Opendata, web and dolomites

ChromoDrive

Investigating how anaphase chromosomal motion is generated during mitosis and meiosis

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 ChromoDrive project word cloud

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

confound    microsurgery    somatic    microscopy    disrupting    renewed    divide    tools    of    live    spontaneous    eggs    copies    meiosis    fertilisation    physically    equally    optogenetics    mouse    whilst    resolution    function    conclusive    mammalian    anaphase    light    daughter    abortion    diseases    power    techniques    disorders    errors    cancer    implications    reproductive    genome    mechanism    suggested    mature    combination    genetic    mammals    movement    protein    fertilised    instability    inactivate    century    shed    technically    division    proteins    poleward    phases    validate    competent    separated    onset    life    single    mitosis    candidate    hallmark    clinical    cell    organism    fundamental    understand    egg    tissues    germ    underlie    celled    unclear    laser    cells    birth    nature    sperm    types    oocytes    underlying    chromosome    occurs    occurring    mechanisms    biological    defects    obvious    transformed    chromosomes   

Project "ChromoDrive" data sheet

The following table provides information about the project.

Coordinator
INSTITUTO DE BIOLOGIA MOLECULAR E CELULAR-IBMC 

Organization address
address: RUA ALFREDO ALLEN 208
city: PORTO
postcode: 4200 135
website: www.ibmc.up.pt

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 Portugal [PT]
 Project website https://www.i3s.up.pt/research-group
 Total cost 148˙635 €
 EC max contribution 148˙635 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2016
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2017
 Duration (year-month-day) from 2017-07-01   to  2019-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    INSTITUTO DE BIOLOGIA MOLECULAR E CELULAR-IBMC PT (PORTO) coordinator 148˙635.00

Map

 Project objective

Cell division is a process essential for life. There are two types of cell division: meiosis and mitosis. Meiosis is a type of cell division specific to germ cells, allowing the formation of fertilisation-competent sperm and eggs. Mitosis allows a single-celled fertilised egg to develop into a mature organism, and also allows tissues to be renewed. During each cell division, the cell must divide two copies of the genome equally between two daughter cells. Errors that occur during this process in oocytes can lead to spontaneous abortion and birth defects, whilst errors occurring in somatic cells can lead to genetic instability, a hallmark of cancer. It is therefore essential to understand how this fundamental process occurs. The phase of cell division during which the chromosomes are physically separated is called anaphase. Although anaphase has been studied for more than a century, the mechanisms that underlie the poleward movement of chromosomes in mammals are still unclear. Several studies have suggested candidate proteins that may power their movement, but there were no conclusive results due to the technically challenging nature of this research. The main challenge is that one must efficiently inactivate the candidate protein(s) only at the onset of anaphase so as to avoid disrupting the previous phases of cell division, which could confound the results. Methods to rapidly inactivate proteins targets have only recently become available. Here, we propose to use these techniques to study the mechanism(s) underlying poleward chromosome movement during anaphase in both meiosis (mouse oocytes) and mitosis (non-transformed mammalian somatic cells). In both cases, we will validate the results using a combination of loss-of-function and optogenetics tools, high-resolution live-cell microscopy, and laser microsurgery. This work will shed light on a fundamental biological process with obvious clinical implications for diseases such as cancer and reproductive disorders.

 Publications

year authors and title journal last update
List of publications.
2019 Olga Afonso, Colleen M Castellani, Liam P Cheeseman, Jorge G Ferreira, Bernardo Orr, Luisa T Ferreira, James J Chambers, Eurico Morais-de-Sá, Thomas J Maresca, Helder Maiato
Spatiotemporal control of mitotic exit during anaphase by an Aurora B-Cdk1 crosstalk
published pages: , ISSN: 2050-084X, DOI: 10.7554/elife.47646
eLife 8 2019-11-13

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "CHROMODRIVE" 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 "CHROMODRIVE" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.3.2.)

MY MITOCOMPLEX (2021)

Functional relevance of mitochondrial supercomplex assembly in myeloid cells

Read More  

LUNG-BIM (2019)

Induction of B cell immunity in the lung mucosa

Read More  

POLINGO (2018)

The Politics of Legitimacy: Non-partisan global governance and networked INGO power in the global governance of post-war states

Read More