MIRLIFE

Molecular Characterization of the microRNA Life-Cycle

 Coordinatore INSTITUT FUER MOLEKULARE BIOTECHNOLOGIE GMBH 

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 Nazionalità Coordinatore Austria [AT]
 Totale costo 1˙499˙631 €
 EC contributo 1˙499˙631 €
 Programma FP7-IDEAS-ERC
Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call ERC-2013-StG
 Funding Scheme ERC-SG
 Anno di inizio 2014
 Periodo (anno-mese-giorno) 2014-02-01   -   2019-01-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    INSTITUT FUER MOLEKULARE BIOTECHNOLOGIE GMBH

 Organization address address: Dr Bohrgasse 3
city: VIENNA
postcode: 1030

contact info
Titolo: Dr.
Nome: Stefan Ludwig
Cognome: Ameres
Email: send email
Telefono: +43 1 79044 4740
Fax: +43 1 79044 110

AT (VIENNA) hostInstitution 1˙499˙631.00
2    INSTITUT FUER MOLEKULARE BIOTECHNOLOGIE GMBH

 Organization address address: Dr Bohrgasse 3
city: VIENNA
postcode: 1030

contact info
Titolo: Ms.
Nome: Tanja
Cognome: Winkler
Email: send email
Telefono: +43 1 79044 4410
Fax: +43 1 79871 53

AT (VIENNA) hostInstitution 1˙499˙631.00

Mappa


 Word cloud

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

determine    micrornas    cell    mirna    function    pathways    microrna    gene    flies    half    protein    therapeutic    enormous    coding    silencing    expression    small    vivo    tools    rna    biochemical    mammals    mechanisms    human    molecular    decay    biological    regulate   

 Obiettivo del progetto (Objective)

'Small silencing RNAs regulate gene expression in nearly all eukaryotes and have enormous biotechnological and therapeutic potential. MicroRNAs belong to the larges family of trans-acting gene regulatory molecules in multicellular organisms. In flies and mammals, they control more than half of the protein-coding transcriptome, and act as key regulators of organismal development, physiology, and disease. Here, we propose to study the molecular mechanisms that regulate microRNA homeostasis. We aim to understand how distinct small RNA profiles are established and maintained to coordinate the expression of more than half of all protein coding genes in flies and mammals. Our studies will provide insight into the processes that regulate the function of miRNAs, determine possible causes for aberrant miRNA levels, that have been associated with human diseases, and provide guidelines how to efficiently inhibit miRNA function for analytical and therapeutic purposes. We aim to identify and characterize the molecular determinants of microRNA stability, to dissect the pathways that promote the sequence-specific degradation of microRNAs, and to understand the biological consequences and therapeutic potential of small RNA decay. We will develop novel tools to obtain a view on the intracellular dynamics of RNA silencing pathways, in order to determine the molecular features associated with small RNA biogenesis and decay. Because of its genetic and biochemical tools, we will use Drosophila melanogaster as a model organism. We will employ a combination of bioinformatics, cell-free biochemical experiments, cell culture methods, and in vivo genetics. What we learn in flies we will test in vitro in mammalian cell extracts, in cultured human cell lines and in vivo in mice to identify where these processes are conserved and where they diverge. Overall, our goal is to determine fundamental biological mechanisms of RNA silencing, a phenomenon with enormous biological and biomedical impact.'

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