Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, the Netherlands.
Inova Translational Medicine Institute (ITMI), Inova Health Systems, Falls Church, Virginia, USA.
Nat Genet. 2016 Aug;48(8):935-9. doi: 10.1038/ng.3597. Epub 2016 Jun 20.
De novo mutations (DNMs) originating in gametogenesis are an important source of genetic variation. We use a data set of 7,216 autosomal DNMs with resolved parent of origin from whole-genome sequencing of 816 parent-offspring trios to investigate differences between maternally and paternally derived DNMs and study the underlying mutational mechanisms. Our results show that the number of DNMs in offspring increases not only with paternal age, but also with maternal age, and that some genome regions show enrichment for maternally derived DNMs. We identify parent-of-origin-specific mutation signatures that become more pronounced with increased parental age, pointing to different mutational mechanisms in spermatogenesis and oogenesis. Moreover, we find DNMs that are spatially clustered to have a unique mutational signature with no significant differences between parental alleles, suggesting a different mutational mechanism. Our findings provide insights into the molecular mechanisms that underlie mutagenesis and are relevant to disease and evolution in humans.
新生突变(DNMs)起源于配子发生,是遗传变异的重要来源。我们利用 816 个亲子三核苷酸组全基因组测序中确定了亲源的 7216 个常染色体 DNMs 数据集,来研究母源和父源 DNMs 之间的差异,并研究潜在的突变机制。我们的研究结果表明,子代中的 DNMs 数量不仅随父亲年龄增加而增加,而且随母亲年龄增加而增加,而且一些基因组区域中母源 DNMs 富集。我们鉴定出了具有亲本特异性的突变特征,这些特征随着亲本年龄的增加而变得更加明显,这表明在精子发生和卵子发生中存在不同的突变机制。此外,我们还发现了空间聚集的 DNMs,它们具有独特的突变特征,且在亲本等位基因之间没有显著差异,这表明存在不同的突变机制。我们的研究结果为突变的分子机制提供了新的见解,与人类疾病和进化有关。