Yu Zhi, Coorens Tim H H, Uddin Md Mesbah, Ardlie Kristin G, Lennon Niall, Natarajan Pradeep
Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Cardiovascular Research Center and Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
Nat Rev Genet. 2024 Aug;25(8):548-562. doi: 10.1038/s41576-024-00709-x. Epub 2024 Mar 28.
Germline variation and somatic mutation are intricately connected and together shape human traits and disease risks. Germline variants are present from conception, but they vary between individuals and accumulate over generations. By contrast, somatic mutations accumulate throughout life in a mosaic manner within an individual due to intrinsic and extrinsic sources of mutations and selection pressures acting on cells. Recent advancements, such as improved detection methods and increased resources for association studies, have drastically expanded our ability to investigate germline and somatic genetic variation and compare underlying mutational processes. A better understanding of the similarities and differences in the types, rates and patterns of germline and somatic variants, as well as their interplay, will help elucidate the mechanisms underlying their distinct yet interlinked roles in human health and biology.
种系变异和体细胞突变紧密相连,共同塑造人类特征和疾病风险。种系变异在个体受孕时就已存在,但个体之间存在差异,并会代代累积。相比之下,由于内在和外在的突变源以及作用于细胞的选择压力,体细胞突变在个体一生中以镶嵌的方式累积。诸如改进检测方法和增加关联研究资源等最新进展,极大地扩展了我们研究种系和体细胞遗传变异以及比较潜在突变过程的能力。更好地理解种系和体细胞变异在类型、发生率和模式上的异同,以及它们之间的相互作用,将有助于阐明它们在人类健康和生物学中独特但相互关联的作用背后的机制。