4.3 Article

The FANCM family Mph1 helicase localizes to the mitochondria and contributes to mtDNA stability

Journal

DNA REPAIR
Volume 82, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.dnarep.2019.102684

Keywords

Mitochondrial DNA repair; Helicase Mph1; Fanconi Anemia-like pathway; Double-strand break; Homologous recombination

Funding

  1. ATIP-Avenir joint program of the CNRS
  2. INSERM
  3. Gustave Roussy Foundation
  4. Fondation ARC pour la Recherche sur le Cancer
  5. LNCC (La Ligue contre le Cancer)
  6. Chinese Scholarship Council
  7. Danish Council for Independent Research (FNU)
  8. Villum Foundation

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Mitochondria are membrane-bound organelles found in eukaryotic cells where they generate energy through the respiratory chain. They contain their own genome that encodes genes critical to the mitochondrial function, but most of their protein content is synthetized from nuclear encoded genes. Damages to the mtDNA can cause mutations and rearrangements with an impact on the respiratory functions of the cell. DNA repair factors are able to localize to mitochondria to restore mtDNA integrity and ensure its proper inheritance. We describe in this article the mitochondrial localization of the Mph1/FANCM helicase that serves critical roles in nuclear DNA repair processes. Mph1 localizes to mitochondria and its functions contribute to the mtDNA integrity under mtDNA damaging conditions.

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