HSV-1 DNA Replication-Coordinated Regulation by Viral and Cellular Factors.
DNA replication
HSV-1
herpes simplex virus
recombination
replication fork
Journal
Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722
Informations de publication
Date de publication:
07 10 2021
07 10 2021
Historique:
received:
15
09
2021
revised:
02
10
2021
accepted:
04
10
2021
entrez:
26
10
2021
pubmed:
27
10
2021
medline:
8
2
2022
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 34696446
pii: v13102015
doi: 10.3390/v13102015
pmc: PMC8539067
pii:
doi:
Substances chimiques
DNA, Viral
0
DNA-Binding Proteins
0
Viral Proteins
0
DNA Primase
EC 2.7.7.-
DNA-Directed DNA Polymerase
EC 2.7.7.7
DNA Helicases
EC 3.6.4.-
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Review
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : NIAID NIH HHS
ID : R21 AI137652
Pays : United States
Organisme : NIH HHS
ID : R21AI137652
Pays : United States
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