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The Transmembrane Domains of Sindbis Virus Envelope Glycoproteins Induce Cell Death

机译:Sindbis病毒包膜糖蛋白的跨膜结构域导致细胞死亡。

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摘要

Sindbis virus, the prototype alphavirus, kills cells by inducing apoptosis. To investigate potential mechanisms by which Sindbis virus induces apoptosis, we examined whether specific viral gene products were able to induce cell death. Genes encoding the three structural proteins—capsid, the precursor E1 (6K plus E1), and the precursor E2 (P62 or E3 plus E2)—were cotransfected with a β-galactosidase reporter plasmid in transient-transfection assays in rat prostate adenocarcinoma AT3 cells. Cell death, as determined by measuring the loss of blue cells, was observed in AT3 cells transfected with 6K plus E1 and with P62 but not in cells transfected with capsid. Deletion mutagenesis of P62 indicated that large regions of the cytoplasmic domain and extracellular domain were not essential for the induction of cell death. However, constructs containing the minimal E3 signal sequence fused to the E2 transmembrane domain and the minimal E3 signal sequence fused to the E1 transmembrane domain induced death as efficiently as full-length P62 and 6K plus E1, whereas no cell death was observed after transfection with a control construct containing the E3 signal sequence linked to the transmembrane domain of murine CD4. These data demonstrate that intracellular expression of the transmembrane domains of the Sindbis virus envelope glycoproteins can kill AT3 cells.
机译:原型α病毒Sindbis病毒通过诱导细胞凋亡杀死细胞。为了研究辛德比斯病毒诱导凋亡的潜在机制,我们检查了特定的病毒基因产物是否能够诱导细胞死亡。在大鼠前列腺腺癌AT3细胞的瞬时转染实验中,将编码三种结构蛋白(衣壳,前体E1(6K加E1)和前体E2(P62或E3加E2)的基因与β-半乳糖苷酶报告质粒共转染。 。通过测量蓝色细胞的损失确定的细胞死亡,在用6K加E1和P62转染的AT3细胞中观察到,但在用衣壳转染的细胞中未观察到。 P62的缺失诱变表明,胞质域和细胞外域的大区域对于诱导细胞死亡不是必需的。然而,含有与E2跨膜结构域融合的最小E3信号序列和与E1跨膜结构域融合的最小E3信号序列的构建体与全长P62和6K加E1一样有效地诱导了死亡,而在以含有与鼠CD4的跨膜结构域连接的E3信号序列的对照构建体。这些数据表明,Sindbis病毒包膜糖蛋白跨膜结构域的细胞内表达可以杀死AT3细胞。

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