Vennström B, Philipson L
J Virol. 1977 May;22(2):290-9. doi: 10.1128/JVI.22.2.290-299.1977.
An in vitro nuclear system from adenovirus type 2-infected cells was developed to study transcription of viral RNA. Nuclei isolated from adenovirus-infected HeLa cells late in the infectious cycle synthesized in vitro only RNA from the r-strand of adenovirus DNA. Around 15% of the virus-specific RNA in isolated nuclei was polyadenylated. Short pulse labeling of nascent RNA followbd by hybrization of size-fractionated RNA to specific restriction endonuclease fragments of the genome suggested that the origin(s) for transcription is located on the r-strand in the left 30% of the adenovirus 2 genome at late times in the infectious cycle. Pulse-chase experiments were used to estimate the elongation rate of adenovirus high-molecular-weight RNA in isolated nuclei. An elongation of a least six nucleotides per second was observed in vitro. Viral RNA synthesis in the vitro nuclei showed several similarities to the in vivo system late in the infectious cycle.
为了研究病毒RNA的转录,构建了一个来自2型腺病毒感染细胞的体外核系统。在感染周期后期从腺病毒感染的HeLa细胞中分离出的细胞核,在体外仅合成腺病毒DNA r链的RNA。分离出的细胞核中约15%的病毒特异性RNA是聚腺苷酸化的。对新生RNA进行短脉冲标记,然后将大小分级的RNA与基因组的特定限制性内切酶片段杂交,结果表明,在感染周期后期,转录起始位点位于腺病毒2基因组左侧30%的r链上。脉冲追踪实验用于估计分离细胞核中腺病毒高分子量RNA的延伸速率。在体外观察到每秒至少延伸六个核苷酸。体外细胞核中的病毒RNA合成与感染周期后期的体内系统有几个相似之处。