Literature DB >> 29969170

Whole genome sequencing and mutation rate analysis of trios with paternal dioxin exposure.

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.
© 2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  LAMA5 gene; dioxin; human de novo mutation rate; mental retardation

Mesh:

Substances:

Year:  2018        PMID: 29969170     DOI: 10.1002/humu.23585

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  6 in total

Review 1.  Inferring evolutionary dynamics of mutation rates through the lens of mutation spectrum variation.

Authors:  Jedidiah Carlson; William S DeWitt; Kelley Harris
Journal:  Curr Opin Genet Dev       Date:  2020-06-30       Impact factor: 5.578

2.  Paternal exposure to benzo(a)pyrene induces genome-wide mutations in mouse offspring.

Authors:  Marc A Beal; Matthew J Meier; Andrew Williams; Andrea Rowan-Carroll; Rémi Gagné; Sarah J Lindsay; Tomas Fitzgerald; Matthew E Hurles; Francesco Marchetti; Carole L Yauk
Journal:  Commun Biol       Date:  2019-06-20

Review 3.  DNA Copy Number Variations as Markers of Mutagenic Impact.

Authors:  Galina Hovhannisyan; Tigran Harutyunyan; Rouben Aroutiounian; Thomas Liehr
Journal:  Int J Mol Sci       Date:  2019-09-24       Impact factor: 5.923

4.  Differences in the number of de novo mutations between individuals are due to small family-specific effects and stochasticity.

Authors:  Jakob M Goldmann; Juliet E Hampstead; Wendy S W Wong; Amy B Wilfert; Tychele N Turner; Marianne A Jonker; Raphael Bernier; Martijn A Huynen; Evan E Eichler; Joris A Veltman; George L Maxwell; Christian Gilissen
Journal:  Genome Res       Date:  2021-07-23       Impact factor: 9.043

Review 5.  Environmental exposures associated with elevated risk for autism spectrum disorder may augment the burden of deleterious de novo mutations among probands.

Authors:  Mark A Bellgrove; Ziarih Hawi; Kealan Pugsley; Stephen W Scherer
Journal:  Mol Psychiatry       Date:  2021-05-17       Impact factor: 15.992

6.  Discovery of genomic variation across a generation.

Authors:  Brett Trost; Livia O Loureiro; Stephen W Scherer
Journal:  Hum Mol Genet       Date:  2021-10-01       Impact factor: 6.150

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.