线粒体相关凝聚物维持线粒体稳态并延长寿命。

IF 19.4 Q1 CELL BIOLOGY
Yan Bai, Tengfei Ma, Shan Zhao, Shalan Li, Xin Wang, Jingyang Li, Wenhao Sun, Yang Yang, Fenglian Liu, Qian Shan, Zizhen Qin, Nan Liu, Jie Zhang, Fei Tian, Mei Duan, Shunkai Chen, Fan Lai, Qingfeng Chen, Xuna Wu, Chonglin Yang
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引用次数: 0

摘要

通过液-液相分离组装的无膜细胞器与多种膜细胞器相互作用,调节不同的细胞过程。目前尚不清楚无膜细胞器是如何参与线粒体稳态的。在这里,我们证明了线粒体相关翻译细胞器(MATOs)介导线粒体结构和功能维持所需的局部蛋白质合成。在秀丽隐杆线虫(Caenorhabditis elegans)中,rna结合蛋白LARP-1 (la -相关蛋白1)通过液-液相分离,协调翻译机制和多种rna结合蛋白的结合,形成以外膜复合体转位酶依赖的方式与线粒体结合的MATOs。LARP-1缺乏显著降低线粒体蛋白水平,损害嵴组织和ATP的产生。具体来说,我们发现在LARP-1 MATOs中合成了形成膜的MICOS亚基imt -1(MIC60)和ATP合成酶β亚基ATP-2,这两个亚基对嵴组织都很重要。在衰老和饥饿过程中,LARP-1 MATOs与线粒体分离;然而,线粒体持久性LARP-1 MATOs保护线粒体健康并大大延长寿命。这些发现提示了线粒体在衰老和应激中的重要调节机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mitochondria-associated condensates maintain mitochondrial homeostasis and promote lifespan.

Membraneless organelles assembled by liquid-liquid phase separation interact with diverse membranous organelles to regulate distinct cellular processes. It remains unknown how membraneless organelles are engaged in mitochondrial homeostasis. Here we demonstrate that mitochondria-associated translation organelles (MATOs) mediate local synthesis of proteins required for structural and functional maintenance of mitochondria. In Caenorhabditis elegans, the RNA-binding protein LARP-1 (La-related protein 1) orchestrates coalescence of translation machinery and multiple RNA-binding proteins via liquid-liquid phase separation into MATOs that associate with mitochondria in a translocase of the outer membrane complex-dependent manner. LARP-1 deficiency markedly reduces mitochondrial protein levels, impairing cristae organization and ATP production. Specifically, we show that the membrane-shaping MICOS subunit IMMT-1(MIC60) and the ATP synthase β subunit ATP-2, both being important for cristae organization, are synthesized in LARP-1 MATOs. During aging and starvation, LARP-1 MATOs dissociate from mitochondria; however, mitochondrion-persistent LARP-1 MATOs protect mitochondrial health and greatly extend lifespan. These findings suggest an important mitochondrion-regulating mechanism in aging and stress.

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CiteScore
14.70
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