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• W3024871567 endingPage "11540" @default.
• W3024871567 startingPage "11531" @default.
• W3024871567 abstract "A polarized architecture is central to both epithelial structure and function. In many cells, polarity involves mutual antagonism between the Par complex and the Scribble (Scrib) module. While molecular mechanisms underlying Par-mediated apical determination are well-understood, how Scrib module proteins specify the basolateral domain remains unknown. Here, we demonstrate dependent and independent activities of Scrib, Discs-large (Dlg), and Lethal giant larvae (Lgl) using the Drosophila follicle epithelium. Our data support a linear hierarchy for localization, but rule out previously proposed protein-protein interactions as essential for polarization. Cortical recruitment of Scrib does not require palmitoylation or polar phospholipid binding but instead an independent cortically stabilizing activity of Dlg. Scrib and Dlg do not directly antagonize atypical protein kinase C (aPKC), but may instead restrict aPKC localization by enabling the aPKC-inhibiting activity of Lgl. Importantly, while Scrib, Dlg, and Lgl are each required, all three together are not sufficient to antagonize the Par complex. Our data demonstrate previously unappreciated diversity of function within the Scrib module and begin to define the elusive molecular functions of Scrib and Dlg." @default.
• W3024871567 created "2020-05-21" @default.
• W3024871567 creator A5014248978 @default.
• W3024871567 creator A5062920414 @default.
• W3024871567 date "2020-05-15" @default.
• W3024871567 modified "2023-10-18" @default.
• W3024871567 title "Distinct activities of Scrib module proteins organize epithelial polarity" @default.
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• W3024871567 doi "https://doi.org/10.1073/pnas.1918462117" @default.
• W3024871567 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7260944" @default.
• W3024871567 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/32414916" @default.
• W3024871567 hasPublicationYear "2020" @default.
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