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PIOMES

Pbx proteins as pioneer factors promoting signal specificity in mesodermal differentiation

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 PIOMES project word cloud

Explore the words cloud of the PIOMES project. It provides you a very rough idea of what is the project "PIOMES" about.

tf    mps    ways    insights    landscape    hescs    central    blood    competence    transcriptional    cellular    esc    opening    date    immunoprecipitation    lineage    pioneer    converting    treating    degenerative    acquisition    cell    routinely    purpose    stem    dystrophies    had    expressed    primitive    critical    vitro    arise    transcription    somitic    shape    mesoderm    differentiation    proteins    analogous    recruitment    signalling    region    muscle    pbx    specification    danstem    strategies    specified    bone    regenerative    mastered    embryo    mouse    specify    regulation    efficiency    limited    conceive    strength    assays    muscular    types    rational    skeletal    cells    question    embryos    murine    mesodermal    embryonic    postdoctoral    organisms    binding    progenitors    dynamics    human    muscles    life    training    wnt    chromatin    tfs    pools    tools    genetic    fate    combat    ultimately    healthy    diseases    extensively    epiblast    streak    combines    promotes   

Project "PIOMES" data sheet

The following table provides information about the project.

Coordinator
KOBENHAVNS UNIVERSITET 

Organization address
address: NORREGADE 10
city: KOBENHAVN
postcode: 1165
website: www.ku.dk

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Denmark [DK]
 Project website http://danstem.ku.dk/research1/ferretti-lab/
 Total cost 200˙194 €
 EC max contribution 200˙194 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2014
 Funding Scheme MSCA-IF-EF-RI
 Starting year 2015
 Duration (year-month-day) from 2015-05-01   to  2017-04-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    KOBENHAVNS UNIVERSITET DK (KOBENHAVN) coordinator 200˙194.00

Map

 Project objective

The development of healthy organisms requires the formation of different cellular systems, such as a blood, bone and muscle. All these different cell types arise during embryonic life from specific pools of mesodermal progenitors (MPs). A central question is how distinct MPs are specified and ultimately why different cells respond to signalling pathways in different ways? Critical insights here are directly relevant to conceive strategies for increasing the efficiency of mesodermal differentiation aimed for treating muscular degenerative diseases. To date, in vitro, somitic mesoderm differentiation for regenerative purpose has had limited success. Wnt signalling promotes Embryonic Stem Cell (ESC) differentiation of all the MPs, including skeletal muscles. The activity of specific pioneer transcription factors (TFs) may be the key for converting Wnt signalling pathways into a specific transcriptional program. Pioneer TFs shape the chromatin landscape by opening the chromatin and allowing the recruitment of lineage specific TFs, and thus ultimately control the TF binding dynamics and the acquisition of a specific cell fate. Pbx proteins are pioneer TFs, which are specifically expressed in the primitive streak, the region of the embryo that will produce all mesoderm, and are critical for promoting mesodermal specification. Here, I will establish how Pbx proteins specify MPs and determine the competence of early mesoderm to respond to Wnt signalling. To this end, I will use mouse embryos and murine epiblast stem cells, which are analogous to human ESC (hESCs). My approach combines the strength of an in vitro ESC differentiation method, routinely used at DanStem, with chromatin immunoprecipitation and transcriptional regulation assays, which I have extensively mastered during my postdoctoral training. I expect that my findings will provide novel tools for rational design of strategies to combat genetic and degenerative muscular diseases, such as muscular dystrophies.

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The information about "PIOMES" are provided by the European Opendata Portal: CORDIS opendata.

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