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ACE-OF-SPACE SIGNED

Analysis, control, and engineering of spatiotemporal pattern formation

Total Cost €

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EC-Contrib. €

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Partnership

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 ACE-OF-SPACE project word cloud

Explore the words cloud of the ACE-OF-SPACE project. It provides you a very rough idea of what is the project "ACE-OF-SPACE" about.

talk    quantitative    orchestrate    stability    precursors    analyze    tissues    begun    sufficient    tgf    first    arise    signal    allocation    independent    symmetry    gain    cell    initially    optogenetics    axis    plan    body    superfamily    opposing    secondary    form    asymmetric    mysterious    colonies    unclear    mammalian    biophysical    insights    temporally    developmental    organizing    biology    experimentally    absence    vertebrate    theoretical    bmp    patterned    organ    mechanisms    small    interact    suggest    minimal    patterns    population    embryos    maternal    engineering    embryonic    modeling    homogeneous    patterning    self    strategies    sources    members    thought    adult    signals    previously    mathematical    zebrafish    organize    molecules    cross    systems    tissue    differentiate    questions    diffusion    unknown    combination    central    identical    risk    engineer    pattern    understand    imaging    mechanism    bacterial    cells    underlying    opens    time    mediated    regulated    mouse    prior    indicates    demonstrated    signaling    embryogenesis    synthetic    stem    beta    reaction    break    asymmetries    extra    space    axes    nodal   

Project "ACE-OF-SPACE" data sheet

The following table provides information about the project.

Coordinator
MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV 

Organization address
address: HOFGARTENSTRASSE 8
city: MUENCHEN
postcode: 80539
website: n.a.

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 Germany [DE]
 Total cost 1˙997˙750 €
 EC max contribution 1˙997˙750 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2019-COG
 Funding Scheme ERC-COG
 Starting year 2020
 Duration (year-month-day) from 2020-07-01   to  2025-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV DE (MUENCHEN) coordinator 1˙997˙750.00

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 Project objective

A central problem in developmental biology is to understand how tissues are patterned in time and space - how do identical cells differentiate to form the adult body plan? Patterns often arise from prior asymmetries in developing embryos, but there is also increasing evidence for self-organizing mechanisms that can break the symmetry of an initially homogeneous cell population. These patterning processes are mediated by a small number of signaling molecules, including the TGF-β superfamily members BMP and Nodal. While we have begun to analyze how biophysical properties such as signal diffusion and stability contribute to axis formation and tissue allocation during vertebrate embryogenesis, three key questions remain. First, how does signaling cross-talk control robust patterning in developing tissues? Opposing sources of Nodal and BMP are sufficient to produce secondary zebrafish axes, but it is unclear how the signals interact to orchestrate this mysterious process. Second, how do signaling systems self-organize to pattern tissues in the absence of prior asymmetries? Recent evidence indicates that axis formation in mammalian embryos is independent of maternal and extra-embryonic tissues, but the mechanism underlying this self-organized patterning is unknown. Third, what are the minimal requirements to engineer synthetic self-organizing systems? Our theoretical analyses suggest that self-organizing reaction-diffusion systems are more common and robust than previously thought, but this has so far not been experimentally demonstrated. We will address these questions in zebrafish embryos, mouse embryonic stem cells, and bacterial colonies using a combination of quantitative imaging, optogenetics, mathematical modeling, and synthetic biology. In addition to providing insights into signaling and development, this high-risk/high-gain approach opens exciting new strategies for tissue engineering by providing asymmetric or temporally regulated signaling in organ precursors.

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The information about "ACE-OF-SPACE" are provided by the European Opendata Portal: CORDIS opendata.

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