Literature DB >> 8807313

Doing the conjugative two-step: evidence of recipient autonomy in retrotransfer.

J A Heinemann1, H E Scott, M Williams.   

Abstract

Bidirectional exchange of genetic information, called retrotransfer, during bouts of bacterial conjugation has drawn the interest of those concerned with the risk of releasing genetically engineered microbes, the fluidity of genes among species, and the mechanism of DNA transport between cells. The phenomenon has generated two models in explanation, both of which yield highly testable predictions. The first model, called the one-step, predicts that the flow of genes from recipient bacteria to donor bacteria is mechanistically distinct from, but dependent on, conjugation between donors and recipients. The second model, called the two-step, predicts that the same genetic requirements and mechanistic constraints apply to the process of gene flow from recipients to donors as for gene flow from donors to recipients. The requirement for expression of at least 10 plasmid-encoded genes in recipients, sensitivity of the reverse flow (recipient to donor) to restriction of DNA transferring from the donor, and the requirement of an additional 30-90 min for DNA to flow from recipients back to donors are predictions of the two-step model and directly refute the one-step model. Retrotransfer of genes to donors during conjugation remains genetically and physically indistinguishable from two successive rounds of conjugation between neighbors.

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Year:  1996        PMID: 8807313      PMCID: PMC1207410     

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  24 in total

1.  Recombination in Bact. coli K 12; unidirectional transfer of genetic material.

Authors:  W HAYES
Journal:  Nature       Date:  1952-01-19       Impact factor: 49.962

2.  Protein transfer into the recipient cell during bacterial conjugation: studies with F and RP4.

Authors:  C E Rees; B M Wilkins
Journal:  Mol Microbiol       Date:  1990-07       Impact factor: 3.501

3.  An upper limit on beta-galactosidase transfer in bacterial conjugation.

Authors:  J L Rosner; E A Adelberg; M B Yarmolinsky
Journal:  J Bacteriol       Date:  1967-11       Impact factor: 3.490

4.  A complementation analysis of the restriction and modification of DNA in Escherichia coli.

Authors:  H W Boyer; D Roulland-Dussoix
Journal:  J Mol Biol       Date:  1969-05-14       Impact factor: 5.469

5.  Redundant transfer of F' plasmids occurs between Escherichia coli cells during nonlethal selections.

Authors:  J E Peters; S A Benson
Journal:  J Bacteriol       Date:  1995-02       Impact factor: 3.490

6.  On the nature of the polymerase responsible for the transcription of released bacterial DNA in plant cells.

Authors:  M Stroun
Journal:  Biochem Biophys Res Commun       Date:  1971-08-06       Impact factor: 3.575

7.  Bacterial conjugative plasmids mobilize DNA transfer between bacteria and yeast.

Authors:  J A Heinemann; G F Sprague
Journal:  Nature       Date:  1989-07-20       Impact factor: 49.962

8.  Chromosomal gene capture mediated by the Pseudomonas putida TOL catabolic plasmid.

Authors:  M I Ramos-González; M A Ramos-Díaz; J L Ramos
Journal:  J Bacteriol       Date:  1994-08       Impact factor: 3.490

9.  Host-specific effects of the korA-korB operon and oriT region on the maintenance of miniplasmid derivatives of broad host-range plasmid RK2.

Authors:  T J Schmidhauser; D H Bechhofer; D H Figurski; D R Helinski
Journal:  Plasmid       Date:  1989-03       Impact factor: 3.466

10.  Mechanism of retrotransfer in conjugation: prior transfer of the conjugative plasmid is required.

Authors:  E A Sia; D M Kuehner; D H Figurski
Journal:  J Bacteriol       Date:  1996-03       Impact factor: 3.490

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  8 in total

1.  Postsegregational killing does not increase plasmid stability but acts to mediate the exclusion of competing plasmids.

Authors:  T F Cooper; J A Heinemann
Journal:  Proc Natl Acad Sci U S A       Date:  2000-11-07       Impact factor: 11.205

2.  Within-host competition selects for plasmid-encoded toxin-antitoxin systems.

Authors:  Tim F Cooper; Tiago Paixão; Jack A Heinemann
Journal:  Proc Biol Sci       Date:  2010-05-26       Impact factor: 5.349

3.  Selection for plasmid post-segregational killing depends on multiple infection: evidence for the selection of more virulent parasites through parasite-level competition.

Authors:  T F Cooper; J A Heinemann
Journal:  Proc Biol Sci       Date:  2005-02-22       Impact factor: 5.349

4.  Gene transfer between Salmonella enterica serovar Typhimurium inside epithelial cells.

Authors:  Gayle C Ferguson; Jack A Heinemann; Martin A Kennedy
Journal:  J Bacteriol       Date:  2002-04       Impact factor: 3.490

5.  Molecular evolution of the Escherichia coli chromosome. V. Recombination patterns among strains of diverse origin.

Authors:  R Milkman; E A Raleigh; M McKane; D Cryderman; P Bilodeau; K McWeeny
Journal:  Genetics       Date:  1999-10       Impact factor: 4.562

6.  Plasmid capture by the Bacillus thuringiensis conjugative plasmid pXO16.

Authors:  Sophie Timmery; Pauline Modrie; Olivier Minet; Jacques Mahillon
Journal:  J Bacteriol       Date:  2009-01-30       Impact factor: 3.490

7.  Recombination speeds adaptation by reducing competition between beneficial mutations in populations of Escherichia coli.

Authors:  Tim F Cooper
Journal:  PLoS Biol       Date:  2007-09       Impact factor: 8.029

8.  Agrichemicals and antibiotics in combination increase antibiotic resistance evolution.

Authors:  Brigitta Kurenbach; Amy M Hill; William Godsoe; Sophie van Hamelsveld; Jack A Heinemann
Journal:  PeerJ       Date:  2018-10-12       Impact factor: 2.984

  8 in total

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