STEMRB

Role of siRNA-mediated DNA methylation in the root stem cell niche

 Coordinatore UNIVERSITEIT UTRECHT 

 Organization address address: Heidelberglaan 8
city: UTRECHT
postcode: 3584 CS

contact info
Titolo: Ms.
Nome: Herminia
Cognome: Erasmo
Email: send email
Telefono: 31-30-2532614
Fax: 31-30-2531645

 Nazionalità Coordinatore Netherlands [NL]
 Totale costo 0 €
 EC contributo 169˙425 €
 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-IEF-2008
 Funding Scheme MC-IEF
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-01-01   -   2011-12-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITEIT UTRECHT

 Organization address address: Heidelberglaan 8
city: UTRECHT
postcode: 3584 CS

contact info
Titolo: Ms.
Nome: Herminia
Cognome: Erasmo
Email: send email
Telefono: 31-30-2532614
Fax: 31-30-2531645

NL (UTRECHT) coordinator 169˙425.40

Mappa


 Word cloud

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

identity    lxcxe    sirna    root    mediated    stem    plant    found    cells    meristem    proteins    animal    retinoblastoma    protein    cell    pathway    rbr    domains    silencing   

 Obiettivo del progetto (Objective)

'Stem cells are undifferentiated cells that can give rise to different cell types in multicellular organisms. Plant and animal stem cells are usually not specified by the same subset of genes, even though the niche organizations are very similar. The Retinoblastoma (Rb) protein and its plant homologue RETINOBLASTOMA-RELATED (RBR) in stem cell identity however constitutes a possible common pathway in both kingdoms (1). We want to further explore possible similarities in stem cell control, so we focused on RBR interactors in order to find conserved mechanisms. RBR shares two main protein-protein interaction domains with its animal homologs; one interacts with the transcription factor E2F and the other with LxCxE containing motif proteins (such as viral proteins and histone deacetylases). Interestingly, we have found that two proteins implicated in siRNA mediated silencing contain LxCxE domains, and both mutants show a root phenotype. Our aim is to characterize the role of siRNA-mediated silencing in the root meristem stem cells, and to identify the role of RBR in this pathway. It has been found that small inhibitory RNAs control the shoot apical meristem and flowering transition as well as root cap cell formation and lateral root formation (2,3). We will try to identify the role that siRNAs have in stem cell identity.'

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