Abstract
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.
Original language | English |
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Article number | 102684 |
Journal | DNA Repair |
Volume | 82 |
Number of pages | 11 |
ISSN | 1568-7864 |
DOIs | |
Publication status | Published - 2019 |
Keywords
- Double-strand break
- Fanconi Anemia-like pathway
- Helicase Mph1
- Homologous recombination
- Mitochondrial DNA repair