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宿主DNA复制叉不是噬菌体Mu转座的首选靶点。

Host DNA replication forks are not preferred targets for bacteriophage Mu transposition.

作者信息

Nakai H, Taylor A L

出版信息

J Bacteriol. 1985 Jul;163(1):282-90. doi: 10.1128/jb.163.1.282-290.1985.

DOI:10.1128/jb.163.1.282-290.1985
PMID:3159718
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC219110/
Abstract

Bacteriophage Mu DNA integration in Escherichia coli strains infected after alignment of chromosomal replication was analyzed by a sandwich hybridization assay. The results indicated that Mu integrated into chromosomal segments at various distances from oriC with similar kinetics. In an extension of these studies, various Hfr strains were infected after alignment of chromosomal replication, and Mu transposition was shut down early after infection. The positions of integrated Mu copies were inferred from the transfer kinetics of Mu to an F- strain. Our analysis indicated that the location of Mu DNA in the host chromosome was not dependent on the positions of host replication forks at the time of infection. However, the procedure for aligning chromosomal replication affected DNA transfer by various Hfr strains differently, and this effect could account for prior results suggesting preferential integration of Mu at host replication forks.

摘要

通过夹心杂交分析,研究了在染色体复制对齐后感染的大肠杆菌菌株中噬菌体Mu DNA的整合情况。结果表明,Mu以相似的动力学整合到距离oriC不同距离的染色体片段中。在这些研究的扩展中,在染色体复制对齐后感染了各种Hfr菌株,并在感染后早期关闭了Mu转座。从Mu转移到F-菌株的动力学推断出整合的Mu拷贝的位置。我们的分析表明,宿主染色体中Mu DNA的位置不依赖于感染时宿主复制叉的位置。然而,对齐染色体复制的程序对各种Hfr菌株的DNA转移影响不同,这种影响可以解释先前表明Mu在宿主复制叉处优先整合的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddac/219110/3753b601e910/jbacter00218-0292-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddac/219110/3753b601e910/jbacter00218-0292-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddac/219110/3753b601e910/jbacter00218-0292-a.jpg

相似文献

1
Host DNA replication forks are not preferred targets for bacteriophage Mu transposition.宿主DNA复制叉不是噬菌体Mu转座的首选靶点。
J Bacteriol. 1985 Jul;163(1):282-90. doi: 10.1128/jb.163.1.282-290.1985.
2
Integration of bacteriophage Mu at host chromosomal replication forks during lytic development.在裂解发育过程中噬菌体Mu在宿主染色体复制叉处的整合。
Proc Natl Acad Sci U S A. 1980 May;77(5):2801-5. doi: 10.1073/pnas.77.5.2801.
3
Replication forks of Escherichia coli are not the preferred sites for lysogenic integration of bacteriophage Mu.大肠杆菌的复制叉不是噬菌体Mu溶原整合的首选位点。
J Bacteriol. 1988 Jul;170(7):3089-93. doi: 10.1128/jb.170.7.3089-3093.1988.
4
[Participation of plasmid F in the replication of the chromosome of an Hfr strain of Escherichia coli K-12].[质粒F参与大肠杆菌K - 12 Hfr菌株染色体的复制]
Genetika. 1983 Mar;19(3):416-24.
5
Association of Mu-containing plasmids with the Escherichia coli chromosome upon prophage induction.原噬菌体诱导后含μ质粒与大肠杆菌染色体的关联
Proc Natl Acad Sci U S A. 1980 Apr;77(4):1778-82. doi: 10.1073/pnas.77.4.1778.
6
Genetic study of Mu transposition and Mu-mediated chromosomal rearrangements.Mu转座及Mu介导的染色体重排的遗传学研究。
Cold Spring Harb Symp Quant Biol. 1981;45 Pt 1:355-63. doi: 10.1101/sqb.1981.045.01.049.
7
Fate of plasmids containing Mu DNA: chromosome association and mobilization.含有Mu DNA的质粒的命运:染色体关联与转移
Mol Gen Genet. 1980;180(2):377-83. doi: 10.1007/BF00425851.
8
Transposition without duplication of infecting bacteriophage Mu DNA.感染性噬菌体Mu DNA的转座而无重复。
Nature. 1984;311(5986):580-1. doi: 10.1038/311580a0.
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The influence of host DNA replication on the formation of infectious and transducing Mu-particles.宿主DNA复制对感染性和转导性Mu颗粒形成的影响。
Mol Gen Genet. 1981;184(2):308-11. doi: 10.1007/BF00272922.
10
Mu gem3 as a tool to investigate the influence of chromosome supercoiling on gene expression in Escherichia coli K12.利用Mu gem3作为工具研究染色体超螺旋对大肠杆菌K12基因表达的影响。
FEMS Microbiol Lett. 1990 Jan 1;54(1-3):135-40. doi: 10.1016/0378-1097(90)90271-q.

引用本文的文献

1
Repair of transposable phage Mu DNA insertions begins only when the E. coli replisome collides with the transpososome.只有当大肠杆菌复制体与转座体发生碰撞时,转座噬菌体Mu DNA插入片段的修复才会开始。
Mol Microbiol. 2015 Aug;97(4):746-58. doi: 10.1111/mmi.13061. Epub 2015 Jun 6.
2
The Mu story: how a maverick phage moved the field forward.缪故事:偏锋噬菌体如何推动领域前进
Mob DNA. 2012 Dec 5;3(1):21. doi: 10.1186/1759-8753-3-21.
3
Mu insertions are repaired by the double-strand break repair pathway of Escherichia coli.Mu 插入序列通过大肠杆菌的双链断裂修复途径进行修复。

本文引用的文献

1
BACTERIOPHAGE-INDUCED MUTATION IN ESCHERICHIA COLI.噬菌体诱导的大肠杆菌突变
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Cloning of a phosphate-regulated hemolysin gene (phospholipase C) from Pseudomonas aeruginosa.从铜绿假单胞菌中克隆一个受磷酸盐调节的溶血素基因(磷脂酶C)。
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The influence of host DNA replication on the formation of infectious and transducing Mu-particles.宿主DNA复制对感染性和转导性Mu颗粒形成的影响。
PLoS Genet. 2012;8(4):e1002642. doi: 10.1371/journal.pgen.1002642. Epub 2012 Apr 12.
4
Replication forks of Escherichia coli are not the preferred sites for lysogenic integration of bacteriophage Mu.大肠杆菌的复制叉不是噬菌体Mu溶原整合的首选位点。
J Bacteriol. 1988 Jul;170(7):3089-93. doi: 10.1128/jb.170.7.3089-3093.1988.
Mol Gen Genet. 1981;184(2):308-11. doi: 10.1007/BF00272922.
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Integration of bacteriophage Mu at host chromosomal replication forks during lytic development.在裂解发育过程中噬菌体Mu在宿主染色体复制叉处的整合。
Proc Natl Acad Sci U S A. 1980 May;77(5):2801-5. doi: 10.1073/pnas.77.5.2801.
5
Linkage map of Escherichia coli K-12, edition 7.大肠杆菌K-12连锁图谱,第7版。
Microbiol Rev. 1983 Jun;47(2):180-230. doi: 10.1128/mr.47.2.180-230.1983.
6
Gene-protein index of Escherichia coli K-12.大肠杆菌K-12的基因-蛋白质索引
Microbiol Rev. 1983 Jun;47(2):231-84. doi: 10.1128/mr.47.2.231-284.1983.
7
Instability of transposase activity: evidence from bacteriophage mu DNA replication.转座酶活性的不稳定性:来自噬菌体μ DNA复制的证据。
Cell. 1982 May;29(1):219-25. doi: 10.1016/0092-8674(82)90106-4.
8
Inititation and termination of chromosome replication in Escherichia coli subjected to amino acid starvation.氨基酸饥饿条件下大肠杆菌染色体复制的起始与终止
J Bacteriol. 1980 Apr;142(1):236-42. doi: 10.1128/jb.142.1.236-242.1980.
9
Growth of bacteriophage Mu in Escherichia coli dnaA mutants.噬菌体Mu在大肠杆菌dnaA突变体中的生长
J Virol. 1982 Nov;44(2):555-64. doi: 10.1128/JVI.44.2.555-564.1982.
10
A membrane-filter technique for the detection of complementary DNA.一种用于检测互补DNA的膜过滤技术。
Biochem Biophys Res Commun. 1966 Jun 13;23(5):641-6. doi: 10.1016/0006-291x(66)90447-5.