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The Role of Protein Disorder in Nuclear Transport and in Its Subversion by Viruses

The transport of host proteins into and out of the nucleus is key to host function. However, nuclear transport is restricted by nuclear pores that perforate the nuclear envelope. Protein intrinsic disorder is an inherent feature of this selective transport barrier and is also a feature of the nuclea...

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Autores principales: Wubben, Jacinta M., Atkinson, Sarah C., Borg, Natalie A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7764567/
https://www.ncbi.nlm.nih.gov/pubmed/33321790
http://dx.doi.org/10.3390/cells9122654
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author Wubben, Jacinta M.
Atkinson, Sarah C.
Borg, Natalie A.
author_facet Wubben, Jacinta M.
Atkinson, Sarah C.
Borg, Natalie A.
author_sort Wubben, Jacinta M.
collection PubMed
description The transport of host proteins into and out of the nucleus is key to host function. However, nuclear transport is restricted by nuclear pores that perforate the nuclear envelope. Protein intrinsic disorder is an inherent feature of this selective transport barrier and is also a feature of the nuclear transport receptors that facilitate the active nuclear transport of cargo, and the nuclear transport signals on the cargo itself. Furthermore, intrinsic disorder is an inherent feature of viral proteins and viral strategies to disrupt host nucleocytoplasmic transport to benefit their replication. In this review, we highlight the role that intrinsic disorder plays in the nuclear transport of host and viral proteins. We also describe viral subversion mechanisms of the host nuclear transport machinery in which intrinsic disorder is a feature. Finally, we discuss nuclear import and export as therapeutic targets for viral infectious disease.
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spelling pubmed-77645672020-12-27 The Role of Protein Disorder in Nuclear Transport and in Its Subversion by Viruses Wubben, Jacinta M. Atkinson, Sarah C. Borg, Natalie A. Cells Review The transport of host proteins into and out of the nucleus is key to host function. However, nuclear transport is restricted by nuclear pores that perforate the nuclear envelope. Protein intrinsic disorder is an inherent feature of this selective transport barrier and is also a feature of the nuclear transport receptors that facilitate the active nuclear transport of cargo, and the nuclear transport signals on the cargo itself. Furthermore, intrinsic disorder is an inherent feature of viral proteins and viral strategies to disrupt host nucleocytoplasmic transport to benefit their replication. In this review, we highlight the role that intrinsic disorder plays in the nuclear transport of host and viral proteins. We also describe viral subversion mechanisms of the host nuclear transport machinery in which intrinsic disorder is a feature. Finally, we discuss nuclear import and export as therapeutic targets for viral infectious disease. MDPI 2020-12-10 /pmc/articles/PMC7764567/ /pubmed/33321790 http://dx.doi.org/10.3390/cells9122654 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Wubben, Jacinta M.
Atkinson, Sarah C.
Borg, Natalie A.
The Role of Protein Disorder in Nuclear Transport and in Its Subversion by Viruses
title The Role of Protein Disorder in Nuclear Transport and in Its Subversion by Viruses
title_full The Role of Protein Disorder in Nuclear Transport and in Its Subversion by Viruses
title_fullStr The Role of Protein Disorder in Nuclear Transport and in Its Subversion by Viruses
title_full_unstemmed The Role of Protein Disorder in Nuclear Transport and in Its Subversion by Viruses
title_short The Role of Protein Disorder in Nuclear Transport and in Its Subversion by Viruses
title_sort role of protein disorder in nuclear transport and in its subversion by viruses
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7764567/
https://www.ncbi.nlm.nih.gov/pubmed/33321790
http://dx.doi.org/10.3390/cells9122654
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