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Longitudinal effects of developmental bisphenol A and variable diet exposures on epigenetic drift in mice.

Citation
Kochmanski, J., et al. “Longitudinal Effects Of Developmental Bisphenol A And Variable Diet Exposures On Epigenetic Drift In Mice.”. Reproductive Toxicology (Elmsford, N.y.), pp. 154-163.
Center University of Michigan
Author Joseph Kochmanski, Elizabeth H Marchlewicz, Matthew Savidge, Luke Montrose, Christopher Faulk, Dana C Dolinoy
Keywords Bisphenol A, DNA methylation, developmental origins of health and disease, Drift, Epigenetics, high fat diet
Abstract

Environmental factors, including exogenous exposures and nutritional status, can affect DNA methylation across the epigenome, but effects of exposures on age-dependent epigenetic drift remain unclear. Here, we tested the hypothesis that early-life exposure to bisphenol A (BPA) and/or variable diet results in altered epigenetic drift, as measured longitudinally via target loci methylation in paired mouse tail tissue (3 wks/10 mos old). Methylation was quantified at two repetitive elements (LINE-1, IAP), two imprinted genes (Igf2, H19), and one non-imprinted gene (Esr1) in isogenic mice developmentally exposed to Control, Control+BPA (50μg/kg diet), Mediterranean, Western, Mediterranean+BPA, or Western+BPA diets. Across age, methylation levels significantly (p<0.050) decreased at LINE-1, IAP, and H19, and increased at Esr1. Igf2 demonstrated Western-specific changes in early-life methylation (p=0.027), and IAP showed marginal negative modification of drift in Western (p=0.058) and Western+BPA (p=0.051). Thus, DNA methylation drifts across age, and developmental nutritional exposures can alter age-related methylation patterns.

Year of Publication
2017
Journal
Reproductive toxicology (Elmsford, N.Y.)
Volume
68
Number of Pages
154-163
Date Published
12/2017
ISSN Number
1873-1708
DOI
10.1016/j.reprotox.2016.07.021
Alternate Journal
Reprod. Toxicol.
PMID
27496716
PMCID
PMC5290281
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