Literature DB >> 19028666

Unbalanced deoxynucleotide pools cause mitochondrial DNA instability in thymidine phosphorylase-deficient mice.

Luis C López1, Hasan O Akman, Angeles García-Cazorla, Beatriz Dorado, Ramón Martí, Ichizo Nishino, Saba Tadesse, Giuseppe Pizzorno, Dikoma Shungu, Eduardo Bonilla, Kurenai Tanji, Michio Hirano.   

Abstract

Replication and repair of DNA require equilibrated pools of deoxynucleoside triphosphate precursors. This concept has been proven by in vitro studies over many years, but in vivo models are required to demonstrate its relevance to multicellular organisms and to human diseases. Accordingly, we have generated thymidine phosphorylase (TP) and uridine phosphorylase (UP) double knockout (TP(-/-)UP(-/-)) mice, which show severe TP deficiency, increased thymidine and deoxyuridine in tissues and elevated mitochondrial deoxythymidine triphosphate. As consequences of the nucleotide pool imbalances, brains of mutant mice developed partial depletion of mtDNA, deficiencies of respiratory chain complexes and encephalopathy. These findings largely account for the pathogenesis of mitochondrial neurogastrointestinal encephalopathy (MNGIE), the first inherited human disorder of nucleoside metabolism associated with somatic DNA instability.

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Year:  2008        PMID: 19028666      PMCID: PMC2638828          DOI: 10.1093/hmg/ddn401

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  42 in total

Review 1.  Biochemical assays of respiratory chain complex activity.

Authors:  Denise M Kirby; David R Thorburn; Douglass M Turnbull; Robert W Taylor
Journal:  Methods Cell Biol       Date:  2007       Impact factor: 1.441

2.  Expression of deoxynucleoside kinases and 5'-nucleotidases in mouse tissues: implications for mitochondrial toxicity.

Authors:  Svetlana N Rylova; Saeedeh Mirzaee; Freidoun Albertioni; Staffan Eriksson
Journal:  Biochem Pharmacol       Date:  2007-04-12       Impact factor: 5.858

3.  A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutations.

Authors:  Weiwei Fan; Katrina G Waymire; Navneet Narula; Peng Li; Christophe Rocher; Pinar E Coskun; Mani A Vannan; Jagat Narula; Grant R Macgregor; Douglas C Wallace
Journal:  Science       Date:  2008-02-15       Impact factor: 47.728

4.  Mutations in mitochondrial-encoded cytochrome c oxidase subunits I, II, and III genes detected in Alzheimer's disease using single-strand conformation polymorphism.

Authors:  Natasha S Hamblet; Brian Ragland; Mervat Ali; Barbara Conyers; Frank J Castora
Journal:  Electrophoresis       Date:  2006-02       Impact factor: 3.535

5.  mtDNA phylogeny and evolution of laboratory mouse strains.

Authors:  Ana Goios; Luísa Pereira; Molly Bogue; Vincent Macaulay; António Amorim
Journal:  Genome Res       Date:  2007-02-06       Impact factor: 9.043

6.  Mitochondrial deoxynucleotide pool sizes in mouse liver and evidence for a transport mechanism for thymidine monophosphate.

Authors:  Paola Ferraro; Luca Nicolosi; Paolo Bernardi; Peter Reichard; Vera Bianchi
Journal:  Proc Natl Acad Sci U S A       Date:  2006-11-21       Impact factor: 11.205

7.  Mitochondrial DNA depletion and thymidine phosphate pool dynamics in a cellular model of mitochondrial neurogastrointestinal encephalomyopathy.

Authors:  Giovanna Pontarin; Paola Ferraro; Maria L Valentino; Michio Hirano; Peter Reichard; Vera Bianchi
Journal:  J Biol Chem       Date:  2006-06-13       Impact factor: 5.157

8.  Thymidine and deoxyuridine accumulate in tissues of patients with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).

Authors:  Maria Lucia Valentino; Ramon Martí; Saba Tadesse; Luis Carlos López; Jose L Manes; Judy Lyzak; Angelika Hahn; Valerio Carelli; Michio Hirano
Journal:  FEBS Lett       Date:  2007-06-27       Impact factor: 4.124

9.  MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion.

Authors:  Antonella Spinazzola; Carlo Viscomi; Erika Fernandez-Vizarra; Franco Carrara; Pio D'Adamo; Sarah Calvo; René Massimiliano Marsano; Claudia Donnini; Hans Weiher; Pietro Strisciuglio; Rossella Parini; Emmanuelle Sarzi; Alicia Chan; Salvatore DiMauro; Agnes Rötig; Paolo Gasparini; Iliana Ferrero; Vamsi K Mootha; Valeria Tiranti; Massimo Zeviani
Journal:  Nat Genet       Date:  2006-04-02       Impact factor: 38.330

10.  Strong purifying selection in transmission of mammalian mitochondrial DNA.

Authors:  James Bruce Stewart; Christoph Freyer; Joanna L Elson; Anna Wredenberg; Zekiye Cansu; Aleksandra Trifunovic; Nils-Göran Larsson
Journal:  PLoS Biol       Date:  2008-01       Impact factor: 8.029

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  60 in total

1.  Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy.

Authors:  Caterina Garone; Saba Tadesse; Michio Hirano
Journal:  Brain       Date:  2011-09-20       Impact factor: 13.501

Review 2.  CoQ(10) deficiencies and MNGIE: two treatable mitochondrial disorders.

Authors:  Michio Hirano; Caterina Garone; Catarina M Quinzii
Journal:  Biochim Biophys Acta       Date:  2012-01-18

3.  Metabolism of deoxypyrimidines and deoxypyrimidine antiviral analogs in isolated brain mitochondria.

Authors:  Kathleen A McCann; David W Williams; Edward E McKee
Journal:  J Neurochem       Date:  2012-05-21       Impact factor: 5.372

4.  Deoxycytidine and Deoxythymidine Treatment for Thymidine Kinase 2 Deficiency.

Authors:  Carlos Lopez-Gomez; Rebecca J Levy; Maria J Sanchez-Quintero; Martí Juanola-Falgarona; Emanuele Barca; Beatriz Garcia-Diaz; Saba Tadesse; Caterina Garone; Michio Hirano
Journal:  Ann Neurol       Date:  2017-05-04       Impact factor: 10.422

Review 5.  Mitochondrial Diseases Part III: Therapeutic interventions in mouse models of OXPHOS deficiencies.

Authors:  Susana Peralta; Alessandra Torraco; Luisa Iommarini; Francisca Diaz
Journal:  Mitochondrion       Date:  2015-01-29       Impact factor: 4.160

6.  Allogeneic hematopoietic SCT as treatment option for patients with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a consensus conference proposal for a standardized approach.

Authors:  J Halter; Wmm Schüpbach; A Gratwohl; M Hirano; C Casali; R Elhasid; K Fay; S Hammans; I Illa; L Kappeler; S Krähenbühl; T Lehmann; H Mandel; R Marti; H Mattle; K Orchard; D Savage; C M Sue; D Valcarcel
Journal:  Bone Marrow Transplant       Date:  2010-05-03       Impact factor: 5.483

7.  Thiamine Deficiency-Mediated Brain Mitochondrial Pathology in Alaskan Huskies with Mutation in SLC19A3.1.

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Journal:  Brain Pathol       Date:  2014-10-29       Impact factor: 6.508

8.  Autocrine amplification of integrin αIIbβ3 activation and platelet adhesive responses by deoxyribose-1-phosphate.

Authors:  Dina S Vara; Michelangelo Campanella; Ilaria Canobbio; Warwick B Dunn; Giuseppe Pizzorno; Michio Hirano; Giordano Pula
Journal:  Thromb Haemost       Date:  2013-03-14       Impact factor: 5.249

Review 9.  Mitochondrial Diseases Part II: Mouse models of OXPHOS deficiencies caused by defects in regulatory factors and other components required for mitochondrial function.

Authors:  Luisa Iommarini; Susana Peralta; Alessandra Torraco; Francisca Diaz
Journal:  Mitochondrion       Date:  2015-01-29       Impact factor: 4.160

10.  Quantitation of cellular deoxynucleoside triphosphates.

Authors:  Paola Ferraro; Elisa Franzolin; Giovanna Pontarin; Peter Reichard; Vera Bianchi
Journal:  Nucleic Acids Res       Date:  2009-12-11       Impact factor: 16.971

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