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A functional nuclear localization sequence in the VP1 capsid protein of coxsackievirus B3
The capsid proteins of some RNA viruses can translocate to the nucleus and interfere with cellular phenotypes. In this study we found that the VP1 capsid protein of coxsackievirus B3 (CVB3) was dominantly localized in the nucleus of the cells transfected with VP1-expressing plasmid. The VP1 nuclear...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111942/ https://www.ncbi.nlm.nih.gov/pubmed/23010168 http://dx.doi.org/10.1016/j.virol.2012.08.040 |
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author | Wang, Tianying Yu, Bohai Lin, Lexun Zhai, Xia Han, Yelu Qin, Ying Guo, Zhiwei Wu, Shuo Zhong, Xiaoyan Wang, Yan Tong, Lei Zhang, Fengmin Si, Xiaoning Zhao, Wenran Zhong, Zhaohua |
author_facet | Wang, Tianying Yu, Bohai Lin, Lexun Zhai, Xia Han, Yelu Qin, Ying Guo, Zhiwei Wu, Shuo Zhong, Xiaoyan Wang, Yan Tong, Lei Zhang, Fengmin Si, Xiaoning Zhao, Wenran Zhong, Zhaohua |
author_sort | Wang, Tianying |
collection | PubMed |
description | The capsid proteins of some RNA viruses can translocate to the nucleus and interfere with cellular phenotypes. In this study we found that the VP1 capsid protein of coxsackievirus B3 (CVB3) was dominantly localized in the nucleus of the cells transfected with VP1-expressing plasmid. The VP1 nuclear localization also occurred in the cells infected with CVB3. Truncation analysis indicated that the VP1 nuclear localization sequence located near the C-terminal. The substitution of His220 with threonine completely abolished its translocation. The VP1 proteins of other CVB types might have the nuclear localization potential because this region was highly conserved. Moreover, the VP1 nuclear localization induced cell cycle deregulation, including a prolonged S phase and shortened G2-M phase. Besides these findings, we also found a domain between Ala72 and Phe106 that caused the VP1 truncates dotted distributed in the cytoplasm. Our results suggest a new pathogenic mechanism of CVB. |
format | Online Article Text |
id | pubmed-7111942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71119422020-04-02 A functional nuclear localization sequence in the VP1 capsid protein of coxsackievirus B3 Wang, Tianying Yu, Bohai Lin, Lexun Zhai, Xia Han, Yelu Qin, Ying Guo, Zhiwei Wu, Shuo Zhong, Xiaoyan Wang, Yan Tong, Lei Zhang, Fengmin Si, Xiaoning Zhao, Wenran Zhong, Zhaohua Virology Article The capsid proteins of some RNA viruses can translocate to the nucleus and interfere with cellular phenotypes. In this study we found that the VP1 capsid protein of coxsackievirus B3 (CVB3) was dominantly localized in the nucleus of the cells transfected with VP1-expressing plasmid. The VP1 nuclear localization also occurred in the cells infected with CVB3. Truncation analysis indicated that the VP1 nuclear localization sequence located near the C-terminal. The substitution of His220 with threonine completely abolished its translocation. The VP1 proteins of other CVB types might have the nuclear localization potential because this region was highly conserved. Moreover, the VP1 nuclear localization induced cell cycle deregulation, including a prolonged S phase and shortened G2-M phase. Besides these findings, we also found a domain between Ala72 and Phe106 that caused the VP1 truncates dotted distributed in the cytoplasm. Our results suggest a new pathogenic mechanism of CVB. Elsevier Inc. 2012-11-25 2012-09-23 /pmc/articles/PMC7111942/ /pubmed/23010168 http://dx.doi.org/10.1016/j.virol.2012.08.040 Text en Copyright © 2012 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 Wang, Tianying Yu, Bohai Lin, Lexun Zhai, Xia Han, Yelu Qin, Ying Guo, Zhiwei Wu, Shuo Zhong, Xiaoyan Wang, Yan Tong, Lei Zhang, Fengmin Si, Xiaoning Zhao, Wenran Zhong, Zhaohua A functional nuclear localization sequence in the VP1 capsid protein of coxsackievirus B3 |
title | A functional nuclear localization sequence in the VP1 capsid protein of coxsackievirus B3 |
title_full | A functional nuclear localization sequence in the VP1 capsid protein of coxsackievirus B3 |
title_fullStr | A functional nuclear localization sequence in the VP1 capsid protein of coxsackievirus B3 |
title_full_unstemmed | A functional nuclear localization sequence in the VP1 capsid protein of coxsackievirus B3 |
title_short | A functional nuclear localization sequence in the VP1 capsid protein of coxsackievirus B3 |
title_sort | functional nuclear localization sequence in the vp1 capsid protein of coxsackievirus b3 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111942/ https://www.ncbi.nlm.nih.gov/pubmed/23010168 http://dx.doi.org/10.1016/j.virol.2012.08.040 |
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