A PINK1 input threshold arises from positive feedback in the PINK1/Parkin mitophagy decision circuit

被引:7
作者
Waters, Christopher S. [1 ]
Angenent, Sigurd B. [2 ]
Altschuler, Steven J. [1 ]
Wu, Lani F. [1 ]
机构
[1] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94158 USA
[2] Univ Wisconsin Madison, Math Dept, Madison, WI 53706 USA
来源
CELL REPORTS | 2023年 / 42卷 / 10期
基金
美国国家科学基金会;
关键词
DAMAGED MITOCHONDRIA; PARKIN; UBIQUITIN; ACTIVATION; MECHANISM; FISSION; USP30; PHOSPHORYLATION; RECRUITMENT; COMPLEX;
D O I
10.1016/j.celrep.2023.113260
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mechanisms that prevent accidental activation of the PINK1/Parkin mitophagy circuit on healthy mitochon-dria are poorly understood. On the surface of damaged mitochondria, PINK1 accumulates and acts as the input signal to a positive feedback loop of Parkin recruitment, which in turn promotes mitochondrial degra-dation via mitophagy. However, PINK1 is also present on healthy mitochondria, where it could errantly recruit Parkin and thereby activate this positive feedback loop. Here, we explore emergent properties of the PINK1/ Parkin circuit by quantifying the relationship between mitochondrial PINK1 concentrations and Parkin recruitment dynamics. We find that Parkin is recruited to mitochondria only if PINK1 levels exceed a threshold and then only after a delay that is inversely proportional to PINK1 levels. Furthermore, these two regulatory properties arise from the input-coupled positive feedback topology of the PINK1/Parkin circuit. These results outline an intrinsic mechanism by which the PINK1/Parkin circuit can avoid errant activation on healthy mito-chondria.
引用
收藏
页数:23
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