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Whole genome sequencing and mutation rate analysis of trios with paternal dioxin exposure.
Ton, Nguyen Dang; Nakagawa, Hidewaki; Ha, Nguyen Hai; Duong, Nguyen Thuy; Nhung, Vu Phuong; Hien, Le Thi Thu; Hue, Huynh Thi Thu; Hoang, Nguyen Huy; Wong, Jing Hao; Nakano, Kaoru; Maejima, Kazuhiro; Sasaki-Oku, Aya; Tsunoda, Tatsuhiko; Fujimoto, Akihiro; Van Hai, Nong.
Afiliación
  • Ton ND; Institute of Genome Research, Vietnam Academy of Science and Technology, Ha Noi, Vietnam.
  • Nakagawa H; Laboratory for Cancer Genomics, RIKEN Center for Integrative Medical Sciences, Tokyo, Japan.
  • Ha NH; Laboratory for Cancer Genomics, RIKEN Center for Integrative Medical Sciences, Tokyo, Japan.
  • Duong NT; Institute of Genome Research, Vietnam Academy of Science and Technology, Ha Noi, Vietnam.
  • Nhung VP; Institute of Genome Research, Vietnam Academy of Science and Technology, Ha Noi, Vietnam.
  • Hien LTT; Institute of Genome Research, Vietnam Academy of Science and Technology, Ha Noi, Vietnam.
  • Hue HTT; Institute of Genome Research, Vietnam Academy of Science and Technology, Ha Noi, Vietnam.
  • Hoang NH; Institute of Genome Research, Vietnam Academy of Science and Technology, Ha Noi, Vietnam.
  • Wong JH; Institute of Genome Research, Vietnam Academy of Science and Technology, Ha Noi, Vietnam.
  • Nakano K; Department of Drug Discovery Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.
  • Maejima K; Laboratory for Cancer Genomics, RIKEN Center for Integrative Medical Sciences, Tokyo, Japan.
  • Sasaki-Oku A; Laboratory for Cancer Genomics, RIKEN Center for Integrative Medical Sciences, Tokyo, Japan.
  • Tsunoda T; Laboratory for Cancer Genomics, RIKEN Center for Integrative Medical Sciences, Tokyo, Japan.
  • Fujimoto A; Laboratory for Medical Science Mathematics, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
  • Van Hai N; Department of Medical Science Mathematics, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
Hum Mutat ; 39(10): 1384-1392, 2018 10.
Article en En | MEDLINE | ID: mdl-29969170
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Exposición Paterna / Dioxinas / Estudio de Asociación del Genoma Completo / Secuenciación Completa del Genoma / Mutación Tipo de estudio: Prognostic_studies Límite: Child / Female / Humans / Male Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Vietnam

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Exposición Paterna / Dioxinas / Estudio de Asociación del Genoma Completo / Secuenciación Completa del Genoma / Mutación Tipo de estudio: Prognostic_studies Límite: Child / Female / Humans / Male Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Vietnam