Exposure-altered gene expression in five candidate imprinted loci for adult disease

成人疾病的五个候选印迹基因座中暴露改变的基因表达

基本信息

批准号：
9106621
负责人：
Zhibin Wang
金额：
$ 34.89万
依托单位：
JOHNS HOPKINS UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2016
资助国家：
美国
起止时间：
2016-07-01 至 2021-06-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/9106621
关键词：
129 Mouse Address Adult Affect Alleles Animal Model Animals Barker Hypothesis Behavior Disorders Binding Binding Sites Cell Differentiation process ChIP-seq Charcot-Marie-Tooth Disease Control Locus DNA Methylation DNA Modification Methylases Data Development Diabetes Mellitus Disease Embryo Endocrine Disruptors Environmental Exposure Environmental Risk Factor Epigenetic Process Epilepsy Exposure to Famines Female Fetal Liver Fetus Gene Expression Genes Genome Genomic Imprinting Growth and Development function Histone Code Histones Human Hunger Individual Knock-out Knowledge Life Link Location Methylation Mus Mutate Neurologic Parents Parkinson Disease Partner in relationship Pathogenesis Pattern Perinatal Exposure Play Predisposition Prevention strategy Process Regulation Resolution Risk Role Schizophrenia Shapes Staging Survivors Testing Tissue-Specific Gene Expression Tissues Toxic Environmental Substances Toxicant exposure base bisphenol A developmental plasticity embryonic stem cell fetal bisphenol-A exposure histone methylation histone modification imprint insight male methylation pattern methylome mouse genome nervous system disorder neuron development novel novel strategies prenatal promoter public health relevance response toxicant

项目摘要

DESCRIPTION (provided by applicant): Increasing evidence from studies of animals and of individuals who suffered from the Dutch Hunger Winter of 1944-45 supports the concept that environmental exposure of early embryos causes increased risk of development of disease in adulthood (Barker hypothesis). For example, exposure of mouse embryos to the endocrine disrupting chemical Bisphenol A (BPA) is known to cause many disorders, including neurological/behavioral disorders. Genomic imprinting (an epigenetic process to control parent-origin-specific expression of genes) has been theorized as the major determinant of these effects. Methylation of Igf2 differentially-methylated-region (DMR; a hallmark of imprinting) is persistently changed in individuals surviving the Dutch famine. Our understanding of the mechanism(s) underlying the "Barker hypothesis" has been hampered by focusing only on a few imprinted loci (i.e. Igf2). However, it is unlikely that all 20 "Barker diseases" are due solely to changes in Igf2 expression; particularly as many "Barker diseases" have no association with known imprinted genes. Using two novel approaches (so-called NORED and Tag-mosaicity), which allow one to analyze base-resolution methylomes of DNA methyltransferase (DNMT) knockout (KO) embryonic stem cells (ESCs), we have successfully identified 20 novel DMRs representing 17 `candidate' imprinted loci. Intriguingly, five of these 17 putative imprinted loci are linked to neurological disorders in humans. Further studies are needed to confirm that these putative loci contain imprinted genes and to determine whether (and then how) environmental exposure-altered DMRs change expression of these putatively imprinted genes within these loci, thereby contributing to the pathogenesis of "Barker diseases." To this end, we confirmed at least one locus (i.e., D2hgdh) via revealing its allelic methylation patterns and found that alleli methylation of five DMRs dictates the binding of insulator CTCF for potentially effecting histone modifications of imprinted genes. Furthermore, fetal exposure of BPA altered multiple DMRs including selected DMRs. Based on our exciting preliminary data, we hypothesized that DMRs dictate the allele-specific binding of CTCF and CTCF insulation subsequently controls the distinct histone modifications at promoters of different imprinted genes in five loci for regulatio. Lastly, BPA exposure-altered DMRs in these loci change gene expression, thereby contributing to the pathogeneses of neurological disorders. We will test our hypothesis through three complementary aims: SA1, Determine whether the putative DMRs dynamically alter gene expression in a tissue-specific manner. SA2, Determine the mechanisms of imprinting of five novel loci. SA3, Determine whether BPA-induced alterations in novel DMRs result in altered tissue-specific gene expression during development. The results of these studies should elucidate how putatively imprinted genes from five `candidate' loci contribute to developmental plasticity during normal growth and development or under environmental exposure-altered conditions and inform the development of prevention strategies to protect the unborn fetus.

描述（由申请人提供）：对遭受 1944-45 年荷兰饥饿冬季的动物和个人的研究越来越多的证据支持这样的观点，即早期胚胎的环境暴露会导致成年后患疾病的风险增加（巴克假说）。例如，已知小鼠胚胎接触内分泌干扰化学物质双酚 A (BPA) 会导致许多疾病，包括神经/行为障碍（一种表观遗传）。控制亲本来源特异性基因表达的过程）被认为是这些效应的主要决定因素，Igf2 差异甲基化区域（DMR；印记的标志）在荷兰饥荒中幸存下来的个体中持续发生变化。由于仅关注少数印记位点（即 Igf2），对“巴克假说”背后机制的理解受到了阻碍。然而，不可能同时关注所有 20 个印记位点。 “巴克病”完全是由于 Igf2 表达的变化；特别是许多“巴克病”与已知的印记基因无关，使用两种新方法（所谓的 NORED 和标签镶嵌性），可以分析 DNA 甲基转移酶 (DNMT) 的碱基分辨率甲基化组。通过敲除 (KO) 胚胎干细胞 (ESC)，我们成功鉴定了 20 个新的 DMR，代表 17 个“候选”印记位点，有趣的是，其中有 5 个。这 17 个假定的印记基因座中的一个与人类的神经系统疾病有关，需要进一步的研究来确认这些假定的基因座包含印记基因，并确定环境暴露改变的 DMR 是否（以及如何）改变这些假定的印记基因的表达。为此，我们通过揭示其等位基因甲基化模式和确认了至少一个基因座（即 D2hgdh）。发现五个 DMR 的等位基因甲基化决定了绝缘子 CTCF 的结合，从而可能影响印记基因的组蛋白修饰。此外，胎儿接触 BPA 改变了多个 DMR，包括选定的 DMR。根据我们令人兴奋的初步数据，我们渴望 DMR 决定等位基因。 CTCF 和 CTCF 绝缘的特异性结合随后控制五个位点中不同印记基因启动子处的不同组蛋白修饰，以进行调节。最后，BPA 暴露发生改变。这些位点中的 DMR 会改变基因表达，从而导致神经系统疾病的发病机制。我们将通过三个互补的目标来检验我们的假设：SA1，确定假定的 DMR 是否以组织特异性方式动态改变基因表达。 SA3 的印记，确定 BPA 诱导的新 DMR 改变是否会导致发育过程中组织特异性基因表达的改变。来自五个“候选”基因座的印记基因有助于正常生长和发育期间或环境暴露改变条件下的发育可塑性，并为保护未出生胎儿的预防策略的制定提供信息。