Ribonucleotide synthesis by NME6 fuels mitochondrial gene expression

Author:

Grotehans Nils1ORCID,McGarry Lynn2ORCID,Nolte Hendrik1,Xavier Vanessa2,Kroker Moritz1,Narbona‐Pérez Álvaro Jesús1ORCID,Deshwal Soni1ORCID,Giavalisco Patrick1,Langer Thomas13ORCID,MacVicar Thomas2ORCID

Affiliation:

1. Max Planck Institute for Biology of Ageing Cologne Germany

2. The CRUK Beatson Institute Glasgow UK

3. Cologne Excellence Cluster on Cellular Stress Responses in Aging‐Associated Diseases (CECAD) University of Cologne Cologne Germany

Abstract

AbstractReplication of the mitochondrial genome and expression of the genes it encodes both depend on a sufficient supply of nucleotides to mitochondria. Accordingly, dysregulated nucleotide metabolism not only destabilises the mitochondrial genome, but also affects its transcription. Here, we report that a mitochondrial nucleoside diphosphate kinase, NME6, supplies mitochondria with pyrimidine ribonucleotides that are necessary for the transcription of mitochondrial genes. Loss of NME6 function leads to the depletion of mitochondrial transcripts, as well as destabilisation of the electron transport chain and impaired oxidative phosphorylation. These deficiencies are rescued by an exogenous supply of pyrimidine ribonucleosides. Moreover, NME6 is required for the maintenance of mitochondrial DNA when the access to cytosolic pyrimidine deoxyribonucleotides is limited. Our results therefore reveal an important role for ribonucleotide salvage in mitochondrial gene expression.

Funder

Cancer Research UK

Max-Planck-Gesellschaft

Publisher

Springer Science and Business Media LLC

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology,General Neuroscience

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