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描述(由申请人提供):DNA甲基化模式在发育过程中如何形成-甲基化和去甲基化如何在特定时间靶向特定基因座-尚不清楚。生殖细胞在擦除从上一代遗传的雄性和雌性特异性标记后,根据性腺的性别建立甲基化印记。我们的主要假设是DNA胞嘧啶5-羟甲基化和染色质组成是印记周期的重要组成部分,参与生殖细胞的擦除和建立阶段以及索马的维持阶段。为了证明这一点,我们将分析DNA甲基化,DNA胞嘧啶羟甲基化和染色质的全球和特定的印记基因在生殖细胞和体细胞。为了测试特定的表观遗传修饰剂在印记周期中的作用,我们将在印记周期的擦除,建立和维护阶段对这些功能进行遗传干扰。这些结果将有助于理解DNA甲基化,DNA羟甲基化和染色质标记如何在生殖细胞的表观遗传重塑以及消除,建立和维持基因组印记中合作。在胚胎-胎儿生殖细胞发育过程中,正确的整体表观遗传重塑和印记重置对于下一代和后代的健康至关重要。
英文摘要
DESCRIPTION (provided by applicant): How DNA methylation patterns are shaped during development - how methylation and demethylation are targeted to specific loci at specific times - is not known. Germ cells establish methylation imprints depending on the sex of the gonad after erasing the male and female -specific marks inherited from the previous generation. Our main hypothesis is that DNA cytosine 5-hydroxymethylation and chromatin composition are important components of the imprint cycle, being involved in the erasure and establishment phases in germ cells and in the maintenance phase in the soma. To demonstrate this, we will analyze DNA methylation, DNA cytosine hydroxymethylation and chromatin globally and at specific imprinted genes in germ cells and somatic cells. To test the role of specific epigenetic modifiers in the cycle of imprinting, we will genetically perturb these functions during the erasure, establishment and maintenance phases of the imprinting cycle. These results collectively will help understand how DNA methylation, DNA hydroxymethylation and chromatin marks collaborate in the epigenetic remodeling of germ cells and in erasing, establishing and maintaining genomic imprints. Correct global epigenetic remodeling and imprint reseting during embryonic-fetal germ cell development is essential for the health of the next generation and for future generations.
期刊论文(29)
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会议论文
DOI: 10.1016/j.ygeno.2014.08.015
发表时间: 2014-11
期刊: GENOMICS
影响因子: 4.4
作者: [Hahn, Maria A., Szabo, Piroska E., Pfeifer, Gerd P.]
通讯作者: Pfeifer, Gerd P.
Allele-specific H3K79 Di- versus trimethylation distinguishes opposite parental alleles at imprinted regions.
等位基因特异性 H3K79 二甲基化与三甲基化可区分印记区域的相反亲本等位基因。
DOI: 10.1128/mcb.01537-09
发表时间: 2010
期刊: Molecular and cellular biology
影响因子: 5.3
作者: [Singh,Purnima, Han,Li, Rivas,GuillermoE, Lee,Dong-Hoon, Nicholson,ThomasB, Larson,GarrettP, Chen,Taiping, Szabo,PiroskaE]
通讯作者: Szabo,PiroskaE
DOI: 10.1126/sciadv.adi2050
发表时间: 2023-09-08
期刊: Science advances
影响因子: 13.6
作者: [Liao J, Song S, Gusscott S, Fu Z, VanderKolk I, Busscher BM, Lau KH, Brind'Amour J, Szabó PE]
通讯作者: Szabó PE
DOI: 10.1016/j.celrep.2021.108729
发表时间: 2021-02-09
期刊: Cell reports
影响因子: 8.8
作者: [Liao J, Zeng TB, Pierce N, Tran DA, Singh P, Mann JR, Szabó PE]
通讯作者: Szabó PE
共 15 条
    A NOVEL PROCESS SAFEGUARDS GENOME INTEGRITY IN THE MAMMALIAN GERM LINE
    • 批准号:
      10445720
    • 项目类别:
    • 资助金额:
      $51.9万
    • 财政年份:
      2022
    • 负责人:
      Piroska Edit Szabó
    • 依托单位:
    A Novel Process Safeguards Genome Integrity In The Mammalian Germ Line-Administrative Supplement to Support Undergraduate Summer Research Experiences
    • 批准号:
      10807301
    • 项目类别:
    • 资助金额:
      $1.24万
    • 财政年份:
      2022
    • 负责人:
      Piroska Edit Szabó
    • 依托单位:
    A NOVEL PROCESS SAFEGUARDS GENOME INTEGRITY IN THE MAMMALIAN GERM LINE
    • 批准号:
      10650391
    • 项目类别:
    • 资助金额:
      $51.9万
    • 财政年份:
      2022
    • 负责人:
      Piroska Edit Szabó
    • 依托单位:
    Epigenetic effects if endocrine disruptors in fetal germ cells
    海外基金