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Identification of NAP1 a Regulatory Subunit of IκB Kinase-Related Kinases That Potentiates NF-κB Signaling

机译:NAP1IκB激酶相关激酶的调节亚基可增强NF-κB信号传导的鉴定

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摘要

The IκB kinase (IKK)-related kinase NAK (also known as TBK or T2K) contributes to the activation of NF-κB-dependent gene expression. Here we identify NAP1 (for NAK-associated protein 1), a protein that interacts with NAK and its relative IKKɛ (also known as IKKi). NAP1 activates NAK and facilitates its oligomerization. Interestingly, the NAK-NAP1 complex itself effectively phosphorylated serine 536 of the p65/RelA subunit of NF-κB, and this activity was stimulated by tumor necrosis factor alpha (TNF-α). Overexpression of NAP1 specifically enhanced cytokine induction of an NF-κB-dependent, but not an AP-1-dependent, reporter. Depletion of NAP1 reduced NF-κB-dependent reporter gene expression and sensitized cells to TNF-α-induced apoptosis. These results define NAP1 as an activator of IKK-related kinases and suggest that the NAK-NAP1 complex may protect cells from TNF-α-induced apoptosis by promoting NF-κB activation.
机译:IκB激酶(IKK)相关的激酶NAK(也称为TBK或T2K)有助于激活NF-κB依赖性基因表达。在这里,我们确定了NAP1(与NAK相关的蛋白1),该蛋白与NAK及其相对的IKKɛ(也称为IKKi)相互作用。 NAP1激活NAK并促进其低聚。有趣的是,NAK-NAP1复合物本身有效地使NF-κB的p65 / RelA亚基的丝氨酸536磷酸化,并且这种活性被肿瘤坏死因子α(TNF-α)刺激。 NAP1的过表达特异性增强了依赖于NF-κB而不是依赖于AP-1的报告基因的细胞因子诱导。 NAP1的消耗减少了NF-κB依赖的报告基因表达,并使细胞对TNF-α诱导的细胞凋亡敏感。这些结果将NAP1定义为IKK相关激酶的激活剂,并表明NAK-NAP1复合物可通过促进NF-κB活化来保护细胞免受TNF-α诱导的细胞凋亡。

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