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Dimerization and a Novel Tax Speckled Structure Localization Signal Are Required for Tax Nuclear Localization

机译:税收核定位需要二聚化和新颖的有斑点结构的定位信号

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摘要

The human T-cell leukemia virus type 1 oncoprotein Tax has pleiotropic activities, a subset of which likely leads to immortalization of T cells. Tax is expressed and known to function in both the cell nucleus and the cytoplasm. Tax has defined nuclear localization (NLS) and nuclear export signals that enable shuttling between the two compartments. In this study, we identified a novel region in Tax that targets the protein to discrete nuclear foci that we have previously termed Tax speckled structures (TSS). We demonstrated that the identified region is both necessary and sufficient for directing proteins to TSS. This novel TSS localization signal (TSLS), spanning amino acids 50 to 75, is separable from and adjacent to the NLS of Tax. Coexpression of a Tax NLS mutant and a Tax TSLS mutant rescued the nuclear entry and subnuclear TSS targeting of both proteins, demonstrating that these signals are independent domains. Our analysis also revealed that Tax proteins deficient for dimerization fail to localize to the nucleus. Consequently, when we restored dimerization via induction of a heterologous “dimerizer” domain, nuclear localization was rescued. Thus, we defined additional domains in Tax specific for nuclear localization and subnuclear targeting. Our results reveal a more complex network for regulation of Tax subcellular localization and subsequent function.
机译:人类T细胞白血病病毒1型癌蛋白Tax具有多效活性,其中一部分可能导致T细胞永生。在细胞核和细胞质中都表达并已知了Tax功能。税收定义了核能定位(NLS)和核能出口信号,可以在两个舱室之间穿梭。在这项研究中,我们确定了Tax中一个新的区域,该区域将蛋白质靶向离散的核病灶,我们先前将其称为Tax斑点结构(TSS)。我们证明了已鉴定的区域对于将蛋白质引导至TSS既必要又充分。这种新颖的TSS定位信号(TSLS)跨越50至75位氨基酸,可与Tax的NLS分离并相邻。 Tax NLS突变体和Tax TSLS突变体的共表达拯救了两种蛋白质的核进入和亚核TSS靶向,证明了这些信号是独立的结构域。我们的分析还显示,缺乏二聚作用的Tax蛋白无法定位到细胞核。因此,当我们通过诱导异源“二聚体”域恢复二聚化时,核定位得以挽救。因此,我们在Tax中定义了特定于核定位和亚核目标的其他域。我们的结果揭示了一个更复杂的网络,用于调节Tax亚细胞定位和后续功能。

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