DISC1 regulates astrogenesis in the embryonic brain via modulation of RAS/MEK/ERK signaling through RASSF7

• DOI: 10.1242/dev.133066
• Publication Date: 2016-06-11T04:31:44Z
• Authors: Shukun Wang; Qingli Liang; Huimin Qiao; Hong Li; Tianjin Shen; Fen Ji; Jianwei Jiao
• Keywords: 0301 basic medicine; Mice, Inbred ICR; 0303 health sciences; MAP Kinase Signaling System; Neurogenesis; Blotting, Western; Brain; Nerve Tissue Proteins; Immunohistochemistry; Cell Line; Mice; 03 medical and health sciences; Animals; Humans; Immunoprecipitation; Female; Signal Transduction; Transcription Factors

Disrupted in schizophrenia 1 (DISC1) is known as a high susceptibility gene for schizophrenia. Recent studies have indicated that schizophrenia might be caused by glia defects and dysfunction. However, there is no direct evidence of a link between the schizophrenia gene DISC1 and gliogenesis defects. Thus, an investigation into the involvement of DISC1 (a ubiquitously expressed brain protein) in astrogenesis during the late stage of mouse embryonic brain development is warranted. Here, we show that suppression of DISC1 expression represses astrogenesis in vitro and in vivo, and that DISC1 overexpression substantially enhances the process. Furthermore, mouse and human DISC1 overexpression rescued the astrogenesis defects caused by DISC1 knockdown. Mechanistically, DISC1 activates the RAS/MEK/ERK signaling pathway via direct association with RASSF7. Also, the pERK complex undergoes nuclear translocation and influences the expression of genes related to astrogenesis. In summary, our results demonstrate that DISC1 regulates astrogenesis by modulating RAS/MEK/ERK signaling via RASSF7 and provide a framework for understanding how DISC1 dysfunction might lead to neuropsychiatric diseases.