FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Citation
Sun, Y., Shui, K., Li, Q., Liu, C., Jin, W., Ni, J.Q., Lu, J., Zhang, L. (2025). Upstream open reading frames dynamically modulate CLOCK protein translation to regulate circadian rhythms and sleep.  PLoS Biol. 23(5): e3003173.
FlyBase ID
FBrf0262553
Publication Type
Research paper
Abstract
The circadian rhythm is an evolutionarily conserved mechanism with translational regulation increasingly recognized as pivotal in its modulation. In this study, we found that upstream open reading frames (uORFs) are enriched in Drosophila circadian rhythm genes, with particularly conserved uORFs present in core circadian clock genes. We demonstrate evidence that the uORFs of the core clock gene, Clock (Clk), rhythmically and substantially attenuate CLK protein translation in Drosophila, with pronounced suppression occurring during daylight hours. Eliminating Clk uORFs leads to increased CLK protein levels during the day and results in a shortened circadian cycle, along with a broad shift in clock gene expression rhythms. Notably, Clk uORF deletion also augments morning sleep by reducing dopaminergic activity. Beyond daily circadian adjustments, Clk uORFs play a role in modulating sleep patterns in response to seasonal daylight variations. Furthermore, the Clk uORFs act as an important regulator to shape the rhythmic expression of a vast array of genes and influence multifaceted physiological outcomes. Collectively, our research sheds light on the intricate ways uORFs dynamically adjust downstream coding sequences to acclimate to environmental shifts.
PubMed ID
PubMed Central ID
PMC12121920 (PMC) (EuropePMC)
Related Publication(s)
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Assignment of cell line based on information provided by the author in the Fast Track Your Paper tool.
FlyBase Curators, 2020-, Assignment of cell line based on information provided by the author in the Fast Track Your Paper tool. [FBrf0247694]

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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    PLoS Biol.
    Title
    PLoS Biology
    Publication Year
    2003-
    ISBN/ISSN
    1545-7885 1544-9173
    Data From Reference
    Alleles (5)
    Chemicals (1)
    Genes (4)
    Cell Lines (2)