Opendata, web and dolomites

PlasmoCycle SIGNED

DNA dynamics in the unusual cell cycle of the malaria parasite Plasmodium falciparum

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 PlasmoCycle project word cloud

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

schizogony    biology    little    inside    reveal    24hrs    diverging    cells    unprecedented    resistance    investigation    mapping    lifecycle    fibres    changing    infected    labelling    asynchronous    sequences    rounds    checkpoints    despite    gametogenesis    protozoan    synthesis    permit    subject    wealth    plasmodium    gametes    basic    cycle    exposure    nascent    transform    prior    spatio    origin    cycles    resolution    cytokinesis    biological    parasite    erythrocytes    spacing    replication    single    speed    cell    molecule    occurs    model    drugs    drug    extremely    elucidate    dynamics    remarkably    host    generates    gametocyte    rapid    inform    characterisation    virulence    replicates    human    environment    nuclei    male    promises    transmission    dna    transmitting    previously    vital    unusual    first    antimalarial    malaria    contrasting    genome    interventions    extraordinarily    necessitating    10mins    sexual    temporal    replicative    blocking    mosquito    copied    independent   

Project "PlasmoCycle" data sheet

The following table provides information about the project.

Coordinator
THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE 

Organization address
address: TRINITY LANE THE OLD SCHOOLS
city: CAMBRIDGE
postcode: CB2 1TN
website: www.cam.ac.uk

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 United Kingdom [UK]
 Project website https://www.path.cam.ac.uk/directory/catherine-merrick/
 Total cost 1˙998˙696 €
 EC max contribution 1˙998˙696 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2016-COG
 Funding Scheme ERC-COG
 Starting year 2017
 Duration (year-month-day) from 2017-06-01   to  2022-05-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE UK (CAMBRIDGE) coordinator 1˙801˙331.00
2    UNIVERSITY OF KEELE UK (KEELE) participant 197˙364.00

Map

 Project objective

This proposal promises to transform our understanding of the basic biology of the malaria parasite Plasmodium, and of how that biology affects virulence. Remarkably little is known about the Plasmodium cell cycle, despite a wealth of knowledge on the subject in model cells. This project will reveal, with unprecedented resolution, how DNA replication is organised in Plasmodium and how changing conditions in the human host and exposure to antimalarial drugs affect it.

Plasmodium is an early-diverging protozoan with a complex lifecycle & unusual cell-biological features. It replicates in its human host by ‘schizogony’: a single parasite generates many nuclei via independent, asynchronous rounds of genome replication prior to cytokinesis. This occurs over ~24hrs inside infected erythrocytes. However, the genome can also be copied extremely rapidly during the sexual cycle in the malaria-transmitting mosquito. Here 8 male gametes are produced from a single gametocyte in less than 10mins, necessitating extraordinarily rapid DNA synthesis.

This project will first elucidate the spatio-temporal dynamics of DNA replication in these contrasting cell cycles. To do this, I have developed a method for labelling nascent DNA replication, which was not previously possible in Plasmodium. It will permit: a) a detailed characterisation, at the whole-cell level, of the asynchronous genome replication that occurs in schizogony; b) a study of replication origin spacing & DNA synthesis speed at single-molecule resolution on DNA fibres, comparing these parameters in schizogony & gametogenesis; c) mapping sequences with replication origin activity in the Plasmodium genome; d) investigation of cell-cycle checkpoints & replicative responses to the changing environment in the human host and to antimalarial drugs. These are crucial issues for understanding parasite virulence and drug-resistance, and the work will inform vital new research into transmission-blocking interventions for malaria.

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

More projects from the same programme (H2020-EU.1.1.)

CoolNanoDrop (2019)

Self-Emulsification Route to NanoEmulsions by Cooling of Industrially Relevant Compounds

Read More  

QLite (2019)

Quantum Light Enterprise

Read More  

QUAMAP (2019)

Quasiconformal Methods in Analysis and Applications

Read More