Circadian regulation of cAMP response element-mediated gene expression in the suprachiasmatic nuclei

J Biol Chem. 1999 Jun 18;274(25):17748-56. doi: 10.1074/jbc.274.25.17748.

Abstract

A program of stringently-regulated gene expression is thought to be a fundamental component of the circadian clock. Although recent work has implicated a role for E-box-dependent transcription in circadian rhythmicity, the contribution of other enhancer elements has yet to be assessed. Here, we report that cells of the suprachiasmatic nuclei (SCN) exhibit a prominent circadian oscillation in cAMP response element (CRE)-mediated gene expression. Maximal reporter gene expression occurred from late-subjective night to mid-subjective day. Cycling of CRE-dependent transcription was not observed in other brain regions, including the supraoptic nucleus and piriform cortex. Levels of the phospho-active form of the transcription factor CREB (P-CREB) varied as a function of circadian time. Peak P-CREB levels occurred during the mid- to late-subjective night. Furthermore, photic stimulation during the subjective night, but not during the subjective day, triggered a marked increase in CRE-mediated gene expression in the SCN. Reporter gene experiments showed that activation of the p44/42 mitogen-activated protein kinase signaling cascade is required for Ca2+-dependent stimulation of CRE-mediated transcription in the SCN. These findings reveal the CREB/CRE transcriptional pathway to be circadian-regulated within the SCN, and raise the possibility that this pathway provides signaling information essential for normal clock function.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Calcium / pharmacology
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism
  • Circadian Rhythm*
  • Cyclic AMP / genetics*
  • Cyclic AMP / metabolism
  • Cyclic AMP Response Element-Binding Protein / genetics
  • Enhancer Elements, Genetic
  • Enzyme Activation
  • Gene Expression Regulation
  • Genes, Reporter
  • Immunohistochemistry
  • Light
  • Mice
  • Mice, Transgenic
  • Mitogen-Activated Protein Kinase 3
  • Mitogen-Activated Protein Kinases*
  • Phosphoproteins / genetics
  • Phosphorylation
  • Signal Transduction
  • Suprachiasmatic Nucleus / metabolism*

Substances

  • Cyclic AMP Response Element-Binding Protein
  • Phosphoproteins
  • Cyclic AMP
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Mitogen-Activated Protein Kinase 3
  • Mitogen-Activated Protein Kinases
  • Calcium