Opendata, web and dolomites

SynarchiC SIGNED

Investigating the functional architecture of microbial genomes with synthetic approaches

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 SynarchiC project word cloud

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

molecules    appeal    actively    functional    networks    limited    intermingled    players    environment    sc    broadly    insights    engineering    duplicated    metabolic    consists    mitosis    microbial    structural    limiting    regulates    chromatids    dynamic    intertwined    functionally    bacteria    innovative    track    organization    layers    infectious    uncovered    host    interplay    redirects    folding    characterization    phylum    conserved    stressful    synarchic    discriminate    entire    unable    reverse    cycle    yeast    folded    difficult    metabolism    genomes    conformation    contacts    patterns    segregation    3d    scientists    maintenance    assortment    replication    smc    topological    capture    interacts    multiple    pathogen    ing    combined    proteins    eukaryotic    perspective    prokaryotic    clade    structures    scs    ranging    chromosomes    gene    synthetic    evolutionary    fundamental    hosts    derivatives    technologies    sister    chromosome    disambiguating    cell    genome    molecular    involve    individualization    expression   

Project "SynarchiC" data sheet

The following table provides information about the project.

Coordinator
INSTITUT PASTEUR 

Organization address
address: RUE DU DOCTEUR ROUX 25-28
city: PARIS CEDEX 15
postcode: 75724
website: http://www.pasteur.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˙995˙557 €
 EC max contribution 1˙995˙557 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2017-COG
 Funding Scheme ERC-COG
 Starting year 2018
 Duration (year-month-day) from 2018-04-01   to  2023-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    INSTITUT PASTEUR FR (PARIS CEDEX 15) coordinator 1˙995˙557.00

Map

 Project objective

The folding of eukaryotic and prokaryotic chromosomes consists of an assortment of intertwined structural features. The resulting complex networks of contacts is highly dynamic and interacts functionally with, or regulates metabolic processes ranging from gene expression to chromosome segregation. Some higher order structures involve evolutionary conserved molecular players, such as structural maintenance of chromosomes (SMC) proteins, while others depend on phylum specific proteins. The functional organization of yeast and bacteria chromosomes are actively investigated, with multiple folded structures uncovered in recent years. However, disambiguating the intermingled structures is a difficult task, limiting their functional characterization. In addition, current technologies are limited and are unable to track the genome-wide folding of duplicated sister chromatids (SC) molecules, limiting the study of genome folding during replication and mitosis.

The overall aim of the SynarchiC project is to characterize, through innovative derivatives of the chromosome conformation capture technology combined with synthetic chromosomes, the folding patterns of microbial genomes during the entire cell cycle, including those of SCs. By reverse engineering chromosomes in bacteria and yeast, we will discriminate the different layers of topological structures and their associated molecular players. We will then investigate how these 3D structures affect SC folding, individualization, and segregation. Finally, we will investigate the interplay between a pathogen and its hosts during an infectious process. How the bacteria redirects its host chromosome metabolism in stressful environment will be addressed from the perspective of genome organization and segregation. Technologies and results from SynarchiC will provide fundamental insights on the cell cycle, and should appeal broadly to scientists working on various aspects genome functional organization in any clade.

 Publications

year authors and title journal last update
List of publications.
2018 Héloïse Muller, Vittore F Scolari, Nicolas Agier, Aurèle Piazza, Agnès Thierry, Guillaume Mercy, Stéphane Descorps‐Declere, Luciana Lazar‐Stefanita, Olivier Espeli, Bertrand Llorente, Gilles Fischer, Julien Mozziconacci, Romain Koszul
Characterizing meiotic chromosomes\' structure and pairing using a designer sequence optimized for Hi‐C
published pages: , ISSN: 1744-4292, DOI: 10.15252/msb.20188293
Molecular Systems Biology 14/7 2019-12-17

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

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

ERC VP CSA (2018)

Support to the Vice-Presidents of the ERC Scientific Council 2018

Read More  

CellProbe (2019)

CellProbe: Microfluidic probe for simultaneous tagging and extraction of single cells

Read More  

CELPRED (2020)

Circuit elements of the cortical circuit for predictive processing

Read More