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4D-GenEx SIGNED

Spatio-temporal Organization and Expression of the Genome

Total Cost €

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EC-Contrib. €

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Partnership

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 4D-GenEx project word cloud

Explore the words cloud of the 4D-GenEx project. It provides you a very rough idea of what is the project "4D-GenEx" about.

genes    hormone    live    signal    experimental    cellular    molecule    impairing    tracking    genome    cutting    single    biology    probing    investigates    modeling    perturbations    noise    functional    coupling    hypothesis    validate    mechanisms    responding    pp7    spatio    domain    space    competition    positions    supercoiling    indicates    tools    hi    enhancers    regulation    color    compartments    physics    preferred    patterns    cluster    innovative    organization    combines    theory    dimensions    statistical    4d    conformational    extract    individual    relation    locus    co    linear    analytical    gene    shared    acting    time    relationship    expression    transcriptional    normal    coordinate    expertise    lack    temporal    pathological    imaging    shape    responsive    experiment    underlying    dynamics    stochastic    local    relates    certain    understand    physical    coordinated    uncover    regulated    organizing    subnuclear    edge    interface    recycling    transcription    critically    chromosomes    signatures    visualize    ms2    appropriate    rna    science    interpreting    fish    first    communicate    labeling    dual    data    microenvironment    building    suggest    pairs    computer    motion    nucleus   

Project "4D-GenEx" 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˙499˙750 €
 EC max contribution 1˙499˙750 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2017-STG
 Funding Scheme ERC-STG
 Starting year 2018
 Duration (year-month-day) from 2018-04-01   to  2023-03-31

 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˙499˙750.00

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 Project objective

This project investigates the two-way relationship between spatio-temporal genome organization and coordinated gene regulation, through an approach at the interface between physics, computer science and biology.

In the nucleus, preferred positions are observed from chromosomes to single genes, in relation to normal and pathological cellular states. Evidence indicates a complex spatio-temporal coupling between co-regulated genes: e.g. certain genes cluster spatially when responding to similar factors and transcriptional noise patterns suggest domain-wide mechanisms. Yet, no individual experiment allows probing transcriptional coordination in 4 dimensions (FISH, live locus tracking, Hi-C...). Interpreting such data also critically requires theory (stochastic processes, statistical physics…). A lack of appropriate experimental/analytical approaches is impairing our understanding of the 4D genome.

Our proposal combines cutting-edge single-molecule imaging, signal-theory data analysis and physical modeling to study how genes coordinate in space and time in a single nucleus. Our objectives are to understand (a) competition/recycling of shared resources between genes within subnuclear compartments, (b) how enhancers communicate with genes domain-wide, and (c) the role of local conformational dynamics and supercoiling in gene co-regulation. Our organizing hypothesis is that, by acting on their microenvironment, genes shape their co-expression with other genes.

Building upon my expertise, we will use dual-color MS2/PP7 RNA labeling to visualize for the first time transcription and motion of pairs of hormone-responsive genes in real time. With our innovative signal analysis tools, we will extract spatio-temporal signatures of underlying processes, which we will investigate with stochastic modeling and validate through experimental perturbations. We expect to uncover how the functional organization of the linear genome relates to its physical properties and dynamics in 4D.

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The information about "4D-GENEX" are provided by the European Opendata Portal: CORDIS opendata.

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