Flint S J, Plumb M A, Yang U C, Stein G S, Stein J L
Mol Cell Biol. 1984 Jul;4(7):1363-71. doi: 10.1128/mcb.4.7.1363-1371.1984.
The influence of adenovirus type 2 infection of HeLa cells upon expression of human histone genes was examined as a function of the period of infection. Histone RNA synthesis was assayed after run-off transcription in nuclei isolated from mock-infected cells and after various periods of adenovirus infection. Histone protein synthesis was measured by [3H]leucine labeling of intact cells and fluorography of electrophoretically fractionated nuclear and cytoplasmic proteins. The cellular representation of RNA species complementary to more than 13 different human histone genes was determined by RNA blot analysis of total cellular, nuclear or cytoplasmic RNA by using a series of 32P-labeled cloned human histone genes as hybridization probes and also by analysis of 3H-labeled histone mRNA species synthesized in intact cells. By 18 h after infection, HeLa cell DNA synthesis and all parameters of histone gene expression, including transcription and the nuclear and cytoplasmic concentrations of core and H1 mRNA species, were reduced to less than 5 to 10% of the control values. By contrast, transcription and processing of other cellular mRNA sequences have been shown to continue throughout this period of infection. The early period of adenovirus infection was marked by an inhibition of transcription of histone genes that accompanied the reduction in rate of HeLa cell DNA synthesis. These results suggest that the adenovirus-induced inhibition of histone gene expression is mediated in part at the transcriptional level. However, the persistence of histone mRNA species at concentrations comparable to those of mock-infected control cells during the early phase of the infection, despite a reduction in histone gene transcription and histone protein synthesis, implies that histone gene expression is also regulated post-transcriptionally in adenovirus-infected cells. These results suggest that the tight coupling between histone mRNA concentrations and the rate of cellular DNA synthesis, observed when DNA replication is inhibited by a variety of drugs, is not maintained after adenovirus infection.
研究了2型腺病毒感染HeLa细胞对人组蛋白基因表达的影响,并将其作为感染时间的函数进行检测。在从模拟感染细胞分离的细胞核中进行径流转录后,以及在腺病毒感染的不同时间段后,检测组蛋白RNA合成。通过对完整细胞进行[3H]亮氨酸标记以及对电泳分离的核蛋白和细胞质蛋白进行荧光显影来测量组蛋白蛋白质合成。通过使用一系列32P标记的克隆人组蛋白基因作为杂交探针,对总细胞、核或细胞质RNA进行RNA印迹分析,以及通过分析在完整细胞中合成的3H标记的组蛋白mRNA种类,来确定与13种以上不同人组蛋白基因互补的RNA种类的细胞表达情况。感染后18小时,HeLa细胞DNA合成以及组蛋白基因表达的所有参数,包括转录以及核心和H1 mRNA种类的核浓度和细胞质浓度,均降至对照值的5%至10%以下。相比之下,已证明其他细胞mRNA序列的转录和加工在整个感染期间持续进行。腺病毒感染的早期阶段的特征是组蛋白基因转录受到抑制,同时HeLa细胞DNA合成速率降低。这些结果表明,腺病毒诱导的组蛋白基因表达抑制部分是在转录水平介导的。然而,尽管组蛋白基因转录和组蛋白蛋白质合成减少,但在感染早期阶段,组蛋白mRNA种类的浓度与模拟感染对照细胞的浓度相当,这意味着组蛋白基因表达在腺病毒感染的细胞中也受到转录后调控。这些结果表明,当DNA复制受到多种药物抑制时观察到的组蛋白mRNA浓度与细胞DNA合成速率之间的紧密耦合,在腺病毒感染后并未维持。