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MyeRIBO SIGNED

Deconstructing the Translational Control of Myelination by Specialized Ribosomes

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EC-Contrib. €

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Partnership

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 MyeRIBO project word cloud

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

genetic    lesions    mrnas    capacity    quantitative    shapes    myelination    heterogeneous    environment    generate    mechanisms    nature    selective    profiling    regulation    disease    lipid    axonal    health    techniques    exceptional    machines    passive    sclerosis    insights    ribosome    relies    membrane    cells    instead    marie    propagation    fuel    ionic    translation    regulate    function    pathogenesis    cell    tooth    decades    ribosomal    sheath    functional    components    preclinical    genome    vivo    profound    glial    mechanism    neurons    neuronal    models    transcriptional    proteomics    specialized    neurological    diabetic    neuropathy    enabled    regulatory    myeribo    disorders    cryo    demands    potentials    rates    drives    discover    translational    multiple    myelinating    preferential    synthesis    ribosomes    demyelination    diversity    devastating    notably    proteome    whereas    uncovered    mouse    neural    little    modern    mrna    employ    obtain    implication    em    layer    push    charcot    specialization    invariant    received    mechanistic    viewed    molecular    energetic    injury    boundaries    composition    strategy    myelin    striking    protein    speed    expansion   

Project "MyeRIBO" data sheet

The following table provides information about the project.

Coordinator
ASOCIACION CENTRO DE INVESTIGACION COOPERATIVA EN BIOCIENCIAS 

Organization address
address: PARQUE TECNOLOGICO EDIFICIO 801 A
city: DERIO VIZCAYA
postcode: 48160
website: www.cicbiogune.es

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 Spain [ES]
 Total cost 1˙874˙996 €
 EC max contribution 1˙874˙996 € (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 2020-06-01   to  2025-05-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    ASOCIACION CENTRO DE INVESTIGACION COOPERATIVA EN BIOCIENCIAS ES (DERIO VIZCAYA) coordinator 1˙874˙996.00

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 Project objective

The myelin sheath is essential for neuronal function and health: myelinating glial cells speed up propagation of axonal potentials, fuel the energetic demands and regulate the ionic environment of neurons. Lesions to the myelin sheath thus result in devastating neurological disorders that include multiple sclerosis, diabetic neuropathy and Charcot-Marie-Tooth disease. Myelination involves a striking expansion of the glial cell membrane that relies on an exceptional increase in protein and lipid synthesis rates. Decades of dedicated research has uncovered a complex transcriptional program that drives this process, whereas translational control mechanisms, on the other hand, have received little attention. There is emerging evidence, enabled by modern techniques, that ribosomes, typically viewed as invariant, passive molecular machines, may instead be heterogeneous in composition, with particular ribosomal components having a ‘specialized’ regulatory capacity for preferential translation of specific mRNAs. In MyeRIBO, I propose that translation control by specialized ribosomes is a novel layer of regulation that shapes the proteome of the myelinating glial cell. I will exploit advances in cryo-EM and quantitative proteomics analyses to discover the nature and diversity of ribosomes in myelinating cells, employ genome-wide ribosome profiling to obtain mechanistic insights into selective mRNA translation by heterogeneous ribosomes, and generate genetic mouse models to determine the functional consequences of this specialization for myelination in vivo. Notably, I will study the implication of this mechanism in pathogenesis of injury-induced demyelination and diabetic neuropathy, and evaluate the targeting of specialized ribosomal components as a preclinical strategy. MyeRIBO will push further the boundaries of our current understanding of the molecular control of myelination, which could have a profound impact for understanding neural development and myelin disorders.

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

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