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在赛氏疱疹病毒转化的淋巴样肿瘤细胞系中的病毒特异性转录

Virus-specific transcription in a Herpesvirus saimiri-transformed lymphoid tumor cell line.

作者信息

Knust E, Dietrich W, Fleckenstein B, Bodemer W

出版信息

J Virol. 1983 Nov;48(2):377-83. doi: 10.1128/JVI.48.2.377-383.1983.

Abstract

Herpesvirus saimiri-transformed lymphoid tumor cell lines contain nonintegrated covalently closed circular viral DNA molecules in high multiplicity. One of those cell lines, 1670, carries large viral DNA circles (202 kilobase pairs) with two stretches of repetitive DNA (70.8% G + C) that are interspersed between two segments of unique DNA (36% G + C). Since it was not known if there is any viral gene expression in H. saimiri-transformed cells, we initiated a study of transcription in cell line 1670. cDNA was generated by reverse transcription of cellular RNA and hybridized with cloned virion DNA fragments. The experiments indicated that appreciable transcription is restricted to a single segment of unique DNA. This sequence is present once only in the circular viral DNA and corresponds to unique DNA between map units 0.89 and 0.93 of virion DNA. By Northern blot hybridizations with labeled cloned probes of virion unique DNA, one predominant virus-specific polyadenylated transcript of, at most, 2.7 kilo-bases could be detected in tumor cell line 1670. The direction of transcription was determined by hybridization with randomly primed cDNA and, in parallel, with oligodeoxythymidylate-primed cDNA probes. Apparently, the patterns of virus-specific RNA synthesis in the H. saimiri-transformed cells are clearly distinct from the transcription program in other herpesvirus transformation systems analyzed before.

摘要

赛氏疱疹病毒转化的淋巴样肿瘤细胞系中含有大量非整合的共价闭合环状病毒DNA分子。其中一个细胞系1670携带大的病毒DNA环(202千碱基对),有两段重复DNA(G + C含量为70.8%)散布于两段单一DNA(G + C含量为36%)之间。由于此前尚不清楚赛氏疱疹病毒转化细胞中是否存在病毒基因表达,我们启动了对1670细胞系转录的研究。通过细胞RNA的逆转录生成cDNA,并与克隆的病毒粒子DNA片段杂交。实验表明,明显的转录仅限于单一的一段单一DNA。该序列在环状病毒DNA中仅出现一次,对应于病毒粒子DNA图谱单位0.89至0.93之间的单一DNA。通过用标记的病毒粒子单一DNA克隆探针进行Northern印迹杂交,在肿瘤细胞系1670中最多可检测到一种主要的病毒特异性多聚腺苷酸化转录本,长度为2.7千碱基。通过与随机引物cDNA以及同时与寡聚脱氧胸苷酸引物cDNA探针杂交来确定转录方向。显然,赛氏疱疹病毒转化细胞中病毒特异性RNA合成模式与之前分析的其他疱疹病毒转化系统中的转录程序明显不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47cd/255362/3f6a5d5bc80f/jvirol00140-0052-a.jpg

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