Transcription factor POU3F2 regulates TRIM8 expression contributing to cellular functions implicated in schizophrenia

基因敲除 生物 转录因子 遗传学 基因 基因沉默
作者
Chaodong Ding,Chunling Zhang,Richard F. Kopp,Liz Kuney,Qingtuan Meng,Le Wang,Yan Xia,Yi Jiang,Rujia Dai,Shishi Min,Wei‐Dong Yao,Ma‐Li Wong,Hongyu Ruan,Chunyu Liu,Chao Chen
出处
期刊:Molecular Psychiatry [Springer Nature]
卷期号:26 (7): 3444-3460 被引量:21
标识
DOI:10.1038/s41380-020-00877-2
摘要

Schizophrenia (SCZ) is a neuropsychiatric disorder with aberrant expression of multiple genes. However, identifying its exact causal genes remains a considerable challenge. The brain-specific transcription factor POU3F2 (POU domain, class 3, transcription factor 2) has been recognized as a risk factor for SCZ, but our understanding of its target genes and pathogenic mechanisms are still limited. Here we report that POU3F2 regulates 42 SCZ-related genes in knockdown and RNA-sequencing experiments of human neural progenitor cells (NPCs). Among those SCZ-related genes, TRIM8 (Tripartite motif containing 8) is located in SCZ-associated genetic locus and is aberrantly expressed in patients with SCZ. Luciferase reporter and electrophoretic mobility shift assays (EMSA) showed that POU3F2 induces TRIM8 expression by binding to the SCZ-associated SNP (single nucleotide polymorphism) rs5011218, which affects POU3F2-binding efficiency at the promoter region of TRIM8. We investigated the cellular functions of POU3F2 and TRIM8 as they co-regulate several pathways related to neural development and synaptic function. Knocking down either POU3F2 or TRIM8 promoted the proliferation of NPCs, inhibited their neuronal differentiation, and impaired the excitatory synaptic transmission of NPC-derived neurons. These results indicate that POU3F2 regulates TRIM8 expression through the SCZ-associated SNP rs5011218, and both genes may be involved in the etiology of SCZ by regulating neural development and synaptic function.
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