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. 1980 Jul;95(3):611–630. doi: 10.1093/genetics/95.3.611

Ultraviolet Mutagenesis Studies of [psi], a Cytoplasmic Determinant of SACCHAROMYCES CEREVISIAE

M F Tuite 1, B S Cox 1
PMCID: PMC1214250  PMID: 7002721

Abstract

UV mutagenesis was used to probe the molecular nature of [psi], a non-mitochondrial cytoplasmic determinant of Saccharomyces cerevisiae involved in the control of nonsense suppression. The UV-induced mutation from [psi+] to [psi-] showed characteristics of forward nuclear gene mutation in terms of frequency, induction kinetics, occurrence of whole and sectored mutant clones and the effect of the stage in the growth cycle on mutation frequency. The involvement of pyrimidine dimers in the premutational lesion giving the [psi-] mutation was demonstrated by photoreactivation. UV-induced damage to the [psi] genetic determinant was shown to be repaired by nuclear-coded repair enzymes that are responsible for the repair of nuclear DNA damage. UV-induced damage to mitochondrial DNA appeared to be, at least partly, under the control of different repair processes. The evidence obtained suggests that the [psi] determinant is DNA.

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Selected References

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

  1. Cox B. S. A recessive lethal super-suppressor mutation in yeast and other psi phenomena. Heredity (Edinb) 1971 Apr;26(2):211–232. doi: 10.1038/hdy.1971.28. [DOI] [PubMed] [Google Scholar]
  2. Cox B. S., Tuite M. F., Mundy C. J. Reversion from suppression to nonsuppression in SUQ5 [psi+] strains of yeast: the classificaion of mutations. Genetics. 1980 Jul;95(3):589–609. doi: 10.1093/genetics/95.3.589. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Hurter J., Gordon M. P., Kirwan J. P., McLaren A. D. In vitro photoreactivation of ultraviolet-inactivated ribonucleic acid from tobacco mosaic virus. Photochem Photobiol. 1974 Mar;19(3):185–190. doi: 10.1111/j.1751-1097.1974.tb06497.x. [DOI] [PubMed] [Google Scholar]
  4. Jackle H., Kalthoff K. Photoreactivation of RNA in UV-irradiated insect eggs (Smittia sp., Chironomidae, Diptera) I. Photosensitized production and light-dependent disappearance of pyrimidine dimers. Photochem Photobiol. 1978 Mar;27(3):309–315. doi: 10.1111/j.1751-1097.1978.tb07605.x. [DOI] [PubMed] [Google Scholar]
  5. James A. P., Kilbey B. J., Prefontaine G. J. The timing of UV mutagenesis in yeast: continuing mutation in an excision-defective (rad1-1) strain. Mol Gen Genet. 1978 Oct 4;165(2):207–212. doi: 10.1007/BF00269908. [DOI] [PubMed] [Google Scholar]
  6. James A. P., Kilbey B. J. The timing of UV mutagenesis in yeast: a pedigree analysis of induced recessive mutation. Genetics. 1977 Oct;87(2):237–248. doi: 10.1093/genetics/87.2.237. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Lachowicz T. M., Kotylak Z., Kolodyński J., Sniegocka Z. New types of respiratory deficient mutants in Saccharomyces cerevisiae. II. Physiology and genetics of a series of segregational mutants induced by ultraviolet irradiation or nitrous acid treatment. Arch Immunol Ther Exp (Warsz) 1969;17(1):72–85. [PubMed] [Google Scholar]
  8. Liebman S. W., Stewart J. W., Sherman F. Serine substitutions caused by an ochre suppressor in yeast. J Mol Biol. 1975 Jun 5;94(4):595–610. doi: 10.1016/0022-2836(75)90324-1. [DOI] [PubMed] [Google Scholar]
  9. McCready S. J., Cox B. S., McLaughlin C. S. The extrachromosomal control of nonsense suppression in yeast: an analysis of the elimination of [psi+] in the presence of a nuclear gene PNM. Mol Gen Genet. 1977 Feb 15;150(3):265–270. doi: 10.1007/BF00268125. [DOI] [PubMed] [Google Scholar]
  10. Moustacchi E., Enteric S. Differential "liquid holding recovery" for the lethal effect and cytoplasmic "petite" induction by UV light in Saccharomyces cerevisiae. Mol Gen Genet. 1970;109(1):69–83. doi: 10.1007/BF00334047. [DOI] [PubMed] [Google Scholar]
  11. Moustacchi E., Perlman P. S., Mahler H. R. A novel class of Saccharomyces cerevisiae mutants specifically UV-sensitive to "petite" induction. Mol Gen Genet. 1976 Nov 17;148(3):251–261. doi: 10.1007/BF00332899. [DOI] [PubMed] [Google Scholar]
  12. Nagley P., Sriprakash K. S., Linnane A. W. Structure, synthesis and genetics of yeast mitochondrial DNA. Adv Microb Physiol. 1977;16:157–277. doi: 10.1016/s0065-2911(08)60049-1. [DOI] [PubMed] [Google Scholar]
  13. Oliver S. G. On the mutability of the yeast mitochondrial genome. J Theor Biol. 1977 Jul 21;67(2):195–201. doi: 10.1016/0022-5193(77)90193-x. [DOI] [PubMed] [Google Scholar]
  14. PATRICK M. H., HAYNES R. H., URETZ R. B. DARK RECOVERY PHENOMENA IN YEAST. 1. COMPARATIVE EFFECTS WITH VARIOUS INACTIVATING AGENTS. Radiat Res. 1964 Jan;21:144–163. [PubMed] [Google Scholar]
  15. Parry J. M., Cox B. S. Photoreactivation of ultraviolet induced reciprocal recombination, gene conversion and mutation to prototrophy in Saccharomyces cerevisiae. J Gen Microbiol. 1965 Aug;40(2):235–241. doi: 10.1099/00221287-40-2-235. [DOI] [PubMed] [Google Scholar]
  16. Prakash L. Lack of chemically induced mutation in repair-deficient mutants of yeast. Genetics. 1974 Dec;78(4):1101–1118. doi: 10.1093/genetics/78.4.1101. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Unrau P., Wheatcroft R., Cox B. S. The excision of pyrimidine dimers from DNA of ultraviolet irradiated yeast. Mol Gen Genet. 1971;113(4):359–362. doi: 10.1007/BF00272336. [DOI] [PubMed] [Google Scholar]
  18. Waters R., Moustacchi E. The fate of ultraviolet-induced pyrimidine dimers in the mitochondrial DNA of Saccharomyces cerevisiae following various post-irradiation cell treatments. Biochim Biophys Acta. 1974 Oct 28;366(3):241–250. doi: 10.1016/0005-2787(74)90282-2. [DOI] [PubMed] [Google Scholar]
  19. Williamson D. H. The effect of environmental and genetic factors on the replication of mitochondrial DNA in yeast. Symp Soc Exp Biol. 1970;24:247–276. [PubMed] [Google Scholar]
  20. Young C. S., Cox B. S. Extrachromosomal elements in a super-suppression system of yeast. II. Relations with other extrachromosomal elements. Heredity (Edinb) 1972 Apr;28(2):189–199. doi: 10.1038/hdy.1972.24. [DOI] [PubMed] [Google Scholar]

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