Meru couples planar cell polarity with apical-basal polarity during asymmetric cell division
Jennifer J Banerjee,
Birgit L Aerne,
Maxine V Holder,
Simon Hauri,
Matthias Gstaiger,
Nicolas Tapon
Affiliations
Jennifer J Banerjee
Apoptosis and Proliferation Control Laboratory, The Francis Crick Institute, London, United Kingdom
Birgit L Aerne
Apoptosis and Proliferation Control Laboratory, The Francis Crick Institute, London, United Kingdom
Maxine V Holder
Apoptosis and Proliferation Control Laboratory, The Francis Crick Institute, London, United Kingdom
Simon Hauri
Department of Biology, Institute of Molecular Systems Biology, ETH Zürich, Zürich, Switzerland; Competence Center Personalized Medicine UZH/ETH, Zürich, Switzerland
Matthias Gstaiger
Department of Biology, Institute of Molecular Systems Biology, ETH Zürich, Zürich, Switzerland; Competence Center Personalized Medicine UZH/ETH, Zürich, Switzerland
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.