Accelerated cell death in Podospora autophagy mutants

被引:87
作者
Pinan-Lucarré, B
Baiguerie, A
Clavé, C
机构
[1] CNRS, Inst Biochim & Genet Cellulaires, Lab Genet Mol Champignons, UMR 5095, F-33077 Bordeaux, France
[2] Univ Bordeaux 2, F-33077 Bordeaux, France
关键词
D O I
10.1128/EC.4.11.1765-1774.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Although autophagy is characteristic of type II programmed cell death (PCD), its role in cell death is currently debated. Both cell death-promoting and prosurvival roles of autophagy have been reported depending on the organism and the cell type. In filamentous fungi, a cell death reaction known as an incompatibility reaction occurs when cells of unlike genotype fuse. Cell death by incompatibility is characterized by a dramatic vacuolar enlargement and cell lysis. In Podospora anserina, autophagy is induced early during this cell death reaction. Cell death by incompatibility in Podospora is a model of type II PCD used here to assess the role of autophagy in this type of cell death. We have inactivated PaATG1, the Podospora ortholog of the Saccharomyces cerevisiae ATG1 gene involved in the early steps of autophagy in yeast. The Delta PaATG1 mutant displays developmental defects characteristic of abrogated autophagy in Podospora. Using the green fluorescent protein-PaATG8 autophagosome marker, we show that autophagy is abolished in this mutant. Neither cell death by incompatibility nor vacuolization are suppressed in Delta PaATG1 and Delta PaATG8 autophagy mutants, indicating that a vacuolar cell death reaction without autophagy occurs in Podospora. Our results thus provide a novel example of a type II PCD reaction in which autophagy is not the cause of cell death. In addition, we found that cell death is accelerated in Delta PaATG null mutants, suggesting that autophagy has a protective role in this type II PCD reaction.
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页码:1765 / 1774
页数:10
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