Opendata, web and dolomites

ChromoSOMe SIGNED

Canonical and Non-canonical modes of Chromosome Segregation in Oocyte Meiosis

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 ChromoSOMe project word cloud

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

segregation    single    unichromosomal    vast    principles    mechanisms    kinetochore    silico    defective    canonical    biochemistry    wealth    capacity    analyze    ploidy    specialized    somatic    obstacle    nematode    oogenesis    nematodes    spindle    reproducing    evolution    parthenogenetic    individuals    combining    disciplinary    gametes    fertilization    analyzing    sexually    genomic    centrosomal    regulate    homeostasis    oocyte    live    wp1    components    organisms    reproduction    dissect    modeling    self    division    leads    multiplication    assembly    microscopy    embryos    oocytes    edge    cell    spontaneous    rounds    machinery    replication    relies    haploid    species    reproductive    follow    constraints    drive    chromosomes    poorly    wp2    incorrect    female    abortion    meiosis    mitosis    resolution    molecular    inaccuracy    coupled    carry    cutting    proliferate    genome    diversity    wp3    scenarios    technologies    proteomic    universal    genomes    chromosome    aneuploid    electron    geometry    diploid    divisions    majority    considering    tissues    decisive    meiotic    cells   

Project "ChromoSOMe" data sheet

The following table provides information about the project.

Coordinator
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS 

Organization address
address: RUE MICHEL ANGE 3
city: PARIS
postcode: 75794
website: www.cnrs.fr

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 France [FR]
 Total cost 1˙561˙563 €
 EC max contribution 1˙561˙563 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-COG
 Funding Scheme ERC-COG
 Starting year 2020
 Duration (year-month-day) from 2020-01-01   to  2024-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS FR (PARIS) coordinator 1˙561˙563.00

Map

 Project objective

Cell division is crucial for the development of complex organisms, for the homeostasis of tissues, and for the reproductive capacity of individuals. While most somatic cells are diploid and proliferate through mitosis, multiplication of sexually reproducing species relies on haploid gametes that are generated through a specialized cell division process called meiosis. To achieve this reduction in ploidy, two rounds of chromosome segregation follow a single phase of genome replication. Inaccuracy in this process leads to gametes that carry an incorrect number of chromosomes and to aneuploid embryos after fertilization. In their vast majority, these are non-viable and lead to spontaneous abortion: defective meiotic division is therefore a major obstacle in achieving reproduction. However, the key principles that drive this process are still poorly understood, one main reason being the diversity of the molecular scenarios that have been adopted across evolution to regulate oocyte chromosome segregation. To dissect the key components of oocyte meiotic chromosome segregation, we propose to carry out a multi-disciplinary approach, combining several nematode species with the use of high-resolution live and electron microscopy, cutting edge genomic and proteomic technologies, and biochemistry coupled to in silico modeling. In Work Package 1 (WP1), we will analyze the molecular mechanisms controlling the self-assembly of the chromosome segregation machinery -the meiotic spindle- in the oocyte. WP2 will focus on defining how chromosome segregation is achieved in oocytes with non-canonical kinetochore geometry. WP3 aims at analyzing meiotic divisions in parthenogenetic nematodes with specific meiotic constraints, such as centrosomal oogenesis and unichromosomal genomes. By considering the wealth of mechanisms that can drive chromosome segregation in oocytes, this project will provide decisive steps towards understanding the essential and universal features of female meiosis.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "CHROMOSOME" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email (fabio@fabiodisconzi.com) and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

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

More projects from the same programme (H2020-EU.1.1.)

CURVE-X (2019)

Industrialisation of curved sensors and related imagers

Read More  

RTMFRM (2019)

Room Temperature Magnetic Resonance Force Microscopy

Read More  

CohoSing (2019)

Cohomology and Singularities

Read More