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Integrating Transcriptomic and Proteomic Data Using Predictive Regulatory Network Models of Host Response to Pathogens

机译:使用宿主对病原体反应的预测性调控网络模型整合转录组和蛋白质组学数据

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摘要

Mammalian host response to pathogenic infections is controlled by a complex regulatory network connecting regulatory proteins such as transcription factors and signaling proteins to target genes. An important challenge in infectious disease research is to understand molecular similarities and differences in mammalian host response to diverse sets of pathogens. Recently, systems biology studies have produced rich collections of omic profiles measuring host response to infectious agents such as influenza viruses at multiple levels. To gain a comprehensive understanding of the regulatory network driving host response to multiple infectious agents, we integrated host transcriptomes and proteomes using a network-based approach. Our approach combines expression-based regulatory network inference, structured-sparsity based regression, and network information flow to infer putative physical regulatory programs for expression modules. We applied our approach to identify regulatory networks, modules and subnetworks that drive host response to multiple influenza infections. The inferred regulatory network and modules are significantly enriched for known pathways of immune response and implicate apoptosis, splicing, and interferon signaling processes in the differential response of viral infections of different pathogenicities. We used the learned network to prioritize regulators and study virus and time-point specific networks. RNAi-based knockdown of predicted regulators had significant impact on viral replication and include several previously unknown regulators. Taken together, our integrated analysis identified novel module level patterns that capture strain and pathogenicity-specific patterns of expression and helped identify important regulators of host response to influenza infection.
机译:哺乳动物宿主对病原体感染的反应是由一个复杂的调控网络控制的,该网络将诸如转录因子和信号蛋白之类的调控蛋白连接到目标基因上。传染病研究的一个重要挑战是了解哺乳动物宿主对多种病原体的反应的分子相似性和差异性。最近,系统生物学研究已经产生了丰富的卵子图谱集合,可测量宿主对多种水平的感染因子(例如流感病毒)的反应。为了全面了解驱动宿主对多种传染原反应的调控网络,我们使用基于网络的方法整合了宿主转录组和蛋白质组。我们的方法结合了基于表达式的监管网络推断,基于结构稀疏的回归和网络信息流,以推断出针对表达式模块的假定物理监管程序。我们采用了我们的方法来识别可导致宿主对多种流感感染做出反应的监管网络,模块和子网。推断的调节网络和模块显着丰富了已知的免疫应答途径,并在不同病原性病毒感染的差异应答中暗示了凋亡,剪接和干扰素信号传导过程。我们使用学习到的网络来划分监管机构的优先级,并研究病毒和特定时间点的网络。基于RNAi的预测调控子的抑制作用对病毒复制具有重大影响,并且包括几个以前未知的调控子。综上所述,我们的综合分析确定了新的模块水平模式,该模式可捕获菌株和特定病原性的表达模式,并有助于确定宿主对流感感染的反应的重要调控因子。

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