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通过RNA测序对感染日本脑炎病毒的小鼠大脑进行微小RNA转录组分析。

MicroRNA transcriptome profiling of mice brains infected with Japanese encephalitis virus by RNA sequencing.

作者信息

Li Xin-Feng, Cao Rui-Bing, Luo Jun, Fan Jian-Ming, Wang Jing-Man, Zhang Yuan-Peng, Gu Jin-Yan, Feng Xiu-Li, Zhou Bin, Chen Pu-Yan

机构信息

College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, China.

Henan Provincial Key Laboratory of Animal Immunology, Henan Academy of Agricultural Sciences, Zhengzhou 450002, China.

出版信息

Infect Genet Evol. 2016 Apr;39:249-257. doi: 10.1016/j.meegid.2016.01.028. Epub 2016 Feb 2.

Abstract

Japanese encephalitis (JE) is a mosquito borne viral disease, caused by Japanese encephalitis virus (JEV) infection producing severe neuroinflammation in the central nervous system (CNS) with the associated disruption of the blood brain barrier. MicroRNAs (miRNAs) are a family of 21-24 nt small non-coding RNAs that play important post-transcriptional regulatory roles in gene expression and have critical roles in virus pathogenesis. We examined the potential roles of miRNAs in JEV-infected suckling mice brains and found that JEV infection changed miRNA expression profiles when the suckling mice began showing nervous symptoms. A total of 1062 known and 71 novel miRNAs were detected in JEV-infected group, accompanied with 1088 known and 75 novel miRNAs in mock controls. Among these miRNAs, one novel and 25 known miRNAs were significantly differentially expressed, including 18 up-regulated and 8 down-regulated miRNAs which were further confirmed by real-time PCR. Gene ontology (GO) and signaling pathway analysis of the predicted target mRNAs of the modulated miRNAs showed that they are correlated with the regulation of apoptosis, neuron differentiation, antiviral immunity and infiltration of mouse brain, and the validated targets of 12 differentially expressed miRNAs were enriched for the regulation of cell programmed death, proliferation, transcription, muscle organ development, erythrocyte differentiation, gene expression, plasma membrane and protein domain specific binding. KEGG analysis further reveals that the validated target genes were involved in the Pathways in cancer, Neurotrophin signaling pathway, Toll like receptor signaling pathway, Endometrial cancer and Jak-STAT signaling pathway. We constructed the interaction networks of miRNAs and their target genes according to GO terms and KEGG pathways and the expression levels of several target genes were examined. Our data provides a valuable basis for further studies on the regulatory roles of miRNAs in JE pathogenesis.

摘要

日本脑炎(JE)是一种由蚊子传播的病毒性疾病,由日本脑炎病毒(JEV)感染引起,可在中枢神经系统(CNS)中产生严重的神经炎症,并伴有血脑屏障的破坏。微小RNA(miRNA)是一类21 - 24个核苷酸的小型非编码RNA,在基因表达中发挥重要的转录后调控作用,并且在病毒发病机制中起关键作用。我们研究了miRNA在JEV感染的乳鼠脑中的潜在作用,发现当乳鼠开始出现神经症状时,JEV感染改变了miRNA表达谱。在JEV感染组中总共检测到1062个已知miRNA和71个新miRNA,模拟对照组中则有1088个已知miRNA和75个新miRNA。在这些miRNA中,1个新miRNA和25个已知miRNA有显著差异表达,其中18个上调和8个下调的miRNA通过实时PCR进一步得到证实。对调控的miRNA预测靶mRNA进行基因本体(GO)和信号通路分析表明,它们与细胞凋亡调控、神经元分化、抗病毒免疫以及小鼠脑浸润相关,并且12个差异表达miRNA的验证靶标在细胞程序性死亡、增殖、转录、肌肉器官发育、红细胞分化、基因表达、质膜和蛋白质结构域特异性结合的调控方面富集。KEGG分析进一步揭示,验证的靶基因参与癌症通路、神经营养因子信号通路、Toll样受体信号通路、子宫内膜癌和Jak - STAT信号通路。我们根据GO术语、KEGG通路构建了miRNA及其靶基因的相互作用网络,并检测了几个靶基因的表达水平。我们的数据为进一步研究miRNA在JE发病机制中的调控作用提供了有价值的基础。

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