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Crumbs 3b promotes tight junctions in an ezrin-dependent manner in mammalian cells Free
Andrew M. Tilston-Lünel1, Kathryn E. Haley2, Nicolas F. Schlecht3, Yanhua Wang3, Abigail L.D. Chatterton2, Susana Moleirinho1,2,6, Ailsa Watson4, Harinder S. Hundal4, Michael B. Prystowsky5, Frank J. Gunn-Moore1,†,*, and Paul A. Reynolds2,†,*
1Medical and Biological Sciences Building, School of Biology, University of St Andrews, St Andrews, KY16 9TF, UK
2Medical and Biological Sciences Building, School of Medicine, University of St Andrews, St Andrews, KY16 9TF, UK
3Department of Epidemiology & Population Health, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA
4School of Life Sciences, University of Dundee, Dundee DD1 5EH, UK
5Department of Pathology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA
6Present address: Scripps Research Institute, Jupiter, FL, USA. *Correspondence to:Paul A. Reynolds, E-mail: par10@st-andrews.ac.uk; Frank J. Gunn-Moore, E-mail: fjg1@st-andrews.ac.uk
J Mol Cell Biol, Volume 8, Issue 5, October 2016, 439-455,  https://doi.org/10.1093/jmcb/mjw020
Keyword: CRB3, crumbs, FERM proteins, FBM, tight junctions, ezrin

Crumbs 3 (CRB3) is a component of epithelial junctions, which has been implicated in apical-basal polarity, apical identity, apical stability, cell adhesion, and cell growth. CRB3 undergoes alternative splicing to yield two variants: CRB3a and CRB3b. Here, we describe novel data demonstrating that, as with previous studies on CRB3a, CRB3b also promotes the formation of tight junctions (TJs). However, significantly we demonstrate that the 4.1-ezrin–radixin–moesin-binding motif of CRB3b is required for CRB3b functionality and that ezrin binds to the FBM of CRB3b. Furthermore, we show that ezrin contributes to CRB3b functionality and the correct distribution of TJ proteins. We demonstrate that both CRB3 isoforms are required for the production of functionally mature TJs and also the localization of ezrin to the plasma membrane. Finally, we demonstrate that reduced CRB3b expression in head and neck squamous cell carcinoma (HNSCC) correlates with cytoplasmic ezrin, a biomarker for aggressive disease, and shows evidence that while CRB3a expression has no effect, low CRB3b and high cytoplasmic ezrin expression combined may be prognostic for HNSCC.