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Scribble, Erbin, and Lano redundantly regulate epithelial polarity and apical adhesion complex
Jongho Choi1, Regina B Troyanovsky1, Indrajyoti Indra1
1Department of Dermatology, Northwestern University, The Feinberg School of Medicine, Chicago, IL.
The Journal of Cell Biology
|June 1, 2019
Summary
Mammalian Scribble (Scrib) protein
Area of Science:
- Cell Biology
- Molecular Biology
- Genetics
Background:
- The basolateral protein Scribble (Scrib) is vital for epithelial apicobasal polarity (ABP) in Drosophila.
- Its conserved function in mammals remained unclear due to compensatory roles of other LAP proteins.
Purpose of the Study:
- To investigate the conserved function of Scribble (Scrib) in mammalian epithelial apicobasal polarity (ABP).
- To elucidate the compensatory mechanisms involving LAP proteins Erbin and Lano in mammalian ABP.
Main Methods:
- Generated a combined knockout of Scrib, Erbin, and Lano in mammalian cells.
- Analyzed cell-cell junctions, cytoskeleton organization, and protein localization.
- Performed structure-function analysis of the conserved
Main Results:
- Combined knockout of Scrib, Erbin, and Lano disrupted cell-cell junctions and cytoskeleton.
- Significant mislocalization of apical (Par6, aPKC, Pals1) and basolateral (Llgl1, Llgl2) proteins observed.
- The conserved
Conclusions:
- The compensatory functions of Erbin and Lano mask Scrib's role in mammalian ABP.
- The conserved LU region, particularly LAPSDb and LAPSDa domains, is crucial for basolateral targeting and identity.
- Llgl mislocalization is less critical for the Scrib ABP phenotype in mammals compared to Drosophila.
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