FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Nan, N., Liu, Y., Yan, Z., Zhang, Y., Li, S., Zhang, J., Qin, G., Sang, N. (2025). dilp2-Mediated Insulin Signaling Pathway Was Involved in O3-Induced Multigenerational Effects of Shortened Lifespan in Drosophila melanogasters.  Environ. Sci. Technol. 59(6): 2937--2947.
FlyBase ID
FBrf0261624
Publication Type
Research paper
Abstract
As a long-standing atmospheric pollutant, ozone (O3) exerts enduring effects on biological health. However, experimental research on its impact on organism lifespan and generational effects is limited. This study exposed three generations of fruit flies (Drosophila melanogaster) to O3, revealing a shortened lifespan across generations. Specifically, after O3 exposure, the lifespan of the F2 generation was significantly reduced compared with F0 and F1 generations, indicating a cumulative multigenerational effect. Transcriptome analysis unveiled significant disruptions in metabolic pathways, notably the insulin signaling pathway. Subsequent qRT-PCR analysis showed elevated mRNA levels of insulin pathway-related genes (dilp2, dilp3, dilp5, InR, and TOR), alongside decreased expression levels of FOXO, 4E-BP, and Atg5 in flies exposed to O3. Notably, knocking down dilp2, rather than dilp3, dilp5, and InR, rescued the O3-induced lifespan shortening. Overall, O3 exposure triggered activation of the dilp2-mediated InR-FOXO/TOR-4E-BP-Atg5 signaling pathway, potentially contributing to shortened lifespan with cumulative effects. This study highlights the viability of employing fruit flies as a model to evaluate the multigenerational toxicity of environmental pollutants, particularly atmospheric pollutants.
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    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Environ. Sci. Technol.
    Title
    Environmental Science and Technology
    Publication Year
    1967-
    ISBN/ISSN
    0013-936X
    Data From Reference
    Chemicals (1)
    Genes (8)
    Human Disease Models (1)