Inheritance patterns of mitochondrial DNA in multi-generational maternal pedigrees: Insights from mitochondrial...

Mitochondrial DNA (mtDNA) exhibits unique advantages in forensic analysis and maternal lineage identification. However, its inherent heteroplasmy presents a moderate limitation to its application in forensic genetics. The purpose of this study is to explore the inheritance patterns of mtDNA across three-generation and two-generation maternal pedigrees. Employing the Ion S5™ XL System in conjunction with the Precision ID mtDNA Whole Genome Panel, we conducted mtDNA whole-genome sequencing on mtDNA extracted from buccal swabs of 248 individuals from 73 maternal pedigrees. Our results indicate that the sequencing depth in the 8622-8796 region was relatively low with the Precision ID mtDNA Whole Genome Panel, leading to a relatively high occurrence of missing variants in this region. We recommend performing multiple checks for this region to ensure accurate variant detection, particularly in maternal lineage identification. Notably, no homoplasmic mutations were detected within the same maternal pedigree, 35 heteroplasmic variants were identified among 30 samples from 18 pedigrees, accounting for 12.10% of individuals. Sanger sequencing corroborated the presence of heteroplasmic variants at the corresponding nucleotide positions in most heteroplasmic samples from three-generation pedigrees. Heteroplasmic variants demonstrated instability during maternal transmission, with allelic frequencies exhibiting erratic fluctuations across different maternal pedigrees. Although some point heteroplasmies were transmitted, no significant correlation was found in the frequencies of variant alleles between mothers and their offspring. Heteroplasmic variants should not be considered as exclusionary indicators in maternal lineage identification. However, when two samples with identical haplotypes exhibit identical point heteroplasmies, particularly when the minor alleles are consistent, these shared variants may serve as corroborative evidence supporting the hypothesis of a common maternal origin.