Skip to main content
Genetics logoLink to Genetics
. 1994 Jul;137(3):671–676. doi: 10.1093/genetics/137.3.671

The Sup35 Omnipotent Suppressor Gene Is Involved in the Maintenance of the Non-Mendelian Determinant [Psi(+)] in the Yeast Saccharomyces Cerevisiae

M D Ter-Avanesyan 1, A R Dagkesamanskaya 1, V V Kushnirov 1, V N Smirnov 1
PMCID: PMC1206026  PMID: 8088512

Abstract

The SUP35 gene of yeast Saccharomyces cerevisiae encodes a 76.5-kD ribosome-associated protein (Sup35p), the C-terminal part of which exhibits a high degree of similarity to EF-1α elongation factor, while its N-terminal region is unique. Mutations in or overexpression of the SUP35 gene can generate an omnipotent suppressor effect. In the present study the SUP35 wild-type gene was replaced with deletion alleles generated in vitro that encode Sup35p lacking all or a part of the unique N-terminal region. These 5'-deletion alleles lead, in a haploid strain, simultaneously to an antisuppressor effect and to loss of the non-Mendelian determinant [psi(+)]. The antisuppressor effect is dominant while the elimination of the [psi(+)] determinant is a recessive trait. A set of the plasmid-borne deletion alleles of the SUP35 gene was tested for the ability to maintain [psi(+)]. It was shown that the first 114 amino acids of Sup35p are sufficient to maintain the [psi(+)] determinant. We propose that the Sup35p serves as a trans-acting factor required for the maintenance of [psi(+)].

Full Text

The Full Text of this article is available as a PDF (3.2 MB).

Selected References

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

  1. Broach J. R., Friedman L., Sherman F. Correspondence of yeast UAA suppressors to cloned tRNASerUCA genes. J Mol Biol. 1981 Aug 15;150(3):375–387. doi: 10.1016/0022-2836(81)90553-2. [DOI] [PubMed] [Google Scholar]
  2. Broach J. R., Strathern J. N., Hicks J. B. Transformation in yeast: development of a hybrid cloning vector and isolation of the CAN1 gene. Gene. 1979 Dec;8(1):121–133. doi: 10.1016/0378-1119(79)90012-x. [DOI] [PubMed] [Google Scholar]
  3. Chernoff Y. O., Inge-Vechtomov S. G., Derkach I. L., Ptyushkina M. V., Tarunina O. V., Dagkesamanskaya A. R., Ter-Avanesyan M. D. Dosage-dependent translational suppression in yeast Saccharomyces cerevisiae. Yeast. 1992 Jul;8(7):489–499. doi: 10.1002/yea.320080702. [DOI] [PubMed] [Google Scholar]
  4. Cox B. S., Tuite M. F., McLaughlin C. S. The psi factor of yeast: a problem in inheritance. Yeast. 1988 Sep;4(3):159–178. doi: 10.1002/yea.320040302. [DOI] [PubMed] [Google Scholar]
  5. 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]
  6. Crouzet M., Tuite M. F. Genetic control of translational fidelity in yeast: molecular cloning and analysis of the allosuppressor gene SAL3. Mol Gen Genet. 1987 Dec;210(3):581–583. doi: 10.1007/BF00327216. [DOI] [PubMed] [Google Scholar]
  7. Culbertson M. R., Gaber R. F., Cummins C. M. Frameshift suppression in Saccharomyces cerevisiae. V. Isolation and genetic properties of nongroup-specific suppressors. Genetics. 1982 Nov;102(3):361–378. doi: 10.1093/genetics/102.3.361. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Dagkesamanskaya A. R., Ter-Avanesyan M. D. Interaction of the yeast omnipotent suppressors SUP1(SUP45) and SUP2(SUP35) with non-mendelian factors. Genetics. 1991 Jul;128(3):513–520. doi: 10.1093/genetics/128.3.513. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Didichenko S. A., Ter-Avanesyan M. D., Smirnov V. N. Ribosome-bound EF-1 alpha-like protein of yeast Saccharomyces cerevisiae. Eur J Biochem. 1991 Jun 15;198(3):705–711. doi: 10.1111/j.1432-1033.1991.tb16070.x. [DOI] [PubMed] [Google Scholar]
  10. Eustice D. C., Wakem L. P., Wilhelm J. M., Sherman F. Altered 40 S ribosomal subunits in omnipotent suppressors of yeast. J Mol Biol. 1986 Mar 20;188(2):207–214. doi: 10.1016/0022-2836(86)90305-0. [DOI] [PubMed] [Google Scholar]
  11. Gerlach W. L. Mutational properties of supP amber-ochre supersuppressors in Saccharomyces cerevisiae. Mol Gen Genet. 1976 Mar 22;144(2):213–215. doi: 10.1007/BF02428111. [DOI] [PubMed] [Google Scholar]
  12. Goldring E. S., Grossman L. I., Krupnick D., Cryer D. R., Marmur J. The petite mutation in yeast. Loss of mitochondrial deoxyribonucleic acid during induction of petites with ethidium bromide. J Mol Biol. 1970 Sep 14;52(2):323–335. doi: 10.1016/0022-2836(70)90033-1. [DOI] [PubMed] [Google Scholar]
  13. Goodman H. M., Olson M. V., Hall B. D. Nucleotide sequence of a mutant eukaryotic gene: the yeast tyrosine-inserting ochre suppressor SUP4-o. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5453–5457. doi: 10.1073/pnas.74.12.5453. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Hoffman C. S., Winston F. A ten-minute DNA preparation from yeast efficiently releases autonomous plasmids for transformation of Escherichia coli. Gene. 1987;57(2-3):267–272. doi: 10.1016/0378-1119(87)90131-4. [DOI] [PubMed] [Google Scholar]
  15. Hoshino S., Miyazawa H., Enomoto T., Hanaoka F., Kikuchi Y., Kikuchi A., Ui M. A human homologue of the yeast GST1 gene codes for a GTP-binding protein and is expressed in a proliferation-dependent manner in mammalian cells. EMBO J. 1989 Dec 1;8(12):3807–3814. doi: 10.1002/j.1460-2075.1989.tb08558.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Ito H., Fukuda Y., Murata K., Kimura A. Transformation of intact yeast cells treated with alkali cations. J Bacteriol. 1983 Jan;153(1):163–168. doi: 10.1128/jb.153.1.163-168.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Kikuchi Y., Shimatake H., Kikuchi A. A yeast gene required for the G1-to-S transition encodes a protein containing an A-kinase target site and GTPase domain. EMBO J. 1988 Apr;7(4):1175–1182. doi: 10.1002/j.1460-2075.1988.tb02928.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Kushnirov V. V., Ter-Avanesyan M. D., Didichenko S. A., Smirnov V. N., Chernoff Y. O., Derkach I. L., Novikova O. N., Inge-Vechtomov S. G., Neistat M. A., Tolstorukov I. I. Divergence and conservation of SUP2 (SUP35) gene of yeast Pichia pinus and Saccharomyces cerevisiae. Yeast. 1990 Nov-Dec;6(6):461–472. doi: 10.1002/yea.320060603. [DOI] [PubMed] [Google Scholar]
  19. Kushnirov V. V., Ter-Avanesyan M. D., Telckov M. V., Surguchov A. P., Smirnov V. N., Inge-Vechtomov S. G. Nucleotide sequence of the SUP2 (SUP35) gene of Saccharomyces cerevisiae. Gene. 1988 Jun 15;66(1):45–54. doi: 10.1016/0378-1119(88)90223-5. [DOI] [PubMed] [Google Scholar]
  20. Masurekar M., Palmer E., Ono B. I., Wilhelm J. M., Sherman F. Misreading of the ribosomal suppressor SUP46 due to an altered 40 S subunit in yeast. J Mol Biol. 1981 Apr 15;147(3):381–390. doi: 10.1016/0022-2836(81)90490-3. [DOI] [PubMed] [Google Scholar]
  21. McCready S. J., Cox B. S. Antisuppressors in yeast. Mol Gen Genet. 1973 Aug 28;124(4):305–320. doi: 10.1007/BF00267660. [DOI] [PubMed] [Google Scholar]
  22. 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]
  23. Ono B. I., Stewart J. W., Sherman F. Yeast UAA suppressors effective in psi+ strains serine-inserting suppressors. J Mol Biol. 1979 Feb 15;128(1):81–100. doi: 10.1016/0022-2836(79)90309-7. [DOI] [PubMed] [Google Scholar]
  24. Ono B., Moriga N., Ishihara K., Ishiguro J., Ishino Y., Shinoda S. Omnipotent Suppressors Effective in psi Strains of SACCHAROMYCES CEREVISIAE: Recessiveness and Dominance. Genetics. 1984 Jun;107(2):219–230. doi: 10.1093/genetics/107.2.219. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Piper P. W., Wasserstein M., Engbaek F., Kaltoft K., Celis J. E., Zeuthen J., Liebman S., Sherman F. Nonsense suppressors of Saccharomyces cerevisiae can be generated by mutation of the tyrosine tRNA anticodon. Nature. 1976 Aug 26;262(5571):757–761. doi: 10.1038/262757a0. [DOI] [PubMed] [Google Scholar]
  26. Surguchov A. P., Beretetskaya Y. V., Fominykch E. S., Pospelova E. M., SmirnovVN, Ter-Avanesyan M. D., Inge-Vechtomov S. G. Recessive suppression in yeast Saccharomyces cerevisiae is mediated by a ribosomal mutation. FEBS Lett. 1980 Feb 25;111(1):175–178. doi: 10.1016/0014-5793(80)80786-1. [DOI] [PubMed] [Google Scholar]
  27. Ter-Avanesyan M. D., Kushnirov V. V., Dagkesamanskaya A. R., Didichenko S. A., Chernoff Y. O., Inge-Vechtomov S. G., Smirnov V. N. Deletion analysis of the SUP35 gene of the yeast Saccharomyces cerevisiae reveals two non-overlapping functional regions in the encoded protein. Mol Microbiol. 1993 Mar;7(5):683–692. doi: 10.1111/j.1365-2958.1993.tb01159.x. [DOI] [PubMed] [Google Scholar]
  28. Wilson P. G., Culbertson M. R. SUF12 suppressor protein of yeast. A fusion protein related to the EF-1 family of elongation factors. J Mol Biol. 1988 Feb 20;199(4):559–573. doi: 10.1016/0022-2836(88)90301-4. [DOI] [PubMed] [Google Scholar]

Articles from Genetics are provided here courtesy of Oxford University Press

RESOURCES