MIRNAEVOL

"MicroRNAs, genomic evolution and the emergence of anatomical complexity."

 Coordinatore UNIVERSITY OF BRISTOL 

 Organization address address: TYNDALL AVENUE SENATE HOUSE
city: BRISTOL
postcode: BS8 1TH

contact info
Titolo: Ms.
Nome: Audrey
Cognome: Michael
Email: send email
Telefono: +44 117 9289000
Fax: +44 117 9250900

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 237˙311 €
 EC contributo 237˙311 €
 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-IOF-2008
 Funding Scheme MC-IOF
 Anno di inizio 2009
 Periodo (anno-mese-giorno) 2009-10-01   -   2012-09-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITY OF BRISTOL

 Organization address address: TYNDALL AVENUE SENATE HOUSE
city: BRISTOL
postcode: BS8 1TH

contact info
Titolo: Ms.
Nome: Audrey
Cognome: Michael
Email: send email
Telefono: +44 117 9289000
Fax: +44 117 9250900

UK (BRISTOL) coordinator 237˙311.95

Mappa

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 Word cloud

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training    junk    micrornas    evolutionary    sponges    class    coding    international    complexity    anatomical    genome    world    fellowship   

 Obiettivo del progetto (Objective)

'The embryological and evolutionary origins of anatomical complexity have been the subject of debate and speculation since the time of the ancients. Large-scale comparative genomic analyses have begun to yield tantalising secrets concerning the mechanisms by which anatomical complexity has emerged. However, this field has recently undergone an epiphany with the realisation that much of the ‘tool-kit’ (i.e. the transcription factors and signalling systems) of more anatomically complex animals such as vertebrates is found in relatively more simple taxa like cnidarians and sponges. Leaving researchers to wonder what accounts for the dramatic increase in anatomical complexity of protostomes and deuterostomes in comparison to sponges. This proposal plans to investigate the evolution and functional constraints of microRNAs, a class of non-coding regulatory elements that lie within a section of the genome originally labelled ‘junk DNA’. However, rather than being ‘junk’ microRNAs have been shown to play important roles in animal development with their misexpression being associated with a variety of medical conditions including, cancer and heart disease. My proposal for an International Outgoing Marie Curie Fellowship aims to provide me with world class training to underpin a world class career researching the fundamental question of how anatomical complexity is coded in the genome, and how that coding has evolved through evolutionary history. This will be realised by gaining skills and techniques lacking in the EU. I outline a programme of research that will act as a vehicle for this training, on which I will be able to make the subsequent steps in realising my aim of establishing my own research laboratory. In the interim, this Fellowship will also foster an international collaboration between the US and the EU and between regional centres within the EU.'

Altri progetti dello stesso programma (FP7-PEOPLE)

GEN ECOL ADAPT (2012)

Adaptation genomics of trophic polymorphism

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TRAHOMGEN (2009)

Reductive evolution of parasite genomes with a focus on the microsporidian Trachipleistophora hominis

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MULTIMOD (2009)

Multiscale Modeling of Chemical and Biochemical Systems

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