High Gestational Folic Acid Supplementation Alters Expression of Imprinted and Candidate Autism Susceptibility Genes in a sex-Specific Manner in Mouse Offspring

被引:0
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作者
Subit Barua
Salomon Kuizon
W. Ted Brown
Mohammed A. Junaid
机构
[1] New York State Institute for Basic Research in Developmental Disabilities,Structural Neurobiology Laboratory, Department of Developmental Biochemistry
[2] Columbia University,Department of Pathology and Cell Biology, College of Physicians and Surgeons
[3] New York State Institute for Basic Research in Developmental Disabilities,Department of Human Genetics
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Folic acid; DNA methylation; Epigenetics; Imprinting; Prenatal nutrition; Autism;
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摘要
Maternal nutrients play critical roles in modulating epigenetic events and exert long-term influences on the progeny’s health. Folic acid (FA) supplementation during pregnancy has decreased the incidence of neural tube defects in newborns, but the influence of high doses of maternal FA supplementation on infants’ brain development is unclear. The present study was aimed at investigating the effects of a high dose of gestational FA on the expression of genes in the cerebral hemispheres (CHs) of 1-day-old pups. One week prior to mating and throughout the entire period of gestation, female C57BL/6J mice were fed a diet, containing FA at either 2 mg/kg (control diet (CD)) or 20 mg/kg (high maternal folic acid (HMFA)). At postnatal day 1, pups from different dams were sacrificed and CH tissues were collected. Quantitative RT-PCR and Western blot analysis confirmed sex-specific alterations in the expression of several genes that modulate various cellular functions (P < 0.05) in pups from the HMFA group. Genomic DNA methylation analysis showed no difference in the level of overall methylation in pups from the HMFA group. These findings demonstrate that HMFA supplementation alters offsprings’ CH gene expression in a sex-specific manner. These changes may influence infants’ brain development.
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页码:277 / 286
页数:9
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