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Grant: Operating Grant

Université Laval

$627,299.00

Function of the FMR1 gene product in protein synthesis

FY 2008-09

Summary
The Fragile X syndrome, one of the most frequent genetic disease, is the most common form of inherited mental retardation. It affects 1 person out of 5000 in the population all over the world. The syndrome results from the absence of the Fragile X mental Retardation Protein (FMRP). This protein is normally involved in the transport and metabolism of messenger RNA that are required for the synthesis of specific proteins necessary for normal neuron circuitry and development. We are currently using normal as well as defective cells in culture to understand the missing functions that leads to mental retardation. We are also studying how FMRP interacts with its RNA targets in order to understand its functions. These studies will provide critical data to better understand the pathology of mental retardation and possibly to device strategies for therapeutic interventions in the future.
Program
Operating Grant
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
179044
Name
Khandjian Edward W
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Genetics
Projecttitle
Function of the FMR1 gene product in protein synthesis
Programtype2
Operating Grants
Orgnameinp2
Université Laval
Cihramount2
$627,299
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Fragile X Syndrome; Gene Regulation; Mental Retardation; Mribonucleoparticle; Neurons-Cultures; Rna-Binding Protein
Abstract
The Fragile X syndrome, one of the most frequent genetic disease, is the most common form of inherited mental retardation. It affects 1 person out of 5000 in the population all over the world. The syndrome results from the absence of the Fragile X mental Retardation Protein (FMRP). This protein is normally involved in the transport and metabolism of messenger RNA that are required for the synthesis of specific proteins necessary for normal neuron circuitry and development. We are currently using normal as well as defective cells in culture to understand the missing functions that leads to mental retardation. We are also studying how FMRP interacts with its RNA targets in order to understand its functions. These studies will provide critical data to better understand the pathology of mental retardation and possibly to device strategies for therapeutic interventions in the future.
Competitiondate
200903
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Khandjian, Edward W
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $627,299~ $0~