The bottleneck for maternal transmission of mtDNA is linked to purifying selection by autophagy

Mammalian mitochondrial DNA (mtDNA) inheritance differs fundamentally from nuclear inheritance owing to exclusive maternal transmission, high mutation rate, and lack of recombination. Two key mechanisms shape this inheritance: the bottleneck, which drives stochastic transmission of maternal mtDNA variants, and purifying selection, which actively removes mutant mtDNA. Whether these mechanisms interact has been unresolved. To address this question, we generated a series of mouse models with random mtDNA mutations alongside alleles altering mtDNA copy number or decreasing autophagy. We demonstrate that tightening the mtDNA bottleneck increases heteroplasmic variance between individuals, causing lower mutational burden and nonsynonymous-to-synonymous ratios. In contrast, reduced autophagy weakens purifying selection, leading to decreased interoffspring heteroplasmic variance and increased mutational burden with higher nonsynonymous-to-synonymous ratios. These findings provide experimental evidence that the mtDNA bottleneck size modulates the efficacy of purifying selection. Our findings yield fundamental insights into the processes governing mammalian mtDNA transmission with direct implications for the origin and propagation of mtDNA mutations causing human disease.

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Publication Details

Journal
Science Advances
Published
2025-11-12
DOI
https://doi.org/10.1126/sciadv.aea4660
Citations
2
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
1.61

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article

The bottleneck for maternal transmission of mtDNA is linked to purifying selection by autophagy

Tom Barton-Owen, Patrick Francis Chinnery, Zoe Golder, Camilla Koolmeister et al.
2 citations
Science Advances
Mitochondrial Function and Pathology
1.61
article

The bottleneck for maternal transmission of mtDNA is linked to purifying selection by autophagy

Tom Barton-Owen, Patrick Francis Chinnery, Zoe Golder, Camilla Koolmeister, Laura S. Kremer, Nils‐Göran Larsson, Polyxeni Papadea
article en
2 citations

Abstract

Mammalian mitochondrial DNA (mtDNA) inheritance differs fundamentally from nuclear inheritance owing to exclusive maternal transmission, high mutation rate, and lack of recombination. Two key mechanisms shape this inheritance: the bottleneck, which drives stochastic transmission of maternal mtDNA variants, and purifying selection, which actively removes mutant mtDNA. Whether these mechanisms interact has been unresolved. To address this question, we generated a series of mouse models with random mtDNA mutations alongside alleles altering mtDNA copy number or decreasing autophagy. We demonstrate that tightening the mtDNA bottleneck increases heteroplasmic variance between individuals, causing lower mutational burden and nonsynonymous-to-synonymous ratios. In contrast, reduced autophagy weakens purifying selection, leading to decreased interoffspring heteroplasmic variance and increased mutational burden with higher nonsynonymous-to-synonymous ratios. These findings provide experimental evidence that the mtDNA bottleneck size modulates the efficacy of purifying selection. Our findings yield fundamental insights into the processes governing mammalian mtDNA transmission with direct implications for the origin and propagation of mtDNA mutations causing human disease.

Science AdvancesVol. 11(46)
University of Cambridge (GB), Karolinska Institutet (SE), Universitätsmedizin Göttingen (DE), University of Göttingen (DE), MRC Mitochondrial Biology Unit (GB)
LifeArc, Swedish Cancer Foundation, Department of Health and Social Care, Rosetrees Trust, Knut och Alice Wallenbergs Stiftelse, Novo Nordisk, Vetenskapsrådet, Novo Nordisk Fonden, Medical Research Council, NIHR Cambridge Biomedical Research Centre
Openalex Percentile: Top 14%
Mitochondrial Function and Pathology
1.61
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