NONCODEVOL

"Evolutionary genomics of long, non-coding RNAs"

 Coordinatore FUNDACIO CENTRE DE REGULACIO GENOMICA 

Spiacenti, non ci sono informazioni su questo coordinatore. Contattare Fabio per maggiori infomrazioni, grazie.

 Nazionalità Coordinatore Spain [ES]
 Totale costo 1˙302˙113 €
 EC contributo 1˙302˙113 €
 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-StG_20111109
 Funding Scheme ERC-SG
 Anno di inizio 2013
 Periodo (anno-mese-giorno) 2013-01-01   -   2017-12-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    FUNDACIO CENTRE DE REGULACIO GENOMICA

 Organization address address: CARRER DOCTOR AIGUADER 88
city: BARCELONA
postcode: 8003

contact info
Titolo: Dr.
Nome: Juan Antonio
Cognome: Gabaldón Estevan
Email: send email
Telefono: 34933160281

ES (BARCELONA) hostInstitution 1˙302˙113.00
2    FUNDACIO CENTRE DE REGULACIO GENOMICA

 Organization address address: CARRER DOCTOR AIGUADER 88
city: BARCELONA
postcode: 8003

contact info
Titolo: Ms.
Nome: Olga
Cognome: Juderías Gil
Email: send email
Telefono: +34 933160298

ES (BARCELONA) hostInstitution 1˙302˙113.00

Mappa


 Word cloud

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despite    lncrnas    genome    recent    genomes    proper    molecules    genes    eukaryotic    mechanisms    sequencing    evolutionary    coding    lack    evolution    protein    techniques   

 Obiettivo del progetto (Objective)

'Recent genomics analyses have facilitated the discovery of a novel major class of stable transcripts, now called long non-coding RNAs (lncRNAs). A growing number of analyses have implicated lncRNAs in the regulation of gene expression, dosage compensation and imprinting, and there is increasing evidence suggesting the involvement of lncRNAs in various diseases such as cancer. Despite recent advances, however, the role of the large majority of lncRNAs remains unknown and there is current debate on what fraction of lncRNAs may just represent transcriptional noise. Moreover, despite a growing number of lncRNAs catalogues for diverse model species, we lack a proper understanding of how these molecules evolve across genomes. Evolutionary analyses of protein-coding genes have proved tremendously useful in elucidating functional relationships and in understanding how the processes in which they are involved are shaped during evolution. Similar insights may be expected from a proper evolutionary characterization of lncRNAs, although the lack of proper tools and basic knowledge of underlying evolutionary mechanisms are a sizable challenge. Here, I propose to combine state-of-the-art computational and sequencing techniques in order to elucidate what evolutionary mechanisms are shaping this enigmatic component of eukaryotic genomes.The first goal is to enable large-scale phylogenomic analyses of lncRNAs by developing, for these molecules, methodologies that are now standard in the evolutionary analysis of protein-coding genes. The second goal is to explore, at high levels of resolution, the evolutionary dynamics of lncRNAs across selected eukaryotic groups for which novel genome-wide data will be produced experimentally using recently developed sequencing techniques that enable obtaining genome-wide footprints of RNA secondary structure. Finally, this dataset will be used to test the impact on lncRNAs evolution of processes known to be important in protein-coding genes.'

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MECHANOSENSATION (2008)

"What is the molecular mechanism of mechanosensation? Mechanosensitive channel of large conductance, MscL, as a model"

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ARISYS (2013)

Engineering an artificial immune system with functional components assembled from prokaryotic parts and modules

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NIPD (2013)

A Novel Non-Invasive Prenatal Diagnosis for Genetic Disorders

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