TY - JOUR AU - Wang, Xin AU - Jiang, Wei AU - Luo, Shuo AU - Yang, Xiaoyu AU - Wang, Changnan AU - Wang, Bingying AU - Dang, Yongjun AU - Shen, Yin AU - Ma, Dengke K. PY - 2021 DA - 2021/03/16 TI - The C. elegans homolog of human panic-disorder risk gene TMEM132D orchestrates neuronal morphogenesis through the WAVE-regulatory complex JO - Molecular Brain SP - 54 VL - 14 IS - 1 AB - TMEM132D is a human gene identified with multiple risk alleles for panic disorders, anxiety and major depressive disorders. Defining a conserved family of transmembrane proteins, TMEM132D and its homologs are still of unknown molecular functions. By generating loss-of-function mutants of the sole TMEM132 ortholog in C. elegans, we identify abnormal morphologic phenotypes in the dopaminergic PDE neurons. Using a yeast two-hybrid screen, we find that NAP1 directly interacts with the cytoplasmic domain of human TMEM132D, and mutations in C. elegans tmem-132 that disrupt interaction with NAP1 cause similar morphologic defects in the PDE neurons. NAP1 is a component of the WAVE regulatory complex (WRC) that controls F-actin cytoskeletal dynamics. Decreasing activity of WRC rescues the PDE defects in tmem-132 mutants, whereas gain-of-function of TMEM132D in mammalian cells inhibits WRC, leading to decreased abundance of select WRC components, impaired actin nucleation and cell motility. We propose that metazoan TMEM132 family proteins play evolutionarily conserved roles in regulating NAP1 protein homologs to restrict inappropriate WRC activity, cytoskeletal and morphologic changes in the cell. SN - 1756-6606 UR - https://doi.org/10.1186/s13041-021-00767-w DO - 10.1186/s13041-021-00767-w ID - Wang2021 ER -