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中文摘要
翻译
描述(申请人提供):这篇论文的长期目标是阐明乙醇的表观遗传效应对胎儿酒精暴露后抑郁和焦虑障碍的发育易感性的贡献。母体酒精消费是一个普遍存在的问题,这项研究将对完成拟议的具体目标后的潜在逆转策略具有很大的指导意义。这些包括确定酒精介导的大脑和胎盘中激素和表观遗传变化的时间进程,以及实验分离表观遗传效应和酒精诱导的母体甲状腺功能减退的影响。我们还将确定乙醇改变印迹和甲状腺激素代谢的表观遗传学机制,揭示未来逆转范例将针对的特定基因组区域。总而言之,获得的关于乙醇暴露的不同但相关的表观遗传学和激素方面的信息将创造一个全面的理解,即乙醇在胎儿大脑中作用的时间和性质。在我们可以实施有针对性的、定时的方法来逆转我们发现的每一种酒精效应之前,我们的数据产生的时间和生理轮廓是绝对必要的。我们高度重视这个项目的健康相关性,因为它是基于适度但持续的胎儿酒精暴露水平。这一范式与母亲饮酒被接受或未被报告的人群高度相关,从而导致后代出现神经问题。这些缺陷在出生后发育和成年期间持续存在,造成了贯穿整个生命周期的公共卫生问题。这些包括儿童学习障碍和多动症对教育系统的负面影响,以及随后成人精神疾病对社会、经济和卫生保健的影响。
英文摘要
DESCRIPTION (provided by applicant): The long-term goal of the thesis work proposed here is to elucidate the contribution of epigenetic effects of ethanol to the developmental susceptibility to depression and anxiety disorders seen after fetal alcohol exposure. Maternal ethanol consumption is a widespread problem and this research will be highly instructive as to potential reversal strategies after completion of the proposed specific aims. These include the determination of the time course of ethanol-mediated hormonal and epigenetic changes in the brain and placenta, and the experimental dissociation of epigenetic effects from the effects of ethanol-induced maternal hypothyroidism. We will also determine the epigenetic mechanism by which ethanol alters imprinting and thyroid hormone metabolism, unveiling the specific genomic regions that will be targeted by future reversal paradigms. Together, the information gained about the distinct but related epigenetic and hormonal aspects of ethanol exposure will create a comprehensive understanding of the timing and nature of ethanol's actions in the fetal brain. The temporal and physiological outline to be generated by our data is absolutely necessary before we can implement targeted, timed approaches to reverse each of the ethanol effects we uncover. We place high value on the health relevance of this project as it is based on a moderate but sustained level of fetal alcohol exposure. This paradigm is highly relevant in human populations in which maternal alcohol consumption is accepted or under-reported, resulting in neurological problems in the offspring. These deficits persist throughout postnatal development and adulthood, creating public health issues that manifest over the entire lifespan. These include negative effects on the education system attributable to childhood learning disabilities and hyperactivity, and subsequently, the social, financial, and health care-related repercussions of adult mental illness.
期刊论文(4)
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科研奖励(0)
会议论文
Fine-tuning notes in the behavioral symphony: parent-of-origin allelic gene expression in the brain.
行为交响曲中的微调音符:大脑中的亲本等位基因表达。
DOI: 10.1016/b978-0-12-800222-3.00005-x
发表时间: 2014
期刊: Advances in genetics
影响因子: --
作者: [Sittig,LauraJ, Redei,EvaE]
通讯作者: Redei,EvaE
Hypothesis: genetic and epigenetic risk factors interact to modulate vulnerability and resilience to FASD.
假设:遗传和表观遗传风险因素相互作用,调节 FASD 的脆弱性和恢复力。
DOI: 10.3389/fgene.2014.00261
发表时间: 2014
期刊: Frontiers in genetics
影响因子: 3.7
作者: [Tunc-Ozcan,Elif, Sittig,LauraJ, Harper,KathrynM, Graf,EvanN, Redei,EvaE]
通讯作者: Redei,EvaE
DOI: 10.3389/fgene.2012.00279
发表时间: 2012
期刊: Frontiers in genetics
影响因子: 3.7
作者: [Dietz WH, Masterson K, Sittig LJ, Redei EE, Herzing LB]
通讯作者: Herzing LB
Novel polymorphisms within the Dlk1-Dio3 imprinted locus in rat: a putative genetic basis for strain-specific allelic gene expression.
大鼠 Dlk1-Dio3 印迹基因座内的新多态性:品系特异性等位基因表达的假定遗传基础。
DOI: 10.3389/fgene.2012.00296
发表时间: 2012
期刊: Frontiers in genetics
影响因子: 3.7
作者: [Sittig,LauraJ, Redei,EvaE]
通讯作者: Redei,EvaE
Mapping Epistatic Modifiers of Human Psychiatric Risk Using Mouse Genetics
Mapping epistatic modifiers of human psychiatric risk using mouse genetics
  • 批准号:
    8829702
  • 项目类别:
  • 资助金额:
    $3.76万
  • 财政年份:
    2014
  • 负责人:
    LAURA J. SITTIG
  • 依托单位:
Mapping epistatic modifiers of human psychiatric risk using mouse genetics
  • 批准号:
    8712849
  • 项目类别:
  • 资助金额:
    $5.58万
  • 财政年份:
    2014
  • 负责人:
    LAURA J. SITTIG
  • 依托单位:
Hormonal Programming and Epigenetic Imprinting in FAE
海外基金