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. 1997 Jan;145(1):75–83. doi: 10.1093/genetics/145.1.75

Apd1(+), a Gene Required for Red Pigment Formation in Ade6 Mutants of Schizosaccharomyces Pombe, Encodes an Enzyme Required for Glutathione Biosynthesis: A Role for Glutathione and a Glutathione-Conjugate Pump

B Chaudhuri 1, S Ingavale 1, A K Bachhawat 1
PMCID: PMC1207786  PMID: 9017391

Abstract

Mutants in the adenine biosynthetic pathway of yeasts (ade1 and ade2 of Saccharomyces cerevisiae, ade6 and ade7 of Schizosaccharomyces pombe) accumulate an intense red pigment in their vacuoles when grown under adenine-limiting conditions. The precise events that determine the formation of the pigment are however, still unknown. We have begun a genetic investigation into the nature and cause of pigmentation of ade6 mutants of S. pombe and have discovered that one of these pigmentation defective mutants, apd1 (adenine pigmentation defective), is a strict glutathione auxotroph. The gene apd1(+) was found to encode the first enzyme in glutathione biosynthesis, γ-glutamylcysteine synthetase, gcs1(+). This gene when expressed in the mutant could confer both glutathione prototrophy and the characteristic red pigmentation, and disruption of the gene led to a loss in both phenotypes. Supplementation of glutathione in the medium, however, could only restore growth but not the pigmentation because the cells were unable to achieve sufficient intracellular levels of glutathione. Disruption of the second enzyme in glutathione biosynthesis, glutathione synthetase, gsh2(+), also led to glutathione auxotrophy, but only a partial defect in pigment formation. A reevaluation of the major amino acids previously reported to be present in the pigment indicated that the pigment is probably a glutathione conjugate. The ability of vanadate to inhibit pigment formation indicated that the conjugate was transported into the vacuole through a glutathione-conjugate pump. This was further confirmed using strains of S. cerevisiae bearing disruptions in the recently identified glutathione-conjugate pump, YCF1, where a significant reduction in pigment formation was observed. The pump of S. pombe is distinct from the previously identified vacuolar pump, hmt1p, for transporting cadystin peptides into vacuoles of S. pombe.

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Selected References

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  1. Anderson M. E. Determination of glutathione and glutathione disulfide in biological samples. Methods Enzymol. 1985;113:548–555. doi: 10.1016/s0076-6879(85)13073-9. [DOI] [PubMed] [Google Scholar]
  2. Barbet N., Muriel W. J., Carr A. M. Versatile shuttle vectors and genomic libraries for use with Schizosaccharomyces pombe. Gene. 1992 May 1;114(1):59–66. doi: 10.1016/0378-1119(92)90707-v. [DOI] [PubMed] [Google Scholar]
  3. Baudin A., Ozier-Kalogeropoulos O., Denouel A., Lacroute F., Cullin C. A simple and efficient method for direct gene deletion in Saccharomyces cerevisiae. Nucleic Acids Res. 1993 Jul 11;21(14):3329–3330. doi: 10.1093/nar/21.14.3329. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Coblenz A., Wolf K. Gcs1, a gene encoding gamma-glutamylcysteine synthetase in the fission yeast Schizosaccharomyces pombe. Yeast. 1995 Sep 30;11(12):1171–1177. doi: 10.1002/yea.320111207. [DOI] [PubMed] [Google Scholar]
  5. Dorfman B. Z. The isolation of adenylosuccinate synthetase mutants in yeast by selection for constitutive behavior in pigmented strains. Genetics. 1969 Feb;61(2):377–389. doi: 10.1093/genetics/61.2.377. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Grill E., Winnacker E. L., Zenk M. H. Phytochelatins: the principal heavy-metal complexing peptides of higher plants. Science. 1985 Nov 8;230(4726):674–676. doi: 10.1126/science.230.4726.674. [DOI] [PubMed] [Google Scholar]
  7. Ishiguro J. An abnormal cell division cycle in an AIR carboxylase-deficient mutant of the fission yeast Schizosaccharomyces pombe. Curr Genet. 1989 Jan;15(1):71–74. doi: 10.1007/BF00445754. [DOI] [PubMed] [Google Scholar]
  8. Ishikawa T. The ATP-dependent glutathione S-conjugate export pump. Trends Biochem Sci. 1992 Nov;17(11):463–468. doi: 10.1016/0968-0004(92)90489-v. [DOI] [PubMed] [Google Scholar]
  9. Klein R. D., Favreau M. A. Transformation of Schwanniomyces occidentalis with an ADE2 gene cloned from S. occidentalis. J Bacteriol. 1988 Dec;170(12):5572–5578. doi: 10.1128/jb.170.12.5572-5578.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Leier I., Jedlitschky G., Buchholz U., Cole S. P., Deeley R. G., Keppler D. The MRP gene encodes an ATP-dependent export pump for leukotriene C4 and structurally related conjugates. J Biol Chem. 1994 Nov 11;269(45):27807–27810. [PubMed] [Google Scholar]
  11. Li Z. S., Szczypka M., Lu Y. P., Thiele D. J., Rea P. A. The yeast cadmium factor protein (YCF1) is a vacuolar glutathione S-conjugate pump. J Biol Chem. 1996 Mar 15;271(11):6509–6517. doi: 10.1074/jbc.271.11.6509. [DOI] [PubMed] [Google Scholar]
  12. Marrs K. A., Alfenito M. R., Lloyd A. M., Walbot V. A glutathione S-transferase involved in vacuolar transfer encoded by the maize gene Bronze-2. Nature. 1995 Jun 1;375(6530):397–400. doi: 10.1038/375397a0. [DOI] [PubMed] [Google Scholar]
  13. Meister A. Glutathione metabolism and its selective modification. J Biol Chem. 1988 Nov 25;263(33):17205–17208. [PubMed] [Google Scholar]
  14. Mutoh N., Nakagawa C. W., Ando S., Tanabe K., Hayashi Y. Cloning and sequencing of the gene encoding the large subunit of glutathione synthetase of Schizosaccharomyces pombe. Biochem Biophys Res Commun. 1991 Nov 27;181(1):430–436. doi: 10.1016/s0006-291x(05)81437-8. [DOI] [PubMed] [Google Scholar]
  15. Ortiz D. F., Ruscitti T., McCue K. F., Ow D. W. Transport of metal-binding peptides by HMT1, a fission yeast ABC-type vacuolar membrane protein. J Biol Chem. 1995 Mar 3;270(9):4721–4728. doi: 10.1074/jbc.270.9.4721. [DOI] [PubMed] [Google Scholar]
  16. Pikula S., Hayden J. B., Awasthi S., Awasthi Y. C., Zimniak P. Organic anion-transporting ATPase of rat liver. II. Functional reconstitution of active transport and regulation by phosphorylation. J Biol Chem. 1994 Nov 4;269(44):27574–27579. [PubMed] [Google Scholar]
  17. Ponticelli A. S., Sena E. P., Smith G. R. Genetic and physical analysis of the M26 recombination hotspot of Schizosaccharomyces pombe. Genetics. 1988 Jul;119(3):491–497. doi: 10.1093/genetics/119.3.491. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Sikorski R. S., Hieter P. A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae. Genetics. 1989 May;122(1):19–27. doi: 10.1093/genetics/122.1.19. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Smirnov M. N., Smirnov V. N., Budowsky E. I., Inge-Vechtomov S. G., Serebrjakov N. G. Red pigment of adenine-deficient yeast Saccharomyces cerevisiae. Biochem Biophys Res Commun. 1967 May 5;27(3):299–304. doi: 10.1016/s0006-291x(67)80096-2. [DOI] [PubMed] [Google Scholar]
  20. Wach A., Brachat A., Pöhlmann R., Philippsen P. New heterologous modules for classical or PCR-based gene disruptions in Saccharomyces cerevisiae. Yeast. 1994 Dec;10(13):1793–1808. doi: 10.1002/yea.320101310. [DOI] [PubMed] [Google Scholar]
  21. Wada Y., Ohsumi Y., Anraku Y. Genes for directing vacuolar morphogenesis in Saccharomyces cerevisiae. I. Isolation and characterization of two classes of vam mutants. J Biol Chem. 1992 Sep 15;267(26):18665–18670. [PubMed] [Google Scholar]
  22. Zonneveld B. J., van der Zanden A. L. The red ade mutants of Kluyveromyces lactis and their classification by complementation with cloned ADE1 or ADE2 genes from Saccharomyces cerevisiae. Yeast. 1995 Jul;11(9):823–827. doi: 10.1002/yea.320110904. [DOI] [PubMed] [Google Scholar]

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