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PMID: 12970434 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Transcription program of murine gammaherpesvirus 68.

Journal of virology ·Vol. 77 ·No. 19 ·2003-10-00 ·Pages 10488-503

Martinez-Guzman D, Rickabaugh T, Wu TT, Brown H, Cole S, Song MJ, Tong L, Sun R

Abstract

Murine gammaherpesvirus 68 (MHV-68 [also referred to as gammaHV68]) is phylogenetically related to Kaposi's sarcoma-associated herpesvirus (KSHV [also referred to as HHV-8]) and Epstein-Barr virus (EBV). However, unlike KSHV or EBV, MHV-68 readily infects fibroblast and epithelial cell lines derived from several mammalian species, providing a system to study productive and latent infections as well as reactivation of gammaherpesviruses in vivo and in vitro. To carry out rapid genome-wide analysis of MHV-68 gene expression, we made DNA arrays containing nearly all of the known and predicted open reading frames (ORFs) of the virus. RNA obtained from an MHV-68 latently infected cell line, from cells lytically infected with MHV-68 in culture, and from the lung tissue of infected mice was used to probe the MHV-68 arrays. Using a tightly latent B-cell line (S11E), the MHV-68 latent transcription program was quantitatively described. Using BHK-21 cells and infected mice, we demonstrated that latent genes are transcribed during lytic replication and are relatively independent of de novo protein synthesis. We determined that the transcription profiles at the peak of lytic gene expression are similar in cultured fibroblast and in the lung of infected mice. Finally, the MHV-68 DNA arrays were used to examine the gene expression profile of a recombinant virus that overexpresses replication and transcription activator (RTA), C-RTA/MHV-68, during lytic replication in cell culture. The recombinant virus replicates faster then the parental strain and the DNA arrays revealed that nearly every MHV-68 ORF examined was activated by RTA overexpression. Examination of the gene expression patterns of C-RTA/MHV-68 over a time course led to the finding that the M3 promoter is RTA responsive in the absence of other viral factors.

MeSH Terms
Animals DNA Replication Gene Expression Profiling Lung/virology Mice Mice, Inbred BALB C Oligonucleotide Array Sequence Analysis Open Reading Frames Rhadinovirus/genetics Transcription, Genetic Viral Proteins/biosynthesis Virus Latency
Chemicals
Viral Proteins
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Martinez-Guzman DeeAnn
Department of Molecular and Medical Pharmacology, University of California at Los Angeles, Los Angeles, California 90095, USA.
Rickabaugh Tammy
Wu Ting-Ting
Brown Helen
Cole Steven
Song Moon Jung
Tong Leming
Sun Ren
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Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
2003-10-00
Pages
10488-503
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC228380
Subset
IM
Grants
NCI NIH HHS · CA83525 · United States
NIDCR NIH HHS · R01 DE014153 · United States
NCI NIH HHS · CA91791 · United States
NIDCR NIH HHS · DE14153 · United States
NCI NIH HHS · R01 CA091791 · United States
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