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Super-resolution microscopy of mitochondrial mRNAs

Author

Listed:
  • Stefan Stoldt

    (RG Mitochondrial Structure and Dynamics
    University Medical Center Göttingen
    University of Göttingen)

  • Frederike Maass

    (RG Mitochondrial Structure and Dynamics
    University Medical Center Göttingen
    University of Göttingen)

  • Michael Weber

    (Max Planck Institute for Multidisciplinary Sciences)

  • Sven Dennerlein

    (University Medical Center Göttingen)

  • Peter Ilgen

    (RG Mitochondrial Structure and Dynamics
    University Medical Center Göttingen
    Translational Neuroinflammation and Automated Microscopy)

  • Jutta Gärtner

    (University of Göttingen
    Translational Neuroinflammation and Automated Microscopy
    University Medical Center Göttingen
    partner site Göttingen)

  • Aysenur Canfes

    (RG Mitochondrial Structure and Dynamics
    University Medical Center Göttingen)

  • Sarah V. Schweighofer

    (RG Mitochondrial Structure and Dynamics
    Translational Neuroinflammation and Automated Microscopy)

  • Daniel C. Jans

    (RG Mitochondrial Structure and Dynamics
    University Medical Center Göttingen)

  • Peter Rehling

    (University of Göttingen
    University Medical Center Göttingen
    Translational Neuroinflammation and Automated Microscopy
    partner site Göttingen)

  • Stefan Jakobs

    (RG Mitochondrial Structure and Dynamics
    University Medical Center Göttingen
    University of Göttingen
    Translational Neuroinflammation and Automated Microscopy)

Abstract

Mitochondria contain their own DNA (mtDNA) and a dedicated gene expression machinery. As the mitochondrial dimensions are close to the diffraction limit of classical light microscopy, the spatial distribution of mitochondrial proteins and in particular of mitochondrial mRNAs remains underexplored. Here, we establish single-molecule fluorescence in situ hybridization (smFISH) combined with STED and MINFLUX super-resolution microscopy (nanoscopy) to visualize individual mitochondrial mRNA molecules and associated proteins. STED nanoscopy reveals the spatial relationships between distinct mRNA species and proteins such as the RNA granule marker GRSF1, demonstrating adaptive changes in mRNA distribution and quantity in challenged mammalian cells and patient-derived cell lines. Notably, STED-smFISH shows the release of mRNAs during apoptosis, while MINFLUX reveals the folding of the mRNAs into variable shapes, as well as their spatial proximity to mitochondrial ribosomes. These protocols are transferable to various cell types and open new avenues for understanding mitochondrial gene regulation in health and disease.

Suggested Citation

  • Stefan Stoldt & Frederike Maass & Michael Weber & Sven Dennerlein & Peter Ilgen & Jutta Gärtner & Aysenur Canfes & Sarah V. Schweighofer & Daniel C. Jans & Peter Rehling & Stefan Jakobs, 2025. "Super-resolution microscopy of mitochondrial mRNAs," Nature Communications, Nature, vol. 16(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-61577-5
    DOI: 10.1038/s41467-025-61577-5
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    References listed on IDEAS

    as
    1. Zbigniew Pietras & Magdalena A. Wojcik & Lukasz S. Borowski & Maciej Szewczyk & Tomasz M. Kulinski & Dominik Cysewski & Piotr P. Stepien & Andrzej Dziembowski & Roman J. Szczesny, 2018. "Dedicated surveillance mechanism controls G-quadruplex forming non-coding RNAs in human mitochondria," Nature Communications, Nature, vol. 9(1), pages 1-15, December.
    2. Nina A. Bonekamp & Bradley Peter & Hauke S. Hillen & Andrea Felser & Tim Bergbrede & Axel Choidas & Moritz Horn & Anke Unger & Raffaella Lucrezia & Ilian Atanassov & Xinping Li & Uwe Koch & Sascha Men, 2020. "Small-molecule inhibitors of human mitochondrial DNA transcription," Nature, Nature, vol. 588(7839), pages 712-716, December.
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