Literature DB >> 8311256

Modulation of the Golgi apparatus in Saccharomyces cerevisiae sec7 mutants as seen by three-dimensional electron microscopy.

A Rambourg1, Y Clermont, F Képès.   

Abstract

The three-dimensional configuration of the Golgi apparatus has been examined with the electron microscope in thick Golgi sections of Saccharomyces cerevisiae prepared from a wild-type strain and from sec7 mutants maintained for various periods of time at the nonpermissive temperature of 37 degrees C and then returned to the permissive temperature of 24 degrees C. Reduced osmium postfixation of glutaraldehyde fixed specimens stained intensely the content of Golgi elements and thus facilitated their three-dimensional characterization. In wild-type S. cerevisiae, the Golgi elements usually appeared as isolated networks of membranous tubules dispersed throughout the cytoplasm. Along such networks, distensions filled with stained material were similar in size to nearby secretory granules, suggesting that the latter formed by fragmentation of the Golgi elements. In sec7 mutants maintained at 37 degrees C in low (0.1%) glucose medium, secretion granules progressively decreased in number and soon disappeared. Concomitantly the networks of Golgi tubules increased in size and complexity, lost their distensions, and then transformed into flattened saccules forming stacks of up to seven or eight saccules that were similar to the Golgi stacks seen in mammalian cells. However in contrast to the latter, connections between the saccules were evident and Golgi-associated small vesicles were generally absent. Following return to the permissive temperature (24 degrees C), secretion granules reappeared, the Golgi stacks progressively decreased in size, and resumed their initial state of separated small tubular networks. Thus in sec7 mutant, grown at 37 degrees C in low glucose medium, segregation of secretory granules is blocked. As a result, Golgi membranes accumulate to form a continuous system of stacked and interconnected saccules.

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Year:  1993        PMID: 8311256     DOI: 10.1002/ar.1092370402

Source DB:  PubMed          Journal:  Anat Rec        ISSN: 0003-276X


  24 in total

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4.  Distinct functions for Arf guanine nucleotide exchange factors at the Golgi complex: GBF1 and BIGs are required for assembly and maintenance of the Golgi stack and trans-Golgi network, respectively.

Authors:  Florin Manolea; Alejandro Claude; Justin Chun; Javier Rosas; Paul Melançon
Journal:  Mol Biol Cell       Date:  2007-11-14       Impact factor: 4.138

5.  Organization and dynamics of the Aspergillus nidulans Golgi during apical extension and mitosis.

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Journal:  Mol Biol Cell       Date:  2009-08-19       Impact factor: 4.138

6.  A presynaptic role for the ADP ribosylation factor (ARF)-specific GDP/GTP exchange factor msec7-1.

Authors:  U Ashery; H Koch; V Scheuss; N Brose; J Rettig
Journal:  Proc Natl Acad Sci U S A       Date:  1999-02-02       Impact factor: 11.205

7.  ARF is required for maintenance of yeast Golgi and endosome structure and function.

Authors:  E C Gaynor; C Y Chen; S D Emr; T R Graham
Journal:  Mol Biol Cell       Date:  1998-03       Impact factor: 4.138

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Authors:  N Yahara; T Ueda; K Sato; A Nakano
Journal:  Mol Biol Cell       Date:  2001-01       Impact factor: 4.138

9.  GRASP55 and GRASP65 play complementary and essential roles in Golgi cisternal stacking.

Authors:  Yi Xiang; Yanzhuang Wang
Journal:  J Cell Biol       Date:  2010-01-18       Impact factor: 10.539

10.  Early stages of the secretory pathway, but not endosomes, are required for Cvt vesicle and autophagosome assembly in Saccharomyces cerevisiae.

Authors:  Fulvio Reggiori; Chao-Wen Wang; Usha Nair; Takahiro Shintani; Hagai Abeliovich; Daniel J Klionsky
Journal:  Mol Biol Cell       Date:  2004-03-05       Impact factor: 4.138

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