Abstract
The hypothalamic suprachiasmatic nucleus is the site of an endogenous circadian clock synchronized by daily light-dark cycles. At some daily phases, light exposure both shifts the clock and alters the expression of several immediate-early genes in cells of the suprachiasmatic nucleus. We have studied both spontaneous circadian and light-induced expression of several immediate-early gene messenger RNAs and proteins in hamsters in constant darkness or in response to brief light exposure. There was no detectable spontaneous expression of NGFI-A messenger RNA in suprachiasmatic nucleus cells at any circadian phase, but light pulses induced its expression selectively during the subjective night, with highest levels of expression 6 h into the night. We also found that there are two independent rhythms of expression of junB messenger RNA and JunB protein, as well as c-fos messenger RNA and c-Fos protein, in the suprachiasmatic nucleus of hamsters: a rhythm of photic sensitivity expressed throughout the night and a spontaneous rhythm of expression triggered around dawn. Induction of NGFI-A messenger RNA and c- fos messenger RNA and c-Fos protein in response to a light pulse were found throughout the suprachiasmatic nucleus, with the highest levels of expression in the ventrolateral subdivision; however, the spontaneous expression of JunB and c-Fos proteins was confined mainly to the dorsomedial suprachiasmatic nucleus. The temporal and anatomical differences in the expression of these immediate-early genes in the mammalian suprachiasmatic nucleus suggest that their protein products may be involved in different signaling mechanisms mediating either photic entrainment or endogenous oscillations within distinct subpopulations of suprachiasmatic nucleus cells.
Original language | English |
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Pages (from-to) | 555-571 |
Number of pages | 17 |
Journal | Neuroscience |
Volume | 90 |
Issue number | 2 |
DOIs | |
Publication status | Published - Feb 22 1999 |
Bibliographical note
Funding Information:We are grateful to Victoria Muise, Kay Murphy, Katie Gilchrist, Tanya Myers, Heather Grant, Brenda Ross and Marc Peterson for their excellent technical assistance, to Dr Rodrigo Bravo for his gift of the JunB antibody, and to two anonymous referees for their helpful comments. This work was supported by grants from the Medical Research Council of Canada (MA8929; MT10644) and a postdoctoral fellowship (M.E.G.) from CONICET of Argentina.
ASJC Scopus Subject Areas
- General Neuroscience
PubMed: MeSH publication types
- Journal Article
- Research Support, Non-U.S. Gov't