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CELLONGATE SIGNED

Unraveling the molecular network that drives cell growth in plants

Total Cost €

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EC-Contrib. €

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Partnership

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 CELLONGATE project word cloud

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

physiology    gravity    sculpture    regulation    consequently    similarly    methodology    roots    effect    chart    onset    migrate    differential    protein    chip    despite    genes    organs    window    types    gradients    acquisition    arabidopsis    mechanism    wall    cellular    skeleton    dynamic    networks    size    steer    turgor    discovery    temporal    optimized    organ    setup    auxin    move    cells    strict    phytohormone    steering    elongation    developmental    light    molecular    microfluidic    vector    absence    unravel    resolution    transcriptome    occurs    am    thaliana    hydrostatic    immobility    physiological    precise    live    strikingly    discover    individual    regulator    equipped    plants    movements    balance    unknown    microscopy    nutrient    optimize    cell    pressurized    tip    correlating    consists    bodies    differ    strength    lab    almost    division    parallel    manipulation    imaging    epicenter    depends    internal    platform    root    central    combine    exemplified    plant    orient    encased    gene    migration    pressure    spatio    though    profiles    map    mechanisms    animals    total    massive    termination    elusive    orientation   

Project "CELLONGATE" data sheet

The following table provides information about the project.

Coordinator
UNIVERZITA KARLOVA 

Organization address
address: OVOCNY TRH 560/5
city: PRAHA 1
postcode: 116 36
website: www.cuni.cz

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 Czech Republic [CZ]
 Total cost 1˙498˙750 €
 EC max contribution 1˙498˙750 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-STG
 Funding Scheme ERC-STG
 Starting year 2019
 Duration (year-month-day) from 2019-01-01   to  2023-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERZITA KARLOVA CZ (PRAHA 1) coordinator 1˙498˙750.00

Map

 Project objective

Plants differ strikingly from animals by the almost total absence of cell migration in their development. Plants build their bodies using a hydrostatic skeleton that consists of pressurized cells encased by a cell wall. Consequently, plant cells cannot migrate and must sculpture their bodies by orientation of cell division and precise regulation of cell growth. Cell growth depends on the balance between internal cell pressure – turgor, and strength of the cell wall. Cell growth is under a strict developmental control, which is exemplified in the Arabidopsis thaliana root tip, where massive cell elongation occurs in a defined spatio-temporal developmental window. Despite the immobility of their cells, plant organs move to optimize light and nutrient acquisition and to orient their bodies along the gravity vector. These movements depend on differential regulation of cell elongation across the organ, and on response to the phytohormone auxin. Even though the control of cell growth is in the epicenter of plant development, protein networks steering the developmental growth onset, coordination and termination remain elusive. Similarly, although auxin is the central regulator of growth, the molecular mechanism of its effect on root growth is unknown. In this project, I will establish a unique microscopy setup for high spatio-temporal resolution live-cell imaging equipped with a microfluidic lab-on-chip platform optimized for growing roots, to enable analysis and manipulation of root growth physiology. I will use developmental gradients in the root to discover genes that steer cellular growth, by correlating transcriptome profiles of individual cell types with the cell size. In parallel, I will exploit the auxin effect on root to unravel molecular mechanisms that control cell elongation. Finally, I am going to combine the live-cell imaging methodology with the gene discovery approaches to chart a dynamic spatio-temporal physiological map of a growing Arabidopsis root.

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The information about "CELLONGATE" are provided by the European Opendata Portal: CORDIS opendata.

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