Skip to main content
Genetics logoLink to Genetics
. 2000 Jan;154(1):83–97. doi: 10.1093/genetics/154.1.83

Synthetic genetic interactions with temperature-sensitive clathrin in Saccharomyces cerevisiae. Roles for synaptojanin-like Inp53p and dynamin-related Vps1p in clathrin-dependent protein sorting at the trans-Golgi network.

E S Bensen 1, G Costaguta 1, G S Payne 1
PMCID: PMC1460916  PMID: 10628971

Abstract

Clathrin is involved in selective protein transport at the Golgi apparatus and the plasma membrane. To further understand the molecular mechanisms underlying clathrin-mediated protein transport pathways, we initiated a genetic screen for mutations that display synthetic growth defects when combined with a temperature-sensitive allele of the clathrin heavy chain gene (chc1-521) in Saccharomyces cerevisiae. Mutations, when present in cells with wild-type clathrin, were analyzed for effects on mating pheromone alpha-factor precursor maturation and sorting of the vacuolar protein carboxypeptidase Y as measures of protein sorting at the yeast trans-Golgi network (TGN) compartment. By these criteria, two classes of mutants were obtained, those with and those without defects in protein sorting at the TGN. One mutant with unaltered protein sorting at the TGN contains a mutation in PTC1, a type 2c serine/threonine phosphatase with widespread influences. The collection of mutants displaying TGN sorting defects includes members with mutations in previously identified vacuolar protein sorting genes (VPS), including the dynamin family member VPS1. Striking genetic interactions were observed by combining temperature-sensitive alleles of CHC1 and VPS1, supporting the model that Vps1p is involved in clathrin-mediated vesicle formation at the TGN. Also in the spectrum of mutants with TGN sorting defects are isolates with mutations in the following: RIC1, encoding a product originally proposed to participate in ribosome biogenesis; LUV1, encoding a product potentially involved in vacuole and microtubule organization; and INP53, encoding a synaptojanin-like inositol polyphosphate 5-phosphatase. Disruption of INP53, but not the related INP51 and INP52 genes, resulted in alpha-factor maturation defects and exacerbated alpha-factor maturation defects when combined with chc1-521. Our findings implicate a wide variety of proteins in clathrin-dependent processes and provide evidence for the selective involvement of Inp53p in clathrin-mediated protein sorting at the TGN.

Full Text

The Full Text of this article is available as a PDF (345.8 KB).

Selected References

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

  1. Altschul S. F., Madden T. L., Schäffer A. A., Zhang J., Zhang Z., Miller W., Lipman D. J. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 1997 Sep 1;25(17):3389–3402. doi: 10.1093/nar/25.17.3389. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Archer J. E., Vega L. R., Solomon F. Rbl2p, a yeast protein that binds to beta-tubulin and participates in microtubule function in vivo. Cell. 1995 Aug 11;82(3):425–434. doi: 10.1016/0092-8674(95)90431-x. [DOI] [PubMed] [Google Scholar]
  3. Barlowe C. COPII and selective export from the endoplasmic reticulum. Biochim Biophys Acta. 1998 Aug 14;1404(1-2):67–76. doi: 10.1016/s0167-4889(98)00047-0. [DOI] [PubMed] [Google Scholar]
  4. Basson M. E., Moore R. L., O'Rear J., Rine J. Identifying mutations in duplicated functions in Saccharomyces cerevisiae: recessive mutations in HMG-CoA reductase genes. Genetics. 1987 Dec;117(4):645–655. doi: 10.1093/genetics/117.4.645. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Becherer K. A., Rieder S. E., Emr S. D., Jones E. W. Novel syntaxin homologue, Pep12p, required for the sorting of lumenal hydrolases to the lysosome-like vacuole in yeast. Mol Biol Cell. 1996 Apr;7(4):579–594. doi: 10.1091/mbc.7.4.579. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Brewster J. L., de Valoir T., Dwyer N. D., Winter E., Gustin M. C. An osmosensing signal transduction pathway in yeast. Science. 1993 Mar 19;259(5102):1760–1763. doi: 10.1126/science.7681220. [DOI] [PubMed] [Google Scholar]
  7. Bryant N. J., Stevens T. H. Vacuole biogenesis in Saccharomyces cerevisiae: protein transport pathways to the yeast vacuole. Microbiol Mol Biol Rev. 1998 Mar;62(1):230–247. doi: 10.1128/mmbr.62.1.230-247.1998. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Christianson T. W., Sikorski R. S., Dante M., Shero J. H., Hieter P. Multifunctional yeast high-copy-number shuttle vectors. Gene. 1992 Jan 2;110(1):119–122. doi: 10.1016/0378-1119(92)90454-w. [DOI] [PubMed] [Google Scholar]
  9. Cleves A. E., Novick P. J., Bankaitis V. A. Mutations in the SAC1 gene suppress defects in yeast Golgi and yeast actin function. J Cell Biol. 1989 Dec;109(6 Pt 1):2939–2950. doi: 10.1083/jcb.109.6.2939. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Cooper A. A., Stevens T. H. Vps10p cycles between the late-Golgi and prevacuolar compartments in its function as the sorting receptor for multiple yeast vacuolar hydrolases. J Cell Biol. 1996 May;133(3):529–541. doi: 10.1083/jcb.133.3.529. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Dell'Angelica E. C., Klumperman J., Stoorvogel W., Bonifacino J. S. Association of the AP-3 adaptor complex with clathrin. Science. 1998 Apr 17;280(5362):431–434. doi: 10.1126/science.280.5362.431. [DOI] [PubMed] [Google Scholar]
  12. Erneux C., Govaerts C., Communi D., Pesesse X. The diversity and possible functions of the inositol polyphosphate 5-phosphatases. Biochim Biophys Acta. 1998 Dec 8;1436(1-2):185–199. doi: 10.1016/s0005-2760(98)00132-5. [DOI] [PubMed] [Google Scholar]
  13. Guarente L. Synthetic enhancement in gene interaction: a genetic tool come of age. Trends Genet. 1993 Oct;9(10):362–366. doi: 10.1016/0168-9525(93)90042-g. [DOI] [PubMed] [Google Scholar]
  14. Guo S., Stolz L. E., Lemrow S. M., York J. D. SAC1-like domains of yeast SAC1, INP52, and INP53 and of human synaptojanin encode polyphosphoinositide phosphatases. J Biol Chem. 1999 May 7;274(19):12990–12995. doi: 10.1074/jbc.274.19.12990. [DOI] [PubMed] [Google Scholar]
  15. Haffner C., Takei K., Chen H., Ringstad N., Hudson A., Butler M. H., Salcini A. E., Di Fiore P. P., De Camilli P. Synaptojanin 1: localization on coated endocytic intermediates in nerve terminals and interaction of its 170 kDa isoform with Eps15. FEBS Lett. 1997 Dec 15;419(2-3):175–180. doi: 10.1016/s0014-5793(97)01451-8. [DOI] [PubMed] [Google Scholar]
  16. Hirst J., Robinson M. S. Clathrin and adaptors. Biochim Biophys Acta. 1998 Aug 14;1404(1-2):173–193. doi: 10.1016/s0167-4889(98)00056-1. [DOI] [PubMed] [Google Scholar]
  17. Horazdovsky B. F., Davies B. A., Seaman M. N., McLaughlin S. A., Yoon S., Emr S. D. A sorting nexin-1 homologue, Vps5p, forms a complex with Vps17p and is required for recycling the vacuolar protein-sorting receptor. Mol Biol Cell. 1997 Aug;8(8):1529–1541. doi: 10.1091/mbc.8.8.1529. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Huang K. N., Symington L. S. Suppressors of a Saccharomyces cerevisiae pkc1 mutation identify alleles of the phosphatase gene PTC1 and of a novel gene encoding a putative basic leucine zipper protein. Genetics. 1995 Dec;141(4):1275–1285. doi: 10.1093/genetics/141.4.1275. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Jiang B., Ram A. F., Sheraton J., Klis F. M., Bussey H. Regulation of cell wall beta-glucan assembly: PTC1 negatively affects PBS2 action in a pathway that includes modulation of EXG1 transcription. Mol Gen Genet. 1995 Aug 21;248(3):260–269. doi: 10.1007/BF02191592. [DOI] [PubMed] [Google Scholar]
  20. Lemmon S. K., Jones E. W. Clathrin requirement for normal growth of yeast. Science. 1987 Oct 23;238(4826):504–509. doi: 10.1126/science.3116672. [DOI] [PubMed] [Google Scholar]
  21. Lemmon S. K., Pellicena-Palle A., Conley K., Freund C. L. Sequence of the clathrin heavy chain from Saccharomyces cerevisiae and requirement of the COOH terminus for clathrin function. J Cell Biol. 1991 Jan;112(1):65–80. doi: 10.1083/jcb.112.1.65. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Lowe M., Kreis T. E. Regulation of membrane traffic in animal cells by COPI. Biochim Biophys Acta. 1998 Aug 14;1404(1-2):53–66. doi: 10.1016/s0167-4889(98)00046-9. [DOI] [PubMed] [Google Scholar]
  23. Luo W. j., Chang A. Novel genes involved in endosomal traffic in yeast revealed by suppression of a targeting-defective plasma membrane ATPase mutant. J Cell Biol. 1997 Aug 25;138(4):731–746. doi: 10.1083/jcb.138.4.731. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Maeda T., Tsai A. Y., Saito H. Mutations in a protein tyrosine phosphatase gene (PTP2) and a protein serine/threonine phosphatase gene (PTC1) cause a synthetic growth defect in Saccharomyces cerevisiae. Mol Cell Biol. 1993 Sep;13(9):5408–5417. doi: 10.1128/mcb.13.9.5408. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Maeda T., Wurgler-Murphy S. M., Saito H. A two-component system that regulates an osmosensing MAP kinase cascade in yeast. Nature. 1994 May 19;369(6477):242–245. doi: 10.1038/369242a0. [DOI] [PubMed] [Google Scholar]
  26. Marcusson E. G., Horazdovsky B. F., Cereghino J. L., Gharakhanian E., Emr S. D. The sorting receptor for yeast vacuolar carboxypeptidase Y is encoded by the VPS10 gene. Cell. 1994 May 20;77(4):579–586. doi: 10.1016/0092-8674(94)90219-4. [DOI] [PubMed] [Google Scholar]
  27. Munn A. L., Silveira L., Elgort M., Payne G. S. Viability of clathrin heavy-chain-deficient Saccharomyces cerevisiae is compromised by mutations at numerous loci: implications for the suppression hypothesis. Mol Cell Biol. 1991 Aug;11(8):3868–3878. doi: 10.1128/mcb.11.8.3868. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Nothwehr S. F., Conibear E., Stevens T. H. Golgi and vacuolar membrane proteins reach the vacuole in vps1 mutant yeast cells via the plasma membrane. J Cell Biol. 1995 Apr;129(1):35–46. doi: 10.1083/jcb.129.1.35. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Payne G. S., Baker D., van Tuinen E., Schekman R. Protein transport to the vacuole and receptor-mediated endocytosis by clathrin heavy chain-deficient yeast. J Cell Biol. 1988 May;106(5):1453–1461. doi: 10.1083/jcb.106.5.1453. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Payne G. S., Hasson T. B., Hasson M. S., Schekman R. Genetic and biochemical characterization of clathrin-deficient Saccharomyces cerevisiae. Mol Cell Biol. 1987 Nov;7(11):3888–3898. doi: 10.1128/mcb.7.11.3888. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Payne G. S., Schekman R. Clathrin: a role in the intracellular retention of a Golgi membrane protein. Science. 1989 Sep 22;245(4924):1358–1365. doi: 10.1126/science.2675311. [DOI] [PubMed] [Google Scholar]
  32. Phan H. L., Finlay J. A., Chu D. S., Tan P. K., Kirchhausen T., Payne G. S. The Saccharomyces cerevisiae APS1 gene encodes a homolog of the small subunit of the mammalian clathrin AP-1 complex: evidence for functional interaction with clathrin at the Golgi complex. EMBO J. 1994 Apr 1;13(7):1706–1717. doi: 10.1002/j.1460-2075.1994.tb06435.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Pishvaee B., Payne G. S. Clathrin coats--threads laid bare. Cell. 1998 Nov 13;95(4):443–446. doi: 10.1016/s0092-8674(00)81611-6. [DOI] [PubMed] [Google Scholar]
  34. Rad M. R., Phan H. L., Kirchrath L., Tan P. K., Kirchhausen T., Hollenberg C. P., Payne G. S. Saccharomyces cerevisiae Apl2p, a homologue of the mammalian clathrin AP beta subunit, plays a role in clathrin-dependent Golgi functions. J Cell Sci. 1995 Apr;108(Pt 4):1605–1615. doi: 10.1242/jcs.108.4.1605. [DOI] [PubMed] [Google Scholar]
  35. Raymond C. K., Howald-Stevenson I., Vater C. A., Stevens T. H. Morphological classification of the yeast vacuolar protein sorting mutants: evidence for a prevacuolar compartment in class E vps mutants. Mol Biol Cell. 1992 Dec;3(12):1389–1402. doi: 10.1091/mbc.3.12.1389. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Reynolds T. B., Hopkins B. D., Lyons M. R., Graham T. R. The high osmolarity glycerol response (HOG) MAP kinase pathway controls localization of a yeast golgi glycosyltransferase. J Cell Biol. 1998 Nov 16;143(4):935–946. doi: 10.1083/jcb.143.4.935. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Robinson J. S., Klionsky D. J., Banta L. M., Emr S. D. Protein sorting in Saccharomyces cerevisiae: isolation of mutants defective in the delivery and processing of multiple vacuolar hydrolases. Mol Cell Biol. 1988 Nov;8(11):4936–4948. doi: 10.1128/mcb.8.11.4936. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Robinson M. S. Coats and vesicle budding. Trends Cell Biol. 1997 Mar;7(3):99–102. doi: 10.1016/S0962-8924(96)10048-9. [DOI] [PubMed] [Google Scholar]
  39. Roeder A. D., Hermann G. J., Keegan B. R., Thatcher S. A., Shaw J. M. Mitochondrial inheritance is delayed in Saccharomyces cerevisiae cells lacking the serine/threonine phosphatase PTC1. Mol Biol Cell. 1998 Apr;9(4):917–930. doi: 10.1091/mbc.9.4.917. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Rothman J. E., Wieland F. T. Protein sorting by transport vesicles. Science. 1996 Apr 12;272(5259):227–234. doi: 10.1126/science.272.5259.227. [DOI] [PubMed] [Google Scholar]
  41. Schmid S. L. Clathrin-coated vesicle formation and protein sorting: an integrated process. Annu Rev Biochem. 1997;66:511–548. doi: 10.1146/annurev.biochem.66.1.511. [DOI] [PubMed] [Google Scholar]
  42. Seaman M. N., McCaffery J. M., Emr S. D. A membrane coat complex essential for endosome-to-Golgi retrograde transport in yeast. J Cell Biol. 1998 Aug 10;142(3):665–681. doi: 10.1083/jcb.142.3.665. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Seeger M., Payne G. S. A role for clathrin in the sorting of vacuolar proteins in the Golgi complex of yeast. EMBO J. 1992 Aug;11(8):2811–2818. doi: 10.1002/j.1460-2075.1992.tb05348.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Sever S., Muhlberg A. B., Schmid S. L. Impairment of dynamin's GAP domain stimulates receptor-mediated endocytosis. Nature. 1999 Apr 8;398(6727):481–486. doi: 10.1038/19024. [DOI] [PubMed] [Google Scholar]
  45. 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]
  46. Silveira L. A., Wong D. H., Masiarz F. R., Schekman R. Yeast clathrin has a distinctive light chain that is important for cell growth. J Cell Biol. 1990 Oct;111(4):1437–1449. doi: 10.1083/jcb.111.4.1437. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Simpson F., Bright N. A., West M. A., Newman L. S., Darnell R. B., Robinson M. S. A novel adaptor-related protein complex. J Cell Biol. 1996 May;133(4):749–760. doi: 10.1083/jcb.133.4.749. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Singer-Krüger B., Nemoto Y., Daniell L., Ferro-Novick S., De Camilli P. Synaptojanin family members are implicated in endocytic membrane traffic in yeast. J Cell Sci. 1998 Nov;111(Pt 22):3347–3356. doi: 10.1242/jcs.111.22.3347. [DOI] [PubMed] [Google Scholar]
  49. Smith A. M., Archer J. E., Solomon F. Regulation of tubulin polypeptides and microtubule function: Luv1p [correction of Rki1p] interacts with the beta-tubulin binding protein Rbl2p. Chromosoma. 1998 Dec;107(6-7):471–478. doi: 10.1007/s004120050331. [DOI] [PubMed] [Google Scholar]
  50. Srinivasan S., Seaman M., Nemoto Y., Daniell L., Suchy S. F., Emr S., De Camilli P., Nussbaum R. Disruption of three phosphatidylinositol-polyphosphate 5-phosphatase genes from Saccharomyces cerevisiae results in pleiotropic abnormalities of vacuole morphology, cell shape, and osmohomeostasis. Eur J Cell Biol. 1997 Dec;74(4):350–360. [PubMed] [Google Scholar]
  51. Stepp J. D., Pellicena-Palle A., Hamilton S., Kirchhausen T., Lemmon S. K. A late Golgi sorting function for Saccharomyces cerevisiae Apm1p, but not for Apm2p, a second yeast clathrin AP medium chain-related protein. Mol Biol Cell. 1995 Jan;6(1):41–58. doi: 10.1091/mbc.6.1.41. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Stevens T., Esmon B., Schekman R. Early stages in the yeast secretory pathway are required for transport of carboxypeptidase Y to the vacuole. Cell. 1982 Sep;30(2):439–448. doi: 10.1016/0092-8674(82)90241-0. [DOI] [PubMed] [Google Scholar]
  53. Stolz L. E., Huynh C. V., Thorner J., York J. D. Identification and characterization of an essential family of inositol polyphosphate 5-phosphatases (INP51, INP52 and INP53 gene products) in the yeast Saccharomyces cerevisiae. Genetics. 1998 Apr;148(4):1715–1729. doi: 10.1093/genetics/148.4.1715. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Sweitzer S. M., Hinshaw J. E. Dynamin undergoes a GTP-dependent conformational change causing vesiculation. Cell. 1998 Jun 12;93(6):1021–1029. doi: 10.1016/s0092-8674(00)81207-6. [DOI] [PubMed] [Google Scholar]
  55. Tang H. Y., Munn A., Cai M. EH domain proteins Pan1p and End3p are components of a complex that plays a dual role in organization of the cortical actin cytoskeleton and endocytosis in Saccharomyces cerevisiae. Mol Cell Biol. 1997 Aug;17(8):4294–4304. doi: 10.1128/mcb.17.8.4294. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Traub L. M., Kornfeld S. The trans-Golgi network: a late secretory sorting station. Curr Opin Cell Biol. 1997 Aug;9(4):527–533. doi: 10.1016/s0955-0674(97)80029-4. [DOI] [PubMed] [Google Scholar]
  57. Vater C. A., Raymond C. K., Ekena K., Howald-Stevenson I., Stevens T. H. The VPS1 protein, a homolog of dynamin required for vacuolar protein sorting in Saccharomyces cerevisiae, is a GTPase with two functionally separable domains. J Cell Biol. 1992 Nov;119(4):773–786. doi: 10.1083/jcb.119.4.773. [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. Vida T. A., Emr S. D. A new vital stain for visualizing vacuolar membrane dynamics and endocytosis in yeast. J Cell Biol. 1995 Mar;128(5):779–792. doi: 10.1083/jcb.128.5.779. [DOI] [PMC free article] [PubMed] [Google Scholar]
  59. Wendland B., Emr S. D. Pan1p, yeast eps15, functions as a multivalent adaptor that coordinates protein-protein interactions essential for endocytosis. J Cell Biol. 1998 Apr 6;141(1):71–84. doi: 10.1083/jcb.141.1.71. [DOI] [PMC free article] [PubMed] [Google Scholar]
  60. Wendland B., McCaffery J. M., Xiao Q., Emr S. D. A novel fluorescence-activated cell sorter-based screen for yeast endocytosis mutants identifies a yeast homologue of mammalian eps15. J Cell Biol. 1996 Dec;135(6 Pt 1):1485–1500. doi: 10.1083/jcb.135.6.1485. [DOI] [PMC free article] [PubMed] [Google Scholar]
  61. Whitters E. A., Cleves A. E., McGee T. P., Skinner H. B., Bankaitis V. A. SAC1p is an integral membrane protein that influences the cellular requirement for phospholipid transfer protein function and inositol in yeast. J Cell Biol. 1993 Jul;122(1):79–94. doi: 10.1083/jcb.122.1.79. [DOI] [PMC free article] [PubMed] [Google Scholar]
  62. Wilsbach K., Payne G. S. Dynamic retention of TGN membrane proteins in Saccharomyces cerevisiae. Trends Cell Biol. 1993 Dec;3(12):426–432. doi: 10.1016/0962-8924(93)90031-u. [DOI] [PubMed] [Google Scholar]
  63. van Zyl W. H., Wills N., Broach J. R. A general screen for mutant of Saccharomyces cerevisiae deficient in tRNA biosynthesis. Genetics. 1989 Sep;123(1):55–68. doi: 10.1093/genetics/123.1.55. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Genetics are provided here courtesy of Oxford University Press

RESOURCES