Literature DB >> 17600062

Secondary structures as predictors of mutation potential in the lacZ gene of Escherichia coli.

Evan Burkala1, Jacqueline M Reimers2, Karen H Schmidt1, Nick Davis1, Ping Wei3, Barbara E Wright1.   

Abstract

Four independent nonsense mutations were engineered into the Escherichia coli chromosomal lacZ gene, and reversion rates back to LacZ(+) phenotypes were determined. The mutation potential of bases within putative DNA secondary structures formed during transcription was predicted by a sliding-window analysis that simulates successive folding of the ssDNA creating these structures. The relative base mutabilities predicted by the mfg computer program correlated with experimentally determined reversion rates in three of the four mutants analysed. The nucleotide changes in revertants at one nonsense codon site consisted of a triple mutation, presumed to occur by a templated repair mechanism. Additionally, the effect of supercoiling on mutation was investigated and, in general, reversion rates increased with higher levels of negative supercoiling. Evidence indicates that predicted secondary structures are in fact formed in vivo and that directed mutation in response to starvation stress is dependent upon the exposure of particular bases, the stability of the structures in which these bases are unpaired and the level of DNA supercoiling within the cell.

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Year:  2007        PMID: 17600062     DOI: 10.1099/mic.0.2007/005470-0

Source DB:  PubMed          Journal:  Microbiology        ISSN: 1350-0872            Impact factor:   2.777


  8 in total

1.  Limits and patterns of cytomegalovirus genomic diversity in humans.

Authors:  Nicholas Renzette; Cornelia Pokalyuk; Laura Gibson; Bornali Bhattacharjee; Mark R Schleiss; Klaus Hamprecht; Aparecida Y Yamamoto; Marisa M Mussi-Pinhata; William J Britt; Jeffrey D Jensen; Timothy F Kowalik
Journal:  Proc Natl Acad Sci U S A       Date:  2015-07-06       Impact factor: 11.205

2.  Functional and metabolic effects of adaptive glycerol kinase (GLPK) mutants in Escherichia coli.

Authors:  M Kenyon Applebee; Andrew R Joyce; Tom M Conrad; Donald W Pettigrew; Bernhard Ø Palsson
Journal:  J Biol Chem       Date:  2011-05-06       Impact factor: 5.157

3.  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

4.  Evolution of coordinated mutagenesis and somatic hypermutation in VH5.

Authors:  Barbara E Wright; Karen H Schmidt; Aaron T Hunt; Dennis K Reschke; Michael F Minnick
Journal:  Mol Immunol       Date:  2011-11-05       Impact factor: 4.407

5.  Stabilised DNA secondary structures with increasing transcription localise hypermutable bases for somatic hypermutation in IGHV3-23.

Authors:  Bhargavi Duvvuri; Venkata R Duvvuri; Jianhong Wu; Gillian E Wu
Journal:  Immunogenetics       Date:  2012-03-06       Impact factor: 2.846

6.  The roles of transcription and genotoxins underlying p53 mutagenesis in vivo.

Authors:  Barbara E Wright; Karen H Schmidt; Aaron T Hunt; J Stephen Lodmell; Michael F Minnick; Dennis K Reschke
Journal:  Carcinogenesis       Date:  2011-07-29       Impact factor: 4.944

7.  Transcription-associated mutagenesis increases protein sequence diversity more effectively than does random mutagenesis in Escherichia coli.

Authors:  Hyunchul Kim; Baek-Seok Lee; Masaru Tomita; Akio Kanai
Journal:  PLoS One       Date:  2010-05-10       Impact factor: 3.240

Review 8.  Transcription-associated mutagenesis.

Authors:  Sue Jinks-Robertson; Ashok S Bhagwat
Journal:  Annu Rev Genet       Date:  2014-09-10       Impact factor: 13.826

  8 in total

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