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Human HERC5 restricts an early stage of HIV-1 assembly by a mechanism correlating with the ISGylation of Gag

机译:人类HERC5通过与Gag的ISGylation相关的机制限制HIV-1装配的早期阶段

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摘要

BackgroundThe identification and characterization of several interferon (IFN)-induced cellular HIV-1 restriction factors, defined as host cellular proteins or factors that restrict or inhibit the HIV-1 life cycle, have provided insight into the IFN response towards HIV-1 infection and identified new therapeutic targets for HIV-1 infection. To further characterize the mechanism underlying restriction of the late stages of HIV-1 replication, we assessed the ability of IFNbeta-induced genes to restrict HIV-1 Gag particle production and have identified a potentially novel host factor called HECT domain and RCC1-like domain-containing protein 5 (HERC5) that blocks a unique late stage of the HIV-1 life cycle.
机译:背景几种干扰素(IFN)诱导的细胞HIV-1限制因子的鉴定和表征,被定义为宿主细胞蛋白或限制或抑制HIV-1生命周期的因子,为IFN对HIV-1感染和确定了HIV-1感染的新治疗靶标。为了进一步表征潜在的限制HIV-1复制后期阶段的机制,我们评估了IFNbeta诱导的基因限制HIV-1 Gag颗粒产生的能力,并确定了潜在的新型宿主因子,称为HECT结构域和RCC1类结构域含有蛋白5(HERC5),可阻止HIV-1生命周期的独特晚期。

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