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Ribonucleotide synthesis by NME6 fuels mitochondrial gene expression

Nils Grotehans, Lynn McGarry, Hendrik Nolte, Moritz Kroker, View ORCID ProfileÁlvaro Jesús Narbona-Pérez, View ORCID ProfileSoni Deshwal, Patrick Giavalisco, View ORCID ProfileThomas Langer, View ORCID ProfileThomas MacVicar
doi: https://doi.org/10.1101/2022.11.29.518352
Nils Grotehans
1Max Planck Institute for Biology of Ageing, Cologne, Germany
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Lynn McGarry
2The CRUK Beatson Institute, Glasgow, United Kingdom
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Hendrik Nolte
1Max Planck Institute for Biology of Ageing, Cologne, Germany
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Moritz Kroker
1Max Planck Institute for Biology of Ageing, Cologne, Germany
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Álvaro Jesús Narbona-Pérez
1Max Planck Institute for Biology of Ageing, Cologne, Germany
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  • ORCID record for Álvaro Jesús Narbona-Pérez
Soni Deshwal
1Max Planck Institute for Biology of Ageing, Cologne, Germany
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Patrick Giavalisco
1Max Planck Institute for Biology of Ageing, Cologne, Germany
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Thomas Langer
1Max Planck Institute for Biology of Ageing, Cologne, Germany
3Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne, Germany
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  • For correspondence: tlanger@age.mpg.de T.MacVicar@beatson.gla.ac.uk
Thomas MacVicar
2The CRUK Beatson Institute, Glasgow, United Kingdom
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  • For correspondence: tlanger@age.mpg.de T.MacVicar@beatson.gla.ac.uk
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Abstract

Replication and expression of the mitochondrial genome depend on the sufficient supply of nucleotide building blocks to mitochondria. Dysregulated nucleotide metabolism is detrimental to mitochondrial genomes and can result in instability of mitochondrial DNA and inflammation. Here, we report that a mitochondrial nucleoside diphosphate kinase, NME6, supplies mitochondria with ribonucleotides to drive the transcription of mitochondrial genes. Moreover, NME6 supports the maintenance of mitochondrial DNA when the access to cytosolic deoxyribonucleotides is limited. Perturbation of NME6 leads to the depletion of mitochondrial transcripts, destabilisation of the electron transport chain and impaired oxidative phosphorylation; deficiencies which are suppressed upon supplementation with pyrimidine ribonucleotides. Our work proposes NME6 and mitochondrial nucleotide metabolism to be untapped therapeutic targets in diseases associated with aberrant mitochondrial gene expression including cancer and autoimmune disorders.

Competing Interest Statement

The authors have declared no competing interest.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted November 30, 2022.
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Ribonucleotide synthesis by NME6 fuels mitochondrial gene expression
Nils Grotehans, Lynn McGarry, Hendrik Nolte, Moritz Kroker, Álvaro Jesús Narbona-Pérez, Soni Deshwal, Patrick Giavalisco, Thomas Langer, Thomas MacVicar
bioRxiv 2022.11.29.518352; doi: https://doi.org/10.1101/2022.11.29.518352
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Ribonucleotide synthesis by NME6 fuels mitochondrial gene expression
Nils Grotehans, Lynn McGarry, Hendrik Nolte, Moritz Kroker, Álvaro Jesús Narbona-Pérez, Soni Deshwal, Patrick Giavalisco, Thomas Langer, Thomas MacVicar
bioRxiv 2022.11.29.518352; doi: https://doi.org/10.1101/2022.11.29.518352

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