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.

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

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.)

CHES (2020)

Resilience of Coastal Human-Environment Systems

Read More  

TheaTheor (2018)

Theorizing the Production of 'Comedia Nueva': The Process of Play Configuration in Spanish Golden Age Theater

Read More  

MarshFlux (2020)

The effect of future global climate and land-use change on greenhouse gas fluxes and microbial processes in salt marshes

Read More