Literature DB >> 6392868

UV-mutagenesis at a cloned target sequence: converted suppressor mutation is insensitive to mutation frequency decline regardless of the gene orientation.

J Engstrom, S Larsen, S Rogers, R Bockrath.   

Abstract

Premutational lesions produced by ultraviolet radiation in the Gln2 tRNA genes of E. coli B/r show differing sensitivities to a mutation avoidance phenomenon known as mutation frequency decline (MFD). A mutation event that changes the wild-type gene to an amber (UAG) suppressor is normally sensitive to MFD. Mutation of this amber suppressor to an ochre (UAA) suppressor is not sensitive to MFD. These two mutation events occur in the same anticodon region of the DNA. The dissimilarity of MFD sensitivity between these two mutations may result because the respective premutational photoproducts for the two are located in opposite strands of duplex DNA. To examine the effect of strand position of the premutational lesions on MFD, recombinant lambda phage were constructed that contained the amber suppressor as a mutation target in the two possible orientations. Comparison of MFD in bacterial lysogens containing either of the two types of recombinant prophage indicated that reversing the orientation of the target sequence relative to adjacent bacterial DNA had no effect on MFD. Since rotational inversion of the target sequence did not alter the sensitivity to MFD of mutation occurring at the cloned target gene, the antimutation process inherent to MFD can not be attributed to an asymmetrical interaction between the template strands and the DNA-replication complex.

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Year:  1984        PMID: 6392868     DOI: 10.1016/0167-8817(84)90032-4

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  10 in total

1.  Escherichia coli mfd mutant deficient in "mutation frequency decline" lacks strand-specific repair: in vitro complementation with purified coupling factor.

Authors:  C P Selby; E M Witkin; A Sancar
Journal:  Proc Natl Acad Sci U S A       Date:  1991-12-15       Impact factor: 11.205

2.  An in vivo complex with DNA photolyase blocks UV mutagenesis targeted at a thymine-cytosine dimer in Escherichia coli.

Authors:  M Ruiz-Rubio; K Yamamoto; R Bockrath
Journal:  J Bacteriol       Date:  1988-11       Impact factor: 3.490

3.  Anti-mutagenic effect of ultraviolet light on spontaneous tyrosine tRNA ochre suppressor mutations in Escherichia coli.

Authors:  R Bockrath; M Ruiz-Rubio
Journal:  Mol Gen Genet       Date:  1988-10

4.  Ultraviolet photoproducts at the ochre suppressor mutation site in the glnU gene of Escherichia coli: relevance to "mutation frequency decline".

Authors:  N Garvey; E M Witkin; D E Brash
Journal:  Mol Gen Genet       Date:  1989-11

Review 5.  Transcription-repair coupling and mutation frequency decline.

Authors:  C P Selby; A Sancar
Journal:  J Bacteriol       Date:  1993-12       Impact factor: 3.490

6.  Mutation frequency decline in Escherichia coli. II. Kinetics support the involvement of transcription-coupled excision repair.

Authors:  R Bockrath; B H Li
Journal:  Mol Gen Genet       Date:  1995-12-20

7.  Mutation frequency decline in Escherichia coli. I. Effects of defects in mismatch repair.

Authors:  B H Li; R Bockrath
Journal:  Mol Gen Genet       Date:  1995-12-20

Review 8.  Mechanisms of transcription-repair coupling and mutation frequency decline.

Authors:  C P Selby; A Sancar
Journal:  Microbiol Rev       Date:  1994-09

9.  Mutation probe of gene structure in E. coli: suppressor mutations in the seven-tRNA operon.

Authors:  R Bockrath; P Mosbaugh
Journal:  Mol Gen Genet       Date:  1986-09

10.  Thermal resistance of UV-mutagenesis to photoreactivation in E. coli B/r uvrA ung: estimate of activation energy and further analysis.

Authors:  D F Fix
Journal:  Mol Gen Genet       Date:  1986-09
  10 in total

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