Literature DB >> 14520667

Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies.

Massimiliano Filosto1, Michelangelo Mancuso, Cristofol Vives-Bauza, Maya R Vilà, Sara Shanske, Michio Hirano, Antoni L Andreu, Salvatore DiMauro.   

Abstract

In 2002, paternal inheritance of muscle mitochondrial DNA (mtDNA) was reported in a patient with exercise intolerance and a mitochondrial DNA (mtDNA) mutation restricted to skeletal muscle. To evaluate whether paternal inheritance is a common phenomenon, we studied 10 sporadic patients with skeletal muscle-restricted mtDNA mutations: five harbored mtDNA point mutations in protein-coding genes and five had single mtDNA deletions. We performed haplotype analysis and direct sequencing of the hypervariable regions 1 and 2 of the D-loop in muscle and blood from the patients and, when available, in blood from their parents. We did not observe paternal inheritance in any of our patients.

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Year:  2003        PMID: 14520667     DOI: 10.1002/ana.10709

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  14 in total

1.  No mitochondrial DNA deletions but more D-loop point mutations in repeated pregnancy loss.

Authors:  Seyed Mohammad Seyedhassani; Massoud Houshmand; Seyed Mehdi Kalantar; Glayol Modabber; Abbas Aflatoonian
Journal:  J Assist Reprod Genet       Date:  2010-05-25       Impact factor: 3.412

Review 2.  Mitochondrial DNA mutations in human disease.

Authors:  Robert W Taylor; Doug M Turnbull
Journal:  Nat Rev Genet       Date:  2005-05       Impact factor: 53.242

3.  A history of mitochondrial diseases.

Authors:  Salvatore Dimauro
Journal:  J Inherit Metab Dis       Date:  2010-05-21       Impact factor: 4.982

Review 4.  Mitochondrial disease in childhood: mtDNA encoded.

Authors:  Russell P Saneto; Margret M Sedensky
Journal:  Neurotherapeutics       Date:  2013-04       Impact factor: 7.620

5.  Biparental Inheritance of Mitochondrial DNA in Humans.

Authors:  Shiyu Luo; C Alexander Valencia; Jinglan Zhang; Ni-Chung Lee; Jesse Slone; Baoheng Gui; Xinjian Wang; Zhuo Li; Sarah Dell; Jenice Brown; Stella Maris Chen; Yin-Hsiu Chien; Wuh-Liang Hwu; Pi-Chuan Fan; Lee-Jun Wong; Paldeep S Atwal; Taosheng Huang
Journal:  Proc Natl Acad Sci U S A       Date:  2018-11-26       Impact factor: 11.205

6.  Rare creation of recombinant mtDNA haplotypes in mammalian tissues.

Authors:  Akitsugu Sato; Kazuto Nakada; Miho Akimoto; Kaori Ishikawa; Tomoko Ono; Hiroshi Shitara; Hiromichi Yonekawa; Jun-Ichi Hayashi
Journal:  Proc Natl Acad Sci U S A       Date:  2005-04-13       Impact factor: 11.205

7.  Recombination of mitochondrial DNA in skeletal muscle of individuals with multiple mitochondrial DNA heteroplasmy.

Authors:  Gábor Zsurka; Yevgenia Kraytsberg; Tatiana Kudina; Cornelia Kornblum; Christian E Elger; Konstantin Khrapko; Wolfram S Kunz
Journal:  Nat Genet       Date:  2005-07-17       Impact factor: 38.330

8.  Keeping in shape the dogma of mitochondrial DNA maternal inheritance.

Authors:  Valerio Carelli
Journal:  PLoS Genet       Date:  2015-05-14       Impact factor: 5.917

Review 9.  The inheritance of pathogenic mitochondrial DNA mutations.

Authors:  L M Cree; D C Samuels; P F Chinnery
Journal:  Biochim Biophys Acta       Date:  2009-03-19

10.  Association of mitochondrial genetic variation with carotid atherosclerosis.

Authors:  Igor A Sobenin; Margarita A Sazonova; Anton Y Postnov; Jukka T Salonen; Yuri V Bobryshev; Alexander N Orekhov
Journal:  PLoS One       Date:  2013-07-09       Impact factor: 3.240

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