GTOXOME

The impact of genotoxic stress on the mRNA-interactome and RNA-regulons

 Coordinatore EUROPEAN MOLECULAR BIOLOGY LABORATORY 

 Organization address address: Meyerhofstrasse 1
city: HEIDELBERG
postcode: 69117

contact info
Titolo: Ms.
Nome: Jillian
Cognome: Rowe
Email: send email
Telefono: 4962210000000
Fax: +49 6221 3878575

 Nazionalità Coordinatore Germany [DE]
 Totale costo 161˙968 €
 EC contributo 161˙968 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2012-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2014
 Periodo (anno-mese-giorno) 2014-01-01   -   2015-12-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    EUROPEAN MOLECULAR BIOLOGY LABORATORY

 Organization address address: Meyerhofstrasse 1
city: HEIDELBERG
postcode: 69117

contact info
Titolo: Ms.
Nome: Jillian
Cognome: Rowe
Email: send email
Telefono: 4962210000000
Fax: +49 6221 3878575

DE (HEIDELBERG) coordinator 161˙968.80

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

stress    rbps    related    dna    responses    cell    damage    cells    rna    proteins    functionally    interactome    mrna    rnas    binding    rbp    regulons    death    genotoxic   

 Obiettivo del progetto (Objective)

'RNA-binding proteins (RBP) play critical roles in stress responses like DNA-damage through interactions with elements in functionally related RNAs, termed regulons. One of the most cytotoxic forms of DNA-damage are DNA double strand breaks (DSB), that can lead to mutagenic events and when improperly repaired to cell death. This proposed project focuses on the dynamics of the global RBP network (mRNA-interactome) and RNA-regulons of mouse fibroblasts (NIH-3T3) cells in response to genotoxic stress. The “RNA-regulon” model implies that RBPs control functionally related mRNAs via cis-regulatory elements in these RNAs. Using mRNA-interactome capture and high-resolution quantitative proteomics, I will comprehensively identify mRNA-binding proteins involved in immediate DNA-repair and cell death responses to genotoxic stress. By employing deep sequencing and crosslink immunoprecipitation approaches, I will highlight the controlled RNA-networks and their influence on cell survival. Taken together, this project aims to address key questions of the role for RBPs in the DNA-damage response at different stages and the identification of their RNA-regulons. Furthermore, it opens new perspectives in posttranscriptional regulation after the cells exposure to genotoxic stress. The innovative nature of this interdisciplinary project involves European collaborators, which creates excellent inter-European-networking. The development of a novel research area will showcase the cutting-edge research performed in the ERA thus directly contribute to the European Work Programme by enhancing the attractiveness of Europe for third country and European top-scientists.'

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