Epigenetic and Behavioral Effects of BPA Exposure
Epigenetic and Behavioral Effects of BPA Exposure
批准号:
8490489
负责人:
JENNIFER T WOLSTENHOLME
金额:
$5.67万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-06-15 至 2014-06-14
关键词:
AdolescentAdultAffectAnimal ModelAnxietyBehaviorBehavioralBloodBrainCandidate Disease GeneCanned FoodsChemicalsComplexDNADNA MethylationDataDevelopmentDietDiseaseDoseEmbryoEndocrineEpigenetic ProcessEstrogen Receptor alphaEstrogensExposure toFemaleGene ExpressionGenesGenetic TranscriptionGenome MappingsHealthHormonalHumanImmunoprecipitationKnockout MiceLeadMalignant neoplasm of prostateMammary NeoplasmsMapsMeasuresMethylationModelingModificationMolecular TargetMusNeurologicNo-Observed-Adverse-Effect LevelObesityPhenotypePit and Fissure SealantsPlasticizersPlasticsPregnancyReproductionResistanceRoleSocial BehaviorTestingTimeValidationWater SupplyWestern BlottingWorkbehavior influencebehavior testbisphenol Abisulfitedrinking watergenome-widein uteroin vivolandfillmalemanmonomernervous system disorderneurodevelopmentprenatal exposurepromoterrelating to nervous systemsexsocial
中文摘要
描述(由申请人提供):双酚A(BPA)是一种主要的环境干扰化合物,在作为增塑剂使用几十年后,它存在于几乎所有发育中和成年人的血液中。暴露于这种内分泌活性化合物会改变正常的激素功能,影响神经组织,最终可能改变行为并导致神经系统疾病。BPA可能起作用的一种机制是通过降低DNA甲基化导致基因表达失调。我将确定子宫内BPA暴露后的持续性、表观遗传和行为变化。BPA诱导的低甲基化和/或其对基因转录的影响的确切靶点尚未完全表征。在这些研究中,我将使用与人类相同剂量的BPA,并通过母体饮食暴露小鼠胚胎。将使用Aim 1中的全基因组甲基化组分析来鉴定BPA诱导的这些小鼠发育中的脑的变化。我将使用亚硫酸氢盐测序确认DNA甲基化水平的表观遗传变化,并测量一致的基因表达改变。从这个,我将创建一个优先的基因列表进行验证。在我们的模型中,BPA暴露降低了雌激素受体α的甲基化。为了直接识别与BPA暴露相关的表观遗传修饰,在第二个目标中,我将测试雌激素受体α基因敲除小鼠在对照组或BPA饮食下的幼年社会行为改变。这些研究将有助于识别BPA的分子靶点,并可能揭示导致行为改变的表观遗传学改变的基因。
英文摘要
DESCRIPTION (provided by applicant): Bisphenol A (BPA) is a major environmental disruptor compound and after several decades in use as a plasticizer it is present in the blood of nearly all developing and adult humans. Exposure to this endocrine- active compound alters normal hormonal function, affects neural organization and ultimately can modify behavior and lead to neurological disorders. One mechanism by which BPA may act is via decreased DNA methylation causing dysregulated gene expression. I will identify persistent, epigenetic and behavioral changes following in utero BPA exposure. The exact targets of BPA-induced hypomethylation and/or its effects on gene transcription have not been fully characterized. In these studies, I will use a dose of BPA equivalent to that noted in humans and expose mouse embryos via maternal diet. BPA-induced changes in the developing brain of these mice will be identified using genome-wide methylome profiling in Aim 1. I will confirm the epigenetic changes at the level of DNA methylation using bisulfite sequencing and measure the concordant altered gene expression. From this, I will create a prioritized gene list for validation. In our model, BPA exposure decreases methylation of estrogen receptor alpha. In order to directly identify epigenetic modifications relevant to changes associated with BPA exposure, in the second aim, I will test estrogen receptor alpha knockout mice gestated on control or BPA diets for alterations in juvenile social behaviors. These studies will aid in the identification of BPA's molecular targets and potentially uncover genes that are epigenetically changed leading to altered behavior.
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会议论文
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