TCDD-induced multi- and transgenerational changes in the methylome of male zebrafish gonads. Issue 1 (27th September 2020)

• Record Type: Journal Article
• Authors: Akemann, Camille; Meyer, Danielle N; Gurdziel, Katherine; Baker, Tracie R
• Editors: Dolinoy, Dana
• Is Part Of: Environmental epigenetics. Volume 6:Issue 1(2020)
• Publication Date: 2020-09-27
• Subjects: zebrafish -- transgenerational -- epigenetics -- methylation -- 2, 3, 7, 8-tetrachlorodibenzo-p-dioxin -- reproduction; Epigenetics -- Periodicals; 572.86505
• DOI: 10.1093/eep/dvaa010
• Languages: English
• ISSNs: 2058-5888

Abstract

Abstract: The legacy endocrine disrupting chemical and aryl hydrocarbon receptor agonist, 2, 3, 7, 8-tetrachlorodibenzo- p -dioxin (TCDD), is produced as a byproduct of industrial processes and causes adverse health effects ranging from skin irritation to cancer. TCDD endpoints are also observed in subsequent, unexposed generations; however, the mechanisms of these multi- and transgenerational effects are unknown. We hypothesized an epigenetic mechanism, specifically DNA methylation for the transgenerational, male-mediated reproductive effects of developmental TCDD exposure. Using whole genome bisulfite sequencing, we evaluated DNA methylation changes in three generations of zebrafish, the first of which was exposed to TCDD during sexual development at 50 ppt for 1 h at both 3- and 7-week post-fertilization. We discovered that TCDD induces multi- and transgenerational methylomic changes in testicular tissue from zebrafish with decreased reproductive capacity, but most significantly in the indirectly exposed F1 generation. In comparing differentially methylated genes to concurrent transcriptomic changes, we identified several genes and pathways through which transgenerational effects of low level TCDD exposure are likely inherited. These include significant differential methylation of genes involved in reproduction, endocrine function, xenobiotic metabolism, and epigenetic processing. Notably, a number of histone modification genes were both differentially methylated and expressed in all generations, and many differentially methylated genes overlapped between multiple generations. Collectively, our results suggest that DNA methylation is a promising mechanism to explain male-mediated transgenerational reproductive effects of TCDD exposure in zebrafish, and these effects are likely inherited through integration of multiple epigenetic pathways.