ASTRIR

Argonaute-associated factors required for translational repression in plant RNA silencing

 Coordinatore EIDGENOESSISCHE TECHNISCHE HOCHSCHULE ZURICH 

 Organization address address: Raemistrasse 101
city: ZUERICH
postcode: 8092

contact info
Titolo: Prof.
Nome: Olivier
Cognome: Voinnet
Email: send email
Telefono: +41 44 633 93 60
Fax: +41 44 632 10 44

 Nazionalità Coordinatore Switzerland [CH]
 Totale costo 177˙601 €
 EC contributo 177˙601 €
 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-2010-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2012
 Periodo (anno-mese-giorno) 2012-03-01   -   2014-03-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    EIDGENOESSISCHE TECHNISCHE HOCHSCHULE ZURICH

 Organization address address: Raemistrasse 101
city: ZUERICH
postcode: 8092

contact info
Titolo: Prof.
Nome: Olivier
Cognome: Voinnet
Email: send email
Telefono: +41 44 633 93 60
Fax: +41 44 632 10 44

CH (ZUERICH) coordinator 177˙601.60

Mappa


 Word cloud

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

risc    transcripts    slice    arabidopsis    class    plant    translational    rnas    sites    silencing    action    host    associate    repression    slicing    regulate    small    ago    mirnas    atago    mrnas    expression    mode    mirna    mad    proteins    uncover    mutants    laboratory    micrornas   

 Obiettivo del progetto (Objective)

'MicroRNAs (miRNAs) are key post-transcriptional regulators of eukaryotic gene expression. In plants, most miRNAs associate with AGO1 as part of RNA-induced-silencing-complexes (RISC) to regulate target mRNAs via perfectly or near-perfecly miRNA-complementarity sites. These sites differ from those found in metazoan miRNA target transcripts, where extensive mis-pairing prevents endonucleolytic cleavage, or ‘slicing’, and favors translational repression as an alternative mode of AGO action. Recently, two classes of miRNA action deficient (mad) mutants have been isolated in Arabidopsis thaliana: class I mutants carry lesions in genes required for slicing, whereas class II mutants are still able to slice but yet, fail to silence miRNA target transcripts at the protein level. Studying many examples of endogenous miRNA/target mRNA interactions in the context of class-II mad mutants, the host laboratory showed that most plant miRNAs may, in fact, concurrently slice and translationally inhibit any given pool of target mRNAs, raising the fundamental question of how slicing is avoided during translational repression? One hypothesis holds that translational repressor proteins specifically associate with AtAGO1 on polysomes and block its slicing activity. The recent purification and preliminary characterization, in the host laboratory, of several possible core components of the AtAGO1 RISC support this idea. Combining biochemical and genetic approaches, I will address (i) how these proteins interact with each other, (ii) how their inactivation/over-expression impacts the mode of action of AtAGO1 and its known functions in the various Arabidopsis silencing pathways, and (iii) how these factors may be exploited to uncover the full suite of small RNAs operating preferentially via translational repression. Parallel investigations in mammalian cell systems will further uncover the extent to which the underlying mechanisms are conserved in metazoans.'

Introduzione (Teaser)

Small RNAs regulate an astonishing number of processes. European research has investigated the action of one prominent class, microRNAs (miRNAs), that play a major role in plant antiviral defence.

Altri progetti dello stesso programma (FP7-PEOPLE)

SEX SEL - VAR (2013)

Sexual selection - How is variation maintained?

Read More  

OZMALNET (2012)

TOWARDS THE ESTABLISHMENT OF A FRAMEWORK IN MALARIA BETWEEN THE AMRN AND EVIMALAR

Read More  

ANGIOBLOCK (2013)

Testing a novel target for anti-angiogenesis therapy in the eye

Read More