New insights into the generation and role of de novo mutations in health and disease

Rocio Acuna-Hidalgo, Joris A. Veltman*, Alexander Hoischen

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Aside from inheriting half of the genome of each of our parents, we are born with a small number of novel mutations that occurred during gametogenesis and postzygotically. Recent genome and exome sequencing studies of parent-offspring trios have provided the first insights into the number and distribution of these de novo mutations in health and disease, pointing to risk factors that increase their number in the offspring. De novo mutations have been shown to be a major cause of severe early-onset genetic disorders such as intellectual disability, autism spectrum disorder, and other developmental diseases. In fact, the occurrence of novel mutations in each generation explains why these reproductively lethal disorders continue to occur in our population. Recent studies have also shown that de novo mutations are predominantly of paternal origin and that their number increases with advanced paternal age. Here, we review the recent literature on de novo mutations, covering their detection, biological characterization, and medical impact.
Original languageEnglish
Article number241
JournalGenome Biology (Online)
Volume17
DOIs
Publication statusPublished - 28 Nov 2016

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