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You inherit mitochondrial DNA only from your mother

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You inherit mitochondrial DNA only from your mother

A 2018 report said fathers could pass on mitochondrial DNA too. A study of 11,035 families found the 'paternal' signal was hiding in the nucleus.

Verified · MedlinePlus Genetics (U.S. National Library of Medicine)

You inherit your mitochondrial DNA (mtDNA) only from your mother: a 2020 study of more than 11,000 families found no evidence that human fathers pass it on, settling a debate reopened in 2018. This small second genome sits inside the mitochondria that power your cells — about 16,500 base pairs carrying 37 genes, all essential for the mitochondria to work.

Because the egg supplies an embryo’s mitochondria, mtDNA passes down the maternal line largely unchanged, skipping the reshuffling that mixes nuclear DNA each generation. That makes it a clean record of maternal ancestry. Men carry it too; they just don’t transmit it.

Did fathers ever pass it on?

Not as far as anyone can find. In 2018, researchers described three families in which children appeared to carry mtDNA from both parents, challenging the textbook rule. A team then analysed whole genomes from 11,035 mother–father–child trios in England’s 100,000 Genomes Project and found the same signature in 7 families. In every case the father had a large, rare stretch of mitochondrial sequence embedded in his nuclear chromosomes — a “mega-NUMT” — inherited the ordinary way. The authors concluded there was no evidence of paternal mtDNA transmission in humans.

Can faulty mitochondrial DNA be kept from a child?

Largely, though not perfectly. Maternal inheritance also hands down harmful mutations: around one in 5,000 children is born with mtDNA mutations that can cause severe disease, particularly in energy-hungry tissues such as the heart, muscle and brain.

The UK legalised mitochondrial donation in 2015, becoming the first country to regulate it. In pronuclear transfer, the parents’ nuclear genome is moved into a fertilised donor egg with healthy mitochondria; the donor contributes less than 1% of the child’s genetics. In July 2025, the Newcastle team reported eight babies born this way, all without signs of mitochondrial disease. Some still carried a little of the mother’s faulty mtDNA — up to 16% in newborn blood — a known limitation of the technique.

37
genes in mitochondrial DNA
11,035
families tested for paternal mtDNA
8
babies born via UK donation by 2025

Sources & references

5 references

Well-established. Corroborated by 5 independent sources.

1 MedlinePlus Genetics (U.S. National Library of Medicine) government In humans, mitochondrial DNA spans about 16,500 DNA building blocks (base pairs), representing a small fraction of the total DNA in cells. Mitochondrial DNA contains 37 genes, all of which are essential for normal mitochondrial function. medlineplus.gov ↗
2 National Human Genome Research Institute government Offspring inherit mitochondria — and as a result mitochondrial DNA — from their mother. genome.gov ↗
3 National Library of Medicine (PMC) Government medical library However, analysing the nuclear whole genome sequence, we observe likely large rare or unique nuclear-mitochondrial DNA segments (mega-NUMTs) transmitted from the father in all 7 families. pmc.ncbi.nlm.nih.gov ↗
4 Newcastle University university press office All eight babies show no signs of having mitochondrial DNA disease. The babies, four girls and four boys, including one set of identical twins, were born to seven women at high risk of transmitting serious disease caused by mutations in mitochondrial DNA. ncl.ac.uk ↗
5 Human Fertilisation and Embryology Authority (UK) government A woman who donates their eggs and/or embryos for use in other women’s mitochondrial donation treatment will not be the genetic parent of the resulting child. This is because the mitochondria that they provide makes up less than 1% of the child’s genetics. hfea.gov.uk ↗
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