Nix interacts with WIPI2 to induce mitophagy

Author:

Bunker Eric N1ORCID,Le Guerroué François1ORCID,Wang Chunxin1,Strub Marie‐Paule2ORCID,Werner Achim3ORCID,Tjandra Nico2,Youle Richard J1ORCID

Affiliation:

1. Surgical Neurology Branch National Institute of Neurological Disorders and Stroke, National Institutes of Health Bethesda MD USA

2. Biochemistry and Biophysics Center National Heart, Lung, and Blood Institute, National Institutes of Health Bethesda MD USA

3. Stem Cell Biochemistry Unit National Institute of Dental and Craniofacial Research, National Institutes of Health Bethesda MD USA

Abstract

AbstractNix 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.

Funder

National Institute of Dental and Craniofacial Research

National Institute of Neurological Disorders and Stroke

NHLBI Division of Intramural Research

Publisher

Springer Science and Business Media LLC

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology,General Neuroscience

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