Cadherin 99C regulates apical expansion and cell rearrangement during epithelial tube elongation
Cadherin 99C regulates apical expansion and cell rearrangement during epithelial tube elongation
Apical and basolateral determinants specify and maintain membrane domains in epithelia. Here, we identify new roles for two apical surface proteins – Cadherin 99C (Cad99C) and Stranded at Second (SAS) – in conferring apical character in Drosophila tubular epithelia. Cad99C, the Drosophila ortholog of human Usher protocadherin PCDH15, is expressed in several embryonic tubular epithelial structures. Through loss-of-function and overexpression studies, we show that Cad99C is required to regulate cell rearrangement during salivary tube elongation. We further show that overexpression of either Cad99C or SAS causes a dramatic increase in apical membrane at the expense of other membrane domains, and that both proteins can do this independently of each other and independently of mislocalization of the apical determinant Crumbs (Crb). Overexpression of Cad99C or SAS results in similar, but distinct effects, suggesting both shared and unique roles for these proteins in conferring apical identity.
- Johns Hopkins Medicine United States
- Johns Hopkins University School of Medicine United States
Cell Nucleus, Embryo, Nonmammalian, Cell Membrane, Cell Polarity, Membrane Proteins, Epithelial Cells, Cadherins, Models, Biological, Epithelium, Salivary Glands, Extracellular Matrix, Protein Structure, Tertiary, Protein Transport, Structure-Activity Relationship, Drosophila melanogaster, Phenotype, Mutation, Animals, Drosophila Proteins, Humans
Cell Nucleus, Embryo, Nonmammalian, Cell Membrane, Cell Polarity, Membrane Proteins, Epithelial Cells, Cadherins, Models, Biological, Epithelium, Salivary Glands, Extracellular Matrix, Protein Structure, Tertiary, Protein Transport, Structure-Activity Relationship, Drosophila melanogaster, Phenotype, Mutation, Animals, Drosophila Proteins, Humans
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