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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.

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

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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