Singer I I, Rhode S L
J Virol. 1978 Jan;25(1):349-60. doi: 10.1128/JVI.25.1.349-360.1978.
The localization of H-1 viral replicative-form double-stranded DNA and progeny single-stranded DNA replication in parasynchronously infected, simian virus 40-transformed newborn human kidney cells was studied with high-resolution electron microscope autoradiography (80-nm silver grains). We analyzed wild-type H-1 and ts1 H-1 (a conditional mutant defective in progeny single-stranded DNA synthesis). The proportion of the total DNA synthesis that was viral was estimated to be >90% by comparing the amount of [(3)H]thymidine uptake in cultures infected with wild-type H-1 versus ts14 (an H-1 mutant defective in DNA replication). Simultaneous staining with cytochrome c-conjugated anti-H-1 immunoglobulin G was performed to ensure that cells incorporating [(3)H]thymidine (2- to 60-min pulses) were H-1 infected. The sites of H-1 replicative-form (in ts1-infected cells) and progeny (in wild-type-infected cells) DNA synthesis were identical. Immunospecifically labeled nuclei at the earliest stages of infection exhibited dense clusters of silver grains over material extruded from nucleolar fibrillar centers. These foci became larger with increasing cellular damage, forming a limited number of H-1 DNA synthetic centers in the euchromatin. Each island-like focus was surrounded by tufts of heterochromatin containing high concentrations of unassembled H-1 capsid proteins. In late phases of infection, the heterochromatin became completely marginated, and the nucleoplasm contained only euchromatin that exhibited randomly distributed sites of H-1 DNA replication. This indicates that H-1 DNA synthesis begins at localized euchromatic or nucleolar sites and then spreads outward. Immunostained heterochromatin and nucleolar chromatin never incorporated [(3)H]thymidine. Our results suggest that H-1 proteins and cellular cofactors associated with the fibrillar component of the nucleolus and the euchromatin may play a role in the regulation of H-1 DNA synthesis.
利用高分辨率电子显微镜放射自显影技术(80纳米银颗粒),研究了猿猴病毒40转化的新生人肾细胞在同步感染H - 1病毒时,其复制型双链DNA和子代单链DNA复制的定位情况。我们分析了野生型H - 1和ts1 H - 1(一种在子代单链DNA合成方面有缺陷的条件突变体)。通过比较感染野生型H - 1与ts14(一种在DNA复制方面有缺陷的H - 1突变体)的培养物中[³H]胸腺嘧啶的摄取量,估计病毒DNA合成占总DNA合成的比例>90%。同时用细胞色素c偶联的抗H - 1免疫球蛋白G进行染色,以确保摄取[³H]胸腺嘧啶(2至60分钟脉冲)的细胞被H - 1感染。H - 1复制型(在ts1感染的细胞中)和子代(在野生型感染的细胞中)DNA合成的位点是相同的。在感染的最早阶段,免疫特异性标记的细胞核在从核仁纤维中心挤出的物质上呈现出密集的银颗粒簇。随着细胞损伤的增加,这些焦点变得更大,在常染色质中形成数量有限的H - 1 DNA合成中心。每个岛状焦点被含有高浓度未组装H - 1衣壳蛋白的异染色质簇包围。在感染后期,异染色质完全边缘化,核质中仅含有呈现H - 1 DNA复制随机分布位点的常染色质。这表明H - 1 DNA合成始于局部的常染色质或核仁位点,然后向外扩散。免疫染色的异染色质和核仁染色质从未摄取[³H]胸腺嘧啶。我们的结果表明,与核仁的纤维成分和常染色质相关的H - 1蛋白和细胞辅助因子可能在H - 1 DNA合成的调控中发挥作用。