EVOBREED

Evolutionary strategy for plant breeding

 Coordinatore THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE 

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 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 2˙497˙061 €
 EC contributo 2˙497˙061 €
 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-2012-ADG_20120314
 Funding Scheme ERC-AG
 Anno di inizio 2013
 Periodo (anno-mese-giorno) 2013-10-01   -   2018-09-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE

 Organization address address: The Old Schools, Trinity Lane
city: CAMBRIDGE
postcode: CB2 1TN

contact info
Titolo: Ms.
Nome: Renata
Cognome: Schaeffer
Email: send email
Telefono: +44 1223 333543
Fax: +44 1223 332988

UK (CAMBRIDGE) hostInstitution 2˙497˙062.00
2    THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE

 Organization address address: The Old Schools, Trinity Lane
city: CAMBRIDGE
postcode: CB2 1TN

contact info
Titolo: Prof.
Nome: Jerzy
Cognome: Paszkowski
Email: send email
Telefono: 441224000000
Fax: 441223000000

UK (CAMBRIDGE) hostInstitution 2˙497˙062.00

Mappa


 Word cloud

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tes    retrotransposition    experimental    breeding    genomes    selected    arabidopsis    retrotransposons    genetic    lyrata    environmental    thaliana    mechanisms    plant    phenotypic    epigenetic    model    diversity   

 Obiettivo del progetto (Objective)

'Large proportions of eukaryotic genomes consist of transposable elements (TEs), predominantly of retrotransposons. They are generally considered as intra-chromosomal parasites. However, their periodical activity bursts influenced organization of host genomes and contributed to beneficial traits. Remarkably, number of transposon generated phenotypic innovations was subsequently selected by humans during plant domestication and breeding. Therefore, retrotransposons could be also considered as attractive endogenous source of genetic variation. Unfortunately so far there is no experimental/technological means to exploit this potential in a controlled fashion.

Recently my laboratory revealed surprisingly selective epigenetic, environmental and developmental mechanisms controlling retrotransposition in Arabidopsis. Here, I intend to build on this knowledge and establish well controlled retrotransposition system a crop plant to liberate its innate genetic diversity buried in silenced TEs.

To achieve this, I propose a stepwise strategy with the following three objectives:

1. Deeper understanding of molecular mechanisms and environmental cues controlling retrotransposition in Arabidopsis thaliana and use this model plant to develop universal methodology for detection of retrotransposition. 2. Transfer the knowledge and methodologies to non model plant. I propose to use Arabidopsis lyrata as close relative of A. thaliana, however with 50% enlarged genome due to expansion of retrotransposon populations. 3. Using methodologies and experimental conditions developed for A. thaliana and A. lyrata we will apply them to maize where we can also take advantage of genetic resources (mutants in epigenetic regulation) in conjunction with responses to selected abiotic stresses.

If the progress towards above listed objectives was swift, I will initiate collaboration with a corn breeding company to create EVOBREED generated population for evaluation of its phenotypic diversity.'

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