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Viral transcription in KB cells infected by temperature-sensitive "early" mutants of adenovirus type 5.被腺病毒5型温度敏感“早期”突变体感染的KB细胞中的病毒转录。
J Virol. 1976 Apr;18(1):156-66. doi: 10.1128/JVI.18.1.156-166.1976.
2
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Autoregulation of adenovirus type 5 early gene expression. III. Transcription studies in isolated nuclei.5型腺病毒早期基因表达的自动调节。III. 分离细胞核中的转录研究。
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Adenovirus DNA-binding protein in cells infected with wild-type 5 adenovirus and two DNA-minus, temperature-sensitive mutants, H5ts125 and H5ts149.感染野生型5型腺病毒以及两种缺失DNA、温度敏感型突变体H5ts125和H5ts149的细胞中的腺病毒DNA结合蛋白。
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Possible role of the 72,000 dalton DNA-binding protein in regulation of adenovirus type 5 early gene expression.72,000道尔顿DNA结合蛋白在调控5型腺病毒早期基因表达中的可能作用。
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Mol Cell Biochem. 1976 Apr 28;11(2):79-95. doi: 10.1007/BF01792789.
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Temperature-sensitive initiation and elongation of adenovirus DNA replication in vitro with nuclear extracts from H5ts36-, H5ts149-, and H5ts125-infected HeLa cells.利用来自感染H5ts36、H5ts149和H5ts125的HeLa细胞的核提取物,在体外对腺病毒DNA复制进行温度敏感起始和延伸。
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本文引用的文献

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Relationship between deoxyribonucleic acid-like ribonucleic acid synthesis and inhibition of host protein synthesis in type 5 adenovirus-infected KB cells.5型腺病毒感染的KB细胞中脱氧核糖核酸样核糖核酸合成与宿主蛋白合成抑制之间的关系
J Virol. 1969 Feb;3(2):106-13. doi: 10.1128/JVI.3.2.106-113.1969.
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Transcription during bacteriophage T4 development: a demonstration that distinct subclasses of the "early" RNA appear at different times and that some are "turned off" at late times.噬菌体T4发育过程中的转录:证明“早期”RNA的不同亚类在不同时间出现,且有些在后期“关闭”。
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Biochemical studies on adenovirus multiplication. XV. Transcription of the adenovirus type II genome during productive infection.腺病毒增殖的生化研究。十五。II型腺病毒基因组在增殖性感染期间的转录。
Virology. 1969 Oct;39(2):205-10. doi: 10.1016/0042-6822(69)90040-3.
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Mechanism of viral carcinogenesis by DNA mammalian viruses. VII. Viral genes transcribed in adenovirus type 2 infected and transformed cells.DNA 哺乳动物病毒的病毒致癌机制。VII. 在 2 型腺病毒感染和转化细胞中转录的病毒基因。
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Biochemical studies on adenovirus multiplication. 18. Resolution of early virus-specific RNA species in Ad 2 infected and transformed cells.腺病毒增殖的生化研究。18. 腺病毒2型感染和转化细胞中早期病毒特异性RNA种类的解析。
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Selection and preliminary characterization of temperature-sensitive mutants of type 5 adenovirus.5型腺病毒温度敏感突变体的筛选及初步鉴定
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被腺病毒5型温度敏感“早期”突变体感染的KB细胞中的病毒转录。

Viral transcription in KB cells infected by temperature-sensitive "early" mutants of adenovirus type 5.

作者信息

Carter T H, Ginsberg H S

出版信息

J Virol. 1976 Apr;18(1):156-66. doi: 10.1128/JVI.18.1.156-166.1976.

DOI:10.1128/JVI.18.1.156-166.1976
PMID:1255869
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC515534/
Abstract

RNA

DNA hybridization was used to study the synthesis of viral RNA in two DNA-minus, temperature-sensitive mutants of type 5 adenovirus (H5ts125 and H5ts149) belonging to two different, non-overlapping complementation groups. Hybridization competition analysis showed that both mutants transcribed all early gene sequences at the restrictive temperature (41 C). In mutant-infected cells at 41 C, the rate of viral transcription was similar to the rate of early RNA synthesis in wild-type virus infection and was dependent on the multiplicity of infection; little or no late transcription was detected. The shutoff of class I early RNA transcription was shown to be a late function during wild-type virus infection and did not occur at 41 C in mutant-infected cells. When mutant-infected cells were incubated at the permissive temperature (32 C) for 25 h and then shifted to 41 C, the rate of viral DNA synthesis decreased rapidly for H5ts125 and slowly for H5ts149. However, the rate of viral transcription remained unchanged in H5ts125-infected cells for at least 3 h after the temperature shift; although the synthesis of viral DNA had stopped by this time, the synthesis of late viral RNA sequences continued.

摘要

RNA

DNA杂交技术被用于研究属于两个不同且不重叠互补组的5型腺病毒的两个DNA缺失型温度敏感突变体(H5ts125和H5ts149)中病毒RNA的合成。杂交竞争分析表明,在限制温度(41℃)下,这两个突变体均转录所有早期基因序列。在41℃下感染突变体的细胞中,病毒转录速率与野生型病毒感染时早期RNA合成速率相似,且依赖于感染复数;几乎检测不到晚期转录。I类早期RNA转录的关闭被证明是野生型病毒感染期间的晚期功能,在41℃下感染突变体的细胞中不会发生。当感染突变体的细胞在允许温度(32℃)下孵育25小时,然后转移到41℃时,H5ts125的病毒DNA合成速率迅速下降,H5ts149的则缓慢下降。然而,在温度转移后至少3小时内,H5ts125感染的细胞中病毒转录速率保持不变;尽管此时病毒DNA合成已经停止,但晚期病毒RNA序列的合成仍在继续。