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Functional Analysis of the Simian Immunodeficiency Virus Vpx Protein: Identification of Packaging Determinants and a Novel Nuclear Targeting Domain

机译:猿猴免疫缺陷病毒Vpx蛋白的功能分析:包装决定因素和新型核靶向域的鉴定。

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摘要

The vpx gene products of human immunodeficiency virus type 2 (HIV-2) and of the closely related simian immunodeficiency viruses from sooty mangabeys (SIVsm) and macaques (SIVmac) comprise a 112-amino-acid virion-associated protein that is critical for efficient virus replication in nondividing cells such as macrophages. When expressed in the absence of other viral proteins, Vpx localizes to the nuclear membrane as well as to the nucleus; however, in the context of virus replication Vpx is packaged into virions via interaction with the p6 domain of the Gag precursor polyprotein (p55gag). To identify the domains essential for virion incorporation and nuclear localization, site-directed mutations were introduced into the vpx gene of SIVsmPBj1.9 and functionally analyzed. Our results show that (i) mutation of two highly conserved L74 and I75 residues impaired both virion incorporation and nuclear localization of Vpx; (ii) substitution of conserved H82, G86, C87, P103, and P106 residues impaired Vpx nuclear localization but not virion incorporation; (iii) mutations of conserved Y66, Y69, and Y71 residues impaired virion incorporation but not the translocation of Vpx to the nucleus; and (iv) a mutation at E30 (predicted to disrupt an N-terminal α-helix) had no effect on either virion incorporation or nuclear localization of Vpx. Importantly, mutations in Vpx which impaired nuclear localization also reduced virus replication in macaque macrophages, suggesting an important role of the carboxyl terminus of Vpx in nuclear translocation of the viral preintegration complex. Analyzing this domain in greater detail, we identified a 26-amino-acid (aa 60 to 85) fragment that was sufficient to mediate the transport of a heterologous protein (green fluorescent protein [GFP]) to the nucleus. Taken together, these results indicate that virion incorporation and nuclear localization are encoded by two partially overlapping domains in the C-terminus of Vpx (aa 60 to 112). The identification of a novel 26-amino-acid nuclear targeting domain provides a new tool to investigate the nuclear import of the HIV-2/SIV preintegration complex.
机译:人类2型免疫缺陷病毒(HIV-2)以及来自黑社会(SIVsm)和猕猴(SIVmac)的紧密相关的猿猴免疫缺陷病毒的vpx基因产物包含112个氨基酸的病毒体相关蛋白,对高效病毒在非分裂细胞(例如巨噬细胞)中复制。当在没有其他病毒蛋白的情况下表达时,Vpx定位于核膜以及细胞核。但是,在病毒复制的情况下,Vpx通过与Gag前体多蛋白(p55gag)的p6域相互作用而被包装到病毒体中。为了鉴定对于病毒体掺入和核定位必不可少的结构域,将定点突变引入SIVsmPBj1.9的vpx基因中并进行功能分析。我们的结果表明:(i)两个高度保守的L74和I75残基的突变会损害病毒颗粒的结合和Vpx的核定位; (ii)替换保守的H82,G86,C87,P103和P106残基会损害Vpx核定位,但不会破坏病毒体掺入; (iii)保守的Y66,Y69和Y71残基的突变会损害病毒体掺入,但不会使Vpx易位至细胞核; (iv)E30处的突变(预计会破坏N端α-螺旋)对病毒颗粒的结合或Vpx的核定位均无影响。重要的是,削弱核定位的Vpx突变也减少了猕猴巨噬细胞中的病毒复制,表明Vpx的羧基末端在病毒预整合复合物的核转运中具有重要作用。更详细地分析此域,我们确定了一个26位氨基酸(从60到85)的片段,足以介导异源蛋白(绿色荧光蛋白[GFP])向细胞核的转运。两者合计,这些结果表明,病毒体的掺入和核定位是由Vpx的C末端(aa 60至112)中的两个部分重叠的域编码的。新型26氨基酸核靶向域的鉴定为研究HIV-2 / SIV预整合复合物的核输入提供了新工具。

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