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PMID: 7796921 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Intracellular transport of inositol-containing sphingolipids in the yeast, Saccharomyces cerevisiae.

FEBS letters ·Vol. 367 ·No. 2 ·1995-06-26 ·Pages 201-4

Hechtberger P, Daum G

Abstract

Organelles of the early protein secretion pathway (ER, Golgi) are involved in biosynthesis and intracellular migration of the yeast sphingolipids, inositolphosphorylceramide (IPC), mannosylinositolphosphorylceramide (MIPC), and mannosyldiinositolphosphorylceramide (M(IP)2C). Cycloheximide and nocodazole neither block biosynthesis of sphingolipids, nor ER to Golgi transport of IPC. In contrast, treatment of yeast cells with brefeldin A, which affects integrity of the Golgi, decreases formation of IPC and MIPC. Interruption of late steps of protein secretion (Golgi to plasma membrane transport) in temperature-sensitive secretory mutants prevents sphingolipids from being transported to the cell periphery.

MeSH Terms
Biological Transport Brefeldin A Cell Membrane/metabolism Ceramides/metabolism Cycloheximide/pharmacology Cyclopentanes/pharmacology Endoplasmic Reticulum/drug effects,metabolism Golgi Apparatus/drug effects,metabolism Inositol/metabolism Nocodazole/pharmacology Saccharomyces cerevisiae/drug effects,growth & development,metabolism
Chemicals
Ceramides Cyclopentanes Brefeldin A Inositol Cycloheximide Nocodazole
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Hechtberger P
Institut für Biochemie und Lebensmittelchemie, Technische Universität Graz, Austria.
Daum G
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
1995-06-26
Pages
201-4
Language
English
Region
England
NLM ID
0155157
Subset
IM
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