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Self-Control SIGNED

Interplay between genetic control and self-organization during embryo morphogenesis

Total Cost €

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EC-Contrib. €

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Partnership

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 Self-Control project word cloud

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

legacies    poorly    accounted    geometric    cellular    explains    occurring    amplifying    tissues    multicellular    perturbations    intertwined    invagination    nature    drosophila    endoderm    contractility    patterns    dynamics    morphogenetic    combining    pulses    description    light    controls    biological    morphogenesis    upstream    curvature    genetic    trigger    physical    regulated    imaging    optogenetic    feedback    conceptual    apical    cells    developmental    embryos    time    capturing    waves    self    model    explore    interactions    effect    local    mechanics    organization    mechano    flows    networks    computational    behaviors    positional    shed    biochemical    asymmetries    emerge    explained    acquire    3d    live    ask    reported    contractile    emergence    flow    unravel    wave    interdisciplinary    contribution    geometry    basal    actomyosin    spatial    mechanical    patterning    molecular    space    newly    parallel    geometrical    chemical    interplay    mechanism    theoretical    cell    variety    understand    tissue    framework    drive    underlying    shape    mediated    coupling   

Project "Self-Control" 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.
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 Coordinator Country France [FR]
 Total cost 2˙862˙571 €
 EC max contribution 2˙862˙571 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2017-ADG
 Funding Scheme ERC-ADG
 Starting year 2018
 Duration (year-month-day) from 2018-11-01   to  2023-10-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS FR (PARIS) coordinator 2˙862˙571.00

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 Project objective

Morphogenesis seeks to understand how information and mechanics emerge from molecular interactions and how they are regulated in space and time. Two parallel legacies are now intertwined: the conceptual framework of developmental patterning that explains how cells acquire positional information during development and control cell behaviors, and the description of biological processes in physical terms. The current framework explains how genetic and biochemical information controls cellular mechanics, in particular contractility mediated by actomyosin networks, and thus cell and tissue shape changes. However, newly reported contractile dynamics, namely pulses, flows and waves, cannot be explained in this framework: they are self-organized in that they depend on local mechano-chemical interactions and feedback that cannot be accounted for by upstream genetic control. This project will explore the interplay between genetic control and self-organization in Drosophila embryos. We will study the emergence of multicellular flow and the mechanism of newly characterized tissue-level trigger wave dynamics associated with endoderm invagination, a poorly studied process. We will ask: 1) how do patterns of apical and basal contractility drive cell dynamics; 2) what is the contribution of geometrical feedback, e.g. tissue curvature, in amplifying the effect of contractile asymmetries; and 3) what is the nature of mechanical feedback and cell spatial coupling underlying trigger wave dynamics in the tissue? We will use an interdisciplinary approach, combining live imaging, capturing the 3D shape of cells/tissues, genetic/optogenetic/mechanical perturbations and theoretical/computational methods to model mechanics and geometry. We expect to unravel how organized multicellular dynamics emerge from genetic, mechanical and geometric “information”, and feedback during morphogenesis. This work will shed new light on a variety of morphogenetic processes occurring during development.

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