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rDNAstress SIGNED

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

Total Cost €

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EC-Contrib. €

0

Partnership

0

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 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.

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combination    live    machinery    chemotherapy    shared    heel    copies    damage    proteomics    functionally    unpublished    syndromes    drugs    achilles    modern    difficult    fuels    guard    grave    innovative    proposes    integrity    receiving    sensor    contains  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

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

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 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.

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