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Role of PARP-1 in Human Cytomegalovirus Infection and Functional Partners Encoded by This Virus

Overview
Journal Viruses
Publisher MDPI
Specialty Microbiology
Date 2022 Sep 23
PMID 36146855
Authors
Affiliations
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Abstract

Human cytomegalovirus (HCMV) is a ubiquitous pathogen that threats the majority of the world's population. Poly (ADP-ribose) polymerase 1 (PARP-1) and protein poly (ADP-ribosyl)ation (PARylation) regulates manifold cellular functions. The role of PARP-1 and protein PARylation in HCMV infection is still unknown. In the present study, we found that the pharmacological and genetic inhibition of PARP-1 attenuated HCMV replication, and PARG inhibition favors HCMV replication. PARP-1 and its enzymatic activity were required for efficient HCMV replication. HCMV infection triggered the activation of PARP-1 and induced the translocation of PARP-1 from nucleus to cytoplasm. PARG was upregulated in HCMV-infected cells and this upregulation was independent of viral DNA replication. Moreover, we found that HCMV UL76, a true late protein of HCMV, inhibited the overactivation of PARP-1 through direct binding to the BRCT domain of PARP-1. In addition, UL76 also physically interacted with poly (ADP-ribose) (PAR) polymers through the RG/RGG motifs of UL76 which mediates its recruitment to DNA damage sites. Finally, PARP-1 inhibition or depletion potentiated HCMV-triggered induction of type I interferons. Our results uncovered the critical role of PARP-1 and PARP-1-mediated protein PARylation in HCMV replication.

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References
1.
Meyer-Ficca M, Meyer R, Coyle D, Jacobson E, Jacobson M . Human poly(ADP-ribose) glycohydrolase is expressed in alternative splice variants yielding isoforms that localize to different cell compartments. Exp Cell Res. 2004; 297(2):521-32. DOI: 10.1016/j.yexcr.2004.03.050. View

2.
Burkle A . Poly(ADP-ribose). The most elaborate metabolite of NAD+. FEBS J. 2005; 272(18):4576-89. DOI: 10.1111/j.1742-4658.2005.04864.x. View

3.
Chen Y, Yao Y, Zhao K, Liu C, Yuan Y, Sun H . DNA Repair Factor Poly(ADP-Ribose) Polymerase 1 Is a Proviral Factor in Hepatitis B Virus Covalently Closed Circular DNA Formation. J Virol. 2022; 96(13):e0058522. PMC: 9278152. DOI: 10.1128/jvi.00585-22. View

4.
Mertens M, Knipe D . Herpes Simplex Virus 1 Manipulates Host Cell Antiviral and Proviral DNA Damage Responses. mBio. 2021; 12(1). PMC: 7885110. DOI: 10.1128/mBio.03552-20. View

5.
Stinski M . Sequence of protein synthesis in cells infected by human cytomegalovirus: early and late virus-induced polypeptides. J Virol. 1978; 26(3):686-701. PMC: 525893. DOI: 10.1128/JVI.26.3.686-701.1978. View