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Grant: Operating Grant

McGill University

$913,670.00

Novel pharmacogenetic strategies to reverse autism-like phenotypes in mouse models of ASD.

EF 2013-14

Résumé
Dysregulated translational control leads to pathological conditions like cancer, obesity, memory impairment and has been hypothesized to cause Autism Spectrum Disorders (ASD); namely through hyperconnectivity of neuronal circuits. Synaptic connections are regulated by translation, thus impaired translational control is postulated to cause ASD. We will study the role of regulation of protein synthesis in the development of autism-like behaviors and in the maintenance of the transmission of information in neurons of mouse models of ASD. To this end we will develop advanced mouse models of proteins that are cardinal in the regulation of protein synthesis and take advantage of compounds designed to modulate protein synthesis. The data from this project can assist in the design of novel therapeutic strategies to modulate ASD-associated behaviors.
Programme
Operating Grant
Bénéficiaire
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
306334
Name
Sonenberg Nahum
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Cell Biology & Mechanisms of Disease
Projecttitle
Novel pharmacogenetic strategies to reverse autism-like phenotypes in mouse models of ASD.
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$913,670
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Animal Models; Autism; Tissue Specific Knockout Mice; Translational Control
Abstract
Dysregulated translational control leads to pathological conditions like cancer, obesity, memory impairment and has been hypothesized to cause Autism Spectrum Disorders (ASD); namely through hyperconnectivity of neuronal circuits. Synaptic connections are regulated by translation, thus impaired translational control is postulated to cause ASD. We will study the role of regulation of protein synthesis in the development of autism-like behaviors and in the maintenance of the transmission of information in neurons of mouse models of ASD. To this end we will develop advanced mouse models of proteins that are cardinal in the regulation of protein synthesis and take advantage of compounds designed to modulate protein synthesis. The data from this project can assist in the design of novel therapeutic strategies to modulate ASD-associated behaviors.
Competitiondate
201403
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Sonenberg, Nahum
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $913,670~ $0~