| Literature DB >> 33087875 |
Ying Zhang1,2, Xu Xu1, Mengxin Hu1, Xin Wang1, Hanhua Cheng3, Rongjia Zhou4,5.
Abstract
Selective autophagic degradation of mitochondria (mitophagy) is important in maintaining proper cellular homeostasis. Here, we found that SPATA33 is a novel autophagy mediator for mitophagy in testis. The SPATA33 protein localizes on mitochondria via its binding of the carboxyl terminal with the outer mitochondrial membrane protein VDAC2. Upon starvation induction, SPATA33 is recruited to autophagosome by binding the autophagy machinery ATG16L1 via its N-terminal along with mitochondria. Notably, Spata33 knockout inhibited autophagy and overexpression can promote autophagosome formation for mitochondrial sequestration. Therefore, SPATA33 confers selectivity for mitochondrial degradation and promotes mitophagy in male germline cells.Entities:
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Year: 2020 PMID: 33087875 PMCID: PMC7937689 DOI: 10.1038/s41418-020-00638-2
Source DB: PubMed Journal: Cell Death Differ ISSN: 1350-9047 Impact factor: 15.828