FB2026_02 , released June 18, 2026
FB2026_02 , released June 18, 2026
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Citation
Joshi, N.S., Sullivan, V.M., Tokamov, S.A., Fehon, R.G. (2026). aPKC and F-actin dynamics promote Hippo pathway polarity in asymmetrically dividing neuroblasts.  Biol. Open 15(3): bio062356.
FlyBase ID
FBrf0264849
Publication Type
Research paper
Abstract
The Hippo signaling pathway is conventionally known to restrict tissue growth in animals. Genetic studies have also shown that loss of Hippo pathway components leads to defects in asymmetric cell division in Drosophila neural stem cells, known as neuroblasts. The hallmark of neuroblast division is the asymmetric localization of aPKC/Bazooka (Par-3)/Par-6 complex, termed the Par complex, to the apical cell cortex. However, the localization of the Hippo pathway components in neuroblasts remains unknown. Here, we report that two key activators of the Hippo pathway, Kibra and Salvador, polarize to the apical cortex of mitotic neuroblasts. We show that apical polarity, via the activity of aPKC, and F-actin dynamics synergize to drive Kibra polarization. Together, these results provide further insights into the relationship between apical polarity and Hippo pathway organization and suggest a possible mechanism by which pathway activity is regulated during neuroblast asymmetric division.
PubMed ID
PubMed Central ID
PMC13035065 (PMC) (EuropePMC)
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    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Biol. Open
    Title
    Biology open
    ISBN/ISSN
    2046-6390
    Data From Reference