Opendata, web and dolomites

rDNAstress SIGNED

Novel insights into DNA damage and stress responses in the nucleolus: Mechanisms and relevance for genomic (in)stability and cancer

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 rDNAstress project word cloud

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

populations    repetitive    synthesis    modern    live    signalling    tumorigenesis    human    repair    imaging    functionally    technological    world    radiation    models    protein    feasible    battle    editing    contains    elucidation    central    nucleolar    genome    insults    heel    sensor    cancer    replication    genomic    stress    exposed    chemotherapy    achilles    cellular    dna    oncogenes    activated    preliminary    diseases    technologies    sequences    damage    grave    proposes    fuels    age    maintenance    pathologies    diverse    stresses    prevent    receiving    drugs    guard    body    transcribed    techniques    exceptionally    ensuing    combination    cell    syndromes    proteomics    machinery    ddr    neurodegeneration    function    copies    premature    vulnerable    phenomena    gene    functional    nucleolus    genes    innovative    centers    cells    defects    strategies    shared    inspire    unpublished    difficult    instability    hypothesis    integrity    aging    incidence    insights    transcription    ribosome    data    treat    fact    causal    rdna    exogenous    biogenesis    enhanced    endogenous   

Project "rDNAstress" data sheet

The following table provides information about the project.

Coordinator
KRAEFTENS BEKAEMPELSE 

Organization address
address: STRANDBOULEVARDEN 49
city: KOEBENHAVN
postcode: 2100
website: http://www.cancer.dk

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 Denmark [DK]
 Total cost 212˙194 €
 EC max contribution 212˙194 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2017
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2019
 Duration (year-month-day) from 2019-01-01   to  2020-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    KRAEFTENS BEKAEMPELSE DK (KOEBENHAVN) coordinator 212˙194.00

Map

 Project objective

Incidence of grave pathologies including neurodegeneration and cancer increases in today’s aging European populations and new approaches to battle these diseases are required. Shared by these pathologies and premature aging syndromes is the enhanced DNA damage and genomic instability, likely causal phenomena that can be better understood by functional elucidation of the cellular DNA damage response (DDR) machinery and its defects. The central hypothesis of this project is that ‘nucleolar genome’ that contains many copies of rDNA genes, the repetitive and most highly transcribed genomic sequences essential for ribosome biogenesis and protein synthesis, may represent an exceptionally vulnerable ‘Achilles heel’ of our genome whose instability fuels aging and tumorigenesis. This project proposes to approach this problem by a combination of innovative cellular models and techniques including gene editing, proteomics and live cell imaging, to assess rDNA damage and the ensuing genomic instability in human cells exposed to exogenous (radiation, chemotherapy drugs) and endogenous (replication and transcription stress, ribosome biogenesis stress, activated oncogenes) insults and identify and functionally characterize signalling and ‘repair’ factors that guard nucleolar integrity and function. This proposal is timely due to the emerging concept of nucleolus as a sensor of diverse stresses and the fact that technological advances now allow analysis of the difficult-to-assess rDNA genes. The applicant is experienced in the DDR field and modern technologies, the receiving institute is among the world leading centers in DNA damage, cancer and cell stress research fields. These aspects, together with the large body of preliminary unpublished data makes this ambitious project feasible. The results will provide novel insights into genome integrity maintenance and cell stress responses, and may inspire novel strategies to treat or even prevent age-related diseases, especially cancer.

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

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

RipGEESE (2020)

Identifying the ripples of gene regulation evolution in the evolution of gene sequences to determine when animal nervous systems evolved

Read More  

SSHelectPhagy (2019)

Regulation of Selective autophagy by sulfide through persulfidation of protein targets.

Read More  

GrowthDevStability (2020)

Characterization of the developmental mechanisms ensuring a robust symmetrical growth in the bilateral model organism Drosophila melanogaster

Read More