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DyNAmecs SIGNED

Early embryonic events, life-long consequences: DNA methylation dynamics in mammalian development

Total Cost €

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EC-Contrib. €

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Partnership

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 DyNAmecs project word cloud

Explore the words cloud of the DyNAmecs project. It provides you a very rough idea of what is the project "DyNAmecs" about.

strive    mark    repression    gain    gene    insights    division    window    phenotype    mouse    ing    previously    epigenetic    proteomics    coding    ascertain    silencing    employ    erased    functions    clear    protein    zdbf2    faithfully    cell    repercussions    largely    undergoes    first    genome    once    novo    commitment    pluripotent    methylation    dramatic    human    mice    lifelong    combinatorial    undergo    canonical    repetitive    utilize    embryogenesis    latent    fertilization    mammalian    immediately    genomics    embryo    lineage    reprogramming    occurs    genes    reshaping    primed    gametic    vivo    exemplified    minority    activation    life    ripple    polycomb    silent    effect    plan    group    antagonism    zygote    wave    events    proteins    model    patterns    programmed    ultimately    genetics    transitions    precision    exhibit    modification    locus    mechanisms    profound    epigenome    genomes    editing    recapitulates    fails    cells    week    deposited    embryonic    dna    de    paradigm    stays    tools    regulation   

Project "DyNAmecs" data sheet

The following table provides information about the project.

Coordinator
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS 

Organization address
address: RUE MICHEL ANGE 3
city: PARIS
postcode: 75794
website: www.cnrs.fr

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country France [FR]
 Total cost 1˙495˙480 €
 EC max contribution 1˙495˙480 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2019-STG
 Funding Scheme ERC-STG
 Starting year 2020
 Duration (year-month-day) from 2020-01-01   to  2024-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS FR (PARIS) coordinator 1˙495˙480.00

Map

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 Project objective

Immediately after fertilization, mammalian genomes undergo a dramatic reshaping of the epigenome as the embryo transitions from the zygote into the pluripotent cells primed for lineage commitment. This is best exemplified by DNA methylation reprogramming, as the gametic patterns are largely erased, and the embryonic genome undergoes a wave of de novo DNA methylation. Moreover, once DNA methylation patterns are established, mechanisms faithfully maintain the mark across cell division. Thus, there is latent potential for DNA methylation deposited in the early embryo to exhibit a lifelong effect. DNA methylation is a modification that is typically associated with gene repression at repetitive elements and at a minority of protein coding genes. I previously described the regulation of the Zdbf2 gene in mice, which is programmed during the de novo DNA methylation program. Challenging the paradigm, in this case DNA methylation is required for activation of a gene via antagonism of the polycomb-group of silencing proteins. If the DNA methylation fails to occur, the gene stays silent throughout life, resulting in a reduced growth phenotype. For my proposed research I will utilize both a cell-based system that recapitulates these early embryonic events as well as an in vivo mouse model to investigate the extent and mechanisms of non-canonical DNA methylation functions. I plan to use a combinatorial approach of genomics, genetics, and proteomics in order to ascertain novel insights into DNA methylation-based regulation. Furthermore, I plan to employ precision epigenome editing tools to address the locus-specific impact of DNA methylation. Ultimately, I strive to gain a clear understanding of the profound epigenetic consequences of DNA methylation on this window of development, which occurs in the first week of mouse embryogenesis, and the second of human, but the repercussions of which can ripple throughout life.

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