The EH-Domain-Containing Protein Pan1 Is Required for Normal Organization of the Actin Cytoskeleton in Saccharomyces cerevisiae

REFERENCES

• Adams, A. E. M., D. Botstein, and D. G. Drubin. 1991. Requirement of yeast fimbrin for actin organization and morphogenesis in vivo. Nature (London) 354:404–408.
   PubMedGoogle Scholar
• Adams, A. E. M., and J. R. Pringle. 1984. Relationship of actin and tubulin distribution to bud growth in wild-type and morphogenetic-mutant Saccha-romyces cerevisiae. J. Cell Biol. 98:934–945.
   PubMed Web of Science ®Google Scholar
• Amatruda, J. F., J. F. Cannon, K. Tatchell, C. Hug, and J. A. Cooper. 1992. Disruption of the actin cytoskeleton in yeast capping protein mutants. Nature (London) 344:352–354.
   Google Scholar
• Babu, Y. S., C. E. Bugg, and W. J. Cook. 1988. Structure of calmodulin refined at 2.2 A resolution. J. Mol. Biol. 204:191–204.
   PubMed Web of Science ®Google Scholar
• Benedetti, H., S. Raths, F. Crausaz, and H. Riezman. 1994. The END3 gene encodes a protein that is required for the internalization step of endocytosis and for actin cytoskeleton organization in yeast. Mol. Biol. Cell 5:1023–1037.
   PubMed Web of Science ®Google Scholar
• Benmerah, A., J. Gagnon, B. Begue, B. Megarbane, A. Dautry-Varsat, and N. Cerf-Bensussan. 1995. The tyrosine kinase substrate eps15 is constitutively associated with the plasma membrane adaptor AP-2. J. Cell Biol. 131:1831–1838.
   PubMedGoogle Scholar
• Benton, B. K., A. H. Tinkelenberg, D. Jean, S. D. Plump, and F. R. Cross. 1993. Genetic analysis of Cln/Cdc28 regulation of cell morphogenesis in budding yeast. EMBO J. 12:5267–5275.
   PubMedGoogle Scholar
• Boeck, R., S. Tarun, Jr., M. Rieger, J. A. Deardorff, S. Muller-Auer, and A. B. Sachs. 1996. The yeast Pan2 protein is required for poly(A)-binding protein-stimulated poly(A)-nuclease activity. J. Biol. Chem. 271:432–438.
   PubMedGoogle Scholar
• Cai, M., and R. W. Davis. 1990. Yeast centromere binding protein CBF1, of the helix-loop-helix protein family, is required for chromosome stability and methionine prototrophy. Cell 61:437–446.
   PubMed Web of Science ®Google Scholar
• Chant, J. 1994. Cell polarity in yeast. Trends Genet. 10:328–333.
   PubMed Web of Science ®Google Scholar
• Chant, J., and I. Herskowitz. 1991. Genetic control of bud site selection in yeast by a set of gene products that constitute a morphogenetic pathway. Cell 65:1203–1212.
   PubMedGoogle Scholar
• Chant, J., and J. R. Pringle. 1995. Patterns of bud-site selection in the yeast Saccharomyces cerevisiae. J. Cell Biol. 129:751–765.
   PubMed Web of Science ®Google Scholar
• Christianson, T. W., R. S. Sikorski, M. Dante, J. H. Shero, and P. Hieter. 1992. Multifunctional yeast high-copy-number shuttle vectors. Gene 110:119–122.
   PubMed Web of Science ®Google Scholar
• Cid, V. J., A. Duran, F. D. Rey, M. P. Snyder, C. Nombela, and M. Sanchez. 1995. Molecular basis of cell integrity and morphogenesis in Saccharomyces cerevisiae. Microbiol. Rev. 59:345–386.
   PubMedGoogle Scholar
• Cleves, A. E., P. J. Novick, and V. A. Bankaitis. 1989. Mutation in the SAC1 gene supress defects in yeast golgi and yeast actin function. J. Cell Biol. 109:2939–2950.
   PubMedGoogle Scholar
• Cooper, J. A. 1987. Effects of cytochalasin and phalloidin on actin. J. Cell Biol. 105:1473–1478.
   PubMed Web of Science ®Google Scholar
• Cross, F. R. 1995. Starting the cell cycle: what’s the point? Curr. Opin. Cell Biol. 7:790–797.
   PubMed Web of Science ®Google Scholar
• Cvrckova, F., C. De Virgilio, E. Manser, J. R. Pringle, and K. Nasmyth. 1995. Ste20-like protein kinases are required for normal localization of cell growth and for cytokinesis in budding yeast. Genes Dev. 9:1817–1830.
   PubMedGoogle Scholar
• Cvrckova, F., and K. Nasmyth. 1993. Yeast G1 cyclins CLN1 and CLN2 and a GAP-like protein have a role in bud formation. EMBO J. 12:5277–5286.
   PubMed Web of Science ®Google Scholar
• Drubin, D. G., H. D. Jones, and K. F. Wertman. 1993. Actin structure and function: roles in mitochondrial organization and morphogenesis in budding yeast and identification of the phalloidin-binding site. Mol. Biol. Cell 4:1277–1294.
   PubMedGoogle Scholar
• Drubin, D. G., J. Mulholland, Z. M. Zhu, and D. Botstein. 1990. Homology of a yeast actin-binding protein to signal transduction proteins and myosin-I. Nature (London) 343:388–390.
   Google Scholar
• Drubin, D. G., and W. J. Nelson. 1996. Origins of cell polarity. Cell 84:335–344.
   PubMed Web of Science ®Google Scholar
• Fazioli, F., L. Minichiello, B. Maťoškovā, W. T. Wong, and P. P. Di Fiore. 1993. eps15, a novel tyrosine kinase substrate, exhibits transforming activity. Mol. Cell. Biol. 13:5814–5828.
   PubMed Web of Science ®Google Scholar
• Geiser, J. R., D. van Tuinen, S. E. Brockerhoff, M. M. Neff, and T. N. Davis. 1991. Can calmodulin function without binding calcium? Cell 65:949–959.
   PubMed Web of Science ®Google Scholar
• Haarer, N. K., S. H. Lillie, A. E. M. Adams, A. E. M. Magdolen, W. Bandlow, and S. S. Brown. 1990. Purification of profilin from Saccharomyces cerevisiae and analysis of profilin-deficient cells. J. Cell Biol. 110:105–114.
   PubMedGoogle Scholar
• Harold, F. M. 1990. To shape a cell: an inquiry into the causes of morphogenesis of microorganisms. Microbiol. Rev. 54:381–431.
   PubMedGoogle Scholar
• Hartwell, L. H., R. K. Mortimer, J. Culotti, and M. Culotti. 1973. Genetic control of the cell division cycle in yeast: V. Genetic analysis of cdc mutants. Genetics 74:267–286.
   PubMed Web of Science ®Google Scholar
• Hereford, L. M., and L. H. Hartwell. 1973. Role of protein synthesis in the replication of yeast DNA. Nature (London) New Biol. 244:129–131.
   PubMedGoogle Scholar
• Holtzman, D. A., S. Yang, and D. G. Drubin. 1993. Synthetic-lethal interactions identify two novel genes, SLA1 and SLA2, that control membrane cytoskeleton assembly in Saccharomyces cerevisiae. J. Cell Biol. 122:635–644.
   PubMed Web of Science ®Google Scholar
• Howell, E. A., M. A. McAlear, D. Rose, and C. Holm. 1994. CDC44, a putative nucleotide-binding protein required for cell cycle progression that has homology to subunits of replication factor C. Mol. Cell. Biol. 14:255–267.
   PubMedGoogle Scholar
• Ito, H., Y. Jukada, K. Murata, and A. Kinura. 1983. Transformation of intact yeast cells treated with alkali cations. J. Bacteriol. 153:163–168.
   PubMed Web of Science ®Google Scholar
• Johnston, L. H., S. L. Eberly, J. W. Chapman, H. Araki, and A. Sugino. 1990. The product of the Saccharomyces cerevisiae cell cycle gene DBF2 has homology with protein kinases and is periodically expressed in the cell cycle. Mol. Cell. Biol. 10:1358–1366.
   PubMedGoogle Scholar
• Kellogg, D. R., and A. W. Murray. 1995. NAP1 acts with Clb2 to perform mitotic functions and to suppress polar bud growth in budding yeast. J. Cell Biol. 130:675–685.
   PubMedGoogle Scholar
• Kilmartin, J. V., and A. E. M. Adams. 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
• Kubler, E., and H. Riezman. 1993. Actin and fimbrin are required for the internalization step of endocytosis in yeast. EMBO J. 12:2855–2862.
   PubMed Web of Science ®Google Scholar
• Kuchler, K., H. G. Dohlman, and J. Thorner. 1993. The a-factor transporter (STE6 gene product) and cell polarity in the yeast Saccharomyces cerevisiae. J. Cell Biol. 120:1203–1215.
   PubMedGoogle Scholar
• Lew, D. J., and S. I. Reed. 1993. Morphogenesis in the yeast cell cycle: regulation by Cdc28 and cyclins. J. Cell Biol. 120:1305–1320.
   PubMed Web of Science ®Google Scholar
• Lew, D. J., and S. I. Reed. 1995. Cell cycle control of morphogenesis in budding yeast. Curr. Opin. Genet. Dev. 5:17–23.
   PubMed Web of Science ®Google Scholar
• Liu, H., and A. Bretscher. 1989. Disruption of the single tropomyosin gene in yeast results in the disappearance of actin cables from the cytoskeleton. Cell 57:233–242.
   PubMedGoogle Scholar
• Madden, K., and M. Snyder. 1992. Specification of sites for polarized growth in Saccharomyces cerevisiae and the influence of external factors on site selection. Mol. Biol. Cell 3:1025–1035.
   PubMedGoogle Scholar
• Mazzoni, C., P. Zarzov, A. Rambourg, and C. Mann. 1993. The SLT2 (MPK1) MAP kinase homolog is involved in polarized cell growth in Saccharomyces cerevisiae. J. Cell Biol. 123:1821–1833.
   PubMedGoogle Scholar
• Munn, A. L., B. J. Stevenson, M. I. Geli, and H. Riezman. 1995. end5, end6, and end7: mutations that cause actin delocalization and block the internalization step of endocytosis in Saccharomyces cerevisiae. Mol. Biol. Cell 6:1721–1742.
   PubMed Web of Science ®Google Scholar
• Nasmyth, K. 1993. Control of the yeast cell cycle by the Cdc28 protein kinase. Curr. Opin. Cell Biol. 5:166–179.
   PubMed Web of Science ®Google Scholar
• Novick, P., and D. Botstein. 1985. Phenotypic analysis of temperature-sensitive yeast actin mutants. Cell 40:405–416.
   PubMedGoogle Scholar
• Novick, P., B. C. Osmond, and D. Botstein. 1989. Suppressors of yeast actin mutations. Genetics 121:659–674.
   PubMedGoogle Scholar
• Palmer, R. E., D. S. Sullivan, T. Huffaker, and D. Koshland. 1992. Role of astral microtubules and actin in spindle orientation and migration in the budding yeast, Saccharomyces cerevisiae. J. Cell Biol. 119:583–593.
   PubMedGoogle Scholar
• Pawson, T. 1995. Protein modules and signalling networks. Nature (London) 373:573–580.
   PubMed Web of Science ®Google Scholar
• Pringle, J. R., and L. H. Hartwell. 1981. The Saccharomyces cerevisiae cell cycle, p. 97–142. In J. N. Strathern, E. W. Jones, and J. R. Broach (ed.), The molecular biology of the yeast Saccharomyces: life cycle and inheritance. Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.
   Google Scholar
• Rose, M. D., P. Novick, J. H. Thomas, D. Botstein, and G. R. Fink. 1987. A Saccharomyces cerevisiae genomic plasmid bank based on a centromere-containing shuttle vector. Gene 60:237–243.
   PubMed Web of Science ®Google Scholar
• Rose, M. D., F. Winston, and P. Hieter. 1990. Methods in yeast genetics: a laboratory course manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.
   Google Scholar
• Rothstein, R. 1991. Targeting, disruption, replacement, and allele rescue: integrative DNA transformation in yeast. Methods Enzymol. 194:281–301.
   PubMed Web of Science ®Google Scholar
• Sachs, A. B., and J. A. Deardorff. 1992. Translation initiation requires the PAB-dependent poly(A) ribonuclease in yeast. Cell 70:961–973.
   PubMedGoogle Scholar
• Sachs, A. B., and J. A. Deardorff. 1995. Erratum. Cell 83:1059.
   PubMedGoogle Scholar
• Sambrook, J., E. F. Fritsch, and T. Maniatis. 1989. Molecular cloning: a laboratory manual, 2nd ed. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.
   Google Scholar
• Schwob, E., T. Bohm, M. D. Mendenhall, and K. Nasmyth. 1994. The B-type cyclin kinase inhibitor p40SIC1 controls the G1 to S transition in S. cerevisiae. Cell 79:233–244.
   PubMed Web of Science ®Google Scholar
• Sikorski, R. S., and P. Hieter. 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
• Surana, U., H. Robitsch, C. Price, T. Schuster, I. Fitch, A. B. Futcher, and K. Nasmyth. 1991. The role of CDC28 and cyclins during mitosis in the budding yeast S. cerevisiae. Cell 65:145–161.
   PubMed Web of Science ®Google Scholar
• Thompson, D. W. 1961. On growth and form. Abridged [J. T. Bonner (ed.)]. Cambridge University Press, London.
   Google Scholar
• Tyers, M., G. Tokiwa, R. Nash, and B. Futcher. 1992. The Cln3-Cdc28 kinase complex of S. cerevisiae is regulated by proteolysis and phosphorylation. EMBO J. 11:1773–1784.
   PubMedGoogle Scholar
• Voss, H., J. Tamames, C. Teodoru, A. Valencia, C. Sensen, S. Wiemann, C. Schwager, J. Zimmermann, C. Sander, and W. Ansorge. 1995. Nucleotide sequence and analysis of the centromeric region of yeast chromosome IX. Yeast 11:61–78.
   PubMedGoogle Scholar
• Wong, W. T., M. H. Kraus, F. Carlomagno, A. Zelano, T. Druck, C. M. Croce, K. Huebner, and P. P. Di Fiore. 1994. The human eps15 gene, encoding a tyrosine kinase substrate, is conserved in evolution and maps to 1p31-p32. Oncogene 9:1591–1597.
   PubMedGoogle Scholar
• Wong, W. T., C. Schumacher, A. E. Salcini, A. Romano, P. Castagnino, P. G. Pelicci, and P. P. Di Fiore. 1995. A protein-binding domain, EH, identified in the receptor tyrosine kinase substrate Eps15 and conserved in evolution. Proc. Natl. Acad. Sci. USA 92:9530–9534.
   PubMedGoogle Scholar
• Yu, F., H. Sun, P. A. Janmey, and H. L. Yin. 1992. Identification of a polyphosphoinositide-binding sequence in an actin monomer-binding domain of gelsolin. J. Biol. Chem. 267:14616–14621.
   PubMed Web of Science ®Google Scholar
• Zarzov, P., C. Mazzoni, and C. Mann. 1996. The SLT2(MPK1) MAP kinase is activated during periods of polarized cell growth in yeast. EMBO J. 15:83–91.
   PubMed Web of Science ®Google Scholar
• Zoladek, T., G. Vaduva, L. A. Hunter, M. Boguta, B. D. Go, N. C. Martin, and N. K. Hopper. 1995. Mutations altering the mitochondrial-cytoplasmic distribution of Mod5p implicate the actin cytoskeleton and mRNA 3′ ends and/or protein synthesis in mitochondrial delivery. Mol. Cell. Biol. 15:6884–6894.
   PubMedGoogle Scholar