Effect of Gene Induction on the Rate of Mutagenesis by ICR-191 in Escherichia coli

Author:

Herman Robert K.1,Dworkin Nomi B.1

Affiliation:

1. Department of Genetics and Cell Biólogy, University of Minnesota, St. Paul, Minnesota 55101

Abstract

ICR-191, an acridine half-mustard known to cause frameshift mutations in bacteria, was used to induce Lac mutations revertible by ICR-191. The reversion rates of several of these mutations were stimulated approximately twofold by the presence of lac inducer. The stimulatory effect of inducer was attributable to gene induction rather than some other effect of inducer, since inducer did not stimulate reversion in a regulator constitutive strain. The stimulatory effect was not observed unless the gene to be reverted was induced during the period of exposure to ICR-191. The presence of a strong polar (nonsense) mutation on the operator side of a frameshift mutation abolished the stimulatory effect of inducer on reversion of the frameshift mutation by ICR-191. (As expected, a nonpolar mutation on the operator side of the frameshift mutation did not affect inducer-stimulated reversion.) It was concluded that some aspect of transcription or translation, or both, in the neighborhood of the ICR-191-induced mutation stimulated reversion by ICR-191. A recA mutation had no effect on reversion by ICR-191 in the presence or absence of inducer. In one mutant, gene induction depressed reversion by ICR-191 about sevenfold. The difference between this exceptional strain and other mutants was not attributable to different genetic backgrounds but seemed to be an inherent difference in the original Lac mutations.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

Reference21 articles.

1. Sequential transcription of the genes of the lactose operon and its regulation by protein synthesis;Alpers D. H.;J. Biol. Chem.,1966

2. Frameshift mutagenesis in Salmonella;Ames B. N.;Cold Spring Harbor Symp. Quant. Biol.,1966

3. Spontaneous and ICR-191-A-induced frameshift mutations in the A gene of Escherichia coli tryptophan synthetase;Berger H.;J. Bacteriol.,1968

4. General nature of the genetic code for proteins;Crick F. H. C.;Nature (London),1961

5. Drake J. W. 1970. The molecular basis of mutation. Holden-Day. San Francisco.

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