Literature DB >> 775287

The effect of dose and time on the induction of genetic alterations in Saccharomyces cerevisiae by aminoacridines in the presence and absence of visible light irradiation in comparison with the dose-effect-curves of mutagens with other type of action.

R Fahrig.   

Abstract

Aminoacridines induce frameshift mutations and are photodynamically active, depending on whether visible light is absent or present. Therefore, a test system which allows to compare quantitatively the genetic effects of aminoacridines irradiated or unirradiated by visible light ought to be susceptible to the different DNA alterations which can be induced by these substances. For this reason in most experiments mitotic gene conversion and only in some selected experiments reverse mutation was chosen as the indicator of genetic activity. In contrast to mutation systems mitotic gene conversion has never shown a response specific to only some types of mutagens. The three aminoacridine derivatives used-acridine orange (AO), proflavine (PF), and acridine yellow (AY)-were successful in the induction of convertants at two different loci. No locus-specificity could be observed. The time-dependent induction of convertants proceeds quickly but soon reaches-especially after treatment without light-a saturation point. The dose/effect-curve after treatment in the dark has a slope increasing with increasing concentration. Irradiation with visible light results in a dose/effect-curve consisting of three parts. Af first the increase of convertants is nearly linear extending one (AY) to three (AO) orders of magnitude. After a saturation effect begins at the point at which an effectiveness of the acridines in the dark is apparent. At high concentrations an induction of convertants can again be observed which is nearly the same as that after treatment in the dark. To determine whether the dose/effect-curves obtained for gene conversion refer to similar curves for gene mutations after treatment with AO at the same locus not only gene conversions but also reverse mutations were scored for. AO-treatment in the dark is ineffective in inducing reverse mutations. Irradiation with visible light results in a dose/effect-curve beeing parallel only in its first part to the dose/effect-curve obtained for gene conversion, while in its second part a mutation frequency decline can be observed. Comparing the dose/effect-curves of AO resulting from the induction of gene conversion and gene mutation, and taking into account that no mutants can be induced by AO-treatment in the dark, the increase in convertants at high acridine-concentrations can be explained as an addition of light-dependent and light-independent effects. That means, in mutation systems at low concentrations of aminoacridines irradiation with visible light should cause transitions, transversions and microlesions, at intermediate concentrations frameshift lesions should begin to appear, and at very high concentrations nearly exclusively frameshift lesions should occur. The dose/effect-curves of aminoacridines compared with those of other mutagens are very complex. The dose/effect-curves of the mutagens of other type of action tested are linear in a double logarithmic scale, and parallel for induced gene conversion and induced gene mutation...

Entities:  

Mesh:

Substances:

Year:  1976        PMID: 775287     DOI: 10.1007/bf02428101

Source DB:  PubMed          Journal:  Mol Gen Genet        ISSN: 0026-8925


  35 in total

1.  THE EFFECT OF ACRIFLAVINE ON PHOTOREVERSAL OF LETHAL AND MUTAGENIC DAMAGE PRODUCED IN BACTERIA BY ULTRAVIOLET LIGHT.

Authors:  E M WITKIN
Journal:  Proc Natl Acad Sci U S A       Date:  1963-09       Impact factor: 11.205

2.  PHOTODYNAMIC DEGRADATION OF GUANINE.

Authors:  J S SUSSENBACH; W BERENDS
Journal:  Biochim Biophys Acta       Date:  1965-01-11

3.  THE ANALYSIS OF GENETIC RECOMBINATION ON THE POLARON HYBRID DNA MODEL.

Authors:  H L WHITEHOUSE; P J HASTINGS
Journal:  Genet Res       Date:  1965-02       Impact factor: 1.588

4.  The structure of the DNA-acridine complex.

Authors:  L S LERMAN
Journal:  Proc Natl Acad Sci U S A       Date:  1963-01-15       Impact factor: 11.205

5.  Damage by visible light to the acridine orange--DNA complex.

Authors:  D FREIFELDER; P F DAVISON; E P GEIDUSCHEK
Journal:  Biophys J       Date:  1961-05       Impact factor: 4.033

6.  [Effect of ultraviolet light on genetic recombination among alleles in yeast].

Authors:  H ROMAN; F JACOB
Journal:  C R Hebd Seances Acad Sci       Date:  1957-09-16

7.  Studies on the induction of mutations in poliovirus by proflavin.

Authors:  R DULBECCO; M VOGT
Journal:  Virology       Date:  1958-04       Impact factor: 3.616

8.  Mutagenesis by acridine orange and proflavine in Escherichia coli strain S.

Authors:  A Zampieri; J Greenberg
Journal:  Mutat Res       Date:  1965-12       Impact factor: 2.433

9.  Genotypic reversion by methylene blue: the orientation of guanine-hydroxymethylcytosine at mutated sites in rII mutants of phage T4.

Authors:  N A Barricelli; G Del Zoppo
Journal:  Mol Gen Genet       Date:  1968

10.  ALLELIC MAPPING IN YEAST BY X-RAY-INDUCED MITOTIC REVERSION.

Authors:  T R MANNEY; R K MORTIMER
Journal:  Science       Date:  1964-02-07       Impact factor: 47.728

View more
  7 in total

Review 1.  Dietary carcinogens, environmental pollution, and cancer: some misconceptions.

Authors:  B N Ames; L S Gold
Journal:  Med Oncol Tumor Pharmacother       Date:  1990

2.  Chemical carcinogenesis: too many rodent carcinogens.

Authors:  B N Ames; L S Gold
Journal:  Proc Natl Acad Sci U S A       Date:  1990-10       Impact factor: 11.205

3.  Evidence that induction and suppression of mutations and recombinations by chemical mutagens in S. cerevisiae during mitosis are jointly correlated.

Authors:  R Fahrig
Journal:  Mol Gen Genet       Date:  1979-01-10

4.  Genetic mode of action of cocarcinogens and tumor promoters in yeast and mice.

Authors:  R Fahrig
Journal:  Mol Gen Genet       Date:  1984

5.  Enhancement of carcinogen-induced mutations or recombinations by 12-O-tetradecanoyl-phorbol-13-acetate in the mammalian spot test.

Authors:  R Fahrig
Journal:  J Cancer Res Clin Oncol       Date:  1987       Impact factor: 4.553

Review 6.  DNA lesions, inducible DNA repair, and cell division: three key factors in mutagenesis and carcinogenesis.

Authors:  B N Ames; M K Shigenaga; L S Gold
Journal:  Environ Health Perspect       Date:  1993-12       Impact factor: 9.031

7.  Genetic effects of dioxins in the spot test with mice.

Authors:  R Fahrig
Journal:  Environ Health Perspect       Date:  1993-10       Impact factor: 9.031

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.