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The Role of NS5 Protein in Determination of Host Cell Range for Yellow Fever Virus

机译:NS5蛋白在黄热病病毒中测定宿主细胞范围中的作用

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Yellow fever virus (YFV) tropism is restricted to human and nonhuman primates. The nonstructural protein 5 (NS5) protein of YFV binds to primate signal transducer and activator of transcription 2 (STAT2) and antagonizes interferon (IFN) signaling. However, YFV NS5 is unable to bind mouse STAT2 and antagonize murine IFN signaling. A similar observation has been made with the NS5 protein of both dengue virus (DENV) and Zika virus (ZIKV). However, the key difference between the NS5 protein of YFV and those of DENV and ZIKV is that YFV NS5 binds human STAT2 in an IFN-dependent manner. In human cells, IFN-I treatment induces K63-linked ubiquitination on lysine (K) 6 of YFV NS5, which is required for binding human STAT2. This IFN-induced ubiquitination of YFV NS5 is absent in murine cells resulting in the lack of binding of YFV NS5 and human STAT2 in murine cells. This highlights the importance of YFV NS5 ubiquitination in determining the host cell range for YFV.
机译:黄热病病毒(YFV)热衷于人类和非人的灵长类动物。 YFV的非结构蛋白5(NS5)蛋白与灵长类会信号传感器和转录2(Stat2)的激活剂结合,并拮抗干扰素(IFN)信号传导。 但是,YFV NS5无法绑定鼠标Stat2并对鼠IFN信令进行绑定。 已经使用登革热病毒(DENV)和ZIKA病毒(ZIKV)的NS5蛋白质进行了类似的观察。 然而,YFV的NS5蛋白与DenV和ZIKV的关键差异是YFV NS5以IFN依赖性方式结合人Stat2。 在人体细胞中,IFN-I处理诱导K63连接的赖氨酸(K)6的YFV NS5上的泛素,这是结合人Stat2所必需的。 在鼠细胞中不存在IFN诱导的YFV NS5的泛素,导致YFV NS5和人Stat2在鼠细胞中缺乏结合。 这突出了YFV NS5 ubiquitch在确定YFV的宿主细胞范围内的重要性。

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