Literature DB >> 9393692

Mutational analysis of the R64 oriT region: requirement for precise location of the NikA-binding sequence.

N Furuya1, T Komano.   

Abstract

Conjugative DNA transfer of IncI1 plasmid R64 is initiated by the introduction of a site- and strand-specific nick into the origin of transfer (oriT). In R64 oriT, 17-bp (repeat A and B) and 8-bp inverted-repeat sequences with mismatches are located 8 bp away from the nick site. The nicking is mediated by R64 NikA and NikB proteins. To analyze the functional organization of the R64 oriT region, various deletion, insertion, and substitution mutations were introduced into a 92-bp minimal R64 oriT sequence and their effects on oriT function were investigated. This detailed analysis confirms our previous prediction that the R64 oriT region consists of an oriT core sequence and additional sequences necessary for full oriT activity. The oriT core sequence consists of the repeat A sequence, which is recognized by R64 NikA protein, and the nick region sequence, which is conserved among various origins of transfer and is most probably recognized by NikB protein. The oriT core sequence is sufficient for NikAB-mediated oriT-specific nicking. Furthermore, it was shown that the repeat A sequence is essential for localization to a precise position relative to the nick site for oriT function. This seems to be required for the formation of a functional ternary complex consisting of NikA and NikB proteins and oriT DNA. The repeat B sequence and 8-bp inverted repeat sequences are suggested to be required for the termination of DNA transfer.

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Year:  1997        PMID: 9393692      PMCID: PMC179678          DOI: 10.1128/jb.179.23.7291-7297.1997

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  34 in total

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2.  A 38 base-pair segment of DNA is required in cis for conjugative mobilization of broad host-range plasmid R1162.

Authors:  M A Brasch; R J Meyer
Journal:  J Mol Biol       Date:  1987-12-05       Impact factor: 5.469

3.  High-copy-number and low-copy-number plasmid vectors for lacZ alpha-complementation and chloramphenicol- or kanamycin-resistance selection.

Authors:  S Takeshita; M Sato; M Toba; W Masahashi; T Hashimoto-Gotoh
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Review 4.  Processing of plasmid DNA during bacterial conjugation.

Authors:  N Willetts; B Wilkins
Journal:  Microbiol Rev       Date:  1984-03

5.  Cloning and nucleotide sequence of the oriT region of the IncI1 plasmid R64.

Authors:  T Komano; A Toyoshima; K Morita; T Nisioka
Journal:  J Bacteriol       Date:  1988-09       Impact factor: 3.490

6.  Conjugative transfer of promiscuous IncP plasmids: interaction of plasmid-encoded products with the transfer origin.

Authors:  J P Fürste; W Pansegrau; G Ziegelin; M Kröger; E Lanka
Journal:  Proc Natl Acad Sci U S A       Date:  1989-03       Impact factor: 11.205

7.  In vitro assembly of relaxosomes at the transfer origin of plasmid RP4.

Authors:  W Pansegrau; D Balzer; V Kruft; R Lurz; E Lanka
Journal:  Proc Natl Acad Sci U S A       Date:  1990-09       Impact factor: 11.205

8.  TraJ protein of plasmid RP4 binds to a 19-base pair invert sequence repetition within the transfer origin.

Authors:  G Ziegelin; J P Fürste; E Lanka
Journal:  J Biol Chem       Date:  1989-07-15       Impact factor: 5.157

9.  Nucleotide sequence and characterization of the trbABC region of the IncI1 Plasmid R64: existence of the pnd gene for plasmid maintenance within the transfer region.

Authors:  N Furuya; T Komano
Journal:  J Bacteriol       Date:  1996-03       Impact factor: 3.490

10.  Transfer region of IncI1 plasmid R64 and role of shufflon in R64 transfer.

Authors:  T Komano; N Funayama; S R Kim; T Nisioka
Journal:  J Bacteriol       Date:  1990-05       Impact factor: 3.490

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  8 in total

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2.  Initiation and termination of DNA transfer during conjugation of IncI1 plasmid R64: roles of two sets of inverted repeat sequences within oriT in termination of R64 transfer.

Authors:  N Furuya; T Komano
Journal:  J Bacteriol       Date:  2000-06       Impact factor: 3.490

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Authors:  E Emond; R Lavallée; G Drolet; S Moineau; G LaPointe
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4.  NikAB- or NikB-dependent intracellular recombination between tandemly repeated oriT sequences of plasmid R64 in plasmid or single-stranded phage vectors.

Authors:  Nobuhisa Furuya; Teruya Komano
Journal:  J Bacteriol       Date:  2003-07       Impact factor: 3.490

5.  Characterization of multiple regions involved in replication and mobilization of plasmid pNZ4000 coding for exopolysaccharide production in Lactococcus lactis.

Authors:  R van Kranenburg; W M de Vos
Journal:  J Bacteriol       Date:  1998-10       Impact factor: 3.490

6.  Investigating the basis of substrate recognition in the pC221 relaxosome.

Authors:  Jamie A Caryl; Christopher D Thomas
Journal:  Mol Microbiol       Date:  2006-06       Impact factor: 3.501

7.  Characteristics of the Conjugative Transfer System of the IncM Plasmid pCTX-M3 and Identification of Its Putative Regulators.

Authors:  Michał Dmowski; Marcin Gołębiewski; Izabela Kern-Zdanowicz
Journal:  J Bacteriol       Date:  2018-08-24       Impact factor: 3.490

8.  Plasmid pEC156, a Naturally Occurring Escherichia coli Genetic Element That Carries Genes of the EcoVIII Restriction-Modification System, Is Mobilizable among Enterobacteria.

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Journal:  PLoS One       Date:  2016-02-05       Impact factor: 3.240

  8 in total

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