Mitochondria-associated condensates maintain mitochondrial homeostasis and promote lifespan

  • Nat Aging. 2025 Sep 10. doi: 10.1038/s43587-025-00942-x.
Yan Bai  #  1 ,  Tengfei Ma  #  1 ,  Shan Zhao  1 ,  Shalan Li  1 ,  Xin Wang  1 ,  Jingyang Li  1 ,  Wenhao Sun  1 ,  Yang Yang  1 ,  Fenglian Liu  1 ,  Qian Shan  1 ,  Zizhen Qin  1 ,  Nan Liu  1 ,  Jie Zhang  1 ,  Fei Tian  1 ,  Mei Duan  1 ,  Shunkai Chen  1 ,  Fan Lai  1  2 ,  Qingfeng Chen  1 ,  Xuna Wu  1 ,  Chonglin Yang  3  4
Affiliations
  • 1. State Key Laboratory of Conservation and Utilization of Bio-resources in Yunnan and Center for Life Sciences, School of Life Sciences, Yunnan University, Kunming, China.
  • 2. Southwest United Graduate School, Kunming, China.
  • 3. State Key Laboratory of Conservation and Utilization of Bio-resources in Yunnan and Center for Life Sciences, School of Life Sciences, Yunnan University, Kunming, China. [email protected].
  • 4. Southwest United Graduate School, Kunming, China. [email protected].
  • # Contributed equally.
Abstract

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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