FB2026_03 , released September 17, 2026
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Zhao, A., Varady, S., O'Kelley-Bangsberg, M., Deng, V., Platenkamp, A., Wijngaard, P., Bern, M., Gormley, W., Kushkowski, E., Thompson, K., Tibbetts, L., Conner, A.T., Noeckel, D., Teran, A., Ritz, A., Applewhite, D.A. (2023). From network analysis to experimental validation: identification of regulators of non-muscle myosin II contractility using the folded-gastrulation signaling pathway.  BMC Mol Cell Biol 24(1): 32.
FlyBase ID
FBrf0257815
Publication Type
Research paper
Abstract
The morphogenetic process of apical constriction, which relies on non-muscle myosin II (NMII) generated constriction of apical domains of epithelial cells, is key to the development of complex cellular patterns. Apical constriction occurs in almost all multicellular organisms, but one of the most well-characterized systems is the Folded-gastrulation (Fog)-induced apical constriction that occurs in Drosophila. The binding of Fog to its cognizant receptors Mist/Smog results in a signaling cascade that leads to the activation of NMII-generated contractility. Despite our knowledge of key molecular players involved in Fog signaling, we sought to explore whether other proteins have an undiscovered role in its regulation. We developed a computational method to predict unidentified candidate NMII regulators using a network of pairwise protein-protein interactions called an interactome. We first constructed a Drosophila interactome of over 500,000 protein-protein interactions from several databases that curate high-throughput experiments. Next, we implemented several graph-based algorithms that predicted 14 proteins potentially involved in Fog signaling. To test these candidates, we used RNAi depletion in combination with a cellular contractility assay in Drosophila S2R + cells, which respond to Fog by contracting in a stereotypical manner. Of the candidates we screened using this assay, two proteins, the serine/threonine phosphatase Flapwing and the putative guanylate kinase CG11811 were demonstrated to inhibit cellular contractility when depleted, suggestive of their roles as novel regulators of the Fog pathway.
PubMed ID
PubMed Central ID
PMC10568788 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    BMC Mol Cell Biol
    Title
    BMC molecular and cell biology
    ISBN/ISSN
    2661-8850
    Data From Reference
    Genes (19)
    Cell Lines (1)