Literature DB >> 2695529

Three-dimensional analysis of morphogenesis induced by mating pheromone alpha factor in Saccharomyces cerevisiae.

M Baba1, N Baba, Y Ohsumi, K Kanaya, M Osumi.   

Abstract

Ultrastructural analyses of cytoplasmic changes in Saccharomyces cerevisiae X2180-1A (MATa) that had been treated with alpha factor were performed by using the freeze-substitution fixation method. After alpha factor treatment, cells exhibited a pointed projection, which is a unique pattern of oriented cell surface growth. The relationship between projection formation and intracellular organelles was examined using serial thin sections and computer-aided three-dimensional reconstructions. Using these analyses membrane vesicles and other organelles were detected, and studies on their dynamic structural reorganization became feasible. Production of membrane vesicles (average 65 nm in diameter) was induced upon exposure of the cells to alpha factor before projection emergence. The total number of membrane vesicles increased at the early stage and decreased at the late stage of projection formation. Three-dimensional analysis indicated that the vesicles were at first dispersed throughout the cell, then accumulated at the site where the projection formed. Morphological changes and multiplication of the Golgi body were seen during the process of projection formation. Other intracellular organelles (nucleus, vacuole, rough endoplasmic reticulum and mitochondria) were also rearranged, showing a polar organization of the cytoplasm during projection formation.

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Year:  1989        PMID: 2695529     DOI: 10.1242/jcs.94.2.207

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  44 in total

1.  Using rapid freeze and freeze-substitution for the preparation of yeast cells for electron microscopy and three-dimensional analysis.

Authors:  T H Giddings; E T O'Toole; M Morphew; D N Mastronarde; J R McIntosh; M Winey
Journal:  Methods Cell Biol       Date:  2001       Impact factor: 1.441

2.  Genetic analysis of default mating behavior in Saccharomyces cerevisiae.

Authors:  R Dorer; C Boone; T Kimbrough; J Kim; L H Hartwell
Journal:  Genetics       Date:  1997-05       Impact factor: 4.562

Review 3.  Electron tomography of yeast cells.

Authors:  Eileen T O'Toole; Mark Winey; J Richard McIntosh; David N Mastronarde
Journal:  Methods Enzymol       Date:  2002       Impact factor: 1.600

Review 4.  To shape a cell: an inquiry into the causes of morphogenesis of microorganisms.

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

Review 5.  Molecules into cells: specifying spatial architecture.

Authors:  Franklin M Harold
Journal:  Microbiol Mol Biol Rev       Date:  2005-12       Impact factor: 11.056

6.  The class V myosin Myo2p is required for Fus2p transport and actin polarization during the yeast mating response.

Authors:  Jason M Sheltzer; Mark D Rose
Journal:  Mol Biol Cell       Date:  2009-04-29       Impact factor: 4.138

7.  An essential role of the yeast pheromone-induced Ca2+ signal is to activate calcineurin.

Authors:  J L Withee; J Mulholland; R Jeng; M S Cyert
Journal:  Mol Biol Cell       Date:  1997-02       Impact factor: 4.138

8.  A synthetic lethal screen identifies SLK1, a novel protein kinase homolog implicated in yeast cell morphogenesis and cell growth.

Authors:  C Costigan; S Gehrung; M Snyder
Journal:  Mol Cell Biol       Date:  1992-03       Impact factor: 4.272

9.  Systematic definition of protein constituents along the major polarization axis reveals an adaptive reuse of the polarization machinery in pheromone-treated budding yeast.

Authors:  Rammohan Narayanaswamy; Emily K Moradi; Wei Niu; G Traver Hart; Matthew Davis; Kriston L McGary; Andrew D Ellington; Edward M Marcotte
Journal:  J Proteome Res       Date:  2009-01       Impact factor: 4.466

10.  Characterization of the Saccharomyces Golgi complex through the cell cycle by immunoelectron microscopy.

Authors:  D Preuss; J Mulholland; A Franzusoff; N Segev; D Botstein
Journal:  Mol Biol Cell       Date:  1992-07       Impact factor: 4.138

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