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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

Producción científica: Articlerevisión exhaustiva

53 Citas (Scopus)

Resumen

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.

Idioma originalEnglish
Páginas (desde-hasta)279-287
Número de páginas9
PublicaciónBrain Research
Volumen964
N.º2
DOI
EstadoPublished - feb 28 2003

Nota bibliográfica

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.

Financiación

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.

FinanciadoresNúmero del financiador
National Institutes of Health (NIH)MH63341, NS-37919
National Eye Institute (NEI)R01EY009256

    ASJC Scopus subject areas

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

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