A novel protein Moat prevents ectopic epithelial folding by limiting Bazooka/Par3-dependent adherens junctions.

Autor: Gu L; School of Life Sciences, University of Nevada, Las Vegas, NV 89154., Sauceda R; School of Life Sciences, University of Nevada, Las Vegas, NV 89154., Brar J; School of Life Sciences, University of Nevada, Las Vegas, NV 89154., Fessahaye F; School of Life Sciences, University of Nevada, Las Vegas, NV 89154., Joo M; School of Life Sciences, University of Nevada, Las Vegas, NV 89154., Lee J; Department of Molecular Biology, Princeton University, Princeton, NJ 08544., Nguyen J; School of Life Sciences, University of Nevada, Las Vegas, NV 89154., Teng M; School of Life Sciences, University of Nevada, Las Vegas, NV 89154., Weng M; School of Life Sciences, University of Nevada, Las Vegas, NV 89154.
Jazyk: angličtina
Zdroj: Molecular biology of the cell [Mol Biol Cell] 2024 Aug 01; Vol. 35 (8), pp. ar110. Date of Electronic Publication: 2024 Jun 26.
DOI: 10.1091/mbc.E24-04-0177
Abstrakt: Contractile myosin and cell adhesion work together to induce tissue shape changes, but how they are patterned to achieve diverse morphogenetic outcomes remains unclear. Epithelial folding occurs via apical constriction, mediated by apical contractile myosin engaged with adherens junctions, as in Drosophila ventral furrow formation. While it has been shown that a multicellular gradient of myosin contractility determines folding shape, the impact of multicellular patterning of adherens junction levels on tissue folding is unknown. We identified a novel Drosophila gene  moat essential for differential apical constriction and folding behaviors across the ventral epithelium which contains both folding ventral furrow and nonfolding ectodermal anterior midgut (ectoAMG). We show that Moat functions to downregulate polarity-dependent adherens junctions through inhibiting cortical clustering of Bazooka/Par3 proteins. Such downregulation of polarity-dependent junctions is critical for establishing a myosin-dependent pattern of adherens junctions, which in turn mediates differential apical constriction in the ventral epithelium. In  moat  mutants, abnormally high levels of polarity-dependent junctions promote ectopic apical constriction in cells with low-level contractile myosin, resulting in expansion of infolding from ventral furrow to ectoAMG, and flattening of ventral furrow constriction gradient. Our results demonstrate that tissue-scale distribution of adhesion levels patterns apical constriction and establishes morphogenetic boundaries.
Competing Interests: Conflicts of interests: The authors declare no financial conflict of interest.
Databáze: MEDLINE