Genetic variants of DISC1 proximal to the NDEL1 binding site affect the interaction between DISC1 and NDEL1, which is required for neurite outgrowth in differentiating PC12 cells.
Genetic variants of DISC1 affect its interaction with NDEL1, which is essential for neurite outgrowth, providing a potential mechanism for its role in major mental conditions.
Disrupted-In-Schizophrenia-1 (DISC1) is a unique susceptibility gene for major mental conditions, because of the segregation of its genetic variant with hereditary psychosis in a Scottish pedigree. Genetic association studies reproducibly suggest involvement of DISC1 in both schizophrenia and bipolar disorder in several ethnic groups. The DISC1 protein is multifunctional, and a pool of DISC1 in the dynein motor complex is required for neurite outgrowth in PC12 cells as well as proper neuronal migration and dendritic arborization in the developing cerebral cortex in vivo. Here, we show that a specific interaction between DISC1 and nuclear distribution element-like (NDEL1/NUDEL) is required for neurite outgrowth in differentiating PC12 cells. Among several components of the dynein motor complex, DISC1 and NDEL1 are selectively upregulated during neurite outgrowth upon differentiation in PC12 cells. The NDEL1 binding site of DISC1 was narrowed down to a small portion of exon 13, corresponding to amino acids 802-835 of DISC1. We demonstrate that genetic variants of DISC1, proximal to the NDEL1 binding site, affect the interaction between DISC1 and NDEL1.
Kamiya et al. (Wed,) conducted a other in Schizophrenia and bipolar disorder. Genetic variants of DISC1 was evaluated on DISC1-NDEL1 interaction and neurite outgrowth. Genetic variants of DISC1 proximal to the NDEL1 binding site affect the interaction between DISC1 and NDEL1, which is required for neurite outgrowth in differentiating PC12 cells.