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Activation of AP-1 signal transduction pathway by SARS coronavirus nucleocapsid protein
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. T...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2003
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111052/ https://www.ncbi.nlm.nih.gov/pubmed/14623261 http://dx.doi.org/10.1016/j.bbrc.2003.10.075 |
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author | He, Runtao Leeson, Andrew Andonov, Anton Li, Yan Bastien, Nathalie Cao, Jingxin Osiowy, Carla Dobie, Frederick Cutts, Todd Ballantine, Melissa Li, Xuguang |
author_facet | He, Runtao Leeson, Andrew Andonov, Anton Li, Yan Bastien, Nathalie Cao, Jingxin Osiowy, Carla Dobie, Frederick Cutts, Todd Ballantine, Melissa Li, Xuguang |
author_sort | He, Runtao |
collection | PubMed |
description | 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-κB 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. |
format | Online Article Text |
id | pubmed-7111052 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71110522020-04-02 Activation of AP-1 signal transduction pathway by SARS coronavirus nucleocapsid protein He, Runtao Leeson, Andrew Andonov, Anton Li, Yan Bastien, Nathalie Cao, Jingxin Osiowy, Carla Dobie, Frederick Cutts, Todd Ballantine, Melissa Li, Xuguang Biochem Biophys Res Commun Article 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-κB 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. Elsevier Inc. 2003-11-28 2003-11-05 /pmc/articles/PMC7111052/ /pubmed/14623261 http://dx.doi.org/10.1016/j.bbrc.2003.10.075 Text en Copyright © 2003 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article He, Runtao Leeson, Andrew Andonov, Anton Li, Yan Bastien, Nathalie Cao, Jingxin Osiowy, Carla Dobie, Frederick Cutts, Todd Ballantine, Melissa Li, Xuguang Activation of AP-1 signal transduction pathway by SARS coronavirus nucleocapsid protein |
title | Activation of AP-1 signal transduction pathway by SARS coronavirus nucleocapsid protein |
title_full | Activation of AP-1 signal transduction pathway by SARS coronavirus nucleocapsid protein |
title_fullStr | Activation of AP-1 signal transduction pathway by SARS coronavirus nucleocapsid protein |
title_full_unstemmed | Activation of AP-1 signal transduction pathway by SARS coronavirus nucleocapsid protein |
title_short | Activation of AP-1 signal transduction pathway by SARS coronavirus nucleocapsid protein |
title_sort | activation of ap-1 signal transduction pathway by sars coronavirus nucleocapsid protein |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111052/ https://www.ncbi.nlm.nih.gov/pubmed/14623261 http://dx.doi.org/10.1016/j.bbrc.2003.10.075 |
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