Translational Control of Cytomegalovirus Gene Expression

描述（由申请方提供）：人巨细胞病毒（HCMV）主要在新生儿和免疫功能低下患者中引起大量发病和死亡。与其他病毒一样，HCMV必须逃避无数的宿主细胞抗病毒防御机制，其中之一是关闭由干扰素诱导的双链RNA（dsRNA）激活的蛋白激酶R（PKR）介导的整体蛋白合成。HCMV编码两种蛋白质，pTRS1和pIRS1，其阻断PKR活化。除了自缔合和与dsRNA和PKR结合之外，这些蛋白质具有使PKR重新定位于细胞核的前所未有的作用。为了阐明pTRS1和pIRS1对PKR作用的机制和意义，本实验拟精确描述pTRS1和pIRS1与RNA和蛋白质相互作用的结构域。这些研究还将揭示pTRS 1和pIRS 1对PKR的核重定位是否作为一种不寻常的病毒策略，用于将PKR从其细胞质靶点中去除，或者作为一种促进PKR尚未鉴定的可能对病毒有益的核功能的手段。最后，实验将直接检验pTRS1或pIRS1，特别是它们与dsRNA和PKR结合的能力，对HCMV复制是必需的这一假设。了解HCMV干扰PKR途径的机制将有助于新的观点到生化相互作用所需的PKR抑制在其他系统中，以及深入了解PKR核再分配活动的意义，迄今为止似乎是一个独特的属性β疱疹病毒。从这些非常规HCMV dsRNA结合蛋白的研究中获得的见解也将有助于在其他系统中识别新的dsRNA结合蛋白，并分析它们在抵消PKR和其他dsRNA激活反应中的功能。最后，由于缺乏阻断PKR激活能力的突变病毒在动物模型中的毒力大大降低，这些研究的结果可能在开发新的抗病毒策略和开发减毒活疫苗中具有应用。

DESCRIPTION (provided by applicant): Human cytomegalovirus (HCMV) causes substantial morbidity and mortality, primarily in newborns and immunocompromised patients. Like other viruses, HCMV must evade myriad host cell antiviral defense mechanisms, among which is the shut off of overall protein synthesis mediated by the interferon-induced, double-stranded RNA (dsRNA)-activated protein kinase R (PKR). HCMV encodes two proteins, pTRS1 and pIRS1, that block PKR activation. In addition to self-associating and to binding to dsRNA and to PKR, these proteins have the unprecedented effect of causing PKR to relocalize to the nucleus. In order to elucidate the mechanism and significance of pTRS1 and pIRS1 effects on PKR, experiments are proposed to precisely delineate the domains of pTRS1 and pIRS1 responsible for their interactions with RNA and proteins. These studies will also reveal whether the nuclear relocalization of PKR by pTRS1 and pIRS1 serves as an unusual viral strategy for removing PKR from its cytoplasmic targets or as a means of facilitating an as-yet-unidentified nuclear function of PKR that may be beneficial to the virus. Finally, experiments will directly test the hypothesis that either pTRS1 or pIRS1, and in particular their ability to bind to dsRNA and PKR, is essential for HCMV replication. Understanding the mechanism by which HCMV interferes with the PKR pathway will contribute new perspectives into biochemical interactions required for PKR inhibition in other systems as well as insights into the significance of the PKR nuclear redistribution activity which thus far seems to be a unique property of betaherpeviruses. The insights gained from studies of these unconventional HCMV dsRNA-binding proteins will also contribute to identifying new dsRNA-binding proteins in other systems and for analyzing their functions in counteracting PKR and other dsRNA-activated responses. Finally, since mutant viruses lacking the ability to block PKR activation have greatly reduced virulence in animal models, results of these studies may have applications in the development of new antiviral strategies and for the development of live attenuated vaccines.