EYE MICRORNAS

Study of the functional role of microRNAs in the eye

Coordinatore	FONDAZIONE TELETHON    more  Organization address address: VIA VARESE 16/B city: ROMA postcode: 185 contact info Titolo: Ms. Nome: Irene Cognome: Mearelli Email: send email Telefono: -44015275 Fax: -44119191
Nazionalità Coordinatore	Italy [IT]
Totale costo	45˙000 €
EC contributo	45˙000 €
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-ERG-2008
Funding Scheme	MC-ERG
Anno di inizio	2008
Periodo (anno-mese-giorno)	2008-10-01   -   2012-02-29

 Partecipanti

#	participant	country	role	EC contrib. [€]
1	FONDAZIONE TELETHON  Organization address address: VIA VARESE 16/B city: ROMA postcode: 185 contact info Titolo: Ms. Nome: Irene Cognome: Mearelli Email: send email Telefono: -44015275 Fax: -44119191	IT (ROMA)	coordinator	45˙000.00

Mappa

 Word cloud

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

 Obiettivo del progetto (Objective)

'The eye is a highly specialized organ whose development and function requires a precise coordination and timing of morphogenetic and cell differentiation events. However, in spite of the recent significant advances in the field, also facilitated by the human and the mouse genomic sequencing efforts, the transcriptional control of this complex network of events is still poorly understood. This project aims at gaining further insights into the control of gene expression in eye tissue and cell types, by identifying novel microRNA-mediated mechanisms that may greatly contribute to this complex function. microRNAs are 21-25 nucleotide small RNAs that negatively regulate gene expression. Although several microRNAs are reported to be expressed in ocular tissues, their role in the eye transcriptome is completely unknown. In this project, we aim at the identification, detailed characterization and functional analysis of microRNAs expressed in the non-retinal parts of the eye, such as lens, cornea and ciliary body. In particular, we will select and characterize microRNAs with a presumptive role in eye development and function, by first carrying out detailed expression analysis in mouse by RNA in situ hybridization to establish their spatiotemporal localization. The selected eye-expressed miRNAs will be further evaluated to identify, by bioinformatics approaches, followed by in vitro experimental validation procedures, their putative target genes. Finally, these miRNAs will be analyzed from a functional point of view, by means of overexpression and loss-of-function studies, both using in vitro (cell cultures) and in vivo (medaka) systems. We believe that this effort should lead to a better understanding of the mechanisms controlling gene expression in the eye and may also contribute to the identification of novel pathogenetic mechanisms for eye pathological conditions.'