Literature DB >> 21097626

Altered regulation of the OmpF porin by Fis in Escherichia coli during an evolution experiment and between B and K-12 strains.

Estelle Crozat1, Thomas Hindré, Lauriane Kühn, Jérome Garin, Richard E Lenski, Dominique Schneider.   

Abstract

The phenotypic plasticity of global regulatory networks provides bacteria with rapid acclimation to a wide range of environmental conditions, while genetic changes in those networks provide additional flexibility as bacteria evolve across long time scales. We previously identified mutations in the global regulator-encoding gene fis that enhanced organismal fitness during a long-term evolution experiment with Escherichia coli. To gain insight into the effects of these mutations, we produced two-dimensional protein gels with strains carrying different fis alleles, including a beneficial evolved allele and one with an in-frame deletion. We found that Fis controls the expression of the major porin-encoding gene ompF in the E. coli B-derived ancestral strain used in the evolution experiment, a relationship that has not been described before. We further showed that this regulatory connection evolved over two different time scales, perhaps explaining why it was not observed before. On the longer time scale, we showed that this regulation of ompF by Fis is absent from the more widely studied K-12 strain and thus is specific to the B strain. On a shorter time scale, this regulatory linkage was lost during 20,000 generations of experimental evolution of the B strain. Finally, we mapped the Fis binding sites in the ompF regulatory region, and we present a hypothetical model of ompF expression that includes its other known regulators.

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Year:  2010        PMID: 21097626      PMCID: PMC3019833          DOI: 10.1128/JB.01341-10

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


  80 in total

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2.  Transcription regulation of ompF and ompC by a single transcription factor, OmpR.

Authors:  Takeshi Yoshida; Ling Qin; Linda A Egger; Masayori Inouye
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3.  DksA is required for growth phase-dependent regulation, growth rate-dependent control, and stringent control of fis expression in Escherichia coli.

Authors:  Prabhat Mallik; Brian J Paul; Steven T Rutherford; Richard L Gourse; Robert Osuna
Journal:  J Bacteriol       Date:  2006-08       Impact factor: 3.490

4.  Parallel changes in global protein profiles during long-term experimental evolution in Escherichia coli.

Authors:  Ludovic Pelosi; Lauriane Kühn; Dorian Guetta; Jérôme Garin; Johannes Geiselmann; Richard E Lenski; Dominique Schneider
Journal:  Genetics       Date:  2006-05-15       Impact factor: 4.562

5.  Defining the roles of the periplasmic chaperones SurA, Skp, and DegP in Escherichia coli.

Authors:  Joseph G Sklar; Tao Wu; Daniel Kahne; Thomas J Silhavy
Journal:  Genes Dev       Date:  2007-10-01       Impact factor: 11.361

Review 6.  Evolution of global regulatory networks during a long-term experiment with Escherichia coli.

Authors:  Nadège Philippe; Estelle Crozat; Richard E Lenski; Dominique Schneider
Journal:  Bioessays       Date:  2007-09       Impact factor: 4.345

7.  Roles for DNA supercoiling and the Fis protein in modulating expression of virulence genes during intracellular growth of Salmonella enterica serovar Typhimurium.

Authors:  Tadhg O Cróinín; Ronan K Carroll; Arlene Kelly; Charles J Dorman
Journal:  Mol Microbiol       Date:  2006-09-25       Impact factor: 3.501

8.  The small nucleoid protein Fis is involved in Vibrio cholerae quorum sensing.

Authors:  Derrick H Lenz; Bonnie L Bassler
Journal:  Mol Microbiol       Date:  2006-12-20       Impact factor: 3.501

9.  The trans-envelope Tol-Pal complex is part of the cell division machinery and required for proper outer-membrane invagination during cell constriction in E. coli.

Authors:  Matthew A Gerding; Yasuyuki Ogata; Nicole D Pecora; Hironori Niki; Piet A J de Boer
Journal:  Mol Microbiol       Date:  2007-02       Impact factor: 3.501

10.  Effects of Fis on Escherichia coli gene expression during different growth stages.

Authors:  Meranda D Bradley; Michael B Beach; A P Jason de Koning; Timothy S Pratt; Robert Osuna
Journal:  Microbiology       Date:  2007-09       Impact factor: 2.777

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  6 in total

1.  Repeatability and contingency in the evolution of a key innovation in phage lambda.

Authors:  Justin R Meyer; Devin T Dobias; Joshua S Weitz; Jeffrey E Barrick; Ryan T Quick; Richard E Lenski
Journal:  Science       Date:  2012-01-27       Impact factor: 47.728

2.  Intergenic sequence comparison of Escherichia coli isolates reveals lifestyle adaptations but not host specificity.

Authors:  A P White; K A Sibley; C D Sibley; J D Wasmuth; R Schaefer; M G Surette; T A Edge; N F Neumann
Journal:  Appl Environ Microbiol       Date:  2011-09-09       Impact factor: 4.792

3.  The multiplicity of divergence mechanisms in a single evolving population.

Authors:  Ram P Maharjan; Thomas Ferenci; Peter R Reeves; Yang Li; Bin Liu; Lei Wang
Journal:  Genome Biol       Date:  2012-06-08       Impact factor: 13.583

4.  Core Genes Evolve Rapidly in the Long-Term Evolution Experiment with Escherichia coli.

Authors:  Rohan Maddamsetti; Philip J Hatcher; Anna G Green; Barry L Williams; Debora S Marks; Richard E Lenski
Journal:  Genome Biol Evol       Date:  2017-04-01       Impact factor: 3.416

5.  AmpC hyperproduction in a Cedecea davisae implant-associated bone infection during treatment: a case report and therapeutic implications.

Authors:  Julia Notter; Salome N Seiffert; Maria Zimmermann-Kogadeeva; Anja Bösch; Robert Wenger; Carol Strahm; Manuel Frischknecht; David M Livermore; Baharak Babouee Flury
Journal:  BMC Infect Dis       Date:  2022-01-06       Impact factor: 3.090

6.  Synonymous Mutations in rpsT Lead to Ribosomal Assembly Defects That Can Be Compensated by Mutations in fis and rpoA.

Authors:  Anna Knöppel; Dan I Andersson; Joakim Näsvall
Journal:  Front Microbiol       Date:  2020-03-06       Impact factor: 5.640

  6 in total

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