Literature DB >> 15009158

Resetting the brain clock: time course and localization of mPER1 and mPER2 protein expression in suprachiasmatic nuclei during phase shifts.

Lily Yan1, Rae Silver.   

Abstract

The mechanism whereby brief light pulses reset the mammalian circadian clock involves acute Per gene induction. In a previous study we investigated light-induced expression of mPer1 and mPer2 mRNA in the suprachiasmatic nuclei (SCN), with the aim of understanding the relationship between gene expression and behavioural phase shifts. In the present study, we examine the protein products of mPer1 and mPer2 genes in the core and shell region of SCN for 34 h following a phase-shifting light pulse, in order to further explore the molecular mechanism of photic entrainment. The results indicate that, during the delay zone of the phase response curve, while endogenous levels of mPER1 and mPER2 protein are falling, a light pulse produces an increase in the expression of both proteins. In contrast, during the advance zone of the phase response curve, while levels of endogenous mPER1 and mPER2 proteins are rising, a light pulse results in a further increase in mPER1 but not mPER2 protein. The regional distribution of mPER1 and mPER2 protein in the SCN follows the same pattern as their respective mRNAs, with mPER1 expression in the shell region of SCN correlated with phase advances and mPER2 in the shell region correlated with phase delays.

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Year:  2004        PMID: 15009158      PMCID: PMC3271804          DOI: 10.1111/j.1460-9568.2004.03189.x

Source DB:  PubMed          Journal:  Eur J Neurosci        ISSN: 0953-816X            Impact factor:   3.386


  24 in total

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Authors:  J C Dunlap
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Journal:  Prog Brain Res       Date:  1996       Impact factor: 2.453

Review 5.  Neural regulation of circadian rhythms.

Authors:  B Rusak; I Zucker
Journal:  Physiol Rev       Date:  1979-07       Impact factor: 37.312

6.  The circadian cycle of mPER clock gene products in the suprachiasmatic nucleus of the siberian hamster encodes both daily and seasonal time.

Authors:  B Nuesslein-Hildesheim; J A O'Brien; F J Ebling; E S Maywood; M H Hastings
Journal:  Eur J Neurosci       Date:  2000-08       Impact factor: 3.386

7.  Analysis of clock proteins in mouse SCN demonstrates phylogenetic divergence of the circadian clockwork and resetting mechanisms.

Authors:  M D Field; E S Maywood; J A O'Brien; D R Weaver; S M Reppert; M H Hastings
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8.  Nuclear entry of the circadian regulator mPER1 is controlled by mammalian casein kinase I epsilon.

Authors:  E Vielhaber; E Eide; A Rivers; Z H Gao; D M Virshup
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Journal:  Proc Natl Acad Sci U S A       Date:  1999-10-12       Impact factor: 11.205

10.  Positional syntenic cloning and functional characterization of the mammalian circadian mutation tau.

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Journal:  Science       Date:  2000-04-21       Impact factor: 47.728

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  62 in total

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Review 3.  Exploring spatiotemporal organization of SCN circuits.

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Journal:  Cold Spring Harb Symp Quant Biol       Date:  2007

4.  Hepatic gene expression profiling of 5'-AMP-induced hypometabolism in mice.

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Journal:  Physiol Genomics       Date:  2011-01-11       Impact factor: 3.107

Review 5.  Linking neural activity and molecular oscillations in the SCN.

Authors:  Christopher S Colwell
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7.  Selective Distribution of Retinal Input to Mouse SCN Revealed in Analysis of Sagittal Sections.

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Review 8.  Sex differences in circadian timing systems: implications for disease.

Authors:  Matthew Bailey; Rae Silver
Journal:  Front Neuroendocrinol       Date:  2013-11-25       Impact factor: 8.606

9.  Aging differentially affects the re-entrainment response of central and peripheral circadian oscillators.

Authors:  Michael T Sellix; Jennifer A Evans; Tanya L Leise; Oscar Castanon-Cervantes; DiJon D Hill; Patrick DeLisser; Gene D Block; Michael Menaker; Alec J Davidson
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10.  Gonadectomy reveals sex differences in circadian rhythms and suprachiasmatic nucleus androgen receptors in mice.

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