Deciphering the Roles of the Salvage and De Novo Pathways of Nucleotide’s Metabolism in Mitochondrial DNA Maintenance

HORIZON.1.2HORIZON-TMA-MSCA-PF-GFID: 101065857
EC Contribution
€2,614
Consortium Size
2 orgs
Summary

Mitochondrion is a crucial integrator of various cellular metabolic pathways in the intermediary metabolism, and it has the ability to produce oxidatively-derived energy by the oxidative phosphorylation (OxPhos) system. The OxPhos complexes are composed of subunits encoded by both mtDNA and nuclear DNA (nDNA), and mutations in either class of genes can cause severe OxPhos defects, leading to mitochondrial diseases (MD). Remarkably, the mitochondrion is unique among the cell's organelles, as it contains its own DNA (mtDNA). The deoxynucleotides triphosphates (dNTPs) required for mtDNA synthesis are produced by the salvage pathway in the own mitochondrion. However, recent data suggest that de novo pathway for dNTPs synthesis is also critical for mtDNA replication. In fact, defects in enzymes involved the de novo pathway have been recently reported as causes of MD. MITO-GARAGE aims to better understand how the different pathways involved in dNTPs metabolism work in mtDNA replication and to develop therapeutic strategies when it is impaired. This will allow us to better comprehend basic metabolic processes and their integration in pathophysiological and therapeutic aspects for MD. With that purpose, we will use unique in vitro and in vivo models with defects in RRM1, GUK1 and COQ2, and a combination of modern and classical reductionist approaches. MITO-GARAGE will be carried out in international-recognized groups at Columbia University and the University of Granada. The workplan includes one key short visit to learn an specific technology; training in basic-clinic and public-private partnerships; training in academic skills; scientific and non-scientific work-packages, tasks, milestones and deliverables; a contingency plan; the landscape for results’ exploitation and the development of a career plan. Overall, MITO-GARAGE clearly define the four-way transfer of knowledge and will achieve significant advances in the progress of the hyper-personalized medicine.

Consortium (2)

Project Results (5)

Source: CORDIS, the EU research results database.

Publications (3)
Coenzyme Q10 deficiency disrupts lipid metabolism by altering cholesterol homeostasis in neurons
Free Radical Biology and Medicine· 2025DOI
Alba Pesini, Eliana Barriocanal-Casado, Giacomo Monzio Compagnoni, Agustin Hidalgo-Gutierrez, Giussepe Yanez, Mohammed Bakkali, Yashpal S. Chhonker, Giulio Kleiner, Delfina Larrea, Saba Tadesse, Luis Carlos Lopez, Daryl J. Murry, Alessio Di Fonzo, Estela Area-Gomez, Catarina M. Quinzii
Early heart and skeletal muscle mitochondrial response to a moderate hypobaric hypoxia environment
Journal of Physiology· 2024DOI
Jerónimo Aragón-Vela, Rafael A. Casuso, Ana Sagrera Aparisi, Julio Plaza-Díaz, Ascensión Rueda-Robles, Agustín Hidalgo-Gutiérrez, Luis Carlos López, Andrea Rodríguez-Carrillo, José Antonio Enriquez, Sara Cogliati, and Jesús R. H
Guanylate Kinase 1 Deficiency: A Novel and Potentially Treatable Mitochondrial DNA Depletion/Deletions Disease
Annals of Neurology· 2024DOI
Agustin Hidalgo-Gutierrez PhD, Jonathan Shintaku, Javier Ramon... Michio Hirano, et al
Deliverables (1)
Data Management Plan
Other Results (1)
Periodic Reporting for period 1 - MITO-GARAGE (Deciphering the Roles of the Salvage and De Novo Pathways of Nucleotide’s Metabolism in Mitochondrial DNA Maintenance)