The Yeast Inositol Polyphosphate 5-Phosphatases Inp52p and Inp53p Translocate to Actin Patches following Hyperosmotic Stress: Mechanism for Regulating Phosphatidylinositol 4,5-Bisphosphate at Plasma Membrane Invaginations

REFERENCES

• Adams, A. E., and Pringle, J. R.. 1984. Relationship of actin and tubulin distribution to bud growth in wild-type and morphogenetic-mutant Saccharomyces cerevisiae. J. Cell Biol. 98:934–945
   PubMed Web of Science ®Google Scholar
• Amatruda, J. F., and Cooper, J. A.. 1992. Purification, characterization, and immunofluorescence localization of Saccharomyces cerevisiae capping protein. J. Cell Biol. 117:1067–1076
   PubMedGoogle Scholar
• Ausubel, F. M., Brent, R., Kingston, R. E., Moore, D. D., Seidman, J. G., Smith, J. A., and Struhl, K.. 1991. Current protocols in molecular biology. John Wiley & Sons, Inc., New York, N.Y
   Google Scholar
• Ayscough, K. R., Stryker, J., Pokala, N., Sanders, M., Crews, P., and Drubin, D. G.. 1997. High rates of actin filament turnover in budding yeast and roles for actin in establishment and maintenance of cell polarity revealed using the actin inhibitor latrunculin-A. J. Cell Biol. 137:399–416
   PubMed Web of Science ®Google Scholar
• Chant, J., and Pringle, J. R.. 1995. Patterns of bud-site selection in the yeast Saccharomyces cerevisiae. J. Cell Biol. 129:751–765
   PubMed Web of Science ®Google Scholar
• Chowdhury, S., Smith, K. W., and Gustin, M. C.. 1992. Osmotic stress and the yeast cytoskeleton: phenotype-specific suppression of an actin mutation. J. Cell Biol. 118:561–571
   PubMed Web of Science ®Google Scholar
• Chung, J. K., Sekiya, F., Kang, H. S., Lee, C., Han, J. S., Kim, S. R., Bae, Y. S., Morris, A. J., and Rhee, S. G.. 1997. Synaptojanin inhibition of phospholipase D activity by hydrolysis of phosphatidylinositol 4,5-bisphosphate. J. Biol. Chem. 272:15980–15985
   PubMed Web of Science ®Google Scholar
• Cleves, A. E., Novick, P. J., and Bankaitis, V. A.. 1989. Mutations in the SAC1 gene suppress defects in yeast Golgi and yeast actin function. J. Cell Biol. 109:2939–2950
   PubMedGoogle Scholar
• Connolly, T. M., Bross, T. E., and Majerus, P. W.. 1985. Isolation of a phosphomonoesterase from human platelets that specifically hydrolyzes the 5-phosphate of inositol 1,4,5-trisphosphate. J. Biol. Chem. 260:7868–7874
   PubMed Web of Science ®Google Scholar
• Cooke, F. T., Dove, S. K., McEwen, R. K., Painter, G., Holmes, A. B., Hall, M. N., Michell, R. H., and Parker, P. J.. 1998. The stress-activated phosphatidylinositol 3-phosphate 5-kinase Fab1p is essential for vacuole function in S. cerevisiae. Curr. Biol. 8:1219–1222
   PubMed Web of Science ®Google Scholar
• Corvera, S., D'Arrigo, A., and Stenmark, H.. 1999. Phosphoinositides in membrane traffic. Curr. Opin. Cell Biol. 11:460–465
   PubMedGoogle Scholar
• De Camilli, P., Emr, S. D., McPherson, P. S., and Novick, P.. 1996. Phosphoinositides as regulators in membrane traffic. Science 271:1533–1539
   PubMed Web of Science ®Google Scholar
• Dove, S. K., Cooke, F. T., Douglas, M. R., Sayers, L. G., Parker, P. J., and Michell, R. H.. 1997. Osmotic stress activates phosphatidylinositol-3,5-bisphosphate synthesis. Nature 390:187–192
   PubMed Web of Science ®Google Scholar
• Downes, C. P., Mussat, M. C., and Michell, R. H.. 1982. The inositol trisphosphate phosphomonoesterase of the human erythrocyte membrane. Biochem. J. 203:169–177
   PubMed Web of Science ®Google Scholar
• Gabriel, M., and Kopecka, M.. 1995. Disruption of the actin cytoskeleton in budding yeast results in formation of an aberrant cell wall. Microbiology 141:891–899
   PubMedGoogle Scholar
• Guo, S., Stolz, L. E., Lemrow, S. M., and York, J. D.. 1999. SAC1-like domains of yeast SAC1, INP52, and INP53 and of human synaptojanin encode polyphosphoinositide phosphatases. J. Biol. Chem. 274:12990–12995
   PubMedGoogle Scholar
• Haarer, B. K., Lillie, S. H., Adams, A. E., Magdolen, V., Bandlow, W., and Brown, S. S.. 1990. Purification of profilin from Saccharomyces cerevisiae and analysis of profilin-deficient cells. J. Cell Biol. 110:105–114
   PubMed Web of Science ®Google Scholar
• Hill, K. L., Catlett, N. L., and Weisman, L. S.. 1996. Actin and myosin function in directed vacuole movement during cell division in Saccharomyces cerevisiae. J. Cell Biol. 135:1535–1549
   PubMedGoogle Scholar
• Iida, K., Moriyama, K., Matsumoto, S., Kawasaki, H., Nishida, E., and Yahara, I.. 1993. Isolation of a yeast essential gene, COF1, that encodes a homologue of mammalian cofilin, a low-M(r) actin-binding and depolymerizing protein. Gene 124:115–120
   PubMedGoogle Scholar
• Jackson, S. P., Schoenwaelder, S. M., Matzaris, M., Brown, S., and Mitchell, C. A.. 1995. Phosphatidylinositol 3,4,5-trisphosphate is a substrate for the 75 kDa inositol polyphosphate 5-phosphatase and a novel 5-phosphatase which forms a complex with the p85/p110 form of phosphoinositide 3-kinase. EMBO J. 14:4490–4500
   PubMedGoogle Scholar
• Johnston, G. C., Prendergast, J. A., and Singer, R. A.. 1991. The Saccharomyces cerevisiae MYO2 gene encodes an essential myosin for vectorial transport of vesicles. J. Cell Biol. 113:539–551
   PubMed Web of Science ®Google Scholar
• Jones, J. S., and Prakash, L.. 1990. Yeast Saccharomyces cerevisiae selectable markers in pUC18 polylinkers. Yeast 6:363–336
   PubMedGoogle Scholar
• Karpova, T. S., McNally, J. G., Moltz, S. L., and Cooper, J. A.. 1998. Assembly and function of the actin cytoskeleton of yeast: relationships between cables and patches. J. Cell Biol. 142:1501–1517
   PubMed Web of Science ®Google Scholar
• Kilmartin, J. V., and Adams, A. E.. 1984. Structural rearrangements of tubulin and actin during the cell cycle of the yeast Saccharomyces. J. Cell Biol. 98:922–933
   PubMed Web of Science ®Google Scholar
• Kopecka, M., and Gabriel, M.. 1995. Actin cortical cytoskeleton and cell wall synthesis in regenerating protoplasts of the Saccharomyces cerevisiae actin mutant DBY 1693. Microbiology 141:1289–1299
   PubMedGoogle Scholar
• Laemmli, U. K.. 1970. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227:680–685
   PubMed Web of Science ®Google Scholar
• Longtine, M. S., McKenzie, A.III, Demarini, D. J., Shah, N. G., Wach, A., Brachat, A., Philippsen, P., and Pringle, J. R.. 1998. Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae. Yeast 14:953–961
   PubMed Web of Science ®Google Scholar
• Majerus, P. W.. 1996. Inositols do it all. Genes Dev. 10:1051–1053
   PubMedGoogle Scholar
• Matzaris, M., Jackson, S. P., Laxminarayan, K. M., Speed, C. J., and Mitchell, C. A.. 1994. Identification and characterization of the phosphatidylinositol-(4, 5)-bisphosphate 5-phosphatase in human platelets. J. Biol. Chem. 269:3397–3402
   PubMedGoogle Scholar
• Mitchell, C. A., Brown, S., Campbell, J. K., Munday, A. D., and Speed, C. J.. 1996. Regulation of second messengers by the inositol polyphosphate 5-phosphatases. Biochem. Soc. Trans. 24:994–1000
   PubMedGoogle Scholar
• Mitchell, C. A., Connolly, T. M., and Majerus, P. W.. 1989. Identification and isolation of a 75-kDa inositol polyphosphate-5-phosphatase from human platelets. J. Biol. Chem. 264:8873–8877
   PubMed Web of Science ®Google Scholar
• Mulholland, J., Konopka, J., Singer-Kruger, B., Zerial, M., and Botstein, D.. 1999. Visualization of receptor-mediated endocytosis in yeast. Mol. Biol. Cell 10:799–817
   PubMedGoogle Scholar
• Mulholland, J., Preuss, D., Moon, A., Wong, A., Drubin, D., and Botstein, D.. 1994. Ultrastructure of the yeast actin cytoskeleton and its association with the plasma membrane. J. Cell Biol. 125:381–391
   PubMed Web of Science ®Google Scholar
• Nemoto, Y., and De Camilli, P.. 1999. Recruitment of an alternatively spliced form of synaptojanin 2 to mitochondria by the interaction with the PDZ domain of a mitochondrial outer membrane protein. EMBO J. 18:2991–3006
   PubMedGoogle Scholar
• Novick, P., Osmond, B. C., and Botstein, D.. 1989. Suppressors of yeast actin mutations. Genetics 121:659–674
   PubMedGoogle Scholar
• Patton, J. L., and Lester, R. L.. 1992. Phosphatidylinositol phosphate, phosphatidylinositol bisphosphate, and the phosphoinositol sphingolipids are found in the plasma membrane and stimulate the plasma membrane H(+)-ATPase of Saccharomyces cerevisiae. Arch. Biochem. Biophys. 292:70–76
   PubMedGoogle Scholar
• Penman, J., and Penman, S.. 1997. Resinless section electron microscopy reveals the yeast cytoskeleton. Proc. Natl. Acad. Sci. USA 94:3732–3735
   PubMedGoogle Scholar
• Pruyne, D., and Bretscher, A.. 2000. Polarization of cell growth in yeast. J. Cell Sci. 113:571–585
   PubMed Web of Science ®Google Scholar
• Raucher, D., Stauffer, T., Chen, W., Shen, K., Guo, S., York, J. D., Sheetz, M. P., and Meyer, T.. 2000. Phosphatidylinositol 4,5-bisphosphate functions as a second messenger that regulates cytoskeleton-plasma membrane adhesion. Cell 100:221–228
   PubMedGoogle Scholar
• Sikorski, R. S., and Hieter, P.. 1989. A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae. Genetics 122:19–27
   PubMed Web of Science ®Google Scholar
• Singer-Kruger, B., Nemoto, Y., Daniell, L., Ferro-Novick, S., and De Camilli, P.. 1998. Synaptojanin family members are implicated in endocytic membrane traffic in yeast. J. Cell Sci. 111:3347–3356
   PubMedGoogle Scholar
• Srinivasan, S., Seaman, M., Nemoto, Y., Daniell, L., Suchy, S. F., Emr, S., De Camilli, P., and Nussbaum, R.. 1997. 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. 74:350–360
   PubMedGoogle Scholar
• Stolz, L. E., Huynh, C. V., Thorner, J., and York, J. D.. 1998. Identification and characterization of an essential family of inositol polyphosphate 5-phosphatases (INP51, INP52 and INP53 gene products) in the yeast Saccharomyces cerevisiae. Genetics 148:1715–1729
   PubMedGoogle Scholar
• Stolz, L. E., Kuo, W. J., Longchamps, J., Sekhon, M. K., and York, J. D.. 1998. INP51, a yeast inositol polyphosphate 5-phosphatase required for phosphatidylinositol 4,5-bisphosphate homeostasis and whose absence confers a cold-resistant phenotype. J. Biol. Chem. 273:11852–11861
   PubMedGoogle Scholar
• Toker, A.. 1998. The synthesis and cellular roles of phosphatidylinositol 4,5-bisphosphate. Curr. Opin. Cell Biol. 10:254–261
   PubMedGoogle Scholar
• Towbin, H., Staehelin, T., and Gordon, J.. 1979. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc. Natl. Acad. Sci. USA 76:4350–4354
   PubMed Web of Science ®Google Scholar
• Waddle, J. A., Karpova, T. S., Waterston, R. H., and Cooper, J. A.. 1996. Movement of cortical actin patches in yeast. J. Cell Biol. 132:861–870
   PubMed Web of Science ®Google Scholar
• Whisstock, J. C., Romero S., Gurung R., Nandurkar H., Ooms L., Bottomley S. P., and Mitchell C. A.. The inositol polyphosphate 5-phosphatases and the apurinic/apyrimidinic base excision repair endonucleases share a common mechanism for catalysis. J. Biol. Chem., in press.
   Google Scholar
• Whitters, E. A., Cleves, A. E., McGee, T. P., Skinner, H. B., and Bankaitis, V. A.. 1993. SAC1p is an integral membrane protein that influences the cellular requirement for phospholipid transfer protein function and inositol in yeast. J. Cell Biol. 122:79–94
   PubMed Web of Science ®Google Scholar
• Yamamoto, A., DeWald, D. B., Boronenkov, I. V., Anderson, R. A., Emr, S. D., and Koshland, D.. 1995. Novel PI(4)P 5-kinase homologue, Fab1p, essential for normal vacuole function and morphology in yeast. Mol. Biol. Cell 6:525–539
   PubMed Web of Science ®Google Scholar