A short half-life GFP mouse model for analysis of suprachiasmatic nucleus organization

Joseph LeSauter, Lily Yan, Bhavana Vishnubhotla, Jorge E. Quintero, Sandra J. Kuhlman, Douglas G. McMahon, Rae Silver

Research output: Contribution to journalArticlepeer-review

52 Scopus citations

Abstract

Period1 (Per1) is one of several clock genes driving the oscillatory mechanisms that mediate circadian rhythmicity. Per1 mRNA and protein are highly expressed in the suprachiasmatic nuclei, which contain oscillator cells that drive circadian rhythmicity in physiological and behavioral responses. We examined a transgenic mouse in which degradable green fluorescent protein (GFP) is driven by the mPer1 gene promoter. This mouse expresses precise free-running rhythms and characteristic light induced phase shifts. GFP protein (reporting Per1 mRNA) is expressed rhythmically as measured by either fluorescence or immunocytochemistry. In addition the animals show predicted rhythms of Per1 mRNA, PER1 and PER2 proteins. The localization of GFP overlaps with that of Per1 mRNA, PER1 and PER2 proteins. Together, these results suggest that GFP reports rhythmic Per1 expression. A surprising finding is that, at their peak expression time GFP, Per1 mRNA, PER1 and PER2 proteins are absent or not detectable in a subpopulation of SCN cells located in the core region of the nucleus.

Original languageEnglish
Pages (from-to)279-287
Number of pages9
JournalBrain Research
Volume964
Issue number2
DOIs
StatePublished - Feb 28 2003

Bibliographical note

Funding Information:
We are grateful to Dr Michael Lehman for his advice on this manuscript. This study was supported by NIH Grants NS-37919 to RS, MH63341 and EY09256 to DGM.

Keywords

  • Circadian rhythm
  • Green fluorescent protein
  • Period gene
  • Suprachiasmatic nucleus
  • Transgenic

ASJC Scopus subject areas

  • General Neuroscience
  • Molecular Biology
  • Clinical Neurology
  • Developmental Biology

Fingerprint

Dive into the research topics of 'A short half-life GFP mouse model for analysis of suprachiasmatic nucleus organization'. Together they form a unique fingerprint.

Cite this