Gravitational and mechanical forces shape mitochondrial translation

Life on Earth has evolved in a form suitable for the gravitational force. Although the pivotal role of gravity in gene expression has been suggested, the molecular details remain unclear. Here, we show that mitochondria utilize gravity to activate protein synthesis within the organelle. Genome-wide ribosome profiling reveals reduced mitochondrial translation in mammalian cells and Caenorhabditis elegans under microgravity. We found that attenuation of cell adhesion through laminin-integrin interactions caused the phenotype. Mitochondrial translation is activated by a signal relayed by FAK, RAC1, PAK1, BAD, and Bcl-2 family proteins in the cytosol, and the mitochondrial fatty acid synthesis (mtFAS) pathway in the matrix. Consumption of mitochondrial malonyl-CoA by mtFAS reduces the malonylation of the translational machinery and accelerates the rates of translational initiation and elongation. Physiologically, this system operates in mechano-response of skeletal muscles. Our work provides mechanistic insights into how cells convert gravitational and mechanical forces into translation in mitochondria.

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Publication Details

Journal
Nature Communications
Published
2026-06-30
DOI
https://doi.org/10.1038/s41467-026-74493-z
Primary Topic
Spaceflight effects on biology
Type
article
Field-Weighted Citation Impact
0.00

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article

Gravitational and mechanical forces shape mitochondrial translation

Tatsuhisa Tsuboi, Nono Takeuchi-Tomita, Taku Saito, Toshiya Tsubaki et al.
Nature Communications
Spaceflight effects on biology
article

Gravitational and mechanical forces shape mitochondrial translation

Tatsuhisa Tsuboi, Nono Takeuchi-Tomita, Taku Saito, Toshiya Tsubaki, Mari Mito, Akira Higashibata, Shintaro Iwasaki, Yusuke Hirabayashi, Koki Nakamura, Taisei Wakigawa, Hironori Saito, Tomokazu Yamazaki, Yuichi Shichino, Atsushi Higashitani, Tohru Yamamori, Muhoon Lee, Abdul Haseeb Khan, Yusuke Kimura
article en

Abstract

Life on Earth has evolved in a form suitable for the gravitational force. Although the pivotal role of gravity in gene expression has been suggested, the molecular details remain unclear. Here, we show that mitochondria utilize gravity to activate protein synthesis within the organelle. Genome-wide ribosome profiling reveals reduced mitochondrial translation in mammalian cells and Caenorhabditis elegans under microgravity. We found that attenuation of cell adhesion through laminin-integrin interactions caused the phenotype. Mitochondrial translation is activated by a signal relayed by FAK, RAC1, PAK1, BAD, and Bcl-2 family proteins in the cytosol, and the mitochondrial fatty acid synthesis (mtFAS) pathway in the matrix. Consumption of mitochondrial malonyl-CoA by mtFAS reduces the malonylation of the translational machinery and accelerates the rates of translational initiation and elongation. Physiologically, this system operates in mechano-response of skeletal muscles. Our work provides mechanistic insights into how cells convert gravitational and mechanical forces into translation in mitochondria.

Nature CommunicationsVol. 17(1)
Pioneer (United States) (US), University of Tsukuba (JP), Tohoku University (JP), Japan Aerospace Exploration Agency (JP), RIKEN (JP), Tsinghua–Berkeley Shenzhen Institute (CN), Japan Space Forum (JP), Institute of Applied Biochemistry (JP), The University of Tokyo (JP)
National Aeronautics and Space Administration, Japan Agency for Medical Research and Development, Ministry of Education, Culture, Sports, Science and Technology, Hokkaido University, National Institutes of Health, Japan Society for the Promotion of Science, Japan Science and Technology Agency, Japan Aerospace Exploration Agency, RIKEN, Common Fund
Openalex Percentile: Top 8%
Spaceflight effects on biology
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