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非法重组发生在质粒pC194的复制起点与正在推进的复制叉之间。

Illegitimate recombination occurs between the replication origin of the plasmid pC194 and a progressing replication fork.

作者信息

Michel B, Ehrlich S D

出版信息

EMBO J. 1986 Dec 20;5(13):3691-6. doi: 10.1002/j.1460-2075.1986.tb04701.x.

DOI:10.1002/j.1460-2075.1986.tb04701.x
PMID:3030736
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1167412/
Abstract

Hybrids between plasmids pC194, pBR322 and the bacteriophage f1 undergo deletions in Escherichia coli. The deletions end most often between nucleotides 1445 and 1446 of pC194. That site probably corresponds to a nick in the replication origin of this plasmid. The localization of the other deletion end appears to be determined by the position of the f1 replication fork. Two models accounting for these data are discussed.

摘要

质粒pC194、pBR322与噬菌体f1之间的杂种在大肠杆菌中会发生缺失。缺失大多在pC194的核苷酸1445和1446之间终止。该位点可能对应于该质粒复制起点处的一个切口。另一个缺失末端的定位似乎由f1复制叉的位置决定。文中讨论了两种解释这些数据的模型。

相似文献

1
Illegitimate recombination occurs between the replication origin of the plasmid pC194 and a progressing replication fork.非法重组发生在质粒pC194的复制起点与正在推进的复制叉之间。
EMBO J. 1986 Dec 20;5(13):3691-6. doi: 10.1002/j.1460-2075.1986.tb04701.x.
2
Generation of deletions through a cis-acting mutation in plasmid pC194.
Mol Gen Genet. 1985;198(3):432-6. doi: 10.1007/BF00332935.
3
Rolling circle replication of single-stranded DNA plasmid pC194.单链DNA质粒pC194的滚环复制
EMBO J. 1987 Dec 1;6(12):3863-9. doi: 10.1002/j.1460-2075.1987.tb02724.x.
4
Illegitimate recombination at the replication origin of bacteriophage M13.噬菌体M13复制起点处的非法重组。
Proc Natl Acad Sci U S A. 1986 May;83(10):3386-90. doi: 10.1073/pnas.83.10.3386.
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Illegitimate recombination in Bacillus subtilis: nucleotide sequences at recombinant DNA junctions.枯草芽孢杆菌中的非法重组:重组DNA接头处的核苷酸序列
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Are single-stranded circles intermediates in plasmid DNA replication?单链环状结构是质粒DNA复制的中间体吗?
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Deletion hot spots in chimeric Escherichia coli plasmids.嵌合型大肠杆菌质粒中的缺失热点
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Replication functions of pC194 are necessary for efficient plasmid transduction by M13 phage.pC194的复制功能对于M13噬菌体高效进行质粒转导是必需的。
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The replication termination signal terB of the Escherichia coli chromosome is a deletion hot spot.大肠杆菌染色体的复制终止信号terB是一个缺失热点。
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[Integration of various plasmids into the Bacillus subtilis chromosome].[各种质粒整合到枯草芽孢杆菌染色体中]
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本文引用的文献

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Sealing of gaps in duplex DNA by T4 DNA ligase.利用T4 DNA连接酶封闭双链DNA中的缺口。
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EMBO J. 1984 Jan;3(1):81-6. doi: 10.1002/j.1460-2075.1984.tb01764.x.
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