Basal spot junctions of Drosophila epithelial tissues respond to morphogenetic forces and regulate Hippo signaling
Organ size is controlled by numerous factors including mechanical forces, which are mediated in part by the Hippo pathway. In growing Drosophila epithelial tissues, cytoskeletal tension influences Hippo signaling by modulating the localization of key pathway proteins to different apical domains. Her...
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Veröffentlicht in: | Developmental cell 2024-01, Vol.59 (2), p.262-279.e6 |
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creator | Kroeger, Benjamin Manning, Samuel A Fonseka, Yoshana Oorschot, Viola Crawford, Simon A Ramm, Georg Harvey, Kieran F |
description | Organ size is controlled by numerous factors including mechanical forces, which are mediated in part by the Hippo pathway. In growing Drosophila epithelial tissues, cytoskeletal tension influences Hippo signaling by modulating the localization of key pathway proteins to different apical domains. Here, we discovered a Hippo signaling hub at basal spot junctions, which form at the basal-most point of the lateral membranes and resemble adherens junctions in protein composition. Basal spot junctions recruit the central kinase Warts via Ajuba and E-cadherin, which prevent Warts activation by segregating it from upstream Hippo pathway proteins. Basal spot junctions are prominent when tissues undergo morphogenesis and are highly sensitive to fluctuations in cytoskeletal tension. They are distinct from focal adhesions, but the latter profoundly influences basal spot junction abundance by modulating the basal-medial actomyosin network and tension experienced by spot junctions. Thus, basal spot junctions couple morphogenetic forces to Hippo pathway activity and organ growth. |
doi_str_mv | 10.1016/j.devcel.2023.11.024 |
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subjects | Adherens Junctions - metabolism Animals Drosophila - metabolism Drosophila Proteins - metabolism Hippo Signaling Pathway Morphogenesis - physiology Signal Transduction Warts - metabolism |
title | Basal spot junctions of Drosophila epithelial tissues respond to morphogenetic forces and regulate Hippo signaling |
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