Opendata, web and dolomites

CHROMDOM SIGNED

Chromosomal domain formation, compartmentalization and architecture

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 CHROMDOM project word cloud

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

basis    folding    dna    insulator    genetic    dynamics    compartments    scaffold    fidelity    confined    dimensional    techniques    structural    insulators    mechanism    folded    structures    gene    scarce    action    eukaryotic    found    bulk    reveal    resolve    chiefly    cohesin    genes    inaccessible    loci    coining    hierarchical    otherwise    underlying    clusters    complexes    regulatory    reconstituted    compartment    domains    organizing    proteins    smc    crosslinking    curtains    expand    assay    interactions    bound    form    nested    molecule    technique    maintenance    constricting    genomic    biochemical    previously    conformation    chromosomes    capture    mutual    complexity    distant    demonstrated    interphase    single    structure    chromosome    experiments    molecular    chromosomal    tads    topologically    regulation    revealed    ctcf    organization    details    3c    platform    experimental    scaffolding    hereditary    throughput    accessible    establishment    contact    chromatin    configuration    loops    hierarchically    drive   

Project "CHROMDOM" data sheet

The following table provides information about the project.

Coordinator
LUDWIG-MAXIMILIANS-UNIVERSITAET MUENCHEN 

Organization address
address: GESCHWISTER SCHOLL PLATZ 1
city: MUENCHEN
postcode: 80539
website: www.uni-muenchen.de

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 Germany [DE]
 Total cost 1˙499˙350 €
 EC max contribution 1˙499˙350 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2017-STG
 Funding Scheme ERC-STG
 Starting year 2018
 Duration (year-month-day) from 2018-07-01   to  2023-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    LUDWIG-MAXIMILIANS-UNIVERSITAET MUENCHEN DE (MUENCHEN) coordinator 1˙499˙350.00

Map

 Project objective

The three-dimensional organization of chromosomes is necessary for hereditary fidelity and gene regulation. Recent studies have found that eukaryotic interphase chromosomes are spatially organized in compartments, chiefly topologically associated domains (TADs), in a hierarchical order of nested chromatin loops, coining the term “chromosome folding”. TADs are clusters of genes and regulatory elements that are confined to their genomic compartment by spatially constricting their accessible range of action. The folded structure of chromosomes through long-range loops enables mutual interactions of distant genomic loci that otherwise would not be in contact. While crosslinking-based chromosome conformation capture (3C) techniques have revealed the underlying structure of interphase chromosomes, the molecular mechanism of how chromosome-organizing proteins, such as the insulator CTCF or the structural maintenance of chromosomes (SMC) complex cohesin build the chromosomal scaffold and contribute to genomic organization, is not understood. Due to the complexity of the processes involved, biochemical information on how chromosomal proteins contribute to the establishment of TADs is scarce. I have previously demonstrated that single molecule techniques can be used to study the interactions of single cohesin complexes with DNA, chromatin and DNA-bound proteins and to resolve processes that are inaccessible in bulk biochemical experiments. In this project, I will use and expand the high-throughput single molecule technique of DNA curtains to study the molecular details of how chromosomal scaffolding proteins and genetic insulators form the basis for the three-dimensional folding of chromosomes. My experiments will build a novel experimental platform to study the dynamics of chromosomal configuration and maintenance in a reconstituted single molecule assay and will reveal the molecular details that drive the organization of chromosomes into hierarchically organized structures.

 Publications

year authors and title journal last update
List of publications.
2019 Pilar Gutierrez-Escribano, Matthew D. Newton, Aida Llauró, Jonas Huber, Loredana Tanasie, Joseph Davy, Isabel Aly, Ricardo Aramayo, Alex Montoya, Holger Kramer, Johannes Stigler, David S. Rueda, Luis Aragon
A conserved ATP- and Scc2/4-dependent activity for cohesin in tethering DNA molecules
published pages: eaay6804, ISSN: 2375-2548, DOI: 10.1126/sciadv.aay6804
Science Advances 5/11 2020-03-05

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

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

TRUST (2018)

Truth and Semantics

Read More  

CohoSing (2019)

Cohomology and Singularities

Read More  

SELECTIONDRIVEN (2019)

Gaining insights into human evolution and disease prevention from adaptive natural selection driven by lethal epidemics

Read More