Literature DB >> 2106132

Pseudomonas chromosomal replication origins: a bacterial class distinct from Escherichia coli-type origins.

T W Yee1, D W Smith.   

Abstract

The bacterial origins of DNA replication have been isolated from Pseudomonas aeruginosa and Pseudomonas putida. These origins comprise a second class of bacterial origins distinct from enteric-type origins: both origins function in both Pseudomonas species, and neither functions in Escherichia coli; enteric origins do not function in either pseudomonad. Both cloned sequences hybridize to chromosomal fragments that show properties expected of replication origins. These origin plasmids are highly unstable, are present at low copy number, and show mutual incompatibility properties. DNA sequence analysis shows that both origins contain several 9-base-pair (bp) E. coli DnaA protein binding sites; four of these are conserved in position and orientation, two of which resemble the R1 and R4 sites of the E. coli origin. Conserved 13-bp direct repeats adjacent to the analogous R1 site are also found. No GATC sites are in the P. aeruginosa origin and only four are in the P. putida origin; no other 4-bp sequence is present in high abundance. Both origins are found between sequences similar to the E. coli and Bacillus subtilis dnaA, dnaN, rpmH, and rnpA genes, a gene organization identical to that for B. subtilis and unlike that of E. coli. A second autonomously replicating sequence was obtained from P. aeruginosa that has some properties of bacterial origins.

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Year:  1990        PMID: 2106132      PMCID: PMC53457          DOI: 10.1073/pnas.87.4.1278

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  40 in total

1.  A replication fork barrier at the 3' end of yeast ribosomal RNA genes.

Authors:  B J Brewer; W L Fangman
Journal:  Cell       Date:  1988-11-18       Impact factor: 41.582

2.  The GenBank genetic sequence data bank.

Authors:  H S Bilofsky; C Burks
Journal:  Nucleic Acids Res       Date:  1988-03-11       Impact factor: 16.971

3.  Coordination of chromosome replication initiation in Escherichia coli: effects of different dnaA alleles.

Authors:  K Skarstad; K von Meyenburg; F G Hansen; E Boye
Journal:  J Bacteriol       Date:  1988-02       Impact factor: 3.490

4.  Duplex opening by dnaA protein at novel sequences in initiation of replication at the origin of the E. coli chromosome.

Authors:  D Bramhill; A Kornberg
Journal:  Cell       Date:  1988-03-11       Impact factor: 41.582

5.  The replicative origin of the E. coli chromosome binds to cell membranes only when hemimethylated.

Authors:  G B Ogden; M J Pratt; M Schaechter
Journal:  Cell       Date:  1988-07-01       Impact factor: 41.582

6.  Insertion mutations in the dam gene of Escherichia coli K-12.

Authors:  M G Marinus; M Carraway; A Z Frey; L Brown; J A Arraj
Journal:  Mol Gen Genet       Date:  1983

7.  Methylation of GATC sites is required for precise timing between rounds of DNA replication in Escherichia coli.

Authors:  A Bakker; D W Smith
Journal:  J Bacteriol       Date:  1989-10       Impact factor: 3.490

8.  Chromosomal initiation in Bacillus subtilis may involve two closely linked origins.

Authors:  A Levine; G Henckes; F Vannier; S J Séror
Journal:  Mol Gen Genet       Date:  1987-06

9.  Klebsiella pneumoniae origin of replication (oriC) is not active in Caulobacter crescentus, Pseudomonas putida, and Rhodobacter sphaeroides.

Authors:  E A O'Neill; R A Bender
Journal:  J Bacteriol       Date:  1988-08       Impact factor: 3.490

10.  A rapid single-stranded cloning strategy for producing a sequential series of overlapping clones for use in DNA sequencing: application to sequencing the corn mitochondrial 18 S rDNA.

Authors:  R M Dale; B A McClure; J P Houchins
Journal:  Plasmid       Date:  1985-01       Impact factor: 3.466

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  31 in total

Review 1.  Essential biological processes of an emerging pathogen: DNA replication, transcription, and cell division in Acinetobacter spp.

Authors:  Andrew Robinson; Anthony J Brzoska; Kylie M Turner; Ryan Withers; Elizabeth J Harry; Peter J Lewis; Nicholas E Dixon
Journal:  Microbiol Mol Biol Rev       Date:  2010-06       Impact factor: 11.056

2.  Localization of alg, opr, phn, pho, 4.5S RNA, 6S RNA, tox, trp, and xcp genes, rrn operons, and the chromosomal origin on the physical genome map of Pseudomonas aeruginosa PAO.

Authors:  U Römling; M Duchéne; D W Essar; D Galloway; C Guidi-Rontani; D Hill; A Lazdunski; R V Miller; K H Schleifer; D W Smith
Journal:  J Bacteriol       Date:  1992-01       Impact factor: 3.490

3.  The impact of two-dimensional pulsed-field gel electrophoresis techniques for the consistent and complete mapping of bacterial genomes: refined physical map of Pseudomonas aeruginosa PAO.

Authors:  U Römling; B Tümmler
Journal:  Nucleic Acids Res       Date:  1991-06-25       Impact factor: 16.971

4.  Sequence diversity of Pseudomonas aeruginosa: impact on population structure and genome evolution.

Authors:  C Kiewitz; B Tümmler
Journal:  J Bacteriol       Date:  2000-06       Impact factor: 3.490

5.  Expression and regulation of a dnaA homologue isolated from Pseudomonas putida.

Authors:  H Ingmer; T Atlung
Journal:  Mol Gen Genet       Date:  1992-04

6.  Transformation of Coxiella burnetii to ampicillin resistance.

Authors:  M L Suhan; S Y Chen; H A Thompson
Journal:  J Bacteriol       Date:  1996-05       Impact factor: 3.490

Review 7.  Maintenance of chromosome structure in Pseudomonas aeruginosa.

Authors:  Valentin V Rybenkov
Journal:  FEMS Microbiol Lett       Date:  2014-06-12       Impact factor: 2.742

8.  Mycobacterium smegmatis dnaA region and autonomous replication activity.

Authors:  M Rajagopalan; M H Qin; D R Nash; M V Madiraju
Journal:  J Bacteriol       Date:  1995-11       Impact factor: 3.490

9.  Combined physical and genetic map of the Pseudomonas putida KT2440 chromosome.

Authors:  M A Ramos-Díaz; J L Ramos
Journal:  J Bacteriol       Date:  1998-12       Impact factor: 3.490

10.  Isolation and characterization of a DNA replication origin from the 1,700-kilobase-pair symbiotic megaplasmid pSym-b of Rhizobium meliloti.

Authors:  W Margolin; S R Long
Journal:  J Bacteriol       Date:  1993-10       Impact factor: 3.490

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