TY - JOUR
T1 - The conserved oligomeric Golgi complex is involved in double-membrane vesicle formation during autophagy
AU - Yen, Wei Lien
AU - Shintani, Takahiro
AU - Nair, Usha
AU - Cao, Yang
AU - Richardson, Brian C.
AU - Li, Zhijian
AU - Hughson, Frederick M.
AU - Baba, Misuzu
AU - Klionsky, Daniel J.
PY - 2010/12/11
Y1 - 2010/12/11
N2 - Macroautophagy is a catabolic pathway used for the turnover of long-lived proteins and organelles in eukaryotic cells. The morphological hallmark of this process is the formation of doublemembrane autophagosomes that sequester cytoplasm. Autophagosome formation is the most complex part of macroautophagy, and it is a dynamic event that likely involves vesicle fusion to expand the initial sequestering membrane, the phagophore; however, essentially nothing is known about this process including the molecular components involved in vesicle tethering and fusion. In this study, we provide evidence that the subunits of the conserved oligomeric Golgi (COG) complex are required for double-membrane cytoplasm to vacuole targeting vesicle and autophagosome formation. COG subunits localized to the phagophore assembly site and interacted with Atg (autophagy related) proteins. In addition, mutations in the COG genes resulted in the mislocalization of Atg8 and Atg9, which are critical components involved in autophagosome formation.
AB - Macroautophagy is a catabolic pathway used for the turnover of long-lived proteins and organelles in eukaryotic cells. The morphological hallmark of this process is the formation of doublemembrane autophagosomes that sequester cytoplasm. Autophagosome formation is the most complex part of macroautophagy, and it is a dynamic event that likely involves vesicle fusion to expand the initial sequestering membrane, the phagophore; however, essentially nothing is known about this process including the molecular components involved in vesicle tethering and fusion. In this study, we provide evidence that the subunits of the conserved oligomeric Golgi (COG) complex are required for double-membrane cytoplasm to vacuole targeting vesicle and autophagosome formation. COG subunits localized to the phagophore assembly site and interacted with Atg (autophagy related) proteins. In addition, mutations in the COG genes resulted in the mislocalization of Atg8 and Atg9, which are critical components involved in autophagosome formation.
UR - http://www.scopus.com/inward/record.url?scp=75749135725&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=75749135725&partnerID=8YFLogxK
U2 - 10.1083/jcb.200904075
DO - 10.1083/jcb.200904075
M3 - Article
C2 - 20065092
AN - SCOPUS:75749135725
SN - 0021-9525
VL - 188
SP - 101
EP - 114
JO - Journal of Cell Biology
JF - Journal of Cell Biology
IS - 1
ER -