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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.

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

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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