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本文引用的文献

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Temporal association of the herpes simplex virus genome with histone proteins during a lytic infection.单纯疱疹病毒基因组在裂解性感染期间与组蛋白的时间关联。
J Virol. 2008 Apr;82(7):3530-7. doi: 10.1128/JVI.00586-07. Epub 2007 Dec 26.
2
Murine gammaherpesvirus 68 open reading frame 24 is required for late gene expression after DNA replication.小鼠γ-疱疹病毒68的开放阅读框24是DNA复制后晚期基因表达所必需的。
J Virol. 2007 Jun;81(12):6761-4. doi: 10.1128/JVI.02726-06. Epub 2007 Mar 28.
3
ORF18 is a transfactor that is essential for late gene transcription of a gammaherpesvirus.开放阅读框18(ORF18)是一种反式作用因子,对γ疱疹病毒的晚期基因转录至关重要。
J Virol. 2006 Oct;80(19):9730-40. doi: 10.1128/JVI.00246-06.
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Identification of viral genes essential for replication of murine gamma-herpesvirus 68 using signature-tagged mutagenesis.利用签名标签诱变技术鉴定对小鼠γ-疱疹病毒68复制至关重要的病毒基因。
Proc Natl Acad Sci U S A. 2005 Mar 8;102(10):3805-10. doi: 10.1073/pnas.0404521102. Epub 2005 Feb 28.
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Viral DNA synthesis-dependent titration of a cellular repressor activates transcription of the human adenovirus type 2 IVa2 gene.细胞阻遏物的病毒DNA合成依赖性滴定激活人2型腺病毒IVa2基因的转录。
Proc Natl Acad Sci U S A. 2004 Dec 21;101(51):17831-6. doi: 10.1073/pnas.0407786101. Epub 2004 Dec 9.
6
Identification of candidate gammaherpesvirus 68 genes required for virus replication by signature-tagged transposon mutagenesis.通过签名标签转座子诱变鉴定病毒复制所需的γ疱疹病毒68候选基因。
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7
During lytic infection herpes simplex virus type 1 is associated with histones bearing modifications that correlate with active transcription.在裂解感染期间,1型单纯疱疹病毒与带有与活跃转录相关修饰的组蛋白相关联。
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8
VP16-dependent association of chromatin-modifying coactivators and underrepresentation of histones at immediate-early gene promoters during herpes simplex virus infection.单纯疱疹病毒感染期间,染色质修饰共激活因子与VP16的依赖性关联以及即刻早期基因启动子处组蛋白的低表达。
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9
Generation of a latency-deficient gammaherpesvirus that is protective against secondary infection.产生一种对二次感染具有保护作用的潜伏期缺陷型γ疱疹病毒。
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10
Identification of cis sequences required for lytic DNA replication and packaging of murine gammaherpesvirus 68.鉴定小鼠γ疱疹病毒68裂解性DNA复制和包装所需的顺式序列。
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ORF30和ORF34对于小鼠γ疱疹病毒68晚期基因的表达至关重要。

ORF30 and ORF34 are essential for expression of late genes in murine gammaherpesvirus 68.

作者信息

Wu Ting-Ting, Park Tina, Kim Hana, Tran Thuy, Tong Leming, Martinez-Guzman DeeAnn, Reyes Nichole, Deng Hongyu, Sun Ren

机构信息

Department of Molecular and Medical Pharmacology, University of California at Los Angeles, Los Angeles, California 90095, USA.

出版信息

J Virol. 2009 Mar;83(5):2265-73. doi: 10.1128/JVI.01785-08. Epub 2008 Dec 17.

DOI:10.1128/JVI.01785-08
PMID:19091863
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2643722/
Abstract

A hallmark of productive infection by DNA viruses is the coupling of viral late gene expression to genome replication. Here we report the identification of open reading frame 30 (ORF30) and ORF34 as viral trans factors crucial for activating late gene transcription following viral DNA replication during lytic infection of murine gammaherpesvirus 68 (MHV-68). The mutant virus lacking either ORF30 or ORF34 underwent normal DNA replication but failed to express viral late gene transcripts, leading to nonproductive infection. In a reporter assay system, ORF30 and ORF34 were required for MHV-68 to activate the viral late gene promoters. Furthermore, studies using chromatin immunoprecipitation assays showed that the recruitment of RNA polymerase II to the viral late promoters during lytic infection was significantly reduced in the absence of ORF30 or ORF34. Together, the results suggest that ORF30 and ORF34 may play an important role in the assembly of the transcription initiation complex at the late gene promoters. Our discovery of the viral mutants that uncouple late gene transcription from DNA replication lays an important foundation to dissect the mechanism of this critical step of gene expression regulation.

摘要

DNA病毒有效感染的一个标志是病毒晚期基因表达与基因组复制的偶联。在此,我们报告了开放阅读框30(ORF30)和开放阅读框34被鉴定为病毒反式作用因子,它们对于小鼠γ疱疹病毒68(MHV - 68)裂解感染期间病毒DNA复制后激活晚期基因转录至关重要。缺失ORF30或ORF34的突变病毒进行了正常的DNA复制,但未能表达病毒晚期基因转录本,导致感染无 productive。在报告基因检测系统中,MHV - 68激活病毒晚期基因启动子需要ORF30和ORF34。此外,使用染色质免疫沉淀分析的研究表明,在裂解感染期间,在没有ORF30或ORF34的情况下,RNA聚合酶II募集到病毒晚期启动子的情况显著减少。总之,结果表明ORF30和ORF34可能在晚期基因启动子处转录起始复合物的组装中起重要作用。我们发现了使晚期基因转录与DNA复制解偶联的病毒突变体,为剖析这一基因表达调控关键步骤的机制奠定了重要基础。