Open AccessOn the Control of Immediate Early ( ) mRNA Survival in Cells Infected with Herpes Simplex Virus
Author(s) -
M. L. Fenwick,
Sarah Owen
Publication year - 1988
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 - 10.1099/0022-1317-69-11-2869
Subject(s) - biology , herpes simplex virus , messenger rna , virology , virus , protein biosynthesis , vero cell , viral tegument , microbiology and biotechnology , recombinant dna , gene , biochemistry
The alpha or immediate early mRNA of herpes simplex virus strain HSV-2(G) had a half-life of about 15 min if made in the absence of viral protein synthesis but was relatively stable if viral protein synthesis occurred, either freely or restricted by the presence of the proline analogue azetidine. In contrast, the alpha mRNA of other strains of the virus is stable, even in the absence of protein synthesis. Studies with recombinant viruses showed that the region of the viral DNA between 0.58 and 0.65 map units [which includes the gene (vhs, UL41) that controls virion-mediated shutoff of host protein synthesis] is important in determining the survival of alpha mRNA. In mixed infection experiments HSV-2(G) inhibited alpha as well as host protein synthesis but the shutoff activity appeared to be short-lived. Within 3 h after infection, as a result of protein synthesis, cells became completely resistant to shutoff by superinfecting virus.