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Control of adenovirus early gene expression: posttranscriptional control mediated by both viral and cellular gene products.腺病毒早期基因表达的调控:由病毒和细胞基因产物介导的转录后调控。
Mol Cell Biol. 1981 Sep;1(9):807-13. doi: 10.1128/mcb.1.9.807-813.1981.
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The product of the adenovirus intermediate gene IX is a transcriptional activator.腺病毒中间基因IX的产物是一种转录激活因子。
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Sequence-mediated regulation of adenovirus gene expression by repression of mRNA accumulation.通过抑制mRNA积累实现的腺病毒基因表达的序列介导调控。
Mol Cell Biol. 1997 Apr;17(4):2207-16. doi: 10.1128/MCB.17.4.2207.
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The initiator element of the adenovirus major late promoter has an important role in transcription initiation in vivo.腺病毒主要晚期启动子的起始元件在体内转录起始过程中起重要作用。
J Virol. 1997 Jan;71(1):102-9. doi: 10.1128/JVI.71.1.102-109.1997.
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The adenovirus death protein (E3-11.6K) is required at very late stages of infection for efficient cell lysis and release of adenovirus from infected cells.腺病毒死亡蛋白(E3-11.6K)在感染的极晚期阶段是有效细胞裂解和腺病毒从受感染细胞中释放所必需的。
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Sequences regulating poly(A) site selection within the adenovirus major late transcription unit influence the interaction of constitutive processing factors with the pre-mRNA.腺病毒主要晚期转录单位内调控聚腺苷酸化位点选择的序列会影响组成型加工因子与前体信使核糖核酸的相互作用。
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Properties of the adenovirus IVa2 gene product, an effector of late-phase-dependent activation of the major late promoter.腺病毒IVa2基因产物的特性,主要晚期启动子晚期依赖性激活的效应因子。
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10
Regulated splicing of adenovirus type 5 E4 transcripts and regulated cytoplasmic accumulation of E4 mRNA.5型腺病毒E4转录本的可变剪接及E4 mRNA在细胞质中的调控积累。
J Virol. 1993 Jun;67(6):3226-31. doi: 10.1128/JVI.67.6.3226-3231.1993.

感染后期腺病毒早期基因表达的调控

Control of adenovirus early gene expression during the late phase of infection.

作者信息

Fessler S P, Young C S

机构信息

Department of Microbiology, Columbia University, New York, New York 10032, USA.

出版信息

J Virol. 1998 May;72(5):4049-56. doi: 10.1128/JVI.72.5.4049-4056.1998.

DOI:10.1128/JVI.72.5.4049-4056.1998
PMID:9557693
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC109633/
Abstract

The adenovirus gene regulatory program occurs in two distinct phases, as defined by the onset of DNA replication. During the early phase, the E1A, E1B, E2, E3, and E4 genes are maximally expressed, while the major late promoter (MLP) is minimally expressed and transcription is attenuated. After the onset of DNA replication, the IVa2 and pIX genes are expressed at high levels, transcription from the MLP is unattenuated and fully activated, and early gene expression is repressed. Although the cis elements and trans-acting factors responsible for the late-phase activation of the MLP have been identified and characterized and the role of DNA replication in activation has been established, the mechanism(s) underlying the commensurate decrease in early gene expression has yet to be elucidated. The results of this study demonstrate that this decrease depends on a fully functional MLP. Specifically, virus mutants with severely deficient transcription from the MLP exhibit a marked increase in expression of the E1A, E1B, and E2 early genes. These increases were observed at the level of transcription initiation, mRNA accumulation, and protein production. In addition, expression from the late gene pIX, which is not contained within the major late transcription unit (MLTU), is also markedly increased. To begin the analysis of the mechanisms underlying these late-phase effects, mixed-infection experiments with mutant and wild-type viruses were performed. The results show that the effects on early gene expression, as measured both at the protein and RNA levels, are mediated in trans and not in cis. These observations are consistent either with a model in which one or more late protein products encoded by the MLTU acts as a repressor of early gene expression or with one in which the wild-type MLP competes with early promoters for limiting transcription factors.

摘要

腺病毒基因调控程序分为两个不同阶段,由DNA复制的起始来界定。在早期阶段,E1A、E1B、E2、E3和E4基因大量表达,而主要晚期启动子(MLP)表达量极低,转录减弱。DNA复制起始后,IVa2和pIX基因高水平表达,MLP的转录不再减弱并被完全激活,早期基因表达受到抑制。尽管已经鉴定并表征了负责MLP晚期激活的顺式元件和反式作用因子,且已确定DNA复制在激活中的作用,但早期基因表达相应降低的机制仍有待阐明。本研究结果表明,这种降低依赖于功能完整的MLP。具体而言,MLP转录严重缺陷的病毒突变体在E1A、E1B和E2早期基因的表达上显著增加。这些增加在转录起始、mRNA积累和蛋白质产生水平均有观察到。此外,主要晚期转录单元(MLTU)中不包含的晚期基因pIX的表达也显著增加。为了开始分析这些晚期效应的潜在机制,进行了突变体和野生型病毒的混合感染实验。结果表明,对早期基因表达的影响,无论是在蛋白质还是RNA水平上测量,都是通过反式作用介导的,而非顺式作用。这些观察结果与以下两种模型之一一致:一种模型是MLTU编码的一种或多种晚期蛋白质产物作为早期基因表达的抑制因子;另一种模型是野生型MLP与早期启动子竞争有限的转录因子。