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整合长链非编码RNA、信使核糖核酸和转录因子进行分析,以确定牛分枝杆菌感染背后的调控网络。

Integrated Analysis of lncRNAs, mRNAs, and TFs to Identify Regulatory Networks Underlying MAP Infection in Cattle.

作者信息

Heidari Maryam, Pakdel Abbas, Bakhtiarizadeh Mohammad Reza, Dehghanian Fariba

机构信息

Department of Animal Sciences, College of Agriculture, Isfahan University of Technology, Isfahan, Iran.

Department of Animal and Poultry Science, College of Aburaihan, University of Tehran, Tehran, Iran.

出版信息

Front Genet. 2021 Jul 5;12:668448. doi: 10.3389/fgene.2021.668448. eCollection 2021.

Abstract

Johne's disease is a chronic infection of ruminants that burdens dairy herds with a significant economic loss. The pathogenesis of the disease has not been revealed clearly due to its complex nature. In order to achieve deeper biological insights into molecular mechanisms involved in MAP infection resulting in Johne's disease, a system biology approach was used. As far as is known, this is the first study that considers lncRNAs, TFs, and mRNAs, simultaneously, to construct an integrated gene regulatory network involved in MAP infection. Weighted gene coexpression network analysis (WGCNA) and functional enrichment analysis were conducted to explore coexpression modules from which nonpreserved modules had altered connectivity patterns. After identification of hub and hub-hub genes as well as TFs and lncRNAs in the nonpreserved modules, integrated networks of lncRNA-mRNA-TF were constructed, and cis and trans targets of lncRNAs were identified. Both cis and trans targets of lncRNAs were found in eight nonpreserved modules. Twenty-one of 47 nonpreserved modules showed significant biological processes related to the immune system and MAP infection. Some of the MAP infection's related pathways in the most important nonpreserved modules comprise "positive regulation of cytokine-mediated signaling pathway," "negative regulation of leukocyte migration," "T-cell differentiation," "neutrophil activation," and "defense response." Furthermore, several genes were identified in these modules, including SLC11A1, MAPK8IP1, HMGCR, IFNGR1, CMPK2, CORO1A, IRF1, LDLR, BOLA-DMB, and BOLA-DMA, which are potentially associated with MAP pathogenesis. This study not only enhanced our knowledge of molecular mechanisms behind MAP infection but also highlighted several promising hub and hub-hub genes involved in macrophage-pathogen interaction.

摘要

约内氏病是反刍动物的一种慢性感染疾病,给奶牛群带来了巨大的经济损失。由于其性质复杂,该疾病的发病机制尚未完全明确。为了更深入地了解导致约内氏病的分枝杆菌感染所涉及的分子机制,采用了系统生物学方法。据我们所知,这是第一项同时考虑长链非编码RNA(lncRNAs)、转录因子(TFs)和信使RNA(mRNAs)来构建分枝杆菌感染相关综合基因调控网络的研究。进行了加权基因共表达网络分析(WGCNA)和功能富集分析,以探索共表达模块,其中未保留的模块具有改变的连接模式。在确定未保留模块中的枢纽基因和枢纽-枢纽基因以及转录因子和长链非编码RNA后,构建了lncRNA-mRNA-TF综合网络,并确定了lncRNAs的顺式和反式靶标。在八个未保留模块中均发现了lncRNAs的顺式和反式靶标。47个未保留模块中的21个显示出与免疫系统和分枝杆菌感染相关的显著生物学过程。最重要的未保留模块中一些与分枝杆菌感染相关的途径包括“细胞因子介导的信号通路的正调控”、“白细胞迁移的负调控”、“T细胞分化”、“中性粒细胞活化”和“防御反应”。此外,在这些模块中鉴定出了几个基因,包括SLC11A1、MAPK8IP1、HMGCR、IFNGR1、CMPK2、CORO1A、IRF1、LDLR、BOLA-DMB和BOLA-DMA,它们可能与分枝杆菌的发病机制有关。这项研究不仅增进了我们对分枝杆菌感染背后分子机制的了解,还突出了几个参与巨噬细胞-病原体相互作用的有前景的枢纽基因和枢纽-枢纽基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e21c/8287970/83e0705b2662/fgene-12-668448-g001.jpg

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