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Trafficking motifs in the SARS-coronavirus nucleocapsid protein

The severe acute respiratory syndrome-coronavirus nucleocapsid (N) protein is involved in virus replication and modulation of cell processes. In this latter respect control may in part be achieved through the sub-cellular localisation of the protein. N protein predominately localises in the cytoplas...

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Detalles Bibliográficos
Autores principales: You, Jae-Hwan, Reed, Mark L., Hiscox, Julian A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Inc. 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7092899/
https://www.ncbi.nlm.nih.gov/pubmed/17524366
http://dx.doi.org/10.1016/j.bbrc.2007.05.036
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author You, Jae-Hwan
Reed, Mark L.
Hiscox, Julian A.
author_facet You, Jae-Hwan
Reed, Mark L.
Hiscox, Julian A.
author_sort You, Jae-Hwan
collection PubMed
description The severe acute respiratory syndrome-coronavirus nucleocapsid (N) protein is involved in virus replication and modulation of cell processes. In this latter respect control may in part be achieved through the sub-cellular localisation of the protein. N protein predominately localises in the cytoplasm (the site of virus replication and assembly) but also in the nucleus/nucleolus. Using a combination of live-cell and confocal microscopy coupled to mutagenesis we identified a cryptic nucleolar localisation signal in the central part of the N protein. In addition, based on structural comparison to the avian coronavirus N protein, a nuclear export signal was identified in the C-terminal region of the protein.
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spelling pubmed-70928992020-03-25 Trafficking motifs in the SARS-coronavirus nucleocapsid protein You, Jae-Hwan Reed, Mark L. Hiscox, Julian A. Biochem Biophys Res Commun Article The severe acute respiratory syndrome-coronavirus nucleocapsid (N) protein is involved in virus replication and modulation of cell processes. In this latter respect control may in part be achieved through the sub-cellular localisation of the protein. N protein predominately localises in the cytoplasm (the site of virus replication and assembly) but also in the nucleus/nucleolus. Using a combination of live-cell and confocal microscopy coupled to mutagenesis we identified a cryptic nucleolar localisation signal in the central part of the N protein. In addition, based on structural comparison to the avian coronavirus N protein, a nuclear export signal was identified in the C-terminal region of the protein. Published by Elsevier Inc. 2007-07-13 2007-05-14 /pmc/articles/PMC7092899/ /pubmed/17524366 http://dx.doi.org/10.1016/j.bbrc.2007.05.036 Text en Copyright © 2007 Published by Elsevier Inc. 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
You, Jae-Hwan
Reed, Mark L.
Hiscox, Julian A.
Trafficking motifs in the SARS-coronavirus nucleocapsid protein
title Trafficking motifs in the SARS-coronavirus nucleocapsid protein
title_full Trafficking motifs in the SARS-coronavirus nucleocapsid protein
title_fullStr Trafficking motifs in the SARS-coronavirus nucleocapsid protein
title_full_unstemmed Trafficking motifs in the SARS-coronavirus nucleocapsid protein
title_short Trafficking motifs in the SARS-coronavirus nucleocapsid protein
title_sort trafficking motifs in the sars-coronavirus nucleocapsid protein
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7092899/
https://www.ncbi.nlm.nih.gov/pubmed/17524366
http://dx.doi.org/10.1016/j.bbrc.2007.05.036
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