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A Network Analysis of Epigenetic and Transcriptional Regulation in a Neurodevelopmental Rat Model of Schizophrenia With Implications for Translational Research

机译:具有转化研究影响的精神分裂症神经发育大鼠模型中表观遗传和转录调控的网络分析

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摘要

Prenatal administration of mitotoxin methylazoxymethanol acetate (MAM) in rats produces behavioral, pharmacological, and anatomical abnormalities once offspring reach adulthood, thus establishing a widely used neurodevelopmental model of schizophrenia. However, the molecular aspects underlying this disease model are not well understood. Therefore, this study examines epigenetic and transcriptional dysregulation in the prefrontal cortex and hippocampus of MAM rats as these are brain regions closely associated with schizophrenia pathogenesis. Upon sequencing messenger and microRNA (mRNA and miRNA, respectively), differential expression was revealed in the prefrontal cortex and hippocampus between MAM- and saline-treated rats; sequencing data were validated by qualitative real-time polymerase chain reaction. Bioinformatic analyses demonstrated that the differentially expressed (DE) genes were strongly enriched in interactive pathways related to schizophrenia, including chemical synaptic transmission, cognition, and inflammatory responses; also, the potential target genes of the DE miRNAs were enriched in pathways related to synapses and inflammation. The blood of schizophrenia patients and healthy controls was further analyzed for several top DE mRNAs: DOPA decarboxylase, ret proto-oncogene, Fc receptor-like 2, interferon lambda receptor 1, and myxovirus (influenza virus) resistance 2. The results demonstrated that the expression of these genes was dysregulated in patients with schizophrenia; combining these mRNAs sufficiently differentiated schizophrenia patients from controls. Taken together, this study suggests that the MAM model has the potential to reproduce hippocampus and prefrontal cortex abnormalities, relevant to schizophrenia, at the epigenetic and transcriptional levels. These data also provide novel targets for schizophrenia diagnoses and treatments.
机译:一旦后代达到成年,大鼠甲基甲蛋白甲醇甲醇乙醇乙酸甲醇亚甲醇(MAM)的产前施用产生行为,药理和解剖学异常,从而建立了广泛使用的精神分裂症的神经发育模型。然而,这种疾病模型的潜在的分子方面尚不清楚。因此,本研究检查了MAM大鼠前额叶皮质和海马的表观遗传和转录失调,因为这些是与精神分裂症发病机制密切相关的脑区。在测序信使和MicroRNA(分别mRNA和miRNA)后,在妈妈和盐水处理的大鼠之间的前额叶皮质和海马中揭示了差异表达;通过定性实时聚合酶链反应验证测序数据。生物信息分析证明差异表达(DE)基因强烈富集在与精神分裂症相关的互动性途径中,包括化学突触传递,认知和炎症反应;此外,DE miRNA的潜在靶基因富集在与突触和炎症有关的途径中。进一步分析了精神分裂症患者的血液和健康对照的几种顶部MRNA:DOPA脱羧酶,RET原癌基因,Fc受体样2,干扰素λ受体1和骨髓病毒(流感病毒)电阻2.结果表明这些基因的表达在精神分裂症患者中诵读了这种基因;结合这些MRNA足够分化的精神分裂症患者免受对照组。这项研究表明,MAM模型具有潜力,潜在的血管和转录和转录水平具有与精神分裂症相关的海马和前额叶皮质异常。这些数据还提供了精神分裂症诊断和治疗的新靶点。

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