Godowski P J, Knipe D M
J Virol. 1985 Aug;55(2):357-65. doi: 10.1128/JVI.55.2.357-365.1985.
The expression of herpes simplex virus gamma 2 (late) genes is inhibited before the onset of viral DNA replication. We report that the block in the expression of certain gamma 2 genes is relieved, at least in part, by defects in the beta ICP8 protein. We have examined the expression of the gamma 2 gene encoding glycoprotein C (gC) in cells infected with a temperature-sensitive ICP8 mutant. Under conditions in which viral DNA replication is inhibited, cells infected with the ICP8 mutant overproduce the gC family of mRNAs relative to the level observed in cells infected with a wild-type virus. The gC mRNA synthesized in cells infected with the ICP8 mutant virus is correctly initiated and spliced and is translated with the same relative efficiency as in cells infected with a replicating wild-type virus. These results suggest that ICP8 is involved in the negative regulation of gamma 2 genes expressed from parental viral genomes. The level of gC expression was greatest in cells infected with a replicating wild-type virus. These data suggest that DNA replication and genome amplification are not absolute requirements for gamma 2 gene expression but may facilitate full-level expression of these genes.
单纯疱疹病毒γ2(晚期)基因的表达在病毒DNA复制开始之前就受到抑制。我们报告称,某些γ2基因表达的阻断至少部分地通过β ICP8蛋白的缺陷得以缓解。我们检测了感染温度敏感型ICP8突变体的细胞中编码糖蛋白C(gC)的γ2基因的表达。在抑制病毒DNA复制的条件下,相对于感染野生型病毒的细胞中观察到的水平,感染ICP8突变体的细胞过量产生gC家族的mRNA。在感染ICP8突变体病毒的细胞中合成的gC mRNA起始和剪接正确,并且与感染复制型野生型病毒的细胞中具有相同的相对翻译效率。这些结果表明ICP8参与了从亲代病毒基因组表达的γ2基因的负调控。gC表达水平在感染复制型野生型病毒的细胞中最高。这些数据表明DNA复制和基因组扩增不是γ2基因表达的绝对必要条件,但可能有助于这些基因的完全表达。