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HSV-1 DNA Replication—Coordinated Regulation by Viral and Cellular Factors
DNA replication is an integral step in the herpes simplex virus type 1 (HSV-1) life cycle that is coordinated with the cellular DNA damage response, repair and recombination of the viral genome, and viral gene transcription. HSV-1 encodes its own DNA replication machinery, including an origin bindin...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8539067/ https://www.ncbi.nlm.nih.gov/pubmed/34696446 http://dx.doi.org/10.3390/v13102015 |
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author | Packard, Jessica E. Dembowski, Jill A. |
author_facet | Packard, Jessica E. Dembowski, Jill A. |
author_sort | Packard, Jessica E. |
collection | PubMed |
description | DNA replication is an integral step in the herpes simplex virus type 1 (HSV-1) life cycle that is coordinated with the cellular DNA damage response, repair and recombination of the viral genome, and viral gene transcription. HSV-1 encodes its own DNA replication machinery, including an origin binding protein (UL9), single-stranded DNA binding protein (ICP8), DNA polymerase (UL30), processivity factor (UL42), and a helicase/primase complex (UL5/UL8/UL52). In addition, HSV-1 utilizes a combination of accessory viral and cellular factors to coordinate viral DNA replication with other viral and cellular processes. The purpose of this review is to outline the roles of viral and cellular proteins in HSV-1 DNA replication and replication-coupled processes, and to highlight how HSV-1 may modify and adapt cellular proteins to facilitate productive infection. |
format | Online Article Text |
id | pubmed-8539067 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85390672021-10-24 HSV-1 DNA Replication—Coordinated Regulation by Viral and Cellular Factors Packard, Jessica E. Dembowski, Jill A. Viruses Review DNA replication is an integral step in the herpes simplex virus type 1 (HSV-1) life cycle that is coordinated with the cellular DNA damage response, repair and recombination of the viral genome, and viral gene transcription. HSV-1 encodes its own DNA replication machinery, including an origin binding protein (UL9), single-stranded DNA binding protein (ICP8), DNA polymerase (UL30), processivity factor (UL42), and a helicase/primase complex (UL5/UL8/UL52). In addition, HSV-1 utilizes a combination of accessory viral and cellular factors to coordinate viral DNA replication with other viral and cellular processes. The purpose of this review is to outline the roles of viral and cellular proteins in HSV-1 DNA replication and replication-coupled processes, and to highlight how HSV-1 may modify and adapt cellular proteins to facilitate productive infection. MDPI 2021-10-07 /pmc/articles/PMC8539067/ /pubmed/34696446 http://dx.doi.org/10.3390/v13102015 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Packard, Jessica E. Dembowski, Jill A. HSV-1 DNA Replication—Coordinated Regulation by Viral and Cellular Factors |
title | HSV-1 DNA Replication—Coordinated Regulation by Viral and Cellular Factors |
title_full | HSV-1 DNA Replication—Coordinated Regulation by Viral and Cellular Factors |
title_fullStr | HSV-1 DNA Replication—Coordinated Regulation by Viral and Cellular Factors |
title_full_unstemmed | HSV-1 DNA Replication—Coordinated Regulation by Viral and Cellular Factors |
title_short | HSV-1 DNA Replication—Coordinated Regulation by Viral and Cellular Factors |
title_sort | hsv-1 dna replication—coordinated regulation by viral and cellular factors |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8539067/ https://www.ncbi.nlm.nih.gov/pubmed/34696446 http://dx.doi.org/10.3390/v13102015 |
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