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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.

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

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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