Department of Genetics, Washington University School of Medicine, St. Louis, MO 63110, USA.
Division of Genetics, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR 97006, USA.
Science. 2023 Apr 14;380(6641):eabn7113. doi: 10.1126/science.abn7113.
Postzygotic mutations (PZMs) begin to accrue in the human genome immediately after fertilization, but how and when PZMs affect development and lifetime health remain unclear. To study the origins and functional consequences of PZMs, we generated a multitissue atlas of PZMs spanning 54 tissue and cell types from 948 donors. Nearly half the variation in mutation burden among tissue samples can be explained by measured technical and biological effects, and 9% can be attributed to donor-specific effects. Through phylogenetic reconstruction of PZMs, we found that their type and predicted functional impact vary during prenatal development, across tissues, and through the germ cell life cycle. Thus, methods for interpreting effects across the body and the life span are needed to fully understand the consequences of genetic variants.
合子后突变 (PZMs) 在受精后立即开始在人类基因组中积累,但 PZMs 如何以及何时影响发育和终生健康尚不清楚。为了研究 PZMs 的起源和功能后果,我们生成了一个跨 54 种组织和细胞类型的 PZMs 多组织图谱,来自 948 个供体。组织样本中突变负担的近一半变异可以用测量的技术和生物学效应来解释,9%可以归因于供体特异性效应。通过 PZMs 的系统发育重建,我们发现它们的类型和预测的功能影响在产前发育、组织间以及生殖细胞生命周期中都有所不同。因此,需要跨身体和寿命解释效应的方法来充分了解遗传变异的后果。