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Starting the zebrafish pineal circadian clock with a single photic transition

  • Robin Vuilleumier
  • , Laurence Besseau
  • , Gilles Boeuf
  • , Aurélien Piparelli
  • , Yoav Gothilf
  • , Walter G. Gehring
  • , David C. Klein
  • , Jack Falcón*
  • *Corresponding author for this work
  • University Pierre and Marie Curie
  • University of Basel
  • National Institutes of Health

Research output: Contribution to journalArticlepeer-review

63 Scopus citations

Abstract

The issue of what starts the circadian clock ticking was addressed by studying the developmental appearance of the daily rhythm in the expression of two genes in the zebrafish pineal gland that are part of the circadian clock system. One encodes the photopigment exorhodopsin and the other the melatonin synthesizing enzyme arylalkylamine N-acetyltransferase (AANAT2). Significant daily rhythms in AANAT2 mRNA abundance were detectable for several days after fertilization in animals maintained in a normal or reversed lighting cycle providing 12 h of light and 12 h of dark. In contrast, these rhythms do not develop if animals are maintained in constant lighting or constant darkness from fertilization. In contrast to exorhodopsin, rhythmicity of AANAT2 can be initiated by a pulse of light against a background of constant darkness, by a pulse of darkness against a background of constant lighting, or by single light-to-dark or dark-to-light transitions. Accordingly, these studies indicate that circadian clock function in the zebrafish pineal gland can be initiated by minimal photic cues, and that single photic transitions can be used as an experimental tool to dissect the mechanism that starts the circadian clock in the pineal gland.

Original languageEnglish
Pages (from-to)2273-2279
Number of pages7
JournalEndocrinology
Volume147
Issue number5
DOIs
StatePublished - May 2006

Funding

FundersFunder number
Eunice Kennedy Shriver National Institute of Child Health and Human DevelopmentZIAHD008837

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