FB2026_02 , released June 18, 2026
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Citation
Hua, Y., Zhu, Y., Hu, Y., Kong, F., Duan, R., Zhang, C., Zhang, C., Zhang, S., Jin, Y., Ye, Y., Cai, Q., Ji, S. (2022). A Feedback Regulatory Loop Involving dTrbd/dTak1 in Controlling IMD Signaling in Drosophila Melanogaster.  Front. Immunol. 13(): 932268.
FlyBase ID
FBrf0254147
Publication Type
Research paper
Abstract
Negative regulators of the inflammatory responses are essential for the maintenance of immune homeostasis and organismal fitness. In Drosophila, the deubiquitinase (Dub) dTrbd selectively restricts the K63-linked ubiquitination modification of dTak1, a pivotal kinase of the IMD signaling pathway, to regulate the IMD innate immune response. However, which domain and how it functions to enable dTrbd's activity remain unexplored. Here, we provide compelling evidence showing that the NZF domain of dTrbd is essential for its association with dTak1. Meanwhile, the Linker region of dTrbd is involved in modulating its condensation, a functional state representing the Dub enzymatical activity of dTrbd. Of interest, the activated IMD signals following bacterial stimuli enhance the dTrbd/dTak1 interaction, as well as the condensate assembly and Dub enzymatical activity of dTrbd. Collectively, our studies shed light on the dual mechanisms by which the IMD signaling-mediated feedback loop of dTrbd/dTak1 precisely regulates the innate immune response in Drosophila.
PubMed ID
PubMed Central ID
PMC9329959 (PMC) (EuropePMC)
Related Publication(s)
Erratum

Corrigendum: A feedback regulatory loop involving dTrbd/dTak1 in controlling IMD signaling in Drosophila Melanogaster.
Hua et al., 2022, Front. Immunol. 13: 993987 [FBrf0254297]

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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Front. Immunol.
    Title
    Frontiers in immunology
    ISBN/ISSN
    1664-3224
    Data From Reference
    Alleles (7)
    Gene Groups (2)
    Genes (8)
    Physical Interactions (4)
    Cell Lines (1)
    Natural transposons (1)
    Insertions (2)
    Experimental Tools (2)
    Transgenic Constructs (4)