Epstein-Barr virus BGLF4 kinase induces premature chromosome condensation through activation of condensin and topoisomerase II
Journal
Journal of Virology
Journal Volume
81
Journal Issue
10
Pages
5166-5180
Date Issued
2007
Author(s)
Abstract
Previous studies of Epstein-Barr virus (EBV) replication focused mainly on the viral and cellular factors involved in replication compartment assembly and controlling the cell cycle. However, little is known about how EBV reorganizes nuclear architecture and the chromatin territories. In EBV-positive nasopharyngeal carcinoma NA cells or Akata cells, we noticed that cellular chromatin becomes highly condensed upon EBV reactivation. In searching for the possible mechanisms involved, we found that transient expression of EBV BGLF4 kinase induces unscheduled chromosome condensation, nuclear lamina disassembly, and stress fiber rearrangements, independently of cellular DNA replication and Cdc2 activity. BGLF4 interacts with condensin complexes, the major components in mitotic chromosome assembly, and induces condensin phosphorylation at Cdc2 consensus motifs. BGLF4 also stimulates the decatenation activity of topoisomerase II, suggesting that it may induce chromosome condensation through condensin and topoisomerase II activation. The ability to induce chromosome condensation is conserved in another gammaherpesvirus kinase, murine herpesvirus 68 ORF36. Together, these findings suggest a novel mechanism by which gammaherpesvirus kinases may induce multiple premature mitotic events to provide more extrachromosomal space for viral DNA replication and successful egress of nucleocapsid from the nucleus. Copyright ? 2007, American Society for Microbiology. All Rights Reserved.
SDGs
Other Subjects
BGLF4 kinase; condensin; cyclin dependent kinase 1; DNA topoisomerase (ATP hydrolysing); phosphotransferase; unclassified drug; article; cancer cell; chromatin; chromosome condensation; controlled study; DNA replication; embryo; enzyme activity; Epstein Barr virus; Herpes virus; human; human cell; nasopharynx carcinoma; nonhuman; nuclear lamina; priority journal; protein expression; protein motif; protein phosphorylation; stress fiber; Adenosine Triphosphatases; Cell Line; Chromosomes, Human; DNA Topoisomerases, Type II; DNA-Binding Proteins; Fluorescent Antibody Technique, Indirect; Herpesvirus 4, Human; Humans; Microscopy, Fluorescence; Models, Biological; Multiprotein Complexes; Nuclear Lamina; Phosphorylation; Protein Binding; Protein-Serine-Threonine Kinases; Rhadinovirus; Stress Fibers; Viral Proteins; Human herpesvirus 4; Murid herpesvirus 4
Type
journal article