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Cellular factors required for papillomavirus DNA replication.乳头瘤病毒DNA复制所需的细胞因子。
J Virol. 1995 Dec;69(12):7857-67. doi: 10.1128/JVI.69.12.7857-7867.1995.
2
Functional interactions between SV40 T antigen and other replication proteins at the replication fork.SV40 T抗原与复制叉处其他复制蛋白之间的功能相互作用。
J Biol Chem. 1993 May 25;268(15):11008-17.
3
Anatomy of a DNA replication fork revealed by reconstitution of SV40 DNA replication in vitro.通过体外重建SV40 DNA复制揭示DNA复制叉的结构
Nature. 1994 May 19;369(6477):207-12. doi: 10.1038/369207a0.
4
The cellular DNA polymerase alpha-primase is required for papillomavirus DNA replication and associates with the viral E1 helicase.细胞DNA聚合酶α-引发酶是乳头瘤病毒DNA复制所必需的,并与病毒E1解旋酶相关联。
Proc Natl Acad Sci U S A. 1994 Aug 30;91(18):8700-4. doi: 10.1073/pnas.91.18.8700.
5
DNA replication machinery: functional characterization of a complex containing DNA polymerase alpha, DNA polymerase delta, and replication factor C suggests an asymmetric DNA polymerase dimer.DNA复制机制:对包含DNA聚合酶α、DNA聚合酶δ和复制因子C的复合物的功能表征表明存在不对称的DNA聚合酶二聚体。
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DNA polymerase switching: I. Replication factor C displaces DNA polymerase alpha prior to PCNA loading.DNA聚合酶转换:I. 在增殖细胞核抗原(PCNA)加载之前,复制因子C取代DNA聚合酶α 。
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Identification of eukaryotic DNA replication proteins using simian virus 40 in vitro replication system.利用猿猴病毒40体外复制系统鉴定真核生物DNA复制蛋白
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Nucleotide excision repair DNA synthesis by DNA polymerase epsilon in the presence of PCNA, RFC, and RPA.在增殖细胞核抗原(PCNA)、复制因子C(RFC)和复制蛋白A(RPA)存在的情况下,由DNA聚合酶ε进行核苷酸切除修复DNA合成。
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J Biol Chem. 1994 Jun 24;269(25):17086-94.

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本文引用的文献

1
DNA polymerases delta and epsilon are required for chromosomal replication in Saccharomyces cerevisiae.DNA聚合酶δ和ε是酿酒酵母染色体复制所必需的。
Mol Cell Biol. 1993 Jan;13(1):496-505. doi: 10.1128/mcb.13.1.496-505.1993.
2
Cooperative assembly of the bovine papilloma virus E1 and E2 proteins on the replication origin requires an intact E2 binding site.牛乳头瘤病毒E1和E2蛋白在复制起点上的协同组装需要完整的E2结合位点。
J Biol Chem. 1993 Jul 25;268(21):15795-803.
3
Completion of mammalian lagging strand DNA replication using purified proteins.使用纯化蛋白完成哺乳动物滞后链DNA复制。
J Biol Chem. 1993 Jul 15;268(20):15136-41.
4
The acidic transcriptional activation domains of VP16 and p53 bind the cellular replication protein A and stimulate in vitro BPV-1 DNA replication.VP16和p53的酸性转录激活结构域与细胞复制蛋白A结合,并在体外刺激牛乳头瘤病毒1型(BPV-1)DNA复制。
Cell. 1993 Jun 18;73(6):1207-21. doi: 10.1016/0092-8674(93)90649-b.
5
The E1 protein of bovine papilloma virus 1 is an ATP-dependent DNA helicase.牛乳头瘤病毒1的E1蛋白是一种依赖ATP的DNA解旋酶。
Proc Natl Acad Sci U S A. 1993 Jun 1;90(11):5086-90. doi: 10.1073/pnas.90.11.5086.
6
The bovine papillomavirus origin of replication requires a binding site for the E2 transcriptional activator.牛乳头瘤病毒复制起点需要E2转录激活因子的结合位点。
Proc Natl Acad Sci U S A. 1993 Feb 1;90(3):898-902. doi: 10.1073/pnas.90.3.898.
7
An interaction between replication protein A and SV40 T antigen appears essential for primosome assembly during SV40 DNA replication.复制蛋白A与SV40 T抗原之间的相互作用对于SV40 DNA复制过程中的引发体组装似乎至关重要。
J Biol Chem. 1993 Feb 15;268(5):3389-95.
8
Bovine papilloma virus (BPV)-encoded E1 protein contains multiple activities required for BPV DNA replication.牛乳头瘤病毒(BPV)编码的E1蛋白含有BPV DNA复制所需的多种活性。
Proc Natl Acad Sci U S A. 1993 Jan 15;90(2):702-6. doi: 10.1073/pnas.90.2.702.
9
Epidemiology of cervical human papillomavirus infections.宫颈人乳头瘤病毒感染的流行病学
Curr Top Microbiol Immunol. 1994;186:55-81. doi: 10.1007/978-3-642-78487-3_4.
10
Molecular pathogenesis of cancer of the cervix and its causation by specific human papillomavirus types.子宫颈癌的分子发病机制及其由特定人乳头瘤病毒类型引起的病因
Curr Top Microbiol Immunol. 1994;186:131-56. doi: 10.1007/978-3-642-78487-3_8.

乳头瘤病毒DNA复制所需的细胞因子。

Cellular factors required for papillomavirus DNA replication.

作者信息

Melendy T, Sedman J, Stenlund A

机构信息

Cold Spring Harbor Laboratory, New York 11724-2206, USA.

出版信息

J Virol. 1995 Dec;69(12):7857-67. doi: 10.1128/JVI.69.12.7857-7867.1995.

DOI:10.1128/JVI.69.12.7857-7867.1995
PMID:7494298
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC189730/
Abstract

In vitro replication of papillomavirus DNA has been carried out with a combination of purified proteins and partially purified extracts made from human cells. DNA synthesis requires the viral E1 protein and the papillomavirus origin of replication. The E2 protein stimulates DNA synthesis in a binding site-independent manner. Papillomavirus DNA replication is also dependent on the cellular factors replication protein A, replication factor C, and proliferating-cell nuclear antigen as well as a phosphocellulose column fraction (IIA). Fraction IIA contains DNA polymerase alpha-primase and DNA polymerase delta. Both of these polymerases are essential for papillomavirus DNA replication in vitro. However, unlike the case with T-antigen-dependent replication from the simian virus 40 origin, purified DNA polymerase alpha-primase and delta cannot efficiently replace fraction IIA in the replication reaction. Hence, additional cellular factors seem to be required for papillomavirus DNA replication. Interestingly, replication factor C and proliferating-cell nuclear antigen are more stringently required for DNA synthesis in the papillomavirus system than in the simian virus 40 in vitro system. These distinctions indicate that there must be mechanistic differences between the DNA replication systems of papillomavirus and simian virus 40.

摘要

乳头瘤病毒DNA的体外复制是通过将纯化蛋白与从人细胞中提取的部分纯化提取物相结合来进行的。DNA合成需要病毒E1蛋白和乳头瘤病毒复制起点。E2蛋白以一种不依赖于结合位点的方式刺激DNA合成。乳头瘤病毒DNA复制还依赖于细胞因子复制蛋白A、复制因子C、增殖细胞核抗原以及磷酸纤维素柱层析组分(IIA)。组分IIA含有DNA聚合酶α-引物酶和DNA聚合酶δ。这两种聚合酶对于乳头瘤病毒DNA的体外复制都是必不可少的。然而,与猿猴病毒40起点的T抗原依赖性复制不同,纯化的DNA聚合酶α-引物酶和δ在复制反应中不能有效地替代组分IIA。因此,乳头瘤病毒DNA复制似乎还需要其他细胞因子。有趣的是,与猿猴病毒40体外系统相比,乳头瘤病毒系统中DNA合成对复制因子C和增殖细胞核抗原的需求更为严格。这些差异表明乳头瘤病毒和猿猴病毒40的DNA复制系统之间一定存在机制上的差异。