Literature DB >> 1381247

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

D Preuss1, J Mulholland, A Franzusoff, N Segev, D Botstein.   

Abstract

The membrane compartments responsible for Golgi functions in wild-type Saccharomyces cerevisiae were identified and characterized by immunoelectron microscopy. Using improved fixation methods, Golgi compartments were identified by labeling with antibodies specific for alpha 1-6 mannose linkages, the Sec7 protein, or the Ypt1 protein. The compartments labeled by each of these antibodies appear as disk-like structures that are apparently surrounded by small vesicles. Yeast Golgi typically are seen as single, isolated cisternae, generally not arranged into parallel stacks. The location of the Golgi structures was monitored by immunoelectron microscopy through the yeast cell cycle. Several Golgi compartments, apparently randomly distributed, were always observed in mother cells. During the initiation of new daughter cells, additional Golgi structures cluster just below the site of bud emergence. These Golgi enter daughter cells at an early stage, raising the possibility that much of the bud's growth might be due to secretory vesicles formed as well as consumed entirely within the daughter. During cytokinesis, the Golgi compartments are concentrated near the site of cell wall synthesis. Clustering of Golgi both at the site of bud formation and at the cell septum suggests that these organelles might be directed toward sites of rapid cell surface growth.

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Year:  1992        PMID: 1381247      PMCID: PMC275635          DOI: 10.1091/mbc.3.7.789

Source DB:  PubMed          Journal:  Mol Biol Cell        ISSN: 1059-1524            Impact factor:   4.138


  58 in total

1.  Vesicle budding: insights from cell-free assays.

Authors:  P Melançon; A Franzusoff; K E Howell
Journal:  Trends Cell Biol       Date:  1991-12       Impact factor: 20.808

2.  GTP-binding Ypt1 protein and Ca2+ function independently in a cell-free protein transport reaction.

Authors:  D Baker; L Wuestehube; R Schekman; D Botstein; N Segev
Journal:  Proc Natl Acad Sci U S A       Date:  1990-01       Impact factor: 11.205

3.  KAR2, a karyogamy gene, is the yeast homolog of the mammalian BiP/GRP78 gene.

Authors:  M D Rose; L M Misra; J P Vogel
Journal:  Cell       Date:  1989-06-30       Impact factor: 41.582

4.  Study of a temperature-sensitive mutant of the ras-related YPT1 gene product in yeast suggests a role in the regulation of intracellular calcium.

Authors:  H D Schmitt; M Puzicha; D Gallwitz
Journal:  Cell       Date:  1988-05-20       Impact factor: 41.582

5.  Reconstitution of SEC gene product-dependent intercompartmental protein transport.

Authors:  D Baker; L Hicke; M Rexach; M Schleyer; R Schekman
Journal:  Cell       Date:  1988-07-29       Impact factor: 41.582

6.  Secretion of invertase in mitotic yeast cells.

Authors:  M Makarow
Journal:  EMBO J       Date:  1988-05       Impact factor: 11.598

7.  The ras-related mouse ypt1 protein can functionally replace the YPT1 gene product in yeast.

Authors:  H Haubruck; R Prange; C Vorgias; D Gallwitz
Journal:  EMBO J       Date:  1989-05       Impact factor: 11.598

8.  A mitotic form of the Golgi apparatus in HeLa cells.

Authors:  J M Lucocq; J G Pryde; E G Berger; G Warren
Journal:  J Cell Biol       Date:  1987-04       Impact factor: 10.539

9.  The GTP-binding protein Ypt1 is required for transport in vitro: the Golgi apparatus is defective in ypt1 mutants.

Authors:  R A Bacon; A Salminen; H Ruohola; P Novick; S Ferro-Novick
Journal:  J Cell Biol       Date:  1989-09       Impact factor: 10.539

10.  Functional compartments of the yeast Golgi apparatus are defined by the sec7 mutation.

Authors:  A Franzusoff; R Schekman
Journal:  EMBO J       Date:  1989-09       Impact factor: 11.598

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  108 in total

1.  Dual prenylation is required for Rab protein localization and function.

Authors:  Monica Calero; Catherine Z Chen; Wenyan Zhu; Nena Winand; Karyn A Havas; Penny M Gilbert; Christopher G Burd; Ruth N Collins
Journal:  Mol Biol Cell       Date:  2003-02-06       Impact factor: 4.138

2.  A modeling approach to the self-assembly of the Golgi apparatus.

Authors:  Jens Kühnle; Julian Shillcock; Ole G Mouritsen; Matthias Weiss
Journal:  Biophys J       Date:  2010-06-16       Impact factor: 4.033

Review 3.  The yeast GRASP Grh1 colocalizes with COPII and is dispensable for organizing the secretory pathway.

Authors:  Stephanie K Levi; Dibyendu Bhattacharyya; Rita L Strack; Jotham R Austin; Benjamin S Glick
Journal:  Traffic       Date:  2010-06-21       Impact factor: 6.215

Review 4.  Modular organization of the mammalian Golgi apparatus.

Authors:  Nobuhiro Nakamura; Jen-Hsuan Wei; Joachim Seemann
Journal:  Curr Opin Cell Biol       Date:  2012-06-20       Impact factor: 8.382

Review 5.  Centrosome positioning in non-dividing cells.

Authors:  Amy R Barker; Kate V McIntosh; Helen R Dawe
Journal:  Protoplasma       Date:  2015-08-30       Impact factor: 3.356

Review 6.  Actin acting at the Golgi.

Authors:  Gustavo Egea; Carla Serra-Peinado; Laia Salcedo-Sicilia; Enric Gutiérrez-Martínez
Journal:  Histochem Cell Biol       Date:  2013-06-27       Impact factor: 4.304

7.  Organization of the yeast Golgi complex into at least four functionally distinct compartments.

Authors:  W T Brigance; C Barlowe; T R Graham
Journal:  Mol Biol Cell       Date:  2000-01       Impact factor: 4.138

8.  Ypt31/32 GTPases and their novel F-box effector protein Rcy1 regulate protein recycling.

Authors:  Shu Hui Chen; Shan Chen; Andrei A Tokarev; Fengli Liu; Gregory Jedd; Nava Segev
Journal:  Mol Biol Cell       Date:  2004-11-10       Impact factor: 4.138

9.  Interaction of the Saccharomyces cerevisiae cortical actin patch protein Rvs167p with proteins involved in ER to Golgi vesicle trafficking.

Authors:  Helena Friesen; Karen Colwill; Karen Robertson; Oliver Schub; Brenda Andrews
Journal:  Genetics       Date:  2005-03-31       Impact factor: 4.562

10.  The dynamics of golgi protein traffic visualized in living yeast cells.

Authors:  S Wooding; H R Pelham
Journal:  Mol Biol Cell       Date:  1998-09       Impact factor: 4.138

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