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The A, B, Cs of Herpesvirus Capsids
Assembly of herpesvirus nucleocapsids shares significant similarities with the assembly of tailed dsDNA bacteriophages; however, important differences exist. A unique feature of herpesviruses is the presence of different mature capsid forms in the host cell nucleus during infection. These capsid for...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4379554/ https://www.ncbi.nlm.nih.gov/pubmed/25730559 http://dx.doi.org/10.3390/v7030899 |
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author | Tandon, Ritesh Mocarski, Edward S. Conway, James F. |
author_facet | Tandon, Ritesh Mocarski, Edward S. Conway, James F. |
author_sort | Tandon, Ritesh |
collection | PubMed |
description | Assembly of herpesvirus nucleocapsids shares significant similarities with the assembly of tailed dsDNA bacteriophages; however, important differences exist. A unique feature of herpesviruses is the presence of different mature capsid forms in the host cell nucleus during infection. These capsid forms, referred to as A-, B-, and C-capsids, represent empty capsids, scaffold containing capsids and viral DNA containing capsids, respectively. The C-capsids are the closest in form to those encapsidated into mature virions and are considered precursors to infectious virus. The evidence supporting A- and B-capsids as either abortive forms or assembly intermediates has been lacking. Interaction of specific capsid forms with viral tegument proteins has been proposed to be a mechanism for quality control at the point of nuclear egress of mature particles. Here, we will review the available literature on these capsid forms and present data to debate whether A- and B-capsids play an important or an extraneous role in the herpesvirus life cycle. |
format | Online Article Text |
id | pubmed-4379554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-43795542015-05-05 The A, B, Cs of Herpesvirus Capsids Tandon, Ritesh Mocarski, Edward S. Conway, James F. Viruses Article Assembly of herpesvirus nucleocapsids shares significant similarities with the assembly of tailed dsDNA bacteriophages; however, important differences exist. A unique feature of herpesviruses is the presence of different mature capsid forms in the host cell nucleus during infection. These capsid forms, referred to as A-, B-, and C-capsids, represent empty capsids, scaffold containing capsids and viral DNA containing capsids, respectively. The C-capsids are the closest in form to those encapsidated into mature virions and are considered precursors to infectious virus. The evidence supporting A- and B-capsids as either abortive forms or assembly intermediates has been lacking. Interaction of specific capsid forms with viral tegument proteins has been proposed to be a mechanism for quality control at the point of nuclear egress of mature particles. Here, we will review the available literature on these capsid forms and present data to debate whether A- and B-capsids play an important or an extraneous role in the herpesvirus life cycle. MDPI 2015-02-26 /pmc/articles/PMC4379554/ /pubmed/25730559 http://dx.doi.org/10.3390/v7030899 Text en © 2015 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 license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Tandon, Ritesh Mocarski, Edward S. Conway, James F. The A, B, Cs of Herpesvirus Capsids |
title | The A, B, Cs of Herpesvirus Capsids |
title_full | The A, B, Cs of Herpesvirus Capsids |
title_fullStr | The A, B, Cs of Herpesvirus Capsids |
title_full_unstemmed | The A, B, Cs of Herpesvirus Capsids |
title_short | The A, B, Cs of Herpesvirus Capsids |
title_sort | a, b, cs of herpesvirus capsids |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4379554/ https://www.ncbi.nlm.nih.gov/pubmed/25730559 http://dx.doi.org/10.3390/v7030899 |
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