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严重急性呼吸综合征冠状病毒的7a蛋白抑制细胞蛋白质合成并激活p38丝裂原活化蛋白激酶。

7a protein of severe acute respiratory syndrome coronavirus inhibits cellular protein synthesis and activates p38 mitogen-activated protein kinase.

作者信息

Kopecky-Bromberg Sarah A, Martinez-Sobrido Luis, Palese Peter

机构信息

Department of Microbiology, Mount Sinai School of Medicine, New York, NY 10029-6574, USA.

出版信息

J Virol. 2006 Jan;80(2):785-93. doi: 10.1128/JVI.80.2.785-793.2006.

Abstract

It was recently shown that the 7a protein of severe acute respiratory syndrome coronavirus induces biochemical changes associated with apoptosis. In this study, the mechanism by which the 7a protein induces apoptosis was examined. The 7a protein was tested for the ability to inhibit cellular gene expression because several proapoptotic viral proteins with this function have previously been identified. 7a protein inhibited expression of luciferase from an mRNA construct that specifically measures translation, whereas inhibitors of transcription and nucleocytoplasmic transport did not. The inhibition of translation and other cellular processes of gene expression have been associated with the induction of a stress response in cells. Western blot analysis using phosphospecific antibodies indicated that 7a protein activated p38 mitogen-activated protein kinase (MAPK), but not c-Jun N-terminal protein kinase/stress-activated protein kinase. Taken together, these data indicate that the induction of apoptosis by the 7a protein may be related to its ability to inhibit cellular translation and activate p38 MAPK.

摘要

最近研究表明,严重急性呼吸综合征冠状病毒的7a蛋白可诱导与细胞凋亡相关的生化变化。在本研究中,对7a蛋白诱导细胞凋亡的机制进行了研究。由于此前已鉴定出几种具有此功能的促凋亡病毒蛋白,因此检测了7a蛋白抑制细胞基因表达的能力。7a蛋白抑制了来自专门测量翻译的mRNA构建体的荧光素酶表达,而转录和核质运输抑制剂则无此作用。翻译抑制和基因表达的其他细胞过程与细胞应激反应的诱导有关。使用磷酸特异性抗体的蛋白质印迹分析表明,7a蛋白激活了p38丝裂原活化蛋白激酶(MAPK),但未激活c-Jun N末端蛋白激酶/应激激活蛋白激酶。综上所述,这些数据表明7a蛋白诱导细胞凋亡可能与其抑制细胞翻译和激活p38 MAPK的能力有关。

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