Differential Regulation of Circadian Pacemaker Output by Separate Clock Genes in Drosophila

Regulation of the Drosophila pigment-dispersing factor (pdf) gene products was analyzed in wild-type and clock mutants. Mutations in the transcription factors CLOCK and CYCLE severely diminish pdf RNA and neuropeptide (PDF) levels in a single cluster of clock-gene-expressing brain cells, called smal...

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Published inProceedings of the National Academy of Sciences - PNAS Vol. 97; no. 7; pp. 3608 - 3613
Main Authors Park, Jae H., Helfrich-Forster, Charlotte, Lee, Gyunghee, Liu, Li, Rosbash, Michael, Hall, Jeffrey C.
Format Journal Article
LanguageEnglish
Published United States National Academy of Sciences of the United States of America 28.03.2000
National Acad Sciences
National Academy of Sciences
The National Academy of Sciences
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Summary:Regulation of the Drosophila pigment-dispersing factor (pdf) gene products was analyzed in wild-type and clock mutants. Mutations in the transcription factors CLOCK and CYCLE severely diminish pdf RNA and neuropeptide (PDF) levels in a single cluster of clock-gene-expressing brain cells, called small ventrolateral neurons (s-LNvS). This clock-gene regulation of specific cells does not operate through an E-box found within pdf regulatory sequences. PDF immunoreactivity exhibits daily cycling, but only within terminals of axons projecting from the s-LNvS. This posttranslational rhythm is eliminated by period or timeless null mutations, which do not affect PDF staining in cell bodies or pdf mRNA levels. Therefore, within these chronobiologically important neurons, separate elements of the central pacemaking machinery regulate pdf or its product in novel and different ways. Coupled with contemporary results showing a pdf-null mutant to be severely defective in its behavioral rhythmicity, the present results reveal PDF as an important circadian mediator whose expression and function are downstream of the clockworks.
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Communicated by Bruce S. Baker, Stanford University, Stanford, CA
To whom reprint requests should be addressed at: Department of Biology, MS-008, Brandeis University, Waltham, MA 02454-9110. E-mail: hall@brandeis.edu.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.070036197