首页> 外文期刊>Molecular BioSystems >vhfRNAi: a web-platform for analysis of hostrngenes involved in viral infections discoveredrnby genome wide RNAi screens
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vhfRNAi: a web-platform for analysis of hostrngenes involved in viral infections discoveredrnby genome wide RNAi screens

机译:vhfRNAi:用于分析与病毒感染有关的宿主基因的网络平台,通过全基因组的RNAi筛选发现

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摘要

Knockdown of host genes using high-throughput genome-wide RNA interference screens has identifiedrnnumerous host factors that affect viral infections, which would be helpful in understanding host–virusrninteractions. We have developed a vhfRNAi web resource based on genome-wide RNAi experiments forrnviruses. It contains experimental details of 12 249 entries (host factors + restriction factors) for 18 viruses.rnSimultaneously, this resource encompasses analysis of overlapping genes, genome wide associationrnstudies, gene ontology (GO), pathogen interacting proteins, interaction networks and pathwayrnenrichment. Using overlap analysis, it was found that Influenza A virus shared overlapping host genesrnwith the majority of viruses including Hepatitis C virus and Dengue virus 2. In the genome widernassociation studies analysis, 429 diseases/traits were mapped, of which obesity-related traits were thernmost common. GO analysis revealed that the major categories belonged to metabolic processes,rnmolecule transport, signal transduction, proteolysis, etc. In the pathogen interacting protein analysis,rnprotein interaction data from different resources can be explored for further understanding of host–virusrnbiology. By pathway enrichment analysis, a total of 8955 genes were mapped on 303 pathways withrnmost of the hits coming from metabolic pathways. We have found 491 genes that are not essential forrnthe host but essential for the virus and can be targeted to inhibit the virus. These may be explored asrnpotential candidates for drug targets. The resource is freely accessible at http://bioinfo.imtech.res.in/manrnojk/vhfrnai and will be useful in understanding host–virus biology as well as identification of targets forrnthe development of antiviral therapeutics.
机译:使用高通量全基因组RNA干扰筛选对宿主基因进行敲除,已鉴定出许多影响病毒感染的宿主因子,这将有助于理解宿主与病毒的相互作用。我们已经基于全病毒的全基因组RNAi实验开发了vhfRNAi网络资源。它包含针对18种病毒的12 249个条目(宿主因子+限制因子)的实验详细信息。同时,该资源还包括重叠基因,全基因组关联研究,基因本体(GO),病原体相互作用蛋白,相互作用网络和途径富集的分析。使用重叠分析,发现甲型流感病毒与大多数病毒(包括丙型肝炎病毒和登革热病毒2)共享宿主基因重叠。在基因组更广泛的关联研究分析中,绘制了429种疾病/特征,其中与肥胖有关的特征最严重共同。 GO分析显示,主要类别属于代谢过程,分子转运,信号转导,蛋白水解等。在病原体相互作用蛋白分析中,可以探索来自不同资源的rn蛋白相互作用数据,以进一步了解宿主-病毒生物学。通过途径富集分析,在303个途径上共绘制了8955个基因,其中大部分命中来自代谢途径。我们发现了491个对宿主不是必需的基因,但对于病毒来说却是必需的,可以靶向抑制该病毒。这些可以作为药物靶标的潜在候选者进行探索。该资源可从http://bioinfo.imtech.res.in/manrnojk/vhfrnai免费获得,并将有助于了解宿主病毒生物学以及确定抗病毒治疗药物开发目标。

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  • 来源
    《Molecular BioSystems》 |2017年第7期|1377-1387|共11页
  • 作者单位

    Bioinformatics Centre, Institute of Microbial Technology, Council of Scientific and Industrial Research, Sector 39-A, Chandigarh-160036, India;

    Bioinformatics Centre, Institute of Microbial Technology, Council of Scientific and Industrial Research, Sector 39-A, Chandigarh-160036, India;

    Bioinformatics Centre, Institute of Microbial Technology, Council of Scientific and Industrial Research, Sector 39-A, Chandigarh-160036, India;

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