Epigenetic Consequences of Prenatal Alcohol Exposure

产前酒精暴露的表观遗传后果

• 批准号: 7737620
• 负责人: Eva E Redei
• 金额: $ 35.88万
• 依托单位: NORTHWESTERN UNIVERSITY AT CHICAGO
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-07-10 至 2014-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7737620
• 关键词: Adult Children; Affect; Alcohol consumption; Alcohols; Animal Model; Animals; Behavioral; Binding; Brain; Candidate Disease Gene; Child; Cognitive; Cognitive deficits; DNA; Defect; Developmental Gene; Diet; Epigenetic Process; Ethanol; Female; Fetal Alcohol Exposure; Functional RNA; Functional disorder; GTP-Binding Proteins; Gene Expression; Generations; Genes; Genetic Polymorphism; Genomic Imprinting; Goals; Guanine Nucleotide Exchange Factors; Human; Impaired cognition; Impairment; Inbred Strains Rats; Inherited; Intervention; Iodide Peroxidase; Laboratories; Lactation; Learning; Long-Term Effects; Memory; Modeling; Mothers; Mus; Norway; Partner in relationship; Pattern; Phenotype; Physiological; Placenta; Protein Subunits; Proteins; Rattus; Regulation; Symptoms; Testing; Ubiquitin-Protein Ligase Complexes; Variant; Weaning; alternative treatment; base; chromatin modification; clinically relevant; dietary supplements; feeding; fetal; histone modification; imprint; male; necdin; novel; offspring; overexpression; prenatal; public health relevance; ras-GRF1; rat genome; response; transcription factor; transmission process; ubiquitin-protein ligase

DESCRIPTION (provided by applicant): Rat models of fetal alcohol exposure (FAE) emulate many symptoms observed in children of alcohol consuming mothers including cognitive impairments of the offspring. We hypothesize that FAE induces epigenetic alterations of neurodevelopmental genes contributing to these impairments in adult offspring. We selected to study imprinted genes that are known to be involved in spatial learning and memory, and whose deficit or overexpression causes cognitive impairment. These genes include, the Delta-like (Dlk), type 3 deiodinase (Dio3), G-protein -subunit, Gs (Gnas) and its variants, necdin (Ndn), ubiquitin protein ligase E3A (Ube3a) and RAS protein-specific guanine nucleotide-releasing factor 1 (Rasgrf1). We will investigate: Specific Aim 1. The epigenetic effects of ethanol exposure in utero on imprinted and total expression of selected genes. We will initially corroborate that these genes are imprinted in the rat and then we will determine the short and long-term effects of FAE on the expression patterns of these imprinted genes. Specific Aim 2. The mechanism of altered expression/imprinting by FAE through characterization of DNA and histone modifications and transcription factor binding at known regulatory loci. We will examine the imprinting mechanisms of candidate genes, which show expression alterations by FAE. Specific Aim 3. Different strategies to reverse FAE-induced epigenetic dysregulation. We will administer dietary supplement regimes, known to affect epigenetic mechanisms, to animals during lactation, or post- weaning, and subsequently screen for improvement in spatial learning and memory as well as gene expression patterns and DNA/chromatin modifications. Specific Aim 4. The trans-generational effects of FAE on the cognitive phenotype and the epigenetic alterations of candidate genes. A two-generational cross will be carried out where only the first generation dam receives alcohol. Reciprocal crossing will tests both maternal and paternal transmission. These aims will bring us closer to understanding the mechanisms by which prenatal ethanol induce behavioral deficits in the offspring. Transgenerational inheritance of FAE effects is a significant question with relevance from treatment alternatives to the sociological consequences of multigenerational dysfunction. Identifying the mechanisms and potential reversibility of transgenerational effects and devising novel interventions in the animal model of FAE is a major goal that could potentially be beneficial for human FAE. PUBLIC HEALTH RELEVANCE: Rat models of fetal alcohol exposure (FAE) emulate many symptoms observed in children of alcohol consuming mothers including cognitive deficits of the offspring. In this application, we hypothesize that epigenetic alterations in response to prenatal alcohol exposure contribute to the cognitive deficits of FAE, and that these alterations are transgenerationally inherited. This latter possibility has multiple implications from the significance of treatment alternatives to the sociological consequences of multigenerational dysfunction. Identifying the mechanisms and potential reversibility of transgenerational effects is an important goal.

描述（由申请人提供）：胎儿酒精暴露（FAE）的大鼠模型模拟了在饮酒母亲的儿童中观察到的许多症状，包括后代的认知障碍。我们假设，FAE诱导的神经发育基因的表观遗传改变，这些损伤在成年后代。我们选择研究已知参与空间学习和记忆的印记基因，其缺陷或过度表达会导致认知障碍。这些基因包括Delta样（Dlk）、3型脱碘酶（Dio 3）、G蛋白亚基、Gs（Gnas）及其变体、necdin（Ndn）、泛素蛋白连接酶E3 A（Ube 3a）和RAS蛋白特异性鸟嘌呤核苷酸释放因子1（Rasgrf 1）。我们将研究：具体目标1。子宫内乙醇暴露对选定基因印迹和总表达的表观遗传学影响。我们将首先证实这些基因在大鼠中是印记的，然后我们将确定FAE对这些印记基因表达模式的短期和长期影响。具体目标2。通过表征DNA和组蛋白修饰以及转录因子在已知调控位点的结合，FAE改变表达/印迹的机制。我们将研究候选基因的印记机制，通过FAE显示表达改变。具体目标3。逆转FAE诱导的表观遗传失调的不同策略。我们将在哺乳期或断奶后对动物施用已知影响表观遗传机制的膳食补充剂方案，随后筛选空间学习和记忆以及基因表达模式和DNA/染色质修饰的改善。具体目标4。FAE对认知表型的跨代影响及候选基因的表观遗传学改变。两代杂交将进行，只有第一代大坝接受酒精。相互杂交将测试母亲和父亲的传播。这些目标将使我们更接近了解产前乙醇诱导后代行为缺陷的机制。FAE效应的跨代遗传是一个重要的问题，从治疗方案到多代功能障碍的社会学后果都有相关性。确定跨代效应的机制和潜在可逆性，并在FAE动物模型中设计新的干预措施，是可能对人类FAE有益的主要目标。公共卫生相关性：胎儿酒精暴露（FAE）的大鼠模型模拟了在饮酒母亲的儿童中观察到的许多症状，包括后代的认知缺陷。在本申请中，我们假设，产前酒精暴露的表观遗传改变有助于FAE的认知缺陷，这些改变是跨代遗传的。后一种可能性具有多重含义，从治疗替代方案的意义到多代功能障碍的社会学后果。查明代际影响的机制和潜在的可逆性是一个重要目标。