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7a protein of severe acute respiratory syndrome coronavirus inhibits cellular protein synthesis and activates p38 mitogen-activated protein kinase.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。
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Protoapigenone, a novel flavonoid, induces apoptosis in human prostate cancer cells through activation of p38 mitogen-activated protein kinase and c-Jun NH2-terminal kinase 1/2.原芹菜素,一种新型黄酮类化合物,通过激活p38丝裂原活化蛋白激酶和c-Jun氨基末端激酶1/2诱导人前列腺癌细胞凋亡。
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本文引用的文献

1
The 3a protein of severe acute respiratory syndrome-associated coronavirus induces apoptosis in Vero E6 cells.严重急性呼吸综合征相关冠状病毒的3a蛋白可诱导Vero E6细胞凋亡。
J Gen Virol. 2005 Jul;86(Pt 7):1921-1930. doi: 10.1099/vir.0.80813-0.
2
The protein X4 of severe acute respiratory syndrome-associated coronavirus is expressed on both virus-infected cells and lung tissue of severe acute respiratory syndrome patients and inhibits growth of Balb/c 3T3 cell line.严重急性呼吸综合征相关冠状病毒的X4蛋白在严重急性呼吸综合征患者的病毒感染细胞和肺组织中均有表达,并抑制Balb/c 3T3细胞系的生长。
Chin Med J (Engl). 2005 Feb 20;118(4):267-74.
3
Structure and intracellular targeting of the SARS-coronavirus Orf7a accessory protein.严重急性呼吸综合征冠状病毒Orf7a辅助蛋白的结构与细胞内靶向作用
Structure. 2005 Jan;13(1):75-85. doi: 10.1016/j.str.2004.10.010.
4
The Birc6 (Bruce) gene regulates p53 and the mitochondrial pathway of apoptosis and is essential for mouse embryonic development.Birc6(布鲁斯)基因调控p53和凋亡的线粒体途径,对小鼠胚胎发育至关重要。
Proc Natl Acad Sci U S A. 2005 Jan 18;102(3):565-70. doi: 10.1073/pnas.0408744102. Epub 2005 Jan 7.
5
Overexpression of 7a, a protein specifically encoded by the severe acute respiratory syndrome coronavirus, induces apoptosis via a caspase-dependent pathway.严重急性呼吸综合征冠状病毒特异性编码的蛋白质7a的过表达通过半胱天冬酶依赖性途径诱导细胞凋亡。
J Virol. 2004 Dec;78(24):14043-7. doi: 10.1128/JVI.78.24.14043-14047.2004.
6
The membrane-associated inhibitor of apoptosis protein, BRUCE/Apollon, antagonizes both the precursor and mature forms of Smac and caspase-9.膜相关凋亡抑制蛋白BRUCE/Apollon可拮抗Smac和半胱天冬酶-9的前体和成熟形式。
J Biol Chem. 2005 Jan 7;280(1):174-82. doi: 10.1074/jbc.M411430200. Epub 2004 Oct 26.
7
Detection and monitoring of SARS coronavirus in the plasma and peripheral blood lymphocytes of patients with severe acute respiratory syndrome.严重急性呼吸综合征患者血浆及外周血淋巴细胞中SARS冠状病毒的检测与监测
Clin Chem. 2004 Jul;50(7):1237-40. doi: 10.1373/clinchem.2004.031237.
8
Characterization of a unique group-specific protein (U122) of the severe acute respiratory syndrome coronavirus.严重急性呼吸综合征冠状病毒一种独特的群特异性蛋白(U122)的特性分析
J Virol. 2004 Jul;78(14):7311-8. doi: 10.1128/JVI.78.14.7311-7318.2004.
9
A novel severe acute respiratory syndrome coronavirus protein, U274, is transported to the cell surface and undergoes endocytosis.一种新型严重急性呼吸综合征冠状病毒蛋白U274被转运至细胞表面并发生内吞作用。
J Virol. 2004 Jul;78(13):6723-34. doi: 10.1128/JVI.78.13.6723-6734.2004.
10
Phosphorylation of p38 MAPK and its downstream targets in SARS coronavirus-infected cells.严重急性呼吸综合征冠状病毒感染细胞中p38丝裂原活化蛋白激酶及其下游靶点的磷酸化作用
Biochem Biophys Res Commun. 2004 Jul 9;319(4):1228-34. doi: 10.1016/j.bbrc.2004.05.107.

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.

DOI:10.1128/JVI.80.2.785-793.2006
PMID:16378980
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1346853/
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。