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PMID: 1803815 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Structure of the yeast endoplasmic reticulum: localization of ER proteins using immunofluorescence and immunoelectron microscopy.

Yeast (Chichester, England) ·Vol. 7 ·No. 9 ·1991-12-00 ·Pages 891-911

Preuss D, Mulholland J, Kaiser CA, Orlean P, Albright C, Rose MD, Robbins PW, Botstein D

Abstract

The endoplasmic reticulum (ER) and other secretory compartments of Saccharomyces cerevisiae have biochemical functions that closely parallel those described in higher eukaryotic cells, yet the morphology of the yeast organelles is quite distinct. In order to associate ER functions with the corresponding cellular structures, we localized several proteins, each of which is expected to be associated with the ER on the basis of enzymatic activity, biological function, or oligosaccharide content. These marker proteins were visualized by immunofluorescence or immunoelectron microscopy, allowing definition of the S. cerevisiae ER structure, both in intact cells and at the ultrastructural level. Each marker protein was most abundant within the membranes that envelop the nucleus and several were also found in extensions of the ER that frequently juxtapose the plasma membrane. Double-labeling experiments were entirely consistent with the idea that the marker proteins reside within the same compartment. This analysis has permitted, for the first time, a detailed characterization of the ER morphology as yeast cells proceed through their growth and division cycles.

Related Genes
MeSH Terms
Cell Cycle Endoplasmic Reticulum/chemistry,enzymology,ultrastructure Fluorescent Antibody Technique Fungal Proteins/analysis Glycoside Hydrolases/analysis,genetics Immunoblotting Mannosyltransferases/analysis,genetics Microscopy, Immunoelectron Protein Conformation Saccharomyces cerevisiae/chemistry,cytology,enzymology,genetics,ultrastructure beta-Fructofuranosidase beta-Galactosidase/analysis
Chemicals
Fungal Proteins Mannosyltransferases dolichyl-phosphate beta-D-mannosyltransferase Glycoside Hydrolases beta-Galactosidase beta-Fructofuranosidase
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Preuss D
Department of Genetics, Stanford University Medical Center, CA 94305.
Mulholland J
Kaiser C A
Orlean P
Albright C
Rose M D
Robbins P W
Botstein D
Article Info
Journal
Yeast (Chichester, England)
Abbr.
Yeast
ISSN
0749-503X
Published
1991-12-00
Pages
891-911
Language
English
Region
England
NLM ID
8607637
Subset
IM
Grants
NIGMS NIH HHS · R01 GM037739 · United States
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