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HERO ID
1411643
Reference Type
Journal Article
Title
Maternal nutrient supplementation counteracts bisphenol A-induced DNA hypomethylation in early development
Author(s)
Dolinoy, DC; Huang, D; Jirtle, RL
Year
2007
Is Peer Reviewed?
1
Journal
Proceedings of the National Academy of Sciences of the United States of America
ISSN:
0027-8424
EISSN:
1091-6490
Volume
104
Issue
32
Page Numbers
13056-13061
Language
English
PMID
17670942
DOI
10.1073/pnas.0703739104
Web of Science Id
WOS:000248650300020
URL
https://www.scopus.com/inward/record.uri?eid=2-s2.0-34548715144&doi=10.1073%2fpnas.0703739104&partnerID=40&md5=809dbf65ae25de3c91420eb0048c16b5
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Abstract
The hypothesis of fetal origins of adult disease posits that early developmental exposures involve epigenetic modifications, such as DNA methylation, that influence adult disease susceptibility. In utero or neonatal exposure to bisphenol A (BPA), a high-production-volume chemical used in the manufacture of polycarbonate plastic, is associated with higher body weight, increased breast and prostate cancer, and altered reproductive function. This study shows that maternal exposure to this endocrine-active compound shifted the coat color distribution of viable yellow agouti (Avy) mouse offspring toward yellow by decreasing CpG (cytosine-guanine dinucleotide) methylation in an intracisternal A particle retrotransposon upstream of the Agouti gene. CpG methylation also was decreased at another metastable locus, the CDK5 activator-binding protein (CabpIAP). DNA methylation at the Avy locus was similar in tissues from the three germ layers, providing evidence that epigenetic patterning during early stem cell development is sensitive to BPA exposure. Moreover, maternal dietary supplementation, with either methyl donors like folic acid or the phytoestrogen genistein, negated the DNA hypomethylating effect of BPA. Thus, we present compelling evidence that early developmental exposure to BPA can change offspring phenotype by stably altering the epigenome, an effect that can be counteracted by maternal dietary supplements.
Keywords
; Animals; Base Sequence; Benzhydryl Compounds; CpG Islands; DNA Methylation/drug effects; Dietary Supplements; Epigenesis; Genetic; Female; Fetus/drug effects; Fetus/metabolism; Hair Color; Maternal Nutritional Physiological Phenomena; Mice; Molecular Sequence Data; Phenols/toxicity; Pregnancy; Index Medicus/
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