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Mutagenesis of the Tra1 core region of RK2 by using Tn5: identification of plasmid-specific transfer genes.

作者信息

Guiney D G, Deiss C, Simnad V, Yee L, Pansegrau W, Lanka E

机构信息

Department of Medicine H811F, UCSD Medical Center, San Diego, California 92103.

出版信息

J Bacteriol. 1989 Jul;171(7):4100-3. doi: 10.1128/jb.171.7.4100-4103.1989.

DOI:10.1128/jb.171.7.4100-4103.1989
PMID:2544570
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC210173/
Abstract

The conjugation system of the IncP alpha plasmid RK2/RP4 is encoded by transfer regions designated Tra1, Tra2, and Tra3. The Tra1 core region, cloned on plasmid pDG4 delta 22, consists of the origin of transfer (oriT) and 2.6 kilobases of flanking DNA providing IncP alpha plasmid-specific functions that allow pDG4 delta 22 to be mobilized by the heterologous IncP beta plasmid R751. Tn5 insertions in pDG4 delta 22 define a minimal 2.2-kilobase region required for plasmid-specific transfer of oriT. The Tra1 core contains the traJ and traK genes as well as an 18-kilodalton open reading frame downstream of traJ. The traJ and traK genes were shown to be required for transfer by complementation of inserts within these genes. Genetic evidence for the role of the 18-kilodalton open reading frame in transfer was obtained, although this protein has not been detected in cell lysates. These studies indicate that at least three transfer proteins are involved in plasmid-specific interactions at oriT.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ed8/210173/720cde22f5fd/jbacter00173-0523-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ed8/210173/720cde22f5fd/jbacter00173-0523-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ed8/210173/720cde22f5fd/jbacter00173-0523-a.jpg

相似文献

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Mutagenesis of the Tra1 core region of RK2 by using Tn5: identification of plasmid-specific transfer genes.
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2
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MobC of conjugative RA3 plasmid from IncU group autoregulates the expression of bicistronic mobC-nic operon and stimulates conjugative transfer.

本文引用的文献

1
Homology in the transfer origins of broad host range IncP plasmids: definition of two subgroups of P plasmids.广泛宿主范围IncP质粒转移起始位点的同源性:P质粒两个亚组的定义。
Mol Gen Genet. 1983;192(3):436-8. doi: 10.1007/BF00392187.
2
Replication of the broad host range plasmid RSF1010: requirement for three plasmid-encoded proteins.广宿主范围质粒RSF1010的复制:对三种质粒编码蛋白的需求。
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3
Location and nucleotide sequence of the transfer origin of the broad host range plasmid RK2.
来自IncU组的接合型RA3质粒的MobC对双顺反子mobC-nic操纵子的表达进行自我调节,并刺激接合转移。
BMC Microbiol. 2014 Sep 4;14:235. doi: 10.1186/s12866-014-0235-1.
4
Plant transformation by coinoculation with a disarmed Agrobacterium tumefaciens strain and an Escherichia coli strain carrying mobilizable transgenes.通过与携带可移动转基因的解除武装的根癌农杆菌菌株和大肠杆菌菌株共接种进行植物转化。
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5
Activity of the Agrobacterium T-DNA transfer machinery is affected by virB gene products.根癌土壤杆菌T-DNA转移机制的活性受virB基因产物的影响。
Proc Natl Acad Sci U S A. 1991 Oct 15;88(20):9350-4. doi: 10.1073/pnas.88.20.9350.
6
The tra region of the nopaline-type Ti plasmid is a chimera with elements related to the transfer systems of RSF1010, RP4, and F.胭脂碱型Ti质粒的tra区域是一个嵌合体,含有与RSF1010、RP4和F的转移系统相关的元件。
J Bacteriol. 1996 Jul;178(14):4233-47. doi: 10.1128/jb.178.14.4233-4247.1996.
7
The mating pair formation system of plasmid RP4 defined by RSF1010 mobilization and donor-specific phage propagation.由RSF1010转移和供体特异性噬菌体繁殖所定义的质粒RP4的配对形成系统。
J Bacteriol. 1993 Oct;175(20):6415-25. doi: 10.1128/jb.175.20.6415-6425.1993.
8
Identification and characterization of RP1 Tra1 cistrons involved in pilus function and plasmid mobilization.参与菌毛功能和质粒转移的RP1 Tra1顺反子的鉴定与表征。
J Bacteriol. 1993 Jan;175(2):448-56. doi: 10.1128/jb.175.2.448-456.1993.
9
Essential motifs of relaxase (TraI) and TraG proteins involved in conjugative transfer of plasmid RP4.参与质粒RP4接合转移的松弛酶(TraI)和TraG蛋白的必需基序。
J Bacteriol. 1994 Jul;176(14):4285-95. doi: 10.1128/jb.176.14.4285-4295.1994.
10
General organization of the conjugal transfer genes of the IncW plasmid R388 and interactions between R388 and IncN and IncP plasmids.IncW 质粒 R388 接合转移基因的总体组织以及 R388 与 IncN 和 IncP 质粒之间的相互作用。
J Bacteriol. 1990 Oct;172(10):5795-802. doi: 10.1128/jb.172.10.5795-5802.1990.
广宿主范围质粒RK2转移起始点的定位及核苷酸序列
Proc Natl Acad Sci U S A. 1983 Jun;80(12):3595-8. doi: 10.1073/pnas.80.12.3595.
4
Plasmid RP4 specifies a deoxyribonucleic acid primase involved in its conjugal transfer and maintenance.质粒RP4编码一种参与其接合转移和维持的脱氧核糖核酸引发酶。
J Bacteriol. 1981 Dec;148(3):769-81. doi: 10.1128/jb.148.3.769-781.1981.
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Processing of plasmid DNA during bacterial conjugation.细菌接合过程中质粒DNA的加工
Microbiol Rev. 1984 Mar;48(1):24-41. doi: 10.1128/mr.48.1.24-41.1984.
6
Conserved regions at the DNA primase locus of IncP alpha and IncP beta plasmids.IncPα和IncPβ质粒DNA引发酶基因座的保守区域。
Plasmid. 1985 Nov;14(3):217-23. doi: 10.1016/0147-619x(85)90005-8.
7
Genetic organization of plasmid R1162 DNA involved in conjugative mobilization.参与接合转移的质粒R1162 DNA的遗传组织。
J Bacteriol. 1986 Aug;167(2):703-10. doi: 10.1128/jb.167.2.703-710.1986.
8
Role and specificity of plasmid RP4-encoded DNA primase in bacterial conjugation.质粒RP4编码的DNA引发酶在细菌接合中的作用与特异性
J Bacteriol. 1986 Jul;167(1):12-7. doi: 10.1128/jb.167.1.12-17.1986.
9
Location of the relaxation complex nick site within the minimal origin of transfer region of RK2.RK2转移区域最小起始点内松弛复合体切口位点的位置。
Plasmid. 1988 Nov;20(3):259-65. doi: 10.1016/0147-619x(88)90032-7.
10
Mobilization of the non-conjugative plasmid RSF1010: a genetic and DNA sequence analysis of the mobilization region.非接合性质粒RSF1010的转移:转移区域的遗传与DNA序列分析
Mol Gen Genet. 1987 Jan;206(1):161-8. doi: 10.1007/BF00326552.