scispace - formally typeset
Open AccessJournal ArticleDOI

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

Charles Field, +1 more
- 01 Jul 1980 - 
- Vol. 86, Iss: 1, pp 123-128
TLDR
The results suggest that secretion reflects a polar mode of yeast cell- surface growth, and that this organization requires the cdc 24 gene product.
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.

read more

Content maybe subject to copyright    Report

Citations
More filters
Journal ArticleDOI

Identification of 23 complementation groups required for post-translational events in the yeast secretory pathway

TL;DR: Electron microscopy of sec mutant cells reveals the temperature-dependent accumulation of membrane-enclosed secretory organelles, and it is suggested that these structures represent intermediates in a pathway in which secretion and plasma membrane assembly are colinear.
Journal ArticleDOI

A ras-like protein is required for a post-Golgi event in yeast secretion

TL;DR: It is proposed that the SEC4 product is a GTP-binding protein that plays an essential role in controlling a late stage of the secretory pathway.
Journal ArticleDOI

Cell Wall and Secreted Proteins of Candida albicans: Identification, Function, and Expression

TL;DR: Surface mannoproteins are strong immunogens that trigger and modulate the host immune response during candidiasis and may play a role in morphogenesis.
Journal ArticleDOI

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

TL;DR: It is reported that the actin assembly inhibitor latrunculin-A (LAT-A) causes complete disruption of the yeast actin cytoskeleton within 2–5 min, suggesting that although yeast are nonmotile, their actin filaments undergo rapid cycles of assembly and disassembly in vivo.
Journal ArticleDOI

Relationship of actin and tubulin distribution to bud growth in wild-type and morphogenetic-mutant Saccharomyces cerevisiae.

TL;DR: Observations are consistent with the hypotheses that actin, tubulin, or both may be involved in the polarization of growth and localization of cell-wall deposition that occurs during the yeast cell cycle.
References
More filters
Journal ArticleDOI

Histochemical methods for acid phosphatase using hexazonium pararosanilin as coupler

TL;DR: ‘[he use of freslsbv diazotizecl pararosanilin w-itim a-msaphthyb pisosphate its a sinmultaneous coupling azo dye method for acid phosphatase resulted in significant improveumment because of the nmaumy desirable characteristics of the final azo dyed (1, 2).
Journal ArticleDOI

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

TL;DR: It is concluded that bud emergence is not a necessary prerequisite for the completion of DNA replication but is apparently necessary for nuclear division and Cytokinesis and cell separation are not necessary prerequisites for bud emergence, DNA replication, or nuclear division.
Journal ArticleDOI

Unequal division in Saccharomyces cerevisiae and its implications for the control of cell division.

TL;DR: The budding yeast, Saccharomyces cerevisiae, was grown exponentially at different rates in the presence of growth rate-limiting concentrations of a protein synthesis inhibitor, cycloheximide, to support the model for the coordination of growth and division.
Journal ArticleDOI

Secretion and cell-surface growth are blocked in a temperature-sensitive mutant of Saccharomyces cerevisiae

TL;DR: Results are consistent with a vesicle intermediate in the yeast secretory pathway and suggest that exocytosis may contribute to cell-surface growth.
Journal ArticleDOI

A Critical Evaluation of the Nitrogen Assimilation Tests Commonly Used in the Classification of Yeasts

TL;DR: The ability of some groups of closely related yeasts to use potassium nitrate as a source of nitrogen was applied successfully by Stelling-Dekker (1931) and later, Lodder added other nitrogen compounds, namely, ammonium sulfate, urea, asparagine, and peptone, in diagnostic tests for her classification of the nonsporogenous, nonfilamentous yeasts.
Related Papers (5)