TY - JOUR
T1 - Atg9 cycles between mitochondria and the pre-autophagosomal structure in yeasts.
AU - Reggiori, Fulvio
AU - Shintani, Takahiro
AU - Nair, Usha
AU - Klionsky, Daniel J.
N1 - Funding Information:
The authors thank R. Tsien for providing the mRFP1 plasmid, and B. Glick, Y. Ohsumi, S. Siniossoglou, P. Stromhaug and W. Wickner for reagents. We are also grateful to Drs. J. Komduur and W.-P. Huang for providing plasmids and H. Chong for providing technical assistance. This work was supported by the National Institutes of Health Public Health Service grant GM53396 (to D.J.K.). F.R. is supported by a Swiss National Foundation Fellowship for advanced researchers.
PY - 2005/7
Y1 - 2005/7
N2 - Autophagy is a degradative process conserved among eukaryotic cells. It allows the elimination of cytoplasm including aberrant protein aggregates and damaged organelles. Accordingly, it is implicated in normal developmental processes and also serves a protective role in tumor suppression and elimination of invading pathogens, whereas defects in autophagy are associated with various human diseases including cancer and neurodegeneration. Atg proteins mediate the sequestration event that occurs at the preautophagosomal structure (PAS) by catalyzing the formation of double-membrane vesicles, termed autophagosomes. In Saccharomyces cerevisiae, the integral membrane protein Atg9 that is required for autophagy cycles through the PAS. Here, we demonstrate that Atg9 shuttles between this location and mitochondria. These data support a new model where mitochondria may provide at least part of the autophagosomal lipids and suggest a novel cellular function for this well-studied organelle.
AB - Autophagy is a degradative process conserved among eukaryotic cells. It allows the elimination of cytoplasm including aberrant protein aggregates and damaged organelles. Accordingly, it is implicated in normal developmental processes and also serves a protective role in tumor suppression and elimination of invading pathogens, whereas defects in autophagy are associated with various human diseases including cancer and neurodegeneration. Atg proteins mediate the sequestration event that occurs at the preautophagosomal structure (PAS) by catalyzing the formation of double-membrane vesicles, termed autophagosomes. In Saccharomyces cerevisiae, the integral membrane protein Atg9 that is required for autophagy cycles through the PAS. Here, we demonstrate that Atg9 shuttles between this location and mitochondria. These data support a new model where mitochondria may provide at least part of the autophagosomal lipids and suggest a novel cellular function for this well-studied organelle.
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U2 - 10.4161/auto.1.2.1840
DO - 10.4161/auto.1.2.1840
M3 - Article
C2 - 16874040
AN - SCOPUS:27644544004
SN - 1554-8627
VL - 1
SP - 101
EP - 109
JO - Autophagy
JF - Autophagy
IS - 2
ER -