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腺病毒RNA转录在分离的HeLa细胞核中的保真度。

Fidelity of adenovirus RNA transcription in isolated HeLa cell nuclei.

作者信息

Vennström B, Philipson L

出版信息

J Virol. 1977 May;22(2):290-9. doi: 10.1128/JVI.22.2.290-299.1977.

Abstract

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.

摘要

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。

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