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Friendly 介导了拟南芥中由膜去极化诱导的线粒体自噬。

Friendly mediates membrane depolarization-induced mitophagy in Arabidopsis.

机构信息

School of Life Sciences, Centre for Cell & Developmental Biology and State Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China.

Gregor Mendel Institute (GMI), Austrian Academy of Sciences, Vienna BioCenter (VBC), Vienna, Austria.

出版信息

Curr Biol. 2021 May 10;31(9):1931-1944.e4. doi: 10.1016/j.cub.2021.02.034. Epub 2021 Mar 11.

DOI:10.1016/j.cub.2021.02.034
PMID:33711250
Abstract

The oxidative environment within the mitochondria makes them particularly vulnerable to proteotoxic stress. To maintain a healthy mitochondrial network, eukaryotes have evolved multi-tiered quality control pathways. If the stress cannot be alleviated, defective mitochondria are selectively removed by autophagy via a process termed mitophagy. Despite significant advances in metazoans and yeast, in plants, the molecular underpinnings of mitophagy are largely unknown. Here, using time-lapse imaging, electron tomography, and biochemical assays, we show that uncoupler treatments cause loss of mitochondrial membrane potential and induce autophagy in Arabidopsis. The damaged mitochondria are selectively engulfed by autophagosomes that are labeled by ATG8 proteins in an ATG5-dependent manner. Friendly, a member of the clustered mitochondria protein family, is recruited to the damaged mitochondria to mediate mitophagy. In addition to the stress, mitophagy is also induced during de-etiolation, a major cellular transformation during photomorphogenesis that involves chloroplast biogenesis. De-etiolation-triggered mitophagy is involved in cotyledon greening, pointing toward an inter-organellar crosstalk mechanism. Altogether, our results demonstrate how plants employ mitophagy to recycle damaged mitochondria during stress and development.

摘要

线粒体内部的氧化环境使它们特别容易受到蛋白毒性应激的影响。为了维持健康的线粒体网络,真核生物已经进化出多层次的质量控制途径。如果应激不能得到缓解,有缺陷的线粒体就会通过自噬作用被选择性地清除,这个过程被称为线粒体自噬。尽管在后生动物和酵母中已经取得了显著的进展,但在植物中,线粒体自噬的分子基础在很大程度上仍是未知的。在这里,我们使用延时成像、电子断层扫描和生化分析,表明解偶联剂处理会导致线粒体膜电位丧失,并在拟南芥中诱导自噬。受损的线粒体被自噬体选择性吞噬,自噬体通过 ATG5 依赖性方式被 ATG8 蛋白标记。Friendly,一个聚集线粒体蛋白家族的成员,被招募到受损的线粒体上,以介导线粒体自噬。除了应激之外,线粒体自噬也会在去黄化过程中被诱导,去黄化是光形态发生过程中一种主要的细胞转化,涉及叶绿体的生物发生。去黄化触发的线粒体自噬参与了子叶的变绿,表明存在细胞器间的串扰机制。总之,我们的研究结果表明,植物如何在应激和发育过程中利用线粒体自噬来回收受损的线粒体。

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