GROWTH AND PATTERN

Coordinated Control of Patterning and Growth: Mechanisms of Transcriptional Regulation and Dynamics of Dpp Signaling in Flies

 Coordinatore UNIVERSITAET BASEL 

 Organization address address: Petersplatz 1
city: BASEL
postcode: 4003

contact info
Titolo: Prof.
Nome: Markus
Cognome: Affolter
Email: send email
Telefono: -2672092
Fax: -2365

 Nazionalità Coordinatore Switzerland [CH]
 Totale costo 0 €
 EC contributo 191˙431 €
 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 2009
 Periodo (anno-mese-giorno) 2009-03-01   -   2011-02-28

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITAET BASEL

 Organization address address: Petersplatz 1
city: BASEL
postcode: 4003

contact info
Titolo: Prof.
Nome: Markus
Cognome: Affolter
Email: send email
Telefono: -2672092
Fax: -2365

CH (BASEL) coordinator 191˙431.30

Mappa


 Word cloud

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

activation    tgf    smad    signaling    beta    dpp    dynamics    vivo    proteins   

 Obiettivo del progetto (Objective)

'Animals and their organs become patterned as they grow. One of the most intriguing and challenging questions in developmental biology today is how patterning and growth are coordinated in time and space. Dpp, a member of TGF-β superfamily, with its ability to regulate both processes, serves as a paradigm to answer this question. Our first aim focuses on the logic of transcriptional regulation by Smad proteins, the nuclear effectors of the TGF-β pathways. The Drosophila Smad proteins, Mad and Medea, lead to activation of some target genes while inhibiting others. The putative cofactors required for Dpp-dependent activation have not been identified thus far. Here, I will test the hypothesis that T-box containing proteins, Dorsocross 1, 2, and 3, fulfill this function. In the second part, I aim to monitor Dpp signaling dynamics in vivo. I will fuse Dpp responsive elements to cDNA constructs that encode highly unstable versions of GFP or RFP allowing us to detect small and transient fluctuations in Dpp response. These experiments aim to achieve a detailed spatio-temporal analysis of the dynamics of Dpp signaling in growing tissues. Such in vivo studies will allow putting forward or excluding certain models of how Dpp exerts its multiple functions.'

Altri progetti dello stesso programma (FP7-PEOPLE)

INTERDRUG (2014)

Epigenetic mechanisms underlying inter-individual differences in drug response and hepatic disease

Read More  

NANOLEDS (2011)

A Novel Approach to the Fabrication of Nanoscale Light Emitting Diodes

Read More  

INTERACTION DESIGN (2012)

"De novo design of affinity, specificity, and multispecificity in synthetic protein interaction networks"

Read More