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Poxvirus DNA replication.痘病毒 DNA 复制。
Cold Spring Harb Perspect Biol. 2013 Sep 1;5(9):a010199. doi: 10.1101/cshperspect.a010199.
2
Methods for analysis of poxvirus DNA replication.痘病毒DNA复制的分析方法。
Methods Mol Biol. 2004;269:169-86. doi: 10.1385/1-59259-789-0:169.
3
Poxvirus uracil-DNA glycosylase-An unusual member of the family I uracil-DNA glycosylases.痘病毒尿嘧啶-DNA糖基化酶——I型尿嘧啶-DNA糖基化酶家族中的一个特殊成员。
Protein Sci. 2016 Dec;25(12):2113-2131. doi: 10.1002/pro.3058. Epub 2016 Nov 2.
4
Poxvirus DNA primase.痘病毒DNA引发酶
Proc Natl Acad Sci U S A. 2007 Nov 20;104(47):18724-9. doi: 10.1073/pnas.0709276104. Epub 2007 Nov 13.
5
Roles of uracil-DNA glycosylase and dUTPase in virus replication.尿嘧啶-DNA糖基化酶和dUTPase在病毒复制中的作用。
J Gen Virol. 2002 Oct;83(Pt 10):2339-2345. doi: 10.1099/0022-1317-83-10-2339.
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Origin-independent plasmid replication occurs in vaccinia virus cytoplasmic factories and requires all five known poxvirus replication factors.不依赖于起源的质粒复制发生在痘苗病毒的细胞质工厂中,并且需要所有五个已知的痘病毒复制因子。
Virol J. 2005 Mar 22;2:23. doi: 10.1186/1743-422X-2-23.
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Identification of Poxvirus Genome Uncoating and DNA Replication Factors with Mutually Redundant Roles.痘病毒基因组脱壳和具有相互冗余作用的DNA复制因子的鉴定
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8
In vitro resolution of poxvirus replicative intermediates into linear minichromosomes with hairpin termini by a virally induced Holliday junction endonuclease.痘病毒复制中间体通过病毒诱导的霍利迪连接内切核酸酶在体外解析为具有发夹末端的线性微型染色体。
J Virol. 1992 Mar;66(3):1551-63. doi: 10.1128/JVI.66.3.1551-1563.1992.
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Domain Organization of Vaccinia Virus Helicase-Primase D5.痘苗病毒解旋酶-引发酶D5的结构域组织
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Organization and expression of the poxvirus genome.痘病毒基因组的组织与表达。
Experientia. 1982 Mar 15;38(3):285-97. doi: 10.1007/BF01949349.

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本文引用的文献

1
Cidofovir Activity against Poxvirus Infections.西多福韦对痘病毒感染的活性。
Viruses. 2010 Dec;2(12):2803-30. doi: 10.3390/v2122803. Epub 2010 Dec 22.
2
Molecular characterization of the host defense activity of the barrier to autointegration factor against vaccinia virus.针对痘苗病毒的屏障抑制因子的宿主防御活性的分子特征分析。
J Virol. 2011 Nov;85(22):11588-600. doi: 10.1128/JVI.00641-11. Epub 2011 Aug 31.
3
Expression profiling of the intermediate and late stages of poxvirus replication.痘病毒复制的中晚期表达谱分析。
J Virol. 2011 Oct;85(19):9899-908. doi: 10.1128/JVI.05446-11. Epub 2011 Jul 27.
4
Vaccinia virus F16 protein, a predicted catalytically inactive member of the prokaryotic serine recombinase superfamily, is targeted to nucleoli.痘苗病毒 F16 蛋白是原核丝氨酸重组酶超家族中一个预测无催化活性的成员,它定位于核仁。
Virology. 2011 Sep 1;417(2):334-42. doi: 10.1016/j.virol.2011.06.017. Epub 2011 Jul 12.
5
Evaluation of the role of the vaccinia virus uracil DNA glycosylase and A20 proteins as intrinsic components of the DNA polymerase holoenzyme.评估牛痘病毒尿嘧啶 DNA 糖基化酶和 A20 蛋白作为 DNA 聚合酶全酶固有成分的作用。
J Biol Chem. 2011 Jul 15;286(28):24702-13. doi: 10.1074/jbc.M111.222216. Epub 2011 May 13.
6
Efficacy of CMX001 as a prophylactic and presymptomatic antiviral agent in New Zealand white rabbits infected with rabbitpox virus, a model for orthopoxvirus infections of humans.CMX001 作为一种预防和症状前抗病毒药物在新西兰白兔中预防感染兔痘病毒的功效,兔痘病毒是人类正痘病毒感染的模型。
Viruses. 2011 Feb;3(2):63-82. doi: 10.3390/v3020063.
7
Vaccinia virus particles mix inefficiently, and in a way that would restrict viral recombination, in coinfected cells.痘苗病毒粒子在感染细胞中混合效率低下,并且以一种限制病毒重组的方式混合。
J Virol. 2010 Mar;84(5):2432-43. doi: 10.1128/JVI.01998-09. Epub 2009 Dec 23.
8
Cellular DNA ligase I is recruited to cytoplasmic vaccinia virus factories and masks the role of the vaccinia ligase in viral DNA replication.细胞 DNA 连接酶 I 被招募到细胞质痘病毒工厂,并掩盖了痘病毒连接酶在病毒 DNA 复制中的作用。
Cell Host Microbe. 2009 Dec 17;6(6):563-9. doi: 10.1016/j.chom.2009.11.005.
9
Predicted poxvirus FEN1-like nuclease required for homologous recombination, double-strand break repair and full-size genome formation.预测的痘病毒FEN1样核酸酶,同源重组、双链断裂修复和全尺寸基因组形成所必需。
Proc Natl Acad Sci U S A. 2009 Oct 20;106(42):17921-6. doi: 10.1073/pnas.0909529106. Epub 2009 Oct 1.
10
The 3'-to-5' exonuclease activity of vaccinia virus DNA polymerase is essential and plays a role in promoting virus genetic recombination.痘苗病毒DNA聚合酶的3'至5'核酸外切酶活性至关重要,并在促进病毒基因重组中发挥作用。
J Virol. 2009 May;83(9):4236-50. doi: 10.1128/JVI.02255-08. Epub 2009 Feb 18.

痘病毒 DNA 复制。

Poxvirus DNA replication.

机构信息

Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Cold Spring Harb Perspect Biol. 2013 Sep 1;5(9):a010199. doi: 10.1101/cshperspect.a010199.

DOI:10.1101/cshperspect.a010199
PMID:23838441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3753712/
Abstract

Poxviruses are large, enveloped viruses that replicate in the cytoplasm and encode proteins for DNA replication and gene expression. Hairpin ends link the two strands of the linear, double-stranded DNA genome. Viral proteins involved in DNA synthesis include a 117-kDa polymerase, a helicase-primase, a uracil DNA glycosylase, a processivity factor, a single-stranded DNA-binding protein, a protein kinase, and a DNA ligase. A viral FEN1 family protein participates in double-strand break repair. The DNA is replicated as long concatemers that are resolved by a viral Holliday junction endonuclease.

摘要

痘病毒是大型包膜病毒,在细胞质中复制,并编码用于 DNA 复制和基因表达的蛋白质。发夹末端连接线性双链 DNA 基因组的两条链。参与 DNA 合成的病毒蛋白包括 117kDa 聚合酶、解旋酶-引发酶、尿嘧啶 DNA 糖基化酶、持续因子、单链 DNA 结合蛋白、蛋白激酶和 DNA 连接酶。一种病毒 FEN1 家族蛋白参与双链断裂修复。DNA 作为长的串联体复制,由病毒 Holliday 连接内切酶解决。