| Literature DB >> 29969170 |
Nguyen Dang Ton1,2, Hidewaki Nakagawa2, Nguyen Hai Ha1, Nguyen Thuy Duong1, Vu Phuong Nhung1, Le Thi Thu Hien1, Huynh Thi Thu Hue1, Nguyen Huy Hoang1, Jing Hao Wong3, Kaoru Nakano2, Kazuhiro Maejima2, Aya Sasaki-Oku2, Tatsuhiko Tsunoda4,5, Akihiro Fujimoto2,3, Nong Van Hai1.
Abstract
2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) or dioxin, is commonly considered the most toxic man-made substance. Dioxin exposure impacts human health and diseases, birth defects and teratogenesis were frequently observed in children of persons who have been exposed to dioxin. However, the impact of dioxin on human mutation rate in trios has not yet been elucidated at the whole genome level. To identify and characterize the genetic alterations in the individuals exposed to dioxin, we performed whole genome sequencing (WGS) of nine Vietnamese trios whose fathers were exposed to dioxin. In total, 846 de novo point mutations, 26 de novo insertions and deletions, 4 de novo structural variations, and 1 de novo copy number variation were identified. The number of point mutations and dioxin concentrations were positively correlated (P-value < 0.05). Considering the substitution pattern, the number of A > T/T > A mutation and the dioxin concentration was positively correlated (P-value < 0.05). Our analysis also identified one possible disease-related mutation in LAMA5 in one trio. These findings suggested that dioxin exposure might affect father genomes of trios leading to de novo mutations in their children. Further analysis with larger sample sizes would be required to better clarify mutation rates and substitution patterns in trios caused by dioxin.Entities:
Keywords: LAMA5 gene; dioxin; human de novo mutation rate; mental retardation
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Year: 2018 PMID: 29969170 DOI: 10.1002/humu.23585
Source DB: PubMed Journal: Hum Mutat ISSN: 1059-7794 Impact factor: 4.878