- Oral presentation
- Open Access
Dishevelled stablisation at the cilium by RPGRIP1L is essential for planar cell polarity
© Schneider-Maunoury et al; licensee BioMed Central Ltd. 2012
- Published: 16 November 2012
- Recent Work
- Protein Complex
- Developmental Biology
- Transition Zone
- Body Position
Cilia are involved in planar polarity in different systems but the mechanisms by which they influence the polarization process are unclear . In order to clarify this issue, we investigated the function of the ciliary gene Rpgrip1l (Ftm/NPHP8/MKS5) in the mammalian cochlear sensory epithelium and in the zebrafish floor plate. We and others have previously shown that mutations in the human RPGRIP1L gene cause Meckel and Joubert type B syndromes . The Rpgrip1l protein is localised at the ciliary transition zone and is required for transduction of the Hh/Gli pathway . Our recent work has shown that Rpgrip1l patterns the telencephalon via the regulation of Gli3 proteolytic cleavage . Here we show that in both the mammalian cochlear sensory epithelium and the zebrafish floor plate, Rpgrip1l is required for correct positioning of the basal body along the planar polarity axis. Our results strongly suggest that Rpgrip1l is essential for stabilizing the adaptor protein dishevelled at the basal body and/or cilium. Finally, we demonstrate that, in the zebrafish floor plate, the function of Rpgrip1l in basal body positioning is mediated by dishevelled. We propose that Rpgrip1l participates in a protein complex required for stabilizing dishevelled at the cilium, and that this stabilization is essential for asymmetric localization of the basal body along the planar polarity axis.
- Wallingford , Mitchell : Genes Dev. 2011, 25: 201-13. 10.1101/gad.2008011.PubMed CentralView ArticlePubMedGoogle Scholar
- Delous, et al: Nat Genet. 2007, 39: 875-81. 10.1038/ng2039.View ArticlePubMedGoogle Scholar
- Vierkotten, et al: Development. 2007, 134: 2569-77. 10.1242/dev.003715.View ArticlePubMedGoogle Scholar
- Besse, et al: Development. 2011, 138: 2079-88. 10.1242/dev.059808.View ArticlePubMedGoogle Scholar
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