2. Academic Validation
  3. The NS1 protein of the parvovirus MVM Aids in the localization of the viral genome to cellular sites of DNA damage

The NS1 protein of the parvovirus MVM Aids in the localization of the viral genome to cellular sites of DNA damage

  • PLoS Pathog. 2020 Oct 16;16(10):e1009002. doi: 10.1371/journal.ppat.1009002.
Kinjal Majumder 1 2,  Maria Boftsi 2 3,  Fawn B Whittle 1 2,  Juexin Wang 2 4,  Matthew S Fuller 5,  Trupti Joshi 2 4 6 7,  David J Pintel 1 2
Affiliations

Affiliations

  • 1 Department of Molecular Microbiology and Immunology, University of Missouri School of Medicine, Columbia, Missouri, United States of America.
  • 2 Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, Missouri, United States of America.
  • 3 Pathobiology Area Graduate Program, University of Missouri, Columbia, Missouri, United States of America.
  • 4 Department of Electrical Engineering and Computer Science, University of Missouri, Columbia, Missouri, United States of America.
  • 5 Ultragenyx Gene Therapy, Cambridge, Massachusetts, United States of America.
  • 6 Department of Health Management and Informatics, University of Missouri School of Medicine, Columbia, Missouri, United States of America.
  • 7 MU Institute of Data Science and Informatics, University of Missouri, Columbia, Missouri, United States of America.
PMID: 33064772 DOI: 10.1371/journal.ppat.1009002
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.

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