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Interaction between SARS-CoV helicase and a multifunctional cellular protein (Ddx5) revealed by yeast and mammalian cell two-hybrid systems
To reveal the putative cellular factors involved in SARS coronavirus replication, the helicase (Hel, nsp13) of SARS coronavirus was used to screen the cDNA library of rat pulmonary epithelial cells using the yeast two-hybrid system. Positively interacting proteins were further tested using a mammali...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087151/ https://www.ncbi.nlm.nih.gov/pubmed/19224332 http://dx.doi.org/10.1007/s00705-009-0323-y |
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author | Chen, Jin-Yan Chen, Wan-Nan Poon, Kwok-Man Vincent Zheng, Bo-Jian Lin, Xu Wang, Yong-Xiang Wen, Yu-Mei |
author_facet | Chen, Jin-Yan Chen, Wan-Nan Poon, Kwok-Man Vincent Zheng, Bo-Jian Lin, Xu Wang, Yong-Xiang Wen, Yu-Mei |
author_sort | Chen, Jin-Yan |
collection | PubMed |
description | To reveal the putative cellular factors involved in SARS coronavirus replication, the helicase (Hel, nsp13) of SARS coronavirus was used to screen the cDNA library of rat pulmonary epithelial cells using the yeast two-hybrid system. Positively interacting proteins were further tested using a mammalian cell hybrid system and co-immunoprecipitation in the human A549 cell line, which has been shown to support SARS coronavirus replication. Out of the seven positive clones observed by yeast two-hybrid assay, only the Ddx5 (Asp-Glu-Ala-Asp box polypeptide 5) protein showed specific interaction with SARS-CoV helicase. When expression of DdX5 was knocked down by small interfering RNA (siRNA), SARS coronavirus replication was significantly inhibited in fetal rhesus kidney (FRhK-4) cells. Since Ddx5 is a multifunctional protein that plays important roles in transcriptional regulation, its interaction with SARS coronavirus helicase provides interesting clues for studying virus–host cell interactions in SARS-CoV infections. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00705-009-0323-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7087151 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-70871512020-03-23 Interaction between SARS-CoV helicase and a multifunctional cellular protein (Ddx5) revealed by yeast and mammalian cell two-hybrid systems Chen, Jin-Yan Chen, Wan-Nan Poon, Kwok-Man Vincent Zheng, Bo-Jian Lin, Xu Wang, Yong-Xiang Wen, Yu-Mei Arch Virol Brief Report To reveal the putative cellular factors involved in SARS coronavirus replication, the helicase (Hel, nsp13) of SARS coronavirus was used to screen the cDNA library of rat pulmonary epithelial cells using the yeast two-hybrid system. Positively interacting proteins were further tested using a mammalian cell hybrid system and co-immunoprecipitation in the human A549 cell line, which has been shown to support SARS coronavirus replication. Out of the seven positive clones observed by yeast two-hybrid assay, only the Ddx5 (Asp-Glu-Ala-Asp box polypeptide 5) protein showed specific interaction with SARS-CoV helicase. When expression of DdX5 was knocked down by small interfering RNA (siRNA), SARS coronavirus replication was significantly inhibited in fetal rhesus kidney (FRhK-4) cells. Since Ddx5 is a multifunctional protein that plays important roles in transcriptional regulation, its interaction with SARS coronavirus helicase provides interesting clues for studying virus–host cell interactions in SARS-CoV infections. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00705-009-0323-y) contains supplementary material, which is available to authorized users. Springer Vienna 2009-02-18 2009 /pmc/articles/PMC7087151/ /pubmed/19224332 http://dx.doi.org/10.1007/s00705-009-0323-y Text en © Springer-Verlag 2009 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Brief Report Chen, Jin-Yan Chen, Wan-Nan Poon, Kwok-Man Vincent Zheng, Bo-Jian Lin, Xu Wang, Yong-Xiang Wen, Yu-Mei Interaction between SARS-CoV helicase and a multifunctional cellular protein (Ddx5) revealed by yeast and mammalian cell two-hybrid systems |
title | Interaction between SARS-CoV helicase and a multifunctional cellular protein (Ddx5) revealed by yeast and mammalian cell two-hybrid systems |
title_full | Interaction between SARS-CoV helicase and a multifunctional cellular protein (Ddx5) revealed by yeast and mammalian cell two-hybrid systems |
title_fullStr | Interaction between SARS-CoV helicase and a multifunctional cellular protein (Ddx5) revealed by yeast and mammalian cell two-hybrid systems |
title_full_unstemmed | Interaction between SARS-CoV helicase and a multifunctional cellular protein (Ddx5) revealed by yeast and mammalian cell two-hybrid systems |
title_short | Interaction between SARS-CoV helicase and a multifunctional cellular protein (Ddx5) revealed by yeast and mammalian cell two-hybrid systems |
title_sort | interaction between sars-cov helicase and a multifunctional cellular protein (ddx5) revealed by yeast and mammalian cell two-hybrid systems |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087151/ https://www.ncbi.nlm.nih.gov/pubmed/19224332 http://dx.doi.org/10.1007/s00705-009-0323-y |
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