FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Citation
Depetris-Chauvin, A., Berni, J., Aranovich, E.J., Muraro, N.I., Beckwith, E.J., Ceriani, M.F. (2011). Adult-specific electrical silencing of pacemaker neurons uncouples molecular clock from circadian outputs.  Curr. Biol. 21(21): 1783--1793.
FlyBase ID
FBrf0216659
Publication Type
Research paper
Abstract
Circadian rhythms regulate physiology and behavior through transcriptional feedback loops of clock genes running within specific pacemaker cells. In Drosophila, molecular oscillations in the small ventral lateral neurons (sLNvs) command rhythmic behavior under free-running conditions releasing the neuropeptide PIGMENT DISPERSING FACTOR (PDF) in a circadian fashion. Electrical activity in the sLNvs is also required for behavioral rhythmicity. Yet, how temporal information is transduced into behavior remains unclear.Here we developed a new tool for temporal control of gene expression to obtain adult-restricted electrical silencing of the PDF circuit, which led to reversible behavioral arrhythmicity. Remarkably, PERIOD (PER) oscillations during the silenced phase remained unaltered, indicating that arrhythmicity is a direct consequence of the silenced activity. Accordingly, circadian axonal remodeling and PDF accumulation were severely affected during the silenced phase.Although electrical activity of the sLNvs is not a clock component, it coordinates circuit outputs leading to rhythmic behavior.
Graphical Abstract
Obtained with permission from Cell Press.
PubMed ID
PubMed Central ID
PMC3226771 (PMC) (EuropePMC)
Related Publication(s)
Note

Circadian pacemakers: how clock properties relate to their cellular properties.
Taghert, 2011, Curr. Biol. 21(21): R894--R896 [FBrf0219133]

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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Curr. Biol.
    Title
    Current Biology
    Publication Year
    1991-
    ISBN/ISSN
    0960-9822
    Data From Reference
    Alleles (4)
    Genes (5)
    Natural transposons (1)
    Experimental Tools (1)
    Transgenic Constructs (4)