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The three-component helicase/primase complex of herpes simplex virus-1

Herpes simplex virus type 1 (HSV-1) is one of the nine herpesviruses that infect humans. HSV-1 encodes seven proteins to replicate its genome in the hijacked human cell. Among these are the herpes virus DNA helicase and primase that are essential components of its replication machinery. In the HSV-1...

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Autores principales: Bermek, Oya, Williams, R. Scott
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8187027/
https://www.ncbi.nlm.nih.gov/pubmed/34102080
http://dx.doi.org/10.1098/rsob.210011
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author Bermek, Oya
Williams, R. Scott
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Williams, R. Scott
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description Herpes simplex virus type 1 (HSV-1) is one of the nine herpesviruses that infect humans. HSV-1 encodes seven proteins to replicate its genome in the hijacked human cell. Among these are the herpes virus DNA helicase and primase that are essential components of its replication machinery. In the HSV-1 replisome, the helicase–primase complex is composed of three components including UL5 (helicase), UL52 (primase) and UL8 (non-catalytic subunit). UL5 and UL52 subunits are functionally interdependent, and the UL8 component is required for the coordination of UL5 and UL52 activities proceeding in opposite directions with respect to the viral replication fork. Anti-viral compounds currently under development target the functions of UL5 and UL52. Here, we review the structural and functional properties of the UL5/UL8/UL52 complex and highlight the gaps in knowledge to be filled to facilitate molecular characterization of the structure and function of the helicase–primase complex for development of alternative anti-viral treatments.
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spelling pubmed-81870272021-06-09 The three-component helicase/primase complex of herpes simplex virus-1 Bermek, Oya Williams, R. Scott Open Biol Review Herpes simplex virus type 1 (HSV-1) is one of the nine herpesviruses that infect humans. HSV-1 encodes seven proteins to replicate its genome in the hijacked human cell. Among these are the herpes virus DNA helicase and primase that are essential components of its replication machinery. In the HSV-1 replisome, the helicase–primase complex is composed of three components including UL5 (helicase), UL52 (primase) and UL8 (non-catalytic subunit). UL5 and UL52 subunits are functionally interdependent, and the UL8 component is required for the coordination of UL5 and UL52 activities proceeding in opposite directions with respect to the viral replication fork. Anti-viral compounds currently under development target the functions of UL5 and UL52. Here, we review the structural and functional properties of the UL5/UL8/UL52 complex and highlight the gaps in knowledge to be filled to facilitate molecular characterization of the structure and function of the helicase–primase complex for development of alternative anti-viral treatments. The Royal Society 2021-06-09 /pmc/articles/PMC8187027/ /pubmed/34102080 http://dx.doi.org/10.1098/rsob.210011 Text en © 2021 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Review
Bermek, Oya
Williams, R. Scott
The three-component helicase/primase complex of herpes simplex virus-1
title The three-component helicase/primase complex of herpes simplex virus-1
title_full The three-component helicase/primase complex of herpes simplex virus-1
title_fullStr The three-component helicase/primase complex of herpes simplex virus-1
title_full_unstemmed The three-component helicase/primase complex of herpes simplex virus-1
title_short The three-component helicase/primase complex of herpes simplex virus-1
title_sort three-component helicase/primase complex of herpes simplex virus-1
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8187027/
https://www.ncbi.nlm.nih.gov/pubmed/34102080
http://dx.doi.org/10.1098/rsob.210011
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