Literature DB >> 2501784

A set of lacZ mutations in Escherichia coli that allow rapid detection of each of the six base substitutions.

C G Cupples1, J H Miller.   

Abstract

We describe the construction of six strains of Escherichia coli with different mutations at the same coding position in the lacZ gene, which specifies the active site glutamic acid residue at position 461 in beta'-galactosidase. Each strain is Lac- and reverts to Lac+ only by restoring the glutamic acid codon. The strains have been designed so that each reverts via one of the six base substitutions. The set of strains allows detection of each transition and transversion simply by monitoring the Lac- to Lac+ frequency, as demonstrated here with characterized mutagens and mutator alleles. These strains are useful for rapidly determining the mutagenic specificity of mutagens at a single site, for detecting low levels of stimulation of certain base substitutions, for monitoring specific base changes in response to various experimental conditions or strain backgrounds, and for isolating new mutator strains.

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Year:  1989        PMID: 2501784      PMCID: PMC297618          DOI: 10.1073/pnas.86.14.5345

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


  30 in total

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3.  Genetic studies of the lac repressor. VII. On the molecular nature of spontaneous hotspots in the lacI gene of Escherichia coli.

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Authors:  L Prakash; J W Stewart; F Sherman
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5.  The unusual mutagenic specificity of an E. Coli mutator gene.

Authors:  C Yanofsky; E C Cox; V Horn
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6.  Mutagenic specificity of ultraviolet light.

Authors:  J H Miller
Journal:  J Mol Biol       Date:  1985-03-05       Impact factor: 5.469

7.  Analysis of spontaneous base substitutions generated in mismatch-repair-deficient strains of Escherichia coli.

Authors:  P M Leong; H C Hsia; J H Miller
Journal:  J Bacteriol       Date:  1986-10       Impact factor: 3.490

8.  Spectra of spontaneous mutations in Escherichia coli strains defective in mismatch correction: the nature of in vivo DNA replication errors.

Authors:  R M Schaaper; R L Dunn
Journal:  Proc Natl Acad Sci U S A       Date:  1987-09       Impact factor: 11.205

9.  Effects of amino acid substitutions at the active site in Escherichia coli beta-galactosidase.

Authors:  C G Cupples; J H Miller
Journal:  Genetics       Date:  1988-11       Impact factor: 4.562

10.  Classifying mutagens as to their specificity in causing the six possible transitions and transversions: a simple analysis using the Salmonella mutagenicity assay.

Authors:  D E Levin; B N Ames
Journal:  Environ Mutagen       Date:  1986
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  211 in total

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2.  Functional expression of hMYH, a human homolog of the Escherichia coli MutY protein.

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Review 5.  Mechanisms of stationary phase mutation: a decade of adaptive mutation.

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7.  Very-short-patch repair in Escherichia coli requires the dam adenine methylase.

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8.  The miaA mutator phenotype of Escherichia coli K-12 requires recombination functions.

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9.  Requirement for Phe36 for DNA binding and mismatch repair by Escherichia coli MutS protein.

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10.  The Escherichia coli methyl-directed mismatch repair system repairs base pairs containing oxidative lesions.

Authors:  Jennifer Wyrzykowski; Michael R Volkert
Journal:  J Bacteriol       Date:  2003-03       Impact factor: 3.490

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