Grant: Operating Grant
McGill University
$808,327.00
Role of translational mechanisms in the retrograde regulation of Synaptic homeostasis
FY 2011-12
Summary
It has been recognized for some time that the stability of neuronal activity in the nervous system hinges on a coordinated action of different molecular mechanisms that respond to changes in synaptic activity. We provide evidence that de novo protein synthesis in response to changes in synaptic activity leads to generation of a signal that feeds back to the nerve terminals to regulate the level of neurotransmitter release. We propose to use the powerful genetic tools available in Drosophila to unravel the molecular mechanisms that participate in the regulation of this process. Our preliminary findings suggests that genes that have been associated with human disease, namely Parkinson's disease, may play an important role in this process. Therefore, our findings may provide important steps towards our understanding of how neuronal activity is regulated and how it could be affected during disease.
Department
Program
Operating Grant
Recipient
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
255880
Name
Haghighi Ali Pejmun
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Molecular & Cellular Neurosciences - B
Projecttitle
Role of translational mechanisms in the retrograde regulation of Synaptic homeostasis
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$808,327
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Cap-Dependent Translation; Electrophysiology; Genetics; Retrograde Signaling; Synaptic Homeostasis; Synaptic Signaling; Target Of Rapamycin; Translation
Abstract
It has been recognized for some time that the stability of neuronal activity in the nervous system hinges on a coordinated action of different molecular mechanisms that respond to changes in synaptic activity. We provide evidence that de novo protein synthesis in response to changes in synaptic activity leads to generation of a signal that feeds back to the nerve terminals to regulate the level of neurotransmitter release. We propose to use the powerful genetic tools available in Drosophila to unravel the molecular mechanisms that participate in the regulation of this process. Our preliminary findings suggests that genes that have been associated with human disease, namely Parkinson's disease, may play an important role in this process. Therefore, our findings may provide important steps towards our understanding of how neuronal activity is regulated and how it could be affected during disease.
Competitiondate
201203
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Haghighi, Ali Pejmun
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $808,327~ $0~