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Transgenerational epigenetic inheritance of longevity

Transgenerational epigenetic inheritance of longevity
长寿的跨代表观遗传
批准号:
9091391
负责人:
ANNE BRUNET
金额:
$78.5万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-09-30 至 2017-09-30

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DESCRIPTION Abstract: The goal of this proposal is to explore the transgenerational epigenetic inheritance of longevity. A fundamental question is whether epigenetic changes that affect lifespan in the parental generation can still impact the lifespan of the subsequent generations even when the factors that led to these changes are no longer present. While some evidence of transgenerational epigenetic inheritance for simple traits exist, very little is known about the transgenerational inheritance of acquired complex traits. Understanding the epigenetic memory of longevity between generations has the potential to revolutionize the current paradigm on the inheritance of complex diseases and will also have a broad impact on our understanding of epigenome reprogramming. We recently made the surprising discovery that mutations in specific regulators of trimethylated lysine 4 on histone H3 (H3K4me3) in parents lead to lifespan extension in descendants for up to three generations, even after the initial mutation is no longer present. This unexpected discovery has led our lab in a new direction. The questions we ask are: what are the mechanisms underlying transgenerational epigenetic inheritance of longevity? Is epigenetic memory of lifespan generalizable to vertebrates? Could environmental factors that affect aging, such as dietary intake, impact subsequent generations even when the environment is back to normal? Could this unconventional mode of inheritance have the evolutionary advantage of 'informing' future generations about the ancestors' environment? We will develop an innovative and exciting framework to address transgenerational inheritance of longevity experimentally. A major goal will be to systematically identify the molecules that are inherited in a transgenerational manner and that mediate this epigenetic memory by combining unbiased genomics, proteomics and metabolomics technologies and single-cell approaches. Another challenge will be to examine the importance of epigenet
期刊论文(10)
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会议论文
DOI: 10.1016/j.molcel.2015.08.004
发表时间: 2015-08
期刊: Molecular cell
影响因子: 16
作者: [Lauren N. Booth;A. Brunet]
通讯作者: Lauren N. Booth;A. Brunet
The impact of common dopamine D2 receptor gene polymorphisms on D2/3 receptor availability: C957T as a key determinant in putamen and ventral striatum.
常见多巴胺 D2 受体基因多态性对 D2/3 受体可用性的影响:C957T 作为壳核和腹侧纹状体的关键决定因素。
DOI: 10.1038/tp.2017.45
发表时间: 2017
期刊: Translational psychiatry
影响因子: 6.8
作者: [Smith,CT, Dang,LC, Buckholtz,JW, Tetreault,AM, Cowan,RL, Kessler,RM, Zald,DH]
通讯作者: Zald,DH
The African Turquoise Killifish Genome Provides Insights into Evolution and Genetic Architecture of Lifespan.
非洲绿松石杀死基因组提供了对生命周期进化和遗传结构的见解。
DOI: 10.1016/j.cell.2015.11.008
发表时间: 2015-12-03
期刊: Cell
影响因子: 64.5
作者: [Valenzano DR, Benayoun BA, Singh PP, Zhang E, Etter PD, Hu CK, Clément-Ziza M, Willemsen D, Cui R, Harel I, Machado BE, Yee MC, Sharp SC, Bustamante CD, Beyer A, Johnson EA, Brunet A]
通讯作者: Brunet A
DOI: 10.1016/j.cell.2015.01.038
发表时间: 2015-02-26
期刊: Cell
影响因子: 64.5
作者: [Harel I, Benayoun BA, Machado B, Singh PP, Hu CK, Pech MF, Valenzano DR, Zhang E, Sharp SC, Artandi SE, Brunet A]
通讯作者: Brunet A
8
    T cells in the aging brain
    • 批准号:
      10424536
    • 项目类别:
    • 资助金额:
      $73.56万
    • 财政年份:
      2021
    • 负责人:
      ANNE BRUNET
    • 依托单位:
    T cells in the aging brain
    • 批准号:
      10184422
    • 项目类别:
    • 资助金额:
      $75.22万
    • 财政年份:
      2021
    • 负责人:
      ANNE BRUNET
    • 依托单位:
    FASEB's Transcription, Chromatin and Epigenetics in Aging Conference
    T cells in the aging brain
    • 批准号:
      10604381
    • 项目类别:
    • 资助金额:
      $72.75万
    • 财政年份:
      2021
    • 负责人:
      ANNE BRUNET
    • 依托单位:
    海外基金