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转化细胞腺病毒感染过程中整合腺病毒序列的调控

Regulation of integrated adenovirus sequences during adenovirus infection of transformed cells.

作者信息

Spector D J, Halbert D N, Raskas H J

出版信息

J Virol. 1980 Dec;36(3):860-71. doi: 10.1128/JVI.36.3.860-871.1980.

Abstract

A human cell line (293) transformed by adenovirus type 5 encodes mRNA's and proteins from the early region 1 (E1) of the viral genome. These products correspond to those synthesized early after adenovirus infection of normal cells. This pattern of expression is different from that observed at later times in the lytic cycle. We have determined whether integrated sequences can undergo the early-late transition during infection of transformed cells. Cultures of 293 cells were infected with mutants of adenovirus type 5 that have deletions in EI genes. In such infections, the integrated sequence complements the deletion mutants so that viral DNA replication, late mRNA and protein synthesis, and viral assembly occur. Because the infecting genomes lack EI sequences, the products synthesized from the integrated DNA could be analyzed. In contrast to the early-late transition that occurs with EI DNA in free viral genomes, the pattern of mRNAs and proteins made from the integrated sequences was restricted to the early pattern. Assuming that the viral sequences in 293 cells have not become altered during the history of the cells, our results suggest that regulation of integrated adenovirus genes may not be determined exclusively by nucleotide sequence recognition. Apparently, during infection certain factors prevent the integrated viral genes from responding to the regulatory signals which control late expression from free EI DNA. The distinction between integrated and free viral sequences might reflect the different fates of viral and host transcripts during the lytic cycle of adenovirus.

摘要

由5型腺病毒转化的人细胞系(293)编码来自病毒基因组早期区域1(E1)的mRNA和蛋白质。这些产物与正常细胞腺病毒感染后早期合成的产物相对应。这种表达模式与在裂解周期后期观察到的不同。我们已经确定整合序列在转化细胞感染期间是否能经历早期到晚期的转变。用E1基因有缺失的5型腺病毒突变体感染293细胞培养物。在这种感染中,整合序列补充缺失突变体,从而发生病毒DNA复制、晚期mRNA和蛋白质合成以及病毒组装。由于感染的基因组缺乏E1序列,因此可以分析从整合DNA合成的产物。与游离病毒基因组中E1 DNA发生的早期到晚期转变相反,从整合序列产生的mRNA和蛋白质模式仅限于早期模式。假设293细胞中的病毒序列在细胞历史过程中没有发生改变,我们的结果表明整合腺病毒基因的调控可能不完全由核苷酸序列识别决定。显然,在感染期间某些因素阻止整合的病毒基因对控制游离E1 DNA晚期表达的调控信号作出反应。整合和游离病毒序列之间的差异可能反映了腺病毒裂解周期中病毒和宿主转录本的不同命运。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48dd/353713/78a9e170a6f0/jvirol00180-0240-a.jpg

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