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体外猿猴病毒40 DNA复制过程中引物-DNA的形成

Primer-DNA formation during simian virus 40 DNA replication in vitro.

作者信息

Denis D, Bullock P A

机构信息

Department of Biochemistry, Tufts University School of Medicine, Boston, Massachusetts 02111.

出版信息

Mol Cell Biol. 1993 May;13(5):2882-90. doi: 10.1128/mcb.13.5.2882-2890.1993.

DOI:10.1128/mcb.13.5.2882-2890.1993
PMID:8097277
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC359681/
Abstract

Studies of simian virus 40 (SV40) DNA replication in vitro have identified a small (approximately 30-nucleotide) RNA-DNA hybrid species termed primer-DNA. Initial experiments indicated that T antigen and the polymerase alpha-primase complex are required to form primer-DNA. Proliferating cell nuclear antigen, and presumably proliferating cell nuclear antigen-dependent polymerases, is not needed to form this species. Herein, we present an investigation of the stages at which primer-DNA functions during SV40 DNA replication in vitro. Hybridization studies indicate that primer-DNA is initially formed in the origin region and is subsequently synthesized in regions distal to the origin. At all time points, primer-DNA is synthesized from templates for lagging-strand DNA replication. These studies indicate that primer-DNA functions during both initiation and elongation stages of SV40 DNA synthesis. Results of additional experiments suggesting a precursor-product relationship between formation of primer-DNA and Okazaki fragments are presented.

摘要

对猿猴病毒40(SV40)体外DNA复制的研究鉴定出一种小的(约30个核苷酸)RNA-DNA杂交分子,称为引物-DNA。最初的实验表明,T抗原和聚合酶α-引发酶复合物是形成引物-DNA所必需的。增殖细胞核抗原以及推测的依赖增殖细胞核抗原的聚合酶在形成该分子时并非必需。在此,我们对引物-DNA在SV40体外DNA复制过程中发挥作用的阶段进行了研究。杂交研究表明,引物-DNA最初在起始区域形成,随后在起始点远端的区域合成。在所有时间点,引物-DNA都是从滞后链DNA复制的模板合成的。这些研究表明,引物-DNA在SV40 DNA合成的起始和延伸阶段均发挥作用。还展示了其他实验结果,这些结果表明引物-DNA的形成与冈崎片段之间存在前体-产物关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1277/359681/22dc9f27ccda/molcellb00017-0262-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1277/359681/a98904d53cfc/molcellb00017-0258-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1277/359681/d91e280ca1ca/molcellb00017-0258-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1277/359681/4d989889e7c8/molcellb00017-0260-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1277/359681/615f5f509294/molcellb00017-0261-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1277/359681/22dc9f27ccda/molcellb00017-0262-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1277/359681/a98904d53cfc/molcellb00017-0258-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1277/359681/d91e280ca1ca/molcellb00017-0258-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1277/359681/4d989889e7c8/molcellb00017-0260-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1277/359681/615f5f509294/molcellb00017-0261-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1277/359681/22dc9f27ccda/molcellb00017-0262-a.jpg

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1
Primer-DNA formation during simian virus 40 DNA replication in vitro.体外猿猴病毒40 DNA复制过程中引物-DNA的形成
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Species-specific functional interactions of DNA polymerase alpha-primase with simian virus 40 (SV40) T antigen require SV40 origin DNA.DNA聚合酶α-引发酶与猿猴病毒40(SV40)T抗原的物种特异性功能相互作用需要SV40起始DNA。
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DNA polymerase alpha stimulates the ATP-dependent binding of simian virus tumor T antigen to the SV40 origin of replication.DNA聚合酶α刺激猿猴病毒肿瘤T抗原与SV40复制起点的ATP依赖性结合。
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本文引用的文献

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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。
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Interactions between telomerase and primase physically link the telomere and chromosome replication machinery.端粒酶与引发酶之间的相互作用将端粒与染色体复制机制物理连接起来。
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In the simian virus 40 in vitro replication system, start site selection by the polymerase alpha-primase complex is not significantly altered by changes in the concentration of ribonucleotides.在猿猴病毒40体外复制系统中,核糖核苷酸浓度的变化不会显著改变聚合酶α-引发酶复合物对起始位点的选择。
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Processivity of the DNA polymerase alpha-primase complex from calf thymus.来自小牛胸腺的DNA聚合酶α-引发酶复合物的持续合成能力。
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