Transcriptome profile of murine gammaherpesvirus-68 lytic infection
Author(s) -
Bahram Ebrahimi,
Bernadette M. Dutia,
Kim L. Roberts,
José Javier GarcíaRamírez,
Paul Dickinson,
James P. Stewart,
Peter Ghazal,
Douglas Roy,
Anthony A. Nash
Publication year - 2003
Publication title -
journal of general virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.55
H-Index - 167
eISSN - 1465-2099
pISSN - 0022-1317
DOI - 10.1099/vir.0.18639-0
Subject(s) - lytic cycle , biology , transcriptome , gene , microarray analysis techniques , virology , cycloheximide , microbiology and biotechnology , open reading frame , microarray , gene expression , dna microarray , rna , gene expression profiling , virus , genetics , protein biosynthesis , peptide sequence
The murine gammaherpesvirus-68 genome encodes 73 protein-coding open reading frames with extensive similarities to human gamma(2) herpesviruses, as well as unique genes and cellular homologues. We performed transcriptome analysis of stage-specific viral RNA during permissive infection using an oligonucleotide-based microarray. Using this approach, M4, K3, ORF38, ORF50, ORF57 and ORF73 were designated as immediate-early genes based on cycloheximide treatment. The microarray analysis also identified 10 transcripts with early expression kinetics, 32 transcripts with early-late expression kinetics and 29 transcripts with late expression kinetics. The latter group consisted mainly of structural proteins, and showed high expression levels relative to other viral transcripts. Moreover, we detected all eight tRNA-like transcripts in the presence of cycloheximide and phosphonoacetic acid. Lytic infection with MHV-68 also resulted in a significant reduction in the expression of cellular transcripts included in the DNA chip. This global approach to viral transcript analysis offers a powerful system for examining molecular transitions between lytic and latent virus infections associated with disease pathogenesis.
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