Document Detail


Autophagy in unicellular eukaryotes.
MedLine Citation:
PMID:  20124347     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Cells need a constant supply of precursors to enable the production of macromolecules to sustain growth and survival. Unlike metazoans, unicellular eukaryotes depend exclusively on the extracellular medium for this supply. When environmental nutrients become depleted, existing cytoplasmic components will be catabolized by (macro)autophagy in order to re-use building blocks and to support ATP production. In many cases, autophagy takes care of cellular housekeeping to sustain cellular viability. Autophagy encompasses a multitude of related and often highly specific processes that are implicated in both biogenetic and catabolic processes. Recent data indicate that in some unicellular eukaryotes that undergo profound differentiation during their life cycle (e.g. kinetoplastid parasites and amoebes), autophagy is essential for the developmental change that allows the cell to adapt to a new host or form spores. This review summarizes the knowledge on the molecular mechanisms of autophagy as well as the cytoplasm-to-vacuole-targeting pathway, pexophagy, mitophagy, ER-phagy, ribophagy and piecemeal microautophagy of the nucleus, all highly selective forms of autophagy that have first been uncovered in yeast species. Additionally, a detailed analysis will be presented on the state of knowledge on autophagy in non-yeast unicellular eukaryotes with emphasis on the role of this process in differentiation.
Authors:
Jan A K W Kiel
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Publication Detail:
Type:  Journal Article; Review    
Journal Detail:
Title:  Philosophical transactions of the Royal Society of London. Series B, Biological sciences     Volume:  365     ISSN:  1471-2970     ISO Abbreviation:  Philos. Trans. R. Soc. Lond., B, Biol. Sci.     Publication Date:  2010 Mar 
Date Detail:
Created Date:  2010-02-03     Completed Date:  2010-04-16     Revised Date:  2013-05-31    
Medline Journal Info:
Nlm Unique ID:  7503623     Medline TA:  Philos Trans R Soc Lond B Biol Sci     Country:  England    
Other Details:
Languages:  eng     Pagination:  819-30     Citation Subset:  IM    
Affiliation:
Molecular Cell Biology, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, PO Box 14, 9750 Haren, The Netherlands. j.a.k.w.kiel@rug.nl
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MeSH Terms
Descriptor/Qualifier:
Autophagy / physiology*
Cell Nucleus / metabolism
Cytoplasm / metabolism
Dictyostelium / cytology,  genetics,  growth & development,  physiology
Endoplasmic Reticulum / metabolism
Entamoeba / cytology,  genetics,  growth & development,  physiology
Eukaryota / cytology*,  genetics,  growth & development,  physiology*
Leishmania / cytology,  genetics,  growth & development,  physiology
Models, Biological
Peroxisomes / metabolism
Phagosomes / metabolism
Ribosomes / metabolism
Saccharomyces cerevisiae / cytology,  genetics,  growth & development,  physiology
Saccharomyces cerevisiae Proteins / metabolism
Trypanosoma / cytology,  genetics,  growth & development,  physiology
Vacuoles / metabolism
Chemical
Reg. No./Substance:
0/Saccharomyces cerevisiae Proteins
Comments/Corrections

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