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. 1982 Nov;102(3):341–359. doi: 10.1093/genetics/102.3.341

Mutations in the PHO80 Gene Confer Permeability to 5'-Mononucleotides in SACCHAROMYCES CEREVISIAE

Linda F Bisson 1,2, Jeremy Thorner 1,2
PMCID: PMC1201945  PMID: 6293915

Abstract

Yeast mutants permeable to dTMP (tup) were selected and two new complementation groups (tup5 and tup7) were identified. Assay of the levels of both acid and alkaline phosphatase in cells grown under either repressing (5 mm PO4-3) or derepressing (0.03 mm PO4-3) conditions indicated that, in general, tup mutations cause cells to be defective in their regulation of phosphatase synthesis. In addition, three of the tup mutations (tup1, tup4 and tup7) displayed markedly elevated rates of inorganic phosphate transport. The tup7 locus was found to be tightly centromere-linked on the right arm of chromosome XV, and was shown to be allelic with the pho80 regulatory locus on the basis of both genetic and biochemical criteria. Analysis of other mutations known to affect phosphatase levels (pho) indicated that some also conferred permeability to dTMP. Possible allelic relationships between tup genes and certain of these pho mutations are discussed. Regardless of the culture conditions, wild-type strains were not permeable to dTMP; in contrast, it was found in the course of this work that normal yeast cells were permeable to dUMP and that dUMP permeability was regulated by the concentration of inorganic phosphate present in the medium used to grow the cells. Thus, permeability to 5'-mononucleotides appears to be under coordinate control with phosphatase synthesis.

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Selected References

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  1. Bisson L., Thorner J. Thymidine 5'-monophosphate-requiring mutants of Saccharomyces cerevisiae are deficient in thymidylate synthetase. J Bacteriol. 1977 Oct;132(1):44–50. doi: 10.1128/jb.132.1.44-50.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Brendel M., Fäth W. W., Laskowski W. Isolation and characterization of mutants of Saccharomyces cerevisiae able to grow after inhibition of dTMP synthesis. Methods Cell Biol. 1975;11:287–294. doi: 10.1016/s0091-679x(08)60329-5. [DOI] [PubMed] [Google Scholar]
  3. Brendel M., Haynes R. H. Exogenous thymidine 5'-monophosphate as a precursor for DNA synthesis in yeast. Mol Gen Genet. 1973 Nov 22;126(4):337–348. doi: 10.1007/BF00269443. [DOI] [PubMed] [Google Scholar]
  4. Elorza M. V., Rodriguez L., Villanueva J. R., Sentandreu R. Regulation of acid phosphatase synthesis in Saccharomyces cerevisiae. Biochim Biophys Acta. 1978 Nov 21;521(1):342–351. doi: 10.1016/0005-2787(78)90276-9. [DOI] [PubMed] [Google Scholar]
  5. Fäth W. W., Brendel M. Isolation and properties of yeast mutants with highly efficient thymidylate utilization. Z Naturforsch C. 1976 Jul-Aug;31(7-8):468–478. doi: 10.1515/znc-1976-7-824. [DOI] [PubMed] [Google Scholar]
  6. Gascón S., Lampen J. O. Purification of the internal invertase of yeast. J Biol Chem. 1968 Apr 10;243(7):1567–1572. [PubMed] [Google Scholar]
  7. Grenson M. The utilization of exogenous pyrimidines and the recycling of uridine-5'-phosphate derivatives in Saccharomyces cerevisiae, as studied by means of mutants affected in pyrimidine uptake and metabolism. Eur J Biochem. 1969 Dec;11(2):249–260. doi: 10.1111/j.1432-1033.1969.tb00767.x. [DOI] [PubMed] [Google Scholar]
  8. Lloyd J. B., Whelan W. J. An improved method for enzymic determination of glucose in the presence of maltose. Anal Biochem. 1969 Sep;30(3):467–470. doi: 10.1016/0003-2697(69)90143-2. [DOI] [PubMed] [Google Scholar]
  9. Mortimer R. K., Hawthorne D. C. Genetic mapping in yeast. Methods Cell Biol. 1975;11:221–233. doi: 10.1016/s0091-679x(08)60325-8. [DOI] [PubMed] [Google Scholar]
  10. Perkins D. D. Biochemical Mutants in the Smut Fungus Ustilago Maydis. Genetics. 1949 Sep;34(5):607–626. doi: 10.1093/genetics/34.5.607. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. RANDERATH K., RANDERATH E. ION-EXCHANGE CHROMATOGRAPHY OF NUCLEOTIDES ON POLY-(ETHYLENEIMINE)-CELLULOSE THIN LAYERS. J Chromatogr. 1964 Oct;16:111–125. doi: 10.1016/s0021-9673(01)82445-6. [DOI] [PubMed] [Google Scholar]
  12. Remer S., Sherman A., Kraig E., Haber J. E. Suppressor of deoxythmidine monophosphate uptake in Saccharomyces cerevisiae. J Bacteriol. 1979 May;138(2):638–641. doi: 10.1128/jb.138.2.638-641.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. SCHMIDT G., BARTSCH G., LAUMONT M. C., HERMAN T., LISS M. Acid phosphatase of bakers' yeast: an enzyme of the external cell surface. Biochemistry. 1963 Jan-Feb;2:126–131. doi: 10.1021/bi00901a022. [DOI] [PubMed] [Google Scholar]
  14. SUTTON D. D., LAMPEN J. O. Localization of sucrose and maltose fermenting systems in Saccharomyces cerevisiae. Biochim Biophys Acta. 1962 Jan 29;56:303–312. doi: 10.1016/0006-3002(62)90567-x. [DOI] [PubMed] [Google Scholar]
  15. Schurr A., Yagil E. Regulation and characterization of acid and alkaline phosphatase in yeast. J Gen Microbiol. 1971 Mar;65(3):291–303. doi: 10.1099/00221287-65-3-291. [DOI] [PubMed] [Google Scholar]
  16. To-E A., Ueda Y., Kakimoto S. I., Oshima Y. Isolation and characterization of acid phosphatase mutants in Saccharomyces cerevisiae. J Bacteriol. 1973 Feb;113(2):727–738. doi: 10.1128/jb.113.2.727-738.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Toh-E A., Oshima Y. Characterization of a dominant, constitutive mutation, PHOO, for the repressible acid phosphatase synthesis in Saccharomyces cerevisiae. J Bacteriol. 1974 Nov;120(2):608–617. doi: 10.1128/jb.120.2.608-617.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Toh-e A., Inouye S., Oshima Y. Structure and function of the PHO82-pho4 locus controlling the synthesis of repressible acid phosphatase of Saccharomyces cerevisiae. J Bacteriol. 1981 Jan;145(1):221–232. doi: 10.1128/jb.145.1.221-232.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Toh-e A., Kobayashi S., Oshima Y. Disturbance of the machinery for the gene expression by acidic pH in the repressible acid phosphatase system of Saccharomyces cerevisiae. Mol Gen Genet. 1978 Jun 14;162(2):139–149. doi: 10.1007/BF00267870. [DOI] [PubMed] [Google Scholar]
  20. Ueda Y., Oshima Y. A constitutive mutation, phoT, of the repressible acid phosphatase synthesis with inability to transport inorganic phosphate in Saccharomyces cerevisiae. Mol Gen Genet. 1975;136(3):255–259. doi: 10.1007/BF00334020. [DOI] [PubMed] [Google Scholar]
  21. Wickner R. B., Leibowitz M. J. Chromosomal genes essential for replication of a double-stranded RNA plasmid of Saccharomyces cerevisiae: the killer character of yeast. J Mol Biol. 1976 Aug 15;105(3):427–443. doi: 10.1016/0022-2836(76)90102-9. [DOI] [PubMed] [Google Scholar]
  22. Wickner R. B. Mutants of Saccharomyces cerevisiae that incorporate deoxythymidine 5'-monophosphate into DNA in vivo. Methods Cell Biol. 1975;11:295–302. doi: 10.1016/s0091-679x(08)60330-1. [DOI] [PubMed] [Google Scholar]
  23. Wickner R. B. Mutants of Saccharomyces cerevisiae that incorporate deoxythymidine-5'-monophosphate into deoxyribonucleic acid in vivo. J Bacteriol. 1974 Jan;117(1):252–260. doi: 10.1128/jb.117.1.252-260.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Yee W. S., Decker R. W., Brunk C. F. Incorporation of tritium-labeled thymidine monophosphate into nuclear DNA by permeabilized yeast cells. Biochim Biophys Acta. 1976 Nov 1;447(4):385–390. doi: 10.1016/0005-2787(76)90075-7. [DOI] [PubMed] [Google Scholar]
  25. Zimmermann F. K., Schmiedt I., ten Berge A. M. Dominance and recessiveness at the protein level in mutant x wildtype crosses in Sacchaomyces cerevisiae. Mol Gen Genet. 1969 Aug 15;104(4):321–330. doi: 10.1007/BF00334231. [DOI] [PubMed] [Google Scholar]

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