Atg20 and Atg24 family proteins promote organelle autophagy in fission yeast

Author:

Zhao Dan12,Liu Xiao-Man2,Yu Zhong-Qiu2,Sun Ling-Ling2,Xiong Xingchuang3,Dong Meng-Qiu2,Du Li-Lin2ORCID

Affiliation:

1. PTN Graduate Program, School of Life Sciences, Peking University, Beijing 100871, China

2. National Institute of Biological Sciences, Beijing 102206, China

3. National Institute of Metrology, Beijing 100013, China

Abstract

Autophagy cargos include not only soluble cytosolic materials but also bulky organelles such as ER and mitochondria. In budding yeast, two proteins that contain the PX domain and the BAR domain, Atg20/Snx42 and Atg24/Snx4, are required for organelle autophagy and contribute to general autophagy in a way that can be compensated. It remains unclear why these proteins are important for organelle autophagy. Here, we show that in a distantly related fungal organism the fission yeast Schizosaccharomyces pombe, autophagy of ER and mitochondria is induced by nitrogen starvation and is promoted by three Atg20 and Atg24 family proteins, Atg20, Atg24, and Atg24b/SPBC1711.11. These proteins localize at the pre-autophagosomal structure/phagophore assembly site (PAS) during starvation. Atg24 forms a homo-oligomer, and acts redundantly with Atg20 and Atg24b, which form a hetero-oligomer. The organelle autophagy defect caused by the loss of these proteins is associated with a reduction of autophagosome size and a decrease of Atg8 accumulation at PAS. These results provide new insights into the autophagic function of Atg20 and Atg24 family proteins.

Funder

National Basic Research Program of China

Publisher

The Company of Biologists

Subject

Cell Biology

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