McVoy Michael A, Nixon Daniel E
Department of Pediatrics, Virginia Commonwealth University School of Medicine, Richmond, 23298-0163, USA.
J Virol. 2005 Sep;79(17):11115-27. doi: 10.1128/JVI.79.17.11115-11127.2005.
Herpesvirus genome maturation is a complex process in which concatemeric DNA molecules are translocated into capsids and cleaved at specific sequences to produce encapsidated-unit genomes. Bacteriophage studies further suggest that important ancillary processes, such as RNA transcription and DNA synthesis, concerned with repeat duplication, recombination, branch resolution, or damage repair may also be involved with the genome maturation process. To gain insight into the biochemical activities needed for herpesvirus genome maturation, 2-bromo-5,6-dichloro-1-beta-d-ribofuranosyl benzimidazole riboside (BDCRB) was used to allow the accumulation of human cytomegalovirus concatemeric DNA while the formation of new genomes was being blocked. Genome formation was restored upon BDCRB removal, and addition of various inhibitors during this time window permitted evaluation of their effects on genome maturation. Inhibitors of protein synthesis, RNA transcription, and the viral DNA polymerase only modestly reduced genome formation, demonstrating that these activities are not required for genome maturation. In contrast, drugs that inhibit both viral and host DNA polymerases potently blocked genome formation. Radioisotope incorporation in the presence of a viral DNA polymerase inhibitor further suggested that significant host-mediated DNA synthesis occurs throughout the viral genome. These results indicate a role for host DNA polymerases in genome maturation and are consistent with a need for terminal repeat duplication, debranching, or damage repair concomitant with DNA packaging or cleavage. Similarities to previously reported effects of BDCRB on guinea pig cytomegalovirus were also noted; however, BDCRB induced low-level formation of a supergenomic species called monomer+ DNA that is unique to human cytomegalovirus. Analysis of monomer+ DNA suggested a model for its formation in which BDCRB permits limited packaging of concatemeric DNA but induces skipping of cleavage sites.
疱疹病毒基因组成熟是一个复杂的过程,在此过程中,串联DNA分子被转运到衣壳中,并在特定序列处切割以产生衣壳化的单位基因组。噬菌体研究进一步表明,与重复复制、重组、分支解析或损伤修复相关的重要辅助过程,如RNA转录和DNA合成,也可能参与基因组成熟过程。为了深入了解疱疹病毒基因组成熟所需的生化活性,使用2-溴-5,6-二氯-1-β-D-呋喃核糖基苯并咪唑核苷(BDCRB)来积累人巨细胞病毒串联DNA,同时阻断新基因组的形成。去除BDCRB后基因组形成得以恢复,在此时间窗口内添加各种抑制剂可评估它们对基因组成熟的影响。蛋白质合成、RNA转录和病毒DNA聚合酶的抑制剂仅适度降低了基因组形成,表明这些活性并非基因组成熟所必需。相反,抑制病毒和宿主DNA聚合酶的药物强烈阻断了基因组形成。在存在病毒DNA聚合酶抑制剂的情况下进行放射性同位素掺入进一步表明,在整个病毒基因组中发生了显著的宿主介导的DNA合成。这些结果表明宿主DNA聚合酶在基因组成熟中发挥作用,并且与DNA包装或切割时伴随的末端重复复制、去分支或损伤修复的需求一致。还注意到与先前报道的BDCRB对豚鼠巨细胞病毒的影响相似;然而,BDCRB诱导了一种称为单体+DNA的超基因组物种的低水平形成,这是人巨细胞病毒特有的。对单体+DNA的分析提出了一种其形成模型,其中BDCRB允许串联DNA的有限包装,但诱导切割位点的跳过。