Meru couples planar cell polarity with apical-basal polarity during asymmetric cell division

Author:

Banerjee Jennifer J1,Aerne Birgit L1,Holder Maxine V1,Hauri Simon23,Gstaiger Matthias23,Tapon Nicolas1ORCID

Affiliation:

1. Apoptosis and Proliferation Control Laboratory, The Francis Crick Institute, London, United Kingdom

2. Department of Biology, Institute of Molecular Systems Biology, ETH Zürich, Zürich, Switzerland

3. Competence Center Personalized Medicine UZH/ETH, Zürich, Switzerland

Abstract

Polarity is a shared feature of most cells. In epithelia, apical-basal polarity often coexists, and sometimes intersects with planar cell polarity (PCP), which orients cells in the epithelial plane. From a limited set of core building blocks (e.g. the Par complexes for apical-basal polarity and the Frizzled/Dishevelled complex for PCP), a diverse array of polarized cells and tissues are generated. This suggests the existence of little-studied tissue-specific factors that rewire the core polarity modules to the appropriate conformation. In Drosophila sensory organ precursors (SOPs), the core PCP components initiate the planar polarization of apical-basal determinants, ensuring asymmetric division into daughter cells of different fates. We show that Meru, a RASSF9/RASSF10 homologue, is expressed specifically in SOPs, recruited to the posterior cortex by Frizzled/Dishevelled, and in turn polarizes the apical-basal polarity factor Bazooka (Par3). Thus, Meru belongs to a class of proteins that act cell/tissue-specifically to remodel the core polarity machinery.

Funder

Francis Crick Institute

Wellcome

Innovative Medicines Initiative project ULTRA-DD

European Union 7th Framework programme

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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