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精神分裂症中一种新型的微小RNA和转录因子介导的调控网络。

A novel microRNA and transcription factor mediated regulatory network in schizophrenia.

作者信息

Guo An-Yuan, Sun Jingchun, Jia Peilin, Zhao Zhongming

机构信息

Department of Biomedical Informatics, Vanderbilt University School of Medicine, Nashville, TN, USA.

出版信息

BMC Syst Biol. 2010 Feb 15;4:10. doi: 10.1186/1752-0509-4-10.

Abstract

BACKGROUND

Schizophrenia is a complex brain disorder with molecular mechanisms that have yet to be elucidated. Previous studies have suggested that changes in gene expression may play an important role in the etiology of schizophrenia, and that microRNAs (miRNAs) and transcription factors (TFs) are primary regulators of this gene expression. So far, several miRNA-TF mediated regulatory modules have been verified. We hypothesized that miRNAs and TFs might play combinatory regulatory roles for schizophrenia genes and, thus, explored miRNA-TF regulatory networks in schizophrenia.

RESULTS

We identified 32 feed-forward loops (FFLs) among our compiled schizophrenia-related miRNAs, TFs and genes. Our evaluation revealed that these observed FFLs were significantly enriched in schizophrenia genes. By converging the FFLs and mutual feedback loops, we constructed a novel miRNA-TF regulatory network for schizophrenia. Our analysis revealed EGR3 and hsa-miR-195 were core regulators in this regulatory network. We next proposed a model highlighting EGR3 and miRNAs involved in signaling pathways and regulatory networks in the nervous system. Finally, we suggested several single nucleotide polymorphisms (SNPs) located on miRNAs, their target sites, and TFBSs, which may have an effect in schizophrenia gene regulation.

CONCLUSIONS

This study provides many insights on the regulatory mechanisms of genes involved in schizophrenia. It represents the first investigation of a miRNA-TF regulatory network for a complex disease, as demonstrated in schizophrenia.

摘要

背景

精神分裂症是一种复杂的脑部疾病,其分子机制尚未阐明。先前的研究表明,基因表达的变化可能在精神分裂症的病因中起重要作用,并且微小RNA(miRNA)和转录因子(TF)是这种基因表达的主要调节因子。到目前为止,已经验证了几个miRNA-TF介导的调控模块。我们假设miRNA和TF可能对精神分裂症相关基因发挥组合调控作用,因此,探索了精神分裂症中的miRNA-TF调控网络。

结果

我们在汇编的精神分裂症相关miRNA、TF和基因中鉴定出32个前馈环(FFL)。我们的评估显示,这些观察到的FFL在精神分裂症相关基因中显著富集。通过整合FFL和相互反馈环,我们构建了一个新的精神分裂症miRNA-TF调控网络。我们的分析表明,EGR3和hsa-miR-195是该调控网络中的核心调节因子。接下来,我们提出了一个模型,突出了EGR3和参与神经系统信号通路和调控网络的miRNA。最后,我们提出了几个位于miRNA、其靶位点和TFBS上的单核苷酸多态性(SNP),它们可能对精神分裂症基因调控有影响。

结论

本研究为精神分裂症相关基因的调控机制提供了许多见解。它代表了对复杂疾病(如精神分裂症)的miRNA-TF调控网络的首次研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7714/2834616/81ffcbd90ab3/1752-0509-4-10-1.jpg

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