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Article ; Online: Interference of nuclear mitochondrial DNA segments in mitochondrial DNA testing resembles biparental transmission of mitochondrial DNA in humans.

Bai, Renkui / Cui, Hong / Devaney, Joseph M / Allis, Katrina M / Balog, Amanda M / Liu, Xinyue / Schnur, Rhonda E / Shapiro, Faye L / Brautbar, Ariel / Estrada-Veras, Juvianee I / Hochstetler, Laurel / McConkie-Rosell, Allyn / McDonald, Marie T / Solomon, Benjamin D / Hofherr, Sean / Richard, Gabriele / Suchy, Sharon F

Genetics in medicine : official journal of the American College of Medical Genetics

2021  Volume 23, Issue 8, Page(s) 1514–1521

Abstract: Purpose: Reports have questioned the dogma of exclusive maternal transmission of human mitochondrial DNA (mtDNA), including the recent report of an admixture of two mtDNA haplogroups in individuals from three multigeneration families. This was ... ...

Abstract Purpose: Reports have questioned the dogma of exclusive maternal transmission of human mitochondrial DNA (mtDNA), including the recent report of an admixture of two mtDNA haplogroups in individuals from three multigeneration families. This was interpreted as being consistent with biparental transmission of mtDNA in an autosomal dominant-like mode. The authenticity and frequency of these findings are debated.
Methods: We retrospectively analyzed individuals with two mtDNA haplogroups from 2017 to 2019 and selected four families for further study.
Results: We identified this phenomenon in 104/27,388 (approximately 1/263) unrelated individuals. Further study revealed (1) a male with two mitochondrial haplogroups transmits only one haplogroup to some of his offspring, consistent with nuclear transmission; (2) the heteroplasmy level of paternally transmitted variants is highest in blood, lower in buccal, and absent in muscle or urine of the same individual, indicating it is inversely correlated with mtDNA content; and (3) paternally transmitted apparent large-scale mtDNA deletions/duplications are not associated with a disease phenotype.
Conclusion: These findings strongly suggest that the observed mitochondrial haplogroup of paternal origin resulted from coamplification of rare, concatenated nuclear mtDNA segments with genuine mtDNA during testing. Evaluation of additional specimen types can help clarify the clinical significance of the observed results.
MeSH term(s) DNA, Mitochondrial/genetics ; Haplotypes ; Humans ; Male ; Mitochondria/genetics ; Phenotype ; Retrospective Studies
Chemical Substances DNA, Mitochondrial
Language English
Publishing date 2021-04-12
Publishing country United States
Document type Journal Article
ZDB-ID 1455352-1
ISSN 1530-0366 ; 1098-3600
ISSN (online) 1530-0366
ISSN 1098-3600
DOI 10.1038/s41436-021-01166-1
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