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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.

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

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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