FB2025_01 , released February 20, 2025
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Citation
Lavalou, J., Mao, Q., Harmansa, S., Kerridge, S., Lellouch, A.C., Philippe, J.M., Audebert, S., Camoin, L., Lecuit, T. (2021). Formation of polarized contractile interfaces by self-organized Toll-8/Cirl GPCR asymmetry.  Dev. Cell 56(11): 1574--1588.e7.
FlyBase ID
FBrf0249144
Publication Type
Research paper
Abstract
Interfaces between cells with distinct genetic identities elicit signals to organize local cell behaviors driving tissue morphogenesis. The Drosophila embryonic axis extension requires planar polarized enrichment of myosin-II powering oriented cell intercalations. Myosin-II levels are quantitatively controlled by GPCR signaling, whereas myosin-II polarity requires patterned expression of several Toll receptors. How Toll receptors polarize myosin-II and how this involves GPCRs remain unknown. Here, we report that differential expression of a single Toll receptor, Toll-8, polarizes myosin-II through binding to the adhesion GPCR Cirl/latrophilin. Asymmetric expression of Cirl is sufficient to enrich myosin-II, and Cirl localization is asymmetric at Toll-8 expression boundaries. Exploring the process dynamically, we reveal that Toll-8 and Cirl exhibit mutually dependent planar polarity in response to quantitative differences in Toll-8 expression between neighboring cells. Collectively, we propose that the cell surface protein complex Toll-8/Cirl self-organizes to generate local asymmetric interfaces essential for planar polarization of contractility.
PubMed ID
PubMed Central ID
PMC8207821 (PMC) (EuropePMC)
Related Publication(s)
Note

For whom the cell tolls.
Noordstra and Yap, 2021, Dev. Cell 56(11): 1555--1557 [FBrf0249220]

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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Dev. Cell
    Title
    Developmental Cell
    Publication Year
    2001-
    ISBN/ISSN
    1534-5807 1878-1551
    Data From Reference
    Alleles (25)
    Genes (8)
    Physical Interactions (1)
    Natural transposons (2)
    Insertions (21)
    Experimental Tools (6)
    Transgenic Constructs (19)