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鉴定需要模板复制以进行表达的腺病毒基因。

Identification of adenovirus genes that require template replication for expression.

作者信息

Crossland L D, Raskas H J

出版信息

J Virol. 1983 Jun;46(3):737-48. doi: 10.1128/JVI.46.3.737-748.1983.

DOI:10.1128/JVI.46.3.737-748.1983
PMID:6854739
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC256550/
Abstract

The relationship between adenovirus type 2 DNA replication and expression of intermediate stage viral genes was investigated. The 1.03-kilobase mRNA from early region 1b (E1b) and the mRNAs coding for proteins IX and IVa2 were first detected between 6 and 8 h postinfection. Inhibition of viral DNA replication with hydroxyurea prevented expression of the IX and IVa2 mRNAs, but not of the E1b mRNA. Pulse-labeling experiments demonstrated that the block of IX and IVa2 expression in hydroxyurea-treated cells was at the level of transcription. By a series of superinfection experiments, it was determined that the viral and cellular factors present during the late stage of adenovirus infection are insufficient to activate IX gene expression. The viral DNA template must first replicate before IX transcription can begin.

摘要

研究了2型腺病毒DNA复制与中期病毒基因表达之间的关系。感染后6至8小时首次检测到来自早期区域1b(E1b)的1.03千碱基mRNA以及编码蛋白质IX和IVa2的mRNA。用羟基脲抑制病毒DNA复制可阻止IX和IVa2 mRNA的表达,但不影响E1b mRNA的表达。脉冲标记实验表明,在羟基脲处理的细胞中,IX和IVa2表达的阻断发生在转录水平。通过一系列的超感染实验确定,腺病毒感染后期存在的病毒和细胞因子不足以激活IX基因的表达。病毒DNA模板必须先复制,IX转录才能开始。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b85/256550/6587ca8d9030/jvirol00147-0075-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b85/256550/dd780ab4732b/jvirol00147-0069-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b85/256550/c390e6e1133a/jvirol00147-0070-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b85/256550/360a99f9a87e/jvirol00147-0071-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b85/256550/75fd3cc204ac/jvirol00147-0072-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b85/256550/0616fbf1922e/jvirol00147-0073-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b85/256550/c276c785d5af/jvirol00147-0074-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b85/256550/ab36334642a7/jvirol00147-0074-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b85/256550/6587ca8d9030/jvirol00147-0075-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b85/256550/dd780ab4732b/jvirol00147-0069-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b85/256550/c390e6e1133a/jvirol00147-0070-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b85/256550/360a99f9a87e/jvirol00147-0071-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b85/256550/75fd3cc204ac/jvirol00147-0072-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b85/256550/0616fbf1922e/jvirol00147-0073-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b85/256550/c276c785d5af/jvirol00147-0074-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b85/256550/ab36334642a7/jvirol00147-0074-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b85/256550/6587ca8d9030/jvirol00147-0075-a.jpg

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本文引用的文献

1
Regulation of integrated adenovirus sequences during adenovirus infection of transformed cells.转化细胞腺病毒感染过程中整合腺病毒序列的调控
J Virol. 1980 Dec;36(3):860-71. doi: 10.1128/JVI.36.3.860-871.1980.
2
Transcripts from the adenovirus-2 major late promoter yield a single early family of 3' coterminal mRNAs and five late families.腺病毒2型主要晚期启动子的转录本产生一个3' 共末端mRNA的早期家族和五个晚期家族。
Cell. 1980 Dec;22(3):905-16. doi: 10.1016/0092-8674(80)90568-1.
3
DNA replication and the early to late transition in adenovirus infection.
FEBS Lett. 2019 Dec;593(24):3531-3550. doi: 10.1002/1873-3468.13695. Epub 2019 Dec 17.
4
Comparison of the Life Cycles of Genetically Distant Species C and Species D Human Adenoviruses Ad6 and Ad26 in Human Cells.遗传距离较远的C型和D型人类腺病毒Ad6和Ad26在人类细胞中的生命周期比较。
J Virol. 2015 Dec;89(24):12401-17. doi: 10.1128/JVI.01534-15. Epub 2015 Sep 30.
5
Strong foreign promoters contribute to innate inflammatory responses induced by adenovirus transducing vectors.强的外源启动子有助于腺病毒转导载体诱导的固有炎症反应。
Virology. 2011 Mar 30;412(1):28-35. doi: 10.1016/j.virol.2010.12.054. Epub 2011 Jan 20.
6
Identification of a previously unrecognized promoter that drives expression of the UXP transcription unit in the human adenovirus type 5 genome.鉴定出一种先前未被识别的启动子,该启动子驱动人腺病毒 5 型基因组中 UXP 转录单元的表达。
J Virol. 2010 Nov;84(21):11470-8. doi: 10.1128/JVI.01338-10. Epub 2010 Aug 25.
7
In vitro dynamic visualization analysis of fluorescently labeled minor capsid protein IX and core protein V by simultaneous detection.通过同步检测对荧光标记的次要衣壳蛋白IX和核心蛋白V进行体外动态可视化分析。
J Mol Biol. 2010 Jan 8;395(1):55-78. doi: 10.1016/j.jmb.2009.10.034. Epub 2009 Oct 21.
8
Adenovirus serotype 5 L4-22K and L4-33K proteins have distinct functions in regulating late gene expression.腺病毒5型L4-22K和L4-33K蛋白在调节晚期基因表达方面具有不同功能。
J Virol. 2009 Apr;83(7):3049-58. doi: 10.1128/JVI.02455-08. Epub 2009 Jan 28.
9
Interaction of the adenovirus L1 52/55-kilodalton protein with the IVa2 gene product during infection.腺病毒L1 52/55千道尔顿蛋白在感染过程中与IVa2基因产物的相互作用。
J Virol. 1996 Sep;70(9):6463-7. doi: 10.1128/JVI.70.9.6463-6467.1996.
10
Nucleoplasmic and nucleolar distribution of the adenovirus IVa2 gene product.腺病毒IVa2基因产物的核质和核仁分布。
J Virol. 1996 Jun;70(6):3449-60. doi: 10.1128/JVI.70.6.3449-3460.1996.
腺病毒感染中的DNA复制及早期到晚期的转变
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4
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J Mol Biol. 1981 May 25;148(3):231-51. doi: 10.1016/0022-2836(81)90537-4.
5
Controls of RNA splicing and termination in the major late adenovirus transcription unit.腺病毒主要晚期转录单元中RNA剪接和终止的调控
Nature. 1981 Jul 30;292(5822):420-6. doi: 10.1038/292420a0.
6
Regulation of adenovirus-2 gene expression at the level of transcriptional termination and RNA processing.腺病毒-2基因表达在转录终止和RNA加工水平上的调控。
Nature. 1981 Mar 12;290(5802):113-8. doi: 10.1038/290113a0.
7
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8
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9
The gene for polypeptide IX of adenovirus type 2 and its unspliced messenger RNA.2型腺病毒多聚肽IX基因及其未剪接的信使核糖核酸。
Cell. 1980 Mar;19(3):671-81. doi: 10.1016/s0092-8674(80)80044-4.
10
Organization and expression of the left third of the genome of adenovirus.腺病毒基因组左三分之一的组织与表达
Cold Spring Harb Symp Quant Biol. 1980;44 Pt 1,:493-508. doi: 10.1101/sqb.1980.044.01.052.