FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Citation
Jia, M., Shan, Z., Yang, Y., Liu, C., Li, J., Luo, Z.G., Zhang, M., Cai, Y., Wen, W., Wang, W. (2015). The structural basis of Miranda-mediated Staufen localization during Drosophila neuroblast asymmetric division.  Nat. Commun. 6(): 8381.
FlyBase ID
FBrf0229741
Publication Type
Research paper
Abstract
During the asymmetric division of Drosophila neuroblasts (NBs), the scaffold Miranda (Mira) coordinates the subcellular distribution of cell-fate determinants including Staufen (Stau) and segregates them into the ganglion mother cells (GMCs). Here we show the fifth double-stranded RNA (dsRNA)-binding domain (dsRBD5) of Stau is necessary and sufficient for binding to a coiled-coil region of Mira cargo-binding domain (CBD). The crystal structure of Mira514-595/Stau dsRBD5 complex illustrates that Mira forms an elongated parallel coiled-coil dimer, and two dsRBD5 symmetrically bind to the Mira dimer through their exposed β-sheet faces, revealing a previously unrecognized protein interaction mode for dsRBDs. We further demonstrate that the Mira-Stau dsRBD5 interaction is responsible for the asymmetric localization of Stau during Drosophila NB asymmetric divisions. Finally, we find the CBD-mediated dimer assembly is likely a common requirement for Mira to recognize and translocate other cargos including brain tumour (Brat).
PubMed ID
PubMed Central ID
PMC4600727 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Nat. Commun.
    Title
    Nature communications
    ISBN/ISSN
    2041-1723
    Data From Reference
    Alleles (5)
    Genes (7)
    Physical Interactions (7)
    Natural transposons (1)
    Experimental Tools (2)
    Transgenic Constructs (5)