Epigenetic transgenerational effects of endocrine disruptors via female germ line

内分泌干​​扰物通过雌性生殖系的表观遗传跨代效应

• 批准号: 8733997
• 负责人: Mehmet Uzumcu
• 金额: $ 19.38万
• 依托单位: RUTGERS, THE STATE UNIV OF N.J.
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-08-12 至 2015-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8733997
• 关键词: Aberrant DNA Methylation; Address; Adult; Affect; Aging; Anxiety; Apoptosis; Behavior; Breeding; Chemical Exposure; Child; DNA Methylation; DNA Methyltransferase; DNA Modification Methylases; DNA Sequence; Development; Disease susceptibility; Dose; Embryo; Endocrine Disruptors; Endogenous Retroviruses; Environment; Epigenetic Process; Event; Exhibits; Exposure to; Female; Fertility; Future; Future Generations; Gene Expression; Gene Expression Profile; Generations; Genes; Germ Cells; Germ Lines; Global Change; Goals; Gonadal structure; H19 gene; Health; Health Care Costs; Inbreeding; Incidence; Individual; Knowledge; Lead; Life; Link; Mediating; Mediator of activation protein; Methods; Methoxychlor; Methylation; Modeling; Morphology; Neonatal; Onset of illness; Oocytes; Ovarian; Ovary; Ovulation; Parents; Partner in relationship; Pathology; Pattern; Perinatal Exposure; Periodicity; Pesticides; Phenotype; Play; Puberty; Public Health; Rattus; Research; Retrotransposon; Reverse Transcriptase Polymerase Chain Reaction; Risk; Role; Sex Ratio; Testing; Time; TimeLine; Tissues; Toxic Environmental Substances; Woman; Women' s Role; base; beryllium trifluoride; bisulfite; demethylation; density; environmental stressor; fetal; folliculogenesis; follow-up; grandchild; imprint; in utero; innovation; male; novel; postnatal; prevent; programs; reproductive; reproductive function; sex; sperm cell; vinclozolin

DESCRIPTION (provided by applicant): It is well established that exposure to environmental stressors or toxicants such as endocrine-disrupting chemicals (EDCs) during in utero and/or neonatal development can result in adult-onset diseases. Such detrimental changes have been linked to aberrant DNA methylation patterns as well as other epigenetic mechanisms. It is of great concern that recent studies have suggested that such disease susceptibilities can be transmitted via epigenetic mechanisms to subsequent generations that were never directly exposed to the EDCs. For example, testicular abnormalities were transmitted to F2-F4 generation males via the male germ line after in utero exposure to an EDC. However, these effects were found to be sex-specific since F2-F3 females exhibited milder phenotypes that required exposure of both parents to the EDC. In this proposal, our objective is to address the critical issue of whether the female germ line is involved in such transgenerational (TG) effects of EDC exposure. Methoxychlor (MXC) is an EDC that has actions mimicking those of many other EDCs in the environment and was shown to cause epigenetic changes in the gonad; it will therefore be used as a model EDC in this proposal. Our hypothesis is that exposure to MXC during the critical window of development, defined here as the period of gonad differentiation through oocyte epigenetic reprogramming, leads to TG effects in the ovary that are mediated by epigenetic changes in the oocyte. To test our hypothesis, the proposal has two interrelated but distinct specific aims: (1) Determine somatic TG epigenetic effects of MXC in the ovary of F3 generation following exposure of F1. F1-generation inbred female rats will be treated with 0, 20 5g/kg/day MXC, or 50-100 mg/kg/day MXC between E11 and PND7. These females will be bred with untreated males, and F2-F4 females will be generated. Initially, ovarian morphology and gene expression and fertility will be assessed only in the F3 females since observation of TG effects in F3 generation is the minimum requirement for establishing TG effects. Gene expression changes and global and gene-specific DNA methylation changes will be investigated using conventional methods as well as array-based approaches. (2) Investigate the epigenetic changes induced by MXC in F1/F2 oocytes that may lead to TG effects in F3. DNA methylation patterns in imprinted genes and parasitic DNA sequences such as retrotransposons in oocytes will be analyzed, as aberrant methylation patterns in these sequences can be pathogenic. Oocytic gene expression patterns will also be examined; any correlation between the changes in gene expression and DNA methylation will be elucidated. The proposed study will be the first to investigate the epigenetic TG effects of EDCs transmitted via the female germ line beyond the F2 generation. We recognize the considerable risk associated with this study, but implications to the health of present and future generations are significant given the widespread presence of EDCs in the environment. A mechanistic understanding of the TG epigenetic actions of MXC will broaden our knowledge of how EDCs, in general, disrupt normal epigenetic programming in females, and facilitate the development of strategies to prevent and treat EDC-induced TG abnormalities.

描述(由申请人提供)：众所周知，在宫内和/或新生儿发育期间暴露于环境应激源或毒物，如内分泌干扰物(EDCs)，可导致成人发病。这种有害的变化与异常的DNA甲基化模式以及其他表观遗传机制有关。令人非常关注的是，最近的研究表明，这种疾病的易感性可以通过表观遗传机制传播给从未直接接触内皮细胞的后代。例如，在宫内暴露于EDC后，睾丸异常通过雄性生殖系传递给F2-F4代雄性。然而，这些影响被发现是性别特有的，因为F2-F3雌性表现出较温和的表型，需要父母双方都接触EDC。在这项建议中，我们的目标是解决关键问题，即女性生殖系是否参与了EDC暴露的这种跨代(TG)影响。甲氧氯胺(MXC)是一种EDC，具有模仿环境中许多其他EDC的作用，并被证明会导致性腺的表观遗传变化；因此，它将在本提案中用作EDC的模型。我们的假设是，在发育的关键窗口(这里定义为通过卵母细胞表观遗传学重编程实现性腺分化的时期)暴露于MXC会导致卵巢中的TG效应，这是由卵母细胞的表观遗传学变化所介导的。为了验证我们的假设，该提议有两个相互关联但又截然不同的具体目标：(1)确定暴露F1后MXC在F3代卵巢中的体细胞TG表观遗传效应。F1代近交系雌性大鼠在胎龄11~7周龄期间分别给予0、20.5g/kg/d或50~100 mg/kg/d的MXC处理。这些雌性将与未经处理的雄性繁殖，并产生F2-F4雌性。最初，卵巢的形态、基因表达和生育能力将只在F3代雌性中进行评估，因为观察F3代的TG效应是建立TG效应的最低要求。将使用常规方法以及基于阵列的方法来研究基因表达变化以及全局和特定于基因的DNA甲基化变化。(2)探讨MXC对F1/F2卵母细胞的表观遗传学改变，从而可能导致F3卵母细胞的Tg效应。将分析印迹基因和寄生DNA序列(如卵母细胞中的反转录转座子)中的DNA甲基化模式，因为这些序列中的异常甲基化模式可能是致病的。还将研究卵母细胞基因表达模式；基因表达变化与DNA甲基化之间的任何关联将被阐明。这项拟议的研究将首次调查通过雌性生殖系传播的EDCs在F2代之后的表观遗传TG效应。我们认识到与这项研究相关的相当大的风险，但鉴于内分泌细胞在环境中的广泛存在，对当代和子孙后代的健康影响重大。从机制上理解MXC的TG表观遗传行为将拓宽我们的知识，一般情况下，EDCs是如何扰乱女性正常的表观遗传程序的，并有助于开发预防和治疗EDC诱导的TG异常的策略。