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A High-Content RNAi Screen Identifies Ubiquitin Modifiers That Regulate TNF-Dependent Nuclear Accumulation of NF-κB

机译:高内涵RNAi筛选确定泛素修饰剂调节NF-κB的TNF依赖性核积累。

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摘要

The mammalian tumor necrosis factor (TNF) cytokine is a central mediator of inflammatory events. Recent studies revealed a number of complex and sophisticated interactions between the TNF pathway and the enzymatic activities encoded by ubiquitin ligases and deubiquitylation enzymes. However, very little is known about the identity of the ubiquitin pathway members that control the extent of ubiquitylation in TNF responses. To address this deficit, we conducted an unbiased, high-content screen of the human ubiquitin pathway for gene products that control defining features of the cellular response to TNF. In particular, we sought to identify ubiquitin modifying enzymes that alter the ability of TNF to regulate the nuclear accumulation of nuclear factor kappa B. In this screen, we identified and validated several novel regulators of the TNF pathway. We believe these regulators constitute potential targets for pharmacological interventions that manipulate TNF-dependent inflammation.
机译:哺乳动物肿瘤坏死因子(TNF)细胞因子是炎症事件的主要介质。最近的研究表明,TNF途径与泛素连接酶和去泛素化酶编码的酶活性之间存在许多复杂和复杂的相互作用。然而,关于控制TNF反应中泛素化程度的泛素途径成员的身份知之甚少。为了解决这一缺陷,我们对人类泛素途径进行了无偏见的高内涵筛选,以检测控制定义为TNF的细胞反应特征的基因产物。特别是,我们寻求鉴定可改变TNF调节核因子kappa B核积累能力的泛素修饰酶。在此筛选中,我们鉴定并验证了TNF途径的几种新型调节剂。我们认为,这些调节剂构成操纵TNF依赖性炎症的药理干预措施的潜在目标。

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