期刊
AUTOPHAGY
卷 6, 期 1, 页码 86-99出版社
TAYLOR & FRANCIS INC
DOI: 10.4161/auto.6.1.10535
关键词
phagophore; PI3K; Atg6; Vps34; Uvrag; isolation membrane; autophagy; pexophagy; VPS pathway
类别
资金
- NIH [GM69373]
- NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM069373] Funding Source: NIH RePORTER
Although it has been established that Atg6/ Beclin 1, the phosphatidylinositol 3-kinase (PI3K) Vps34, and associated proteins have direct or indirect roles in autophagic pathways in both mammals and yeasts, the elucidation of these roles and the proteins required for them is ongoing. The involvement of the Beclin 1-binding protein, UVRAG, has been a particular source of disagreement. We found that PpAtg6 is required for all autophagic pathways that have been identified in the yeast Pichia pastoris, as well as for the carboxypeptidase Y (PpCPY) vacuolar protein sorting pathway. We localized PpAtg6 to the phagophore assembly site ( PAS) and observed its continued presence at that site as the isolation membrane grew from it and matured into a pexophagosome. PpUvrag, however, was required for proper PpCPY sorting, but not for any autophagic pathway. Rather, the defects in all autophagic pathways observed when PpUvrag was overexpressed support its presence in a complex that competes with the PI3K complex required for autophagy.
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