Atg8 controls phagophore expansion during autophagosome formation

被引:563
作者
Xie, Zhiping [1 ,2 ]
Nair, Usha [1 ,2 ]
Klionsky, Daniel J. [1 ,2 ,3 ]
机构
[1] Univ Michigan, Inst Life Sci, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Biol Chem, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1091/mbc.E07-12-1292
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Autophagy is a potent intracellular degradation process with pivotal roles in health and disease. Atg8, a lipid-conjugated ubiquitin-like protein, is required for the formation of autophagosomes, double-membrane vesicles responsible for the delivery of cytoplasmic material to lysosomes. How and when Atg8 functions in this process, however, is not clear. Here we show that Atg8 controls the expansion of the autophagosome precursor, the phagophore, and give the first real-time, observation-based temporal dissection of the autophagosome formation process. We demonstrate that the amount of Atg8 determines the size of autophagosomes. During autophagosome biogenesis, Atg8 forms an expanding structure and later dissociates from the site of vesicle formation. On the basis of the dynamics of Atg8, we present a multistage model of autophagosome formation. This model provides a foundation for future analyses of the functions and dynamics of known autophagy-related proteins and for screening new genes.
引用
收藏
页码:3290 / 3298
页数:9
相关论文
共 41 条
[1]   Dissection of autophagosome biogenesis into distinct nucleation and expansion steps [J].
Abeliovich, H ;
Dunn, WA ;
Kim, J ;
Klionsky, DJ .
JOURNAL OF CELL BIOLOGY, 2000, 151 (05) :1025-1033
[2]   Two distinct pathways for targeting proteins from the cytoplasm to the vacuole/lysosome [J].
Baba, M ;
Osumi, M ;
Scott, SV ;
Klionsky, DJ ;
Ohsumi, Y .
JOURNAL OF CELL BIOLOGY, 1997, 139 (07) :1687-1695
[3]  
Boland Barry, 2006, Molecular Aspects of Medicine, V27, P503, DOI 10.1016/j.mam.2006.08.009
[4]   The Atg12-Atg5 conjugate has a novel E3-like activity for protein lipidation in autophagy [J].
Hanada, Takao ;
Noda, Nobuo N. ;
Satomi, Yoshinori ;
Ichimura, Yoshinobu ;
Fujioka, Yuko ;
Takao, Toshifumi ;
Inagaki, Fuyuhiko ;
Ohsumi, Yoshinori .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (52) :37298-37302
[5]   A single protease, Apg4B, is specific for the autophagy-related ubiquitin-like proteins GATE-16, MAP1-LC3, GABARAP, and Apg8L [J].
Hemelaar, J ;
Lelyveld, VS ;
Kessler, BM ;
Ploegh, HL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (51) :51841-51850
[6]   The itinerary of a vesicle component, Aut7p/Cvt5p, terminates in the yeast vacuole via the autophagy/Cvt pathways [J].
Huang, WP ;
Scott, SV ;
Kim, J ;
Klionsky, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (08) :5845-5851
[7]   A ubiquitin-like system mediates protein lipidation [J].
Ichimura, Y ;
Kirisako, T ;
Takao, T ;
Satomi, Y ;
Shimonishi, Y ;
Ishihara, N ;
Mizushima, N ;
Tanida, I ;
Kominami, E ;
Ohsumi, M ;
Noda, T ;
Ohsumi, Y .
NATURE, 2000, 408 (6811) :488-492
[8]   LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing [J].
Kabeya, Y ;
Mizushima, N ;
Uero, T ;
Yamamoto, A ;
Kirisako, T ;
Noda, T ;
Kominami, E ;
Ohsumi, Y ;
Yoshimori, T .
EMBO JOURNAL, 2000, 19 (21) :5720-5728
[9]   LC3, GABARAP and GATE16 localize to autophagosomal membrane depending on form-II formation [J].
Kabeya, Y ;
Mizushima, N ;
Yamamoto, A ;
Oshitani-Okamoto, S ;
Ohsumi, Y ;
Yoshimori, T .
JOURNAL OF CELL SCIENCE, 2004, 117 (13) :2805-2812
[10]   Apg14p and Apg6/Vps30p form a protein complex essential for autophagy in the yeast, Saccharomyces cerevisiae [J].
Kametaka, S ;
Okano, T ;
Ohsumi, M ;
Ohsumi, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (35) :22284-22291