Literature DB >> 6998984

Localized secretion of acid phosphatase reflects the pattern of cell surface growth in Saccharomyces cerevisiae.

C Field, R Schekman.   

Abstract

Secretion of cell wall-bound acid phosphatase by Saccharomyces cerevisiae occurs along a restricted portion of the cell surface. Acid phosphatase activity produced during derepressed synthesis on a phosphate-limited growth medium is detected with an enzyme-specific stain and is localized initially to the bud portion of a dividing cell. After two to three generations of phosphate-limited growth, most of the cells can be stained; if further phosphatase synthesis is repressed by growth in excess phosphate, dividing cells are produced in which the parent but not the bud can be stained. Budding growth is interrupted in alpha-mating-type cells by a pheromone (alpha-factor) secreted by the opposite mating type; cell surface growth continues in the presence of alpha-factor and produces a characteristic cell tip. When acid phosphatase synthesis is initiated during alpha-factor treatment, only the cell tip can br stained; when phosphate synthesis is repressed during alpha-factor treatment, the cell body but not the tip can be stained. A mixture of derepressed alpha cells and phosphatase-negative alpha cells form zygotes in which mainly one parent cell surface can be stained. The cell cycle mutant, cdc 24 (Hartwell, L.H. 1971. Exp. Cell Res. 69:265-276), fails to bud and, instead, expands symmetrically as a sphere at a nonpermissive temperature (37 degrees C). This mutant does not form a cell tip during alpha-factor treatment at 37 degrees C, and although acid phosphatade secretion occurs at this temperature, it is not localized. These results suggest that secretion reflects a polar mode of yeast cell- surface growth, and that this organization requires the cdc 24 gene product.

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Year:  1980        PMID: 6998984      PMCID: PMC2110663          DOI: 10.1083/jcb.86.1.123

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  30 in total

Review 1.  Analytical methods for yeasts.

Authors:  P R Stewart
Journal:  Methods Cell Biol       Date:  1975       Impact factor: 1.441

2.  Biosynthesis of acid phosphatase of baker's yeast. Factors influencing its production by protoplasts and characterization of the secreted enzyme.

Authors:  H J Van Rijn; P Boer; E P Steyn-Parvé
Journal:  Biochim Biophys Acta       Date:  1972-05-12

3.  Isolation of glucanase-containing vesicles from budding yeast.

Authors:  M Cortat; P Matile; A Wiemken
Journal:  Arch Mikrobiol       Date:  1972

Review 4.  Biosynthesis of cell walls of fungi.

Authors:  V Farkas
Journal:  Microbiol Rev       Date:  1979-06

5.  Genetic control of the cell division cycle in yeast. IV. Genes controlling bud emergence and cytokinesis.

Authors:  L H Hartwell
Journal:  Exp Cell Res       Date:  1971-12       Impact factor: 3.905

6.  Localization of acid phosphatase in Saccharomyces cerevisiae: a clue to cell wall formation.

Authors:  W A Linnemans; P Boer; P F Elbers
Journal:  J Bacteriol       Date:  1977-08       Impact factor: 3.490

7.  Lysis of yeast cell walls induced by 2-deoxyglucose at their sites of glucan synthesis.

Authors:  B F Johnson
Journal:  J Bacteriol       Date:  1968-03       Impact factor: 3.490

8.  Gene duplication in Saccharomyces cerevisiae.

Authors:  P E Hansche; V Beres; P Lange
Journal:  Genetics       Date:  1978-04       Impact factor: 4.562

9.  Porosity of the yeast cell wall and membrane.

Authors:  R Scherrer; L Louden; P Gerhardt
Journal:  J Bacteriol       Date:  1974-05       Impact factor: 3.490

10.  Regulation of mating in the cell cycle of Saccharomyces cerevisiae.

Authors:  B J Reid; L H Hartwell
Journal:  J Cell Biol       Date:  1977-11       Impact factor: 10.539

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  75 in total

1.  The Rho GTPase Rho3 has a direct role in exocytosis that is distinct from its role in actin polarity.

Authors:  J E Adamo; G Rossi; P Brennwald
Journal:  Mol Biol Cell       Date:  1999-12       Impact factor: 4.138

2.  Exocyst is involved in cystogenesis and tubulogenesis and acts by modulating synthesis and delivery of basolateral plasma membrane and secretory proteins.

Authors:  J H Lipschutz; W Guo; L E O'Brien; Y H Nguyen; P Novick; K E Mostov
Journal:  Mol Biol Cell       Date:  2000-12       Impact factor: 4.138

Review 3.  To shape a cell: an inquiry into the causes of morphogenesis of microorganisms.

Authors:  F M Harold
Journal:  Microbiol Rev       Date:  1990-12

4.  The Rho-GEF Rom2p localizes to sites of polarized cell growth and participates in cytoskeletal functions in Saccharomyces cerevisiae.

Authors:  B D Manning; R Padmanabha; M Snyder
Journal:  Mol Biol Cell       Date:  1997-10       Impact factor: 4.138

5.  Tethering molecules in membrane traffic.

Authors:  B Sönnichsen
Journal:  Protoplasma       Date:  1999       Impact factor: 3.356

6.  Extracellular Enzymes Produced by the Cultivated Mushroom Lentinus edodes during Degradation of a Lignocellulosic Medium.

Authors:  G F Leatham
Journal:  Appl Environ Microbiol       Date:  1985-10       Impact factor: 4.792

7.  Effect of ARS1 mutations on chromosome stability in Saccharomyces cerevisiae.

Authors:  F Srienc; J E Bailey; J L Campbell
Journal:  Mol Cell Biol       Date:  1985-07       Impact factor: 4.272

8.  Regulation of galactokinase (GAL1) enzyme accumulation in Saccharomyces cerevisiae.

Authors:  J G Yarger; H O Halvorson; J E Hopper
Journal:  Mol Cell Biochem       Date:  1984       Impact factor: 3.396

Review 9.  Protein transport and compartmentation in yeast.

Authors:  J Horák
Journal:  Folia Microbiol (Praha)       Date:  1991       Impact factor: 2.099

10.  AKR1 encodes a candidate effector of the G beta gamma complex in the Saccharomyces cerevisiae pheromone response pathway and contributes to control of both cell shape and signal transduction.

Authors:  P M Pryciak; L H Hartwell
Journal:  Mol Cell Biol       Date:  1996-06       Impact factor: 4.272

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