The PVD neuron has male-specific structure and mating function in C. elegans

Abstract

Neurons display unique shapes and establish intricate networks, which may differ between sexes. In complex organisms, studying sex differences in structure and function of individual neurons is difficult. The nematode Caenorhabditis elegans hermaphrodites and males present an exceptional model for studying neuronal morphogenesis in a simple, sexually-dimorphic system. We focus on the polymodal sensory bilateral neuron pair PVD, which forms a complex but stereotypic dendritic tree composed of multiple subunits that resemble candelabra. PVD is well studied in hermaphrodites, but not in males. We show here that during larval development, male PVDs extend a similar architecture to the hermaphrodite utilizing the sexually-shared Menorin patterning mechanism. In early adulthood, however, male PVD develops a unique extension into the copulatory tail structure. Alongside established tail ray neurons RnA and RnB, we show PVD is a third, previously unrecognized, neuron within the tail rays. Unlike RnA and RnB, PVD extends anterogradely, branches and turns within the ray hypodermis, and is non-ciliated. This PVD sexually-dimorphic arborization is absent in mutant backgrounds which perturb the Menorin guidance complex. SAX-7/L1CAM, a hypodermal component of this complex, shows a male-specific expression pattern which precedes PVD extension, and its presence allows PVD to enter the tail rays. Further, our results reveal that genetically altered arborization or ablation of the PVD result in male mating behavioral defects, particularly as males turn around the hermaphrodite. These results uncover an adult-stage sexual dimorphism of dendritic branching and uncover a function for PVD in male sexual behavior. Significance StatementNeurons form intricate shapes and networks, which may display sexual differences. Pinpointing these changes at the single cell level, however, is challenging. In C. elegans, the PVD neuron is a powerful model for stereotypical neuron shaping, yet most studies concern only one of two sexes. Our research focuses on the understudied male, where we show an adult-stage extension of PVD into the male copulatory tail organ. We further show how this stems from a sex-shared patterning complex, progressing independently and in a different environment compared with nearby male-specific neurons. We further find PVD has a role in the male adult-specific mating behavior. PVD thus presents a unique example of a highly arborized neuron showing sexually dimorphic behavioral function and structure.