创伤后应激障碍、帕金森病和精神分裂症基因表达谱的RNA-seq分析确定了常见和独特的生物学途径的作用

Sian M J Hemmings, Patricia Swart, Jacqueline S Womersely, Ellen S Ovenden, Leigh L van den Heuvel, Nathaniel W McGregor, Stuart Meier, Soraya Bardien, Shameemah Abrahams, Gerard Tromp, Robin Emsley, Jonathan Carr, Soraya Seedat
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引用次数: 4

摘要

有证据表明,神经精神疾病(NPD)的共同病理生理机制可能有助于风险和恢复力。我们使用单基因和网络水平的转录组学方法来研究南非样本中创伤后应激障碍(PTSD)、帕金森病(PD)和精神分裂症的共同和特异性过程。对从每个队列的病例和对照组获得的血液进行RNA-seq。分别使用DESeq2和CEMiTool进行基因表达和加权基因相关网络分析(WGCNA)。基因表达的显著差异仅限于PTSD队列。然而,WGCNA暗示核糖体表达、炎症和泛素化是所研究的NPD的关键因素。在PTSD和PD队列中观察到核糖体相关通路的差异表达,局灶性粘附和细胞外基质通路与PD和精神分裂症有关。我们提出,尽管表型表现不同,但核心转导机制可能在NPD的分子病因中发挥重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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RNA-seq analysis of gene expression profiles in posttraumatic stress disorder, Parkinson's disease and schizophrenia identifies roles for common and distinct biological pathways.

Evidence suggests that shared pathophysiological mechanisms in neuropsychiatric disorders (NPDs) may contribute to risk and resilience. We used single-gene and network-level transcriptomic approaches to investigate shared and disorder-specific processes underlying posttraumatic stress disorder (PTSD), Parkinson's disease (PD) and schizophrenia in a South African sample. RNA-seq was performed on blood obtained from cases and controls from each cohort. Gene expression and weighted gene correlation network analyses (WGCNA) were performed using DESeq2 and CEMiTool, respectively. Significant differences in gene expression were limited to the PTSD cohort. However, WGCNA implicated, amongst others, ribosomal expression, inflammation and ubiquitination as key players in the NPDs under investigation. Differential expression in ribosomal-related pathways was observed in the PTSD and PD cohorts, and focal adhesion and extracellular matrix pathways were implicated in PD and schizophrenia. We propose that, despite different phenotypic presentations, core transdiagnostic mechanisms may play important roles in the molecular aetiology of NPDs.

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