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Five families of diverse DNA viruses comprehensively restructure the nucleus.

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  • Author(s): Rosemarie Q;Rosemarie Q; Sugden B; Sugden B
  • Source:
    PLoS biology [PLoS Biol] 2023 Nov 06; Vol. 21 (11), pp. e3002347. Date of Electronic Publication: 2023 Nov 06 (Print Publication: 2023).
  • Publication Type:
    Journal Article
  • Language:
    English
  • Additional Information
    • Source:
      Publisher: Public Library of Science Country of Publication: United States NLM ID: 101183755 Publication Model: eCollection Cited Medium: Internet ISSN: 1545-7885 (Electronic) Linking ISSN: 15449173 NLM ISO Abbreviation: PLoS Biol Subsets: MEDLINE
    • Publication Information:
      Original Publication: San Francisco, CA : Public Library of Science, [2003]-
    • Subject Terms:
    • Abstract:
      Many viruses have evolved ways to restructure their host cell's nucleus profoundly and unexpectedly upon infection. In particular, DNA viruses that need to commandeer their host's cellular synthetic functions to produce their progeny can induce the condensation and margination of host chromatin during productive infection, a phenomenon known as virus-induced reorganization of cellular chromatin (ROCC). These ROCC-inducing DNA viruses belong to 5 families (herpesviruses, baculoviruses, adenoviruses, parvoviruses, and geminiviruses) that infect a wide range of hosts and are important for human and ecosystem health, as well as for biotechnology. Although the study of virus-induced ROCC is in its infancy, investigations are already raising important questions, such as why only some DNA viruses that replicate their genomes in the nucleus elicit ROCC. Studying the shared and distinct properties of ROCC-inducing viruses will provide valuable insights into viral reorganization of host chromatin that could have implications for future therapies that target the viral life cycle.
      Competing Interests: BS is an Academic Editor of PLoS Biology.
      (Copyright: © 2023 Rosemarie, Sugden. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)
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    • Grant Information:
      P01 CA022443 United States CA NCI NIH HHS
    • Accession Number:
      0 (Chromatin)
    • Publication Date:
      Date Created: 20231106 Date Completed: 20231108 Latest Revision: 20240210
    • Publication Date:
      20240210
    • Accession Number:
      PMC10627436
    • Accession Number:
      10.1371/journal.pbio.3002347
    • Accession Number:
      37930945