Identification and Functional Evaluation of Cellular and Viral Factors Involved in the Alteration of Nuclear Architecture during Herpes Simplex Virus 1 Infection

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Published in:Journal of Virology Vol. 79; no. 20; pp. 12840 - 12851
Main Authors: SIMPSON-HOLLEY, Martha, COLGROVE, Robert C, NALEPA, Grzegorz, HARPER, J. Wade, KNIPE, David M
Format: Journal Article
Language:English
Published: Washington, DC American Society for Microbiology 01-10-2005
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Abstract Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue Spotlights in the Current Issue JVI About JVI Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy JVI RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 0022-538X Online ISSN: 1098-5514 Copyright © 2014 by the American Society for Microbiology.   For an alternate route to JVI .asm.org, visit: JVI       
AbstractList Herpes simplex virus 1 (HSV-1) replicates in the nucleus of host cells and radically alters nuclear architecture as part of its replication process. Replication compartments (RCs) form, and host chromatin is marginalized. Chromatin is later dispersed, and RCs spread past it to reach the nuclear edge. Using a lamin A-green fluorescent protein fusion, we provide direct evidence that the nuclear lamina is disrupted during HSV-1 infection and that the UL31 and UL34 proteins are required for this. We show nuclear expansion from 8 h to 24 h postinfection and place chromatin rearrangement and disruption of the lamina in the context of this global change in nuclear architecture. We show HSV-1-induced disruption of the localization of Cdc14B, a cellular protein and component of a putative nucleoskeleton. We also show that UL31 and UL34 are required for nuclear expansion. Studies with inhibitors of globular actin (G-actin) indicate that G-actin plays an essential role in nuclear expansion and chromatin dispersal but not in lamina alterations induced by HSV-1 infection. From analyses of HSV infections under various conditions, we conclude that nuclear expansion and chromatin dispersal are dispensable for optimal replication, while lamina rearrangement is associated with efficient replication.
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Author Robert C. Colgrove
Martha Simpson-Holley
Grzegorz Nalepa
David M. Knipe
J. Wade Harper
AuthorAffiliation Departments of Microbiology and Molecular Genetics, 1 Pathology, Harvard University Medical School, Boston, Massachusetts 02115 2
AuthorAffiliation_xml – name: Departments of Microbiology and Molecular Genetics, 1 Pathology, Harvard University Medical School, Boston, Massachusetts 02115 2
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  organization: Department of Microbiology and Molecular Genetics, Harvard University Medical School, Boston, Massachusetts 02115, United States
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  givenname: Robert C
  surname: COLGROVE
  fullname: COLGROVE, Robert C
  organization: Department of Microbiology and Molecular Genetics, Harvard University Medical School, Boston, Massachusetts 02115, United States
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  givenname: Grzegorz
  surname: NALEPA
  fullname: NALEPA, Grzegorz
  organization: Department of Pathology, Harvard University Medical School, Boston, Massachusetts 02115, United States
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  givenname: J. Wade
  surname: HARPER
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  surname: KNIPE
  fullname: KNIPE, David M
  organization: Department of Microbiology and Molecular Genetics, Harvard University Medical School, Boston, Massachusetts 02115, United States
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Issue 20
Keywords Infection
Virus
Microbiology
Herpesviridae
Viral disease
Alphaherpesvirinae
Herpes
Human herpesvirus 1
Identification
Virology
Language English
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Corresponding author. Mailing address: Department of Microbiology and Molecular Genetics, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115. Phone: (617) 432-1934. Fax: (617) 432-0223. E-mail: david_knipe@hms.harvard.edu.
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Snippet Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley...
Herpes simplex virus 1 (HSV-1) replicates in the nucleus of host cells and radically alters nuclear architecture as part of its replication process....
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SubjectTerms Actins - physiology
Animals
Biological and medical sciences
Cell Line
Cell Nucleus - metabolism
Chromatin - metabolism
Cytoplasm - metabolism
Dual-Specificity Phosphatases
Fundamental and applied biological sciences. Psychology
Herpes Simplex - virology
Herpes simplex virus 1
Herpesvirus 1, Human - physiology
Human viral diseases
Humans
Infectious diseases
Medical sciences
Microbiology
Miscellaneous
Nuclear Lamina - metabolism
Nuclear Proteins - physiology
Protein Tyrosine Phosphatases - metabolism
Time Factors
Viral diseases
Viral diseases with cutaneous or mucosal lesions and viral diseases of the eye
Viral Proteins - physiology
Virology
Virus Replication
Virus-Cell Interactions
Title Identification and Functional Evaluation of Cellular and Viral Factors Involved in the Alteration of Nuclear Architecture during Herpes Simplex Virus 1 Infection
URI http://jvi.asm.org/content/79/20/12840.abstract
https://www.ncbi.nlm.nih.gov/pubmed/16188986
https://search.proquest.com/docview/17395942
https://search.proquest.com/docview/68628256
https://pubmed.ncbi.nlm.nih.gov/PMC1235858
Volume 79
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