Literature DB >> 16087914

Mitochondrial DNA copy number threshold in mtDNA depletion myopathy.

S E Durham1, E Bonilla, D C Samuels, S DiMauro, P F Chinnery.   

Abstract

The authors measured the absolute amount of mitochondrial DNA (mtDNA) within single muscle fibers from two patients with thymidine kinase 2 (TK2) deficiency and two healthy controls. TK2 deficient fibers containing more than 0.01 mtDNA/microm3 had residual cytochrome c oxidase (COX) activity. This defines the minimum amount of wild-type mtDNA molecules required to maintain COX activity in skeletal muscle and provides an explanation for the mosaic histochemical pattern seen in patients with mtDNA depletion syndrome.

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Year:  2005        PMID: 16087914     DOI: 10.1212/01.wnl.0000171861.30277.88

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  17 in total

1.  Normal levels of wild-type mitochondrial DNA maintain cytochrome c oxidase activity for two pathogenic mitochondrial DNA mutations but not for m.3243A-->G.

Authors:  Steve E Durham; David C Samuels; Lynsey M Cree; Patrick F Chinnery
Journal:  Am J Hum Genet       Date:  2007-05-23       Impact factor: 11.025

2.  Mutant POLG2 disrupts DNA polymerase gamma subunits and causes progressive external ophthalmoplegia.

Authors:  Matthew J Longley; Susanna Clark; Cynthia Yu Wai Man; Gavin Hudson; Steve E Durham; Robert W Taylor; Simon Nightingale; Douglass M Turnbull; William C Copeland; Patrick F Chinnery
Journal:  Am J Hum Genet       Date:  2006-05-04       Impact factor: 11.025

3.  Previous estimates of mitochondrial DNA mutation level variance did not account for sampling error: comparing the mtDNA genetic bottleneck in mice and humans.

Authors:  Passorn Wonnapinij; Patrick F Chinnery; David C Samuels
Journal:  Am J Hum Genet       Date:  2010-04-01       Impact factor: 11.025

4.  Fall in circulating mononuclear cell mitochondrial DNA content in human sepsis.

Authors:  Angela Pyle; David J Burn; Charlotte Gordon; Catherine Swan; Patrick F Chinnery; Simon V Baudouin
Journal:  Intensive Care Med       Date:  2010-03-12       Impact factor: 17.440

5.  Cytochrome c oxidase-intermediate fibres: importance in understanding the pathogenesis and treatment of mitochondrial myopathy.

Authors:  Julie L Murphy; Thiloka E Ratnaike; Ersong Shang; Gavin Falkous; Emma L Blakely; Charlotte L Alston; Tanja Taivassalo; Ronald G Haller; Robert W Taylor; Doug M Turnbull
Journal:  Neuromuscul Disord       Date:  2012-05-28       Impact factor: 4.296

6.  Transient systemic mtDNA damage leads to muscle wasting by reducing the satellite cell pool.

Authors:  Xiao Wang; Alicia M Pickrell; Susana G Rossi; Milena Pinto; Lloye M Dillon; Aline Hida; Richard L Rotundo; Carlos T Moraes
Journal:  Hum Mol Genet       Date:  2013-06-10       Impact factor: 6.150

7.  Polymerase γ gene POLG determines the risk of sodium valproate-induced liver toxicity.

Authors:  Joanna D Stewart; Rita Horvath; Enrico Baruffini; Iliana Ferrero; Stefanie Bulst; Paul B Watkins; Robert J Fontana; Christopher P Day; Patrick F Chinnery
Journal:  Hepatology       Date:  2010-11       Impact factor: 17.425

8.  Sensitivity of mitochondrial transcription and resistance of RNA polymerase II dependent nuclear transcription to antiviral ribonucleosides.

Authors:  Jamie J Arnold; Suresh D Sharma; Joy Y Feng; Adrian S Ray; Eric D Smidansky; Maria L Kireeva; Aesop Cho; Jason Perry; Jennifer E Vela; Yeojin Park; Yili Xu; Yang Tian; Darius Babusis; Ona Barauskus; Blake R Peterson; Averell Gnatt; Mikhail Kashlev; Weidong Zhong; Craig E Cameron
Journal:  PLoS Pathog       Date:  2012-11-15       Impact factor: 6.823

9.  In vitro supplementation with deoxynucleoside monophosphates rescues mitochondrial DNA depletion.

Authors:  Stefanie Bulst; Elke Holinski-Feder; Brendan Payne; Angela Abicht; Sabine Krause; Hanns Lochmüller; Patrick F Chinnery; Maggie C Walter; Rita Horvath
Journal:  Mol Genet Metab       Date:  2012-05-03       Impact factor: 4.797

10.  Thymidine kinase 2 deficiency-induced mtDNA depletion in mouse liver leads to defect β-oxidation.

Authors:  Xiaoshan Zhou; Kristina Kannisto; Sophie Curbo; Ulrika von Döbeln; Kjell Hultenby; Sindra Isetun; Mats Gåfvels; Anna Karlsson
Journal:  PLoS One       Date:  2013-03-07       Impact factor: 3.240

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