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精神分裂症患者全血中的基因共表达网络与抗精神病药物使用无关,且富集了大脑表达的基因。

A gene co-expression network in whole blood of schizophrenia patients is independent of antipsychotic-use and enriched for brain-expressed genes.

机构信息

Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.

出版信息

PLoS One. 2012;7(6):e39498. doi: 10.1371/journal.pone.0039498. Epub 2012 Jun 27.

Abstract

Despite large-scale genome-wide association studies (GWAS), the underlying genes for schizophrenia are largely unknown. Additional approaches are therefore required to identify the genetic background of this disorder. Here we report findings from a large gene expression study in peripheral blood of schizophrenia patients and controls. We applied a systems biology approach to genome-wide expression data from whole blood of 92 medicated and 29 antipsychotic-free schizophrenia patients and 118 healthy controls. We show that gene expression profiling in whole blood can identify twelve large gene co-expression modules associated with schizophrenia. Several of these disease related modules are likely to reflect expression changes due to antipsychotic medication. However, two of the disease modules could be replicated in an independent second data set involving antipsychotic-free patients and controls. One of these robustly defined disease modules is significantly enriched with brain-expressed genes and with genetic variants that were implicated in a GWAS study, which could imply a causal role in schizophrenia etiology. The most highly connected intramodular hub gene in this module (ABCF1), is located in, and regulated by the major histocompatibility (MHC) complex, which is intriguing in light of the fact that common allelic variants from the MHC region have been implicated in schizophrenia. This suggests that the MHC increases schizophrenia susceptibility via altered gene expression of regulatory genes in this network.

摘要

尽管进行了大规模的全基因组关联研究(GWAS),但精神分裂症的潜在基因仍知之甚少。因此,需要额外的方法来确定这种疾病的遗传背景。在这里,我们报告了一项针对精神分裂症患者和对照者外周血基因表达的大型研究结果。我们应用系统生物学方法,对 92 名接受药物治疗和 29 名未接受抗精神病药物治疗的精神分裂症患者以及 118 名健康对照者的全血基因组表达数据进行了分析。我们发现,全血中的基因表达谱可以识别出与精神分裂症相关的 12 个大的基因共表达模块。这些与疾病相关的模块中的几个可能反映了由于抗精神病药物治疗而导致的表达变化。然而,其中两个疾病模块可以在涉及未接受抗精神病药物治疗的患者和对照者的独立第二数据集得到复制。这些稳健定义的疾病模块之一显著富集了大脑表达的基因和与 GWAS 研究相关的遗传变异,这可能意味着它们在精神分裂症病因学中具有因果作用。该模块中连接性最高的内模块枢纽基因(ABCF1)位于主要组织相容性复合体(MHC)中,并受其调控,鉴于 MHC 区域的常见等位基因变异与精神分裂症有关,这一点令人感兴趣。这表明,MHC 通过改变该网络中调节基因的表达,增加了精神分裂症的易感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2895/3384650/ee0b744d87e1/pone.0039498.g001.jpg

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