Stinski M F
J Virol. 1978 Jun;26(3):686-701. doi: 10.1128/JVI.26.3.686-701.1978.
At least 10 distinct early virus-induced polypeptides were synthesized within 0 to 6 h after infection of permissive cells with cytomegalovirus. These virus-induced polypeptides were synthesized before and independently of viral DNA replication. A majority of these early virus-induced polypeptides were also synthesized in nonpermissive cells, which do not permit viral DNA replication. The virus-induced polypeptides synthesized before viral DNA replication were hypothesized to be nonstructural proteins coded for by the cytomegalovirus genome. Their synthesis was found to be a sequential process, since three proteins preceded the synthesis of the others. Synthesis of all early cytomegalovirus-induced proteins was a transient process; the proteins reached their highest molar ratios before the onset of viral DNA replication. Late viral proteins were synthesized at the time of the onset of viral DNA replication, which was approximately 15 h after infection. Their synthesis was continuous and increased in molar ratios with the accumulation of newly synthesized viral DNA in the cells. The presence of the amino acid analog canavanine or azetadine during the early stage of infection suppressed viral DNA replication. The amount of viral DNA synthesis was directly correlated to the relative amount of late viral protein synthesis. Because synthesis of late viral proteins depended upon viral DNA replication, the proteins were not detected in permissive cells treated with an inhibitor of viral DNA synthesis or in nonpermissive cells that are restrictive for cytomegalovirus DNA replication.
在用巨细胞病毒感染允许性细胞后的0至6小时内,至少合成了10种不同的早期病毒诱导多肽。这些病毒诱导多肽在病毒DNA复制之前合成,且与病毒DNA复制无关。这些早期病毒诱导多肽中的大多数也在不允许病毒DNA复制的非允许性细胞中合成。在病毒DNA复制之前合成的病毒诱导多肽被推测为由巨细胞病毒基因组编码的非结构蛋白。发现它们的合成是一个顺序过程,因为有三种蛋白质先于其他蛋白质合成。所有早期巨细胞病毒诱导蛋白的合成都是一个短暂过程;这些蛋白在病毒DNA复制开始前达到最高摩尔比。晚期病毒蛋白在病毒DNA复制开始时合成,这大约在感染后15小时。它们的合成是持续的,并且随着细胞中新合成病毒DNA的积累,摩尔比增加。在感染早期存在氨基酸类似物刀豆氨酸或氮杂环丁烷会抑制病毒DNA复制。病毒DNA合成量与晚期病毒蛋白合成的相对量直接相关。由于晚期病毒蛋白的合成依赖于病毒DNA复制,因此在用病毒DNA合成抑制剂处理的允许性细胞或对巨细胞病毒DNA复制有抑制作用的非允许性细胞中未检测到这些蛋白。