Skip to main content
The EMBO Journal logoLink to The EMBO Journal
. 1997 Mar 17;16(6):1164–1172. doi: 10.1093/emboj/16.6.1164

A specific screen for oligosaccharyltransferase mutations identifies the 9 kDa OST5 protein required for optimal activity in vivo and in vitro.

G Reiss 1, S te Heesen 1, R Gilmore 1, R Zufferey 1, M Aebi 1
PMCID: PMC1169715  PMID: 9135133

Abstract

The central reaction in the process of N-linked protein glycosylation in eukaryotic cells, the transfer of the oligosaccharide Glc(3)Man(9)GlcNAc(2) from the lipid dolicholpyrophosphate to selected asparagine residues, is catalyzed by the oligosaccharyltransferase (OTase). This enzyme consists of multiple subunits; however, purification of the complex has revealed different results with respect to its protein composition. To determine how many different loci are required for OTase activity in vivo, we performed a novel, specific screen for mutants with altered OTase activity. Based on the synthetic lethal phenotype of OTase mutants in combination with a deficiency of dolicholphosphoglucose biosynthesis which results in non-glucosylated lipid-linked oligosaccharide, we identified seven complementation groups with decreased OTase activity. Beside the known OTase loci, STT3, OST1, WBP1, OST3, SWP1 and OST2, a novel locus, OST5, was identified. OST5 is an intron-containing gene encoding a putative membrane protein of 9.5 kDa present in highly purified OTase preparations. OST5 protein is not essential for growth but its depletion results in a reduced OTase activity. Suppression of an ost1 mutation by overexpression of OST5 indicates that this small membrane protein directly interacts with other OTase components, most likely with Ost1p. A strong genetic interaction with a stt3 mutation implies a role in complex assembly.

Full Text

The Full Text of this article is available as a PDF (327.4 KB).

Selected References

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

  1. Allen S., Naim H. Y., Bulleid N. J. Intracellular folding of tissue-type plasminogen activator. Effects of disulfide bond formation on N-linked glycosylation and secretion. J Biol Chem. 1995 Mar 3;270(9):4797–4804. doi: 10.1074/jbc.270.9.4797. [DOI] [PubMed] [Google Scholar]
  2. 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]
  3. Bause E. Model studies on N-glycosylation of proteins. Biochem Soc Trans. 1984 Jun;12(3):514–517. doi: 10.1042/bst0120514. [DOI] [PubMed] [Google Scholar]
  4. Boeke J. D., LaCroute F., Fink G. R. A positive selection for mutants lacking orotidine-5'-phosphate decarboxylase activity in yeast: 5-fluoro-orotic acid resistance. Mol Gen Genet. 1984;197(2):345–346. doi: 10.1007/BF00330984. [DOI] [PubMed] [Google Scholar]
  5. Breuer W., Bause E. Oligosaccharyl transferase is a constitutive component of an oligomeric protein complex from pig liver endoplasmic reticulum. Eur J Biochem. 1995 Mar 15;228(3):689–696. [PubMed] [Google Scholar]
  6. Buu-Hoï N. P., Jacquignon P., Mangane M. Carcinogenic nitrogen compounds. LXX. Polycyclic naphthyridines by means of the Ullmann-Fetvadjian reaction. J Chem Soc Perkin 1. 1971;10:1991–1993. doi: 10.1039/j39710001991. [DOI] [PubMed] [Google Scholar]
  7. Chi J. H., Roos J., Dean N. The OST4 gene of Saccharomyces cerevisiae encodes an unusually small protein required for normal levels of oligosaccharyltransferase activity. J Biol Chem. 1996 Feb 9;271(6):3132–3140. doi: 10.1074/jbc.271.6.3132. [DOI] [PubMed] [Google Scholar]
  8. Das R. C., Heath E. C. Dolichyldiphosphoryloligosaccharide--protein oligosaccharyltransferase; solubilization, purification, and properties. Proc Natl Acad Sci U S A. 1980 Jul;77(7):3811–3815. doi: 10.1073/pnas.77.7.3811. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Fiedler K., Simons K. The role of N-glycans in the secretory pathway. Cell. 1995 May 5;81(3):309–312. doi: 10.1016/0092-8674(95)90380-1. [DOI] [PubMed] [Google Scholar]
  10. Finke K., Plath K., Panzner S., Prehn S., Rapoport T. A., Hartmann E., Sommer T. A second trimeric complex containing homologs of the Sec61p complex functions in protein transport across the ER membrane of S. cerevisiae. EMBO J. 1996 Apr 1;15(7):1482–1494. [PMC free article] [PubMed] [Google Scholar]
  11. Franzusoff A., Rothblatt J., Schekman R. Analysis of polypeptide transit through yeast secretory pathway. Methods Enzymol. 1991;194:662–674. doi: 10.1016/0076-6879(91)94048-h. [DOI] [PubMed] [Google Scholar]
  12. Gavel Y., von Heijne G. Sequence differences between glycosylated and non-glycosylated Asn-X-Thr/Ser acceptor sites: implications for protein engineering. Protein Eng. 1990 Apr;3(5):433–442. doi: 10.1093/protein/3.5.433. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Hasilik A., Tanner W. Carbohydrate moiety of carboxypeptidase Y and perturbation of its biosynthesis. Eur J Biochem. 1978 Nov 15;91(2):567–575. doi: 10.1111/j.1432-1033.1978.tb12710.x. [DOI] [PubMed] [Google Scholar]
  14. Heesen S., Lehle L., Weissmann A., Aebi M. Isolation of the ALG5 locus encoding the UDP-glucose:dolichyl-phosphate glucosyltransferase from Saccharomyces cerevisiae. Eur J Biochem. 1994 Aug 15;224(1):71–79. doi: 10.1111/j.1432-1033.1994.tb19996.x. [DOI] [PubMed] [Google Scholar]
  15. Helenius A. How N-linked oligosaccharides affect glycoprotein folding in the endoplasmic reticulum. Mol Biol Cell. 1994 Mar;5(3):253–265. doi: 10.1091/mbc.5.3.253. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Hill J. E., Myers A. M., Koerner T. J., Tzagoloff A. Yeast/E. coli shuttle vectors with multiple unique restriction sites. Yeast. 1986 Sep;2(3):163–167. doi: 10.1002/yea.320020304. [DOI] [PubMed] [Google Scholar]
  17. Hill K. J., Stevens T. H. Vma21p is a yeast membrane protein retained in the endoplasmic reticulum by a di-lysine motif and is required for the assembly of the vacuolar H(+)-ATPase complex. Mol Biol Cell. 1994 Sep;5(9):1039–1050. doi: 10.1091/mbc.5.9.1039. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Holst B., Bruun A. W., Kielland-Brandt M. C., Winther J. R. Competition between folding and glycosylation in the endoplasmic reticulum. EMBO J. 1996 Jul 15;15(14):3538–3546. [PMC free article] [PubMed] [Google Scholar]
  19. Huffaker T. C., Robbins P. W. Yeast mutants deficient in protein glycosylation. Proc Natl Acad Sci U S A. 1983 Dec;80(24):7466–7470. doi: 10.1073/pnas.80.24.7466. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Iwata S., Ostermeier C., Ludwig B., Michel H. Structure at 2.8 A resolution of cytochrome c oxidase from Paracoccus denitrificans. Nature. 1995 Aug 24;376(6542):660–669. doi: 10.1038/376660a0. [DOI] [PubMed] [Google Scholar]
  21. Kalies K. U., Hartmann E. Membrane topology of the 12- and the 25-kDa subunits of the mammalian signal peptidase complex. J Biol Chem. 1996 Feb 16;271(7):3925–3929. doi: 10.1074/jbc.271.7.3925. [DOI] [PubMed] [Google Scholar]
  22. Karaoglu D., Kelleher D. J., Gilmore R. Functional characterization of Ost3p. Loss of the 34-kD subunit of the Saccharomyces cerevisiae oligosaccharyltransferase results in biased underglycosylation of acceptor substrates. J Cell Biol. 1995 Aug;130(3):567–577. doi: 10.1083/jcb.130.3.567. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Kassenbrock C. K., Cao W., Douglas M. G. Genetic and biochemical characterization of ISP6, a small mitochondrial outer membrane protein associated with the protein translocation complex. EMBO J. 1993 Aug;12(8):3023–3034. doi: 10.1002/j.1460-2075.1993.tb05971.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Kelleher D. J., Gilmore R. The Saccharomyces cerevisiae oligosaccharyltransferase is a protein complex composed of Wbp1p, Swp1p, and four additional polypeptides. J Biol Chem. 1994 Apr 29;269(17):12908–12917. [PubMed] [Google Scholar]
  25. Kendall R. L., Yamada R., Bradshaw R. A. Cotranslational amino-terminal processing. Methods Enzymol. 1990;185:398–407. doi: 10.1016/0076-6879(90)85035-m. [DOI] [PubMed] [Google Scholar]
  26. Kumar V., Heinemann F. S., Ozols J. Purification and characterization of avian oligosaccharyltransferase. Complete amino acid sequence of the 50-kDa subunit. J Biol Chem. 1994 May 6;269(18):13451–13457. [PubMed] [Google Scholar]
  27. Kyte J., Doolittle R. F. A simple method for displaying the hydropathic character of a protein. J Mol Biol. 1982 May 5;157(1):105–132. doi: 10.1016/0022-2836(82)90515-0. [DOI] [PubMed] [Google Scholar]
  28. Rost B., Casadio R., Fariselli P., Sander C. Transmembrane helices predicted at 95% accuracy. Protein Sci. 1995 Mar;4(3):521–533. doi: 10.1002/pro.5560040318. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Runge K. W., Huffaker T. C., Robbins P. W. Two yeast mutations in glucosylation steps of the asparagine glycosylation pathway. J Biol Chem. 1984 Jan 10;259(1):412–417. [PubMed] [Google Scholar]
  30. Sharma C. B., Lehle L., Tanner W. N-Glycosylation of yeast proteins. Characterization of the solubilized oligosaccharyl transferase. Eur J Biochem. 1981 May;116(1):101–108. doi: 10.1111/j.1432-1033.1981.tb05306.x. [DOI] [PubMed] [Google Scholar]
  31. Silberstein S., Collins P. G., Kelleher D. J., Gilmore R. The essential OST2 gene encodes the 16-kD subunit of the yeast oligosaccharyltransferase, a highly conserved protein expressed in diverse eukaryotic organisms. J Cell Biol. 1995 Oct;131(2):371–383. doi: 10.1083/jcb.131.2.371. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Silberstein S., Collins P. G., Kelleher D. J., Rapiejko P. J., Gilmore R. The alpha subunit of the Saccharomyces cerevisiae oligosaccharyltransferase complex is essential for vegetative growth of yeast and is homologous to mammalian ribophorin I. J Cell Biol. 1995 Feb;128(4):525–536. doi: 10.1083/jcb.128.4.525. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Silberstein S., Gilmore R. Biochemistry, molecular biology, and genetics of the oligosaccharyltransferase. FASEB J. 1996 Jun;10(8):849–858. [PubMed] [Google Scholar]
  34. Silberstein S., Kelleher D. J., Gilmore R. The 48-kDa subunit of the mammalian oligosaccharyltransferase complex is homologous to the essential yeast protein WBP1. J Biol Chem. 1992 Nov 25;267(33):23658–23663. [PubMed] [Google Scholar]
  35. Spiess M. Heads or tails--what determines the orientation of proteins in the membrane. FEBS Lett. 1995 Aug 1;369(1):76–79. doi: 10.1016/0014-5793(95)00551-j. [DOI] [PubMed] [Google Scholar]
  36. Spiro R. G., Spiro M. J., Bhoyroo V. D. Lipid-saccharide intermediates in glycoprotein biosynthesis. II. Studies on the structure of an oligosaccharide-lipid from thyroid. J Biol Chem. 1976 Oct 25;251(20):6409–6419. [PubMed] [Google Scholar]
  37. Stagljar I., te Heesen S., Aebi M. New phenotype of mutations deficient in glucosylation of the lipid-linked oligosaccharide: cloning of the ALG8 locus. Proc Natl Acad Sci U S A. 1994 Jun 21;91(13):5977–5981. doi: 10.1073/pnas.91.13.5977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Struhl K., Davis R. W. Transcription of the his3 gene region in Saccharomyces cerevisiae. J Mol Biol. 1981 Nov 5;152(3):535–552. doi: 10.1016/0022-2836(81)90267-9. [DOI] [PubMed] [Google Scholar]
  39. Trimble R. B., Byrd J. C., Maley F. Effect of glucosylation of lipid intermediates on oligosaccharide transfer in solubilized microsomes from Saccharomyces cerevisiae. J Biol Chem. 1980 Dec 25;255(24):11892–11895. [PubMed] [Google Scholar]
  40. Varki A. Biological roles of oligosaccharides: all of the theories are correct. Glycobiology. 1993 Apr;3(2):97–130. doi: 10.1093/glycob/3.2.97. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Vijayraghavan U., Company M., Abelson J. Isolation and characterization of pre-mRNA splicing mutants of Saccharomyces cerevisiae. Genes Dev. 1989 Aug;3(8):1206–1216. doi: 10.1101/gad.3.8.1206. [DOI] [PubMed] [Google Scholar]
  42. Wimmer C., Doye V., Grandi P., Nehrbass U., Hurt E. C. A new subclass of nucleoporins that functionally interact with nuclear pore protein NSP1. EMBO J. 1992 Dec;11(13):5051–5061. doi: 10.1002/j.1460-2075.1992.tb05612.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Winther J. R., Stevens T. H., Kielland-Brandt M. C. Yeast carboxypeptidase Y requires glycosylation for efficient intracellular transport, but not for vacuolar sorting, in vivo stability, or activity. Eur J Biochem. 1991 May 8;197(3):681–689. doi: 10.1111/j.1432-1033.1991.tb15959.x. [DOI] [PubMed] [Google Scholar]
  44. Yu Y. H., Sabatini D. D., Kreibich G. Antiribophorin antibodies inhibit the targeting to the ER membrane of ribosomes containing nascent secretory polypeptides. J Cell Biol. 1990 Oct;111(4):1335–1342. doi: 10.1083/jcb.111.4.1335. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Zufferey R., Knauer R., Burda P., Stagljar I., te Heesen S., Lehle L., Aebi M. STT3, a highly conserved protein required for yeast oligosaccharyl transferase activity in vivo. EMBO J. 1995 Oct 16;14(20):4949–4960. doi: 10.1002/j.1460-2075.1995.tb00178.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. te Heesen S., Janetzky B., Lehle L., Aebi M. The yeast WBP1 is essential for oligosaccharyl transferase activity in vivo and in vitro. EMBO J. 1992 Jun;11(6):2071–2075. doi: 10.1002/j.1460-2075.1992.tb05265.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. te Heesen S., Knauer R., Lehle L., Aebi M. Yeast Wbp1p and Swp1p form a protein complex essential for oligosaccharyl transferase activity. EMBO J. 1993 Jan;12(1):279–284. doi: 10.1002/j.1460-2075.1993.tb05654.x. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The EMBO Journal are provided here courtesy of Nature Publishing Group

RESOURCES