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The 3a Protein of SARS-coronavirus Induces Apoptosis in Vero E6 Cells

机译:SARS-CORONAVIRUS的3A蛋白在VERO E6细胞中诱导细胞凋亡

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An outbreak of severe acute respiratory syndrome (SARS) occurred in China and the first case emerged in mid November 2002. The etiologic agent of this disease was found to be a previously unknown coronavirus, SARS-CoV. The detailed pathology of SARS-CoV infection and the host response to the viral infection are still not known. The 3a gene encodes a non-structural viral protein which is predicted to be a transmembrane protein. In this study, we showed that the 3a protein was localized to the endoplasmic reticulum (ER) in 3a-transfected monkey kidney Vero E6 cells. In vitro experiments of chromatin condensation and DNA fragmentation suggest that the 3a protein may trigger apoptosis. Our data show that over-expression of a single SARS-CoV protein can induce apoptosis in vitro. Thus GFP-3a fusion protein could also be used as a biosensor for monitoring the cytopathic features of SARS infection, e.g. lymphopenia, in animal model systems, similar to nucleocapsid and 7a proteins.
机译:在中国发生了严重急性呼吸综合征(SARS)的爆发,2002年11月中旬出现的第一个案例。发现这种疾病的病因因子是先前未知的冠状病毒,SARS-COV。 SARS-COV感染和对病毒感染的宿主反应的详细病理仍然不知道。 3A基因编码非结构性病毒蛋白,其预测是跨膜蛋白。在这项研究中,我们认为3A蛋白质在3A转染的猴子肾VERO E6细胞中局部定位于内质网(ER)。染色质缩合和DNA碎片的体外实验表明,3A蛋白可能引发凋亡。我们的数据表明,单个SARS-COV蛋白的过表达可以在体外诱导细胞凋亡。因此,GFP-3A融合蛋白也可以用作用于监测SARS感染的细胞传感器的生物传感器,例如,SARS感染。淋巴细胞,在动物模型系统中,类似于核衣壳和7A蛋白。

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