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ROMO1 overexpression protects the mitochondrial cysteinome from oxidations in aging

Author

Listed:
  • Fengli Xu

    (Peking University
    Peking University)

  • Haipeng Huang

    (Peking University
    PKU-Nanjing Institute of Translational Medicine)

  • Kun Peng

    (Peking University
    Peking University)

  • Chongshu Jian

    (Peking University)

  • Hao Wu

    (Peking University)

  • Zhiwen Jing

    (Peking University)

  • Shan Qiu

    (Peking University)

  • Ying Chen

    (Peking University)

  • Keke Liu

    (Beijing Institute of Lifeomics)

  • Ling Fu

    (Beijing Institute of Lifeomics)

  • Yanru Wang

    (Peking University)

  • Jing Yang

    (Beijing Institute of Lifeomics)

  • Xiaotao Duan

    (Beijing Institute of Pharmacology and Toxicology)

  • Chu Wang

    (Peking University
    Peking University)

  • Heping Cheng

    (Peking University
    Peking University
    PKU-Nanjing Institute of Translational Medicine)

  • Xianhua Wang

    (Peking University
    Peking University
    PKU-Nanjing Institute of Translational Medicine)

Abstract

Reactive thiols of proteinaceous cysteines are vital to cell biology by serving as sensor, effector and buffer of environmental redox fluctuations. Being the major source, as well as the prime target, of reactive oxygen species (ROS), mitochondria confront great challenges in preserving their thiol pool. Here we show that ROS modulator 1 (ROMO1), a small inner mitochondrial membrane protein, plays a role in protecting the mitochondrial cysteinome. ROMO1 is redox sensitive and reactive and overexpression can prevent deleterious oxidation of proteinaceous thiols. ROMO1 upregulation leads to a reductive shift of the mitochondrial cysteinome, exerting beneficial effects on mitochondria, such as promoting energy metabolism and Ca2+ uniport while inhibiting vicious membrane permeability transition. Importantly, ROMO1 overexpression reverses mitochondrial cysteinome oxidations in multiple organs and slows functional decline in aged male mice. These findings unravel a redox regulatory mechanism of the mitochondrial cysteinome and mark ROMO1 as a potential target for combating oxidative stress and improving healthspan.

Suggested Citation

  • Fengli Xu & Haipeng Huang & Kun Peng & Chongshu Jian & Hao Wu & Zhiwen Jing & Shan Qiu & Ying Chen & Keke Liu & Ling Fu & Yanru Wang & Jing Yang & Xiaotao Duan & Chu Wang & Heping Cheng & Xianhua Wang, 2025. "ROMO1 overexpression protects the mitochondrial cysteinome from oxidations in aging," Nature Communications, Nature, vol. 16(1), pages 1-20, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-60503-z
    DOI: 10.1038/s41467-025-60503-z
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