Topoisomerase 3 α is required for decatenation and segregation of human mitochondrial DNA
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D. Turnbull | E. Larsson | C. Gustafsson | J. Griffith | M. Falkenberg | S. Basu | N. Larsson | G. Gorman | E. Hoberg | E. Motori | E. Sommerville | T. Nicholls | Chinnery | Taylor | C. Nadalutti | W. Robert | F. Patrick | D. Turnbull
[1] M. Zeviani,et al. MtDNA-maintenance defects: syndromes and genes , 2017, Journal of Inherited Metabolic Disease.
[2] Y. Pommier,et al. Roles of eukaryotic topoisomerases in transcription, replication and genomic stability , 2016, Nature Reviews Molecular Cell Biology.
[3] J. Nunnari,et al. ER-mitochondria contacts couple mtDNA synthesis with mitochondrial division in human cells , 2016, Science.
[4] H. Houlden,et al. Pathological ribonuclease H1 causes R-loop depletion and aberrant DNA segregation in mitochondria , 2016, Proceedings of the National Academy of Sciences.
[5] C. Gustafsson,et al. Maintenance and Expression of Mammalian Mitochondrial DNA. , 2016, Annual review of biochemistry.
[6] T. Hsieh,et al. Drosophila mitochondrial topoisomerase III alpha affects the aging process via maintenance of mitochondrial function and genome integrity , 2016, Journal of Biomedical Science.
[7] Karl R. Clauser,et al. MitoCarta2.0: an updated inventory of mammalian mitochondrial proteins , 2015, Nucleic Acids Res..
[8] S. Jakobs,et al. Cross-strand binding of TFAM to a single mtDNA molecule forms the mitochondrial nucleoid , 2015, Proceedings of the National Academy of Sciences.
[9] M. Zeviani,et al. RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial Encephalomyopathy. , 2015, American journal of human genetics.
[10] Maki Maeda,et al. Dynamics of Mitochondrial DNA Nucleoids Regulated by Mitochondrial Fission Is Essential for Maintenance of Homogeneously Active Mitochondria during Neonatal Heart Development , 2014, Molecular and Cellular Biology.
[11] S. West,et al. Holliday junction processing enzymes as guardians of genome stability. , 2014, Trends in biochemical sciences.
[12] Y. Pommier,et al. Increased negative supercoiling of mtDNA in TOP1mt knockout mice and presence of topoisomerases IIα and IIβ in vertebrate mitochondria , 2014, Nucleic acids research.
[13] J. Nunnari,et al. Mitochondrial form and function , 2014, Nature.
[14] S. Carr,et al. Proteomic Mapping of Mitochondria in Living Cells via Spatially Restricted Enzymatic Tagging , 2013, Science.
[15] S. Kowalczykowski,et al. Decatenation of DNA by the S. cerevisiae Sgs1-Top3-Rmi1 and RPA complex: a mechanism for disentangling chromosomes. , 2012, Molecular cell.
[16] Y. Pommier,et al. Mitochondrial Topoisomerase I is Critical for Mitochondrial Integrity and Cellular Energy Metabolism , 2012, PloS one.
[17] Steven L Salzberg,et al. Fast gapped-read alignment with Bowtie 2 , 2012, Nature Methods.
[18] J. Pouget,et al. The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype. , 2012, Brain : a journal of neurology.
[19] S. Jakobs,et al. Super-resolution microscopy reveals that mammalian mitochondrial nucleoids have a uniform size and frequently contain a single copy of mtDNA , 2011, Proceedings of the National Academy of Sciences.
[20] M. Frith,et al. Adaptive seeds tame genomic sequence comparison. , 2011, Genome research.
[21] P. Chinnery,et al. OPA1 links human mitochondrial genome maintenance to mtDNA replication and distribution. , 2011, Genome research.
[22] S. Kowalczykowski,et al. Rmi1 stimulates decatenation of double Holliday junctions during dissolution by Sgs1–Top3 , 2010, Nature Structural &Molecular Biology.
[23] Grant W. Brown,et al. Human Topoisomerase IIIα Is a Single-stranded DNA Decatenase That Is Stimulated by BLM and RMI1* , 2010, The Journal of Biological Chemistry.
[24] T. Prolla,et al. Mitochondrial Fusion Is Required for mtDNA Stability in Skeletal Muscle and Tolerance of mtDNA Mutations , 2010, Cell.
[25] T. Hsieh,et al. Drosophila topo IIIα is required for the maintenance of mitochondrial genome and male germ-line stem cells , 2010, Proceedings of the National Academy of Sciences.
[26] T. Lithgow,et al. Importing Mitochondrial Proteins: Machineries and Mechanisms , 2009, Cell.
[27] A. Reyes,et al. Analysis of mitochondrial DNA by two-dimensional agarose gel electrophoresis. , 2009, Methods in molecular biology.
[28] Catherine Suski,et al. Resolution of converging replication forks by RecQ and topoisomerase III. , 2008, Molecular cell.
[29] Robert W. Taylor,et al. Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance. , 2008, Brain : a journal of neurology.
[30] R. Schwarzenbacher,et al. OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes. , 2008, Brain : a journal of neurology.
[31] G. Lenaz,et al. Isolation and subfractionation of mitochondria from animal cells and tissue culture lines. , 2007, Methods in cell biology.
[32] T. Hsieh,et al. Drosophila melanogaster Topoisomerase IIIα Preferentially Relaxes a Positively or Negatively Supercoiled Bubble Substrate and Is Essential during Development* , 2005, Journal of Biological Chemistry.
[33] D. Friedman,et al. A truncated form of DNA topoisomerase IIbeta associates with the mtDNA genome in mammalian mitochondria. , 2003, European Journal of Biochemistry.
[34] Robert W. Taylor,et al. Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCR. , 2002, Nucleic acids research.
[35] James C. Wang,et al. Dual localization of human DNA topoisomerase IIIalpha to mitochondria and nucleus. , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[36] Y. Pommier,et al. Human mitochondrial topoisomerase I , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[37] F. Harmon,et al. RecQ helicase and topoisomerase III comprise a novel DNA strand passage function: a conserved mechanism for control of DNA recombination. , 1999, Molecular cell.
[38] J. Riou,et al. Purification and characterization of human DNA topoisomerase IIIalpha. , 1999, Nucleic acids research.
[39] Detlef D. Leipe,et al. Toprim--a conserved catalytic domain in type IA and II topoisomerases, DnaG-type primases, OLD family nucleases and RecR proteins. , 1998, Nucleic acids research.
[40] W G Hol,et al. A model for the mechanism of human topoisomerase I. , 1998, Science.
[41] J. Wang,et al. Human TOP3: a single-copy gene encoding DNA topoisomerase III. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[42] J. Griffith,et al. Electron microscopic visualization of DNA and DNA-protein complexes as adjunct to biochemical studies. , 1992, Methods in enzymology.
[43] T. Kuroiwa,et al. Organization of multiple nucleoids and DNA molecules in mitochondria of a human cell. , 1991, Experimental cell research.
[44] S. Dimauro,et al. An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region , 1989, Nature.
[45] J. Griffith,et al. Association of a protein structure of probable membrane derivation with HeLa cell mitochondrial DNA near its origin of replication. , 1977, Proceedings of the National Academy of Sciences of the United States of America.
[46] J. Vinograd,et al. Catenated Circular DNA Molecules in HeLa Cell Mitochondria , 1967, Nature.