» Articles » PMID: 33064772

The NS1 Protein of the Parvovirus MVM Aids in the Localization of the Viral Genome to Cellular Sites of DNA Damage

Overview
Journal PLoS Pathog
Specialty Microbiology
Date 2020 Oct 16
PMID 33064772
Citations 23
Authors
Affiliations
Soon will be listed here.
Abstract

The autonomous parvovirus Minute Virus of Mice (MVM) localizes to cellular DNA damage sites to establish and sustain viral replication centers, which can be visualized by focal deposition of the essential MVM non-structural phosphoprotein NS1. How such foci are established remains unknown. Here, we show that NS1 localized to cellular sites of DNA damage independently of its ability to covalently bind the 5' end of the viral genome, or its consensus DNA binding sequence. Many of these sites were identical to those occupied by virus during infection. However, localization of the MVM genome to DNA damage sites occurred only when wild-type NS1, but not its DNA-binding mutant was expressed. Additionally, wild-type NS1, but not its DNA binding mutant, could localize a heterologous DNA molecule containing the NS1 binding sequence to DNA damage sites. These findings suggest that NS1 may function as a bridging molecule, helping the MVM genome localize to cellular DNA damage sites to facilitate ongoing virus replication.

Citing Articles

Canine parvovirus NS1 induces host translation shutoff by reducing mTOR phosphorylation.

Wang X, Hao X, Zhao Y, Xiao X, Li S, Zhou P J Virol. 2024; 99(1):e0146324.

PMID: 39601560 PMC: 11784071. DOI: 10.1128/jvi.01463-24.


Inactivation of checkpoint kinase 1 (Chk1) during parvovirus minute virus of mice (MVM) infection inhibits cellular homologous recombination repair and facilitates viral genome replication.

Etingov I, Pintel D J Virol. 2024; 98(12):e0088924.

PMID: 39565136 PMC: 11650968. DOI: 10.1128/jvi.00889-24.


NS1-mediated DNMT1 degradation regulates human bocavirus 1 replication and RNA processing.

Qin S, Chen H, Tian C, Chen Z, Zuo L, Zhang X PLoS Pathog. 2024; 20(11):e1012682.

PMID: 39541416 PMC: 11594422. DOI: 10.1371/journal.ppat.1012682.


Intracellular delivery of oncolytic viruses with engineered Salmonella causes viral replication and cell death.

Khanduja S, Bloom S, Raman V, Deshpande C, Hall C, Forbes N iScience. 2024; 27(6):109813.

PMID: 38799578 PMC: 11126981. DOI: 10.1016/j.isci.2024.109813.


Novel mutation N588 residue in the NS1 protein of feline parvovirus greatly augments viral replication.

Li L, Liu Z, Liang R, Yang M, Yan Y, Jiao Y J Virol. 2024; 98(5):e0009324.

PMID: 38591899 PMC: 11092363. DOI: 10.1128/jvi.00093-24.


References
1.
Jang M, Shen K, McBride A . Papillomavirus genomes associate with BRD4 to replicate at fragile sites in the host genome. PLoS Pathog. 2014; 10(5):e1004117. PMC: 4022725. DOI: 10.1371/journal.ppat.1004117. View

2.
Majumder K, Wang J, Boftsi M, Fuller M, Rede J, Joshi T . Parvovirus minute virus of mice interacts with sites of cellular DNA damage to establish and amplify its lytic infection. Elife. 2018; 7. PMC: 6095691. DOI: 10.7554/eLife.37750. View

3.
Dettwiler S, Rommelaere J, Nuesch J . DNA unwinding functions of minute virus of mice NS1 protein are modulated specifically by the lambda isoform of protein kinase C. J Virol. 1999; 73(9):7410-20. PMC: 104268. DOI: 10.1128/JVI.73.9.7410-7420.1999. View

4.
Ruiz Z, Mihaylov I, Cotmore S, Tattersall P . Recruitment of DNA replication and damage response proteins to viral replication centers during infection with NS2 mutants of Minute Virus of Mice (MVM). Virology. 2011; 410(2):375-84. PMC: 3072075. DOI: 10.1016/j.virol.2010.12.009. View

5.
Cater J, Pintel D . The small non-structural protein NS2 of the autonomous parvovirus minute virus of mice is required for virus growth in murine cells. J Gen Virol. 1992; 73 ( Pt 7):1839-43. DOI: 10.1099/0022-1317-73-7-1839. View