Department of Microbiology & Immunology, University of Western Ontario, London, Ontario, Canada.
Department of Microbiology & Immunology, University of Western Ontario, London, Ontario, Canada
mBio. 2018 May 1;9(3):e00390-18. doi: 10.1128/mBio.00390-18.
As obligate intracellular parasites, viruses are dependent on their infected hosts for survival. Consequently, viruses are under enormous selective pressure to utilize available cellular components and processes to their own advantage. As most, if not all, cellular activities are regulated at some level via protein interactions, host protein interaction networks are particularly vulnerable to viral exploitation. Indeed, viral proteins frequently target highly connected "hub" proteins to "hack" the cellular network, defining the molecular basis for viral control over the host. This widespread and successful strategy of network intrusion and exploitation has evolved convergently among numerous genetically distinct viruses as a result of the endless evolutionary arms race between pathogens and hosts. Here we examine the means by which a particularly well-connected viral hub protein, human adenovirus E1A, compromises and exploits the vulnerabilities of eukaryotic protein interaction networks. Importantly, these interactions identify critical regulatory hubs in the human proteome and help define the molecular basis of their function.
作为专性细胞内寄生虫,病毒的生存依赖于受感染的宿主。因此,病毒承受着巨大的选择压力,需要利用可用的细胞成分和过程来为自己谋取利益。由于大多数(如果不是全部的话)细胞活动都在某种程度上受到蛋白质相互作用的调控,因此宿主蛋白相互作用网络特别容易受到病毒的利用。事实上,病毒蛋白经常针对高度连接的“枢纽”蛋白,以“入侵”细胞网络,从而定义了病毒对宿主进行控制的分子基础。由于病原体和宿主之间无休止的进化军备竞赛,这种广泛而成功的网络入侵和利用策略在众多遗传上不同的病毒中趋同进化。在这里,我们研究了一种特别连接良好的病毒枢纽蛋白——人腺病毒 E1A——如何损害和利用真核生物蛋白质相互作用网络的脆弱性。重要的是,这些相互作用确定了人类蛋白质组中的关键调控枢纽,并有助于定义它们功能的分子基础。