Literature DB >> 30478036

Biparental Inheritance of Mitochondrial DNA in Humans.

Shiyu Luo1,2, C Alexander Valencia1, Jinglan Zhang3, Ni-Chung Lee4, Jesse Slone1, Baoheng Gui1,2, Xinjian Wang1, Zhuo Li1, Sarah Dell1, Jenice Brown1, Stella Maris Chen3, Yin-Hsiu Chien4, Wuh-Liang Hwu4, Pi-Chuan Fan5, Lee-Jun Wong3, Paldeep S Atwal6, Taosheng Huang7.   

Abstract

Although there has been considerable debate about whether paternal mitochondrial DNA (mtDNA) transmission may coexist with maternal transmission of mtDNA, it is generally believed that mitochondria and mtDNA are exclusively maternally inherited in humans. Here, we identified three unrelated multigeneration families with a high level of mtDNA heteroplasmy (ranging from 24 to 76%) in a total of 17 individuals. Heteroplasmy of mtDNA was independently examined by high-depth whole mtDNA sequencing analysis in our research laboratory and in two Clinical Laboratory Improvement Amendments and College of American Pathologists-accredited laboratories using multiple approaches. A comprehensive exploration of mtDNA segregation in these families shows biparental mtDNA transmission with an autosomal dominantlike inheritance mode. Our results suggest that, although the central dogma of maternal inheritance of mtDNA remains valid, there are some exceptional cases where paternal mtDNA could be passed to the offspring. Elucidating the molecular mechanism for this unusual mode of inheritance will provide new insights into how mtDNA is passed on from parent to offspring and may even lead to the development of new avenues for the therapeutic treatment for pathogenic mtDNA transmission.

Entities:  

Keywords:  biparental inheritance; human genetics; mitochondria; mtDNA; paternal transmission

Mesh:

Substances:

Year:  2018        PMID: 30478036      PMCID: PMC6304937          DOI: 10.1073/pnas.1810946115

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  37 in total

1.  Genetic counseling and prenatal diagnosis for the mitochondrial DNA mutations at nucleotide 8993.

Authors:  S L White; V R Collins; R Wolfe; M A Cleary; S Shanske; S DiMauro; H H Dahl; D R Thorburn
Journal:  Am J Hum Genet       Date:  1999-08       Impact factor: 11.025

2.  Paternal inheritance of mitochondrial DNA.

Authors:  Marianne Schwartz; John Vissing
Journal:  N Engl J Med       Date:  2002-08-22       Impact factor: 91.245

3.  Recombination of human mitochondrial DNA.

Authors:  Yevgenya Kraytsberg; Marianne Schwartz; Timothy A Brown; Konstantin Ebralidse; Wolfram S Kunz; David A Clayton; John Vissing; Konstantin Khrapko
Journal:  Science       Date:  2004-05-14       Impact factor: 47.728

4.  Failure of elimination of paternal mitochondrial DNA in abnormal embryos.

Authors:  J St John; D Sakkas; K Dimitriadi; A Barnes; V Maclin; J Ramey; C Barratt; C De Jonge
Journal:  Lancet       Date:  2000-01-15       Impact factor: 79.321

5.  No evidence for paternal inheritance of mtDNA in patients with sporadic mtDNA mutations.

Authors:  Marianne Schwartz; John Vissing
Journal:  J Neurol Sci       Date:  2004-03-15       Impact factor: 3.181

6.  Versatile and open software for comparing large genomes.

Authors:  Stefan Kurtz; Adam Phillippy; Arthur L Delcher; Michael Smoot; Martin Shumway; Corina Antonescu; Steven L Salzberg
Journal:  Genome Biol       Date:  2004-01-30       Impact factor: 13.583

7.  Mitochondrial transcription factor A regulates mtDNA copy number in mammals.

Authors:  Mats I Ekstrand; Maria Falkenberg; Anja Rantanen; Chan Bae Park; Martina Gaspari; Kjell Hultenby; Pierre Rustin; Claes M Gustafsson; Nils-Göran Larsson
Journal:  Hum Mol Genet       Date:  2004-03-11       Impact factor: 6.150

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

Authors:  Massimiliano Filosto; Michelangelo Mancuso; Cristofol Vives-Bauza; Maya R Vilà; Sara Shanske; Michio Hirano; Antoni L Andreu; Salvatore DiMauro
Journal:  Ann Neurol       Date:  2003-10       Impact factor: 10.422

9.  Genotypes from patients indicate no paternal mitochondrial DNA contribution.

Authors:  Robert W Taylor; Martina T McDonnell; Emma L Blakely; Patrick F Chinnery; Geoffrey A Taylor; Neil Howell; Massimo Zeviani; Egill Briem; Franco Carrara; Douglass M Turnbull
Journal:  Ann Neurol       Date:  2003-10       Impact factor: 10.422

10.  Impaired ATP synthase assembly associated with a mutation in the human ATP synthase subunit 6 gene.

Authors:  L G Nijtmans; N S Henderson; G Attardi; I J Holt
Journal:  J Biol Chem       Date:  2000-11-13       Impact factor: 5.157

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  77 in total

Review 1.  The unresolved role of mitochondrial DNA in Parkinson's disease: An overview of published studies, their limitations, and future prospects.

Authors:  Amica C Müller-Nedebock; Rebecca R Brennan; Marianne Venter; Ilse S Pienaar; Francois H van der Westhuizen; Joanna L Elson; Owen A Ross; Soraya Bardien
Journal:  Neurochem Int       Date:  2019-06-21       Impact factor: 3.921

Review 2.  Mitochondrial DNA heteroplasmy in disease and targeted nuclease-based therapeutic approaches.

Authors:  Nadee Nissanka; Carlos T Moraes
Journal:  EMBO Rep       Date:  2020-02-19       Impact factor: 8.807

Review 3.  Selfish Mitonuclear Conflict.

Authors:  Justin C Havird; Evan S Forsythe; Alissa M Williams; John H Werren; Damian K Dowling; Daniel B Sloan
Journal:  Curr Biol       Date:  2019-06-03       Impact factor: 10.834

4.  Quasi-Mendelian paternal inheritance of mitochondrial DNA: A notorious artifact, or anticipated behavior?

Authors:  Sofia Annis; Zoe Fleischmann; Mark Khrapko; Melissa Franco; Kevin Wasko; Dori Woods; Wolfram S Kunz; Peter Ellis; Konstantin Khrapko
Journal:  Proc Natl Acad Sci U S A       Date:  2019-07-16       Impact factor: 11.205

5.  Reply to Annis et al.: Is quasi-Mendelian mtDNA competition enough to drive transmission of paternal mtDNA?

Authors:  Jesse Slone; Shiyu Luo; Paldeep S Atwal; Taosheng Huang
Journal:  Proc Natl Acad Sci U S A       Date:  2019-07-16       Impact factor: 11.205

6.  No further evidence for paternal leakage of mitochondrial DNA in humans yet.

Authors:  Sabine Lutz-Bonengel; Walther Parson
Journal:  Proc Natl Acad Sci U S A       Date:  2019-01-23       Impact factor: 11.205

7.  Reply to Lutz-Bonengel et al.: Biparental mtDNA transmission is unlikely to be the result of nuclear mitochondrial DNA segments.

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:  2019-01-23       Impact factor: 11.205

Review 8.  Sex differences in renal mitochondrial function: a hormone-gous opportunity for research.

Authors:  Regina F Sultanova; Ryan Schibalski; Irina A Yankelevich; Krisztian Stadler; Daria V Ilatovskaya
Journal:  Am J Physiol Renal Physiol       Date:  2020-11-02

9.  Cell-free mitochondrial DNA increases in maternal circulation during healthy pregnancy: a prospective, longitudinal study.

Authors:  Spencer C Cushen; Marc L Sprouse; Alexandra Blessing; Jie Sun; Sara S Jarvis; Yoshiyuki Okada; Qi Fu; Steven A Romero; Nicole R Phillips; Styliani Goulopoulou
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2020-01-08       Impact factor: 3.619

Review 10.  Mitochondrial pathways in human health and aging.

Authors:  Rebecca Bornstein; Brenda Gonzalez; Simon C Johnson
Journal:  Mitochondrion       Date:  2020-07-30       Impact factor: 4.160

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