Mutation signatures in germline mitochondrial genome provide insights into human mitochondrial evolution and disease
- 9 April 2019
- journal article
- research article
- Published by Springer Science and Business Media LLC in Human Genetics
- Vol. 138 (6), 613-624
- https://doi.org/10.1007/s00439-019-02009-5
Abstract
Variations in mitochondrial DNA (mtDNA) have been fundamental for understanding human evolution and are causative for a plethora of inherited mitochondrial diseases, but the mutation signatures of germline mtDNA and their value in understanding mitochondrial pathogenicity remain unknown. Here, we carried out a systematic analysis of mutation patterns in germline mtDNA based on 97,566 mtDNA variants from 45,494 full-length sequences and revealed a highly non-stochastic and replication-coupled mutation signature characterized by nucleotide-specific mutation pressure (G > T>A > C) and position-specific selection pressure, suggesting the existence of an intensive mutation–selection interplay in germline mtDNA. We provide evidence that this mutation–selection interplay has strongly shaped the mtDNA sequence during evolution, which not only manifests as an oriented alteration of amino acid compositions of mitochondrial encoded proteins, but also explains the long-lasting mystery of CpG depletion in mitochondrial genome. Finally, we demonstrated that these insights may be integrated to better understand the pathogenicity of disease-implicated mitochondrial variants.Funding Information
- the Fundamental Research Funds for the Central Universities
- Scientific Research Foundation for Returned Scholars of Shaanxi Province
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