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GET 途径通过 Ppg1-Far 复合物靶向内质网激活 Atg32 介导的线粒体自噬。

The GET pathway serves to activate Atg32-mediated mitophagy by ER targeting of the Ppg1-Far complex.

机构信息

Laboratory of Mitochondrial Dynamics, Graduate School of Frontier Biosciences, Osaka University, Suita, Japan.

Laboratory of Mitochondrial Dynamics, Graduate School of Frontier Biosciences, Osaka University, Suita, Japan

出版信息

Life Sci Alliance. 2023 Jan 25;6(4). doi: 10.26508/lsa.202201640. Print 2023 Apr.

Abstract

Mitophagy removes defective or superfluous mitochondria via selective autophagy. In yeast, the pro-mitophagic protein Atg32 localizes to the mitochondrial surface and interacts with the scaffold protein Atg11 to promote degradation of mitochondria. Although Atg32-Atg11 interactions are thought to be stabilized by Atg32 phosphorylation, how this posttranslational modification is regulated remains obscure. Here, we show that cells lacking the guided entry of the tail-anchored protein (GET) pathway exhibit reduced Atg32 phosphorylation and Atg32-Atg11 interactions, which can be rescued by additional loss of the ER-resident Ppg1-Far complex, a multi-subunit phosphatase negatively acting in mitophagy. In GET-deficient cells, Ppg1-Far is predominantly localized to mitochondria. An artificial ER anchoring of Ppg1-Far in GET-deficient cells significantly ameliorates defects in Atg32-Atg11 interactions and mitophagy. Moreover, disruption of GET and Msp1, an AAA-ATPase that extracts non-mitochondrial proteins localized to the mitochondrial surface, elicits synthetic defects in mitophagy. Collectively, we propose that the GET pathway mediates ER targeting of Ppg1-Far, thereby preventing dysregulated suppression of mitophagy activation.

摘要

线粒体自噬通过选择性自噬去除有缺陷或多余的线粒体。在酵母中,促线粒体自噬蛋白 Atg32 定位于线粒体表面,并与支架蛋白 Atg11 相互作用,促进线粒体的降解。尽管 Atg32-Atg11 相互作用被认为是通过 Atg32 磷酸化稳定的,但这种翻译后修饰如何被调节仍然不清楚。在这里,我们表明,缺乏尾部锚定蛋白(GET)途径引导进入的细胞表现出 Atg32 磷酸化和 Atg32-Atg11 相互作用减少,这可以通过额外缺失 ER 驻留的多亚基磷酸酶 Ppg1-Far 复合物得到挽救,Ppg1-Far 复合物在线粒体自噬中起负调控作用。在 GET 缺陷细胞中,Ppg1-Far 主要定位于线粒体。在 GET 缺陷细胞中人为地将 Ppg1-Far 锚定在 ER 上,可显著改善 Atg32-Atg11 相互作用和线粒体自噬缺陷。此外,GET 和 Msp1 的破坏,一种提取定位于线粒体表面的非线粒体蛋白的 AAA-ATP 酶,会引发线粒体自噬的合成缺陷。总之,我们提出 GET 途径介导 Ppg1-Far 的 ER 靶向,从而防止线粒体自噬激活的失调抑制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c3c/9880027/66d30c99fc58/LSA-2022-01640_Fig1.jpg

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