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ChromoSOMe SIGNED

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

Total Cost €

0

EC-Contrib. €

0

Partnership

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 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.

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

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

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 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.

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

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