Yorkie controls tube length and apical barrier integrity in the developingDrosophilaairways

crossref(2019)

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摘要
AbstractEpithelial organ size and shape depend on cell shape changes, cell-matrix communication and apical membrane growth. TheDrosophilaembryonic tracheal network is an excellent model to study these processes. Here, we show that the transcriptional co-activator of the Hippo pathway, Yorkie (YAP in vertebrates), plays distinct roles in the developingDrosophilaairways. Yorkie exerts a cytoplasmic function by bindingDrosophilaTwinstar, the orthologue of the vertebrate actin-severing protein Cofilin, to regulate F-actin levels and apical cell membrane size, which are required for proper tracheal tube elongation. Second, Yorkie controls water-tightness of tracheal tubes by transcriptional regulation of the enzymeδ-aminolevulinate synthase(Alas). We conclude that Yorkie has a dual role in tracheal development to ensure proper tracheal growth and functionality.Short SummaryThis work identified an alternative role of the transcriptional co-activator Yorkie (Yki) in controlling water impermeability and tube size of the developingDrosophilaairways. Tracheal impermeability is triggered by Yki-mediated transcriptional regulation ofδ-aminolevulinate synthase,Alas, whereas tube elongation is controlled by binding of Yki to the actin severing factor Twinstar.
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