School of Public Health of Guangxi Medical University, 22 Shuangyong Road, Nanning, 530021, Guangxi, China.
J Mol Neurosci. 2022 Aug;72(8):1622-1635. doi: 10.1007/s12031-022-02013-x. Epub 2022 May 11.
Schizophrenia (SCZ) is a complex psychiatric syndrome with uncertain etiology. This study aimed to uncover the expression profiles and related regulatory networks of circular RNA (circRNA) in SCZ. Whole transcriptome sequencing was performed to assess the expression profiles of circRNAs and microRNAs (miRNAs) in the peripheral blood of three patients with SCZ and three healthy controls. Five circRNAs were validated by quantitative real-time PCR (RT-qPCR). TargetScan, RNAhybrid, and miRanda were performed to predict the target miRNAs of the top 10 dysregulated circRNAs. MiRTarBase was applied to predict the target mRNAs of miRNAs to construct circRNA-miRNA-mRNA (ceRNA) networks. CatRAPID and StarBase were used to predict the target RNA-binding proteins (RBPs) of circRNAs to construct circRNA-RBP networks. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were performed to predict the potential functions of the maternal genes of circRNAs and target mRNAs. In total, 450 circRNAs and 160 miRNAs were found to be significantly differentially expressed, with hsa_circ_0003999 and hsa_circ_0030042 being significantly different between patients with SCZ and healthy controls (P < 0.05). The PI3K-AKT, MAPK, and cell cycle pathways were predicted to be associated with SCZ. GO analysis showed that focal adhesion was related to SCZ. The ceRNA networks, especially hsa_circ_0006151/hsa-miR-4685-3p/ZBTB16, hsa_circ_0000008/hsa-miR-1976/ZBTB16, and the hsa_circ_0007963/hsa-miR-3127-3p/UBE2K axes have the greatest probability of being involved in the pathophysiology of SCZ. The RBP networks, FXR1, FXR2, DGCR8, XRN2, FMR1, and QKI were the RBPs associated with SCZ. In conclusion, the circRNAs, ceRNAs, and RBP network expression patterns and related pathways indicate the potential role of circRNAs in the pathogenesis and development of SCZ.
精神分裂症 (SCZ) 是一种病因不明的复杂精神综合征。本研究旨在揭示 SCZ 中环状 RNA (circRNA) 的表达谱和相关调控网络。通过对 3 名 SCZ 患者和 3 名健康对照者外周血中的 circRNA 和 microRNA (miRNA) 进行全转录组测序,评估 circRNA 和 miRNA 的表达谱。通过实时定量 PCR (RT-qPCR) 验证了 5 个 circRNA。通过 TargetScan、RNAhybrid 和 miRanda 预测 top10 差异表达 circRNA 的靶 miRNA。利用 MiRTarBase 预测 miRNA 的靶 mRNAs,构建 circRNA-miRNA-mRNA (ceRNA) 网络。利用 CatRAPID 和 StarBase 预测 circRNA 的靶 RNA 结合蛋白 (RBP),构建 circRNA-RBP 网络。通过 Gene Ontology (GO) 和 Kyoto Encyclopedia of Genes and Genomes (KEGG) 通路分析预测 circRNA 母基因和靶 mRNAs 的潜在功能。共发现 450 个 circRNA 和 160 个 miRNA 表达显著差异,hsa_circ_0003999 和 hsa_circ_0030042 在 SCZ 患者与健康对照者之间差异显著(P<0.05)。预测 PI3K-AKT、MAPK 和细胞周期通路与 SCZ 相关。GO 分析表明,粘着斑与 SCZ 相关。ceRNA 网络,特别是 hsa_circ_0006151/hsa-miR-4685-3p/ZBTB16、hsa_circ_0000008/hsa-miR-1976/ZBTB16 和 hsa_circ_0007963/hsa-miR-3127-3p/UBE2K 轴最有可能参与 SCZ 的病理生理学过程。RBP 网络中,FXR1、FXR2、DGCR8、XRN2、FMR1 和 QKI 是与 SCZ 相关的 RBP。综上所述,circRNA、ceRNA 和 RBP 网络表达模式及相关通路表明 circRNA 可能在 SCZ 的发病机制和发展中发挥作用。