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Mutation Induction by Excess Deoxyribonucleotides in Saccharomyces Cerevisiae

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Genetic Consequences of Nucleotide Pool Imbalance

Part of the book series: Basic Life Sciences ((BLSC,volume 31))

Summary

Excess dTMP is toxic and mutagenic with exponentially growing dTMP efficient uptaking yeast strains 831 rho+ and 833 rho. The respiratory deficient strain 833 exhibits a tenfold sensitivity to the genotoxicity of excess dTMP. Mutant yield in the forward mutation system CAN1canl after dTMP excess is comparable to that found after irradiation with UV254nm. Excess dTMP is a poor mutagen in stationary phase cells of both strains. Mutagenicity of excess dTMP is not found in an ochre mutant allele (ade2-l). Exposure of exponentially growing cells to other deoxyribonucleotides (dCMP, dAMP, and dGMP) reveal these nucleotides to have mutagenic potential as well.

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References

  1. B. J. Barclay and J. G. Little Mutation induction in yeast by deoxythymidine monophosphate: A model, Mol. Gen. Genet., 181: 279–281 (1981).

    Article  CAS  Google Scholar 

  2. M. Brendel and R. H. Haynes, Exogenous thymidine 5′-monophosphate as a precursor for DNA synthesis in yeast, Mol. Gen. Genet., 126: 337–348 (1973).

    Article  PubMed  CAS  Google Scholar 

  3. M. Brendel and U. G. Langjahr, Thymineless death in a strain of Saccharomyces cerevisiaeauxotrophic for deoxythymidine 5′-monophosphate, Mol. Gen. Genet., 131: 351–358 (1974).

    Article  PubMed  CAS  Google Scholar 

  4. M. Brendel, W. W. Fäth, and R. Toper, in: “Radiation and Cellular Control Processes” (J. Kiefer, ed.), pp. 35–40, Springer-Verlag, Berlin-Heidelberg-New York (1976).

    Chapter  Google Scholar 

  5. F. Eckardt and R. H. Haynes, Quantitative measures of mutagenicity and mutability based on mutant yield data, Mutat. Res., 74: 439–558 (1980).

    PubMed  CAS  Google Scholar 

  6. F. Eckardt, B. A. Kunz, and R. H. Haynes, Variation of mutation and recombination frequencies over a range of thymidylate concentrations in a diploid thymidylate auxotroph, Curr. Genet., 7: 399–402 (1983).

    Article  CAS  Google Scholar 

  7. W. W. Fäth, and M. Brendel, Isolation and properties of yeast mutants with highly efficient thymidylate utilization, Z. Naturforsch., 31c:468–478 (1976).

    Google Scholar 

  8. W. W. Fäth, and M. Brendel, Nucleic acid metabolism in yeast. V. Excretion of thymidylate, Mol. Gen. Genet., 188: 115–120 (1982).

    Article  PubMed  Google Scholar 

  9. W. W. Fäth and M. Brendel, Nucleic acid metabolism in yeast. VI. Utilization of exogenous dAMP, Mol. Gen. Genet., 188: 121–127 (1982).

    Article  PubMed  Google Scholar 

  10. W. W. Fäth, M. Brendel, W. Laskowski, and E. Lehmann-Brauns, Economizing DNA-specific labelling by exogenous deoxythymidine 5′-monophosphate in Saccharomyces cerevisiae, Mol. Gen. Genet., 132: 335–345 (1974).

    Article  PubMed  Google Scholar 

  11. E. Gocke and T. R. Manney, Expression of radiation-induced mutations at the arginine permease (CAN1) locus in Saccharomyces cerevisiae, Genetics, 91: 53–66 (1979).

    PubMed  CAS  Google Scholar 

  12. B. A. Kunz, Genetic effects of deoxyribonucleotide pool imbalances, Environmental Mutagenesis, 4: 695–725 (1982).

    Article  PubMed  CAS  Google Scholar 

  13. U. G. Langjahr, E. M. Hartman, and M. Brendel, Nucleic acid metabolism in yeast. I. Inhibition of RNA and DNA biosynthesis by high concentrations of exogenous deoxythymidine 5′-monophosphate in 5′-dTMP low requiring strains, Mol. Gen. Genet., 143: 113–118 (1975).

    Article  PubMed  CAS  Google Scholar 

  14. J. F. Lemontt and S. V. Lair, Plate assay for chemical- and radiation-induced mutagenesis of CAN1in yeast as a function of post-treatment DNA replication: The effect of rad6-1, Mutat. Res., 93: 339–352 (1982).

    Article  CAS  Google Scholar 

  15. R. Toper, W. W. Fäth, and M. Brendel, Nucleic acid metabolism in yeast. II. Metabolism of thymidylate during thymidylate excess death, Mol. Gen. Genet., 182: 60–64 (1981).

    Article  PubMed  CAS  Google Scholar 

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© 1985 Plenum Press, New York

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Brendel, M. (1985). Mutation Induction by Excess Deoxyribonucleotides in Saccharomyces Cerevisiae . In: de Serres, F.J. (eds) Genetic Consequences of Nucleotide Pool Imbalance. Basic Life Sciences, vol 31. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-2449-2_26

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  • DOI: https://doi.org/10.1007/978-1-4613-2449-2_26

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4612-9488-7

  • Online ISBN: 978-1-4613-2449-2

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