Cnpy1 is a candidate endoplasmic reticulum chaperone of Vomeronasal type 2 GPCRs.

Abstract

Mouse vomeronasal sensory neurons are continuously generated from stem cells and differentiate to express either V1R or V2R G-protein coupled receptors (GPCRs), along with their respective Gi2 or Go G-protein subunits. We previously reported that Go-type neurons exhibit elevated expression of endoplasmic reticulum (ER) chaperones and a distinctive hypertrophic, gyroid ER architecture, suggesting specialized proteostatic demands. Here we identify a transcript for the mouse Cnpy1 gene that yields full-length Cnpy1 protein selectively expressed in and localized to the ER of Go neurons. Immunoprecipitation coupled with mass spectrometry revealed that Cnpy1 associates specifically with V2R GPCRs and multiple ER chaperones. Cnpy1 deletion resulted in mice that were deficient in Go neuronal activation upon exposure to vomeronasal stimuli and a marked reduction in male-male aggressive behavior. In the absence of Cnpy1, Go neurons develop normally till birth but undergo selective, progressive apoptosis during postnatal development. Unexpectedly, Cnpy1-null vomeronasal neurons displayed neither an obvious unfolded protein response nor defects in V2R GPCR traffic to dendritic tips, indicating that Cnpy1 is required for V2R assembly or functional maturation but dispensable for their ER export. Together, these findings identify Cnpy1 as a previously unrecognized component of an ER chaperone complex that is essential for Go neuron signaling and survival.