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J Cell Biol. 2019 Jul 1;218(7):2277-2293. doi: 10.1083/jcb.201804201. Epub 2019 May 30.

Scribble, Erbin, and Lano redundantly regulate epithelial polarity and apical adhesion complex.

Author information

1
Department of Dermatology, Northwestern University, The Feinberg School of Medicine, Chicago, IL.
2
Department of Cell and Molecular Biology, The Feinberg School of Medicine, Chicago, IL.
3
Department of Dermatology, Northwestern University, The Feinberg School of Medicine, Chicago, IL s-troyanovsky@northwestern.edu.
#
Contributed equally

Abstract

The basolateral protein Scribble (Scrib), a member of the LAP protein family, is essential for epithelial apicobasal polarity (ABP) in Drosophila However, a conserved function for this protein in mammals is unclear. Here we show that the crucial role for Scrib in ABP has remained obscure due to the compensatory function of two other LAP proteins, Erbin and Lano. A combined Scrib/Erbin/Lano knockout disorganizes the cell-cell junctions and the cytoskeleton. It also results in mislocalization of several apical (Par6, aPKC, and Pals1) and basolateral (Llgl1 and Llgl2) identity proteins. These defects can be rescued by the conserved "LU" region of these LAP proteins. Structure-function analysis of this region determined that the so-called LAPSDb domain is essential for basolateral targeting of these proteins, while the LAPSDa domain is essential for supporting the membrane basolateral identity and binding to Llgl. In contrast to the key role in Drosophila, mislocalization of Llgl proteins does not appear to be critical in the scrib ABP phenotype.

PMID:
31147384
PMCID:
PMC6605793
[Available on 2020-01-01]
DOI:
10.1083/jcb.201804201

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