Literature DB >> 19393297

Compartmentalized expression of light-induced clock genes in the suprachiasmatic nucleus of the diurnal grass rat (Arvicanthis niloticus).

C Ramanathan1, A Campbell, A Tomczak, A A Nunez, L Smale, L Yan.   

Abstract

Photic responses of the circadian system are mediated through light-induced clock gene expression in the suprachiasmatic nucleus (SCN). In nocturnal rodents, depending on the timing of light exposure, Per1 and Per2 gene expression shows distinct compartmentalized patterns that correspond to the behavioral responses. Whether the gene- and region-specific induction patterns are unique to nocturnal animals, or are also present in diurnal species is unknown. We explored this question by examining the light-induced Per1 and Per2 gene expression in functionally distinct SCN subregions, using diurnal grass rats Arvicanthis niloticus. Light exposure during nighttime induced Per1 and Per2 expression in the SCN, showing unique spatiotemporal profiles depending on the phase of the light exposure. After a phase delaying light pulse (LP) in the early night, strong Per1 induction was observed in the retinorecipient core region of the SCN, while strong Per2 induction was observed throughout the entire SCN. After a phase advancing LP in the late night, Per1 was first induced in the core and then extended into the whole SCN, accompanied by a weak Per2 induction. This compartmentalized expression pattern is very similar to that observed in nocturnal rodents, suggesting that the same molecular and intercellular pathways underlying acute photic responses are present in both diurnal and nocturnal species. However, after an LP in early subjective day, which induces phase advances in diurnal grass rats, but not in nocturnal rodents, we did not observe any Per1 or Per2 induction in the SCN. This result suggests that in spite of remarkable similarities in the SCN of diurnal and nocturnal rodents, unique mechanisms are involved in mediating the phase shifts of diurnal animals during the subjective day.

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Year:  2009        PMID: 19393297      PMCID: PMC2753486          DOI: 10.1016/j.neuroscience.2009.04.040

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  62 in total

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2.  Expression of Period genes: rhythmic and nonrhythmic compartments of the suprachiasmatic nucleus pacemaker.

Authors:  T Hamada; J LeSauter; J M Venuti; R Silver
Journal:  J Neurosci       Date:  2001-10-01       Impact factor: 6.167

3.  Expression of the Per1 gene in the hamster: brain atlas and circadian characteristics in the suprachiasmatic nucleus.

Authors:  S Yamamoto; Y Shigeyoshi; Y Ishida; T Fukuyama; S Yamaguchi; K Yagita; T Moriya; S Shibata; N Takashima; H Okamura
Journal:  J Comp Neurol       Date:  2001-02-19       Impact factor: 3.215

4.  Phase response curve and light-induced fos expression in the suprachiasmatic nucleus and adjacent hypothalamus of Arvicanthis niloticus.

Authors:  M Mahoney; A Bult; L Smale
Journal:  J Biol Rhythms       Date:  2001-04       Impact factor: 3.182

5.  MPer1 and mper2 are essential for normal resetting of the circadian clock.

Authors:  U Albrecht; B Zheng; D Larkin; Z S Sun; C C Lee
Journal:  J Biol Rhythms       Date:  2001-04       Impact factor: 3.182

6.  Per1 and Per2 gene expression in the rat suprachiasmatic nucleus: circadian profile and the compartment-specific response to light.

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7.  Vasoactive intestinal polypeptide (VIP) phase-shifts the rat suprachiasmatic nucleus clock in vitro.

Authors:  H E Reed; A Meyer-Spasche; D J Cutler; C W Coen; H D Piggins
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8.  Suprachiasmatic nucleus in the mouse: retinal innervation, intrinsic organization and efferent projections.

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9.  Altered behavioral rhythms and clock gene expression in mice with a targeted mutation in the Period1 gene.

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  7 in total

1.  The response of Per1 to light in the suprachiasmatic nucleus of the diurnal degu (Octodon degus).

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Review 3.  Circadian and photic modulation of daily rhythms in diurnal mammals.

Authors:  Lily Yan; Laura Smale; Antonio A Nunez
Journal:  Eur J Neurosci       Date:  2018-10-24       Impact factor: 3.386

4.  Sustained activation of GABAA receptors in the suprachiasmatic nucleus mediates light-induced phase delays of the circadian clock: a novel function of ionotropic receptors.

Authors:  Daniel L Hummer; J Christopher Ehlen; Tony E Larkin; John K McNeill; John R Pamplin; Colton A Walker; Phillip V Walker; Daryl R Dhanraj; H Elliott Albers
Journal:  Eur J Neurosci       Date:  2015-05-12       Impact factor: 3.386

5.  Uncovering the proteome response of the master circadian clock to light using an AutoProteome system.

Authors:  Ruijun Tian; Matias Alvarez-Saavedra; Hai-Ying M Cheng; Daniel Figeys
Journal:  Mol Cell Proteomics       Date:  2011-08-22       Impact factor: 5.911

Review 6.  The dynamics of GABA signaling: Revelations from the circadian pacemaker in the suprachiasmatic nucleus.

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7.  Intrinsic photosensitive retinal ganglion cells in the diurnal rodent, Arvicanthis ansorgei.

Authors:  Diana Karnas; David Hicks; Jérôme Mordel; Paul Pévet; Hilmar Meissl
Journal:  PLoS One       Date:  2013-08-09       Impact factor: 3.240

  7 in total

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