Literature DB >> 20012584

The mitochondrial DNA polymerase in health and disease.

William C Copeland1.   

Abstract

Since mutations in mitochondrial DNA (mtDNA) have been shown to be a cause of many mitochondrial diseases as well as aging, it is important to understand the origin of these mutations and how replication proteins modulate this process. DNA polymerase gamma (pol gamma) is the polymerase that is responsible for replication and repair of mtDNA. Pol gamma has three main roles in mtDNA maintenance and mutagenesis. As the only known DNA polymerase in mitochondria, pol gamma is required for all replication and repair functions and is the main source of errors produced in human mtDNA. Pol gamma is also sensitive to a host of antiviral nucleoside analogs used to treat HIV-1 infections, which can cause an induced mitochondrial toxicity. Finally, the gene for pol gamma, POLG, is a genetic locus for several mitochondrial disease with over 150 genetic mutations currently identified.

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Year:  2010        PMID: 20012584      PMCID: PMC3960799          DOI: 10.1007/978-90-481-3471-7_11

Source DB:  PubMed          Journal:  Subcell Biochem        ISSN: 0306-0225


  49 in total

1.  The spectrum of clinical disease caused by the A467T and W748S POLG mutations: a study of 26 cases.

Authors:  Charalampos Tzoulis; Bernt A Engelsen; Wenche Telstad; Jan Aasly; Massimo Zeviani; Synnøve Winterthun; Gianfrancesco Ferrari; Jan H Aarseth; Laurence A Bindoff
Journal:  Brain       Date:  2006-04-25       Impact factor: 13.501

Review 2.  Functions of DNA polymerases.

Authors:  Katarzyna Bebenek; Thomas A Kunkel
Journal:  Adv Protein Chem       Date:  2004

Review 3.  Mitochondrial DNA and disease.

Authors:  Salvatore Dimauro; Guido Davidzon
Journal:  Ann Med       Date:  2005       Impact factor: 4.709

Review 4.  DNA polymerases and human diseases.

Authors:  Joann B Sweasy; Julia M Lauper; Kristin A Eckert
Journal:  Radiat Res       Date:  2006-11       Impact factor: 2.841

Review 5.  DNA polymerase gamma in mitochondrial DNA replication and repair.

Authors:  Maria A Graziewicz; Matthew J Longley; William C Copeland
Journal:  Chem Rev       Date:  2006-02       Impact factor: 60.622

6.  Origins of human mitochondrial point mutations as DNA polymerase gamma-mediated errors.

Authors:  Weiming Zheng; Konstantin Khrapko; Hilary A Coller; William G Thilly; William C Copeland
Journal:  Mutat Res       Date:  2006-02-20       Impact factor: 2.433

7.  Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European origin.

Authors:  Anna H Hakonen; Silja Heiskanen; Vesa Juvonen; Ilse Lappalainen; Petri T Luoma; Maria Rantamaki; Gert Van Goethem; Ann Lofgren; Peter Hackman; Anders Paetau; Seppo Kaakkola; Kari Majamaa; Teppo Varilo; Bjarne Udd; Helena Kaariainen; Laurence A Bindoff; Anu Suomalainen
Journal:  Am J Hum Genet       Date:  2005-07-27       Impact factor: 11.025

8.  The common A467T mutation in the human mitochondrial DNA polymerase (POLG) compromises catalytic efficiency and interaction with the accessory subunit.

Authors:  Sherine S L Chan; Matthew J Longley; William C Copeland
Journal:  J Biol Chem       Date:  2005-07-16       Impact factor: 5.157

Review 9.  Mitochondrial diseases in man and mouse.

Authors:  D C Wallace
Journal:  Science       Date:  1999-03-05       Impact factor: 47.728

10.  Molecular diagnosis of Alpers syndrome.

Authors:  Khue V Nguyen; Farida S Sharief; Sherine S L Chan; William C Copeland; Robert K Naviaux
Journal:  J Hepatol       Date:  2006-02-20       Impact factor: 25.083

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  32 in total

1.  Presteady state kinetic investigation of the incorporation of anti-hepatitis B nucleotide analogues catalyzed by noncanonical human DNA polymerases.

Authors:  Jessica A Brown; Lindsey R Pack; Jason D Fowler; Zucai Suo
Journal:  Chem Res Toxicol       Date:  2011-12-16       Impact factor: 3.739

Review 2.  Replication proteins and human disease.

Authors:  Andrew P Jackson; Ronald A Laskey; Nicholas Coleman
Journal:  Cold Spring Harb Perspect Biol       Date:  2014-01-01       Impact factor: 10.005

3.  Synergistic Effects of the in cis T251I and P587L Mitochondrial DNA Polymerase γ Disease Mutations.

Authors:  Karen L DeBalsi; Matthew J Longley; Kirsten E Hoff; William C Copeland
Journal:  J Biol Chem       Date:  2017-02-02       Impact factor: 5.157

Review 4.  Neurodevelopmental manifestations of mitochondrial disease.

Authors:  Marni J Falk
Journal:  J Dev Behav Pediatr       Date:  2010-09       Impact factor: 2.225

5.  The Perirolandic Sign: A Unique Imaging Finding Observed in Association with Polymerase γ-Related Disorders.

Authors:  F G Gonçalves; B Hill; Y Guo; C C Muraresku; E McCormick; C A P F Alves; S R Teixeira; J S Martin-Saavedra; Z Zolkipli-Cunningham; M J Falk; A Vossough; A Goldstein; G Zuccoli
Journal:  AJNR Am J Neuroradiol       Date:  2020-05-07       Impact factor: 3.825

Review 6.  Bioenergetic origins of complexity and disease.

Authors:  D C Wallace
Journal:  Cold Spring Harb Symp Quant Biol       Date:  2011-12-22

Review 7.  DNA polymerases and cancer.

Authors:  Sabine S Lange; Kei-ichi Takata; Richard D Wood
Journal:  Nat Rev Cancer       Date:  2011-02       Impact factor: 60.716

Review 8.  Mutator phenotypes due to DNA replication infidelity.

Authors:  Mercedes E Arana; Thomas A Kunkel
Journal:  Semin Cancer Biol       Date:  2010-10-08       Impact factor: 15.707

9.  PCR based determination of mitochondrial DNA copy number in multiple species.

Authors:  John P Rooney; Ian T Ryde; Laurie H Sanders; Evan H Howlett; Meryl D Colton; Kaylyn E Germ; Greg D Mayer; J Timothy Greenamyre; Joel N Meyer
Journal:  Methods Mol Biol       Date:  2015

10.  Polg2 is essential for mammalian embryogenesis and is required for mtDNA maintenance.

Authors:  Margaret M Humble; Matthew J Young; Julie F Foley; Arun R Pandiri; Greg S Travlos; William C Copeland
Journal:  Hum Mol Genet       Date:  2012-11-29       Impact factor: 6.150

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