Literature DB >> 2041784

Site-specific mutagenesis in cells with normal DNA repair systems: transitions produced from DNA carrying a single O6-alkylguanine.

R W Chambers1.   

Abstract

This paper describes a systematic study of transition frequencies produced in vivo when a homologous series of O6-alkylguanine residues located at a preselected position in gene G of phi X174 form I' DNA (double-stranded, circular, covalently-closed, relaxed) is transfected into spheroplasts from two strains of Escherichia coli having normal DNA repair systems. Mutant frequencies were measured as percent of total phage produced by single bursts. The results are: (A) Synthetic DNA without any alkyl group gave a transition frequency of 0.02%. (B) In E. coli AB1157, the frequencies fall into two groups depending on the alkyl group: methyl and ethyl, 8-11%; n-propyl and n-butyl approximately 0.9%. (C) The average transition frequencies were higher in AB1157 than in C600. These data demonstrate that a single O6-alkylguanine residue can produce a specific transition at significant frequencies in cells with normal repair systems and that the mutant frequency depends upon the nature of the alkyl group and the cell type.

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Year:  1991        PMID: 2041784      PMCID: PMC329461          DOI: 10.1093/nar/19.9.2485

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  14 in total

1.  Observations on the infection of bacterial protoplasts with the deoxyribonucleic acid of bacteriophage phi X174.

Authors:  G D GUTHRIE; R L SINSHEIMER
Journal:  Biochim Biophys Acta       Date:  1963-06-25

2.  Repair of O6-methylguanine in adapted Escherichia coli.

Authors:  P F Schendel; P E Robins
Journal:  Proc Natl Acad Sci U S A       Date:  1978-12       Impact factor: 11.205

3.  Storage of spheroplasts at -70 degrees C for transfection with phi X174 RF DNA.

Authors:  H V Malling; M C Fater; J G Burkhart; S C Hardies; C A Hutchison; M H Edgell
Journal:  Gene Anal Tech       Date:  1987 Mar-Apr

4.  Lysis inhibition of phi-X174-, M12-, and Q-beta-infected Escherichia coli bacteria by magnesium ions.

Authors:  H H Gschwender; P H Hofschneider
Journal:  Biochim Biophys Acta       Date:  1969-10-22

5.  Site-specific mutagenesis in vivo by single methylated or deaminated purine bases.

Authors:  M Hill-Perkins; M D Jones; P Karran
Journal:  Mutat Res       Date:  1986-09       Impact factor: 2.433

6.  On the nature of suppression by Escherichia coli HF4714.

Authors:  R W Chambers
Journal:  Mutat Res       Date:  1989-01       Impact factor: 2.433

7.  A study of side reactions occurring during synthesis of oligodeoxynucleotides containing O6-alkyldeoxyguanosine residues at preselected sites.

Authors:  H Borowy-Borowski; R W Chambers
Journal:  Biochemistry       Date:  1987-05-05       Impact factor: 3.162

8.  uvrA and recA mutations inhibit a site-specific transition produced by a single O6-methylguanine in gene G of bacteriophage phi X174.

Authors:  R W Chambers; E Sledziewska-Gojska; S Hirani-Hojatti; H Borowy-Borowski
Journal:  Proc Natl Acad Sci U S A       Date:  1985-11       Impact factor: 11.205

9.  In vivo effect of DNA repair on the transition frequency produced from a single O6-methyl- or O6-n-butyl-guanine in a T:G base pair.

Authors:  R W Chambers; E Sledziewska-Gojska; S Hirani-Hojatti
Journal:  Mol Gen Genet       Date:  1988-08

10.  The in vivo mutagenic frequency and specificity of O6-methylguanine in phi X174 replicative form DNA.

Authors:  O S Bhanot; A Ray
Journal:  Proc Natl Acad Sci U S A       Date:  1986-10       Impact factor: 11.205

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  2 in total

Review 1.  Chemical biology of mutagenesis and DNA repair: cellular responses to DNA alkylation.

Authors:  Nidhi Shrivastav; Deyu Li; John M Essigmann
Journal:  Carcinogenesis       Date:  2009-10-29       Impact factor: 4.944

2.  Site-specific mutagenesis induced by single O6-alkylguanines (O6-n-propyl, O6-n-butyl, O6-n-octyl) in vivo.

Authors:  P M Baumgart; H C Kliem; J Gottfried-Anacker; M Wiessler; H H Schmeiser
Journal:  Nucleic Acids Res       Date:  1993-08-11       Impact factor: 16.971

  2 in total

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