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增加质粒重组体频率的遗传元件的分离。

Isolation of genetic elements that increase frequencies of plasmid recombinants.

作者信息

James A A, Morrison P T, Kolodner R

出版信息

Nature. 1983;303(5914):256-9. doi: 10.1038/303256a0.

DOI:10.1038/303256a0
PMID:6341860
Abstract

Some plasmid DNAs, when maintained in wild-type Escherichia coli strains, form high levels of oligomeric species while others remain primarily monomers. One explanation of this observation is that the plasmids that do not form circular oligomers lack a DNA sequence necessary for the formation or maintenance of circular oligomeric species. Here we describe the isolation of segments of DNA from the E. coli genome and other sources that through a recA+ -dependent process: (1) stimulate the conversion of monomeric plasmids to different oligomeric forms, (2) stimulate the conversion of an oligomeric plasmid to a mixture of monomeric and different oligomeric forms, and (3) increase the frequency of recovery of figure-8 molecules. Both cis-acting and trans-acting elements were found. These elements seen to act by stimulating either the frequency of the recombination events that lead to the interconversion of different oligomeric plasmid DNA molecules or some process involved in the maintenance of newly-formed recombinant molecules.

摘要

一些质粒DNA在野生型大肠杆菌菌株中保存时会形成高水平的寡聚体,而其他质粒则主要保持为单体。对这一现象的一种解释是,不形成环状寡聚体的质粒缺乏形成或维持环状寡聚体所需的DNA序列。在此,我们描述了从大肠杆菌基因组和其他来源分离DNA片段的过程,这些片段通过recA+依赖的过程:(1)刺激单体质粒向不同寡聚体形式的转化;(2)刺激寡聚体质粒向单体和不同寡聚体形式混合物的转化;(3)增加8字形分子的回收频率。发现了顺式作用元件和反式作用元件。这些元件似乎通过刺激导致不同寡聚体质粒DNA分子相互转化的重组事件的频率或参与维持新形成的重组分子的某些过程来发挥作用。

相似文献

1
Isolation of genetic elements that increase frequencies of plasmid recombinants.增加质粒重组体频率的遗传元件的分离。
Nature. 1983;303(5914):256-9. doi: 10.1038/303256a0.
2
Genetic recombination of bacterial plasmid DNA. Physical and genetic analysis of the products of plasmid recombination in Escherichia coli.细菌质粒DNA的基因重组。大肠杆菌中质粒重组产物的物理和遗传学分析。
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Enzymatic formation of biparental figure-eight molecules from plasmid DNA and their resolution in E. coli.由质粒DNA酶促形成双亲性8字形分子及其在大肠杆菌中的拆分
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EMBO J. 1988 Dec 20;7(13):4389-95. doi: 10.1002/j.1460-2075.1988.tb03338.x.
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[Thermosensitive vector derived from RP1 plasmid for detection of transposable elements].[用于检测转座元件的源自RP1质粒的热敏载体]
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引用本文的文献

1
recB recJ mutants of Salmonella typhimurium are deficient in transductional recombination, DNA repair and plasmid maintenance.鼠伤寒沙门氏菌的recB recJ突变体在转导重组、DNA修复和质粒维持方面存在缺陷。
Mol Gen Genet. 1996 Mar 20;250(5):570-80. doi: 10.1007/BF02174445.
2
Host RecJ is required for growth of P22 erf bacteriophage.宿主RecJ是P22 erf噬菌体生长所必需的。
J Bacteriol. 1993 Jan;175(1):288-90. doi: 10.1128/jb.175.1.288-290.1993.
3
Recombination between repeated DNA sequences occurs more often in plasmids than in the chromosome of Bacillus subtilis.
重复DNA序列之间的重组在质粒中比在枯草芽孢杆菌的染色体中更频繁发生。
Mol Gen Genet. 1984;197(1):46-54. doi: 10.1007/BF00327921.
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Transformation of Neurospora crassa with recombinant plasmids containing the cloned glutamate dehydrogenase (am) gene: evidence for autonomous replication of the transforming plasmid.用含有克隆的谷氨酸脱氢酶(am)基因的重组质粒转化粗糙脉孢菌:转化质粒自主复制的证据。
Mol Cell Biol. 1984 Oct;4(10):2041-51. doi: 10.1128/mcb.4.10.2041-2051.1984.
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Hyperrecombination at a specific DNA sequence in pneumococcal transformation.肺炎球菌转化中特定DNA序列处的超重组
Proc Natl Acad Sci U S A. 1984 Aug;81(16):5184-8. doi: 10.1073/pnas.81.16.5184.
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Alteration of the gene for xanthine dehydrogenase in Drosophila following treatment with wildtype DNA.用野生型DNA处理后果蝇中黄嘌呤脱氢酶基因的改变。
Mol Gen Genet. 1985;199(1):89-94. doi: 10.1007/BF00327515.
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Folia Microbiol (Praha). 1987;32(3):185-93. doi: 10.1007/BF02881098.
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Mol Cell Biol. 1986 Oct;6(10):3401-9. doi: 10.1128/mcb.6.10.3401-3409.1986.
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