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ChromoSOMe SIGNED

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

Total Cost €

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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.

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

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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