Nix interacts with WIPI2 to induce mitophagy

被引:20
作者
Bunker, Eric N. [1 ]
Le Guerroue, Francois [1 ]
Wang, Chunxin [1 ]
Strub, Marie-Paule [2 ]
Werner, Achim [3 ]
Tjandra, Nico [2 ]
Youle, Richard J. [1 ]
机构
[1] Natl Inst Neurol Disorders & Stroke, Surg Neurol Branch, NIH, Bethesda, MD 20892 USA
[2] NHLBI, Biochem & Biophys Ctr, NIH, Bethesda, MD USA
[3] Natl Inst Dent & Craniofacial Res, Stem Cell Biochem Unit, NIH, Bethesda, MD USA
关键词
Autophagy; BNIP3; FIP200; LIR; p62; AUTOPHAGOSOME FORMATION; MITOCHONDRIAL AUTOPHAGY; PROTEIN; BNIP3; ACTIVATION; CLEARANCE; TARGET; MOTIF; PHOSPHORYLATION; SPECIFICITY;
D O I
10.15252/embj.2023113491
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nix is a membrane-anchored outer mitochondrial protein that induces mitophagy. While Nix has an LC3-interacting (LIR) motif that binds to ATG8 proteins, it also contains a minimal essential region (MER) that induces mitophagy through an unknown mechanism. We used chemically induced dimerization (CID) to probe the mechanism of Nix-mediated mitophagy and found that both the LIR and MER are required for robust mitophagy. We find that the Nix MER interacts with the autophagy effector WIPI2 and recruits WIPI2 to mitochondria. The Nix LIR motif is also required for robust mitophagy and converts a homogeneous WIPI2 distribution on the surface of the mitochondria into puncta, even in the absence of ATG8s. Together, this work reveals unanticipated mechanisms in Nix-induced mitophagy and the elusive role of the MER, while also describing an interesting example of autophagy induction that acts downstream of the canonical initiation complexes.
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页数:19
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