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严重急性呼吸综合征冠状病毒核衣壳蛋白激活AP-1信号转导通路。

Activation of AP-1 signal transduction pathway by SARS coronavirus nucleocapsid protein.

作者信息

He Runtao, Leeson Andrew, Andonov Anton, Li Yan, Bastien Nathalie, Cao Jingxin, Osiowy Carla, Dobie Frederick, Cutts Todd, Ballantine Melissa, Li Xuguang

机构信息

National Microbiology Laboratory, Health Canada, 1015 Arlington Street, R3E 3R2, Winnipeg, MB, Canada.

出版信息

Biochem Biophys Res Commun. 2003 Nov 28;311(4):870-6. doi: 10.1016/j.bbrc.2003.10.075.

Abstract

In March 2003, a novel coronavirus was isolated from patients exhibiting atypical pneumonia and subsequently proven to be the causative agent of the disease now referred to as severe acute respiratory syndrome (SARS). The complete genome of the SARS coronavirus (SARS-CoV) has since been sequenced. The SARS-CoV nucleocapsid (SARS-CoV N) shares little homology with other members of the coronavirus family. To determine if the N protein is involved in the regulation of cellular signal transduction, an ELISA-based assay on transcription factors was used. We found that the amount of transcription factors binding to promoter sequences of c-Fos, ATF2, CREB-1, and FosB was increased by the expression of SARS-CoV N. Since these factors are related to AP-1 signal transduction pathway, we investigated whether the AP-1 pathway was activated by SARS-CoV N protein using the PathDetect system. The results demonstrated that the expression of N protein, not the membrane protein (M), activated AP-1 pathway. We also found that SARS-CoV N protein does not activate NF-kappaB pathway, demonstrating that activation of important cellular pathways by SAS-CoV N protein is selective. Thus our data for the first time indicate that SARS-CoV has encoded a strategy to regulate cellular signaling process.

摘要

2003年3月,一种新型冠状病毒从表现出非典型肺炎症状的患者身上分离出来,随后被证实是现在被称为严重急性呼吸综合征(SARS)的致病因子。此后,SARS冠状病毒(SARS-CoV)的完整基因组已被测序。SARS-CoV核衣壳(SARS-CoV N)与冠状病毒家族的其他成员几乎没有同源性。为了确定N蛋白是否参与细胞信号转导的调节,我们使用了基于ELISA的转录因子检测方法。我们发现,与c-Fos、ATF2、CREB-1和FosB启动子序列结合的转录因子数量因SARS-CoV N的表达而增加。由于这些因子与AP-1信号转导途径相关,我们使用PathDetect系统研究了SARS-CoV N蛋白是否激活了AP-1途径。结果表明,是N蛋白而非膜蛋白(M)激活了AP-1途径。我们还发现SARS-CoV N蛋白不会激活NF-κB途径,这表明SARS-CoV N蛋白对重要细胞途径的激活具有选择性。因此,我们的数据首次表明SARS-CoV编码了一种调节细胞信号传导过程的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9f7/7111052/174c7c4a30e6/gr1.jpg

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