Literature DB >> 12010495

The effect of genomic position on reversion of a lac frameshift mutation (lacIZ33) during non-lethal selection (adaptive mutation).

E Susan Slechta1, Jennifer Harold, Dan I Andersson, John R Roth.   

Abstract

In a system described by Cairns and Foster, starvation of a particular leaky lac mutant (lacIZ33) in the presence of lactose appears to direct mutation in non-growing cells to sites that allow growth (adaptive mutation). This behaviour requires that the lac operon be located on an F' plasmid. This position effect was investigated by placing the mutant lac operon at many sites in the genome of Salmonella enterica (Typhimurium; LT2) and testing reversion behaviour. Genomic position did not affect reversion during non-selective growth. When lac was at any of 550 chromosomal sites, starvation caused little or no enhancement of reversion. In the 28 strains with the lac on Salmonella's conjugative plasmid (pSLT), selection enhanced reversion strongly, just as seen for strains with lac on an F' plasmid. In 46 strains, the lac operon was inserted within a small chromosomal duplication, and selection stimulated RecA-dependent partial reversion by simple amplification (about 8x) of the mutant lac region. The position of lac on a conjugative plasmid is important to reversion because it allows more frequent gene duplication and amplification. These events are central to growth and reversion under selection because they increase the number of replicating lac alleles within each developing revertant clone.

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Year:  2002        PMID: 12010495     DOI: 10.1046/j.1365-2958.2002.02934.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  16 in total

1.  Evidence that selected amplification of a bacterial lac frameshift allele stimulates Lac(+) reversion (adaptive mutation) with or without general hypermutability.

Authors:  E Susan Slechta; Jing Liu; Dan I Andersson; John R Roth
Journal:  Genetics       Date:  2002-07       Impact factor: 4.562

2.  Adaptive mutation: general mutagenesis is not a programmed response to stress but results from rare coamplification of dinB with lac.

Authors:  E Susan Slechta; Kim L Bunny; Elisabeth Kugelberg; Eric Kofoid; Dan I Andersson; John R Roth
Journal:  Proc Natl Acad Sci U S A       Date:  2003-10-14       Impact factor: 11.205

3.  Adaptive mutation: how growth under selection stimulates Lac(+) reversion by increasing target copy number.

Authors:  John R Roth; Dan I Andersson
Journal:  J Bacteriol       Date:  2004-08       Impact factor: 3.490

4.  Distinct signatures for mutator sensitivity of lacZ reversions and for the spectrum of lacI/lacO forward mutations on the chromosome of nondividing Escherichia coli.

Authors:  Shanti M Bharatan; Manjula Reddy; J Gowrishankar
Journal:  Genetics       Date:  2004-02       Impact factor: 4.562

5.  The amplification model for adaptive mutation: simulations and analysis.

Authors:  Mats E Pettersson; Dan I Andersson; John R Roth; Otto G Berg
Journal:  Genetics       Date:  2004-10-16       Impact factor: 4.562

6.  Amplification of lac cannot account for adaptive mutation to Lac+ in Escherichia coli.

Authors:  Jeffrey D Stumpf; Anthony R Poteete; Patricia L Foster
Journal:  J Bacteriol       Date:  2007-01-05       Impact factor: 3.490

7.  Selection-Enhanced Mutagenesis of lac Genes Is Due to Their Coamplification with dinB Encoding an Error-Prone DNA Polymerase.

Authors:  Itsugo Yamayoshi; Sophie Maisnier-Patin; John R Roth
Journal:  Genetics       Date:  2018-01-04       Impact factor: 4.562

8.  Insights into mutagenesis using Escherichia coli chromosomal lacZ strains that enable detection of a wide spectrum of mutational events.

Authors:  Tracey Seier; Dana R Padgett; Gal Zilberberg; Vincent A Sutera; Noor Toha; Susan T Lovett
Journal:  Genetics       Date:  2011-03-24       Impact factor: 4.562

9.  Roles of YqjH and YqjW, homologs of the Escherichia coli UmuC/DinB or Y superfamily of DNA polymerases, in stationary-phase mutagenesis and UV-induced mutagenesis of Bacillus subtilis.

Authors:  Huang-Mo Sung; Gabriel Yeamans; Christian A Ross; Ronald E Yasbin
Journal:  J Bacteriol       Date:  2003-04       Impact factor: 3.490

10.  Methanol-dependent gene expression demonstrates that methyl-coenzyme M reductase is essential in Methanosarcina acetivorans C2A and allows isolation of mutants with defects in regulation of the methanol utilization pathway.

Authors:  Michael Rother; Paolo Boccazzi; Arpita Bose; Matthew A Pritchett; W W Metcalf
Journal:  J Bacteriol       Date:  2005-08       Impact factor: 3.490

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