Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
Biochemistry and Biophysics Center, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
EMBO J. 2023 Nov 15;42(22):e113491. doi: 10.15252/embj.2023113491. Epub 2023 Aug 25.
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.
Nix 是一种膜锚定的线粒体外膜蛋白,能诱导细胞自噬。虽然 Nix 含有一个与 ATG8 蛋白结合的 LC3 相互作用 (LIR) 基序,但它还包含一个最小必需区域 (MER),通过未知的机制诱导细胞自噬。我们使用化学诱导二聚化 (CID) 来探究 Nix 介导的细胞自噬的机制,发现 LIR 和 MER 两者对于强烈的细胞自噬都是必需的。我们发现 Nix MER 与自噬效应因子 WIPI2 相互作用,并将 WIPI2 招募到线粒体上。Nix LIR 基序对于强烈的细胞自噬也是必需的,它将线粒体表面均匀分布的 WIPI2 转化为斑点,即使在没有 ATG8s 的情况下也是如此。总的来说,这项工作揭示了 Nix 诱导的细胞自噬中意想不到的机制和 MER 的难以捉摸的作用,同时也描述了一个有趣的自噬诱导的例子,它作用于经典起始复合物的下游。