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• W2152800905 abstract "The asymmetric distribution of proteins to basolateral and apical membranes is an important feature of epithelial cell polarity. To investigate how basolateral LAP proteins (LRR (for leucine‐rich repeats) and PDZ (for PSD‐95/Discs‐large/ZO‐1), which play key roles in cell polarity, reach their target membrane, we carried out a structure–function study of three LAP proteins: Caenorhabditis elegans LET‐413, human Erbin and human Scribble (hScrib). Deletion and point mutation analyses establish that their LRR domain is crucial for basolateral membrane targeting. This property is specific to the LRR domain of LAP proteins, as the non‐LAP protein SUR‐8 does not localize at the basolateral membrane of epithelial cells, despite having a closely related LRR domain. Importantly, functional studies of LET‐413 in C. elegans show that although its PDZ domain is dispensable during embryogenesis, its LRR domain is essential. Our data establish a novel paradigm for protein localization by showing that a subset of LRR domains direct subcellular localization in polarized cells." @default.
• W2152800905 created "2016-06-24" @default.
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• W2152800905 date "2003-10-01" @default.
• W2152800905 modified "2023-10-17" @default.
• W2152800905 title "Basolateral targeting by leucine‐rich repeat domains in epithelial cells" @default.
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• W2152800905 doi "https://doi.org/10.1038/sj.embor.7400006" @default.
• W2152800905 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/1326376" @default.
• W2152800905 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/14578922" @default.
• W2152800905 hasPublicationYear "2003" @default.
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