Skip to main content
Genetics logoLink to Genetics
. 1979 Jan;91(1):53–66. doi: 10.1093/genetics/91.1.53

Expression of Radiation-Induced Mutations at the Arginine Permease (CAN1) Locus in SACCHAROMYCES CEREVISIAE

Elmar Gocke 1, Thomas R Manney 1
PMCID: PMC1213931  PMID: 372046

Abstract

In the yeast Saccharomyces cerevisiae, the expression of resistance to the L-arginine analog, L-canavanine, after mutagenesis, is strongly dependent on the metabolic state of the cell. The frequency of mutations recovered after exposure to ultraviolet light or X rays was measured under a variety of culture conditions. The results indicate that the frequency of mutants recovered is determined by the following three factors: (1) The potential mutants still possess enough permease activity to take up some of the cell poison, and some are therefore killed before they can express the mutant genotype. The sensitivity is strongly influenced by the endogenous free arginine, which is in turn influenced by the growth medium. (2) The rapid decay of the permease molecules and the inability of the potential mutants to resynthesize this protein results in a rapidly increasing chance of expression when selection is delayed. (3) During the time when the permease activity is decaying, repair of the mutagen-induced damage appears to occur.

Full Text

The Full Text of this article is available as a PDF (831.5 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Neuhäuser A., Klingmüller W., Kaudewitz F. Selektion Actidion-resistenter Mutanten bei Neurospora crassa sowie ihre genetische und biochemische Analyse. Mol Gen Genet. 1970;106(2):180–194. doi: 10.1007/BF00323837. [DOI] [PubMed] [Google Scholar]
  2. SRB A. M. Effet antibiotique de la canavanine sur la levure. C R Hebd Seances Acad Sci. 1954 Aug 2;239(5):447–448. [PubMed] [Google Scholar]
  3. Schachtele C. F., Rogers P. Canavanine death in Escherichia coli. J Mol Biol. 1965 Dec;14(2):474–489. doi: 10.1016/s0022-2836(65)80197-8. [DOI] [PubMed] [Google Scholar]

Articles from Genetics are provided here courtesy of Oxford University Press

RESOURCES