Abstract
Abstract
Non-canonical Wnt pathways provide directional cues for cell polarity, but the mechanisms that translate these cues into asymmetric cellular organisation remain incompletely defined. We previously showed that a non-canonical EGL-20/Wnt-CAM-1/Ror-DSH-1/Dishevelled pathway establishes polarised membrane compartments in
Caenorhabditis elegans
body wall muscles. However, how EGL-20/Wnt signalling is translated into muscle polarity remains unknown. Here, we identify PZLS-1, the
C. elegans
ortholog of human PDZRN3, PDZRN4 and PDZD4, as a regulator of muscle polarity. Although PDZRN proteins are known targets of non-canonical Wnt-Ror signalling, how they are spatially organised within polarised cells and how their protein domains contribute to their function remain largely unknown. We reveal that PZLS-1 is itself asymmetrically localised by Wnt-Ror-Dvl signalling, and is closely associated with DSH-1. PZLS-1 and DSH-1 colocalise in intracellular puncta and are mutually required for their localisation.
In vivo
structure-function analyses reveal conserved protein motifs that differentially control PZLS-1 localisation, abundance and function. This includes a previously uncharacterized highly conserved sequence that regulates PZLS-1 abundance in a DSH-1-dependent manner. We further show that PZLS-1 and DSH-1 control the abundance and polarised localisation of VAB-8/KIF26b, another conserved target of Wnt-Ror signalling. Together, these findings indicate that Wnt-Ror-Dvl signalling can control the spatial organisation and abundance of PDZRN- and KIF26B-family proteins
in vivo
, providing a mechanism to translate extracellular polarity cues into intracellular asymmetry.