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Nup153 and Nup98 bind the HIV-1 core and contribute to the early steps of HIV-1 replication

机译:Nup153和Nup98结合HIV-1核心并有助于HIV-1复制的早期步骤

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摘要

The early steps of HIV-1 replication involve the entry of HIV-1 into the nucleus, which is characterized by viral interactions with nuclear pore components. HIV-1 developed an evolutionary strategy to usurp the nuclear pore machinery and chromatin in order to integrate and efficiently express viral genes. In the current work, we studied the role of nucleoporins 153 and 98 (Nup153 and Nup98) in infection of human Jurkat lymphocytes by HIV-1. We showed that Nup153-depleted cells exhibited a defect in nuclear import, while depletion of Nup 98 caused a slight defect in HIV integration. To explore the biochemical viral determinants for the requirement of Nup153 and Nup98 during HIV-1 infection, we tested the ability of these nucleoporins to interact with HIV-1 cores. Our findings showed that both nucleoporins bind HIV-1 cores suggesting that this interaction is important for HIV-1 nuclear import and/or integration. Distribution analysis of integration sites in Nup153-depleted cells revealed a reduced tendency of HIV-1 to integrate in intragenic sites, which in part could account for the large infectivity defect observed in Nup153-depleted cells. Our work strongly supports a role for Nup153 in HIV-1 nuclear import and integration.
机译:HIV-1复制的早期步骤涉及HIV-1进入细胞核,其特征是病毒与核孔成分的相互作用。 HIV-1开发了一种进化策略来篡夺核孔机制和染色质,以整合并有效表达病毒基因。在当前的工作中,我们研究了核孔蛋白153和98(Nup153和Nup98)在HIV-1感染人Jurkat淋巴细胞中的作用。我们显示,耗尽Nup153的细胞在核输入方面表现出缺陷,而耗尽Nup 98则导致HIV整合略有缺陷。为了探索在HIV-1感染期间对Nup153和Nup98的需求的生化病毒决定因素,我们测试了这些核孔蛋白与HIV-1核心相互作用的能力。我们的研究结果表明,两个核孔蛋白均结合HIV-1核,这表明这种相互作用对HIV-1核的导入和/或整合很重要。 Nup153缺失细胞中整合位点的分布分析显示,HIV-1整合入基因内位点的趋势有所降低,这部分可以解释Nup153耗尽细胞中观察到的巨大感染力缺陷。我们的工作强烈支持Nup153在HIV-1核进口和整合中的作用。

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