Herpes simplex virus VP16, but Not ICP0, is required to reduce histone occupancy and enhance histone acetylation on viral genomes in U2OS osteosarcoma cells

Meaghan Hancock, Anna R. Cliffe, David M. Knipe, James R. Smiley

Research output: Contribution to journalArticle

30 Citations (Scopus)

Abstract

The herpes simplex virus (HSV) genome rapidly becomes associated with histones after injection into the host cell nucleus. The viral proteins ICP0 and VP16 are required for efficient viral gene expression and have been implicated in reducing the levels of underacetylated histones on the viral genome, raising the possibility that high levels of underacetylated histones inhibit viral gene expression. The U2OS osteosarcoma cell line is permissive for replication of ICP0 and VP16 mutants and appears to lack an innate antiviral repression mechanism present in other cell types. We therefore used chromatin immunoprecipitation to determine whether U2OS cells are competent to load histones onto HSV DNA and, if so, whether ICP0 and/or VP16 are required to reduce histone occupancy and enhance acetylation in this cell type. High levels of underacetylated histone H3 accumulated at several locations on the viral genome in the absence of VP16 activation function; in contrast, an ICP0 mutant displayed markedly reduced histone levels and enhanced acetylation, similar to wild-type HSV. These results demonstrate that U2OS cells are competent to load underacetylated histones onto HSV DNA and uncover an unexpected role for VP16 in modulating chromatin structure at viral early and late loci. One interpretation of these findings is that ICP0 and VP16 affect viral chromatin structure through separate pathways, and the pathway targeted by ICP0 is defective in U2OS cells. We also show that HSV infection results in decreased histone levels on some actively transcribed genes within the cellular genome, demonstrating that viral infection alters cellular chromatin structure.

Original languageEnglish (US)
Pages (from-to)1366-1375
Number of pages10
JournalJournal of Virology
Volume84
Issue number3
DOIs
StatePublished - Feb 2010
Externally publishedYes

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herpes simplex
osteosarcoma
Viral Genome
acetylation
Osteosarcoma
Simplexvirus
Acetylation
histones
Histones
viruses
genome
chromatin
cells
Chromatin
DNA viruses
Viral Structures
Viral Genes
Virus Diseases
Genome
Gene Expression

ASJC Scopus subject areas

  • Immunology
  • Virology

Cite this

Herpes simplex virus VP16, but Not ICP0, is required to reduce histone occupancy and enhance histone acetylation on viral genomes in U2OS osteosarcoma cells. / Hancock, Meaghan; Cliffe, Anna R.; Knipe, David M.; Smiley, James R.

In: Journal of Virology, Vol. 84, No. 3, 02.2010, p. 1366-1375.

Research output: Contribution to journalArticle

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