Literature DB >> 23430519

Inheritance of the m.3243A>G mutation.

Paul de Laat1, Saskia Koene, Lambert P W J Vd Heuvel, Richard J T Rodenburg, Mirian C H Janssen, Jan A M Smeitink.   

Abstract

The m.3243A>G is the most prevalent pathogenic mtDNA mutation but little is known about its inheritance. We studied 34 families containing 56 mother-child relations and 82 intersibling relations to investigate its transmission. We found a significant correlation between mother and child heteroplasmy levels (r = 0.679, p < 0.001). In mothers with a heteroplasmy level of below 25% we found 30% offspring without detectable mutation, while in mothers with a heteroplasmy level of above 25%, 100% of the offspring showed the m.3243A>G mutation. Heteroplasmy levels between siblings also correlated (r = 0.512, p < ;0.001), but had limited extra predictive value because of outliers. These new data on inheritance of the m.3243A>G mutation might be of value in counseling patients and preventing transmission of the mutation.

Entities:  

Year:  2012        PMID: 23430519      PMCID: PMC3565654          DOI: 10.1007/8904_2012_159

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  21 in total

1.  The epidemiology of pathogenic mitochondrial DNA mutations.

Authors:  P F Chinnery; M A Johnson; T M Wardell; R Singh-Kler; C Hayes; D T Brown; R W Taylor; L A Bindoff; D M Turnbull
Journal:  Ann Neurol       Date:  2000-08       Impact factor: 10.422

2.  Maternally inherited diabetes and deafness: a multicenter study.

Authors:  P J Guillausseau; P Massin; D Dubois-LaForgue; J Timsit; M Virally; H Gin; E Bertin; J F Blickle; B Bouhanick; J Cahen; S Caillat-Zucman; G Charpentier; P Chedin; C Derrien; P H Ducluzeau; A Grimaldi; B Guerci; E Kaloustian; A Murat; F Olivier; M Paques; V Paquis-Flucklinger; B Porokhov; J Samuel-Lajeunesse; B Vialettes
Journal:  Ann Intern Med       Date:  2001-05-01       Impact factor: 25.391

3.  A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

Authors:  Y Goto; I Nonaka; S Horai
Journal:  Nature       Date:  1990-12-13       Impact factor: 49.962

4.  Clinical features of mitochondrial DNA m.3243A>G mutation in 47 Chinese families.

Authors:  Yinan Ma; Fang Fang; Yanyan Cao; Yanling Yang; Liping Zou; Ying Zhang; Songtao Wang; Sainan Zhu; Yufeng Xu; Pei Pei; Yu Qi
Journal:  J Neurol Sci       Date:  2010-02-09       Impact factor: 3.181

5.  Mitochondrial tRNALeu(UUR) mutation in a patient with steroid-resistant nephrotic syndrome and focal segmental glomerulosclerosis.

Authors:  M M Löwik; F A Hol; E J Steenbergen; J F M Wetzels; L P W J van den Heuvel
Journal:  Nephrol Dial Transplant       Date:  2004-12-07       Impact factor: 5.992

6.  The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both?

Authors:  P F Chinnery; D R Thorburn; D C Samuels; S L White; H M Dahl; D M Turnbull; R N Lightowlers; N Howell
Journal:  Trends Genet       Date:  2000-11       Impact factor: 11.639

7.  Autonomic symptoms in carriers of the m.3243A>G mitochondrial DNA mutation.

Authors:  Timothy Parsons; Louis Weimer; Kristin Engelstad; Alex Linker; Vanessa Battista; Ying Wei; Michio Hirano; Salvatore Dimauro; Darryl C De Vivo; Petra Kaufmann
Journal:  Arch Neurol       Date:  2010-08

8.  Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

Authors:  K Majamaa; J S Moilanen; S Uimonen; A M Remes; P I Salmela; M Kärppä; K A Majamaa-Voltti; H Rusanen; M Sorri; K J Peuhkurinen; I E Hassinen
Journal:  Am J Hum Genet       Date:  1998-08       Impact factor: 11.025

9.  Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness.

Authors:  J M van den Ouweland; H H Lemkes; W Ruitenbeek; L A Sandkuijl; M F de Vijlder; P A Struyvenberg; J J van de Kamp; J A Maassen
Journal:  Nat Genet       Date:  1992-08       Impact factor: 38.330

10.  Clinical presentations of mitochondrial cardiomyopathies.

Authors:  D Lev; A Nissenkorn; E Leshinsky-Silver; M Sadeh; A Zeharia; B-Z Garty; L Blieden; V Barash; T Lerman-Sagie
Journal:  Pediatr Cardiol       Date:  2004-06-08       Impact factor: 1.655

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  5 in total

Review 1.  Genetic Counselling for Maternally Inherited Mitochondrial Disorders.

Authors:  Joanna Poulton; Josef Finsterer; Patrick Yu-Wai-Man
Journal:  Mol Diagn Ther       Date:  2017-08       Impact factor: 4.074

2.  Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families: support for a variable-size bottleneck.

Authors:  Mingkun Li; Rebecca Rothwell; Martijn Vermaat; Manja Wachsmuth; Roland Schröder; Jeroen F J Laros; Mannis van Oven; Paul I W de Bakker; Jasper A Bovenberg; Cornelia M van Duijn; Gert-Jan B van Ommen; P Eline Slagboom; Morris A Swertz; Cisca Wijmenga; Manfred Kayser; Dorret I Boomsma; Sebastian Zöllner; Peter de Knijff; Mark Stoneking
Journal:  Genome Res       Date:  2016-02-25       Impact factor: 9.043

3.  Darwinian selection within an individual or somatic selection: facts and models.

Authors:  Reiner A Veitia
Journal:  J Mol Cell Biol       Date:  2019-08-19       Impact factor: 6.216

4.  Five non-mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes phenotype adult patients with m.3243A>G mutation after kidney transplantation: follow-up and review of the literature.

Authors:  Paul de Laat; Nienke van Engelen; Jack F Wetzels; Jan A M Smeitink; Mirian C H Janssen
Journal:  Clin Kidney J       Date:  2019-04-21

5.  Three families with 'de novo' m.3243A > G mutation.

Authors:  Paul de Laat; Mirian C H Janssen; Charlotte L Alston; Robert W Taylor; Richard J T Rodenburg; Jan A M Smeitink
Journal:  BBA Clin       Date:  2016-04-29
  5 in total

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