Epigenetics of fetal alcohol syndrome

胎儿酒精综合征的表观遗传学

基本信息

批准号：
7487444
负责人：
FENG C. ZHOU
金额：
$ 24.63万
依托单位：
INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS
依托单位国家：
美国
项目类别：
财政年份：
2006
资助国家：
美国
起止时间：
2006-09-30 至 2010-08-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7487444
关键词：
Acetaldehyde Acetic Acid Acetic Acids Acetylation Acute Address Alcohol consumption Alcoholism Alcohols Apoptosis Appendix Area BCL-2 Protein BCL2 gene Binding Proteins Biological Biological Assay C57BL/6 Mouse Cancer Etiology Candidate Disease Gene Cell Cycle Cessation of life Characteristics Choline Chromatin Chromatin Structure Complex CpG Islands CpG dinucleotide Cytosine DNA DNA Methylation DNA Methyltransferase DNA Modification Methylases DNA Modification Process Data Defect Depth Detection Development Disease Dysmorphology Embryo Environmental Risk Factor Epigenetic Process Ethanol Ethanol Metabolism Etiology Event Evolution Fetal Alcohol Exposure Fetal Alcohol Syndrome Fetal Development Fetus Folate Future Gene Expression Genes Genetic Genetic Transcription Genome Histone Acetylation Histones Homeobox Hypermethylation In Vitro Individual Injury Lead Link Lysine Malignant Neoplasms Mediating Mental Retardation Metabolism Methionine Methionine Metabolism Pathway Methods Methylation Microarray Analysis Modeling Modification Mus Numbers Pathway interactions Patient currently pregnant Pattern Phenotype Phosphotransferases Play Polymerase Chain Reaction Pregnancy Promoter Regions Proteins Regulation Reporting Research Personnel Reverse Transcriptase Polymerase Chain Reaction Role Scanning Schizophrenia Staging Standards of Weights and Measures System Techniques Technology Time Tissue-Specific Gene Expression Tissues Vitamin B Complex Western Blotting alcohol abuse therapy alcohol exposure base chromatin immunoprecipitation cohort day dietary supplements embryo culture embryonic stem cell fetal genetic manipulation genome-wide analysis imprint in utero in vivo Model inhibitor/antagonist maternal imprint methionine methyl ester next generation novel outcome forecast prenatal programs promoter relating to nervous system trait tumor progression tumorigenesis vapor young adult

项目摘要

DESCRIPTION (provided by applicant): Alcoholism and fetal alcohol syndrome are the result of the complex interaction of multiple genetic and environmental factors. Recently, it has become apparent that in addition to genetic and environmental factors, epigenetic mechanisms play crucial roles in the etiology of a large number of diseases such as cancer and schizophrenia. Furthermore, developmental abnormalities are known to be associated with aberrant epigenetic changes in DNA and chromatin. Covalent histone modifications and DNA cytosine methylation, particularly in gene promoter regions, are key epigenetic modifications that control chromatin structure and gene expression. Alcohol and its metabolite acetic acid have strong propensity to deregulate methylation donor by inhibiting a key folate-methionine metabolism pathway leading to altered methylation. Thus, fetal development actively engaged in DNA transcription and cell cycling would be a prime target by alcoholinduced epigenetic abnormalities. This proposal will determine if alcohol cause aberrant epigenetic changes in the fetus, and if the alcohol-induced epigenetic abnormalities lead to fetal alcohol syndrome. Our preliminary data indicates that prenatal alcohol exposure causes decreased multiple linker and core histone genes expression, changes histone methylation, and altered gene expression leading to neural specification. In this proposal, we will study alcohol-mediated epigenetic changes in developing embryos. The alcohol exposure level will be carefully controlled, and our analysis will be able to distinguish maternal imprinting from epigenetic effects due to direct alcohol exposure. We will use a C57BL//6J mice whole embryonic culture model, differential methylation hybridization, and novel ChlP-chip technology to determine genome wide epigenetic changes induced by alcohol. Second, we will identify cohort of genes with promoter methylation and transcriptional alterations, confirm the findings using standard RT-PCR / western blot, and determine their functional pathways. Furthermore, the biological significance of the confirmed key genes will be determined using pharmacological inhibitors of DNA methylation and histone acetylation or genetic manipulation, along with phenotypic analysis. The effect of these epigenetic key genes will be confirmed in the in vivo model exposed to alcohol vapor chamber with alcohol exposure pattern and paradigms similar to the whole embryonic culture.

描述（由申请人提供）：酒精中毒和胎儿酒精综合症是多种遗传和环境因素复杂相互作用的结果。最近，人们发现，除了遗传和环境因素外，表观遗传机制在癌症和精神分裂症等大量疾病的病因学中也发挥着至关重要的作用。此外，已知发育异常与 DNA 和染色质的异常表观遗传变化有关。共价组蛋白修饰和 DNA 胞嘧啶甲基化，特别是在基因启动子区域，是控制染色质结构和基因表达的关键表观遗传修饰。酒精及其代谢物乙酸具有强烈的倾向，通过抑制导致甲基化改变的关键叶酸-蛋氨酸代谢途径来解除甲基化供体的管制。因此，积极参与 DNA 转录和细胞周期的胎儿发育将成为酒精诱导的表观遗传异常的主要目标。该提案将确定酒精是否会导致胎儿异常的表观遗传变化，以及酒精引起的表观遗传异常是否会导致胎儿酒精综合症。我们的初步数据表明，产前酒精暴露会导致多个接头和核心组蛋白基因表达减少，改变组蛋白甲基化，并改变基因表达，从而导致神经特化。在这项提案中，我们将研究发育中胚胎中酒精介导的表观遗传变化。酒精暴露水平将受到仔细控制，我们的分析将能够区分母体印记和直接酒精暴露造成的表观遗传效应。我们将使用 C57BL//6J 小鼠全胚胎培养模型、差异甲基化杂交和新型 ChlP 芯片技术来确定酒精诱导的全基因组表观遗传变化。其次，我们将鉴定具有启动子甲基化和转录改变的基因组，使用标准 RT-PCR/蛋白质印迹确认结果，并确定它们的功能途径。此外，已确认的关键基因的生物学意义将通过DNA甲基化和组蛋白乙酰化的药理学抑制剂或遗传操作以及表型分析来确定。这些表观遗传关键基因的作用将在暴露于酒精蒸汽室的体内模型中得到证实，该模型具有与整个胚胎培养相似的酒精暴露模式和范式。