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1
Mapping of the pin locus coding for a site-specific recombinase that causes flagellar-phase variation in Escherichia coli K-12.编码一种导致大肠杆菌K-12鞭毛相变异的位点特异性重组酶的pin基因座定位。
J Bacteriol. 1983 Nov;156(2):663-8. doi: 10.1128/jb.156.2.663-668.1983.
2
Integration, at hag or elsewhere, of H2 (phase-2 flagellin) genes transduced from Salmonella to Escherichia coli.从沙门氏菌转导至大肠杆菌的H2(第二阶段鞭毛蛋白)基因在哈格或其他地方的整合。
Genetics. 1975 Dec;81(4):595-614. doi: 10.1093/genetics/81.4.595.
3
A gene for DNA invertase and an invertible DNA in Escherichia coli K-12.大肠杆菌K-12中DNA转化酶基因及可反转DNA
Gene. 1985;34(2-3):343-50. doi: 10.1016/0378-1119(85)90143-x.
4
Mapping nonselectable genes of Escherichia coli by using transposon Tn10: location of a gene affecting pyruvate oxidase.利用转座子Tn10对大肠杆菌的非选择基因进行定位:一个影响丙酮酸氧化酶的基因的定位
J Bacteriol. 1982 Sep;151(3):1279-89. doi: 10.1128/jb.151.3.1279-1289.1982.
5
DNA sequence adjacent to flagellar genes and evolution of flagellar-phase variation.鞭毛基因相邻的DNA序列与鞭毛相变异的进化
J Bacteriol. 1983 Jul;155(1):74-81. doi: 10.1128/jb.155.1.74-81.1983.
6
Site-specific recombinase genes in three Shigella subgroups and nucleotide sequences of a pinB gene and an invertible B segment from Shigella boydii.三个志贺氏菌亚群中的位点特异性重组酶基因以及鲍氏志贺氏菌pinB基因和一个可逆B片段的核苷酸序列。
J Bacteriol. 1991 Jul;173(13):4079-87. doi: 10.1128/jb.173.13.4079-4087.1991.
7
[Chromosomal inversion accompanied by an enhancement of uridine phosphorylase gene expression in Escherichia coli K-12].[大肠杆菌K-12中伴随着尿苷磷酸化酶基因表达增强的染色体倒位]
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Interactions between chemotaxis genes and flagellar genes in Escherichia coli.大肠杆菌中趋化性基因与鞭毛基因之间的相互作用。
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Genetic mapping of the minB locus in Escherichia coli K-12.大肠杆菌K-12中minB基因座的遗传图谱
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A Mu gin complementing function and an invertible DNA region in Escherichia coli K-12 are situated on the genetic element e14.在大肠杆菌K-12中,一个Mu Gin互补功能和一个可反转的DNA区域位于遗传元件e14上。
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1
Analysis of the lambdoid prophage element e14 in the E. coli K-12 genome.大肠杆菌K-12基因组中λ样原噬菌体元件e14的分析。
BMC Microbiol. 2004 Jan 20;4:4. doi: 10.1186/1471-2180-4-4.
2
Linkage map of Escherichia coli K-12, edition 10: the traditional map.大肠杆菌K-12连锁图谱,第10版:传统图谱。
Microbiol Mol Biol Rev. 1998 Sep;62(3):814-984. doi: 10.1128/MMBR.62.3.814-984.1998.
3
Cloning and characterization of the region III flagellar operons of the four Shigella subgroups: genetic defects that cause loss of flagella of Shigella boydii and Shigella sonnei.四个志贺氏菌亚群Ⅲ区鞭毛操纵子的克隆与特性分析:导致鲍氏志贺氏菌和宋内氏志贺氏菌鞭毛缺失的遗传缺陷
J Bacteriol. 1997 Jul;179(14):4493-500. doi: 10.1128/jb.179.14.4493-4500.1997.
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J Bacteriol. 1996 Jul;178(13):3722-6. doi: 10.1128/jb.178.13.3722-3726.1996.
5
Nucleotide sequence and regulated expression of the Salmonella fljA gene encoding a repressor of the phase 1 flagellin gene.编码1型鞭毛蛋白基因阻遏物的沙门氏菌fljA基因的核苷酸序列及调控表达
Mol Gen Genet. 1993 Jan;236(2-3):260-6. doi: 10.1007/BF00277121.
6
Conversion of the Salmonella phase 1 flagellin gene fliC to the phase 2 gene fljB on the Escherichia coli K-12 chromosome.沙门氏菌1相鞭毛蛋白基因fliC在大肠杆菌K-12染色体上向2相基因fljB的转变。
J Bacteriol. 1993 Feb;175(3):758-66. doi: 10.1128/jb.175.3.758-766.1993.
7
Phase variation and the Hin protein: in vivo activity measurements, protein overproduction, and purification.相变与Hin蛋白:体内活性测定、蛋白过量表达及纯化
J Bacteriol. 1984 Jul;159(1):71-9. doi: 10.1128/jb.159.1.71-79.1984.
8
Expression of an Escherichia coli flagellin gene, hag48, in the presence of a Salmonella H1-repressor.大肠杆菌鞭毛蛋白基因hag48在沙门氏菌H1阻遏物存在情况下的表达
Mol Gen Genet. 1985;201(1):133-5. doi: 10.1007/BF00397999.
9
The invertible P-DNA segment in the chromosome of Escherichia coli.大肠杆菌染色体中的可逆P-DNA片段。
EMBO J. 1985 Jan;4(1):237-42. doi: 10.1002/j.1460-2075.1985.tb02341.x.
10
A naturally occurring large chromosomal inversion in Escherichia coli K12.大肠杆菌K12中自然发生的大型染色体倒位。
Mol Gen Genet. 1986 Nov;205(2):376-9. doi: 10.1007/BF00430454.

本文引用的文献

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Hfr formation directed by tn10.由 tn10 指导的高频转导形成。
Genetics. 1979 Apr;91(4):639-55. doi: 10.1093/genetics/91.4.639.
2
A Stabilizer of Antigenic Phases in Salmonella Abortus-Equi.马流产沙门氏菌抗原相的稳定剂
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3
Phase Variation in Salmonella.沙门氏菌的相变
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4
A trans-acting factor mediates inversion of a specific DNA segment in flagellar phase variation of Salmonella.一种反式作用因子介导沙门氏菌鞭毛相变中特定DNA片段的倒位。
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5
Inversions of specific DNA segments in flagellar phase variation of Salmonella and inversion systems of bacteriophages P1 and Mu.沙门氏菌鞭毛相变中特定DNA片段的倒位以及噬菌体P1和Mu的倒位系统
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6
Selection for loss of tetracycline resistance by Escherichia coli.大肠杆菌对四环素抗性丧失的选择。
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Linkage map of Escherichia coli K-12, edition 6.大肠杆菌K-12连锁图谱,第6版。
Microbiol Rev. 1980 Mar;44(1):1-56. doi: 10.1128/mr.44.1.1-56.1980.
8
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Genetics. 1980 Feb;94(2):277-90. doi: 10.1093/genetics/94.2.277.
9
Analysis of the nucleotide sequence of an invertible controlling element.对一个可逆控制元件的核苷酸序列的分析。
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10
Phase variation: genetic analysis of switching mutants.相变:转换突变体的遗传分析
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编码一种导致大肠杆菌K-12鞭毛相变异的位点特异性重组酶的pin基因座定位。

Mapping of the pin locus coding for a site-specific recombinase that causes flagellar-phase variation in Escherichia coli K-12.

作者信息

Enomoto M, Oosawa K, Momota H

出版信息

J Bacteriol. 1983 Nov;156(2):663-8. doi: 10.1128/jb.156.2.663-668.1983.

DOI:10.1128/jb.156.2.663-668.1983
PMID:6355064
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC217881/
Abstract

Although the vh2 mutation almost entirely prevents phase variation in Salmonella spp., an Escherichia coli strain that carried the Salmonella H1 and H2 region, including the vh2 mutation, showed phase variation. From this strain, EJ1076, a number of mutants defective in phase variation were isolated, and the symbol pin was assigned to their mutant gene. The pin locus was mapped between purB and trp near purB by interrupted matings using Tn10 sites inserted near pin. The locus was cotransduced with purB by P1 vir at a frequency of around 0.33. All the mutations tested were clustered at this locus. Three E. coli K-12 strains probably derived via different lines from the wild type have been tested for the presence of pin+ by introducing the two Salmonella H regions; two were pin+, and one was a pin mutant.

摘要

尽管vh2突变几乎完全阻止了沙门氏菌属的相变,但携带沙门氏菌H1和H2区域(包括vh2突变)的大肠杆菌菌株却表现出相变。从该菌株EJ1076中分离出了许多相变缺陷型突变体,并将其突变基因命名为pin。通过使用插入在pin附近的Tn10位点进行中断杂交,将pin位点定位在purB和trp之间靠近purB的位置。该位点通过P1噬菌体以约0.33的频率与purB共转导。所有测试的突变都聚集在该位点。通过引入两个沙门氏菌H区域,对可能通过不同品系从野生型衍生而来的三株大肠杆菌K-12菌株进行了pin+存在情况的测试;其中两株为pin+,一株为pin突变体。