TY - JOUR
T1 - Longitudinal effects of developmental bisphenol A and variable diet exposures on epigenetic drift in mice
AU - Kochmanski, Joseph
AU - Marchlewicz, Elizabeth H.
AU - Savidge, Matthew
AU - Montrose, Luke
AU - Faulk, Christopher
AU - Dolinoy, Dana C.
N1 - Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2017/3/1
Y1 - 2017/3/1
N2 - 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 (50 μg/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.
AB - 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 (50 μg/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.
KW - Bisphenol A
KW - DNA methylation
KW - Developmental origins of health and disease
KW - Drift
KW - Epigenetics
KW - High fat diet
UR - http://www.scopus.com/inward/record.url?scp=84995639233&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84995639233&partnerID=8YFLogxK
U2 - 10.1016/j.reprotox.2016.07.021
DO - 10.1016/j.reprotox.2016.07.021
M3 - Article
C2 - 27496716
AN - SCOPUS:84995639233
SN - 0890-6238
VL - 68
SP - 154
EP - 163
JO - Reproductigve Toxicoloy
JF - Reproductigve Toxicoloy
ER -