106:1976;291-331.
21. Pittendrigh C.S., Minis D.H. The entrainment of circadian oscillations by light and their role as photoperiodic clocks. Am. Nat. 98:1964;261-294.
22. Rosenwasser A.M., Boulos Z., Terman M. Circadian feeding and drinking rhythms in the rat under complete and skeleton photoperiods. Physiol. Behav. 30:1983;353-359.
23. Sakamoto K. Photoperiod differentially affects the expression of three mPer genes in the mouse heart. Biol. Rhythm Res. 33:2002;75-81.
24. Sakamoto K., Ishida N. Circadian expression of serotonin N-acetyltransferase mRNA in the rat retina. Neurosci. Lett. 245:1998;113-116.
25. Sakamoto K., Ishida N. Light-induced phase-shifts in the circadian expression rhythm of mammalian Period genes in the mouse heart. Eur. J. Neurosci. 12:2000;4003-4006.
26. Sakamoto K., Nagase T., Fukui H., Horikawa K., Okada T., Tanaka H., Sato K., Miyake Y., Ohara O., Kako K., Ishida N. Multitissue circadian expression of rat period homolog (rPer2) mRNA is governed by the mammalian circadian clock, the suprachiasmatic nucleus in the brain. J. Biol. Chem. 273:1998;27039-27042.
27. Schwartz W.J., Peters R.V., Aronin N., Bennett M.R. Unexpected c-fos gene expression in the suprachiasmatic nucleus of mice entrained to a skeleton photoperiod. J. Biol. Rhythms. 11:1996;35-44.
28. Shearman L.P., Jin X., Lee C., Reppert S.M., Weaver D.R. Targeted disruption of the mPer3 gene: subtle effects on circadian clock function. Mol. Cell. Biol. 20:2000;6269-6275.
29. 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 mammalian circadian clock is associated with rapid induction of the mPer1 transcript. Cell. 91:1997;1043-1053.
30. Silver R., LeSauter J., Tresco P.A., Lehman M.N. A diffusible coupling signal from the transplanted suprachiasmatic nucleus controlling circadian locomotor rhythms. Nature. 382:1996;810-813.
31. Tamaru T., Isojima Y., Yamada T., Okada M., Nagai K., Takamatsu K. Light and glutamate-induced degradation of the circadian oscillating protein BMAL1 during the mammalian clock resetting. J. Neurosci. 20:2000;7525-7530.
32. van Esseveldt K.E., Lehman M.N., Boer G.J. The suprachiasmatic nucleus and the circadian time-keeping system revisited. Brain Res. Rev. 33:2000;34-77.
33. Zanello S.B., Jackson D.M., Holick M.F. Expression of the circadian clock genes clock and period1 in human skin. J. Invest. Dermatol. 115:2000;757-760.
34. Zheng B., Albrecht U., Kaasik K., Sage M., Lu W., Vaishnav S., Li Q., Sun Z.S., Eichele G., Bradley A., Lee C.C. Nonredundant roles of the mPer1 and mPer2 genes in the mammalian circadian clock. Cell. 105:2001;683-694.
35. 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.