Courcelle C T, Courcelle J, Prichard M N, Mocarski E S
Department of Microbiology and Immunology, Stanford University, Stanford, California 94305, USA.
J Virol. 2001 Aug;75(16):7592-601. doi: 10.1128/JVI.75.16.7592-7601.2001.
Cytomegalovirus gene UL114, a homolog of mammalian uracil-DNA glycosylase (UNG), is required for efficient viral DNA replication. In quiescent fibroblasts, UNG mutant virus replication is delayed for 48 h and follows the virus-induced expression of cellular UNG. In contrast, mutant virus replication proceeds without delay in actively growing fibroblasts that express host cell UNG. In the absence of viral or host cell UNG expression, mutant virus fails to proceed to late-phase DNA replication, characterized by rapid DNA amplification. The data suggest that uracil incorporated early during wild-type viral DNA replication must be removed by virus or host UNG prior to late-phase amplification and encapsidation into progeny virions. The process of uracil incorporation and excision may introduce strand breaks to facilitate the transition from early-phase replication to late-phase amplification.
巨细胞病毒基因UL114是哺乳动物尿嘧啶-DNA糖基化酶(UNG)的同源物,是病毒DNA高效复制所必需的。在静止的成纤维细胞中,UNG突变病毒的复制延迟48小时,并跟随病毒诱导的细胞UNG表达。相反,在表达宿主细胞UNG的活跃生长的成纤维细胞中,突变病毒的复制没有延迟地进行。在没有病毒或宿主细胞UNG表达的情况下,突变病毒无法进入以快速DNA扩增为特征的晚期DNA复制阶段。数据表明,在野生型病毒DNA复制早期掺入的尿嘧啶必须在晚期扩增和包装到子代病毒粒子之前被病毒或宿主UNG去除。尿嘧啶掺入和切除的过程可能会引入链断裂,以促进从早期复制到晚期扩增的转变。